(Q34979278)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

title

Immunoreactivity of valosin-containing protein in sporadic amyotrophic lateral sclerosis and in a case of its novel mutant (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

amyotrophic lateral sclerosis

24 February 2020

main subject

0 references

author

Hiroyuki Morino

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Masafumi Ihara

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Riki Matsumoto

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Makoto Urushitani

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Hideshi Kawakami

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

5

Takayuki Kondo

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

author name string

Takashi Ayaki

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Hidefumi Ito

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Hiroko Fukushima

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Takeshi Inoue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Akito Ikemoto

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Takeshi Asano

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Akemi Shodai

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Takuji Fujita

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Satoshi Fukui

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Satoshi Nakano

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Hirofumi Kusaka

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Hirofumi Yamashita

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Jun Kawamata

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

Ryosuke Takahashi

20

1 reference

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24 February 2020

language of work or name

1 reference

10 December 2014

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

Acta Neuropathologica Communications

24 February 2020

published in

1 reference

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24 February 2020

volume

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

page(s)

172

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

Creative Commons Attribution 4.0 International

24 February 2020

copyright license

start time

1 December 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Aggregation of polyglutamine-expanded ataxin-3 sequesters its specific interacting partners into inclusions: implication in a loss-of-function pathology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

Drosophila Valosin-Containing Protein is required for dendrite pruning through a regulatory role in mRNA metabolism

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

Role of p97/VCP (Cdc48) in genome stability

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

Motor neuron involvement in multisystem proteinopathy: implications for ALS

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

Heteromeric p97/p97R155C complexes induce dominant negative changes in wild-type and autophagy 9-deficient Dictyostelium strains

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

Phenotypic variability in three families with valosin-containing protein mutation.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

Emerging functions of the VCP/p97 AAA-ATPase in the ubiquitin system

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

UBQLN2/P62 cellular recycling pathways in amyotrophic lateral sclerosis and frontotemporal dementia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

Mutational analysis of the VCP gene in Parkinson's disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

Recent advances in p97/VCP/Cdc48 cellular functions

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

A harmonized classification system for FTLD-TDP pathology

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

Phosphorylation of the autophagy receptor optineurin restricts Salmonella growth

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

Cdc48/p97 mediates UV-dependent turnover of RNA Pol II.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

Exome sequencing reveals VCP mutations as a cause of familial ALS

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

Functional diversity of the hnRNPs: past, present and perspectives

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

TDP-43 mediates degeneration in a novel Drosophila model of disease caused by mutations in VCP/p97.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

VCP/p97 is essential for maturation of ubiquitin-containing autophagosomes and this function is impaired by mutations that cause IBMPFD

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

Valosin-containing protein (VCP) is required for autophagy and is disrupted in VCP disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

A ubiquitin-selective AAA-ATPase mediates transcriptional switching by remodelling a repressor-promoter DNA complex

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

VCP mutations causing frontotemporal lobar degeneration disrupt localization of TDP-43 and induce cell death

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

Mechanisms of Cdc48/VCP-mediated cell death: from yeast apoptosis to human disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

Pathological consequences of VCP mutations on human striated muscle

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

p97/p47-Mediated biogenesis of Golgi and ER

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

p47 is a cofactor for p97-mediated membrane fusion

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

Fragmentation of the Golgi apparatus of motor neurons in amyotrophic lateral sclerosis revealed by organelle-specific antibodies

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

Fragmentation of the Golgi apparatus of motor neurons in amyotrophic lateral sclerosis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4297454

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

8 July 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0172-0

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0172-0

A novel VCP mutation underlies scapuloperoneal muscular dystrophy and dropped head syndrome featuring lobulated fibers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0172-0

Valosin-containing protein mutation and Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0172-0

Hereditary spastic paraplegia caused by a mutation in the VCP gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0172-0

Characterization of the Asian myopathy patients with VCP mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0172-0

TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0172-0

Valosin-containing protein immunoreactivity in tauopathies, synucleinopathies, polyglutamine diseases and intranuclear inclusion body disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0172-0

Increased expression of valosin-containing protein in the skin of patients with amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0172-0

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0172-0

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0172-0

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0172-0

Inclusion body myopathy, Paget's disease of the bone and frontotemporal dementia: recurrence of the VCP R155H mutation in an Italian family and implications for genetic counselling.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0172-0

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0172-0

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0172-0

VCP mutations in familial and sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0172-0

Cdc48/p97 promotes reformation of the nucleus by extracting the kinase Aurora B from chromatin

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40478-014-0172-0

Autophagy in spinal cord motor neurons in sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

12 December 2020

Endoplasmic reticulum stress in motor neurons of the spinal cord in sporadic amyotrophic lateral sclerosis

1 reference

12 December 2020

Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

APOE is a potential modifier gene in an autosomal dominant form of frontotemporal dementia (IBMPFD)

1 reference

12 December 2020

Oxidative and endoplasmic reticulum stress interplay in sporadic amyotrophic lateral sclerosis

1 reference

12 December 2020

The fragmented neuronal Golgi apparatus in amyotrophic lateral sclerosis includes the trans-Golgi-network: functional implications

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1186/S40478-014-0172-0

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

24 February 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

PubMed publication ID

25492614

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25492614%20AND%20SRC:MED&resulttype=core&format=json