A Calsequestrin-1 Mutation Associated with a Skeletal Muscle Disease Alters Sarcoplasmic Ca2+ Release.

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DNA Hypomethylation in Intragenic and Intergenic Enhancer Chromatin of Muscle-Specific Genes Usually Correlates with their Expression.Calsequestrin depolymerizes when calcium is depleted in the sarcoplasmic reticulum of working muscle.

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Q37517522-BCE2A7AA-8103-4404-81DE-B69CFB096AF3 Q37612539-9869B362-16AE-4E9D-AD32-D50F438A5430

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A Calsequestrin-1 Mutation Associated with a Skeletal Muscle Disease Alters Sarcoplasmic Ca2+ Release.

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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A Calsequestrin-1 Mutation Ass ...... ers Sarcoplasmic Ca2+ Release.

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A Calsequestrin-1 Mutation Ass ...... ers Sarcoplasmic Ca2+ Release.

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A Calsequestrin-1 Mutation Ass ...... ers Sarcoplasmic Ca2+ Release.

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A Calsequestrin-1 Mutation Ass ...... ers Sarcoplasmic Ca2+ Release.

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A Calsequestrin-1 Mutation Ass ...... ers Sarcoplasmic Ca2+ Release.

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A Calsequestrin-1 Mutation Ass ...... ers Sarcoplasmic Ca2+ Release.

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A Calsequestrin-1 Mutation Ass ...... ers Sarcoplasmic Ca2+ Release.

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P2093

Alessandro Grottesi

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Fabio Franciolini

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

Lanfranco Corazzi

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Lara Macchioni

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Llenio Servettini

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Luca Guglielmi

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Maurizio Curcio

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P2860

High-capacity Ca2+ binding of human skeletal calsequestrin

Crystal structure of calsequestrin from rabbit skeletal muscle sarcoplasmic reticulum

Fractional SR Ca release is regulated by trigger Ca and SR Ca content in cardiac myocytes

Contribution of the central hydrophobic residue in the PXP motif of voltage-dependent K+ channels to S6 flexibility and gating properties

Reorganized stores and impaired calcium handling in skeletal muscle of mice lacking calsequestrin-1

Mice null for calsequestrin 1 exhibit deficits in functional performance and sarcoplasmic reticulum calcium handling.

Potentiation of fractional sarcoplasmic reticulum calcium release by total and free intra-sarcoplasmic reticulum calcium concentration

A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates.

Cultured muscle from myotonic muscular dystrophy patients: altered membrane electrical properties

The couplonopathies: A comparative approach to a class of diseases of skeletal and cardiac muscle.

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e0155516

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scholarly article

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10.1371/JOURNAL.PONE.0155516

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English

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Chiara De Nuccio

Marina Mora

Maria Cristina D'Adamo

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2016-05-19T00:00:00Z

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27196359

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4873205

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A Calsequestrin-1 Mutation Associated with a Skeletal Muscle Disease Alters Sarcoplasmic Ca2+ Release.

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P2860

P2860

A Calsequestrin-1 Mutation Associated with a Skeletal Muscle Disease Alters Sarcoplasmic Ca2+ Release.

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