(Q42855085)

English

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

scientific article published on January 2003

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

8 November 2017

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

1 reference

Europe PubMed Central

PMC publication ID

8 November 2017

Elisabeth Tournier-Lasserve

6

1 reference

Europe PubMed Central

PMC publication ID

8 November 2017

object named as

Anne Joutel

7

0 references

author name string

Marie Magdeleine Ruchoux

1

1 reference

Europe PubMed Central

PMC publication ID

8 November 2017

Valérie Domenga

2

1 reference

Europe PubMed Central

PMC publication ID

8 November 2017

Peggy Brulin

3

1 reference

Europe PubMed Central

PMC publication ID

8 November 2017

Jacqueline Maciazek

4

1 reference

Europe PubMed Central

PMC publication ID

8 November 2017

Sylvie Limol

5

1 reference

Europe PubMed Central

PMC publication ID

8 November 2017

language of work or name

0 references

publication date

1 January 2003

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Europe PubMed Central

PMC publication ID

8 November 2017

The American Journal of Pathology

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Europe PubMed Central

PMC publication ID

8 November 2017

162

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Europe PubMed Central

PMC publication ID

8 November 2017

1

1 reference

Europe PubMed Central

PMC publication ID

8 November 2017

329-342

1 reference

Europe PubMed Central

PMC publication ID

8 November 2017

CADASIL Notch3 mutant proteins localize to the cell surface and bind ligand

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

27 May 2018

Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

27 May 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

27 May 2018

Left ventricular hypertrophy in ascending aortic stenosis mice: anoikis and the progression to early failure.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

27 May 2018

De novo mutation in the Notch3 gene causing CADASIL

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

27 May 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

27 May 2018

CADASIL: Notch signaling defect or protein accumulation problem?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

27 May 2018

CADASIL: hereditary disease of arteries causing brain infarcts and dementia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

27 May 2018

Notch signaling: cell fate control and signal integration in development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

27 May 2018

Patterns of MRI lesions in CADASIL.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

27 May 2018

Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

27 May 2018

CADASIL: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

27 May 2018

Loss of matrix adhesion triggers rapid transformation-selective apoptosis in fibroblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

27 May 2018

CADASIL: skin biopsy allows diagnosis in early stages.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

27 May 2018

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

27 May 2018

The SM 22 promoter directs tissue-specific expression in arterial but not in venous or visceral smooth muscle cells in transgenic mice.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

27 May 2018

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

27 May 2018

Disruption of epithelial cell-matrix interactions induces apoptosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

27 May 2018

Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

27 May 2018

Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

27 May 2018

Morphometric analysis of ultrastructural vascular changes in CADASIL: analysis of 50 skin biopsy specimens and pathogenic implications.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

16 August 2018

Small in-frame deletions and missense mutations in CADASIL: 3D models predict misfolding of Notch3 EGF-like repeat domains

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

16 August 2018

Phenotypic variability of CADASIL and novel morphologic findings.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

16 August 2018

Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1851116

16 August 2018

The phenotypic spectrum of CADASIL: clinical findings in 102 cases

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963824-2

7 January 2021

The natural history of CADASIL: a pooled analysis of previously published cases

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963824-2

7 January 2021

Diagnostic Notch3 sequence analysis in CADASIL: three new mutations in Dutch patients. Dutch CADASIL Research Group

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963824-2

7 January 2021

De novo mutation in theNotch3 gene causing CADASIL

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963824-2

7 January 2021

Presence of ultrastructural arterial lesions in muscle and skin vessels of patients with CADASIL

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963824-2

7 January 2021

Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963824-2

7 January 2021

Identification of the characteristic vascular changes in a sural nerve biopsy of a case with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963824-2

7 January 2021

Muscle and skin biopsies are a sensitive diagnostic tool in the diagnosis of CADASIL

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963824-2

7 January 2021

Endothelial changes in muscle and skin biopsies in patients with CADASIL

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963824-2

7 January 2021

Identifiers

10.1016/S0002-9440(10)63824-2

1 reference

Europe PubMed Central

PMC publication ID

8 November 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

8 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

8 November 2017

ResearchGate publication ID

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