(Q43232375)

English

Myopathy caused by HRAS germline mutations: implications for disturbed myogenic differentiation in the presence of constitutive HRas activation

scientific article published on 5 April 2007

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scholarly article

1 reference

Europe PubMed Central

16 November 2017

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Myopathy caused by HRAS germline mutations: implications for disturbed myogenic differentiation in the presence of constitutive HRas activation (English)

1 reference

Europe PubMed Central

16 November 2017

10

object named as

Martin Zenker

1 reference

Europe PubMed Central

16 November 2017

author name string

Ineke van der Burgt

1

1 reference

Europe PubMed Central

16 November 2017

William Kupsky

2

1 reference

Europe PubMed Central

16 November 2017

Stephani Stassou

3

1 reference

Europe PubMed Central

16 November 2017

Ali Nadroo

4

1 reference

Europe PubMed Central

16 November 2017

Cândida Barroso

5

1 reference

Europe PubMed Central

16 November 2017

Angelika Diem

6

1 reference

Europe PubMed Central

16 November 2017

Christian P Kratz

7

1 reference

Europe PubMed Central

16 November 2017

Radovan Dvorsky

8

1 reference

Europe PubMed Central

16 November 2017

Mohammad Reza Ahmadian

9

1 reference

Europe PubMed Central

16 November 2017

language of work or name

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publication date

5 April 2007

1 reference

Europe PubMed Central

16 November 2017

Journal of Medical Genetics

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Europe PubMed Central

16 November 2017

44

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Europe PubMed Central

16 November 2017

7

1 reference

Europe PubMed Central

16 November 2017

459-462

1 reference

Europe PubMed Central

16 November 2017

Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598013

25 May 2018

Noonan syndrome and related disorders: dysregulated RAS-mitogen activated protein kinase signal transduction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598013

25 May 2018

The cardiofaciocutaneous syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598013

25 May 2018

Genotype-phenotype correlation in Costello syndrome: HRAS mutation analysis in 43 cases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598013

25 May 2018

Ras activation of a Rac1 exchange factor, Tiam1, mediates neurotrophin-3-induced Schwann cell migration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598013

25 May 2018

Germline mutations in HRAS proto-oncogene cause Costello syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598013

25 May 2018

Glial cell-line derived neurotrophic factor-dependent fusimotor neuron survival during development

1 reference

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25 May 2018

Neuregulin induces the expression of transcription factors and myosin heavy chains typical of muscle spindles in cultured human muscle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598013

25 May 2018

Costello syndrome: an overview

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598013

25 May 2018

A role for neuregulin1 signaling in muscle spindle differentiation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598013

25 May 2018

A novel activating mutation of the K-ras gene in human primary colon adenocarcinoma

1 reference

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25 May 2018

Signaling complexes and protein-protein interactions involved in the activation of the Ras and phosphatidylinositol 3-kinase pathways by the c-Ret receptor tyrosine kinase.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598013

25 May 2018

Involvement of the switch 2 domain of Ras in its interaction with guanine nucleotide exchange factors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598013

25 May 2018

Expression of myosin heavy chain isoforms and myogenesis of intrafusal fibres in rat muscle spindles.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598013

25 May 2018

Ras p21Val inhibits myogenesis without altering the DNA binding or transcriptional activities of the myogenic basic helix-loop-helix factors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598013

25 May 2018

Lack of neurotrophin-3 leads to deficiencies in the peripheral nervous system and loss of limb proprioceptive afferents

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598013

25 May 2018

Analysis of the transforming potential of the human H-ras gene by random mutagenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598013

25 May 2018

The oncogenic forms of N-ras or H-ras prevent skeletal myoblast differentiation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598013

25 May 2018

Transformation by activated ras or fos prevents myogenesis by inhibiting expression of MyoD1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598013

25 May 2018

The role of Gln61 and Glu63 of Ras GTPases in their activation by NF1 and Ras GAP.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598013

25 May 2018

HRAS mutations in Costello syndrome: detection of constitutional activating mutations in codon 12 and 13 and loss of wild-type allele in malignancy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598013

15 August 2018

HRAS mutation analysis in Costello syndrome: genotype and phenotype correlation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598013

15 August 2018

Myopathology in patients with a Noonan phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/17412879

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new syndrome of myopathy with muscle spindle excess

1 reference

https://pubmed.ncbi.nlm.nih.gov/17412879

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myopathy with muscle spindle excess: A new congenital neuromuscular syndrome?

1 reference

https://pubmed.ncbi.nlm.nih.gov/17412879

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuregulin-induced association of Sos Ras exchange protein with HER2(erbB2)/HER3(erbB3) receptor complexes in Schwann cells through a specific Grb2-HER2(erbB2) interaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/17412879

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Skeletal myopathy in transgenic mice carrying human prototype c-Ha-ras gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/17412879

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Noonan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17412879

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.2007.049270

1 reference

Europe PubMed Central

16 November 2017

1 reference

Europe PubMed Central

16 November 2017

1 reference

Europe PubMed Central

16 November 2017

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0 references

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