(Q48953016)

17 February 2018

title

Myotonic dystrophy kinase modulates skeletal muscle but not cardiac voltage-gated sodium channels. (English)

1 reference

17 February 2018

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Chahine M

1

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17 February 2018

George AL Jr

series ordinal

2

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17 February 2018

language of work or name

English

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publication date

1 August 1997

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17 February 2018

published in

FEBS Letters

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17 February 2018

volume

412

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17 February 2018

issue

3

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17 February 2018

page(s)

621-624

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17 February 2018

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

cites work

1 reference

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

21 January 2018

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

21 January 2018

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Modulation of skeletal muscle sodium channels by human myotonin protein kinase

21 January 2018

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Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel

21 January 2018

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Characterization of the myotonic dystrophy region predicts multiple protein isoform-encoding mRNAs

21 January 2018

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In vitro RNA synthesis with SP6 RNA polymerase

21 January 2018

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A molecular basis for gating mode transitions in human skeletal muscle Na+ channels.

21 January 2018

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Myotonic dystrophy: will the real gene please step forward!

21 January 2018

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Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy.

21 January 2018

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Hereditary dysfunction of voltage-gated sodium channels: from clinical phenotype to molecular mechanisms

21 January 2018

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The skeletal muscle chloride channel in dominant and recessive human myotonia

21 January 2018

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Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita).

21 January 2018

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Abnormalities of the fast sodium current in myotonic dystrophy, recessive generalized myotonia, and adynamia episodica

21 January 2018

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The long QT syndrome. A review of recent molecular genetic and physiologic discoveries

21 January 2018

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Pathology of the cardiac conduction system in myotonic dystrophy: a study of 12 cases

21 January 2018

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Multiple domains contribute to the distinct inactivation properties of human heart and skeletal muscle Na+ channels

21 January 2018

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Effect of the myotonic dystrophy (DM) mutation on mRNA levels of the DM gene

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0014-5793%2897%2900869-7

Phosphorylation reactions of recombinant human myotonic dystrophy protein kinase and their inhibition

7 January 2021

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Cardiac abnormalities in myotonic dystrophy. Electrophysiologic and histopathologic studies

7 January 2021

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10.1016/S0014-5793(97)00869-7

7 January 2021

Identifiers

DOI

1 reference

17 February 2018

1 reference

17 February 2018