Potassium currents in human myogenic cells from healthy and congenital myotonic dystrophy foetuses

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Functional KCa1.1 channels are crucial for regulating the proliferation, migration and differentiation of human primary skeletal myoblasts

P2860

Q30830556-19699083-00FB-4356-9CF6-635D85FD28F7

P2860

Potassium currents in human myogenic cells from healthy and congenital myotonic dystrophy foetuses

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http://www.wikidata.org/entity/Q57268499

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im Februar 2009 veröffentlichter wissenschaftlicher Artikel

@de

scientific article published on 04 February 2009

@en

wetenschappelijk artikel

@nl

наукова стаття, опублікована в січні 2009

@uk

name

Potassium currents in human my ...... al myotonic dystrophy foetuses

@en

Potassium currents in human my ...... al myotonic dystrophy foetuses

@nl

type

Item

label

Potassium currents in human my ...... al myotonic dystrophy foetuses

@en

Potassium currents in human my ...... al myotonic dystrophy foetuses

@nl

prefLabel

Potassium currents in human my ...... al myotonic dystrophy foetuses

@en

Potassium currents in human my ...... al myotonic dystrophy foetuses

@nl

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Potassium currents in human my ...... al myotonic dystrophy foetuses

@en

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Andrew Constanti

http://www.w3.org/2001/XMLSchema#string

Fabio Ruzzier

http://www.w3.org/2001/XMLSchema#string

Paola Lorenzon

http://www.w3.org/2001/XMLSchema#string

P2860

Muscleblind proteins regulate alternative splicing

Molecular basis for impaired muscle differentiation in myotonic dystrophy

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

Structure and function of cardiac potassium channels.

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

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

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

Foci of trinucleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues.

Human myoblast fusion requires expression of functional inward rectifier Kir2.1 channels

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

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s11658-009-0006-4

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336-346

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scholarly article

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10.2478/S11658-009-0006-4

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http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

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2009-02-04T00:00:00Z

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1010405408

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19194665

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P932

6275736

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Potassium currents in human myogenic cells from healthy and congenital myotonic dystrophy foetuses

about

P2860

P2860

Potassium currents in human myogenic cells from healthy and congenital myotonic dystrophy foetuses

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P6179

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P6179

P698

P932