A Novel CCM2 Gene Mutation Associated with Familial Cerebral Cavernous Malformation

about

A Novel CCM2 Gene Mutation Associated with Familial Cerebral Cavernous Malformation

Item

http://www.wikidata.org/entity/Q37270784

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 21 September 2016

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

A Novel CCM2 Gene Mutation Associated with Familial Cerebral Cavernous Malformation

@en

A Novel CCM2 Gene Mutation Associated with Familial Cerebral Cavernous Malformation.

@nl

type

Item

label

A Novel CCM2 Gene Mutation Associated with Familial Cerebral Cavernous Malformation

@en

A Novel CCM2 Gene Mutation Associated with Familial Cerebral Cavernous Malformation.

@nl

prefLabel

A Novel CCM2 Gene Mutation Associated with Familial Cerebral Cavernous Malformation

@en

A Novel CCM2 Gene Mutation Associated with Familial Cerebral Cavernous Malformation.

@nl

P1476

A Novel CCM2 Gene Mutation Associated with Familial Cerebral Cavernous Malformation

@en

P2093

Chi-Meng Tzeng

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

Cong-Xia Lu

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

Han Wang

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

Ke-Hui Yi

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

Liang-Liang Cai

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

Ming-Li Li

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

Qing Lin

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

Wen-Qing Huang

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

Ya Zhang

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

P2860

Susceptibility-Weighted Imaging for the Evaluation of Patients with Familial Cerebral Cavernous Malformations: A Comparison with T2-Weighted Fast Spin-Echo and Gradient-Echo Sequences

Structural studies of cerebral cavernous malformations 2 (CCM2) reveal a folded helical domain at its C-terminus

CCM1 and CCM2 protein interactions in cell signaling: implications for cerebral cavernous malformations pathogenesis

Crystal structure of CCM3, a cerebral cavernous malformation protein critical for vascular integrity

CCM3 interacts with CCM2 indicating common pathogenesis for cerebral cavernous malformations

Mutations in a gene encoding a novel protein containing a phosphotyrosine-binding domain cause type 2 cerebral cavernous malformations.

A two-hit mechanism causes cerebral cavernous malformations: complete inactivation of CCM1, CCM2 or CCM3 in affected endothelial cells

Structural basis of the junctional anchorage of the cerebral cavernous malformations complex

Structural basis for the disruption of the cerebral cavernous malformations 2 (CCM2) interaction with Krev interaction trapped 1 (KRIT1) by disease-associated mutations

Genetics of cavernous angiomas.

P304

220

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

P31

scholarly article

case report

P356

10.3389/FNAGI.2016.00220

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

P478

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

P577

2016-09-21T00:00:00Z

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

P698

27708576

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

P932

5030299

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