Skeletal muscle repair in a mouse model of nemaline myopathy (Q34552514)

3 August 2017

title

Skeletal muscle repair in a mouse model of nemaline myopathy (English)

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3 August 2017

Despina Sanoudou

1

1 reference

3 August 2017

Mark A Corbett

2

1 reference

3 August 2017

Mei Han

3

1 reference

3 August 2017

Majid Ghoddusi

4

1 reference

3 August 2017

Mai-Anh T Nguyen

5

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3 August 2017

Nicole Vlahovich

6

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3 August 2017

Edna C Hardeman

7

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3 August 2017

Alan H Beggs

8

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3 August 2017

publication date

28 July 2006

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3 August 2017

published in

Human Molecular Genetics

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3 August 2017

volume

15

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3 August 2017

issue

17

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3 August 2017

page(s)

2603-2612

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The differential gene expression profiles of proximal and distal muscle groups are altered in pre-pathological dysferlin-deficient mice

3 August 2017

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Expression profiling reveals altered satellite cell numbers and glycolytic enzyme transcription in nemaline myopathy muscle

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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Clinical and genetic heterogeneity in nemaline myopathy--a disease of skeletal muscle thin filaments

7 July 2018

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7 July 2018

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7 July 2018

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A mutation in alpha-tropomyosin(slow) affects muscle strength, maturation and hypertrophy in a mouse model for nemaline myopathy

7 July 2018

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7 July 2018

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7 July 2018

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Acetylation of MyoD directed by PCAF is necessary for the execution of the muscle program

7 July 2018

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Mena is required for neurulation and commissure formation

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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

7 July 2018

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An alphaTropomyosin mutation alters dimer preference in nemaline myopathy.

7 July 2018

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Conserved and muscle-group-specific gene expression patterns shape postnatal development of the novel extraocular muscle phenotype

27 October 2018

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The Ankrd2 Protein, a Link Between the Sarcomere and the Nucleus in Skeletal Muscle

27 October 2018

1 reference

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Molecular classification of nemaline myopathies: "nontyping" specimens exhibit unique patterns of gene expression

27 October 2018

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Temporal gene expression profiling of dystrophin-deficient (mdx) mouse diaphragm identifies conserved and muscle group-specific mechanisms in the pathogenesis of muscular dystrophy

27 October 2018

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De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy

27 October 2018

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27 October 2018

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Mutations of the slow muscle alpha-tropomyosin gene, TPM3, are a rare cause of nemaline myopathy

27 October 2018

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Muscle weakness in a mouse model of nemaline myopathy can be reversed with exercise and reveals a novel myofiber repair mechanism

27 October 2018

1 reference

12 December 2020

Identification, distribution, and myosin subunit composition of type IIX fibers in mouse muscles

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12 December 2020

Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene

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12 December 2020

Variations in gene expression among different types of human skeletal muscle

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12 December 2020

The influence of muscle type and dystrophin deficiency on murine expression profiles

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12 December 2020

Altered expression of ARPP protein in skeletal muscles of patients with muscular dystrophy, congenital myopathy and spinal muscular atrophy

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12 December 2020

Identifiers

DOI

10.1093/HMG/DDL186

1 reference

3 August 2017

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3 August 2017

1 reference