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Stela Gengrinovitch

Researcher at Technion – Israel Institute of Technology

Publications -  6
Citations -  4369

Stela Gengrinovitch is an academic researcher from Technion – Israel Institute of Technology. The author has contributed to research in topics: Vascular endothelial growth factor A & Vascular endothelial growth factor. The author has an hindex of 5, co-authored 6 publications receiving 4239 citations.

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Vascular endothelial growth factor (VEGF) and its receptors

TL;DR: Recent developments that have widened considerably the understanding of the mechanisms that control V EGF production and VEGF signal transduction are focused on and recent studies that have shed light on the mechanisms by which VEGf regulates angiogenesis are reviewed.
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Platelet factor-4 inhibits the mitogenic activity of vegf121 and vegf165 using several concurrent mechanisms

TL;DR: PF4 can bind to heparin binding proteins such as VEGF165 leading to an inhibition of their receptor binding ability, and it is observed that PF4 inhibits efficiently the V EGF165 induced proliferation of vascular endothelial cells.
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Glypican-1 Is a VEGF165 Binding Proteoglycan That Acts as an Extracellular Chaperone for VEGF165

TL;DR: It is suggested that glypican-1 may play an important role in the control of angiogenesis by regulating the activity of VEGF165, a regulation that may be critical under conditions such as wound repair, in which oxidizing agents that can impair theActivity of V EGF are produced, and in situations were the concentrations of active VEGf are limiting.
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Selective Binding of VEGF121 to One of the Three Vascular Endothelial Growth Factor Receptors of Vascular Endothelial Cells (

TL;DR: Experiments suggest that alternative splicing can generate a diversity in growth factor signaling by determining receptor recognition patterns and indicate that the heparin binding ability of VEGF may enable the restoration of damaged V EGF function in processes such as inflammation or wound healing.
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Abnormal deposition of collagen around hepatocytes in Wilson's disease is associated with hepatocyte specific expression of lysyl oxidase and lysyl oxidase like protein-2.

TL;DR: The upregulation of Lox and Loxl2 in Wilson's disease could perhaps be utilized for diagnostic purposes since their expression is up-regulated in hepatocytes even before the onset of fibrosis.