Mice carrying a R142C Notch 3 knock-in mutation do not develop a CADASIL-like phenotype (Q45220730)

11 December 2017

Mice carrying a R142C Notch 3 knock-in mutation do not develop a CADASIL-like phenotype (English)

1 reference

11 December 2017

15

1 reference

11 December 2017

8

Helena Karlström

1 reference

11 December 2017

11

Björn Rozell

1 reference

11 December 2017

Johan Lundkvist

1

1 reference

11 December 2017

Shunwei Zhu

2

1 reference

11 December 2017

Emil M Hansson

3

1 reference

11 December 2017

Petra Schweinhardt

4

1 reference

11 December 2017

Qing Miao

5

1 reference

11 December 2017

Paul Beatus

6

1 reference

11 December 2017

Karin Dannaeus

7

1 reference

11 December 2017

Clas B Johansson

9

1 reference

11 December 2017

Matti Viitanen

10

1 reference

11 December 2017

Christian Spenger

12

1 reference

11 December 2017

Abdul Mohammed

13

1 reference

11 December 2017

Hannu Kalimo

14

1 reference

11 December 2017

1 January 2005

1 reference

11 December 2017

1 reference

11 December 2017

41

1 reference

11 December 2017

1

1 reference

11 December 2017

13-22

1 reference

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

11 December 2017

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20091

Expression of dominant negative cadherin in the adult mouse brain modifies rearing behavior.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20091

Notch signaling in development and disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20091

HES and HERP families: multiple effectors of the Notch signaling pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20091

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20091

Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20091

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

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20091

The temporal evolution of hypoglycemic brain damage. III. Light and electron microscopic findings in the rat caudoputamen.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20091

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20091

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20091

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20091

The human NOTCH1, 2, and 3 genes are located at chromosome positions 9q34, 1p13-p11, and 19p13.2-p13.1 in regions of neoplasia-associated translocation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20091

The role of Notch in tumorigenesis: oncogene or tumour suppressor?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20091

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20091

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20091

7 January 2021

Patterns of MRI lesions in CADASIL.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20091

7 January 2021

The phenotypic spectrum of CADASIL: clinical findings in 102 cases

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20091

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20091

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/10.1002%2FGENE.20091

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/10.1002%2FGENE.20091

7 January 2021

Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutation

1 reference

https://api.crossref.org/works/10.1002%2FGENE.20091

7 January 2021

Identifiers

DOI

10.1002/GENE.20091

1 reference

11 December 2017

1 reference