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Genetic and Pharmacological Manipulation of Urotensin II Ameliorate the Metabolic and Atherosclerosis Sequalae in Mice
Author(s) -
Zhipeng You,
Jacques Genest,
Pierre-Olivier Barrette,
Anouar Hafiane,
David J. Behm,
Pedro D’Orléans-Juste,
Adel Schwertani
Publication year - 2012
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.112.252973
Subject(s) - urotensin ii , hyperlipidemia , endocrinology , medicine , knockout mouse , apolipoprotein b , receptor , ldl receptor , lipoprotein , biology , cholesterol , diabetes mellitus
Urotensin II (UII) is a potent vasoactive peptide that binds to the urotensin receptor-coupled receptor-14 (known as UT) and exerts a wide range of actions in humans and experimental animals. We tested the hypothesis that UII gene deletion or UT blockade ameliorate experimental atherosclerosis.

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