Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21
about
CCM1 and CCM2 protein interactions in cell signaling: implications for cerebral cavernous malformations pathogenesisCrystal structure of CCM3, a cerebral cavernous malformation protein critical for vascular integrityMutations in a gene encoding a novel protein containing a phosphotyrosine-binding domain cause type 2 cerebral cavernous malformations.Krit1 missense mutations lead to splicing errors in cerebral cavernous malformationLocalization of a susceptibility gene for common forms of stroke to 5q12Deletions in CCM2 are a common cause of cerebral cavernous malformationsFamilial hemiplegic migraine and spreading depressionMechanism for KRIT1 Release of ICAP1-Mediated Suppression of Integrin ActivationStructural Basis for Small G Protein Effector Interaction of Ras-related Protein 1 (Rap1) and Adaptor Protein Krev Interaction Trapped 1 (KRIT1)Cerebral Cavernous Malformations: Review of the Genetic and Protein-Protein Interactions Resulting in Disease PathogenesisMutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)2006 expressed-sequence tags derived from human chromosome 7-enriched cDNA librariesSupratentorial cavernous haemangiomas and epilepsy: a review of the literature and case series.Hereditary haemorrhagic telangiectasia with extensive liver involvement is not caused by either HHT1 or HHT2.Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27.Loss of p53 sensitizes mice with a mutation in Ccm1 (KRIT1) to development of cerebral vascular malformations.Extra-axial cavernous hemangioma: two case reports.Genetics of cerebral cavernous malformations: current status and future prospectsCCM3/SERPINI1 bidirectional promoter variants in patients with cerebral cavernous malformations: a molecular and functional studyFamilial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7q.Familial cavernous angiomas masquerading as multiple sclerosis.Differential gene expression in human cerebrovascular malformations.Brainstem cavernous malformations.Signaling pathways and the cerebral cavernous malformations proteins: lessons from structural biology.Genetic and cellular basis of cerebral cavernous malformations: implications for clinical management.PTEN/PI3K/Akt/VEGF signaling and the cross talk to KRIT1, CCM2, and PDCD10 proteins in cerebral cavernous malformations.The gene encoding phosphodiesterase 4D confers risk of ischemic stroke.A comparison of the clinical profile of cavernous malformations with and without associated venous malformations.Molecular Basis of Vascular Birthmarks.
P2860
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P2860
Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21
description
1995 nî lūn-bûn
@nan
1995 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1995年の論文
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1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21
@ast
Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21
@en
Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21
@nl
type
label
Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21
@ast
Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21
@en
Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21
@nl
prefLabel
Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21
@ast
Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21
@en
Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21
@nl
P2093
P2860
P3181
P356
P1476
Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21
@en
P2093
P2860
P304
P3181
P356
10.1073/PNAS.92.14.6620
P407
P577
1995-07-03T00:00:00Z