Differential gene expression in human cerebrovascular malformations. - Wikidata - awgldk - TriplyDB

Differential gene expression in human cerebrovascular malformations.

Differential gene expression in human cerebrovascular malformations.

http://www.wikidata.org/entity/Q37258927

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Differential gene expression in relation to the clinical characteristics of human brain arteriovenous malformations Ephrin B2 and EphB4 selectively mark arterial and venous vessels in cerebral arteriovenous malformation.EPHB4 gene polymorphisms and risk of intracranial hemorrhage in patients with brain arteriovenous malformations.A novel mouse model of cerebral cavernous malformations based on the two-hit mutation hypothesis recapitulates the human disease.Polymorphisms in inflammatory and immune response genes associated with cerebral cavernous malformation type 1 severity.Gene expression profiling of blood in brain arteriovenous malformation patients.The role of SDF-1/CXCR4 in the vasculogenesis and remodeling of cerebral arteriovenous malformation.Familial occurrence of brain arteriovenous malformations: a systematic review Array analysis of viral gene transcription during lytic infection of cells in tissue culture with Varicella-Zoster virus.Increased tissue perfusion promotes capillary dysplasia in the ALK1-deficient mouse brain following VEGF stimulation.Soluble endoglin modulates aberrant cerebral vascular remodeling Immune response in human cerebral cavernous malformations.Brain arteriovenous malformation pathogenesis: a response-to-injury paradigm.Developmental origins of cerebrovascular disease I: prenatal cerebrovascular development--classic findings in the context of advances in genetic and fetal surveillance evaluations.Neurovascular patterning cues and implications for central and peripheral neurological disease.Evidence of inflammatory cell involvement in brain arteriovenous malformations.An early venous abnormality: a potential cause of arteriovenous malformation recurrence.Evidence of endothelial progenitor cells in the human brain and spinal cord arteriovenous malformations.In vivo imaging of endothelial cell adhesion molecule expression after radiosurgery in an animal model of arteriovenous malformation.Aberrant angiogenic characteristics of human brain arteriovenous malformation endothelial cells.Characterization of the integrin alpha v beta3 in arteriovenous malformations and cavernous malformations.Testing the angiogenic potential of cerebrovascular malformations by use of a rat cornea model: usefulness and novel assessment of changes over time.The relationship of cortical folding and brain arteriovenous malformations.

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Differential gene expression in human cerebrovascular malformations.

http://www.wikidata.org/entity/Q37258927

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

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scientific article published on February 2003

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Differential gene expression in human cerebrovascular malformations.

@en

Differential gene expression in human cerebrovascular malformations.

@nl

type

label

Differential gene expression in human cerebrovascular malformations.

@en

Differential gene expression in human cerebrovascular malformations.

@nl

prefLabel

Differential gene expression in human cerebrovascular malformations.

@en

Differential gene expression in human cerebrovascular malformations.

@nl

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01.NEU.0000044131.03495.22

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Differential gene expression in human cerebrovascular malformations.

@en

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Issam A Awad

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

J Paul Elliott

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Judith Gault

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Katrina Diener

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Ling-Jia Hu

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Randall J Cohrs

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Robert E Breeze

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Robert Shenkar

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Tzulip Phang

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P2860

Nonsyndromic hearing impairment is associated with a mutation in DFNA5

T6BP, a TRAF6-interacting protein involved in IL-1 signaling

Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

Molecular classification of cancer: class discovery and class prediction by gene expression monitoring

Selenoprotein P: properties, functions, and regulation

Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas

Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)

Gene expression patterns in the lungs of patients with primary pulmonary hypertension: a gene microarray analysis

Interaction between krit1 and icap1alpha infers perturbation of integrin beta1-mediated angiogenesis in the pathogenesis of cerebral cavernous malformation

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465-77; discussion 477-8

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scholarly article

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10.1227/01.NEU.0000044131.03495.22

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2

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52

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Lawrence Hunter

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2003-02-01T00:00:00Z

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10944737

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12535382

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2709524

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