About: Dysferlin associates with the developing T-tubule system in rodent and human skeletal muscle

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rdf:type	Item
description	article (en) wetenschappelijk artikel (nl) наукова стаття, опублікована в лютому 2010 (uk) im Februar 2010 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q57390058-69A45F5C-3C79-4D06-9C4A-5870F34D7FC5
publication date	2010-02-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q57390058-63A6C759-185F-49C8-AFB1-85F47580F03B wds:Q57390058-BF6D0548-7A33-49F9-9056-C596F5C0F101 wds:Q57390058-E6B2C566-C2D9-4994-9D6B-72CA62654443
cites work	The earliest pathologic alterations in dysferlinopathy Dysferlin interacts with affixin (beta-parvin) at the sarcolemma Caveolinopathies: mutations in caveolin-3 cause four distinct autosomal dominant muscle diseases
author name string	wds:Q57390058-1ED61A8F-F4C7-448C-9B2A-B133EB48B67B wds:Q57390058-26A5F788-97D7-499F-8E89-C832C870DB51 wds:Q57390058-32408151-3BE3-4835-9DEF-EFBB3A578F53 wds:Q57390058-3B44E3F8-6AE5-43C8-A3C9-B26A2750FD62 wds:Q57390058-4CB45304-0586-460B-B87B-7507A9372DEF wds:Q57390058-79A88CD3-EE8B-45C9-A265-EAADD620C25F wds:Q57390058-C64F5327-8B6F-43B0-9DED-B04BA4E7A401 wds:Q57390058-DFFFE76C-278E-4B72-9D97-174FADAD9136 wds:Q57390058-E97FA19F-76FA-4983-9690-572C571A037D wds:Q57390058-EC19C544-8E15-4EB2-9829-CFCCFBF5EB14
author name string	John Harris Kate Bushby Caroline Sewry Rita Barresi Lars Klinge Richard Charlton Yen-Hui Chiu Louise Anderson Steve Laval Mark Hornsey
rdfs:label	Dysferlin associates with the developing T-tubule system in rodent and human skeletal muscle (en) Dysferlin associates with the developing T-tubule system in rodent and human skeletal muscle (nl)
skos:prefLabel	Dysferlin associates with the developing T-tubule system in rodent and human skeletal muscle (en) Dysferlin associates with the developing T-tubule system in rodent and human skeletal muscle (nl)
name	Dysferlin associates with the developing T-tubule system in rodent and human skeletal muscle (en) Dysferlin associates with the developing T-tubule system in rodent and human skeletal muscle (nl)
author	wds:Q57390058-772E1BBF-B2C7-4E6F-9D4E-CFB68B8B51C7 wds:Q57390058-A03A49E7-4821-403D-96F2-3301724CDC63
author	Volker Straub Hanns Lochmüller
title	wds:Q57390058-21E15239-DF86-4B85-BDF8-ED3B34791420
title	Dysferlin associates with the developing T-tubule system in rodent and human skeletal muscle (en)
page(s)	wds:Q57390058-44B320E0-6A28-4CF9-9F08-4E43A90C8E38
page(s)	166-173
instance of	wds:Q57390058-E55651A6-B901-4560-82A1-CE3C85F20ED0
instance of	scholarly article
PubMed ID	wds:Q57390058-5EFD00A7-5550-44CF-AA28-87BFE8823718
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/20082313
PubMed ID	20082313
published in	wds:Q57390058-244168AD-7469-46C1-8709-CA97BB0D474E
published in	Muscle and Nerve
issue	wds:Q57390058-13A86BFE-CA14-4FEA-9634-B122ED15B23A
volume	wds:Q57390058-81EFDD50-780D-41F5-BD74-9CA901784A9F
issue	2
volume	41
DOI	wds:Q57390058-83FC0020-BFDB-4B6B-98D8-3AADFEBA3A1D
DOI	http://dx.doi.org/10.1002/MUS.21166
DOI	10.1002/MUS.21166
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57390058
is cites work of	Dysferlin deficiency blunts β-adrenergic-dependent lusitropic function of mouse heart Unmasking potential intracellular roles for dysferlin through improved immunolabeling methods A naturally occurring human minidysferlin protein repairs sarcolemmal lesions in a mouse model of dysferlinopathy. Alternate splicing of dysferlin C2A confers Ca²⁺-dependent and Ca²⁺-independent binding for membrane repair Membrane damage-induced vesicle-vesicle fusion of dysferlin-containing vesicles in muscle cells requires microtubules and kinesin. Modular dispensability of dysferlin C2 domains reveals rational design for mini-dysferlin molecules Dysferlin stabilizes stress-induced Ca2+ signaling in the transverse tubule membrane Dysferlin and myoferlin regulate transverse tubule formation and glycerol sensitivity. Ferlins: regulators of vesicle fusion for auditory neurotransmission, receptor trafficking and membrane repair T-tubule biogenesis and triad formation in skeletal muscle and implication in human diseases Dynamin 2 the rescue for centronuclear myopathy. A comparison of AAV strategies distinguishes overlapping vectors for efficient systemic delivery of the 6.2 kb Dysferlin coding sequence Defective membrane remodeling in neuromuscular diseases: insights from animal models Retracted: Dysferlin Interacts with Histone Deacetylase 6 and Increases alpha-Tubulin Acetylation Dysferlin rescue by spliceosome-mediated pre-mRNA trans-splicing targeting introns harbouring weakly defined 3' splice sites New aspects on patients affected by dysferlin deficient muscular dystrophy Ferlin proteins in myoblast fusion and muscle growth. Muscle membrane repair and inflammatory attack in dysferlinopathy. EHD1 mediates vesicle trafficking required for normal muscle growth and transverse tubule development Treatment with Recombinant Human MG53 Protein Increases Membrane Integrity in a Mouse Model of Limb Girdle Muscular Dystrophy 2B. Lack of correlation between outcomes of membrane repair assay and correction of dystrophic changes in experimental therapeutic strategy in dysferlinopathy An actin-dependent annexin complex mediates plasma membrane repair in muscle A novel dysferlin mutant pseudoexon bypassed with antisense oligonucleotides Junctophilin-2 is necessary for T-tubule maturation during mouse heart development. Dysferlin at transverse tubules regulates Ca(2+) homeostasis in skeletal muscle Dysferlin and animal models for dysferlinopathy The absence of dysferlin induces the expression of functional connexin-based hemichannels in human myotubes Translational research and therapeutic perspectives in dysferlinopathies. Membrane fusion in muscle development and repair Amphiphysin (BIN1) negatively regulates dynamin 2 for normal muscle maturation. Altered splicing of the BIN1 muscle-specific exon in humans and dogs with highly progressive centronuclear myopathy Animal models of muscular dystrophy Fibroadipogenic progenitors are responsible for muscle loss in limb girdle muscular dystrophy 2B Ultrastructural myopathology in the molecular era. From proteins to genes: immunoanalysis in the diagnosis of muscular dystrophies Dysferlin-deficient muscular dystrophy and innate immune activation. Contribution of dysferlin deficiency to skeletal muscle pathology in asymptomatic and severe dystroglycanopathy models: generation of a new model for Fukuyama congenital muscular dystrophy Plasma Membrane Repair in Health and Disease

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