Keywords: |
protein expression; treatment response; leukemia; gene mutation; mutation; proto-oncogene proteins; clinical trial; erlotinib; drug efficacy; note; imatinib; melanoma; neoplasm recurrence, local; map kinase signaling system; lung cancer; enzyme activation; drug resistance, neoplasm; dasatinib; chronic myeloid leukemia; cancer therapy; cancer resistance; protein kinase inhibitors; cancer inhibition; oncogene; gene expression regulation, neoplastic; sulfonamides; tumor cell; extracellular signal-regulated map kinases; adenosine triphosphate; nilotinib; indoles; b raf kinase; mitogen-activated protein kinase kinases; drug binding; proto-oncogene proteins b-raf; plx 4032; proto-oncogene proteins c-raf; gastrointestinal tumor; map kinase kinase kinases; mitogen activated protein kinase 11
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