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Primary and Secondary Kinase Genotypes Correlate With the Biological and Clinical Activity of Sunitinib in Imatinib-Resistant Gastrointestinal Stromal Tumor

Data up to Jan 2025

Published2008
Citations726
References41

Total Citations Per Year

Abstract

References (41)

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2006 • 793 citations

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Polyclonal Evolution of Multiple Secondary KIT Mutations in Gastrointestinal Stromal Tumors under Treatment with Imatinib Mesylate

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2007 • 338 citations

A Missense Mutation in KIT Kinase Domain 1 Correlates with Imatinib Resistance in Gastrointestinal Stromal Tumors

2004 • 338 citations

A new mutation in the KIT ATP pocket causes acquired resistance to imatinib in a gastrointestinal stromal tumor patient

2004 • 324 citations

SU11248 inhibits tumor growth and CSF-1R-dependent osteolysis in an experimental breast cancer bone metastasis model

2003 • 305 citations

An Orally Administered Multitarget Tyrosine Kinase Inhibitor, SU11248, Is a Novel Potent Inhibitor of Thyroid Oncogenic RET/Papillary Thyroid Cancer Kinases

2006 • 284 citations

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2005 • 280 citations

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2006 • 274 citations

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2005 • 188 citations

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2004 • 180 citations

Sorafenib Inhibits the Imatinib-Resistant KIT T670I Gatekeeper Mutation in Gastrointestinal Stromal Tumor

2007 • 142 citations

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2005 • 111 citations

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2006 • 110 citations

Late resistance to imatinib therapy in a metastatic gastrointestinal stromal tumour is associated with a second KIT mutation

2004 • 93 citations

Sunitinib (SU) response in imatinib-resistant (IM-R) GIST correlates with KIT and PDGFRA mutation status

2006 • 84 citations

Imatinib binding and cKIT inhibition is abrogated by the cKIT kinase domain I missense mutation Val654Ala

2005 • 74 citations

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2005 • 10 citations

Synthesis and Antimelanoma Activity of Reversed Amide Analogues of N-Acetyl-4-S-cysteaminylphenol

2006 • 9 citations

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Primary and Secondary Kinase Genotypes Correlate With the Biological and Clinical… (2008) – Journal of Clinical Oncology | Metascience Observatory Explorer