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Karen Fox-Talbot

Researcher at Johns Hopkins University

Publications -  41
Citations -  2091

Karen Fox-Talbot is an academic researcher from Johns Hopkins University. The author has contributed to research in topics: Antibody & Transplantation. The author has an hindex of 25, co-authored 41 publications receiving 1884 citations. Previous affiliations of Karen Fox-Talbot include New York University.

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Nuclear miRNA Regulates the Mitochondrial Genome in the Heart

TL;DR: The data show for the first time that nuclear miR-181c translocates into the mitochondria and regulates mitochondrial genome expression, ultimately causing electron transport chain complex IV remodeling and mitochondrial dysfunction.
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Antibody to human leukocyte antigen triggers endothelial exocytosis

TL;DR: The data show that antibody to host antigens can activate human endothelial cell exocytosis and leukocyte trafficking, and by triggering vascular inflammation, antibody activation of exocyTosis may play a role in transplant rejection.
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Adenoviral transfer of HIF-1α enhances vascular responses to critical limb ischemia in diabetic mice

TL;DR: Intramuscular injection of AdCA5 into the ischemic limb of db/db mice increased the recovery of limb perfusion and function, reduced tissue necrosis, rescued the diabetes-associated impairment of circulating angiogenic cells, enhanced endothelial nitric oxide synthase activation, and increased vessel density and luminal area in the isChemic limb.
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Endothelial expression of hypoxia-inducible factor 1 protects the murine heart and aorta from pressure overload by suppression of TGF-β signaling

TL;DR: It is reported that Hif1af/f;Tie2-Cre conditional knockout mice, which lack HIF-1α expression only in Tie2+ lineage cells, develop normally, but when subjected to pressure overload induced by transaortic constriction, they manifest rapid cardiac decompensation.
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MicroRNA profiling of diverse endothelial cell types

TL;DR: EC miRNA expression levels are generally consistent across EC types, and polycistronic miRNA chromosomal clusters have common expression levels within a given cell type.