Targeted-capture massively-parallel sequencing enables robust detection of clinically informative mutations from formalin-fixed tumours-Reference-Cited by-同舟云学术

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Targeted-capture massively-parallel sequencing enables robust detection of clinically informative mutations from formalin-fixed tumours

Published:2013-12 Issue:1 Volume:3 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Wong Stephen Q.,Li Jason,Salemi Renato,Sheppard Karen E.,Hongdo Do ,Tothill Richard W.,McArthur Grant A.,Dobrovic Alexander

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep03494.pdf

Reference47 articles.

1. Hirota, S. et al. Gain-of-function mutations of c-kit in human gastrointestinal stromal tumors. Science 279, 577–580 (1998).

2. Davies, H. et al. Mutations of the BRAF gene in human cancer. Nature 417, 949–954 (2002).

3. Paez, J. G. et al. EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy. Science 304, 1497–1500 (2004).

4. Zhang, L. & Daly, R. J. Targeting the human kinome for cancer therapy: current perspectives. Critical reviews in oncogenesis 17, 233–246 (2012).

5. Ferte, C., Andre, F. & Soria, J. C. Molecular circuits of solid tumors: prognostic and predictive tools for bedside use. Nat Rev Clin Oncol 7, 367–380 (2010).

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