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SCIENTIFIC REPORTS (2019)
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FAK Inhibition Abrogates the Malignant Phenotype in Aggressive Pediatric Renal Tumors
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Abstract A249: BI 853520, a potent and highly selective inhibitor of protein tyrosine kinase 2 (focal adhesion kinase), shows efficacy in multiple xenograft models of human cancer.
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Adrenergic modulation of focal adhesion kinase protects human ovarian cancer cells from anoikis
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Proline-rich tyrosine kinase-2 is critical for CD8 T-cell short-lived effector fate
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Sunitinib and PF-562,271 (FAK/Pyk2 inhibitor) effectively block growth and recovery of human hepatocellular carcinoma in a rat xenograft model
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CANCER BIOLOGY & THERAPY (2009)
Regulation of heterochromatin remodelling and myogenin expression during muscle differentiation by FAK interaction with MBD2
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EMBO JOURNAL (2009)
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CANCER RESEARCH (2008)
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JOURNAL OF CELL BIOLOGY (2008)
PyK2 and FAK connections to p190Rho guanine nucleotide exchange factor regulate RhoA activity, focal adhesion formation, and cell motility
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JOURNAL OF CELL BIOLOGY (2008)
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JOURNAL OF MEDICINAL CHEMISTRY (2008)
Nuclear FAK promotes cell proliferation and survival through FERM-enhanced p53 degradation
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MOLECULAR CELL (2008)
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JOURNAL OF CELL SCIENCE (2007)
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JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
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