Correction of ClC-1 splicing eliminates chloride channelopathy and myotonia in mouse models of myotonic dystrophy (Q24679378)

22 June 2017

Correction of ClC-1 splicing eliminates chloride channelopathy and myotonia in mouse models of myotonic dystrophy (English)

1 reference

22 June 2017

1 reference

Maurice S Swanson

3

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author name string

Thurman M Wheeler

1

1 reference

22 June 2017

John D Lueck

2

1 reference

22 June 2017

Robert T Dirksen

4

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22 June 2017

Charles A Thornton

5

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22 June 2017

language of work or name

English

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publication date

1 December 2007

1 reference

Journal of Clinical Investigation

22 June 2017

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22 June 2017

117

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22 June 2017

12

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22 June 2017

3952-3957

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describes a project that uses

22 June 2017

ImageQuant

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2075481/fullTextXML

inferred from PubMed Central ID database lookup

cites work

Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy

1 reference

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Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy

7 April 2017

1 reference

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Ion transport in human skeletal muscle cells: disturbances in myotonic dystrophy and Brody's disease

7 April 2017

1 reference

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Restoration of correct splicing in thalassemic pre-mRNA by antisense oligonucleotides

7 April 2017

1 reference

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Drug treatment for myotonia

7 April 2017

1 reference

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Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches

7 April 2017

1 reference

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RNA leaching of transcription factors disrupts transcription in myotonic dystrophy

7 April 2017

1 reference

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A muscleblind knockout model for myotonic dystrophy

7 April 2017

1 reference

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Myotonic dystrophy protein kinase is involved in the modulation of the Ca2+ homeostasis in skeletal muscle cells

7 April 2017

1 reference

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Muscle chloride channel dysfunction in two mouse models of myotonic dystrophy.

7 April 2017

1 reference

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28 September 2017

RNA-dominant diseases

1 reference

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Reversal of RNA missplicing and myotonia after muscleblind overexpression in a mouse poly(CUG) model for myotonic dystrophy

28 September 2017

1 reference

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Altered skeletal muscle phenotypes in calcineurin Aalpha and Abeta gene-targeted mice

28 September 2017

1 reference

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Modification of alternative splicing by antisense oligonucleotides as a potential chemotherapy for cancer and other diseases

28 September 2017

1 reference

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Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing

28 September 2017

1 reference

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Expanded CUG repeats trigger aberrant splicing of ClC-1 chloride channel pre-mRNA and hyperexcitability of skeletal muscle in myotonic dystrophy

28 September 2017

1 reference

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Specific removal of the nonsense mutation from the mdx dystrophin mRNA using antisense oligonucleotides.

28 September 2017

1 reference

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Modification of splicing in the dystrophin gene in cultured Mdx muscle cells by antisense oligoribonucleotides

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2075481

Disruption of splicing regulated by a CUG-binding protein in myotonic dystrophy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2075481

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2075481

Characteristics of Na+ channels and Cl- conductance in resealed muscle fibre segments from patients with myotonic dystrophy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2075481

Systemic delivery of morpholino oligonucleotide restores dystrophin expression bodywide and improves dystrophic pathology

30 May 2018

1 reference

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Quantitative evaluation of mammalian skeletal muscle as a heterologous protein expression system.

28 November 2018

1 reference

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Altered mRNA splicing of the skeletal muscle ryanodine receptor and sarcoplasmic/endoplasmic reticulum Ca2+-ATPase in myotonic dystrophy type 1.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2075481

Truncated ClC-1 mRNA in myotonic dystrophy exerts a dominant-negative effect on the Cl current.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2075481

Optimisation of electrotransfer of plasmid into skeletal muscle by pretreatment with hyaluronidase -- increased expression with reduced muscle damage

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2075481

Expression of apamin receptor in muscles of patients with myotonic muscular dystrophy.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2075481

The pathophysiology of myotonia produced by aromatic carboxylic acids

28 November 2018

1 reference

12 December 2020

Possible role of apamin-sensitive K+ channels in myotonic dystrophy

1 reference

12 December 2020

Chloride channelopathy in myotonic dystrophy resulting from loss of posttranscriptional regulation for CLCN1

1 reference

12 December 2020

Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat

1 reference

12 December 2020

Identifiers

DOI

10.1172/JCI33355

1 reference

OpenCitations bibliographic resource ID

22 June 2017

2391602

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference