2009 Fiscal Year Final Research Report
Mechanism of Ductus arteriosus through an endogenous inhibitor of NOS
Project/Area Number |
20790778
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
Embryonic/Neonatal medicine
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Research Institution | Kurume University |
Principal Investigator |
KAJIMOTO Hidemi Kurume University, 循環器病研究所, 助教 (50349700)
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Project Period (FY) |
2008 – 2009
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Keywords | 新生児医学 / 動脈管 |
Research Abstract |
Dimethylarginine dimethylaminohydrolase that metabolizes endogenous NOS inhibitor increases after ductus arteriosus closure. Analysis of the comprehensive gene expression profile changes provided new insight into understanding the mechanism of DA closure.
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[Journal Article] Exaggerated blood pressure variability superimposed on hypertension aggravates cardiac remodeling in rats via angiotensin II system-mediated chronic inflammation2009
Author(s)
Kudo H, Kai H, Kajimoto H, Koga M, Takayama N, Mori T, Ikeda A, Yasuoka S, Anegawa T, Mifune H, Kato S, Hirooka Y, Imaizumi T
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Journal Title
Hypertension 54(4)
Pages: 832-838
Peer Reviewed
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[Presentation] Enhanced cardiac inflammation and myocardial fibrosis in ovariectomized, pressure-overloaded rats -A possible mechanism of aggravation of diastolic dysfunction in the post-menopause: Circulation2009
Author(s)
Mori H, Kai H, Kajimoto H, Kudo H, Takayama N, Ikeda A, Yasuoka S, Anegawa T, Imaizumi T
Organizer
American Heart Association's Scientific Sessions
Place of Presentation
Orlando, USA
Year and Date
20091115-20091117
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