Dysregulation of RNF213 promotes cerebral hypoperfusion.

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Dysregulation of RNF213 promotes cerebral hypoperfusion.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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Dysregulation of RNF213 promotes cerebral hypoperfusion.

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Dysregulation of RNF213 promotes cerebral hypoperfusion.

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label

Dysregulation of RNF213 promotes cerebral hypoperfusion.

@en

Dysregulation of RNF213 promotes cerebral hypoperfusion.

@nl

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Dysregulation of RNF213 promotes cerebral hypoperfusion.

@en

Dysregulation of RNF213 promotes cerebral hypoperfusion.

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P1476

Dysregulation of RNF213 promotes cerebral hypoperfusion

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P2093

Akio Koizumi

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Hiroko Okuda

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Jun-Ichiro Enmi

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Satoshi Iguchi

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Satoshi Saito

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Shohab Youssefian

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Susumu Miyamoto

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Takaaki Morimoto

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Yasushi Takagi

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Yohei Mineharu

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P2860

Identification of RNF213 as a susceptibility gene for moyamoya disease and its possible role in vascular development.

Substantial Reduction of Parenchymal Cerebral Blood Flow in Mice with Bilateral Common Carotid Artery Stenosis.

A new horizon of moyamoya disease and associated health risks explored through RNF213

Moyamoya disease-associated protein mysterin/RNF213 is a novel AAA+ ATPase, which dynamically changes its oligomeric state

Biochemical and Functional Characterization of RNF213 (Mysterin) R4810K, a Susceptibility Mutation of Moyamoya Disease, in Angiogenesis In Vitro and In Vivo

Caveolae and caveolins in the cardiovascular system

Caveolin-1 deficiency increases cerebral ischemic injury

White matter lesions and glial activation in a novel mouse model of chronic cerebral hypoperfusion.

Significant association of RNF213 p.R4810K, a moyamoya susceptibility variant, with coronary artery disease

A genome-wide association study identifies RNF213 as the first Moyamoya disease gene.

P304

3607

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P31

scholarly article

P356

10.1038/S41598-018-22064-8

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P407

English

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P478

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P577

2018-02-26T00:00:00Z

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P698

29483617

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P932

5827518

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