(Q42825763)

English

CADASIL-associated Notch3 mutations have differential effects both on ligand binding and ligand-induced Notch3 receptor signaling through RBP-Jk

scientific article published on October 2004

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scholarly article

1 reference

Europe PubMed Central

8 November 2017

CADASIL-associated Notch3 mutations have differential effects both on ligand binding and ligand-induced Notch3 receptor signaling through RBP-Jk (English)

1 reference

Europe PubMed Central

8 November 2017

Notch receptor 3

1 reference

GOA release 2020-03-11

signaling receptor activity

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GOA release 2020-03-11

1 reference

based on heuristic

inferred from title

4

object named as

Anja Capell

1 reference

Europe PubMed Central

8 November 2017

Martin Dichgans

6

object named as

Martin Dichgans

1 reference

Europe PubMed Central

8 November 2017

Christian Opherk

2

object named as

Christian Opherk

1 reference

Europe PubMed Central

8 November 2017

author name string

Nils Peters

1

1 reference

Europe PubMed Central

8 November 2017

Simone Zacherle

3

1 reference

Europe PubMed Central

8 November 2017

Petra Gempel

5

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Europe PubMed Central

8 November 2017

language of work or name

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publication date

1 October 2004

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Europe PubMed Central

8 November 2017

Experimental Cell Research

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Europe PubMed Central

8 November 2017

299

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Europe PubMed Central

8 November 2017

454-464

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Europe PubMed Central

8 November 2017

2

1 reference

Europe PubMed Central

8 November 2017

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

The phenotypic spectrum of CADASIL: clinical findings in 102 cases

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

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%2FJ.YEXCR.2004.06.004

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

Notch signaling: cell fate control and signal integration in development

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

Specific EGF repeats of Notch mediate interactions with Delta and serrate: Implications for notch as a multifunctional receptor

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

A ligand-induced extracellular cleavage regulates gamma-secretase-like proteolytic activation of Notch1

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

Notch signal transduction: a real rip and more

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

CSL-independent Notch signalling: a checkpoint in cell fate decisions during development?

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

NOTCH3 mutation involving three cysteine residues in a family with typical CADASIL

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

Notch3 signaling in vascular smooth muscle cells induces c-FLIP expression via ERK/MAPK activation. Resistance to Fas ligand-induced apoptosis

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

Coordinate Notch3-hairy-related transcription factor pathway regulation in response to arterial injury. Mediator role of platelet-derived growth factor and ERK

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

Determinants of Notch-3 receptor expression and signaling in vascular smooth muscle cells: implications in cell-cycle regulation.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

The novel Notch homologue mouse Notch 3 lacks specific epidermal growth factor-repeats and is expressed in proliferating neuroepithelium

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

Fringe differentially modulates Jagged1 and Delta1 signalling through Notch1 and Notch2.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

Notch receptor activation inhibits oligodendrocyte differentiation.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

Signal transduction by activated mNotch: importance of proteolytic processing and its regulation by the extracellular domain.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

Notch-1 signalling requires ligand-induced proteolytic release of intracellular domain

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

Conservation of the biochemical mechanisms of signal transduction among mammalian Notch family members

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

Missense mutations impair intracellular processing of fibrillin and microfibril assembly in Marfan syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

Cysteine substitutions in epidermal growth factor-like domains of fibrillin-1: distinct effects on biochemical and clinical phenotypes

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

Deletion in cysteine-rich region of LDL receptor impedes transport to cell surface in WHHL rabbit

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

An individual with a healthy phenotype in spite of a pathogenic LDL receptor mutation (C240F)

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

Integration of endoplasmic reticulum signaling in health and disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

Characterization of Notch3-deficient mice: normal embryonic development and absence of genetic interactions with a Notch1 mutation.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

F3/contactin acts as a functional ligand for Notch during oligodendrocyte maturation

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

HERP1 is a cell type-specific primary target of Notch

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

Inherent toxicity of aggregates implies a common mechanism for protein misfolding diseases

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.06.004

7 January 2021

Paradigm shifts in Alzheimer's disease and other neurodegenerative disorders: the emerging role of oligomeric assemblies

1 reference

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7 January 2021

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10.1016/J.YEXCR.2004.06.004

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Europe PubMed Central

8 November 2017

release_3y3nyokr2nae3f6e3grmjuwdsu

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https://api.fatcat.wiki/v0/release/3y3nyokr2nae3f6e3grmjuwdsu

24 November 2022

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Europe PubMed Central

8 November 2017

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