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American Journal of Human Genetics|December 23, 2006
Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardationPatrick S Tarpey, Claire Stevens, Jon Teague, et al.Science Translational Medicine|August 9, 2013
Genome-wide mutational signatures of aristolochic acid and its application as a screening toolSong Ling Poon, See-Tong Pang, John R McPherson, et al.Nature Communications|April 10, 2014
Processed pseudogenes acquired somatically during cancer developmentSusanna L Cooke, Adam Shlien, John Marshall, et al.Genome Medicine|August 13, 2010
Predictive biomarker discovery through the parallel integration of clinical trial and functional genomics datasetsCharles Swanton, James M Larkin, Marco Gerlinger, et al.Nature|October 25, 2019
Somatic mutations and clonal dynamics in healthy and cirrhotic human liverSimon F Brunner, Nicola D Roberts, Luke A Wylie, et al.Nature Medicine|May 26, 2022
A cellular hierarchy framework for understanding heterogeneity and predicting drug response in acute myeloid leukemiaAndy G X Zeng, Suraj Bansal, Liqing Jin, et al.Human Genetics|April 12, 2008
Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genesLane J Jaeckle Santos, Chao Xing, Robert B Barnes, et al.Science (New York, N.Y.)|May 23, 2015
Tumor evolution. High burden and pervasive positive selection of somatic mutations in normal human skinIñigo Martincorena, Amit Roshan, Moritz Gerstung, et al.Nucleic Acids Research|October 31, 2014
COSMIC: exploring the world's knowledge of somatic mutations in human cancerSimon A Forbes, David Beare, Prasad Gunasekaran, et al.Journal of Experimental & Clinical Cancer Research : CR|May 13, 2022
Immunogenomic intertumor heterogeneity across primary and metastatic sites in a patient with lung adenocarcinomaRunzhe Chen, Jun Li, Junya Fujimoto, et al.Pageof 40