A transcriptomic approach to search for novel phenotypic regulators in McArdle disease. - Wikidata - wikimedia - TriplyDB

A transcriptomic approach to search for novel phenotypic regulators in McArdle disease.

A transcriptomic approach to search for novel phenotypic regulators in McArdle disease.

http://www.wikidata.org/entity/Q34162933

about

Omics-Based Strategies in Precision Medicine: Toward a Paradigm Shift in Inborn Errors of Metabolism Investigations Quantitative analysis of proteins of metabolism by reverse phase protein microarrays identifies potential biomarkers of rare neuromuscular diseases.Rodent models for resolving extremes of exercise and health.McArdle disease: a unique study model in sports medicine.Genes and exercise intolerance: insights from McArdle disease.Differential glucose metabolism in mice and humans affected by McArdle disease.Differential Muscle Involvement in Mice and Humans Affected by McArdle Disease.Low versus high carbohydrates in the diet of the world-class athlete: insights from McArdle's disease.

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A transcriptomic approach to search for novel phenotypic regulators in McArdle disease.

http://www.wikidata.org/entity/Q34162933

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2012 nî lūn-bûn

@nan

2012 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի փետրվարին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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name

A transcriptomic approach to search for novel phenotypic regulators in McArdle disease.

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A transcriptomic approach to search for novel phenotypic regulators in McArdle disease.

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A transcriptomic approach to search for novel phenotypic regulators in McArdle disease.

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type

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A transcriptomic approach to search for novel phenotypic regulators in McArdle disease.

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A transcriptomic approach to search for novel phenotypic regulators in McArdle disease.

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A transcriptomic approach to search for novel phenotypic regulators in McArdle disease.

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prefLabel

A transcriptomic approach to search for novel phenotypic regulators in McArdle disease.

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A transcriptomic approach to search for novel phenotypic regulators in McArdle disease.

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A transcriptomic approach to search for novel phenotypic regulators in McArdle disease.

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A transcriptomic approach to search for novel phenotypic regulators in McArdle disease

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Alejandro Lucia

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Antoni L Andreu

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Elena García-Arumí

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Inés Consuegra-García

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Javier Torres-Torronteras

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Juan C Rubio

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Marc Cuadros

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P2860

Quantification of the glycogen cascade system: the ultrasensitive responses of liver glycogen synthase and muscle phosphorylase are due to distinctive regulatory designs.

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

Expression of glycogen phosphorylase isoforms in cultured muscle from patients with McArdle's disease carrying the p.R771PfsX33 PYGM mutation

Ca2+ uptake coupled to glycogen phosphorolysis in the glycogenolytic-sarcoplasmic reticulum complex from rat skeletal muscle

New insights into the role and mechanism of glycogen synthase activation by insulin.

SERCA pump isoforms: their role in calcium transport and disease.

Control of phosphorylase activity in a muscle glycogen particle. I. Isolation and characterization of the protein-glycogen complex.

The effect of oral sucrose on exercise tolerance in patients with McArdle's disease.

Myophosphorylase deficiency (glycogenosis type V; McArdle disease).

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e31718

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Carmen Fiuza-Luces

Miguel Angel Martín

Joaquín Arenas

Yolanda Cámara

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2012-02-09T00:00:00Z

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