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Dusko Ilic

Researcher at King's College London

Publications -  208
Citations -  14204

Dusko Ilic is an academic researcher from King's College London. The author has contributed to research in topics: Stem cell & Regenerative medicine. The author has an hindex of 47, co-authored 188 publications receiving 13276 citations. Previous affiliations of Dusko Ilic include University of Cambridge & Kumamoto University.

Papers
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Journal ArticleDOI

Reduced cell motility and enhanced focal adhesion contact formation in cells from FAK-deficient mice

TL;DR: Surprisingly, the number of focal adhesions was increased in FAK-deficient cells, suggesting that FAK may be involved in the turnover of focalAdhesion contacts during cell migration.

FAK integrates growth-factor and integrin signals to promote cell

TL;DR: In this article, the authors show that cells lacking focal adhesion kinase (FAK) are refractory to motility signals from platelet-derived and epidermal growth factors (PDGF and EGF respectively), and that stable re-expression of FAK rescues these defects.
Journal ArticleDOI

FAK integrates growth-factor and integrin signals to promote cell migration

TL;DR: It is shown that cells lacking focal adhesion kinase (FAK) are refractory to motility signals from platelet-derived and epidermal growth factors (PDGF and EGF respectively), and that stable re-expression of FAK rescues these defects.
Journal ArticleDOI

Differential regulation of cell motility and invasion by FAK

TL;DR: It is shown that viral Src transformation of FAK−/− cells promotes integrin-stimulated motility equal to stable FAK reexpression, and a dual role for FAK in promoting cell motility and invasion through the activation of distinct signaling pathways.
Journal ArticleDOI

Extracellular Matrix Survival Signals Transduced by Focal Adhesion Kinase Suppress p53-mediated Apoptosis

TL;DR: It is reported that survival signals from fibronectin are transduced by the focal adhesion kinase (FAK) in anchorage- dependent cells, and this is the first report that p53 monitors survival signal from ECM/FAK in anch Anchorage-dependent cells.