Dystrophic cardiomyopathy: role of TRPV2 channels in stretch-induced cell damage. - Wikidata - wikimedia - TriplyDB

Dystrophic cardiomyopathy: role of TRPV2 channels in stretch-induced cell damage.

Dystrophic cardiomyopathy: role of TRPV2 channels in stretch-induced cell damage.

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Current understanding of molecular pathology and treatment of cardiomyopathy in duchenne muscular dystrophy Cardiac Mechano-Gated Ion Channels and Arrhythmias.Dystrophic Cardiomyopathy-Potential Role of Calcium in Pathogenesis, Treatment and Novel Therapies Chronic Dosing with Membrane Sealant Poloxamer 188 NF Improves Respiratory Dysfunction in Dystrophic Mdx and Mdx/Utrophin-/- Mice Axial stretch-dependent cation entry in dystrophic cardiomyopathy: Involvement of several TRPs channels Pathoproteomic profiling of the skeletal muscle matrisome in dystrophinopathy associated myofibrosis.Piezo channels and GsMTx4: Two milestones in our understanding of excitatory mechanosensitive channels and their role in pathology.Can Human Pluripotent Stem Cell-Derived Cardiomyocytes Advance Understanding of Muscular Dystrophies?Mechano-chemo-transduction in cardiac myocytes.Mitochondrial Mechanosensor Microdomains in Cardiovascular Disorders.Ups and downs of calcium in the heart.Blocking transient receptor potential vanilloid 2 channel in astrocytes enhances astrocyte-mediated neuroprotection after oxygen-glucose deprivation and reoxygenation.Probenecid Improves Cardiac Function in Patients With Heart Failure With Reduced Ejection Fraction In Vivo and Cardiomyocyte Calcium Sensitivity In Vitro.A TRPV2 interactome-based signature for prognosis in glioblastoma patients.

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Dystrophic cardiomyopathy: role of TRPV2 channels in stretch-induced cell damage.

http://www.wikidata.org/entity/Q53636857

description

2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年學術文章

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2015年學術文章

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2015年學術文章

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name

Dystrophic cardiomyopathy: role of TRPV2 channels in stretch-induced cell damage.

@en

Dystrophic cardiomyopathy: role of TRPV2 channels in stretch-induced cell damage.

@nl

type

label

Dystrophic cardiomyopathy: role of TRPV2 channels in stretch-induced cell damage.

@en

Dystrophic cardiomyopathy: role of TRPV2 channels in stretch-induced cell damage.

@nl

prefLabel

Dystrophic cardiomyopathy: role of TRPV2 channels in stretch-induced cell damage.

@en

Dystrophic cardiomyopathy: role of TRPV2 channels in stretch-induced cell damage.

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Cardiovascular Research

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Dystrophic cardiomyopathy: role of TRPV2 channels in stretch-induced cell damage.

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Charlotte Lorin

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Isabelle Vögeli

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P2860

A capsaicin-receptor homologue with a high threshold for noxious heat

Leaky RyR2 trigger ventricular arrhythmias in Duchenne muscular dystrophy

Hierarchical accumulation of RyR post-translational modifications drives disease progression in dystrophic cardiomyopathy

Hypernitrosylated ryanodine receptor calcium release channels are leaky in dystrophic muscle

International Union of Basic and Clinical Pharmacology. LXXVI. Current progress in the mammalian TRP ion channel family

Stretch-activated ion channels: what are they?

X-linked dilated cardiomyopathy and the dystrophin gene.

TRPV2 is critical for the maintenance of cardiac structure and function in mice.

The anti-influenza drug oseltamivir exhibits low potential to induce pharmacokinetic drug interactions via renal secretion-correlation of in vivo and in vitro studies.

Genetic inhibition of PKA phosphorylation of RyR2 prevents dystrophic cardiomyopathy.

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153-162

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scholarly article

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10.1093/CVR/CVV021

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1

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106

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25616416

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