The ER-bound RING finger protein 5 (RNF5/RMA1) causes degenerative myopathy in transgenic mice and is deregulated in inclusion body myositis (Q27301955)

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scientific article (publication date: 2008)

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English	The ER-bound RING finger protein 5 (RNF5/RMA1) causes degenerative myopathy in transgenic mice and is deregulated in inclusion body myositis	scientific article (publication date: 2008)

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2 January 2020

The ER-bound RING finger protein 5 (RNF5/RMA1) causes degenerative myopathy in transgenic mice and is deregulated in inclusion body myositis (English)

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2 January 2020

inclusion body myositis

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Massimiliano Mirabella

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2 January 2020

Roberta Morosetti

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Pier Lorenzo Puri

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2 January 2020

Aldobrando Broccolini

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Aldobrando Broccolini

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Agnès Delaunay

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Kenneth D Bromberg

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Yukiko Hayashi

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Denise Burch

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Brian Kirkwood

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Carlo Serra

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May C Malicdan

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Andrew P Mizisin

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Ling T Guo

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Stephen N Jones

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Sergio A Lira

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G Diane Shelton

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2 January 2020

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13 February 2008

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2 January 2020

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2 January 2020

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2 January 2020

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Creative Commons Attribution 4.0 International

13 February 2008

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Sequential quality-control checkpoints triage misfolded cystic fibrosis transmembrane conductance regulator

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A novel ubiquitin-binding protein ZNF216 functioning in muscle atrophy

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RNF5, a RING finger protein that regulates cell motility by targeting paxillin ubiquitination and altered localization

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Limb-girdle muscular dystrophy type 2H associated with mutation in TRIM32, a putative E3-ubiquitin-ligase gene

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Cloning, expression and mapping of a novel RING-finger gene (RNF5), a human homologue of a putative zinc-finger gene from Caenorhabditis elegans

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Ozz-E3, a muscle-specific ubiquitin ligase, regulates beta-catenin degradation during myogenesis

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Trim32 is a ubiquitin ligase mutated in limb girdle muscular dystrophy type 2H that binds to skeletal muscle myosin and ubiquitinates actin

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Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

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Loss of muscle-specific RING-finger 3 predisposes the heart to cardiac rupture after myocardial infarction

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Inclusion-body myositis: a myodegenerative conformational disorder associated with Abeta, protein misfolding, and proteasome inhibition

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10.1371/JOURNAL.PONE.0001609

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2 January 2020

2008PLoSO...3.1609D

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