Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease. - Wikidata - wikimedia - TriplyDB

Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease.

Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease.

http://www.wikidata.org/entity/Q30408291

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Cerebral small vessel disease and Alzheimer's disease Microvascular pathology and morphometrics of sporadic and hereditary small vessel diseases of the brain Genetics of subcortical vascular dementia Genetics of age-related white matter lesions from linkage to genome wide association studies Age and the metabolic syndrome as risk factors for ischemic stroke: improving preclinical models of ischemic stroke White Matter Lesion Progression: Genome-Wide Search for Genetic Influences Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease NOTCH3 variants and risk of ischemic stroke.Cerebral small vessel disease: insights and opportunities from mouse models of collagen IV-related small vessel disease and cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.Personalized management of atrial fibrillation: Proceedings from the fourth Atrial Fibrillation competence NETwork/European Heart Rhythm Association consensus conference.Longitudinal change of small-vessel disease-related brain abnormalities Cardiovascular risk factors and small vessel disease of the brain: Blood pressure, white matter lesions, and functional decline in older persons Stroke genetics: a review and update.Genetics of cerebral small vessel disease Common NOTCH3 Variants and Cerebral Small-Vessel Disease.R54C Mutation of NOTCH3 Gene in the First Rungus Family with CADASIL.Association of Notch3 single-nucleotide polymorphisms and lacunar infarctions in patients.Stroke injury, cognitive impairment and vascular dementia Up-regulation of serotonin receptor 2B mRNA and protein in the peri-infarcted area of aged rats and stroke patients.Immunolocalization of platelet-derived growth factor receptor-β (PDGFR-β) and pericytes in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).Archetypal NOTCH3 mutations frequent in public exome: implications for CADASIL.Neurovascular signaling in the brain and the pathological consequences of hypertension.Mechanisms of sporadic cerebral small vessel disease: insights from neuroimaging.Small vessel disease and memory loss: what the clinician needs to know to preserve patients' brain health.Interpretation of NOTCH3 mutations in the diagnosis of CADASIL.Genetic factors in cerebral small vessel disease and their impact on stroke and dementia.Monogenic causes of stroke: now and the future.Genetics of ischaemic stroke.Prognostic value of Notch receptors in postsurgical patients with hepatitis B virus-related hepatocellular carcinoma.Combined effects of age and polymorphisms in Notch3 in the pathogenesis of cerebral infarction disease.A population neuroscience approach to the study of cerebral small vessel disease in mid- and late-life: an Invited Review.Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3.

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Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease.

http://www.wikidata.org/entity/Q30408291

description

2011 nî lūn-bûn

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2011 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2011 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Genetic variants of the NOTCH3 ...... cerebral small vessel disease.

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Genetic variants of the NOTCH3 ...... cerebral small vessel disease.

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Genetic variants of the NOTCH3 ...... cerebral small vessel disease.

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Genetic variants of the NOTCH3 ...... cerebral small vessel disease.

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Genetic variants of the NOTCH3 ...... cerebral small vessel disease.

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Genetic variants of the NOTCH3 ...... cerebral small vessel disease.

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Genetic variants of the NOTCH3 ...... cerebral small vessel disease.

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CHARGE consortium Neurology working group

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Christian Enzinger

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Katja Petrovic

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Marco Wiltgen

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Margherita Cavalieri

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Marion Zeginigg

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Paul Freudenberger

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Pierre Gider

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Reinhold Schmidt

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Stephanie Debette

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P2860

“Mini-mental state”

SWISS-MODEL and the Swiss-PdbViewer: an environment for comparative protein modeling

Protein structure prediction on the Web: a case study using the Phyre server

Haploview: analysis and visualization of LD and haplotype maps

Notch signaling: cell fate control and signal integration in development

Cerebral small vessel disease: from pathogenesis and clinical characteristics to therapeutic challenges

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

Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts

Cerebrovascular dysfunction and microcirculation rarefaction precede white matter lesions in a mouse genetic model of cerebral ischemic small vessel disease

The protein data bank. Bridging the gap between the sequence and 3D structure world.

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3384-3397

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scholarly article

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10.1093/BRAIN/AWR252

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P433

Pt 11

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P478

134

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Jerome I Rotter

Lenore J Launer

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2011-10-17T00:00:00Z

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51721405

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22006983

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3212720

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