Functional analysis of a recurrent missense mutation in Notch3 in CADASIL - Wikidata - wikimedia - TriplyDB

Functional analysis of a recurrent missense mutation in Notch3 in CADASIL

Functional analysis of a recurrent missense mutation in Notch3 in CADASIL

http://www.wikidata.org/entity/Q35489815

about

Conserved signal peptide of Notch3 inhibits interaction with proteasome Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain CADASIL and CARASIL.Statistical platform to discern spatial and temporal coordination of endothelial sprouting.NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling.Genetic factors in cerebral small vessel disease and their impact on stroke and dementia.The archetypal R90C CADASIL-NOTCH3 mutation retains NOTCH3 function in vivo.A Next-Generation Sequencing of the NOTCH3 and HTRA1 Genes in CADASIL Patients.Skin and sural nerve biopsies: ultrastructural findings in the first genetically confirmed cases of CADASIL in Serbia.

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P2860

Functional analysis of a recurrent missense mutation in Notch3 in CADASIL

http://www.wikidata.org/entity/Q35489815

description

2005 nî lūn-bûn

@nan

2005 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2005 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年论文

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name

Functional analysis of a recurrent missense mutation in Notch3 in CADASIL

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Functional analysis of a recurrent missense mutation in Notch3 in CADASIL

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type

label

Functional analysis of a recurrent missense mutation in Notch3 in CADASIL

@ast

Functional analysis of a recurrent missense mutation in Notch3 in CADASIL

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prefLabel

Functional analysis of a recurrent missense mutation in Notch3 in CADASIL

@ast

Functional analysis of a recurrent missense mutation in Notch3 in CADASIL

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Journal of Neurology, Neurosurgery and Psychiatry

P1476

Functional analysis of a recurrent missense mutation in Notch3 in CADASIL

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P2093

C Schanen

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D Ghavimi

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D M St Clair

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G Weinmaster

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J T Nichols

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R P J De Lange

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T Chow

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T Haritunians

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P2860

Dll4, a novel Notch ligand expressed in arterial endothelium

Physical interaction of Delta1, Jagged1, and Jagged2 with Notch1 and Notch3 receptors

Members of the Jagged/Notch gene families are expressed in injured arteries and regulate cell phenotype via alterations in cell matrix and cell-cell interaction

Expression patterns of Jagged, Delta1, Notch1, Notch2, and Notch3 genes identify ligand-receptor pairs that may function in neural development

An antisense oligonucleotide to the notch ligand jagged enhances fibroblast growth factor-induced angiogenesis in vitro

A CADASIL-mutated Notch 3 receptor exhibits impaired intracellular trafficking and maturation but normal ligand-induced signaling.

The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients

Truncated mammalian Notch1 activates CBF1/RBPJk-repressed genes by a mechanism resembling that of Epstein-Barr virus EBNA2

The Notch1 receptor is cleaved constitutively by a furin-like convertase

A novel proteolytic cleavage involved in Notch signaling: the role of the disintegrin-metalloprotease TACE

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