Myotonic dystrophy kinase modulates skeletal muscle but not cardiac voltage‐gated sodium channels (Q48953016)

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scientific article published on August 4, 1997

Language	Label	Description	Also known as
English	Myotonic dystrophy kinase modulates skeletal muscle but not cardiac voltage‐gated sodium channels	scientific article published on August 4, 1997

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/9276478

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

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/9276478

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

1 reference

10.1016/S0014-5793(97)00869-7

https://api.crossref.org/works/10.1016/S0014-5793(97)00869-7

13 November 2024

myotonic dystrophy

1 reference

based on heuristic

inferred from title

ion channel gating

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9276478

13 November 2024

author name string

George AL Jr

2

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/9276478

M. Chahine

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9276478

13 November 2024

A. L. George

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9276478

13 November 2024

language of work or name

0 references

publication date

1 August 1997

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/9276478

4 August 1997

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9276478

13 November 2024

full work available at URL

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1016%2FS0014-5793%2897%2900869-7

1 reference

10.1016/S0014-5793(97)00869-7

https://api.crossref.org/works/10.1016/S0014-5793(97)00869-7

13 November 2024

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1016%2FS0014-5793(97)00869-7

1 reference

10.1016/S0014-5793(97)00869-7

https://api.crossref.org/works/10.1016/S0014-5793(97)00869-7

13 November 2024

https://febs.onlinelibrary.wiley.com/doi/pdf/10.1016/S0014-5793%2897%2900869-7

1 reference

10.1016/S0014-5793(97)00869-7

https://api.crossref.org/works/10.1016/S0014-5793(97)00869-7

13 November 2024

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/9276478

412

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/9276478

3

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/9276478

621-624

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/9276478

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Modulation of skeletal muscle sodium channels by human myotonin protein kinase

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

In vitro RNA synthesis with SP6 RNA polymerase

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Myotonic dystrophy: will the real gene please step forward!

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

The skeletal muscle chloride channel in dominant and recessive human myotonia

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

Cardiac abnormalities in myotonic dystrophy. Electrophysiologic and histopathologic studies

1 reference

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

7 January 2021

Identifiers

10.1016/S0014-5793(97)00869-7

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/9276478

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/9276478

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