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class="organization-publication-list__group" aria-label="2024 publications"><h2 class="organization-publication-list__group-title">2024</h2><ul class="organization-publication-list__group-list"><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/38924775" class="research-list-item__link"><span>Single-Cell Analysis Reveals Novel Immune Perturbations in Fibrotic Hypersensitivity Pneumonitis.</span></a><span class="research-list-item__text">Zhao A, Unterman A, Abu Hussein N, Sharma P, Nikola F, Flint J, Yan X, Adams T, Justet A, Sumida T, Zhao J, Schupp J, Raredon M, Ahangari F, Deluliis G, Zhang Y, Buendia-Roldan I, Adegunsoye A, Sperling A, Prasse A, Ryu C, Herzog E, Selman M, Pardo A, <strong>Kaminski N</strong>. Single-Cell Analysis Reveals Novel Immune Perturbations in Fibrotic Hypersensitivity Pneumonitis. American Journal Of Respiratory And Critical Care Medicine 2024, 210: 1252-1266. <a href="https://pubmed.ncbi.nlm.nih.gov/38924775" target="_blank">PMID: 38924775</a>, <a href="https://doi.org/10.1164/rccm.202401-0078oc" target="_blank">DOI: 10.1164/rccm.202401-0078oc</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39522891" class="research-list-item__link"><span>GPR68 supports AML cells through the calcium/calcineurin pro-survival pathway and confers chemoresistance by mediating glucose metabolic symbiosis</span></a><span class="research-list-item__text">He X, Hawkins C, Lawley L, Phan T, Park I, Joven N, Zhang J, Wunderlich M, Mizukawa B, Pei S, Patel A, VanOudenhove J, <strong>Halene S</strong>, Fang J. GPR68 supports AML cells through the calcium/calcineurin pro-survival pathway and confers chemoresistance by mediating glucose metabolic symbiosis. Biochimica Et Biophysica Acta (BBA) - Molecular Basis Of Disease 2024, 167565. <a href="https://pubmed.ncbi.nlm.nih.gov/39522891" target="_blank">PMID: 39522891</a>, <a href="https://doi.org/10.1016/j.bbadis.2024.167565" target="_blank">DOI: 10.1016/j.bbadis.2024.167565</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39514636" class="research-list-item__link"><span>A B cell screen against endogenous retroviruses identifies glycan-reactive IgM that recognizes a broad array of enveloped viruses</span></a><span class="research-list-item__text">Yang Y, Treger R, Hernandez-Bird J, Lu P, Mao T, <strong>Iwasaki A</strong>. A B cell screen against endogenous retroviruses identifies glycan-reactive IgM that recognizes a broad array of enveloped viruses. Science Immunology 2024, 9: eadd6608. <a href="https://pubmed.ncbi.nlm.nih.gov/39514636" target="_blank">PMID: 39514636</a>, <a href="https://doi.org/10.1126/sciimmunol.add6608" target="_blank">DOI: 10.1126/sciimmunol.add6608</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39504356" class="research-list-item__link"><span>Integrative multiomic analysis identifies distinct molecular subtypes of NAFLD in a Chinese population</span></a><span class="research-list-item__text">Ding J, Liu H, Zhang X, Zhao N, Peng Y, Shi J, Chen J, Chi X, Li L, Zhang M, Liu W, Zhang L, Ouyang J, Yuan Q, Liao M, Tan Y, Li M, Xu Z, Tang W, Xie C, Li Y, Pan Q, Xu Y, Cai S, Byrne C, Targher G, <strong>Ouyang X</strong>, Zhang L, Jiang Z, Zheng M, Sun F, Chai J. Integrative multiomic analysis identifies distinct molecular subtypes of NAFLD in a Chinese population. 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Experimental Hematology 2024, 140: 104655. <a href="https://pubmed.ncbi.nlm.nih.gov/39393608" target="_blank">PMID: 39393608</a>, <a href="https://doi.org/10.1016/j.exphem.2024.104655" target="_blank">DOI: 10.1016/j.exphem.2024.104655</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39388546" class="research-list-item__link"><span>Somatic mosaicism in schizophrenia brains reveals prenatal mutational processes</span></a><span class="research-list-item__text">Maury E, Jones A, Seplyarskiy V, Nguyen T, Rosenbluh C, Bae T, Wang Y, Abyzov A, Khoshkhoo S, Chahine Y, Zhao S, Venkatesh S, Root E, Voloudakis G, Roussos P, Network B, Park P, Akbarian S, <strong>Brennand K</strong>, <strong>Reilly S</strong>, Lee E, Sunyaev S, Walsh C, Chess A. 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Science 2024, 386: 217-224. <a href="https://pubmed.ncbi.nlm.nih.gov/39388546" target="_blank">PMID: 39388546</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11490355" target="_blank">PMCID: PMC11490355</a>, <a href="https://doi.org/10.1126/science.adq1456" target="_blank">DOI: 10.1126/science.adq1456</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39384951" class="research-list-item__link"><span>Steering research on mRNA splicing in cancer towards clinical translation</span></a><span class="research-list-item__text">Anczukow O, Allain F, Angarola B, Black D, Brooks A, Cheng C, Conesa A, Crosse E, Eyras E, Guccione E, Lu S, <strong>Neugebauer K</strong>, Sehgal P, Song X, Tothova Z, Valcárcel J, Weeks K, Yeo G, Thomas-Tikhonenko A. 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Nature Reviews Cancer 2024, 1-19. <a href="https://pubmed.ncbi.nlm.nih.gov/39384951" target="_blank">PMID: 39384951</a>, <a href="https://doi.org/10.1038/s41568-024-00750-2" target="_blank">DOI: 10.1038/s41568-024-00750-2</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39382073" class="research-list-item__link"><span>Tumor-specific antigen delivery for T-cell therapy via a pH-sensitive peptide conjugate.</span></a><span class="research-list-item__text">Yurkevicz A, Liu Y, Katz S, <strong>Glazer P</strong>. 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Molecular Cancer Therapeutics 2024, of1-of13. <a href="https://pubmed.ncbi.nlm.nih.gov/39382073" target="_blank">PMID: 39382073</a>, <a href="https://doi.org/10.1158/1535-7163.mct-23-0809" target="_blank">DOI: 10.1158/1535-7163.mct-23-0809</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39378873" class="research-list-item__link"><span>Early Release - Dengue Outbreak Caused by Multiple Virus Serotypes and Lineages, Colombia, 2023–2024 - Volume 30, Number 11—November 2024 - Emerging Infectious Diseases journal - CDC</span></a><span class="research-list-item__text"><strong>Grubaugh N</strong>, Torres-Hernández D, Murillo-Ortiz M, Dávalos D, Lopez P, Hurtado I, Breban M, Bourgikos E, Hill V, López-Medina E. 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Emerging Infectious Diseases 2024, 30: 2391-2395. <a href="https://pubmed.ncbi.nlm.nih.gov/39378873" target="_blank">PMID: 39378873</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11521178" target="_blank">PMCID: PMC11521178</a>, <a href="https://doi.org/10.3201/eid3011.241031" target="_blank">DOI: 10.3201/eid3011.241031</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://doi.org/10.1007/978-3-031-72111-3_15" class="research-list-item__link"><span>CUTS: A Deep Learning and Topological Framework for Multigranular Unsupervised Medical Image Segmentation</span></a><span class="research-list-item__text">Liu C, Amodio M, Shen L, Gao F, Avesta A, Aneja S, Wang J, Del Priore L, <strong>Krishnaswamy S</strong>. 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CCR2+ monocytes are dispensable to resolve acute pulmonary Pseudomonas aeruginosa infections in WT and Cystic Fibrosis mice. Journal Of Leukocyte Biology 2024, qiae218. <a href="https://pubmed.ncbi.nlm.nih.gov/39365279" target="_blank">PMID: 39365279</a>, <a href="https://doi.org/10.1093/jleuko/qiae218" target="_blank">DOI: 10.1093/jleuko/qiae218</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39362854" class="research-list-item__link"><span>Targeting Pseudomonas aeruginosa biofilm with an evolutionary trained bacteriophage cocktail exploiting phage resistance trade-offs</span></a><span class="research-list-item__text">Kunisch F, Campobasso C, Wagemans J, Yildirim S, Chan B, Schaudinn C, Lavigne R, <strong>Turner P</strong>, Raschke M, Trampuz A, Gonzalez Moreno M. Targeting Pseudomonas aeruginosa biofilm with an evolutionary trained bacteriophage cocktail exploiting phage resistance trade-offs. Nature Communications 2024, 15: 8572. <a href="https://pubmed.ncbi.nlm.nih.gov/39362854" target="_blank">PMID: 39362854</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11450229" target="_blank">PMCID: PMC11450229</a>, <a href="https://doi.org/10.1038/s41467-024-52595-w" target="_blank">DOI: 10.1038/s41467-024-52595-w</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39413460" class="research-list-item__link"><span>Keratin 17 and A2ML1 are negative prognostic biomarkers in non-small cell lung cancer</span></a><span class="research-list-item__text">Babu S, Horowitz M, Delgado-Coka L, Roa-Peña L, Akalin A, <strong>Escobar-Hoyos L</strong>, Shroyer K. 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Pathology - Research And Practice 2024, 263: 155643. <a href="https://pubmed.ncbi.nlm.nih.gov/39413460" target="_blank">PMID: 39413460</a>, <a href="https://doi.org/10.1016/j.prp.2024.155643" target="_blank">DOI: 10.1016/j.prp.2024.155643</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://doi.org/10.1016/j.chest.2024.06.2020" class="research-list-item__link"><span>INTERACTIONS BETWEEN MITOCHONDRIAL DNA AND TOLL-LIKE RECEPTOR 9 MEDIATES PULMONARY FIBROSIS</span></a><span class="research-list-item__text">LEE C, TRUJILLO G, REGUEIRO-REN A, LIU C, HU B, SUN Y, KHOURY J, KHOURY J, AHANGARI F, ISHIKAWA G, WALIA A, PIVARNIK T, YU S, WOO S, FIORINI V, MCGOVERN J, AL JUMAILY K, SUN H, PENG X, ANTIN-OZERKIS D, SAULER M, <strong>KAMINSKI N</strong>, HERZOG E. INTERACTIONS BETWEEN MITOCHONDRIAL DNA AND TOLL-LIKE RECEPTOR 9 MEDIATES PULMONARY FIBROSIS. CHEST Journal 2024, 166: a3384-a3386. <a href="https://doi.org/10.1016/j.chest.2024.06.2020" target="_blank">DOI: 10.1016/j.chest.2024.06.2020</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39352803" class="research-list-item__link"><span>Next-generation cell-penetrating antibodies for tumor targeting and RAD51 inhibition</span></a><span class="research-list-item__text">Rackear M, Quijano E, Ianniello Z, Colón-Ríos D, Krysztofiak A, Abdullah R, Liu Y, Rogers F, Ludwig D, Dwivedi R, Bleichert F, <strong>Glazer P</strong>. 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Molecular Cell 2024, 84: 3967-3978.e8. <a href="https://pubmed.ncbi.nlm.nih.gov/39317199" target="_blank">PMID: 39317199</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11490368" target="_blank">PMCID: PMC11490368</a>, <a href="https://doi.org/10.1016/j.molcel.2024.08.032" target="_blank">DOI: 10.1016/j.molcel.2024.08.032</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39322118" class="research-list-item__link"><span>Contemporary Approach to the Diagnosis and Classification of Myelodysplastic Neoplasms/Syndromes—Recommendations From the International Consortium for Myelodysplastic Neoplasms/Syndromes (MDS [icMDS])</span></a><span class="research-list-item__text">Aakash F, Gisriel S, Zeidan A, Bennett J, Bejar R, Bewersdorf J, Borate U, Boultwood J, Brunner A, Buckstein R, Carraway H, Churpek J, Daver N, DeZern A, Efficace F, Fenaux P, Figueroa M, Garcia-Manero G, Gore S, Greenberg P, Griffiths E, <strong>Halene S</strong>, Hourigan C, Kim T, Kim N, Komrokji R, Kutchroo V, List A, Little R, Majeti R, Nazha A, Nimer S, Odenike O, Padron E, Patnaik M, Platzbecker U, Della Porta M, Roboz G, Sallman D, Santini V, Sanz G, Savona M, Sekeres M, Stahl M, Starczynowski D, Steensma D, Taylor J, Abdel-Wahab O, Wei A, Xie Z, Xu M, Hasserjian R, Loghavi S. Contemporary Approach to the Diagnosis and Classification of Myelodysplastic Neoplasms/Syndromes—Recommendations From the International Consortium for Myelodysplastic Neoplasms/Syndromes (MDS [icMDS]). Modern Pathology 2024, 37: 100615. <a href="https://pubmed.ncbi.nlm.nih.gov/39322118" target="_blank">PMID: 39322118</a>, <a href="https://doi.org/10.1016/j.modpat.2024.100615" target="_blank">DOI: 10.1016/j.modpat.2024.100615</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39302113" class="research-list-item__link"><span>IL-1β Induces Human Endothelial Surface Expression of IL-15 by Relieving let-7c-3p Suppression of Protein Translation.</span></a><span class="research-list-item__text">Mullan C, Summer L, Lopez-Giraldez F, Tobiasova Z, Manes T, Yasothan S, Song G, Jane-Wit D, <strong>Saltzman W</strong>, Pober J. IL-1β Induces Human Endothelial Surface Expression of IL-15 by Relieving let-7c-3p Suppression of Protein Translation. The Journal Of Immunology 2024, 213: 1338-1348. <a href="https://pubmed.ncbi.nlm.nih.gov/39302113" target="_blank">PMID: 39302113</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11493510" target="_blank">PMCID: PMC11493510</a>, <a href="https://doi.org/10.4049/jimmunol.2400331" target="_blank">DOI: 10.4049/jimmunol.2400331</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39372273" class="research-list-item__link"><span>Diagnostic values of BALF metagenomic next-generation sequencing, BALF real-time PCR and serum BDG for Pneumocystis jirovecii pneumonia in HIV-infected patients</span></a><span class="research-list-item__text">Chen Q, Chen X, Mo P, Chen L, Du Q, Hu W, Jiang Q, Zhang Z, Zhang Y, Guo Q, <strong>Xiong Y</strong>, Deng L. Diagnostic values of BALF metagenomic next-generation sequencing, BALF real-time PCR and serum BDG for Pneumocystis jirovecii pneumonia in HIV-infected patients. Frontiers In Microbiology 2024, 15: 1421660. <a href="https://pubmed.ncbi.nlm.nih.gov/39372273" target="_blank">PMID: 39372273</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11449763" target="_blank">PMCID: PMC11449763</a>, <a href="https://doi.org/10.3389/fmicb.2024.1421660" target="_blank">DOI: 10.3389/fmicb.2024.1421660</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39302833" class="research-list-item__link"><span>A comparative roadmap of PIWI-interacting RNAs across seven species reveals insights into de novo piRNA-precursor formation in mammals</span></a><span class="research-list-item__text">Konstantinidou P, Loubalova Z, Ahrend F, Friman A, Almeida M, Poulet A, Horvat F, Wang Y, Losert W, Lorenzi H, Svoboda P, Miska E, <strong>van Wolfswinkel J</strong>, Haase A. A comparative roadmap of PIWI-interacting RNAs across seven species reveals insights into de novo piRNA-precursor formation in mammals. Cell Reports 2024, 43: 114777. <a href="https://pubmed.ncbi.nlm.nih.gov/39302833" target="_blank">PMID: 39302833</a>, <a href="https://doi.org/10.1016/j.celrep.2024.114777" target="_blank">DOI: 10.1016/j.celrep.2024.114777</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39298321" class="research-list-item__link"><span>Protocol for detecting glycoRNAs using metabolic labeling and northwestern blot</span></a><span class="research-list-item__text">Li L, Zhang N, Pantoja C, Wang Y, <strong>Lu J</strong>. Protocol for detecting glycoRNAs using metabolic labeling and northwestern blot. STAR Protocols 2024, 5: 103321. <a href="https://pubmed.ncbi.nlm.nih.gov/39298321" target="_blank">PMID: 39298321</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11426122" target="_blank">PMCID: PMC11426122</a>, <a href="https://doi.org/10.1016/j.xpro.2024.103321" target="_blank">DOI: 10.1016/j.xpro.2024.103321</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39360312" class="research-list-item__link"><span>Improved methods for genetic manipulation of the alkaliphile Halalkalibacterium halodurans</span></a><span class="research-list-item__text">Wencker F, Lyon S, <strong>Breaker R</strong>. Improved methods for genetic manipulation of the alkaliphile Halalkalibacterium halodurans. Frontiers In Microbiology 2024, 15: 1465811. <a href="https://pubmed.ncbi.nlm.nih.gov/39360312" target="_blank">PMID: 39360312</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11445130" target="_blank">PMCID: PMC11445130</a>, <a href="https://doi.org/10.3389/fmicb.2024.1465811" target="_blank">DOI: 10.3389/fmicb.2024.1465811</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39288189" class="research-list-item__link"><span>Genome-wide association study between SARS-CoV-2 single nucleotide polymorphisms and virus copies during infections</span></a><span class="research-list-item__text">Li K, Chaguza C, Stamp J, Chew Y, Chen N, Ferguson D, Pandya S, Kerantzas N, Schulz W, Initiative Y, Hahn A, Ogbunugafor C, Pitzer V, Crawford L, Weinberger D, <strong>Grubaugh N</strong>. Genome-wide association study between SARS-CoV-2 single nucleotide polymorphisms and virus copies during infections. PLOS Computational Biology 2024, 20: e1012469. <a href="https://pubmed.ncbi.nlm.nih.gov/39288189" target="_blank">PMID: 39288189</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11432881" target="_blank">PMCID: PMC11432881</a>, <a href="https://doi.org/10.1371/journal.pcbi.1012469" target="_blank">DOI: 10.1371/journal.pcbi.1012469</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39283942" class="research-list-item__link"><span>A new lineage nomenclature to aid genomic surveillance of dengue virus</span></a><span class="research-list-item__text">Hill V, Cleemput S, Pereira J, Gifford R, Fonseca V, Tegally H, Brito A, Ribeiro G, de Souza V, Brcko I, Ribeiro I, De Lima I, Slavov S, Sampaio S, Elias M, Tran V, Kien D, Huynh T, Yacoub S, Dieng I, Salvato R, Wallau G, Gregianini T, Godinho F, Vogels C, Breban M, Leguia M, Jagtap S, Roy R, Hapuarachchi C, Mwanyika G, Giovanetti M, Alcantara L, Faria N, Carrington C, Hanley K, Holmes E, Dumon W, Lima A, de Oliveira T, <strong>Grubaugh N</strong>. A new lineage nomenclature to aid genomic surveillance of dengue virus. PLOS Biology 2024, 22: e3002834. <a href="https://pubmed.ncbi.nlm.nih.gov/39283942" target="_blank">PMID: 39283942</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11426435" target="_blank">PMCID: PMC11426435</a>, <a href="https://doi.org/10.1371/journal.pbio.3002834" target="_blank">DOI: 10.1371/journal.pbio.3002834</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://doi.org/10.1158/1538-7445.pancreatic24-pr-05" class="research-list-item__link"><span>Abstract PR-05: Endocrine beta-cell stress promotes pancreatic ductal adenocarcinoma through endocrine-exocrine cell crosstalk</span></a><span class="research-list-item__text">Garcia C, Venkat A, McQuaid D, Agabiti S, Tong A, Cardone R, Kibbey R, <strong>Krishnaswamy S</strong>, Muzumdar M. Abstract PR-05: Endocrine beta-cell stress promotes pancreatic ductal adenocarcinoma through endocrine-exocrine cell crosstalk. Cancer Research 2024, 84: pr-05-pr-05. <a href="https://doi.org/10.1158/1538-7445.pancreatic24-pr-05" target="_blank">DOI: 10.1158/1538-7445.pancreatic24-pr-05</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://doi.org/10.1158/1538-7445.pancreatic24-pr-01" class="research-list-item__link"><span>Abstract PR-01: Systemic targeting of therapeutic RNA to pancreatic ductal adenocarcinoma via a novel, cell-penetrating, and nucleic acid-binding monoclonal antibody</span></a><span class="research-list-item__text">Martinez-Saucedo D, Quijano E, Ianniello Z, Rackear M, Liu Y, Hegan D, Chen H, Shan X, Tseng R, Yugawa D, Pinto-Medici N, Chowdhury S, Bindra R, Robert M, <strong>Saltzman W</strong>, <strong>Escobar-Hoyos L</strong>, <strong>Glazer P</strong>. Abstract PR-01: Systemic targeting of therapeutic RNA to pancreatic ductal adenocarcinoma via a novel, cell-penetrating, and nucleic acid-binding monoclonal antibody. Cancer Research 2024, 84: pr-01-pr-01. <a href="https://doi.org/10.1158/1538-7445.pancreatic24-pr-01" target="_blank">DOI: 10.1158/1538-7445.pancreatic24-pr-01</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://doi.org/10.1158/1538-7445.pancreatic24-c030" class="research-list-item__link"><span>Abstract C030: Evolutionary and epistatic analyses reveal genic interactions with KRAS during malignant progression of pancreatic ductal adenocarcinoma</span></a><span class="research-list-item__text">Fisk N, Song D, Moore M, Jensen C, Cannataro V, Nagib M, Mandell J, <strong>Escobar-Hoyos L</strong>, Kunstman J, Townsend J. Abstract C030: Evolutionary and epistatic analyses reveal genic interactions with KRAS during malignant progression of pancreatic ductal adenocarcinoma. Cancer Research 2024, 84: c030-c030. <a href="https://doi.org/10.1158/1538-7445.pancreatic24-c030" target="_blank">DOI: 10.1158/1538-7445.pancreatic24-c030</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://doi.org/10.1158/1538-7445.pancreatic24-pr-11" class="research-list-item__link"><span>Abstract PR-11: Altered mRNA splicing mimics chromosome loss and drives pancreatic cancer</span></a><span class="research-list-item__text">Medici N, Martinez-Saucedo D, Lee D, Chu T, Tseng R, Cannataro V, Townsend J, Iacobuzio-Donahue C, Robert M, Abdel-Wahab O, Leach S, <strong>Escobar-Hoyos L</strong>. Abstract PR-11: Altered mRNA splicing mimics chromosome loss and drives pancreatic cancer. Cancer Research 2024, 84: pr-11-pr-11. <a href="https://doi.org/10.1158/1538-7445.pancreatic24-pr-11" target="_blank">DOI: 10.1158/1538-7445.pancreatic24-pr-11</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://doi.org/10.1158/1538-7445.pancreatic24-b083" class="research-list-item__link"><span>Abstract B083: The splicing factor SMNDC1 facilitates alternative RNA splicing, contributing to therapy resistance in pancreatic cancer</span></a><span class="research-list-item__text">Siraj M, Zhang Y, Yugawa D, Giri G, Chakraborty P, Goda G, Rao G, Dominguez D, Kubicek S, Bhattacharya R, <strong>Escobar-Hoyos L</strong>, Mukherjee P. Abstract B083: The splicing factor SMNDC1 facilitates alternative RNA splicing, contributing to therapy resistance in pancreatic cancer. Cancer Research 2024, 84: b00-b00. <a href="https://doi.org/10.1158/1538-7445.pancreatic24-b083" target="_blank">DOI: 10.1158/1538-7445.pancreatic24-b083</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://doi.org/10.1158/1538-7445.pancreatic24-b079" class="research-list-item__link"><span>Abstract B079: Disassembly of embryonic keratin filaments promotes pancreatic cancer metastases</span></a><span class="research-list-item__text">Yugawa D, Kawalerski R, Gonçalves M, Pan C, Tseng R, Roa-Pena L, Leiton C, Torre-Healy L, Boyle T, Chowdhury S, Snider N, Shroyer K, <strong>Escobar-Hoyos L</strong>. Abstract B079: Disassembly of embryonic keratin filaments promotes pancreatic cancer metastases. Cancer Research 2024, 84: b079-b079. <a href="https://doi.org/10.1158/1538-7445.pancreatic24-b079" target="_blank">DOI: 10.1158/1538-7445.pancreatic24-b079</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://doi.org/10.1158/1538-7445.pancreatic24-c031" class="research-list-item__link"><span>Abstract C031: Keratin 17 promotes pancreatic cancer chemoresistance through mitochondrial translocation and stabilization of dihydroorotate dehydrogenase (DHODH)</span></a><span class="research-list-item__text">Lyu Y, Ghosh M, Pan C, Sarkar S, Rajacharya G, Chen B, Marchenko N, Singh P, Shroyer K, <strong>Escobar-Hoyos L</strong>. Abstract C031: Keratin 17 promotes pancreatic cancer chemoresistance through mitochondrial translocation and stabilization of dihydroorotate dehydrogenase (DHODH). Cancer Research 2024, 84: c031-c031. <a href="https://doi.org/10.1158/1538-7445.pancreatic24-c031" target="_blank">DOI: 10.1158/1538-7445.pancreatic24-c031</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://doi.org/10.1158/1538-7445.pancreatic24-c070" class="research-list-item__link"><span>Abstract C070: Keratin 17 and GATA6 correlate with diffusely infiltrative versus gland-forming components of PDAC: Uncovering the transitional state in pancreatic ductal adenocarcinoma</span></a><span class="research-list-item__text">Delgado- Coka L, Nelson B, Horowitz M, Sarkar S, Marchenko N, Powers S, <strong>Escobar-Hoyos L</strong>, Shroyer K. Abstract C070: Keratin 17 and GATA6 correlate with diffusely infiltrative versus gland-forming components of PDAC: Uncovering the transitional state in pancreatic ductal adenocarcinoma. Cancer Research 2024, 84: c070-c070. <a href="https://doi.org/10.1158/1538-7445.pancreatic24-c070" target="_blank">DOI: 10.1158/1538-7445.pancreatic24-c070</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://doi.org/10.1183/13993003.congress-2024.oa953" class="research-list-item__link"><span>Dissecting the immune cell niche in pulmonary sarcoidosis – CXCL10+ monocyte-derived macrophages are potential drivers of TH17.1 inflammation</span></a><span class="research-list-item__text">Ruwisch J, Schupp J, Bartkute B, Artysh N, <strong>Kaminski N</strong>, Prasse A. Dissecting the immune cell niche in pulmonary sarcoidosis – CXCL10+ monocyte-derived macrophages are potential drivers of TH17.1 inflammation. 2024, oa953. <a href="https://doi.org/10.1183/13993003.congress-2024.oa953" target="_blank">DOI: 10.1183/13993003.congress-2024.oa953</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://doi.org/10.1183/13993003.congress-2024.oa985" class="research-list-item__link"><span>Single-nuclei RNA-seq reveals aberrant cell populations in restrictive allograft syndrome after lung transplantation</span></a><span class="research-list-item__text">Leiber L, Christian L, Neubert L, Yilmaz H, Kamp J, Plucinski E, Welte T, Falk C, <strong>Kaminski N</strong>, Jonigk* D, Gottlieb* J, Schupp* J. Single-nuclei RNA-seq reveals aberrant cell populations in restrictive allograft syndrome after lung transplantation. 2024, oa985. <a href="https://doi.org/10.1183/13993003.congress-2024.oa985" target="_blank">DOI: 10.1183/13993003.congress-2024.oa985</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39261628" class="research-list-item__link"><span>Organization of a functional glycolytic metabolon on mitochondria for metabolic efficiency</span></a><span class="research-list-item__text">Wang H, Vant J, Zhang A, Sanchez R, Wu Y, Micou M, Luczak V, Whiddon Z, Carlson N, Yu S, Jabbo M, Yoon S, Abushawish A, Ghassemian M, Masubuchi T, Gan Q, Watanabe S, Griffis E, <strong>Hammarlund M</strong>, Singharoy A, Pekkurnaz G. Organization of a functional glycolytic metabolon on mitochondria for metabolic efficiency. Nature Metabolism 2024, 6: 1712-1735. <a href="https://pubmed.ncbi.nlm.nih.gov/39261628" target="_blank">PMID: 39261628</a>, <a href="https://doi.org/10.1038/s42255-024-01121-9" target="_blank">DOI: 10.1038/s42255-024-01121-9</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39258548" class="research-list-item__link"><span>HIV-1 usurps mixed-charge domain-dependent CPSF6 phase separation for higher-order capsid binding, nuclear entry and viral DNA integration</span></a><span class="research-list-item__text">Jang S, Bedwell G, Singh S, Yu H, Arnarson B, Singh P, Radhakrishnan R, Douglas A, Ingram Z, Freniere C, Akkermans O, Sarafianos S, Ambrose Z, <strong>Xiong Y</strong>, Anekal P, Llopis P, KewalRamani V, Francis A, Engelman A. HIV-1 usurps mixed-charge domain-dependent CPSF6 phase separation for higher-order capsid binding, nuclear entry and viral DNA integration. Nucleic Acids Research 2024, 52: 11060-11082. <a href="https://pubmed.ncbi.nlm.nih.gov/39258548" target="_blank">PMID: 39258548</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11472059" target="_blank">PMCID: PMC11472059</a>, <a href="https://doi.org/10.1093/nar/gkae769" target="_blank">DOI: 10.1093/nar/gkae769</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39241085" class="research-list-item__link"><span>RluA is the major mRNA pseudouridine synthase in Escherichia coli</span></a><span class="research-list-item__text">Schaening-Burgos C, LeBlanc H, Fagre C, Li G, <strong>Gilbert W</strong>. RluA is the major mRNA pseudouridine synthase in Escherichia coli. PLOS Genetics 2024, 20: e1011100. <a href="https://pubmed.ncbi.nlm.nih.gov/39241085" target="_blank">PMID: 39241085</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11421799" target="_blank">PMCID: PMC11421799</a>, <a href="https://doi.org/10.1371/journal.pgen.1011100" target="_blank">DOI: 10.1371/journal.pgen.1011100</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39232138" class="research-list-item__link"><span>Endothelial γ-protocadherins inhibit KLF2 and KLF4 to promote atherosclerosis</span></a><span class="research-list-item__text">Joshi D, Coon B, Chakraborty R, Deng H, Yang Z, Babar M, Fernandez-Tussy P, Meredith E, Attanasio J, Joshi N, Traylor J, Orr A, <strong>Fernandez-Hernando C</strong>, Libreros S, Schwartz M. Endothelial γ-protocadherins inhibit KLF2 and KLF4 to promote atherosclerosis. Nature Cardiovascular Research 2024, 3: 1035-1048. <a href="https://pubmed.ncbi.nlm.nih.gov/39232138" target="_blank">PMID: 39232138</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11399086" target="_blank">PMCID: PMC11399086</a>, <a href="https://doi.org/10.1038/s44161-024-00522-z" target="_blank">DOI: 10.1038/s44161-024-00522-z</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39230381" class="research-list-item__link"><span>Beyond the “spine of hydration”: Chiral SFG spectroscopy detects DNA first hydration shell and base pair structures</span></a><span class="research-list-item__text">Perets E, Konstantinovsky D, Santiago T, Videla P, Tremblay M, Velarde L, Batista V, Hammes-Schiffer S, <strong>Yan E</strong>. Beyond the “spine of hydration”: Chiral SFG spectroscopy detects DNA first hydration shell and base pair structures. The Journal Of Chemical Physics 2024, 161: 095104. <a href="https://pubmed.ncbi.nlm.nih.gov/39230381" target="_blank">PMID: 39230381</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11377083" target="_blank">PMCID: PMC11377083</a>, <a href="https://doi.org/10.1063/5.0220479" target="_blank">DOI: 10.1063/5.0220479</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39225418" class="research-list-item__link"><span>Aplastic anemia in association with multiple myeloma: clinical and pathophysiological insights</span></a><span class="research-list-item__text">Muradashvili T, Liu Y, VanOudenhove J, Gu S, <strong>Krause D</strong>, Montanari F, Carlino M, Mancuso R, Stempel J, <strong>Halene S</strong>, Zeidan A, Podoltsev N, Neparidze N. Aplastic anemia in association with multiple myeloma: clinical and pathophysiological insights. Leukemia & Lymphoma 2024, ahead-of-print: 1-8. <a href="https://pubmed.ncbi.nlm.nih.gov/39225418" target="_blank">PMID: 39225418</a>, <a href="https://doi.org/10.1080/10428194.2024.2393260" target="_blank">DOI: 10.1080/10428194.2024.2393260</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39101673" class="research-list-item__link"><span>Akt is a mediator of artery specification during zebrafish development</span></a><span class="research-list-item__text">Zhou W, Ghersi J, Ristori E, Semanchik N, Prendergast A, Zhang R, Carneiro P, Baldissera G, <strong>Sessa W</strong>, <strong>Nicoli S</strong>. Akt is a mediator of artery specification during zebrafish development. Development 2024, 151: dev202727. <a href="https://pubmed.ncbi.nlm.nih.gov/39101673" target="_blank">PMID: 39101673</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11441982" target="_blank">PMCID: PMC11441982</a>, <a href="https://doi.org/10.1242/dev.202727" target="_blank">DOI: 10.1242/dev.202727</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39230702" class="research-list-item__link"><span>Predicting spatially resolved gene expression via tissue morphology using adaptive spatial GNNs</span></a><span class="research-list-item__text">Song T, Cosatto E, Wang G, Kuang R, <strong>Gerstein M</strong>, Min M, Warrell J. Predicting spatially resolved gene expression via tissue morphology using adaptive spatial GNNs. Bioinformatics 2024, 40: ii111-ii119. <a href="https://pubmed.ncbi.nlm.nih.gov/39230702" target="_blank">PMID: 39230702</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11373608" target="_blank">PMCID: PMC11373608</a>, <a href="https://doi.org/10.1093/bioinformatics/btae383" target="_blank">DOI: 10.1093/bioinformatics/btae383</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://doi.org/10.1016/s1569-1993(24)01125-1" class="research-list-item__link"><span>285 Development of an electrochemiluminescence CFTR immunoassay</span></a><span class="research-list-item__text">Browne J, Lee J, Peterec K, Garrison A, Bruscia E, <strong>Saltzman W</strong>, Egan M. 285 Development of an electrochemiluminescence CFTR immunoassay. Journal Of Cystic Fibrosis 2024, 23: s152. <a href="https://doi.org/10.1016/s1569-1993(24)01125-1" target="_blank">DOI: 10.1016/s1569-1993(24)01125-1</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://doi.org/10.1016/s1569-1993(24)01235-9" class="research-list-item__link"><span>395 Altered hematopoiesis and functional decline of hematopoietic stem cells in cystic fibrosis mice</span></a><span class="research-list-item__text">Braga C, Mancuso R, Thompson E, Oez H, Gudneppannavar R, Zhang P, Huang P, Egan M, Murray T, <strong>Krause D</strong>, Bruscia E. 395 Altered hematopoiesis and functional decline of hematopoietic stem cells in cystic fibrosis mice. Journal Of Cystic Fibrosis 2024, 23: s207-s208. <a href="https://doi.org/10.1016/s1569-1993(24)01235-9" target="_blank">DOI: 10.1016/s1569-1993(24)01235-9</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://doi.org/10.1016/s1569-1993(24)01104-4" class="research-list-item__link"><span>264 Poly(amine-co-ester) nanoparticle delivery of CFTR mRNA shows restoration of CFTR activity in cystic fibrosis airway models</span></a><span class="research-list-item__text">Garrison A, Lee J, Browne J, Akhtar L, Peterec K, Suberi A, Eaton D, Ene M, Zhang X, Whang C, Oez H, Kizilirmak T, Bruscia E, Piotrowski-Daspit A, <strong>Saltzman W</strong>, Egan M. 264 Poly(amine-co-ester) nanoparticle delivery of CFTR mRNA shows restoration of CFTR activity in cystic fibrosis airway models. Journal Of Cystic Fibrosis 2024, 23: s140-s141. <a href="https://doi.org/10.1016/s1569-1993(24)01104-4" target="_blank">DOI: 10.1016/s1569-1993(24)01104-4</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://doi.org/10.1016/s1569-1993(24)01135-4" class="research-list-item__link"><span>295 Polymeric nanoparticles for in utero gene delivery in non-human primates</span></a><span class="research-list-item__text">Piotrowski-Daspit A, Lynn A, Eaton D, Bracaglia L, Mortlock R, Tarantal A, Glazer P, <strong>Saltzman W</strong>. 295 Polymeric nanoparticles for in utero gene delivery in non-human primates. Journal Of Cystic Fibrosis 2024, 23: s157. <a href="https://doi.org/10.1016/s1569-1993(24)01135-4" target="_blank">DOI: 10.1016/s1569-1993(24)01135-4</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://doi.org/10.1016/s2152-2650(24)01991-8" class="research-list-item__link"><span>P-088 Evaluating T-cell Fitness Pre B-Cell Maturation Antigen (BCMA)-Targeted T-Cell Redirection Therapies (TRT) as a Predictive Marker for Efficacy/Toxicity in Relapsed/Refractory Multiple Myeloma (RRMM)</span></a><span class="research-list-item__text">Theprungsirikul P, Yu M, Liu Y, Rall K, Matthews M, Neparidze N, Parker T, Browning S, Anderson T, Stevens E, Foss F, Gowda L, <strong>Pillai M</strong>, Isufi I, Seropian S, Mirza S, Bar N. P-088 Evaluating T-cell Fitness Pre B-Cell Maturation Antigen (BCMA)-Targeted T-Cell Redirection Therapies (TRT) as a Predictive Marker for Efficacy/Toxicity in Relapsed/Refractory Multiple Myeloma (RRMM). Clinical Lymphoma Myeloma & Leukemia 2024, 24: s92-s93. <a href="https://doi.org/10.1016/s2152-2650(24)01991-8" target="_blank">DOI: 10.1016/s2152-2650(24)01991-8</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://doi.org/10.1016/j.ajmo.2024.100078" class="research-list-item__link"><span>Post-Acute sequelae of COVID-19 in pediatric patients within the United States: A Scoping Review</span></a><span class="research-list-item__text">Miller C, Borre C, Green A, Funaro M, Oliveira C, <strong>Iwasaki A</strong>. Post-Acute sequelae of COVID-19 in pediatric patients within the United States: A Scoping Review. American Journal Of Medicine Open 2024, 100078. <a href="https://doi.org/10.1016/j.ajmo.2024.100078" target="_blank">DOI: 10.1016/j.ajmo.2024.100078</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39217658" class="research-list-item__link"><span>Massively parallel approaches for characterizing noncoding functional variation in human evolution</span></a><span class="research-list-item__text">Rong S, Root E, <strong>Reilly S</strong>. Massively parallel approaches for characterizing noncoding functional variation in human evolution. Current Opinion In Genetics & Development 2024, 88: 102256. <a href="https://pubmed.ncbi.nlm.nih.gov/39217658" target="_blank">PMID: 39217658</a>, <a href="https://doi.org/10.1016/j.gde.2024.102256" target="_blank">DOI: 10.1016/j.gde.2024.102256</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39192734" class="research-list-item__link"><span>Disulfide Tethering to Map Small Molecule Binding Sites Transcriptome-wide</span></a><span class="research-list-item__text">Moon M, Vock I, Streit A, Connor L, Senkina J, Ellman J, <strong>Simon M</strong>. Disulfide Tethering to Map Small Molecule Binding Sites Transcriptome-wide. ACS Chemical Biology 2024, 19: 2081-2086. <a href="https://pubmed.ncbi.nlm.nih.gov/39192734" target="_blank">PMID: 39192734</a>, <a href="https://doi.org/10.1021/acschembio.4c00538" target="_blank">DOI: 10.1021/acschembio.4c00538</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39189851" class="research-list-item__link"><span>Toll-like Receptor 9 Inhibition Mitigates Fibroproliferative Responses in Translational Models of Pulmonary Fibrosis.</span></a><span class="research-list-item__text">Trujillo G, Regueiro-Ren A, Liu C, Hu B, Sun Y, Ahangari F, Fiorini V, Ishikawa G, Al Jumaily K, Khoury J, McGovern J, Lee C, Peng X, Pivarnik T, Sun H, Walia A, Woo S, Yu S, Antin-Ozerkis D, Sauler M, <strong>Kaminski N</strong>, Herzog E, Ryu C. Toll-like Receptor 9 Inhibition Mitigates Fibroproliferative Responses in Translational Models of Pulmonary Fibrosis. American Journal Of Respiratory And Critical Care Medicine 2024 <a href="https://pubmed.ncbi.nlm.nih.gov/39189851" target="_blank">PMID: 39189851</a>, <a href="https://doi.org/10.1164/rccm.202401-0065oc" target="_blank">DOI: 10.1164/rccm.202401-0065oc</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39190492" class="research-list-item__link"><span>miR-33 deletion in hepatocytes attenuates NAFLD-NASH-HCC progression</span></a><span class="research-list-item__text">Fernández-Tussy P, Cardelo M, Zhang H, Sun J, Price N, Boutagy N, Goedeke L, Cadena-Sandoval M, Xirouchaki C, Brown W, Yang X, Pastor-Rojo O, Haeusler R, Bennett A, Tiganis T, <strong>Suárez Y</strong>, <strong>Fernández-Hernando C</strong>. miR-33 deletion in hepatocytes attenuates NAFLD-NASH-HCC progression. JCI Insight 2024, 9: e168476. <a href="https://pubmed.ncbi.nlm.nih.gov/39190492" target="_blank">PMID: 39190492</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11466198" target="_blank">PMCID: PMC11466198</a>, <a href="https://doi.org/10.1172/jci.insight.168476" target="_blank">DOI: 10.1172/jci.insight.168476</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39186078" class="research-list-item__link"><span>Similarity Metrics for Subcellular Analysis of FRET Microscopy Videos</span></a><span class="research-list-item__text">Burke M, Batista V, <strong>Davis C</strong>. Similarity Metrics for Subcellular Analysis of FRET Microscopy Videos. The Journal Of Physical Chemistry B 2024, 128: 8344-8354. <a href="https://pubmed.ncbi.nlm.nih.gov/39186078" target="_blank">PMID: 39186078</a>, <a href="https://doi.org/10.1021/acs.jpcb.4c02859" target="_blank">DOI: 10.1021/acs.jpcb.4c02859</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39174298" class="research-list-item__link"><span>Characterization and implementation of the MarathonRT template-switching reaction to expand the capabilities of RNA-Seq</span></a><span class="research-list-item__text">Guo L, Grinko A, Olson S, Leipold A, Graveley B, Saliba A, <strong>Pyle A</strong>. Characterization and implementation of the MarathonRT template-switching reaction to expand the capabilities of RNA-Seq. RNA 2024, 30: rna.080032.124. <a href="https://pubmed.ncbi.nlm.nih.gov/39174298" target="_blank">PMID: 39174298</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11482623" target="_blank">PMCID: PMC11482623</a>, <a href="https://doi.org/10.1261/rna.080032.124" target="_blank">DOI: 10.1261/rna.080032.124</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39173635" class="research-list-item__link"><span>Spatial transcriptomic validation of a biomimetic model of fibrosis enables re-evaluation of a therapeutic antibody targeting LOXL2</span></a><span class="research-list-item__text">Bell J, Davies E, Brereton C, Vukmirovic M, Roberts J, Lunn K, Wickens L, Conforti F, Ridley R, Ceccato J, Sayer L, Johnston D, Vallejo A, Alzetani A, Jogai S, Marshall B, Fabre A, Richeldi L, Monk P, Skipp P, <strong>Kaminski N</strong>, Offer E, Wang Y, Davies D, Jones M. Spatial transcriptomic validation of a biomimetic model of fibrosis enables re-evaluation of a therapeutic antibody targeting LOXL2. Cell Reports Medicine 2024, 5: 101695. <a href="https://pubmed.ncbi.nlm.nih.gov/39173635" target="_blank">PMID: 39173635</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11524965" target="_blank">PMCID: PMC11524965</a>, <a href="https://doi.org/10.1016/j.xcrm.2024.101695" target="_blank">DOI: 10.1016/j.xcrm.2024.101695</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39246333" class="research-list-item__link"><span>Exfoliation of a metal–organic framework enabled by post-synthetic cleavage of a dipyridyl dianthracene ligand</span></a><span class="research-list-item__text">Logelin M, Schreiber E, Mercado B, Burke M, <strong>Davis C</strong>, Bartholomew A. Exfoliation of a metal–organic framework enabled by post-synthetic cleavage of a dipyridyl dianthracene ligand. Chemical Science 2024, 15: 15198-15204. <a href="https://pubmed.ncbi.nlm.nih.gov/39246333" target="_blank">PMID: 39246333</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11378025" target="_blank">PMCID: PMC11378025</a>, <a href="https://doi.org/10.1039/d4sc03524k" target="_blank">DOI: 10.1039/d4sc03524k</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/38800659" class="research-list-item__link"><span>Identifying the minimal sets of distance restraints for FRET‐assisted protein structural modeling</span></a><span class="research-list-item__text">Liu Z, Grigas A, Sumner J, Knab E, <strong>Davis C</strong>, O'Hern C. Identifying the minimal sets of distance restraints for FRET‐assisted protein structural modeling. Protein Science 2024, 33 <a href="https://pubmed.ncbi.nlm.nih.gov/38800659" target="_blank">PMID: 38800659</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11118665" target="_blank">PMCID: PMC11118665</a>, <a href="https://doi.org/10.1002/pro.5219" target="_blank">DOI: 10.1002/pro.5219</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11389620" class="research-list-item__link"><span>Corrigendum: Translation regulation by a guanidine-II riboswitch is highly tunable in sensitivity, dynamic range, and apparent cooperativity</span></a><span class="research-list-item__text">Focht C, Hiller D, Grunseich S, <strong>Strobel S</strong>. Corrigendum: Translation regulation by a guanidine-II riboswitch is highly tunable in sensitivity, dynamic range, and apparent cooperativity. RNA 2024, 30: 1259-2-1259-2. <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11389620" target="_blank">PMCID: PMC11389620</a>, <a href="https://doi.org/10.1261/rna.080150.124" target="_blank">DOI: 10.1261/rna.080150.124</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/38717443" class="research-list-item__link"><span>Single-Cell Profiling Reveals Immune Aberrations in Progressive Idiopathic Pulmonary Fibrosis.</span></a><span class="research-list-item__text">Unterman A, Zhao A, Neumark N, Schupp J, Ahangari F, Cosme C, Sharma P, Flint J, Stein Y, Ryu C, Ishikawa G, Sumida T, Gomez J, Herazo-Maya J, Dela Cruz C, Herzog E, <strong>Kaminski N</strong>. Single-Cell Profiling Reveals Immune Aberrations in Progressive Idiopathic Pulmonary Fibrosis. American Journal Of Respiratory And Critical Care Medicine 2024, 210: 484-496. <a href="https://pubmed.ncbi.nlm.nih.gov/38717443" target="_blank">PMID: 38717443</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11351796" target="_blank">PMCID: PMC11351796</a>, <a href="https://doi.org/10.1164/rccm.202306-0979oc" target="_blank">DOI: 10.1164/rccm.202306-0979oc</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39151428" class="research-list-item__link"><span>Individual variation in the emergence of anterior-to-posterior neural fates from human pluripotent stem cells</span></a><span class="research-list-item__text">Kim S, Seo S, Stein-O’Brien G, Jaishankar A, Ogawa K, Micali N, Luria V, Karger A, Wang Y, Kim H, Hyde T, Kleinman J, Voss T, Fertig E, Shin J, Bürli R, Cross A, Brandon N, Weinberger D, Chenoweth J, Hoeppner D, <strong>Sestan N</strong>, Colantuoni C, McKay R. Individual variation in the emergence of anterior-to-posterior neural fates from human pluripotent stem cells. Stem Cell Reports 2024, 19: 1336-1350. <a href="https://pubmed.ncbi.nlm.nih.gov/39151428" target="_blank">PMID: 39151428</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11411333" target="_blank">PMCID: PMC11411333</a>, <a href="https://doi.org/10.1016/j.stemcr.2024.07.004" target="_blank">DOI: 10.1016/j.stemcr.2024.07.004</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39389673" class="research-list-item__link"><span>A user guide to RT-based mapping of RNA modifications</span></a><span class="research-list-item__text">Fang D, Babich J, Dangelmaier E, Wall V, <strong>Nachtergaele S</strong>. A user guide to RT-based mapping of RNA modifications. Methods In Enzymology 2024, 705: 51-79. <a href="https://pubmed.ncbi.nlm.nih.gov/39389673" target="_blank">PMID: 39389673</a>, <a href="https://doi.org/10.1016/bs.mie.2024.07.006" target="_blank">DOI: 10.1016/bs.mie.2024.07.006</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39205939" class="research-list-item__link"><span>Editorial: Synthetic biology and therapeutic applications of transfer RNA</span></a><span class="research-list-item__text"><strong>Söll D</strong>, O’Donoghue P, Heinemann I. Editorial: Synthetic biology and therapeutic applications of transfer RNA. Frontiers In Genetics 2024, 15: 1468891. <a href="https://pubmed.ncbi.nlm.nih.gov/39205939" target="_blank">PMID: 39205939</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11349731" target="_blank">PMCID: PMC11349731</a>, <a href="https://doi.org/10.3389/fgene.2024.1468891" target="_blank">DOI: 10.3389/fgene.2024.1468891</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39134804" class="research-list-item__link"><span>CAR-T and CAR-NK as cellular cancer immunotherapy for solid tumors</span></a><span class="research-list-item__text">Peng L, Sferruzza G, Yang L, Zhou L, <strong>Chen S</strong>. CAR-T and CAR-NK as cellular cancer immunotherapy for solid tumors. Cellular & Molecular Immunology 2024, 21: 1089-1108. <a href="https://pubmed.ncbi.nlm.nih.gov/39134804" target="_blank">PMID: 39134804</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11442786" target="_blank">PMCID: PMC11442786</a>, <a href="https://doi.org/10.1038/s41423-024-01207-0" target="_blank">DOI: 10.1038/s41423-024-01207-0</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39134824" class="research-list-item__link"><span>DNA methylation in mammalian development and disease</span></a><span class="research-list-item__text"><strong>Smith Z</strong>, Hetzel S, Meissner A. DNA methylation in mammalian development and disease. Nature Reviews Genetics 2024, 1-24. <a href="https://pubmed.ncbi.nlm.nih.gov/39134824" target="_blank">PMID: 39134824</a>, <a href="https://doi.org/10.1038/s41576-024-00760-8" target="_blank">DOI: 10.1038/s41576-024-00760-8</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39121194" class="research-list-item__link"><span>The human CD47 checkpoint is targeted by an immunosuppressive Aedes aegypti salivary factor to enhance arboviral skin infectivity</span></a><span class="research-list-item__text">Marin-Lopez A, Huck J, Esterly A, Azcutia V, Rosen C, Garcia-Milian R, Sefik E, Vidal-Pedrola G, Raduwan H, Chen T, Arora G, <strong>Halene S</strong>, Shaw A, Palm N, <strong>Flavell R</strong>, Parkos C, Thangamani S, Ring A, Fikrig E. The human CD47 checkpoint is targeted by an immunosuppressive Aedes aegypti salivary factor to enhance arboviral skin infectivity. Science Immunology 2024, 9: eadk9872. <a href="https://pubmed.ncbi.nlm.nih.gov/39121194" target="_blank">PMID: 39121194</a>, <a href="https://doi.org/10.1126/sciimmunol.adk9872" target="_blank">DOI: 10.1126/sciimmunol.adk9872</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39123049" class="research-list-item__link"><span>Fast, sensitive detection of protein homologs using deep dense retrieval</span></a><span class="research-list-item__text">Hong L, Hu Z, Sun S, Tang X, Wang J, Tan Q, Zheng L, Wang S, Xu S, King I, <strong>Gerstein M</strong>, Li Y. 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Nature Biotechnology 2024, 1-13. <a href="https://pubmed.ncbi.nlm.nih.gov/39123049" target="_blank">PMID: 39123049</a>, <a href="https://doi.org/10.1038/s41587-024-02353-6" target="_blank">DOI: 10.1038/s41587-024-02353-6</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39122965" class="research-list-item__link"><span>Long COVID science, research and policy</span></a><span class="research-list-item__text">Al-Aly Z, Davis H, McCorkell L, Soares L, Wulf-Hanson S, <strong>Iwasaki A</strong>, Topol E. Long COVID science, research and policy. Nature Medicine 2024, 30: 2148-2164. <a href="https://pubmed.ncbi.nlm.nih.gov/39122965" target="_blank">PMID: 39122965</a>, <a href="https://doi.org/10.1038/s41591-024-03173-6" target="_blank">DOI: 10.1038/s41591-024-03173-6</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39122142" class="research-list-item__link"><span>Enhanced intratumoral delivery of immunomodulator MPLA via hyperbranched polyglycerol-coated biodegradable nanoparticles</span></a><span class="research-list-item__text">Chang J, Shin K, Lewis J, Suh H, Lee J, Damsky W, Xu S, Bosenberg M, <strong>Saltzman W</strong>, Girardi M. Enhanced intratumoral delivery of immunomodulator MPLA via hyperbranched polyglycerol-coated biodegradable nanoparticles. Journal Of Investigative Dermatology 2024 <a href="https://pubmed.ncbi.nlm.nih.gov/39122142" target="_blank">PMID: 39122142</a>, <a href="https://doi.org/10.1016/j.jid.2024.07.019" target="_blank">DOI: 10.1016/j.jid.2024.07.019</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39117421" class="research-list-item__link"><span>Plasma collagen neoepitopes are associated with multiorgan disease in the ACCESS and GRADS sarcoidosis cohorts</span></a><span class="research-list-item__text">Sand J, Jessen H, Leeming D, Yu S, Lee C, Hu B, Sun Y, Adams T, Pivarnik T, Liu A, Woo S, McGovern J, Fiorini V, Saber T, Higuero-Sevilla J, Gulati M, <strong>Kaminski N</strong>, Damsky W, Shaw A, Mohanty S, Goobie G, Zhang Y, Herzog E, Ryu C. Plasma collagen neoepitopes are associated with multiorgan disease in the ACCESS and GRADS sarcoidosis cohorts. Thorax 2024, 79: thorax-2023-221095. <a href="https://pubmed.ncbi.nlm.nih.gov/39117421" target="_blank">PMID: 39117421</a>, <a href="https://doi.org/10.1136/thorax-2023-221095" target="_blank">DOI: 10.1136/thorax-2023-221095</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39107154" class="research-list-item__link"><span>Next generation triplex-forming PNAs for site-specific genome editing of the F508del CFTR mutation</span></a><span class="research-list-item__text">Gupta A, Barone C, Quijano E, Piotrowski-Daspit A, Perera J, Riccardi A, Jamali H, Turchick A, Zao W, <strong>Saltzman W</strong>, <strong>Glazer P</strong>, Egan M. Next generation triplex-forming PNAs for site-specific genome editing of the F508del CFTR mutation. Journal Of Cystic Fibrosis 2024 <a href="https://pubmed.ncbi.nlm.nih.gov/39107154" target="_blank">PMID: 39107154</a>, <a href="https://doi.org/10.1016/j.jcf.2024.07.009" target="_blank">DOI: 10.1016/j.jcf.2024.07.009</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11296858" class="research-list-item__link"><span>BSLM-03 BRANCHED-CHAIN KETO ACIDS PROMOTE AN IMMUNE-SUPPRESSIVE AND NEURODEGENERATIVE MICROENVIRONMENT IN LEPTOMENINGEAL DISEASE</span></a><span class="research-list-item__text">Khaled M, Ren Y, Kundalia R, Alhaddad H, Chen Z, Wallace G, Evernden B, Ospina O, Hall M, Liu M, Darville L, Izumi V, Chen Y, Pilon-Thomas S, Stewart P, Koomen J, Corallo S, Jain M, <strong>Robinson T</strong>, Locke F, Forsyth P, Smalley I. BSLM-03 BRANCHED-CHAIN KETO ACIDS PROMOTE AN IMMUNE-SUPPRESSIVE AND NEURODEGENERATIVE MICROENVIRONMENT IN LEPTOMENINGEAL DISEASE. Neuro-Oncology Advances 2024, 6: i5-i5. <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11296858" target="_blank">PMCID: PMC11296858</a>, <a href="https://doi.org/10.1093/noajnl/vdae090.014" target="_blank">DOI: 10.1093/noajnl/vdae090.014</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/38900452" class="research-list-item__link"><span>Perioperative Modified FOLFIRINOX for Resectable Pancreatic Cancer</span></a><span class="research-list-item__text">Cecchini M, Salem R, Robert M, Czerniak S, Blaha O, Zelterman D, Rajaei M, Townsend J, Cai G, Chowdhury S, Yugawa D, Tseng R, Arbelaez C, Jiao J, Shroyer K, Thumar J, Kortmansky J, Zaheer W, Fischbach N, Persico J, Stein S, Khan S, Cha C, Billingsley K, Kunstman J, Johung K, Wiess C, Muzumdar M, Spickard E, Aushev V, Laliotis G, Jurdi A, Liu M, <strong>Escobar-Hoyos L</strong>, Lacy J. Perioperative Modified FOLFIRINOX for Resectable Pancreatic Cancer. JAMA Oncology 2024, 10: 1027-1035. <a href="https://pubmed.ncbi.nlm.nih.gov/38900452" target="_blank">PMID: 38900452</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11190830" target="_blank">PMCID: PMC11190830</a>, <a href="https://doi.org/10.1001/jamaoncol.2024.1575" target="_blank">DOI: 10.1001/jamaoncol.2024.1575</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39195572" class="research-list-item__link"><span>Challenges in LncRNA Biology: Views and Opinions</span></a><span class="research-list-item__text">Adjeroh D, Zhou X, Paschoal A, <strong>Dimitrova N</strong>, Derevyanchuk E, Shkurat T, Loeb J, Martinez I, Lipovich L. Challenges in LncRNA Biology: Views and Opinions. Non-Coding RNA 2024, 10: 43. <a href="https://pubmed.ncbi.nlm.nih.gov/39195572" target="_blank">PMID: 39195572</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11357347" target="_blank">PMCID: PMC11357347</a>, <a href="https://doi.org/10.3390/ncrna10040043" target="_blank">DOI: 10.3390/ncrna10040043</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li><li class="organization-publication-list__group-list-item"><div class="research-list-item research-list-item--with-link"><div class="research-list-item__icon-wrapper"><svg xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24" focusable="false" class="research-list-item__icon"><path d="M22.5 21.75a1.5 1.5 0 0 1-1.5 1.5H3a1.5 1.5 0 0 1-1.5-1.5V2.25A1.5 1.5 0 0 1 3 .75h15.045a1.5 1.5 0 0 1 1.048.426l2.954 2.883a1.5 1.5 0 0 1 .453 1.074ZM6.045 8.25h12M6.045 12.75h12M6.045 17.25h6" style="fill:none;stroke:currentColor;stroke-linecap:round;stroke-linejoin:round;stroke-width:1.5px"></path></svg></div><div class="research-list-item__content-container"><a href="https://pubmed.ncbi.nlm.nih.gov/39075235" class="research-list-item__link"><span>SARS-CoV-2-related bat viruses evade human intrinsic immunity but lack efficient transmission capacity</span></a><span class="research-list-item__text">Peña-Hernández M, Alfajaro M, Filler R, Moriyama M, Keeler E, Ranglin Z, Kong Y, Mao T, Menasche B, Mankowski M, Zhao Z, Vogels C, Hahn A, Kalinich C, Zhang S, Huston N, Wan H, Araujo-Tavares R, Lindenbach B, Homer R, <strong>Pyle A</strong>, Martinez D, <strong>Grubaugh N</strong>, Israelow B, <strong>Iwasaki A</strong>, <strong>Wilen C</strong>. SARS-CoV-2-related bat viruses evade human intrinsic immunity but lack efficient transmission capacity. Nature Microbiology 2024, 9: 2038-2050. <a href="https://pubmed.ncbi.nlm.nih.gov/39075235" target="_blank">PMID: 39075235</a>, <a href="https://doi.org/10.1038/s41564-024-01765-z" target="_blank">DOI: 10.1038/s41564-024-01765-z</a>.</span><div class="organization-publication-list__list-item-badges"></div></div></div></li></ul></section><div class="organization-publication-list__button-container"><div class="organization-publication-list__button"><button type="button" class="button button--large button--primary button--color-mode--blue" tabindex="0"><span class="button__label">Show More</span></button></div><div class="organization-publication-list__button"><a href="/organization-publication/csv/?organizationId=110394&orderBy=PublicationDate" tabindex="0" class="button button--large button--secondary button--color-mode--blue button--link" rel="nofollow"><span class="button__label">Download Full List</span></a></div></div></section></div></div><div class="sidebar 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Adegunsoye A, Sperling A, Prasse A, Ryu C, Herzog E, Selman M, Pardo A, <strong>Kaminski N</strong>. Single-Cell Analysis Reveals Novel Immune Perturbations in Fibrotic Hypersensitivity Pneumonitis. American Journal Of Respiratory And Critical Care Medicine 2024, 210: 1252-1266. <a href=\"https://pubmed.ncbi.nlm.nih.gov/38924775\" target=\"_blank\">PMID: 38924775</a>, <a href=\"https://doi.org/10.1164/rccm.202401-0078oc\" target=\"_blank\">DOI: 10.1164/rccm.202401-0078oc</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/38924775","text":"Single-Cell Analysis Reveals Novel Immune Perturbations in Fibrotic Hypersensitivity Pneumonitis."}},{"pubMedUid":39522891,"doi":"10.1016/j.bbadis.2024.167565","id":null,"title":"GPR68 supports AML cells through the calcium/calcineurin pro-survival pathway and confers chemoresistance by mediating glucose metabolic symbiosis","citation":"He X, Hawkins C, Lawley L, Phan T, Park I, Joven N, Zhang J, Wunderlich M, Mizukawa B, Pei S, Patel A, VanOudenhove J, <strong>Halene S</strong>, Fang J. GPR68 supports AML cells through the calcium/calcineurin pro-survival pathway and confers chemoresistance by mediating glucose metabolic symbiosis. Biochimica Et Biophysica Acta (BBA) - Molecular Basis Of Disease 2024, 167565. <a href=\"https://pubmed.ncbi.nlm.nih.gov/39522891\" target=\"_blank\">PMID: 39522891</a>, <a href=\"https://doi.org/10.1016/j.bbadis.2024.167565\" target=\"_blank\">DOI: 10.1016/j.bbadis.2024.167565</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/39522891","text":"GPR68 supports AML cells through the calcium/calcineurin pro-survival pathway and confers chemoresistance by mediating glucose metabolic symbiosis"}},{"pubMedUid":39514636,"doi":"10.1126/sciimmunol.add6608","id":null,"title":"A B cell screen against endogenous retroviruses identifies glycan-reactive IgM that recognizes a broad array of enveloped viruses","citation":"Yang Y, Treger R, Hernandez-Bird J, Lu P, Mao T, <strong>Iwasaki A</strong>. A B cell screen against endogenous retroviruses identifies glycan-reactive IgM that recognizes a broad array of enveloped viruses. Science Immunology 2024, 9: eadd6608. <a href=\"https://pubmed.ncbi.nlm.nih.gov/39514636\" target=\"_blank\">PMID: 39514636</a>, <a href=\"https://doi.org/10.1126/sciimmunol.add6608\" target=\"_blank\">DOI: 10.1126/sciimmunol.add6608</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/39514636","text":"A B cell screen against endogenous retroviruses identifies glycan-reactive IgM that recognizes a broad array of enveloped viruses"}},{"pubMedUid":39504356,"doi":"10.1126/scitranslmed.adh9940","id":null,"title":"Integrative multiomic analysis identifies distinct molecular subtypes of NAFLD in a Chinese population","citation":"Ding J, Liu H, Zhang X, Zhao N, Peng Y, Shi J, Chen J, Chi X, Li L, Zhang M, Liu W, Zhang L, Ouyang J, Yuan Q, Liao M, Tan Y, Li M, Xu Z, Tang W, Xie C, Li Y, Pan Q, Xu Y, Cai S, Byrne C, Targher G, <strong>Ouyang X</strong>, Zhang L, Jiang Z, Zheng M, Sun F, Chai J. Integrative multiomic analysis identifies distinct molecular subtypes of NAFLD in a Chinese population. Science Translational Medicine 2024, 16: eadh9940. <a href=\"https://pubmed.ncbi.nlm.nih.gov/39504356\" target=\"_blank\">PMID: 39504356</a>, <a href=\"https://doi.org/10.1126/scitranslmed.adh9940\" target=\"_blank\">DOI: 10.1126/scitranslmed.adh9940</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/39504356","text":"Integrative multiomic analysis identifies distinct molecular subtypes of NAFLD in a Chinese population"}},{"pubMedUid":0,"doi":"10.1136/jitc-2024-sitc2024.0065","id":null,"title":"65 High-fidelity enhanced AsCas12a knock-in mice for efficient multiplexed gene editing, disease modeling and orthogonal immunogenetics","citation":"Tang K, Zhou X, Fang S, Vandenbulcke E, Du A, Shen J, Cao H, Zhou J, Chen K, Xin S, Zhou L, Lin S, Majety M, Lin X, Lam S, Chow R, Bai S, Nottoli T, Booth C, Liu C, Dong M, <strong>Chen S</strong>. 65 High-fidelity enhanced AsCas12a knock-in mice for efficient multiplexed gene editing, disease modeling and orthogonal immunogenetics. 2024, a72-a72. <a href=\"https://doi.org/10.1136/jitc-2024-sitc2024.0065\" target=\"_blank\">DOI: 10.1136/jitc-2024-sitc2024.0065</a>.","year":2024,"link":{"url":"https://doi.org/10.1136/jitc-2024-sitc2024.0065","text":"65 High-fidelity enhanced AsCas12a knock-in mice for efficient multiplexed gene editing, disease modeling and orthogonal immunogenetics"}},{"pubMedUid":39482410,"doi":"10.1038/s42003-024-07045-0","id":null,"title":"REliable PIcking by Consensus (REPIC): a consensus methodology for harnessing multiple cryo-EM particle pickers","citation":"Cameron C, Seager S, Sigworth F, Tagare H, <strong>Gerstein M</strong>. REliable PIcking by Consensus (REPIC): a consensus methodology for harnessing multiple cryo-EM particle pickers. Communications Biology 2024, 7: 1421. <a href=\"https://pubmed.ncbi.nlm.nih.gov/39482410\" target=\"_blank\">PMID: 39482410</a>, <a href=\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11528043\" target=\"_blank\">PMCID: PMC11528043</a>, <a href=\"https://doi.org/10.1038/s42003-024-07045-0\" target=\"_blank\">DOI: 10.1038/s42003-024-07045-0</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/39482410","text":"REliable PIcking by Consensus (REPIC): a consensus methodology for harnessing multiple cryo-EM particle pickers"}},{"pubMedUid":39475571,"doi":"10.1126/scitranslmed.abo1997","id":null,"title":"Single-cell transcriptomic and proteomic analysis of Parkinson’s disease brains","citation":"Zhu B, Park J, Coffey S, Russo A, Hsu I, Wang J, Su C, Chang R, Lam T, <strong>Gopal P</strong>, Ginsberg S, Zhao H, Hafler D, Chandra S, Zhang L. Single-cell transcriptomic and proteomic analysis of Parkinson’s disease brains. Science Translational Medicine 2024, 16: eabo1997. <a href=\"https://pubmed.ncbi.nlm.nih.gov/39475571\" target=\"_blank\">PMID: 39475571</a>, <a href=\"https://doi.org/10.1126/scitranslmed.abo1997\" target=\"_blank\">DOI: 10.1126/scitranslmed.abo1997</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/39475571","text":"Single-cell transcriptomic and proteomic analysis of Parkinson’s disease brains"}},{"pubMedUid":39102635,"doi":"10.1182/blood.2024023963","id":null,"title":"CDK9 phosphorylates RUNX1 to promote megakaryocytic fate in megakaryocytic-erythroid progenitors","citation":"Kwon N, Lu Y, Thompson E, Mancuso R, Wang L, Zhang P, <strong>Krause D</strong>. CDK9 phosphorylates RUNX1 to promote megakaryocytic fate in megakaryocytic-erythroid progenitors. Blood 2024, 144: 1800-1812. <a href=\"https://pubmed.ncbi.nlm.nih.gov/39102635\" target=\"_blank\">PMID: 39102635</a>, <a href=\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11530366\" target=\"_blank\">PMCID: PMC11530366</a>, <a href=\"https://doi.org/10.1182/blood.2024023963\" target=\"_blank\">DOI: 10.1182/blood.2024023963</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/39102635","text":"CDK9 phosphorylates RUNX1 to promote megakaryocytic fate in megakaryocytic-erythroid progenitors"}},{"pubMedUid":0,"doi":"10.1038/s43586-024-00354-y","id":null,"title":"Image-based 3D genomics through chromatin tracing","citation":"Yang T, <strong>Wang S</strong>. Image-based 3D genomics through chromatin tracing. Nature Reviews Methods Primers 2024, 4: 76. <a href=\"https://doi.org/10.1038/s43586-024-00354-y\" target=\"_blank\">DOI: 10.1038/s43586-024-00354-y</a>.","year":2024,"link":{"url":"https://doi.org/10.1038/s43586-024-00354-y","text":"Image-based 3D genomics through chromatin tracing"}},{"pubMedUid":0,"doi":"10.3390/v16111653","id":null,"title":"Analysis of Powassan Virus Genome Sequences from Human Cases Reveals Substantial Genetic Diversity with Implications for Molecular Assay Development","citation":"Klontz E, Chowdhury N, Holbrook N, Solomon I, Telford S, Aliota M, Vogels C, <strong>Grubaugh N</strong>, Helgager J, Hughes H, Velez J, Piantadosi A, Chiu C, Lemieux J, Branda J. Analysis of Powassan Virus Genome Sequences from Human Cases Reveals Substantial Genetic Diversity with Implications for Molecular Assay Development. Viruses 2024, 16: 1653. <a href=\"https://doi.org/10.3390/v16111653\" target=\"_blank\">DOI: 10.3390/v16111653</a>.","year":2024,"link":{"url":"https://doi.org/10.3390/v16111653","text":"Analysis of Powassan Virus Genome Sequences from Human Cases Reveals Substantial Genetic Diversity with Implications for Molecular Assay Development"}},{"pubMedUid":39443793,"doi":"10.1038/s41586-024-08070-z","id":null,"title":"Machine-guided design of cell-type-targeting cis-regulatory elements","citation":"Gosai S, Castro R, Fuentes N, Butts J, Mouri K, Alasoadura M, Kales S, Nguyen T, Noche R, Rao A, Joy M, Sabeti P, <strong>Reilly S</strong>, Tewhey R. Machine-guided design of cell-type-targeting cis-regulatory elements. Nature 2024, 634: 1211-1220. <a href=\"https://pubmed.ncbi.nlm.nih.gov/39443793\" target=\"_blank\">PMID: 39443793</a>, <a href=\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11525185\" target=\"_blank\">PMCID: PMC11525185</a>, <a href=\"https://doi.org/10.1038/s41586-024-08070-z\" target=\"_blank\">DOI: 10.1038/s41586-024-08070-z</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/39443793","text":"Machine-guided design of cell-type-targeting cis-regulatory elements"}},{"pubMedUid":0,"doi":"10.1038/s42256-024-00913-8","id":null,"title":"Epitope-anchored contrastive transfer learning for paired CD8+ T cell receptor–antigen recognition","citation":"Zhang Y, Wang Z, Jiang Y, Littler D, <strong>Gerstein M</strong>, Purcell A, Rossjohn J, Ou H, Song J. Epitope-anchored contrastive transfer learning for paired CD8+ T cell receptor–antigen recognition. Nature Machine Intelligence 2024, 1-15. <a href=\"https://doi.org/10.1038/s42256-024-00913-8\" target=\"_blank\">DOI: 10.1038/s42256-024-00913-8</a>.","year":2024,"link":{"url":"https://doi.org/10.1038/s42256-024-00913-8","text":"Epitope-anchored contrastive transfer learning for paired CD8+ T cell receptor–antigen recognition"}},{"pubMedUid":39438113,"doi":"10.1101/gr.279037.124","id":null,"title":"Binding profiles for 961 Drosophila and C. elegans transcription factors reveal tissue-specific regulatory relationships.","citation":"Kudron M, Gewirtzman L, Victorsen A, Lear B, Vafeados D, Gao J, Xu J, Samanta S, Frink E, Tran-Pearson A, Hyunh C, Hammonds A, Fisher W, Wall M, Wesseling G, Hernandez V, Lin Z, Kasparian M, White K, Allada R, Gerstein M, Hillier L, Celniker S, <strong>Reinke V</strong>, Waterston R. Binding profiles for 961 Drosophila and C. elegans transcription factors reveal tissue-specific regulatory relationships. Genome Research 2024, gr.279037.124. <a href=\"https://pubmed.ncbi.nlm.nih.gov/39438113\" target=\"_blank\">PMID: 39438113</a>, <a href=\"https://doi.org/10.1101/gr.279037.124\" target=\"_blank\">DOI: 10.1101/gr.279037.124</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/39438113","text":"Binding profiles for 961 Drosophila and C. elegans transcription factors reveal tissue-specific regulatory relationships."}},{"pubMedUid":39433914,"doi":"10.1038/s41580-024-00784-2","id":null,"title":"All the sites we cannot see: Sources and mitigation of false negatives in RNA modification studies","citation":"Oberdoerffer S, <strong>Gilbert W</strong>. All the sites we cannot see: Sources and mitigation of false negatives in RNA modification studies. Nature Reviews Molecular Cell Biology 2024, 1-12. <a href=\"https://pubmed.ncbi.nlm.nih.gov/39433914\" target=\"_blank\">PMID: 39433914</a>, <a href=\"https://doi.org/10.1038/s41580-024-00784-2\" target=\"_blank\">DOI: 10.1038/s41580-024-00784-2</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/39433914","text":"All the sites we cannot see: Sources and mitigation of false negatives in RNA modification studies"}},{"pubMedUid":39431827,"doi":"10.1128/mbio.02811-24","id":null,"title":"Rab6a enables BICD2/dynein-mediated trafficking of human papillomavirus from the trans-Golgi network during virus entry","citation":"Choi J, Speckhart K, Tsai B, <strong>DiMaio D</strong>. Rab6a enables BICD2/dynein-mediated trafficking of human papillomavirus from the trans-Golgi network during virus entry. MBio 2024, 15: e02811-24. <a href=\"https://pubmed.ncbi.nlm.nih.gov/39431827\" target=\"_blank\">PMID: 39431827</a>, <a href=\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11559006\" target=\"_blank\">PMCID: PMC11559006</a>, <a href=\"https://doi.org/10.1128/mbio.02811-24\" target=\"_blank\">DOI: 10.1128/mbio.02811-24</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/39431827","text":"Rab6a enables BICD2/dynein-mediated trafficking of human papillomavirus from the trans-Golgi network during virus entry"}},{"pubMedUid":39456630,"doi":"10.3390/cancers16203536","id":null,"title":"A TRilogy of ATR’s Non-Canonical Roles Throughout the Cell Cycle and Its Relation to Cancer","citation":"Joo Y, Ramirez C, <strong>Kabeche L</strong>. A TRilogy of ATR’s Non-Canonical Roles Throughout the Cell Cycle and Its Relation to Cancer. Cancers 2024, 16: 3536. <a href=\"https://pubmed.ncbi.nlm.nih.gov/39456630\" target=\"_blank\">PMID: 39456630</a>, <a href=\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11506335\" target=\"_blank\">PMCID: PMC11506335</a>, <a href=\"https://doi.org/10.3390/cancers16203536\" target=\"_blank\">DOI: 10.3390/cancers16203536</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/39456630","text":"A TRilogy of ATR’s Non-Canonical Roles Throughout the Cell Cycle and Its Relation to Cancer"}},{"pubMedUid":39402626,"doi":"10.1186/s13059-024-03416-2","id":null,"title":"SDePER: a hybrid machine learning and regression method for cell-type deconvolution of spatial barcoding-based transcriptomic data","citation":"Liu Y, Li N, Qi J, Xu G, Zhao J, Wang N, Huang X, Jiang W, Wei H, Justet A, Adams T, Homer R, Amei A, Rosas I, <strong>Kaminski N</strong>, Wang Z, Yan X. SDePER: a hybrid machine learning and regression method for cell-type deconvolution of spatial barcoding-based transcriptomic data. Genome Biology 2024, 25: 271. <a href=\"https://pubmed.ncbi.nlm.nih.gov/39402626\" target=\"_blank\">PMID: 39402626</a>, <a href=\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11475911\" target=\"_blank\">PMCID: PMC11475911</a>, <a href=\"https://doi.org/10.1186/s13059-024-03416-2\" target=\"_blank\">DOI: 10.1186/s13059-024-03416-2</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/39402626","text":"SDePER: a hybrid machine learning and regression method for cell-type deconvolution of spatial barcoding-based transcriptomic data"}},{"pubMedUid":39419034,"doi":"10.1016/j.devcel.2024.09.023","id":null,"title":"Ataxin-2 polyglutamine expansions aberrantly sequester TDP-43 ribonucleoprotein condensates disrupting mRNA transport and local translation in neurons","citation":"Wijegunawardana D, Nayak A, Vishal S, Venkatesh N, <strong>Gopal P</strong>. Ataxin-2 polyglutamine expansions aberrantly sequester TDP-43 ribonucleoprotein condensates disrupting mRNA transport and local translation in neurons. Developmental Cell 2024 <a href=\"https://pubmed.ncbi.nlm.nih.gov/39419034\" target=\"_blank\">PMID: 39419034</a>, <a href=\"https://doi.org/10.1016/j.devcel.2024.09.023\" target=\"_blank\">DOI: 10.1016/j.devcel.2024.09.023</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/39419034","text":"Ataxin-2 polyglutamine expansions aberrantly sequester TDP-43 ribonucleoprotein condensates disrupting mRNA transport and local translation in neurons"}},{"pubMedUid":39393608,"doi":"10.1016/j.exphem.2024.104655","id":null,"title":"Splicing the Difference: Harnessing the Complexity of the Transcriptome in Hematopoiesis","citation":"Maul-Newby H, <strong>Halene S</strong>. Splicing the Difference: Harnessing the Complexity of the Transcriptome in Hematopoiesis. 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The Journal Of Immunology 2024, 213: 1338-1348. <a href=\"https://pubmed.ncbi.nlm.nih.gov/39302113\" target=\"_blank\">PMID: 39302113</a>, <a href=\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11493510\" target=\"_blank\">PMCID: PMC11493510</a>, <a href=\"https://doi.org/10.4049/jimmunol.2400331\" target=\"_blank\">DOI: 10.4049/jimmunol.2400331</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/39302113","text":"IL-1β Induces Human Endothelial Surface Expression of IL-15 by Relieving let-7c-3p Suppression of Protein Translation."}},{"pubMedUid":39372273,"doi":"10.3389/fmicb.2024.1421660","id":null,"title":"Diagnostic values of BALF metagenomic next-generation sequencing, BALF real-time PCR and serum BDG for Pneumocystis jirovecii pneumonia in HIV-infected patients","citation":"Chen Q, Chen X, Mo P, Chen L, Du Q, Hu W, Jiang Q, Zhang Z, Zhang Y, Guo Q, <strong>Xiong Y</strong>, Deng L. Diagnostic values of BALF metagenomic next-generation sequencing, BALF real-time PCR and serum BDG for Pneumocystis jirovecii pneumonia in HIV-infected patients. Frontiers In Microbiology 2024, 15: 1421660. <a href=\"https://pubmed.ncbi.nlm.nih.gov/39372273\" target=\"_blank\">PMID: 39372273</a>, <a href=\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11449763\" target=\"_blank\">PMCID: PMC11449763</a>, <a href=\"https://doi.org/10.3389/fmicb.2024.1421660\" target=\"_blank\">DOI: 10.3389/fmicb.2024.1421660</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/39372273","text":"Diagnostic values of BALF metagenomic next-generation sequencing, BALF real-time PCR and serum BDG for Pneumocystis jirovecii pneumonia in HIV-infected patients"}},{"pubMedUid":39302833,"doi":"10.1016/j.celrep.2024.114777","id":null,"title":"A comparative roadmap of PIWI-interacting RNAs across seven species reveals insights into de novo piRNA-precursor formation in mammals","citation":"Konstantinidou P, Loubalova Z, Ahrend F, Friman A, Almeida M, Poulet A, Horvat F, Wang Y, Losert W, Lorenzi H, Svoboda P, Miska E, <strong>van Wolfswinkel J</strong>, Haase A. A comparative roadmap of PIWI-interacting RNAs across seven species reveals insights into de novo piRNA-precursor formation in mammals. Cell Reports 2024, 43: 114777. <a href=\"https://pubmed.ncbi.nlm.nih.gov/39302833\" target=\"_blank\">PMID: 39302833</a>, <a href=\"https://doi.org/10.1016/j.celrep.2024.114777\" target=\"_blank\">DOI: 10.1016/j.celrep.2024.114777</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/39302833","text":"A comparative roadmap of PIWI-interacting RNAs across seven species reveals insights into de novo piRNA-precursor formation in mammals"}},{"pubMedUid":39298321,"doi":"10.1016/j.xpro.2024.103321","id":null,"title":"Protocol for detecting glycoRNAs using metabolic labeling and northwestern blot","citation":"Li L, Zhang N, Pantoja C, Wang Y, <strong>Lu J</strong>. Protocol for detecting glycoRNAs using metabolic labeling and northwestern blot. STAR Protocols 2024, 5: 103321. <a href=\"https://pubmed.ncbi.nlm.nih.gov/39298321\" target=\"_blank\">PMID: 39298321</a>, <a href=\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11426122\" target=\"_blank\">PMCID: PMC11426122</a>, <a href=\"https://doi.org/10.1016/j.xpro.2024.103321\" target=\"_blank\">DOI: 10.1016/j.xpro.2024.103321</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/39298321","text":"Protocol for detecting glycoRNAs using metabolic labeling and northwestern blot"}},{"pubMedUid":39360312,"doi":"10.3389/fmicb.2024.1465811","id":null,"title":"Improved methods for genetic manipulation of the alkaliphile Halalkalibacterium halodurans","citation":"Wencker F, Lyon S, <strong>Breaker R</strong>. Improved methods for genetic manipulation of the alkaliphile Halalkalibacterium halodurans. Frontiers In Microbiology 2024, 15: 1465811. <a href=\"https://pubmed.ncbi.nlm.nih.gov/39360312\" target=\"_blank\">PMID: 39360312</a>, <a href=\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11445130\" target=\"_blank\">PMCID: PMC11445130</a>, <a href=\"https://doi.org/10.3389/fmicb.2024.1465811\" target=\"_blank\">DOI: 10.3389/fmicb.2024.1465811</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/39360312","text":"Improved methods for genetic manipulation of the alkaliphile Halalkalibacterium halodurans"}},{"pubMedUid":39288189,"doi":"10.1371/journal.pcbi.1012469","id":null,"title":"Genome-wide association study between SARS-CoV-2 single nucleotide polymorphisms and virus copies during infections","citation":"Li K, Chaguza C, Stamp J, Chew Y, Chen N, Ferguson D, Pandya S, Kerantzas N, Schulz W, Initiative Y, Hahn A, Ogbunugafor C, Pitzer V, Crawford L, Weinberger D, <strong>Grubaugh N</strong>. Genome-wide association study between SARS-CoV-2 single nucleotide polymorphisms and virus copies during infections. PLOS Computational Biology 2024, 20: e1012469. <a href=\"https://pubmed.ncbi.nlm.nih.gov/39288189\" target=\"_blank\">PMID: 39288189</a>, <a href=\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11432881\" target=\"_blank\">PMCID: PMC11432881</a>, <a href=\"https://doi.org/10.1371/journal.pcbi.1012469\" target=\"_blank\">DOI: 10.1371/journal.pcbi.1012469</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/39288189","text":"Genome-wide association study between SARS-CoV-2 single nucleotide polymorphisms and virus copies during infections"}},{"pubMedUid":39283942,"doi":"10.1371/journal.pbio.3002834","id":null,"title":"A new lineage nomenclature to aid genomic surveillance of dengue virus","citation":"Hill V, Cleemput S, Pereira J, Gifford R, Fonseca V, Tegally H, Brito A, Ribeiro G, de Souza V, Brcko I, Ribeiro I, De Lima I, Slavov S, Sampaio S, Elias M, Tran V, Kien D, Huynh T, Yacoub S, Dieng I, Salvato R, Wallau G, Gregianini T, Godinho F, Vogels C, Breban M, Leguia M, Jagtap S, Roy R, Hapuarachchi C, Mwanyika G, Giovanetti M, Alcantara L, Faria N, Carrington C, Hanley K, Holmes E, Dumon W, Lima A, de Oliveira T, <strong>Grubaugh N</strong>. A new lineage nomenclature to aid genomic surveillance of dengue virus. PLOS Biology 2024, 22: e3002834. <a href=\"https://pubmed.ncbi.nlm.nih.gov/39283942\" target=\"_blank\">PMID: 39283942</a>, <a href=\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11426435\" target=\"_blank\">PMCID: PMC11426435</a>, <a href=\"https://doi.org/10.1371/journal.pbio.3002834\" target=\"_blank\">DOI: 10.1371/journal.pbio.3002834</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/39283942","text":"A new lineage nomenclature to aid genomic surveillance of dengue virus"}},{"pubMedUid":0,"doi":"10.1158/1538-7445.pancreatic24-pr-05","id":null,"title":"Abstract PR-05: Endocrine beta-cell stress promotes pancreatic ductal adenocarcinoma through endocrine-exocrine cell crosstalk","citation":"Garcia C, Venkat A, McQuaid D, Agabiti S, Tong A, Cardone R, Kibbey R, <strong>Krishnaswamy S</strong>, Muzumdar M. Abstract PR-05: Endocrine beta-cell stress promotes pancreatic ductal adenocarcinoma through endocrine-exocrine cell crosstalk. Cancer Research 2024, 84: pr-05-pr-05. <a href=\"https://doi.org/10.1158/1538-7445.pancreatic24-pr-05\" target=\"_blank\">DOI: 10.1158/1538-7445.pancreatic24-pr-05</a>.","year":2024,"link":{"url":"https://doi.org/10.1158/1538-7445.pancreatic24-pr-05","text":"Abstract PR-05: Endocrine beta-cell stress promotes pancreatic ductal adenocarcinoma through endocrine-exocrine cell crosstalk"}},{"pubMedUid":0,"doi":"10.1158/1538-7445.pancreatic24-pr-01","id":null,"title":"Abstract PR-01: Systemic targeting of therapeutic RNA to pancreatic ductal adenocarcinoma via a novel, cell-penetrating, and nucleic acid-binding monoclonal antibody","citation":"Martinez-Saucedo D, Quijano E, Ianniello Z, Rackear M, Liu Y, Hegan D, Chen H, Shan X, Tseng R, Yugawa D, Pinto-Medici N, Chowdhury S, Bindra R, Robert M, <strong>Saltzman W</strong>, <strong>Escobar-Hoyos L</strong>, <strong>Glazer P</strong>. Abstract PR-01: Systemic targeting of therapeutic RNA to pancreatic ductal adenocarcinoma via a novel, cell-penetrating, and nucleic acid-binding monoclonal antibody. Cancer Research 2024, 84: pr-01-pr-01. <a href=\"https://doi.org/10.1158/1538-7445.pancreatic24-pr-01\" target=\"_blank\">DOI: 10.1158/1538-7445.pancreatic24-pr-01</a>.","year":2024,"link":{"url":"https://doi.org/10.1158/1538-7445.pancreatic24-pr-01","text":"Abstract PR-01: Systemic targeting of therapeutic RNA to pancreatic ductal adenocarcinoma via a novel, cell-penetrating, and nucleic acid-binding monoclonal antibody"}},{"pubMedUid":0,"doi":"10.1158/1538-7445.pancreatic24-c030","id":null,"title":"Abstract C030: Evolutionary and epistatic analyses reveal genic interactions with KRAS during malignant progression of pancreatic ductal adenocarcinoma","citation":"Fisk N, Song D, Moore M, Jensen C, Cannataro V, Nagib M, Mandell J, <strong>Escobar-Hoyos L</strong>, Kunstman J, Townsend J. Abstract C030: Evolutionary and epistatic analyses reveal genic interactions with KRAS during malignant progression of pancreatic ductal adenocarcinoma. Cancer Research 2024, 84: c030-c030. <a href=\"https://doi.org/10.1158/1538-7445.pancreatic24-c030\" target=\"_blank\">DOI: 10.1158/1538-7445.pancreatic24-c030</a>.","year":2024,"link":{"url":"https://doi.org/10.1158/1538-7445.pancreatic24-c030","text":"Abstract C030: Evolutionary and epistatic analyses reveal genic interactions with KRAS during malignant progression of pancreatic ductal adenocarcinoma"}},{"pubMedUid":0,"doi":"10.1158/1538-7445.pancreatic24-pr-11","id":null,"title":"Abstract PR-11: Altered mRNA splicing mimics chromosome loss and drives pancreatic cancer","citation":"Medici N, Martinez-Saucedo D, Lee D, Chu T, Tseng R, Cannataro V, Townsend J, Iacobuzio-Donahue C, Robert M, Abdel-Wahab O, Leach S, <strong>Escobar-Hoyos L</strong>. Abstract PR-11: Altered mRNA splicing mimics chromosome loss and drives pancreatic cancer. Cancer Research 2024, 84: pr-11-pr-11. <a href=\"https://doi.org/10.1158/1538-7445.pancreatic24-pr-11\" target=\"_blank\">DOI: 10.1158/1538-7445.pancreatic24-pr-11</a>.","year":2024,"link":{"url":"https://doi.org/10.1158/1538-7445.pancreatic24-pr-11","text":"Abstract PR-11: Altered mRNA splicing mimics chromosome loss and drives pancreatic cancer"}},{"pubMedUid":0,"doi":"10.1158/1538-7445.pancreatic24-b083","id":null,"title":"Abstract B083: The splicing factor SMNDC1 facilitates alternative RNA splicing, contributing to therapy resistance in pancreatic cancer","citation":"Siraj M, Zhang Y, Yugawa D, Giri G, Chakraborty P, Goda G, Rao G, Dominguez D, Kubicek S, Bhattacharya R, <strong>Escobar-Hoyos L</strong>, Mukherjee P. Abstract B083: The splicing factor SMNDC1 facilitates alternative RNA splicing, contributing to therapy resistance in pancreatic cancer. Cancer Research 2024, 84: b00-b00. <a href=\"https://doi.org/10.1158/1538-7445.pancreatic24-b083\" target=\"_blank\">DOI: 10.1158/1538-7445.pancreatic24-b083</a>.","year":2024,"link":{"url":"https://doi.org/10.1158/1538-7445.pancreatic24-b083","text":"Abstract B083: The splicing factor SMNDC1 facilitates alternative RNA splicing, contributing to therapy resistance in pancreatic cancer"}},{"pubMedUid":0,"doi":"10.1158/1538-7445.pancreatic24-b079","id":null,"title":"Abstract B079: Disassembly of embryonic keratin filaments promotes pancreatic cancer metastases","citation":"Yugawa D, Kawalerski R, Gonçalves M, Pan C, Tseng R, Roa-Pena L, Leiton C, Torre-Healy L, Boyle T, Chowdhury S, Snider N, Shroyer K, <strong>Escobar-Hoyos L</strong>. Abstract B079: Disassembly of embryonic keratin filaments promotes pancreatic cancer metastases. Cancer Research 2024, 84: b079-b079. <a href=\"https://doi.org/10.1158/1538-7445.pancreatic24-b079\" target=\"_blank\">DOI: 10.1158/1538-7445.pancreatic24-b079</a>.","year":2024,"link":{"url":"https://doi.org/10.1158/1538-7445.pancreatic24-b079","text":"Abstract B079: Disassembly of embryonic keratin filaments promotes pancreatic cancer metastases"}},{"pubMedUid":0,"doi":"10.1158/1538-7445.pancreatic24-c031","id":null,"title":"Abstract C031: Keratin 17 promotes pancreatic cancer chemoresistance through mitochondrial translocation and stabilization of dihydroorotate dehydrogenase (DHODH)","citation":"Lyu Y, Ghosh M, Pan C, Sarkar S, Rajacharya G, Chen B, Marchenko N, Singh P, Shroyer K, <strong>Escobar-Hoyos L</strong>. Abstract C031: Keratin 17 promotes pancreatic cancer chemoresistance through mitochondrial translocation and stabilization of dihydroorotate dehydrogenase (DHODH). Cancer Research 2024, 84: c031-c031. <a href=\"https://doi.org/10.1158/1538-7445.pancreatic24-c031\" target=\"_blank\">DOI: 10.1158/1538-7445.pancreatic24-c031</a>.","year":2024,"link":{"url":"https://doi.org/10.1158/1538-7445.pancreatic24-c031","text":"Abstract C031: Keratin 17 promotes pancreatic cancer chemoresistance through mitochondrial translocation and stabilization of dihydroorotate dehydrogenase (DHODH)"}},{"pubMedUid":0,"doi":"10.1158/1538-7445.pancreatic24-c070","id":null,"title":"Abstract C070: Keratin 17 and GATA6 correlate with diffusely infiltrative versus gland-forming components of PDAC: Uncovering the transitional state in pancreatic ductal adenocarcinoma","citation":"Delgado- Coka L, Nelson B, Horowitz M, Sarkar S, Marchenko N, Powers S, <strong>Escobar-Hoyos L</strong>, Shroyer K. Abstract C070: Keratin 17 and GATA6 correlate with diffusely infiltrative versus gland-forming components of PDAC: Uncovering the transitional state in pancreatic ductal adenocarcinoma. Cancer Research 2024, 84: c070-c070. <a href=\"https://doi.org/10.1158/1538-7445.pancreatic24-c070\" target=\"_blank\">DOI: 10.1158/1538-7445.pancreatic24-c070</a>.","year":2024,"link":{"url":"https://doi.org/10.1158/1538-7445.pancreatic24-c070","text":"Abstract C070: Keratin 17 and GATA6 correlate with diffusely infiltrative versus gland-forming components of PDAC: Uncovering the transitional state in pancreatic ductal adenocarcinoma"}},{"pubMedUid":0,"doi":"10.1183/13993003.congress-2024.oa953","id":null,"title":"Dissecting the immune cell niche in pulmonary sarcoidosis – CXCL10+ monocyte-derived macrophages are potential drivers of TH17.1 inflammation","citation":"Ruwisch J, Schupp J, Bartkute B, Artysh N, <strong>Kaminski N</strong>, Prasse A. Dissecting the immune cell niche in pulmonary sarcoidosis – CXCL10+ monocyte-derived macrophages are potential drivers of TH17.1 inflammation. 2024, oa953. <a href=\"https://doi.org/10.1183/13993003.congress-2024.oa953\" target=\"_blank\">DOI: 10.1183/13993003.congress-2024.oa953</a>.","year":2024,"link":{"url":"https://doi.org/10.1183/13993003.congress-2024.oa953","text":"Dissecting the immune cell niche in pulmonary sarcoidosis – CXCL10+ monocyte-derived macrophages are potential drivers of TH17.1 inflammation"}},{"pubMedUid":0,"doi":"10.1183/13993003.congress-2024.oa985","id":null,"title":"Single-nuclei RNA-seq reveals aberrant cell populations in restrictive allograft syndrome after lung transplantation","citation":"Leiber L, Christian L, Neubert L, Yilmaz H, Kamp J, Plucinski E, Welte T, Falk C, <strong>Kaminski N</strong>, Jonigk* D, Gottlieb* J, Schupp* J. Single-nuclei RNA-seq reveals aberrant cell populations in restrictive allograft syndrome after lung transplantation. 2024, oa985. <a href=\"https://doi.org/10.1183/13993003.congress-2024.oa985\" target=\"_blank\">DOI: 10.1183/13993003.congress-2024.oa985</a>.","year":2024,"link":{"url":"https://doi.org/10.1183/13993003.congress-2024.oa985","text":"Single-nuclei RNA-seq reveals aberrant cell populations in restrictive allograft syndrome after lung transplantation"}},{"pubMedUid":39261628,"doi":"10.1038/s42255-024-01121-9","id":null,"title":"Organization of a functional glycolytic metabolon on mitochondria for metabolic efficiency","citation":"Wang H, Vant J, Zhang A, Sanchez R, Wu Y, Micou M, Luczak V, Whiddon Z, Carlson N, Yu S, Jabbo M, Yoon S, Abushawish A, Ghassemian M, Masubuchi T, Gan Q, Watanabe S, Griffis E, <strong>Hammarlund M</strong>, Singharoy A, Pekkurnaz G. Organization of a functional glycolytic metabolon on mitochondria for metabolic efficiency. Nature Metabolism 2024, 6: 1712-1735. <a href=\"https://pubmed.ncbi.nlm.nih.gov/39261628\" target=\"_blank\">PMID: 39261628</a>, <a href=\"https://doi.org/10.1038/s42255-024-01121-9\" target=\"_blank\">DOI: 10.1038/s42255-024-01121-9</a>.","year":2024,"link":{"url":"https://pubmed.ncbi.nlm.nih.gov/39261628","text":"Organization of a functional glycolytic metabolon on mitochondria for metabolic efficiency"}},{"pubMedUid":39258548,"doi":"10.1093/nar/gkae769","id":null,"title":"HIV-1 usurps mixed-charge domain-dependent CPSF6 phase separation for higher-order capsid binding, nuclear entry and viral DNA integration","citation":"Jang S, Bedwell G, Singh S, Yu H, Arnarson B, Singh P, Radhakrishnan R, Douglas A, Ingram Z, Freniere C, Akkermans O, Sarafianos S, Ambrose Z, <strong>Xiong Y</strong>, Anekal P, Llopis P, KewalRamani V, Francis A, Engelman A. HIV-1 usurps mixed-charge domain-dependent CPSF6 phase separation for higher-order capsid binding, nuclear entry and viral DNA integration. 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