A defective SERCA1 protein is responsible for congenital pseudomyotonia in Chianina cattle. - Wikidata - awgldk - TriplyDB

A defective SERCA1 protein is responsible for congenital pseudomyotonia in Chianina cattle.

A defective SERCA1 protein is responsible for congenital pseudomyotonia in Chianina cattle.

http://www.wikidata.org/entity/Q37071895

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Dystonia and Paroxysmal Dyskinesias: Under-Recognized Movement Disorders in Domestic Animals? A Comparison with Human Dystonia/Paroxysmal Dyskinesias.Analysis of a zebrafish behavioral mutant reveals a dominant mutation in atp2a1/SERCA1.Pseudomyotonia in Romagnola cattle caused by novel ATP2A1 mutations Microarray gene expression profiling of neural tissues in bovine spastic paresis Calcium pumps in health and disease.Endoplasmic-reticulum calcium depletion and disease.Inhibition of ubiquitin proteasome system rescues the defective sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA1) protein causing Chianina cattle pseudomyotonia.HDAC Inhibition Improves the Sarcoendoplasmic Reticulum Ca2+-ATPase Activity in Cardiac Myocytes.

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A defective SERCA1 protein is responsible for congenital pseudomyotonia in Chianina cattle.

http://www.wikidata.org/entity/Q37071895

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 30 December 2008

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

A defective SERCA1 protein is ...... domyotonia in Chianina cattle.

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A defective SERCA1 protein is ...... domyotonia in Chianina cattle.

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A defective SERCA1 protein is ...... domyotonia in Chianina cattle.

@en

A defective SERCA1 protein is ...... domyotonia in Chianina cattle.

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A defective SERCA1 protein is ...... domyotonia in Chianina cattle.

@en

A defective SERCA1 protein is ...... domyotonia in Chianina cattle.

@nl

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AJPATH.2009.080659

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The American Journal of Pathology

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A defective SERCA1 protein is ...... domyotonia in Chianina cattle.

@en

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Arcangelo Gentile

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Cord Drögemüller

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Ernesto Damiani

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Francesco Mascarello

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Marco Rossi

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Roberta Sacchetto

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Rocco Liguori

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Stefania Testoni

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P2860

Protein measurement with the Folin phenol reagent

The mutation of Pro789 to Leu reduces the activity of the fast-twitch skeletal muscle sarco(endo)plasmic reticulum Ca2+ ATPase (SERCA1) and is associated with Brody disease

Mutations in the gene-encoding SERCA1, the fast-twitch skeletal muscle sarcoplasmic reticulum Ca2+ ATPase, are associated with Brody disease

Ca2+ homeostasis in Brody's disease. A study in skeletal muscle and cultured muscle cells and the effects of dantrolene an verapamil

Cleavage of structural proteins during the assembly of the head of bacteriophage T4

Protein degradation by the ubiquitin-proteasome pathway in normal and disease states

Two Ca2+ ATPase genes: homologies and mechanistic implications of deduced amino acid sequences

Ca2+-ATPase deficiency in a patient with an exertional muscle pain syndrome

Muscle contracture induced by exercise. A syndrome attributable to decreased relaxing factor.

Highly effective SNP-based association mapping and management of recessive defects in livestock.

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565-573

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10.2353/AJPATH.2009.080659

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23713569

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19116366

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