VCP Associated Inclusion Body Myopathy and Paget Disease of Bone Knock-In Mouse Model Exhibits Tissue Pathology Typical of Human Disease (Q33721995)

28 July 2017

title

VCP associated inclusion body myopathy and paget disease of bone knock-in mouse model exhibits tissue pathology typical of human disease (English)

1 reference

28 July 2017

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

1 reference

10.1371/JOURNAL.PONE.0013183

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DOI

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0013183

5 August 2024

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13

Virginia E Kimonis

1 reference

28 July 2017

5

Masashi Kitazawa

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20957154

5 August 2024

10

Jogeshwar Mukherjee

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5 August 2024

author name string

Mallikarjun Badadani

1

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28 July 2017

Angèle Nalbandian

2

1 reference

28 July 2017

Jouni Vesa

4

1 reference

28 July 2017

Hailing Su

6

1 reference

28 July 2017

Jasmin Tanaja

7

1 reference

28 July 2017

Eric Dec

8

1 reference

28 July 2017

Vincent Caiozzo

11

1 reference

28 July 2017

Matthew Warman

12

1 reference

28 July 2017

Giles D. Watts

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20957154

5 August 2024

Douglas C. Wallace

9

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5 August 2024

Virginia E. Kimonis

13

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5 August 2024

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English

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publication date

5 October 2010

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full work available at URL

28 July 2017

https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0013183&type=printable

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open access

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20957154

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20957154/pdf/?tool=EBI

5 August 2024

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Portable Document Format

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https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20957154/?tool=EBI

5 August 2024

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20957154

https://europepmc.org/articles/PMC2950155

5 August 2024

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https://europepmc.org/articles/PMC2950155?pdf=render

5 August 2024

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Portable Document Format

online access status

open access

content deliverer

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5 August 2024

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28 July 2017

volume

5

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28 July 2017

issue

10

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Creative Commons Attribution 4.0 International

28 July 2017

copyright license

start time

5 October 2010

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April 2022 Public Data File from Crossref

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cites work

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

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21 June 2018

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

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

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

30 October 2018

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

30 October 2018

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LAMP-2 deficient mice show depressed cardiac contractile function without significant changes in calcium handling.

30 October 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950155

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

30 October 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950155

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

30 October 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950155

Coxarthrosis. c) 12-15 year results with intertrochanteric osteotomies in patients with coxarthrosis

30 October 2018

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RNA interference of valosin-containing protein (VCP/p97) reveals multiple cellular roles linked to ubiquitin/proteasome-dependent proteolysis

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950155

Cdc48p is required for the cell cycle commitment point at Start via degradation of the G1-CDK inhibitor Far1p

30 October 2018

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

30 October 2018

1 reference

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Dissociation in retrograde memory for object discriminations and object recognition in rats with perirhinal cortex damage.

30 October 2018

1 reference

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Endoplasmic reticulum stress-induced cell death requires mitochondrial membrane permeabilization

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950155

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950155

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950155

Functional analysis of the trypanosomal AAA protein TbVCP with trans-dominant ATP hydrolysis mutants

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950155

Morphological study of the femur in osteopetrotic (op/op) mice using microcomputed tomography.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950155

Quantitative neurohistological features of frontotemporal degeneration

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950155

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

30 October 2018

1 reference

12 December 2020

A series of ubiquitin binding factors connects CDC48/p97 to substrate multiubiquitylation and proteasomal targeting

1 reference

12 December 2020

AAA-ATPases at the crossroads of protein life and death

1 reference

12 December 2020

Heterogenous immunohistochemical expression of microglia-specific ionized calcium binding adaptor protein (Iba1) in the mouse olfactory bulb

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0013183

Identifiers

DOI

1 reference

28 July 2017

0 references

1 reference

28 July 2017

1 reference