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Cell Reports. Medicine|April 12, 2023
MYC activation impairs cell-intrinsic IFNγ signaling and confers resistance to anti-PD1/PD-L1 therapy in lung cancerJuan J Alburquerque-Bejar, Pablo Navajas-Chocarro, Maria Saigi, et al.
Thorax|July 13, 2021
Latent class analysis-derived subphenotypes are generalisable to observational cohorts of acute respiratory distress syndrome: a prospective studyPratik Sinha, Kevin L Delucchi, Yue Chen, et al.
Nature Communications|July 15, 2021
SMARCA4 deficient tumours are vulnerable to KDM6A/UTX and KDM6B/JMJD3 blockadeOctavio A Romero, Andrea Vilarrubi, Juan J Alburquerque-Bejar, et al.
American Journal of Respiratory and Critical Care Medicine|January 20, 2022
Cigarette Smoke Exposure and Acute Respiratory Distress Syndrome in Sepsis: Epidemiology, Clinical Features, and Biologic MarkersFarzad Moazed, Carolyn Hendrickson, Alejandra Jauregui, et al.
American Journal of Respiratory and Critical Care Medicine|January 8, 2024
Host and Microbe Blood Metagenomics Reveals Key Pathways Characterizing Critical Illness PhenotypesLucile P A Neyton, Pratik Sinha, Aartik Sarma, et al.
Frontiers in Oncology|May 22, 2024
Outcomes and patterns of use of Radium-223 in metastatic castration-resistant prostate cancerUrbano Anido-Herranz, Ovidio Fernandez-Calvo, Juan Ruiz-Bañobre, et al.
Cancer Research|August 10, 2014
A comprehensive DNA methylation profile of epithelial-to-mesenchymal transitionF Javier Carmona, Veronica Davalos, Enrique Vidal, et al.
The Journal of Clinical Investigation|September 18, 2018
Ubiquitin ligase RNF8 suppresses Notch signaling to regulate mammary development and tumorigenesisLi Li, Kiran Kumar Naidu Guturi, Brandon Gautreau, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 9, 2016
Epigenetic inactivation of the p53-induced long noncoding RNA TP53 target 1 in human cancerAngel Diaz-Lagares, Ana B Crujeiras, Paula Lopez-Serra, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2015
Mutations in JMJD1C are involved in Rett syndrome and intellectual disabilityMauricio A Sáez, Juana Fernández-Rodríguez, Catia Moutinho, et al.
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