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Gregory L. Shipley

Researcher at University of Texas Health Science Center at Houston

Publications -  43
Citations -  15751

Gregory L. Shipley is an academic researcher from University of Texas Health Science Center at Houston. The author has contributed to research in topics: Endometrium & Estrogen. The author has an hindex of 28, co-authored 41 publications receiving 13668 citations. Previous affiliations of Gregory L. Shipley include University of Texas MD Anderson Cancer Center & University of Texas at Austin.

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Uncoupling protein 3 transcription is regulated by peroxisome proliferator-activated receptor α in the adult rodent heart

TL;DR: Results suggest that in the adult rodent heart, UCP‐3 expression is regu¬lated by PPARα, in contrast, cardiac U CP‐2 expression is regulated in part by a fatty acid‐dependent, PPAR α‐independent mechanism.
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Localization of pendrin in mouse kidney.

TL;DR: Pendrin is expressed in the mouse distal convoluted tubule, CCD, and CNT along the apical plasma membrane of non-A-non-B intercalated cells and in subapical cytoplasmic vesicles of type B intercalate cells.
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Downregulation of Metabolic Gene Expression in Failing Human Heart before and after Mechanical Unloading

TL;DR: Although LVAD treatment improved clinical markers of heart failure, only UCP3 expression reversed to non-failing transcript levels following mechanical unloading, which may be an important mechanism for reducing the formation of oxygen-derived free radicals.
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Metabolic effects of rexinoids: tissue-specific regulation of lipoprotein lipase activity.

TL;DR: These studies demonstrate that RXR ligands can have dramatic effects on the post-translational processing of LPL and suggest that skeletal muscle may be an important target of rexinoid action, which is distinct from either retinoic acid receptor or peroxisome proliferator-activated receptor activation.
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Coordinate regulation of the production and signaling of retinoic acid by estrogen in the human endometrium

TL;DR: The results suggest that estrogen coordinately up-regulates RA production and signaling in the human endometrium, and this coordinate mechanism may play a role in the antiproliferative effects that counterbalance the estrogen-induced endometrial proliferation.