Ontology highlight
ABSTRACT:
SUBMITTER: Greenman C
PROVIDER: S-EPMC2712719 | biostudies-literature | 2007 Mar
REPOSITORIES: biostudies-literature
Greenman Christopher C Stephens Philip P Smith Raffaella R Dalgliesh Gillian L GL Hunter Christopher C Bignell Graham G Davies Helen H Teague Jon J Butler Adam A Stevens Claire C Edkins Sarah S O'Meara Sarah S Vastrik Imre I Schmidt Esther E EE Avis Tim T Barthorpe Syd S Bhamra Gurpreet G Buck Gemma G Choudhury Bhudipa B Clements Jody J Cole Jennifer J Dicks Ed E Forbes Simon S Gray Kris K Halliday Kelly K Harrison Rachel R Hills Katy K Hinton Jon J Jenkinson Andy A Jones David D Menzies Andy A Mironenko Tatiana T Perry Janet J Raine Keiran K Richardson Dave D Shepherd Rebecca R Small Alexandra A Tofts Calli C Varian Jennifer J Webb Tony T West Sofie S Widaa Sara S Yates Andy A Cahill Daniel P DP Louis David N DN Goldstraw Peter P Nicholson Andrew G AG Brasseur Francis F Looijenga Leendert L Weber Barbara L BL Chiew Yoke-Eng YE DeFazio Anna A Greaves Mel F MF Green Anthony R AR Campbell Peter P Birney Ewan E Easton Douglas F DF Chenevix-Trench Georgia G Tan Min-Han MH Khoo Sok Kean SK Teh Bin Tean BT Yuen Siu Tsan ST Leung Suet Yi SY Wooster Richard R Futreal P Andrew PA Stratton Michael R MR
Nature 20070301 7132
Cancers arise owing to mutations in a subset of genes that confer growth advantage. The availability of the human genome sequence led us to propose that systematic resequencing of cancer genomes for mutations would lead to the discovery of many additional cancer genes. Here we report more than 1,000 somatic mutations found in 274 megabases (Mb) of DNA corresponding to the coding exons of 518 protein kinase genes in 210 diverse human cancers. There was substantial variation in the number and patt ...[more]