scispace - formally typeset
Y

Yaowu Zheng

Researcher at Northeast Normal University

Publications -  63
Citations -  7439

Yaowu Zheng is an academic researcher from Northeast Normal University. The author has contributed to research in topics: Gene & Thrombin. The author has an hindex of 22, co-authored 58 publications receiving 7022 citations. Previous affiliations of Yaowu Zheng include University of California, San Francisco & United States Department of Veterans Affairs.

Papers
More filters
Journal ArticleDOI

Identification of a gene encoding an acyl CoA:diacylglycerol acyltransferase, a key enzyme in triacylglycerol synthesis

TL;DR: An expressed sequence tag clone that shared regions of similarity with acyl CoA:cholesterol acyltransferase, an enzyme that also uses fatty acyl coA as a substrate was identified, which will greatly facilitate studies of cellular glycerolipid metabolism and its regulation.
Journal ArticleDOI

A dual thrombin receptor system for platelet activation

TL;DR: It is reported that thrombin responses in platelets from PAR3-deficient mice were markedly delayed and diminished but not absent, and the identification of a two-receptor system for platelet activation byThrombin has important implications for the development of antithrombotic therapies.
Journal ArticleDOI

Protease-activated receptor 3 is a second thrombin receptor in humans.

TL;DR: Cl cloning and characterization of a new human thrombin receptor, designated protease-activated receptor 3 (PAR3) is reported, which can mediate throm-bin-triggered phosphoinositide hydrolysis and is expressed in a variety of tissues, making it a candidate for the sought-after second platelet throm bin receptor.
Journal ArticleDOI

Promotion of Lymphocyte Egress into Blood and Lymph by Distinct Sources of Sphingosine-1-Phosphate

TL;DR: Separate sources provide S1P to plasma and lymph to help lymphocytes exit the low-S1P environment of lymphoid organs, and disruption of compartmentalized S 1P signaling is a plausible mechanism by which S1p-receptor-1 agonists function as immunosuppressives.
Journal ArticleDOI

PAR3 is a cofactor for PAR4 activation by thrombin

TL;DR: This article showed that mPAR3 does not itself mediate transmembrane signalling but instead functions as a cofactor for the cleavage and activation of mPAR4 by thrombin.