Matthew J. Hart - Concepedia

Author

Matthew J. Hart

The University of Texas Health Science Center at San Antonio ORCID

Also Known As

Hart, M, Hart, Matthew J, Hussong, Stacy A, J. Hart, Matthew, M Hart, M J Hart, M Papakonstantinou, M. Hart, M. J. Hart, M.J. Hart

Publications

8.9K

Citations

H-Index

Concepts

All Affiliations

The University of Texas Health Science Center at San Antonio Cornell University Geriatric Research Education and Clinical Center University of California, San Francisco South Texas Veterans Health Care System

About

Matthew J. Hart is an author at The University of Texas Health Science Center at San Antonio specializing in medicine, cell biology, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	24	4.4K
2	Natural Sciences	14	15	3.2K
3	Biochemistry	9	9	1.7K
4	Social Sciences	2	2	294
5	Health Sciences	1	1	26

Matthew J. Hart

Publications

8.4K

Citations

H-Index

Page 1

	Year	Citations
Inhibition of mTOR by Rapamycin Abolishes Cognitive Deficits and Reduces Amyloid-β Levels in a Mouse Model of Alzheimer's Disease Patricia Spilman, Natalia Podlutskaya, Matthew J. Hart, PLoS ONE	2010	993
p115 RhoGEF, a GTPase Activating Protein for Gα <sub>12</sub> and Gα <sub>13</sub> Tohru Kozasa, Xuejun Jiang, Matthew J. Hart, Science Molecular RegulationMolecular BiologyAlpha SubunitsSignaling PathwayCell Signaling	1998	849
Downregulation of β-catenin by human Axin and its association with the APC tumor suppressor, β-catenin and GSK3β Matthew J. Hart, Rico de los Santos, Iris Albert, Current Biology Tumor BiologyHuman AxinApc Tumor SuppressorSignaling PathwayMedicine	1998	844
Direct Stimulation of the Guanine Nucleotide Exchange Activity of p115 RhoGEF by Gα <sub>13</sub> Matthew J. Hart, Xuejun Jiang, Tohru Kozasa, Science	1998	773
The F-box protein β-TrCP associates with phosphorylated β-catenin and regulates its activity in the cell Matthew J. Hart, Jean‐Paul Concordet, Irina Lassot, Current Biology Transcriptional RegulationSignal TransductionSignaling PathwayMolecular RegulationNatural Sciences	1999	667
Catalysis of guanine nucleotide exchange on the CDC42Hs protein by the dbloncogene product Matthew J. Hart, Alessandra Eva, Tony Evans, Nature BiochemistryNatural SciencesEnzyme CatalysisOligonucleotideMolecular Biology	1991	421
IQGAP1, a calmodulin-binding protein with a rasGAP-related domain, is a potential effector for cdc42Hs. Matthew J. Hart, Marinella Callow, Brian Souza, The EMBO Journal Calmodulin-binding ProteinSignal TransductionProtein FunctionMolecular RegulationPotential Effector	1996	385
Cellular transformation and guanine nucleotide exchange activity are catalyzed by a common domain on the dbl oncogene product. Matthew J. Hart, Alessandra Eva, D Zangrilli, Journal of Biological Chemistry Common DomainMolecular RegulationGdp DissociationMolecular BiologyMolecular Research	1994	314
IQGAP1, a Rac- and Cdc42-binding Protein, Directly Binds and Cross-links Microfilaments Anne-Marie Bashour, Aaron T. Fullerton, Matthew J. Hart, The Journal of Cell Biology	1997	246
Chronic inhibition of mammalian target of rapamycin by rapamycin modulates cognitive and non-cognitive components of behavior throughout lifespan in mice Jonathan J. Halloran, Stacy A. Hussong, Raquel R Burbank, Neuroscience Lifespan ExtensionMammalian TargetNeuropsychologyCognitive ScienceAging	2012	213

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