未登录 The genetic heterogeneity and mutational burden of engineered melanomas in zebrafish models Yen, Jennifer; White, Richard M.; Wedge, David C.; Van Loo, Peter; de Ridder, Jeroen; Capper, Amy; Richardson, Jennifer; Jones, David; Raine, Keiran; Watson, Ian R.; Wu, Chang-Jiun; Cheng, Jiqiu; Martincorena, Inigo; Nik-Zainal, Serena; Mudie, Laura; Moreau, Yves; Marshall, John; Ramakrishna, Manasa; Tarpey, Patrick; Shlien, Adam; Whitmore, Ian; Gamble, Steve; Latimer, Calli; Langdon, Erin; Kaufman, Charles; Dovey, Mike; Taylor, Alison; Menzies, Andy; McLaren, Stuart; O'Meara, Sarah; Butler, Adam; Teague, Jon; Lister, James; Chin, Lynda; Campbell, Peter; Adams, David J.; Zon, Leonard I.; Patton, E. Elizabeth; Stemple, Derek L.; Futreal, P. Andy 分享 收藏
Cancer Genomics, Epigenetics and Genomic Instability. Mutational Processes Shaping the Genomes of Twenty-one Breast Cancers Nik-Zainal, S.; Alexandrov, L.; Wedge, D.; Van Loo, P.; Raine, K.; Jones, D. R.; Futreal, P. A.; Campbell, P. J.; Stratton, M. R. 分享 收藏
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Data mining using the Catalogue of Somatic Mutations in Cancer BioMart Shepherd, Rebecca; Forbes, Simon A.; Beare, David; Bamford, S.; Cole, Charlotte G.; Ward, Sari; Bindal, Nidhi; Gunasekaran, Prasad; Jia, Mingming; Kok, Chai Yin; Leung, Kenric; Menzies, Andrew; Butler, Adam P.; Teague, Jon W.; Campbell, Peter J.; Stratton, Michael R.; Futreal, P. Andrew 分享 收藏
DICER1 syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndrome Slade, Ingrid; Bacchelli, Chiara; Davies, Helen; Murray, Anne; Abbaszadeh, Fatemeh; Hanks, Sandra; Barfoot, Rita; Burke, Amos; Chisholm, Julia; Hewitt, Martin; Jenkinson, Helen; King, Derek; Morland, Bruce; Pizer, Barry; Prescott, Katrina; Saggar, Anand; Side, Lucy; Traunecker, Heidi; Vaidya, Sucheta; Ward, Paul; Futreal, P. Andrew; Vujanic, Gordan; Nicholson, Andrew G.; Sebire, Neil; Turnbull, Clare; Priest, John R.; Pritchard-Jones, Kathryn; Houlston, Richard; Stiller, Charles; Stratton, Michael R.; Douglas, Jenny; Rahman, Nazneen 分享 收藏
The original Lujan syndrome family has a novel missense mutation (p. N1007S) in the MED12 gene Schwartz, Charles E.; Tarpey, Patrick S.; Lubs, Herbert A.; Verloes, Alain; May, Melanie M.; Risheg, Hiba; Friez, Michael J.; Futreal, P. Andrew; Edkins, Sarah; Teague, Jon; Briault, Sylvain; Skinner, Cindy; Bauer-Carlin, Astrid; Simensen, Richard J.; Joseph, Sumy M.; Jones, Julie R.; Gecz, Josef; Stratton, Michael R.; Raymond, Lucy; Stevenson, Roger E. 分享 收藏
COSMIC 2005 Forbes, S; Clements, J; Dawson, E; Bamford, S; Webb, T; Dogan, A; Flanagan, A; Teague, J; Wooster, R; Futreal, PA; Stratton, MR 分享 收藏
The COSMIC (Catalogue of Somatic Mutations in Cancer) database and website COSMIC (癌症体细胞突变目录) 数据库和网站 Bamford, S; Dawson, E; Forbes, S; Clements, J; Pettett, R; Dogan, A; Flanagan, A; Teague, J; Futreal, PA; Stratton, MR; Wooster, R 分享 收藏
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