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Hao Zhou

Researcher at Regeneron

Publications -  5
Citations -  3993

Hao Zhou is an academic researcher from Regeneron. The author has contributed to research in topics: Vascular endothelial growth factor & Angiopoietin. The author has an hindex of 5, co-authored 5 publications receiving 3909 citations. Previous affiliations of Hao Zhou include University of Texas Southwestern Medical Center.

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Angiopoietin-1 protects the adult vasculature against plasma leakage.

TL;DR: It is shown that acute administration of angiopoietin-1 does indeed protect adult vasculature from leaking, countering the potentially lethal actions of VEGF and inflammatory agents.
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Essential role for oncogenic Ras in tumour maintenance

TL;DR: The results provide genetic evidence that H-RasV12G is important in both the genesis and maintenance of solid tumours, and the failure of persistent endogenous and enforced VEGF expression to sustain tumour viability indicates that the tumour-maintaining actions of activated Ras extend beyond the regulation of V EGF expression in vivo.
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Increased Vascularization in Mice Overexpressing Angiopoietin-1

TL;DR: It is shown that transgenic overexpression of angiopoietin-1 in the skin of mice produces larger, more numerous, and more highly branched vessels, raising the possibility that angioietins can be used, alone or in combination with VEGF to promote therapeutic angiogenesis.
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Angiopoietins 3 and 4: Diverging gene counterparts in mice and humans

TL;DR: The angiopoietins have recently joined the members of the vascular endothelial growth factor family as the only known growth factors largely specific for vascular endothelium as discussed by the authors, and they include a naturally occurring agonist, angioietin-1, as well as an naturally occurring antagonist, angiopooietin2, both of which act by means of the Tie2 receptor.

Angiopoietins 3 and 4: Diverging gene counterparts in mice and humans (angiogenesisytie receptor tyrosine kinaseyvascular endothelial growth factor)

TL;DR: Attempts to use homology-based cloning approaches to identify new members of the angiopoietin family are reported, leading to the identification of two new angioietins that appear to represent the mouse and human counterparts of the same gene locus.