(Q50471241)

14 March 2018

title

Transgenic expression of inclusion body myopathy associated mutant p97/VCP causes weakness and ubiquitinated protein inclusions in mice. (English)

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14 March 2018

main subject

protein ubiquitination

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Conrad C Weihl

1

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14 March 2018

Sara E Miller

series ordinal

2

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14 March 2018

Phyllis I Hanson

series ordinal

3

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14 March 2018

Alan Pestronk

series ordinal

4

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14 March 2018

publication date

28 February 2007

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14 March 2018

published in

Human Molecular Genetics

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14 March 2018

volume

16

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14 March 2018

issue

8

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14 March 2018

page(s)

919-928

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14 March 2018

Molecular pathology and pathogenesis of inclusion-body myositis

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM037

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM037

Autosomal dominant inclusion body myopathy, Paget disease of bone, and frontotemporal dementia

21 January 2018

1 reference

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Pathological consequences of VCP mutations on human striated muscle.

21 January 2018

1 reference

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Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM037

Mutant valosin-containing protein causes a novel type of frontotemporal dementia

21 January 2018

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Proteasome inhibition and aggresome formation in sporadic inclusion-body myositis and in amyloid-beta precursor protein-overexpressing cultured human muscle fibers

21 January 2018

1 reference

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Endoplasmic reticulum stress and unfolded protein response in inclusion body myositis muscle.

21 January 2018

1 reference

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Molecular perspectives on p97-VCP: progress in understanding its structure and diverse biological functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM037

Valosin-containing protein is a multi-ubiquitin chain-targeting factor required in ubiquitin-proteasome degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM037

Interaction of U-box-type ubiquitin-protein ligases (E3s) with molecular chaperones

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM037

AAA ATPase p97/valosin-containing protein interacts with gp78, a ubiquitin ligase for endoplasmic reticulum-associated degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM037

AAA-ATPase p97/Cdc48p, a cytosolic chaperone required for endoplasmic reticulum-associated protein degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM037

Distinct roles for the AAA ATPases NSF and p97 in the secretory pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM037

Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM037

E-box sites and a proximal regulatory region of the muscle creatine kinase gene differentially regulate expression in diverse skeletal muscles and cardiac muscle of transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM037

Inclusion body myositis-like phenotype induced by transgenic overexpression of beta APP in skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM037

Valosin-containing protein gene mutations: clinical and neuropathologic features.

21 January 2018

1 reference

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Three mouse models of muscular dystrophy: the natural history of strength and fatigue in dystrophin-, dystrophin/utrophin-, and laminin α2-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM037

Visualization of dystrophic muscle fibers in mdx mouse by vital staining with Evans blue: evidence of apoptosis in dystrophin-deficient muscle.

21 January 2018

1 reference

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Animal models for muscular dystrophy show different patterns of sarcolemmal disruption.

21 January 2018

1 reference

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Tubular aggregates are from whole sarcoplasmic reticulum origin: alterations in calcium binding protein expression in mouse skeletal muscle during aging

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM037

Inclusion-body myositis and myopathies: different etiologies, possibly similar pathogenic mechanisms

21 January 2018

1 reference

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

21 January 2018

1 reference

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Protein accumulation and neurodegeneration in the woozy mutant mouse is caused by disruption of SIL1, a cochaperone of BiP

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM037

Caveolinopathies: mutations in caveolin-3 cause four distinct autosomal dominant muscle diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM037

Limb-girdle muscular dystrophy (LGMD-1C) mutants of caveolin-3 undergo ubiquitination and proteasomal degradation. Treatment with proteasomal inhibitors blocks the dominant negative effect of LGMD-1C mutanta and rescues wild-type caveolin-3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM037

Enhanced detection of congo-red-positive amyloid deposits in muscle fibers of inclusion body myositis and brain of Alzheimer's disease using fluorescence technique

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM037

Doxycycline attenuates and delays toxicity of the oculopharyngeal muscular dystrophy mutation in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM037

21 January 2018

Identifiers

DOI

10.1093/HMG/DDM037

1 reference

14 March 2018

1 reference

14 March 2018