CADASIL: a critical look at a Notch disease (Q36409731)

14 August 2017

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title

CADASIL: a critical look at a Notch disease (English)

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Spiros Artavanis-Tsakonas

14 August 2017

author

series ordinal

object named as

Spyros Artavanis-Tsakonas

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14 August 2017

Angeliki Louvi

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14 August 2017

Joseph F Arboleda-Velasquez

series ordinal

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14 August 2017

publication date

1 January 2006

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Developmental Neuroscience

14 August 2017

published in

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14 August 2017

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14 August 2017

issue

1-2

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14 August 2017

page(s)

5-12

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Notch signaling: cell fate control and signal integration in development

14 August 2017

cites work

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Glycosylation regulates Notch signalling.

21 January 2018

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Notch1 and Notch3 instructively restrict bFGF-responsive multipotent neural progenitor cells to an astroglial fate

21 January 2018

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Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

21 January 2018

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Mutations in the human delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis

21 January 2018

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C455R notch3 mutation in a Colombian CADASIL kindred with early onset of stroke

21 January 2018

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Differential lesion patterns in CADASIL and sporadic subcortical arteriosclerotic encephalopathy: MR imaging study with statistical parametric group comparison.

21 January 2018

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Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study

21 January 2018

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Splice site mutation causing a seven amino acid Notch3 in-frame deletion in CADASIL

21 January 2018

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Sclerosing vasculopathy of the central nervous system in nonelderly demented patients

21 January 2018

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Vascular expression of Notch pathway receptors and ligands is restricted to arterial vessels.

21 January 2018

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CADASIL in a North American family: clinical, pathologic, and radiologic findings

21 January 2018

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Genetic, clinical and pathological studies of CADASIL in Japan: a partial contribution of Notch3 mutations and implications of smooth muscle cell degeneration for the pathogenesis

21 January 2018

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Mutations of the notch3 gene in non-caucasian patients with suspected CADASIL syndrome

21 January 2018

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An animal model for the molecular genetics of CADASIL. (Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy).

21 January 2018

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Pathogenic mutations associated with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy differently affect Jagged1 binding and Notch3 activity via the RBP/JK signaling Pathway

21 January 2018

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Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

21 January 2018

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21 January 2018

Identifiers

DOI

10.1159/000090748

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release_vf7j22hblbg77ghdse2xkdvrby

14 August 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/vf7j22hblbg77ghdse2xkdvrby

mapped directly with Wikidata item

24 November 2022

based on heuristic

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