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Matthew J. Hart

Researcher at University of Texas Health Science Center at San Antonio

Publications -  65
Citations -  8264

Matthew J. Hart is an academic researcher from University of Texas Health Science Center at San Antonio. The author has contributed to research in topics: GTPase & Guanine nucleotide exchange factor. The author has an hindex of 32, co-authored 55 publications receiving 7912 citations. Previous affiliations of Matthew J. Hart include Harvard University & Buck Institute for Research on Aging.

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Downregulation of β-catenin by human Axin and its association with the APC tumor suppressor, β-catenin and GSK3β

TL;DR: Overexpression of hAxin strongly promoted the downregulation of wild-type β -catenin in colon cancer cells, whereas mutant oncogenic β -Catenin was unaffected, suggesting that APC may function to derepress Axin activity.
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p115 RhoGEF, a GTPase activating protein for Gα12 and Gα13

TL;DR: Members of the regulators of G protein signaling (RGS) family stimulate the intrinsic guanosine triphosphatase (GTPase) activity of the α subunits of certain heterotrimeric guanine nucleotide–binding proteins (G proteins).
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Direct Stimulation of the Guanine Nucleotide Exchange Activity of p115 RhoGEF by Gα13

TL;DR: The GTPase activities of two G protein alpha subunits, Galpha12 and Galpha13, are stimulated by the Rho guanine nucleotide exchange factor p115 RhoGEF, which can directly link heterotrimeric G proteinalpha subunits to regulation of Rho.
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The F-box protein β-TrCP associates with phosphorylated β-catenin and regulates its activity in the cell

TL;DR: It is concluded that β-TrCP is a component of an E3 ubiquitin ligase that is responsible for the targeted degradation of phosphorylated β-catenin.