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PLX4032

Known as: B-Raf inhibitor PLX4032, PLX 4032, PLX-4032 
National Institutes of Health

Papers overview

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Highly Cited
2014
Highly Cited
2014
Tumor angiogenesis is essential for tumor growth and metastasis and is dependent on key angiogenic factors. Angiogenin (ANG), a… 
Highly Cited
2013
Highly Cited
2013
Resistance to BRAF inhibitor therapy places priority on developing BRAF inhibitor-based combinations that will overcome de novo… 
Highly Cited
2010
Highly Cited
2010
3534 Background: The BRAF activating mutation is present in up to 10% of metastatic colorectal carcinomas (mCRC) and is… 
Review
2010
Review
2010
The promise of personalised medicine is now a clinical reality, with colorectal cancer genetics at the forefront of this next… 
Highly Cited
2010
Highly Cited
2010
Blocking oncogenic signaling induced by the BRAFV600E mutation is a promising approach for melanoma treatment. We tested the anti… 
Highly Cited
2010
Highly Cited
2010
Targeted intervention of the B‐Raf V600E gene product that is prominent in melanoma has been met with modest success. Here, we… 
Review
2010
Review
2010
PLX-4032 is a small-molecule, orally available B-Raf kinase inhibitor being developed by Plexxikon Inc and Hoffman-La Roche Ltd… 
Highly Cited
2008
Highly Cited
2008
BRAF-activating mutations have been reported in several types of cancer, including melanoma (∼70% of cases), thyroid (30-70…