Notch3 gene polymorphism and ischaemic cerebrovascular disease

Journal of Neurology Neurosurgery and Psychiatry

Volumn 72, Issue 3, 2002, Pages 382-384

  Ito, D ^a   Tanahashi, N ^a   Murata, M ^a   Sato, H ^a   Saito, I ^a   Watanabe, K ^a   Fukuuchi, Y ^a  

^a KEIO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

NOTCH RECEPTOR;

ADULT; AGED; ARTERY DISEASE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRAIN INFARCTION; BRAIN ISCHEMIA; CEREBROVASCULAR DISEASE; COMPUTER ASSISTED TOMOGRAPHY; CONTROLLED STUDY; DEMENTIA; EUROPE; FEMALE; GENE FREQUENCY; GENETIC POLYMORPHISM; GENETIC RISK; GENOTYPE; HUMAN; JAPAN; LEUKOENCEPHALOPATHY; MAJOR CLINICAL STUDY; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; STROKE;

AGED; AMINO ACID SUBSTITUTION; CEREBRAL INFARCTION; CHROMOSOME ABERRATIONS; DEMENTIA, MULTI-INFARCT; FEMALE; GENE FREQUENCY; GENES, DOMINANT; HUMANS; ISCHEMIC ATTACK, TRANSIENT; MALE; MIDDLE AGED; POLYMORPHISM, GENETIC; PROTO-ONCOGENE PROTEINS; RECEPTORS, CELL SURFACE; RECEPTORS, NOTCH; RISK; SIGNAL TRANSDUCTION;

EID: 0036189174     PISSN: 00223050     EISSN: None     Source Type: Journal    
DOI: 10.1136/jnnp.72.3.382     Document Type: Article

References (6)

1. Notch 3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementio
2. The ins and outs of notch signaling
3. Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients
4. Association between platelet glycoprotein Ibá genotype and ischemic cerebrovascular disease
5. C242T polymorphism of NADPH oxidase p22 PHOX gene and ischemic cerebrovascular disease in the Japanese population
6. Polymorphism in the promoter of lipopolysaccharide receptor CD14 and ischemic cerebrovascular disease