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Nature Genetics|March 26, 2013
Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexityAustin M Dulak, Petar Stojanov, Shouyong Peng, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 21, 2012
Discovery and prioritization of somatic mutations in diffuse large B-cell lymphoma (DLBCL) by whole-exome sequencingJens G Lohr, Petar Stojanov, Michael S Lawrence, et al.
Nature Genetics|September 6, 2011
Genomic sequencing of colorectal adenocarcinomas identifies a recurrent VTI1A-TCF7L2 fusionAdam J Bass, Michael S Lawrence, Lear E Brace, et al.
Cancer Cell|July 4, 2009
AKT-independent signaling downstream of oncogenic PIK3CA mutations in human cancerKrishna M Vasudevan, David A Barbie, Michael A Davies, et al.
American Journal of Human Genetics|August 5, 2005
A high-density screen for linkage in multiple sclerosisStephen Sawcer, Maria Ban, Mel Maranian, et al.
Cell|July 27, 2019
Small Molecule Targets TMED9 and Promotes Lysosomal Degradation to Reverse ProteinopathyMoran Dvela-Levitt, Maria Kost-Alimova, Maheswarareddy Emani, et al.
Nature Communications|August 25, 2018
Deep-coverage whole genome sequences and blood lipids among 16,324 individualsPradeep Natarajan, Gina M Peloso, Seyedeh Maryam Zekavat, et al.
Nature|October 14, 2011
A high-resolution map of human evolutionary constraint using 29 mammalsKerstin Lindblad-Toh, Manuel Garber, Or Zuk, et al.
Science (New York, N.Y.)|July 30, 2011
The mutational landscape of head and neck squamous cell carcinomaNicolas Stransky, Ann Marie Egloff, Aaron D Tward, et al.
Cell|July 24, 2012
A landscape of driver mutations in melanomaEran Hodis, Ian R Watson, Gregory V Kryukov, et al.
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