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Molecular Oncology
Volume 2, Issue 2
, Pages 161-163
, August 2008
Unlucky number 13? Differential effects of KIT exon 13 mutation in gastrointestinal stromal tumors
References
- A missense mutation in KIT kinase domain 1 correlates with imatinib resistance in gastrointestinal stromal tumors. Cancer Research. 2004;64:5913–5919
- Clonal evolution of resistance to imatinib in patients with metastatic gastrointestinal stromal tumors. Clinical Cancer Research. 2007;13:5398–5405
- Molecular correlates of imatinib resistance in gastrointestinal stromal tumors. Journal of Clinical Oncology. 2006;24:4764–4774
- Clinicopathologic profile of gastrointestinal stromal tumors (GISTs) with primary KIT exon 13 or exon 17 mutations: a multicenter study on 54 cases. Modern Pathology. 2008;
- Prognostic value of KIT mutation type, mitotic activity, and histologic subtype in gastrointestinal stromal tumors. Journal of Clinical Oncology. 2002;20:3898–3905
- Functional analyses and molecular modeling of two c-Kit mutations responsible for imatinib secondary resistance in GIST patients. Oncogene. 2006;25:6140–6146
☆ Funding Source: This work was supported by an institutional Physician-Scientist Award (JCT, AJFL), NIH/NCI grant 1K23CA109060-02 (JCT), The Amschwand Sarcoma Cancer Foundation (JCT), NIH TL1 RR 024147 from the Center of Clinical and Translational Sciences at The University of Texas-Houston Health Science Center (JCM), and NIH/NCI grant K12 CA090891 (JCM). The DNA Sequencing Core Facility is supported by an NCI Cancer Center Support Grant CA-16672.
☆☆ Conflicts of Interest: None to declare.
PII: S1574-7891(08)00061-6
doi: 10.1016/j.molonc.2008.05.002
© 2008 Federation of European Biochemical Societies. Published by Elsevier Inc. All rights reserved.
« Previous
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Molecular Oncology
Volume 2, Issue 2
, Pages 161-163
, August 2008

