Pages that link to "Q74623160"
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The following pages link to Irreversible inhibition of epidermal growth factor receptor tyrosine kinase with in vivo activity by N-[4-[(3-bromophenyl)amino]-6-quinazolinyl]-2-butynamide (CL-387,785) (Q74623160):
Displaying 28 items.
- Oncogenic transformation by inhibitor-sensitive and -resistant EGFR mutants (Q24810573) (← links)
- Induction of lateral lumens through disruption of a monoleucine-based basolateral-sorting motif in betacellulin (Q27339929) (← links)
- Importance of epidermal growth factor receptor signaling in establishment of adenomas and maintenance of carcinomas during intestinal tumorigenesis (Q28593435) (← links)
- Epidermal growth factor receptor mutations in lung cancer (Q29615474) (← links)
- Complexity of signal transduction mediated by ErbB2: clues to the potential of receptor-targeted cancer therapy. (Q33801908) (← links)
- Irreversible inhibitors of the EGF receptor may circumvent acquired resistance to gefitinib (Q33821320) (← links)
- Chemical genetics identifies small-molecule modulators of neuritogenesis involving neuregulin-1/ErbB4 signaling (Q33863150) (← links)
- A genome-wide RNA interference screen reveals an essential CREB3L2-ATF5-MCL1 survival pathway in malignant glioma with therapeutic implications (Q33900952) (← links)
- Inhibition of drug-resistant mutants of ABL, KIT, and EGF receptor kinases (Q33906140) (← links)
- The 4-anilinoquinazoline class of inhibitors of the erbB family of receptor tyrosine kinases (Q34248529) (← links)
- Epidermal growth factor receptor variant III mutations in lung tumorigenesis and sensitivity to tyrosine kinase inhibitors (Q34589789) (← links)
- Targeting the function of the HER2 oncogene in human cancer therapeutics (Q34766486) (← links)
- Perinatal epidermal growth factor receptor blockade prevents peripheral nerve disruption in a mouse model reminiscent of benign world health organization grade I neurofibroma (Q35088274) (← links)
- Induction of BIM is essential for apoptosis triggered by EGFR kinase inhibitors in mutant EGFR-dependent lung adenocarcinomas (Q36026392) (← links)
- EGFR Inhibition in the Treatment of Non-Small Cell Lung Cancer (Q37240726) (← links)
- ErbBs in lung cancer (Q37249978) (← links)
- HER-2-directed, small-molecule antagonists (Q37336019) (← links)
- The soluble protease ADAMDEC1 released from activated platelets hydrolyzes platelet membrane pro-epidermal growth factor (EGF) to active high-molecular-weight EGF. (Q38705556) (← links)
- Cellular Response to Titanium Dioxide Nanoparticles in Intestinal Epithelial Caco-2 Cells is Dependent on Endocytosis-Associated Structures and Mediated by EGFR (Q38708542) (← links)
- EGFR and myosin II inhibitors cooperate to suppress EGFR-T790M-mutant NSCLC cells (Q39390169) (← links)
- Hsp90 inhibition suppresses mutant EGFR-T790M signaling and overcomes kinase inhibitor resistance (Q39960713) (← links)
- Syntheses and EGFR and HER-2 kinase inhibitory activities of 4-anilinoquinoline-3-carbonitriles: analogues of three important 4-anilinoquinazolines currently undergoing clinical evaluation as therapeutic antitumor agents (Q40702060) (← links)
- Tumor-targeting of EGFR inhibitors by hypoxia-mediated activation (Q42173414) (← links)
- MEK (MAPKK) inhibitors. Part 2: structure-activity relationships of 4-anilino-3-cyano-6,7-dialkoxyquinolines (Q43621540) (← links)
- EGF receptor tyrosine kinase inhibition attenuates the development of PKD in Han:SPRD rats (Q44609775) (← links)
- Microwave assisted synthesis of N-arylheterocyclic substituted-4-aminoquinazoline derivatives (Q46930084) (← links)
- Combinatorial chemoprevention of intestinal neoplasia (Q74268548) (← links)
- Soluble E-cadherin promotes cell survival by activating epidermal growth factor receptor (Q83143406) (← links)