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Nature Genetics|March 14, 2017
Disruption of the ATXN1-CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humansHsiang-Chih Lu, Qiumin Tan, Maxime W C Rousseaux, et al.
Clinical and Translational Medicine|June 15, 2024
Integrative genomic analyses of European intrahepatic cholangiocarcinoma: Novel ROS1 fusion gene and PBX1 as prognostic markerPatrick S Plum, Timo Hess, Denis Bertrand, et al.
Cancer Discovery|September 13, 2017
VHL Deficiency Drives Enhancer Activation of Oncogenes in Clear Cell Renal Cell CarcinomaXiaosai Yao, Jing Tan, Kevin Junliang Lim, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 6, 2022
Transcriptome-wide subtyping of pediatric and adult T cell acute lymphoblastic leukemia in an international study of 707 casesYu-Ting Dai, Fan Zhang, Hai Fang, et al.
Nature Cell Biology|April 24, 2023
PBRM1-deficient PBAF complexes target aberrant genomic loci to activate the NF-κB pathway in clear cell renal cell carcinomaXiaosai Yao, Jing Han Hong, Amrita M Nargund, et al.
Science Translational Medicine|April 1, 2026
Uncovering BAP1 deubiquitination landscape enhances mechanism elucidation and therapeutic precision for BAP1-deficient pancancersJing Han Hong, Chern Han Yong, Hong Lee Heng, et al.
Medrxiv : the Preprint Server for Health Sciences|August 1, 2026
Human inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneityIris Fagniez, Miyuki Tsumura, Antoine Guerin, et al.
Gastroenterology|August 15, 2024
Spatially Resolved Niche and Tumor Microenvironmental Alterations in Gastric Cancer Peritoneal MetastasesJoseph J Zhao, Chin-Ann Johnny Ong, Supriya Srivastava, et al.
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