Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease. - Wikidata - awgldk - TriplyDB

Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease.

Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease.

http://www.wikidata.org/entity/Q35140102

about

Genetic Risk Factors for Ischemic and Hemorrhagic Stroke Stroke Risk Factors, Genetics, and Prevention.Genetic variation at 16q24.2 is associated with small vessel stroke.Cardiovascular risk factors and small vessel disease of the brain: Blood pressure, white matter lesions, and functional decline in older persons Perturbations of the cerebrovascular matrisome: A convergent mechanism in small vessel disease of the brain?FOXE3 mutations predispose to thoracic aortic aneurysms and dissections.Clarification of mural cell coverage of vascular endothelial cells by live imaging of zebrafish.A role for PDGF-C/PDGFRα signaling in the formation of the meningeal basement membranes surrounding the cerebral cortex.Foxc1 and Foxc2 deletion causes abnormal lymphangiogenesis and correlates with ERK hyperactivation Vascular Contributions to Cognitive Impairment and Dementia: Topical Review of Animal Models.Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies Genetic factors in cerebral small vessel disease and their impact on stroke and dementia.Monogenic causes of stroke: now and the future.Pathogenetic significance and possibility as a therapeutic target of platelet derived growth factor.Cerebrovascular defects in Foxc1 mutants correlate with aberrant WNT and VEGF-A pathways downstream of retinoic acid from the meninges.Cilia Control Vascular Mural Cell Recruitment in Vertebrates.Knockdown of long non-coding RNA XIST increases blood-tumor barrier permeability and inhibits glioma angiogenesis by targeting miR-137.Atrial fibrillation is associated with anterior predominant white matter lesions in patients presenting with embolic stroke.

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P2860

Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease.

http://www.wikidata.org/entity/Q35140102

description

2014 nî lūn-bûn

@nan

2014 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2014年の論文

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2014年論文

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2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease.

@ast

Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease.

@en

type

label

Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease.

@ast

Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease.

@en

prefLabel

Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease.

@ast

Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease.

@en

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Journal of Clinical Investigation

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Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease.

@en

P2093

Andrew J Waskiewicz

http://www.w3.org/2001/XMLSchema#string

Anita L Destefano

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Corey R Arnold

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Curtis R French

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Derek J Emery

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Jonathan M Skarie

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Marten Hofker

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Ordan J Lehmann

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Ting Liu

http://www.w3.org/2001/XMLSchema#string

Tsutomu Kume

http://www.w3.org/2001/XMLSchema#string

P2860

Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

Forkhead box transcription factor FoxC1 preserves corneal transparency by regulating vascular growth

The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus

Systematic identification of trans eQTLs as putative drivers of known disease associations

FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation

Endothelial/pericyte interactions

Leukoaraiosis: an independent risk factor for stroke?

Variants conferring risk of atrial fibrillation on chromosome 4q25.

The clinical importance of white matter hyperintensities on brain magnetic resonance imaging: systematic review and meta-analysis

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4877-4881

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10.1172/JCI75109

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11

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124

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William B. Dobyns

Kathleen J Millen

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2014-09-24T00:00:00Z

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25250569

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4347243

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