Genes, endothelial function and cerebral small vessel disease in man. (Q36969770)

17 August 2017

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title

Genes, endothelial function and cerebral small vessel disease in man. (English)

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17 August 2017

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Hugh S Markus

1

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17 August 2017

12 October 2007

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17 August 2017

Experimental Physiology

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17 August 2017

93

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17 August 2017

1

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17 August 2017

121-127

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Evidence for genetic variance in white matter hyperintensity volume in normal elderly male twins.

17 August 2017

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Factor V Leiden mutation and completed stroke.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Genetic association studies in stroke: methodological issues and proposed standard criteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Impaired vascular mechanotransduction in a transgenic mouse model of CADASIL arteriopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Association between the Glu298Asp polymorphism in the endothelial constitutive nitric oxide synthase gene and brain infarction. The GENIC Investigators

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Efficacy of galantamine in probable vascular dementia and Alzheimer's disease combined with cerebrovascular disease: a randomised trial

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

White matter lesions in an unselected cohort of the elderly: molecular pathology suggests origin from chronic hypoperfusion injury.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

The arterial lesions underlying lacunes

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Polymorphisms in genes of the endothelin system and cerebral small-vessel disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Polymorphisms in genes of the renin-angiotensin system and cerebral small vessel disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Increased blood-brain barrier permeability in white matter lesions of Binswanger's disease evaluated by contrast-enhanced MRI.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Endothelial nitric oxide gene haplotypes and risk of cerebral small-vessel disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Homocysteine is a risk factor for cerebral small vessel disease, acting via endothelial dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Markers of endothelial dysfunction in lacunar infarction and ischaemic leukoaraiosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Angiotensin converting enzyme insertion/deletion genotype is associated with leukoaraiosis in lacunar syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Association of a 27-bp repeat polymorphism in ecNOS gene with ischemic stroke in Chinese patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Evaluating the genetic component of ischemic stroke subtypes: a family history study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Risk factor profile of cerebral small vessel disease and its subtypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Impaired cerebral vasoreactivity in a transgenic mouse model of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy arteriopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Reduced cerebral blood flow in white matter in ischaemic leukoaraiosis demonstrated using quantitative exogenous contrast based perfusion MRI.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Endothelial nitric oxide synthase exon 7 polymorphism, ischemic cerebrovascular disease, and carotid atheroma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Patterns of cerebral blood flow reduction in patients with ischemic leukoaraiosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Arterial changes in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in relation to pathogenesis of diffuse myelin loss of cerebral white matter: examination of cerebral medullary arteries by recon

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Family history of stroke in stroke types and subtypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Flow-mediated dilatation and intima-media thickness in patients with lacunar infarctions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Increased blood-brain barrier permeability in type II diabetes demonstrated by gadolinium magnetic resonance imaging

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Evaluation of the interactions of common genetic mutations in stroke subtypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Reduced vasomotor reactivity in cerebral microangiopathy : a study with near-infrared spectroscopy and transcranial Doppler sonography.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Intracellular processing of endothelial nitric oxide synthase isoforms associated with differences in severity of cardiopulmonary diseases: cleavage of proteins with aspartate vs. glutamate at position 298.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Haplotype-specific effects on endothelial NO synthase promoter efficiency: modifiable by cigarette smoking

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Is breakdown of the blood-brain barrier responsible for lacunar stroke, leukoaraiosis, and dementia?

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

The effect of the nitric oxide synthase inhibitor L-NMMA on basal CBF and vasoneuronal coupling in man: a PET study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Role of C/A polymorphism at -20 on the expression of human angiotensinogen gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

Measured Haplotype Analysis of the Angiotensin-I Converting Enzyme Gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1113%2FEXPPHYSIOL.2007.038752

10.1113/EXPPHYSIOL.2007.038752

21 January 2018

Identifiers

DOI

1 reference

17 August 2017

1 reference

PubMed ID

17933861