Results 11 to 20 of about 52,035 (209)

FAK deletion promotes p53-mediated induction of p21, DNA-damage responses and radio-resistance in advanced squamous cancer cells. [PDF]

open access: yesPLoS ONE, 2011
Focal adhesion kinase (FAK) is a cytoplasmic tyrosine kinase that is elevated in a variety of human cancers. While FAK is implicated in many cellular processes that are perturbed in cancer, including proliferation, actin and adhesion dynamics ...
Kathryn Graham   +4 more
doaj   +2 more sources

The direct effect of Focal Adhesion Kinase (FAK), dominant-negative FAK, FAK-CD and FAK siRNA on gene expression and human MCF-7 breast cancer cell tumorigenesis [PDF]

open access: yesBMC Cancer, 2009
Background Focal adhesion kinase (FAK) is a non-receptor tyrosine kinase that plays an important role in survival signaling. FAK has been shown to be overexpressed in breast cancer tumors at early stages of tumorigenesis.
Zhang Li   +4 more
doaj   +3 more sources

Altering FAK-paxillin interactions reduces adhesion, migration and invasion processes. [PDF]

open access: yesPLoS ONE, 2014
Focal adhesion kinase (FAK) plays an important role in signal transduction pathways initiated at sites of integrin-mediated cell adhesion to the extracellular matrix.
Thérèse B Deramaudt   +6 more
doaj   +3 more sources

Modelling stromal FAK regulation of tumour growth, angiogenesis and progression [PDF]

open access: yes, 2012
PhDThe growth of tumours within a whole organism depends on the tumour microenvironment. This involves both resident stromal cells, such as endothelial cells and fibroblasts, and also bone marrow derived stromal cells.
Batista, Silvia
core   +4 more sources

Transcending Traditional Treatment: The Therapeutical Potential of Nanovesicles for Transdermal Baclofen Delivery in Repeated Traumatic Brain Injury [PDF]

open access: yesAdvanced Pharmaceutical Bulletin
Purpose: The repositioning of previously approved drugs is occupying the researchers’ plans. Baclofen (Bac) was our candidate for its established neuroprotective capacity, with a proposal of efficient drug delivery as non-ionic surfactant-based ...
Nermin M. Sheta   +5 more
doaj   +1 more source

Epidermal Growth Factor Receptor substrate 8 (Eps8) controls Src/FAK-dependent phenotypes in squamous carcinoma cells [PDF]

open access: yes, 2014
Eps8 is an actin regulatory scaffold protein increased in Squamous Cell Carcinoma (SCC) cells. It forms a complex with both Focal Adhesion Kinase (FAK) and c-Src in SCC cells derived from the DMBA/TPA model of skin carcinogenesis.
Schoenherr, Christina   +13 more
core   +1 more source

ZINC40099027 activates human focal adhesion kinase by accelerating the enzymatic activity of the FAK kinase domain

open access: yesPharmacology Research & Perspectives, 2021
Focal adhesion kinase (FAK) regulates gastrointestinal epithelial restitution and healing. ZINC40099027 (Zn27) activates cellular FAK and promotes intestinal epithelial wound closure in vitro and in mice.
Rashmi   +5 more
doaj   +1 more source

Cortactin as a target for FAK in the regulation of focal adhesion dynamics. [PDF]

open access: yesPLoS ONE, 2012
Efficient cell movement requires the dynamic regulation of focal adhesion (FA) formation and turnover. FAs are integrin-associated sites of cell attachment and establish linkages to the cellular actin cytoskeleton.
Alok Tomar   +3 more
doaj   +1 more source

Drug Discovery Targeting Focal Adhesion Kinase (FAK) as a Promising Cancer Therapy

open access: yesMolecules, 2021
FAK is a nonreceptor intracellular tyrosine kinase which plays an important biological function. Many studies have found that FAK is overexpressed in many human cancer cell lines, which promotes tumor cell growth by controlling cell adhesion, migration ...
Xiao-Jing Pang   +10 more
doaj   +1 more source

Focal Adhesion Kinase (FAK) tyrosine 397E mutation restores the vascular leakage defect in endothelium-specific FAK-kinase dead mice [PDF]

open access: yes, 2017
Focal adhesion kinase (FAK) inhibitors have been developed as potential anti-cancer agents and are in clinical trials. In vitro activation of FAK kinase domain triggers autophosphorylation of tyrosine 397 (Y397), Src activation and subsequent ...
Lees, Delphine M   +33 more
core   +1 more source

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