Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein (Q29619232)

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scientific article (publication date: April 2004)

Language	Label	Description	Also known as
English	Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein	scientific article (publication date: April 2004)

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scholarly article

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

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=15034582

30 April 2017

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frontotemporal dementia

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based on heuristic

inferred from title

Michael P. Whyte

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object named as

Whyte MP

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=15034582

30 April 2017

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object named as

Mumm S

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=15034582

30 April 2017

author name string

Watts GD

1

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=15034582

30 April 2017

Wymer J

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=15034582

30 April 2017

Kovach MJ

3

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30 April 2017

Mehta SG

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Darvish D

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Pestronk A

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Kimonis VE

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language of work or name

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30 April 2017

publication date

April 2004

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30 April 2017

Nature Genetics

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36

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377-81

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30 April 2017

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/10.1038%2FNG1332

21 January 2018

The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

Mutations in the human UDP-N-acetylglucosamine 2-epimerase gene define the disease sialuria and the allosteric site of the enzyme

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

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/10.1038%2FNG1332

21 January 2018

Sequence analysis of the AAA protein family

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

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/10.1038%2FNG1332

21 January 2018

Mobilization of processed, membrane-tethered SPT23 transcription factor by CDC48(UFD1/NPL4), a ubiquitin-selective chaperone

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

Structure of the AAA ATPase p97

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

Hexamerization of p97-VCP is promoted by ATP binding to the D1 domain and required for ATPase and biological activities

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

Distinct AAA-ATPase p97 complexes function in discrete steps of nuclear assembly

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

Syntaxin 5 is a common component of the NSF- and p97-mediated reassembly pathways of Golgi cisternae from mitotic Golgi fragments in vitro

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

p47 is a cofactor for p97-mediated membrane fusion

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

A complex of mammalian ufd1 and npl4 links the AAA-ATPase, p97, to ubiquitin and nuclear transport pathways

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

VCP/p97 in abnormal protein aggregates, cytoplasmic vacuoles, and cell death, phenotypes relevant to neurodegeneration

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

Functional ATPase activity of p97/valosin-containing protein (VCP) is required for the quality control of endoplasmic reticulum in neuronally differentiated mammalian PC12 cells

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

Identification of ter94, Drosophila VCP, as a modulator of polyglutamine-induced neurodegeneration

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

The ubiquitin protein catabolic disorders.

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

Hassles with taking out the garbage: aggravating aggresomes.

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

Ubiquitin-mediated sequestration of normal cellular proteins into polyglutamine aggregates

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

Protein aggregation in motor neurone disorders.

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

SVIP is a novel VCP/p97-interacting protein whose expression causes cell vacuolation

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

Vacuole-creating protein in neurodegenerative diseases in humans

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1332

7 January 2021

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=15034582

30 April 2017

Consolidated OpenCitations Corpus – April 2017

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Consolidated OpenCitations Corpus – April 2017

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2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=15034582

30 April 2017

Consolidated OpenCitations Corpus – April 2017

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