(Q33923247)

30 July 2017

title

Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophy (English)

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Becker muscular dystrophy

30 July 2017

main subject

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ORCID Public Data File 2021

author name string

Kerst B

1

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30 July 2017

Mennerich D

2

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30 July 2017

Schuelke M

3

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30 July 2017

Stoltenburg-Didinger G

4

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30 July 2017

von Moers A

5

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30 July 2017

Gossrau R

6

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30 July 2017

van Landeghem FK

7

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30 July 2017

Speer A

8

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30 July 2017

Braun T

9

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30 July 2017

Hübner C

10

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30 July 2017

publication date

1 December 2000

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30 July 2017

published in

Neuromuscular Disorders

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30 July 2017

volume

10

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30 July 2017

issue

8

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30 July 2017

page(s)

572-577

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The MyoD DNA binding domain contains a recognition code for muscle-specific gene activation

30 July 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

Dimerization specificity of myogenic helix-loop-helix DNA-binding factors directed by nonconserved hydrophilic residues

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

Crystal structure of MyoD bHLH domain-DNA complex: perspectives on DNA recognition and implications for transcriptional activation

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

Skeletal muscle determination and differentiation: story of a core regulatory network and its context

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

In situ hybridization analysis for expression of myogenic regulatory factors in regenerating muscle of mdx mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

MyoD is required for myogenic stem cell function in adult skeletal muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

A role for FGF-6 in skeletal muscle regeneration.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s)

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

Dystrophin characterization in BMD patients: correlation of abnormal protein with clinical phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

Dystrophin expression in a Duchenne muscular dystrophy patient with a frame shift deletion

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

Undetectable dystrophin can still result in a relatively benign phenotype of dystrophinopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

Yield of mtDNA mutation analysis in 2,000 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

Myf-6, a new member of the human gene family of myogenic determination factors: evidence for a gene cluster on chromosome 12

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

The four human muscle regulatory helix-loop-helix proteins Myf3-Myf6 exhibit similar hetero-dimerization and DNA binding properties

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

Transcriptional activation domain of the muscle-specific gene-regulatory protein myf5.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

Muscle histology in becker muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

Muscle differentiation: more complexity to the network of myogenic regulators.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

Dilated cardiomyopathy requiring cardiac transplantation as initial manifestation of Xp21 Becker type muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

Rare combination of Becker muscular dystrophy and Klinefelter's syndrome in one patient

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

Severe cardiomyopathy in mice lacking dystrophin and MyoD

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

Know your neighbors: three phenotypes in null mutants of the myogenic bHLH gene MRF4.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

Human bHLH transcription factor gene myogenin (MYOG): genomic sequence and negative mutation analysis in patients with severe congenital myopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900150-4

7 January 2021

10.1016/S0960-8966(00)00150-4

Identifiers

DOI

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30 July 2017

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