Phospholemman is a substrate for myotonic dystrophy protein kinase. - Wikidata - wikimedia - TriplyDB

Phospholemman is a substrate for myotonic dystrophy protein kinase.

Phospholemman is a substrate for myotonic dystrophy protein kinase.

http://www.wikidata.org/entity/Q30305657

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Divergent mitochondrial and endoplasmic reticulum association of DMPK splice isoforms depends on unique sequence arrangements in tail anchors.Structure of the Na,K-ATPase regulatory protein FXYD1 in micelles Muscle wasting in myotonic dystrophies: a model of premature aging Structure of dystrophia myotonica protein kinase Hypertrophy, increased ejection fraction, and reduced Na-K-ATPase activity in phospholemman-deficient mice Phospholemman expression in extraglomerular mesangium and afferent arteriole of the juxtaglomerular apparatus Phospholemman deficiency in postinfarct hearts: enhanced contractility but increased mortality.A tail-anchored myotonic dystrophy protein kinase isoform induces perinuclear clustering of mitochondria, autophagy, and apoptosis FXYD proteins: new tissue-specific regulators of the ubiquitous Na,K-ATPase.Phospholemman: a novel cardiac stress protein.Brain region-specific expression of Fxyd1, an Mecp2 target gene, is regulated by epigenetic mechanisms.FXYD proteins: new regulators of Na-K-ATPase.Phospholemman regulates cardiac Na+/Ca2+ exchanger by interacting with the exchanger's proximal linker domain Can Human Pluripotent Stem Cell-Derived Cardiomyocytes Advance Understanding of Muscular Dystrophies?Phosphorylation target site specificity for AGC kinases DMPK E and Lats2.Cytoplasmic targeting signals mediate delivery of phospholemman to the plasma membrane.In vivo assessment of muscle membrane properties in myotonic dystrophy.Phospholemman modulates Na+/Ca2+ exchange in adult rat cardiac myocytes.Sarcolemmal excitability in the myotonic dystrophies.Role of phospholemman and the 70 kDa inhibitor protein in regulating Na+/K+ ATPase activity in pulmonary artery smooth muscle cells under U46619 stimulation.

P2860

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P2860

Phospholemman is a substrate for myotonic dystrophy protein kinase.

http://www.wikidata.org/entity/Q30305657

description

2000 nî lūn-bûn

@nan

2000 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2000 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2000年の論文

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2000年論文

@yue

2000年論文

@zh-hant

2000年論文

@zh-hk

2000年論文

@zh-mo

2000年論文

@zh-tw

2000年论文

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name

Phospholemman is a substrate for myotonic dystrophy protein kinase.

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Phospholemman is a substrate for myotonic dystrophy protein kinase.

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type

label

Phospholemman is a substrate for myotonic dystrophy protein kinase.

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Phospholemman is a substrate for myotonic dystrophy protein kinase.

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prefLabel

Phospholemman is a substrate for myotonic dystrophy protein kinase.

@ast

Phospholemman is a substrate for myotonic dystrophy protein kinase.

@en

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P1433

Journal of Biological Chemistry

P1476

Phospholemman is a substrate for myotonic dystrophy protein kinase.

@en

P2093

Bush EW

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

Gilbert J

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

Helmke SM

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

John JE 3rd

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

Jones LR

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

Moorman JR

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

Mounsey JP

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

Perryman MB

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

Roses AD

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

P2860

The skeletal muscle chloride channel in dominant and recessive human myotonia

Cloning and chromosomal location of a novel member of the myotonic dystrophy family of protein kinases

Mat-8, a novel phospholemman-like protein expressed in human breast tumors, induces a chloride conductance in Xenopus oocytes

Characterization of the human and rat phospholemman (PLM) cDNAs and localization of the human PLM gene to chromosome 19q13.1

Protein kinase C and cyclic AMP-dependent protein kinase phosphorylate phospholemman, an insulin and adrenaline-regulated membrane phosphoprotein, at specific sites in the carboxy terminal domain

Theoretical reconstruction of myotonia and paralysis caused by incomplete inactivation of sodium channels.

Sodium, potassium, and chloride fluxes in intercostal muscle from normal goats and goats with hereditary myotonia

The product of the Saccharomyces cerevisiae cell cycle gene DBF2 has homology with protein kinases and is periodically expressed in the cell cycle

The cell-cycle-regulated budding yeast gene DBF2, encoding a putative protein kinase, has a homologue that is not under cell-cycle control.

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

P304

23362-23367

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scholarly article

P356

10.1074/JBC.M000899200

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P407

P433

30

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P478

275

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P577

2000-07-01T00:00:00Z

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P698

10811636

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