The multiple faces of valosin-containing protein-associated diseases: inclusion body myopathy with Paget's disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis. (Q37926529)

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scientific article published on 03 September 2011

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English	The multiple faces of valosin-containing protein-associated diseases: inclusion body myopathy with Paget's disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis.	scientific article published on 03 September 2011

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12 February 2020

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The multiple faces of valosin-containing protein-associated diseases: inclusion body myopathy with Paget's disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis (English)

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12 February 2020

amyotrophic lateral sclerosis

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frontotemporal dementia

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based on heuristic

inferred from title

Paget's disease of bone

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based on heuristic

inferred from title

Jogeshwar Mukherjee

8

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12 February 2020

Virginia Kimonis

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Virginia E Kimonis

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Charles D. Smith

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Charles Smith

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12 February 2020

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Angèle Nalbandian

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Sandra Donkervoort

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Eric Dec

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Mallikarjun Badadani

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Veeral Katheria

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Prachi Rana

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Christopher Nguyen

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12 February 2020

Vincent Caiozzo

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Barbara Martin

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Giles D Watts

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Jouni Vesa

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3 September 2011

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Journal of Molecular Neuroscience

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12 February 2020

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12 February 2020

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12 February 2020

522-531

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12 February 2020

Interplay of IKK/NF-kappaB signaling in macrophages and myofibers promotes muscle degeneration in Duchenne muscular dystrophy

1 reference

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Nuclear factor-kappaB: the enemy within

1 reference

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21 January 2018

UBXD7 binds multiple ubiquitin ligases and implicates p97 in HIF1alpha turnover

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Incidence and lifetime risk of motor neuron disease in the United Kingdom: a population-based study.

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21 January 2018

Quantitative neurohistological features of frontotemporal degeneration

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

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VCP Associated Inclusion Body Myopathy and Paget Disease of Bone Knock-In Mouse Model Exhibits Tissue Pathology Typical of Human Disease

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

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Adapting proteostasis for disease intervention

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Therapeutic targeting of signaling pathways in muscular dystrophy

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TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions

1 reference

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Pathogenic VCP/TER94 alleles are dominant actives and contribute to neurodegeneration by altering cellular ATP level in a Drosophila IBMPFD model

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

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A 200‐amino acid ATPase module in search of a basic function

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https://api.crossref.org/works/10.1007/S12031-011-9627-Y

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The small heat shock protein B8 (HspB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS).

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

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Transgenic mice expressing mutant forms VCP/p97 recapitulate the full spectrum of IBMPFD including degeneration in muscle, brain and bone

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Involvement of valosin-containing protein, an ATPase Co-purified with IkappaBalpha and 26 S proteasome, in ubiquitin-proteasome-mediated degradation of IkappaBalpha

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Mechanisms of disease: genetics of Paget's disease of bone and related disorders

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Central pore residues mediate the p97/VCP activity required for ERAD

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

A novel mutation in the VCP gene (G157R) in a German family with inclusion-body myopathy with Paget disease of bone and frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Imbalances in p97 co-factor interactions in human proteinopathy

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene.

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Excessive collagen accumulation in dystrophic (mdx) respiratory musculature is independent of enhanced activation of the NF-kappaB pathway

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Valosin-containing protein gene mutations: clinical and neuropathologic features

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

The RAGE pathway in inflammatory myopathies and limb girdle muscular dystrophy

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Signaling to NF-kappaB

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Pathological consequences of VCP mutations on human striated muscle

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

The ubiquitin-selective chaperone CDC-48/p97 links myosin assembly to human myopathy

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Protein dislocation from the endoplasmic reticulum--pulling out the suspect

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Exome sequencing reveals VCP mutations as a cause of familial ALS

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Inclusion body myopathy, Paget's disease of the bone and fronto-temporal dementia: a disorder of autophagy

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Roles of VCP in human neurodegenerative disorders

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Identification of a novel valosin-containing protein polymorphism in late-onset Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Inclusion body myopathy with Paget disease of bone and frontotemporal dementia linked to VCP p.Arg155Cys in a Korean family

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia: review of a unique disorder

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia.

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

p47 is a cofactor for p97-mediated membrane fusion

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Autophagy inhibition compromises degradation of ubiquitin-proteasome pathway substrates.

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Two Australian families with inclusion-body myopathy, Paget's disease of bone and frontotemporal dementia: novel clinical and genetic findings

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

ALS-associated mutations in TDP-43 increase its stability and promote TDP-43 complexes with FUS/TLS.

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Descriptive epidemiology of amyotrophic lateral sclerosis: new evidence and unsolved issues

1 reference

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21 January 2018

Are amyotrophic lateral sclerosis patients cognitively normal?

1 reference

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21 January 2018

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1 reference

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In vivo analysis of autophagy in response to nutrient starvation using transgenic mice expressing a fluorescent autophagosome marker

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Targeted deletion of p97 (VCP/CDC48) in mouse results in early embryonic lethality.

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1 reference

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1 reference

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1 reference

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Clinical trials for neuroprotection in ALS.

1 reference

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Comparative study of alendronate versus etidronate for the treatment of Paget's disease of bone.

1 reference

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TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

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Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget's disease of bone and frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

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Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His

1 reference

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Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

1 reference

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1 reference

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

1 reference

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Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

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

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Autophagy gone awry in neurodegenerative diseases

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

The AAA ATPase Cdc48/p97 and its partners transport proteins from the ER into the cytosol

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Loss of brain tau defines novel sporadic and familial tauopathies with frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene

1 reference

https://api.crossref.org/works/10.1007/S12031-011-9627-Y

21 January 2018

Radiological features of Paget disease of bone associated with VCP myopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/21892620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A role of small heat shock protein B8 (HspB8) in the autophagic removal of misfolded proteins responsible for neurodegenerative diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/21892620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inclusion body myopathy with Paget disease and frontotemporal dementia (IBMPFD): clinical features including sphincter disturbance in a large pedigree

1 reference

https://pubmed.ncbi.nlm.nih.gov/21892620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21892620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frontotemporal dementias: Recent advances and current controversies

1 reference

https://pubmed.ncbi.nlm.nih.gov/21892620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incidence of amyotrophic lateral sclerosis in three counties in western Washington state

1 reference

https://pubmed.ncbi.nlm.nih.gov/21892620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Brain imaging and neuropsychology in late-onset dementia due to a novel mutation (R93C) of valosin-containing protein.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21892620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of bone

1 reference

https://pubmed.ncbi.nlm.nih.gov/21892620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Motor neuron disease: focusing the mind on ALS: updated practice parameters

1 reference

https://pubmed.ncbi.nlm.nih.gov/21892620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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