Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations.

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Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations.

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http://www.wikidata.org/entity/Q39079343

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2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

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Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations.

@en

Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations.

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Item

label

Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations.

@en

Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations.

@nl

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Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations.

@en

Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations.

@nl

P1476

Update on Novel CCM Gene Mutations in Patients with Cerebral Cavernous Malformations

@en

P2093

Antonina Sidoti

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

Carmela Rinaldi

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Concetta Alafaci

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Concetta Scimone

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Federica Greco

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Francesca Granata

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Francesco Piva

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Placido Bramanti

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P2860

Adaptor protein cerebral cavernous malformation 3 (CCM3) mediates phosphorylation of the cytoskeletal proteins ezrin/radixin/moesin by mammalian Ste20-4 to protect cells from oxidative stress

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

Loss of CCM3 impairs DLL4-Notch signalling: implication in endothelial angiogenesis and in inherited cerebral cavernous malformations

Cerebral cavernous malformation protein CCM1 inhibits sprouting angiogenesis by activating DELTA-NOTCH signaling.

Krit1 missense mutations lead to splicing errors in cerebral cavernous malformation

Identification of the Kelch family protein Nd1-L as a novel molecular interactor of KRIT1

Genetics of cavernous angiomas.

Cerebral cavernous malformations. Incidence and familial occurrence.

Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27.

KRIT1 protein depletion modifies endothelial cell behavior via increased vascular endothelial growth factor (VEGF) signaling.

P2888

s12031-016-0863-z

P304

189-198

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P31

scholarly article

P356

10.1007/S12031-016-0863-Z

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P433

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

P478

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P50

Rosalia D'Angelo

Luigi Donato

P577

2016-12-20T00:00:00Z

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P698

28000143

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