Myogenic defects in myotonic dystrophy (Q35633172)

9 August 2017

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title

Myogenic defects in myotonic dystrophy (English)

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9 August 2017

Jeffrey D Amack

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9 August 2017

Mani S Mahadevan

series ordinal

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9 August 2017

language of work or name

English

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publication date

1 January 2004

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9 August 2017

published in

Developmental Biology

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9 August 2017

volume

265

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9 August 2017

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9 August 2017

page(s)

294-301

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The myotonic dystrophy expanded CUG repeat tract is necessary but not sufficient to disrupt C2C12 myoblast differentiation

9 August 2017

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Mutant DMPK 3'-UTR transcripts disrupt C2C12 myogenic differentiation by compromising MyoD.

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The muscleblind gene participates in the organization of Z-bands and epidermal attachments of Drosophila muscles and is regulated by Dmef2.

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Muscle-specific alternative splicing of myotubularin-related 1 gene is impaired in DM1 muscle cells

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

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Expansion of a CUG trinucleotide repeat in the 3' untranslated region of myotonic dystrophy protein kinase transcripts results in nuclear retention of transcripts

7 January 2021

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An unstable triplet repeat in a gene related to myotonic muscular dystrophy

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Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice.

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Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9

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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

7 January 2021

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

7 January 2021

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

7 January 2021

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Over expression of the murine myotonic dystrophy protein kinase in the mouse myogenic C2C12 cell line leads to inhibition of terminal differentiation.

7 January 2021

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7 January 2021

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Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathy

7 January 2021

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Overexpression of 3′-Untranslated Region of the Myotonic Dystrophy Kinase cDNA Inhibits Myoblast Differentiation in Vitro

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Aberrant regulation of insulin receptor alternative splicing is associated with insulin resistance in myotonic dystrophy

7 January 2021

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7 January 2021

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Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities

7 January 2021

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Phosphorylation of nuclear MyoD is required for its rapid degradation

7 January 2021

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7 January 2021

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7 January 2021

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Expanded CUG repeat RNAs form hairpins that activate the double-stranded RNA-dependent protein kinase PKR

7 January 2021

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7 January 2021

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Molecular basis for impaired muscle differentiation in myotonic dystrophy

7 January 2021

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Myotonic dystrophy: the role of the CUG triplet repeats in splicing of a novel DMPK exon and altered cytoplasmic DMPK mRNA isoform ratios

7 January 2021

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The myotubular myopathies: differential diagnosis of the X linked recessive, autosomal dominant, and autosomal recessive forms and present state of DNA studies

7 January 2021

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Serial passaging and differentiation of myogenic cells isolated from dystrophic mouse muscle

7 January 2021

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Direct inhibition of G(1) cdk kinase activity by MyoD promotes myoblast cell cycle withdrawal and terminal differentiation

7 January 2021

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10.1016/J.YDBIO.2003.07.021

7 January 2021

Identifiers

DOI

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9 August 2017

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