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Another VCP interactor: NF is enough
scientific article
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
3226341
retrieved
12 September 2017
title
Another VCP interactor: NF is enough
(English)
1 reference
stated in
Europe PubMed Central
PMCID
3226341
retrieved
12 September 2017
author name string
Conrad C Weihl
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
3226341
retrieved
12 September 2017
language of work or name
English
0 references
publication date
21 November 2011
1 reference
stated in
Europe PubMed Central
PMCID
3226341
retrieved
12 September 2017
published in
Journal of Clinical Investigation
1 reference
stated in
Europe PubMed Central
PMCID
3226341
retrieved
12 September 2017
volume
121
1 reference
stated in
Europe PubMed Central
PMCID
3226341
retrieved
12 September 2017
issue
12
1 reference
stated in
Europe PubMed Central
PMCID
3226341
retrieved
12 September 2017
page(s)
4627-4630
1 reference
stated in
Europe PubMed Central
PMCID
3226341
retrieved
12 September 2017
cites work
Valosin-containing protein and neurofibromin interact to regulate dendritic spine density
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
retrieved
12 September 2017
Mutational analysis of the VCP gene in Parkinson's disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
retrieved
12 September 2017
Endolysosomal sorting of ubiquitylated caveolin-1 is regulated by VCP and UBXD1 and impaired by VCP disease mutations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
retrieved
12 September 2017
Neuronal remodeling and apoptosis require VCP-dependent degradation of the apoptosis inhibitor DIAP1.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
retrieved
12 September 2017
Valosin containing protein associated fronto-temporal lobar degeneration: clinical presentation, pathologic features and pathogenesis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
retrieved
12 September 2017
Proteasome and p97 mediate mitophagy and degradation of mitofusins induced by Parkin
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
retrieved
12 September 2017
Exome sequencing reveals VCP mutations as a cause of familial ALS
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
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12 September 2017
Imbalances in p97 co-factor interactions in human proteinopathy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
retrieved
12 September 2017
Molecular and cellular mechanisms of learning disabilities: a focus on NF1.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
retrieved
12 September 2017
The RasGAP proteins Ira2 and neurofibromin are negatively regulated by Gpb1 in yeast and ETEA in humans
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
retrieved
12 September 2017
Valosin-containing protein (VCP) is required for autophagy and is disrupted in VCP disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
retrieved
12 September 2017
Impaired protein aggregate handling and clearance underlie the pathogenesis of p97/VCP-associated disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
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12 September 2017
The UNC-45 chaperone mediates sarcomere assembly through myosin degradation in Caenorhabditis elegans
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
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12 September 2017
Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
retrieved
12 September 2017
p97: The cell's molecular purgatory?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
retrieved
12 September 2017
Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
retrieved
12 September 2017
p97 and close encounters of every kind: a brief review
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
retrieved
12 September 2017
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
retrieved
12 September 2017
AAA-ATPase p97/Cdc48p, a cytosolic chaperone required for endoplasmic reticulum-associated protein degradation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
retrieved
12 September 2017
Specificity of Ca2+-dependent protein interactions mediated by the C2A domains of synaptotagmins
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
retrieved
12 September 2017
Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseases.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
retrieved
14 September 2017
The ubiquitin-selective chaperone CDC-48/p97 links myosin assembly to human myopathy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3226341
retrieved
14 September 2017
Cdc48/p97 promotes reformation of the nucleus by extracting the kinase Aurora B from chromatin
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22105166
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1172/JCI61126
1 reference
stated in
Europe PubMed Central
PMCID
3226341
retrieved
12 September 2017
PMCID
3226341
1 reference
stated in
Europe PubMed Central
PMCID
3226341
retrieved
12 September 2017
PubMed ID
22105166
1 reference
stated in
Europe PubMed Central
PMCID
3226341
retrieved
12 September 2017
ResearchGate publication ID
51819940
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