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Paper Details

Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
Nat Biotechnol
534
2016
275 genes, 470 somatic substitution hotspots, Mutational hotspots, RAC1, RRAS2, Ras, allele, amino acid, cancer, hotspots, human, human tumors, mutant allele, mutational hotspots, recurrently mutated genes, small GTPases, tumor, tumor samples, tumors
Author NameAffiliation
Saurabh AsthanaUniversity of California san francisco
Saurabh AsthanaUniversity of California san francisco
Cyriac KandothMarie-Josee and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center
Jianjiong GaoMarie-Josee and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center
Jianjiong GaoMarie-Josee and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center
Nicholas D SocciMarie-Josee and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center
Nicholas D SocciMemorial Sloan Kettering Cancer Center
Adam B OlshenUniversity of California san francisco
Adam B OlshenHelen Diller Family Comprehensive Cancer Center, University of California san francisco
Nikolaus SchultzMemorial Sloan Kettering Cancer Center
Nikolaus SchultzMarie-Josee and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center
Nikolaus SchultzMemorial Sloan Kettering Cancer Center
Nikolaus SchultzMarie-Josee and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center
Barry S TaylorMemorial Sloan Kettering Cancer Center
Barry S TaylorMemorial Sloan Kettering Cancer Center
Barry S TaylorMarie-Josee and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center
Barry S TaylorMemorial Sloan Kettering Cancer Center
Barry S TaylorMemorial Sloan Kettering Cancer Center
Barry S TaylorMarie-Josee and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center
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