(Q35142864)

6 August 2017

title

Mice lacking microRNA 133a develop dynamin 2–dependent centronuclear myopathy (English)

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6 August 2017

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10

James A Richardson

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6 August 2017

Ning Liu

1

1 reference

6 August 2017

Svetlana Bezprozvannaya

2

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6 August 2017

John M Shelton

3

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6 August 2017

Madlyn I Frisard

4

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6 August 2017

Matthew W Hulver

5

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6 August 2017

Ryan P McMillan

6

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6 August 2017

Yaru Wu

7

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6 August 2017

Kevin A Voelker

8

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6 August 2017

Robert W Grange

9

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6 August 2017

Rhonda Bassel-Duby

11

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6 August 2017

Eric N Olson

12

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6 August 2017

language of work or name

English

0 references

publication date

1 August 2011

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Journal of Clinical Investigation

6 August 2017

published in

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6 August 2017

volume

121

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6 August 2017

issue

8

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6 August 2017

page(s)

3258-3268

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describes a project that uses

6 August 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3148737/fullTextXML

inferred from PubMed Central ID database lookup

cites work

Dynamin GTPase regulation is altered by PH domain mutations found in centronuclear myopathy patients

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Dynamin 2 mutants linked to centronuclear myopathies form abnormally stable polymers

13 July 2018

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MicroRNA regulatory networks in cardiovascular development

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Mitochondrial DNA alterations and reduced mitochondrial function in aging

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Centronuclear myopathies: a widening concept

13 July 2018

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Toll-like receptor 4 modulates skeletal muscle substrate metabolism

13 July 2018

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13 July 2018

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MicroRNA-206 delays ALS progression and promotes regeneration of neuromuscular synapses in mice

13 July 2018

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T-tubule disorganization and defective excitation-contraction coupling in muscle fibers lacking myotubularin lipid phosphatase

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13 July 2018

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Loss of myotubularin function results in T-tubule disorganization in zebrafish and human myotubular myopathy

13 July 2018

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miRNAS in normal and diseased skeletal muscle

13 July 2018

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microRNA-133a regulates cardiomyocyte proliferation and suppresses smooth muscle gene expression in the heart

13 July 2018

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Centronuclear (myotubular) myopathy

13 July 2018

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AAV-mediated intramuscular delivery of myotubularin corrects the myotubular myopathy phenotype in targeted murine muscle and suggests a function in plasma membrane homeostasis

13 July 2018

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Protein kinase D1 stimulates MEF2 activity in skeletal muscle and enhances muscle performance

13 July 2018

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Genetic and pharmacologic inhibition of mitochondrial-dependent necrosis attenuates muscular dystrophy

13 July 2018

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Role of mitochondrial dysfunction in insulin resistance

13 July 2018

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Mechanisms of post-transcriptional regulation by microRNAs: are the answers in sight?

13 July 2018

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13 July 2018

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Ablation of sarcolipin enhances sarcoplasmic reticulum calcium transport and atrial contractility

13 July 2018

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Distinctive patterns of microRNA expression in primary muscular disorders

13 July 2018

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Dysregulation of cardiogenesis, cardiac conduction, and cell cycle in mice lacking miRNA-1-2

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148737

Muscle stem cells in development, regeneration, and disease

13 July 2018

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Signaling pathways in skeletal muscle remodeling

13 July 2018

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The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation

13 July 2018

1 reference

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Mutations in dynamin 2 cause dominant centronuclear myopathy

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148737

Elevated stearoyl-CoA desaturase-1 expression in skeletal muscle contributes to abnormal fatty acid partitioning in obese humans

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148737

Centronuclear myopathy in mice lacking a novel muscle-specific protein kinase transcriptionally regulated by MEF2

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148737

The lipid phosphatase myotubularin is essential for skeletal muscle maintenance but not for myogenesis in mice

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148737

Stimulation of slow skeletal muscle fiber gene expression by calcineurin in vivo

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148737

Correlation of muscle fiber type measurements with clinical and molecular genetic data in Duchenne muscular dystrophy

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148737

Analysis of muscle creatine kinase gene regulatory elements in skeletal and cardiac muscles of transgenic mice

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148737

Structure and development of E-C coupling units in skeletal muscle

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148737

Identification of upstream and intragenic regulatory elements that confer cell-type-restricted and differentiation-specific expression on the muscle creatine kinase gene

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148737

Fast muscle fibers are preferentially affected in Duchenne muscular dystrophy.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148737

Mitochondrial alterations in dynamin 2-related centronuclear myopathy.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148737

Mitochondrial respiratory chain dysfunction in various neuromuscular diseases

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148737

Glucose tolerance and skeletal muscle gene expression in response to alternate day fasting

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148737

Defects in amphiphysin 2 (BIN1) and triads in several forms of centronuclear myopathies

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148737

A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice

25 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3148737

A new centronuclear myopathy phenotype due to a novel dynamin 2 mutation

8 December 2018

1 reference

12 December 2020

Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosis

1 reference

12 December 2020

Regulation of mitochondrial biogenesis in skeletal muscle by CaMK

1 reference

12 December 2020

Muscle hypertrophy in Duchenne muscular dystrophy. A pathological and morphometric study

1 reference

12 December 2020

Mitochondrial dysfunction in adult-onset myopathies with structural abnormalities

1 reference

12 December 2020

Organelle isolation: functional mitochondria from mouse liver, muscle and cultured filroblasts

1 reference

12 December 2020

Dynamin 2 mutations cause sporadic centronuclear myopathy with neonatal onset

1 reference

12 December 2020

Identifiers

DOI

10.1172/JCI46267

1 reference

6 August 2017

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6 August 2017

1 reference