D
Denise A. Dorsey
Researcher at Washington University in St. Louis
Publications - 33
Citations - 2251
Denise A. Dorsey is an academic researcher from Washington University in St. Louis. The author has contributed to research in topics: Sympathetic nervous system & Diabetic Autonomic Neuropathy. The author has an hindex of 22, co-authored 33 publications receiving 1989 citations. Previous affiliations of Denise A. Dorsey include Regeneron & Wistar Institute.
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Journal ArticleDOI
A complement–microglial axis drives synapse loss during virus-induced memory impairment
Michael J. Vasek,Charise Garber,Denise A. Dorsey,Douglas M. Durrant,Douglas M. Durrant,Bryan Bollman,Allison Soung,Jinsheng Yu,Carlos J. Perez-Torres,Arnaud Frouin,Daniel K. Wilton,Kristen E. Funk,Bette K. DeMasters,Xiaoping Jiang,James R. Bowen,Steven Mennerick,John K. Robinson,Joel R. Garbow,Kenneth L. Tyler,Mehul S. Suthar,Robert E. Schmidt,Beth Stevens,Robyn S. Klein +22 more
TL;DR: It is shown that viral infection of adult hippocampal neurons induces complement-mediated elimination of presynaptic terminals in a murine WNV neuroinvasive disease model, which provides a new murine model of WNV-induced spatial memory impairment, and identifies a potential mechanism underlying neurocognitive impairment in patients recovering from WNV Neuroinvasive Disease.
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CXCR7 influences leukocyte entry into the CNS parenchyma by controlling abluminal CXCL12 abundance during autoimmunity
Lillian Cruz-Orengo,David W. Holman,Denise A. Dorsey,Liang Zhou,Penglie Zhang,Melissa Wright,Erin E. McCandless,Jigisha R. Patel,Gary D. Luker,Dan R. Littman,John H. Russell,Robyn S. Klein +11 more
TL;DR: During CNS autoimmunity, brain endothelial cell CXCR7 internalizes CXCL12 from the perivascular space, thereby permitting leukocyte migration into the CNS parenchyma.
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CXCR4 promotes differentiation of oligodendrocyte progenitors and remyelination
TL;DR: Data indicate that CXCR4 activation, by promoting the differentiation of OPCs into oligodendrocytes, is critical for remyelination of the injured adult CNS.
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Regional CNS responses to IFN-γ determine lesion localization patterns during EAE pathogenesis
TL;DR: It is demonstrated, using an adoptive transfer system, that the ability of the central nervous system (CNS) to sense pathogenic T cell–produced IFN-γ during EAE initiation determines the sites of CNS pathogenesis.
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Enhanced sphingosine-1-phosphate receptor 2 expression underlies female CNS autoimmunity susceptibility
Lillian Cruz-Orengo,Brian P. Daniels,Denise A. Dorsey,Sarah Alison Basak,Jose G. Grajales-Reyes,Erin E. McCandless,Laura Piccio,Robert E. Schmidt,Anne H. Cross,Seth D. Crosby,Robyn S. Klein +10 more
TL;DR: This work has identified sphingosine-1-phosphate receptor 2 (S1PR2) as a sex- and strain-specific, disease-modifying molecule that regulates BBB permeability by destabilizing adherens junctions and implicate S1 PR2 in sex-specific patterns of disease during CNS autoimmunity.