(Q41667459)

6 October 2017

TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementia (English)

1 reference

6 October 2017

0 references

frontotemporal dementia

1 reference

8

V Kimonis

1 reference

6 October 2017

1

C C Weihl

1 reference

6 October 2017

5

C Smith

1 reference

6 October 2017

P Temiz

2

1 reference

6 October 2017

S E Miller

3

1 reference

6 October 2017

G Watts

4

1 reference

6 October 2017

M Forman

6

1 reference

6 October 2017

P I Hanson

7

1 reference

6 October 2017

A Pestronk

9

1 reference

6 October 2017

language of work or name

English

0 references

publication date

1 October 2008

1 reference

Journal of Neurology, Neurosurgery and Psychiatry

6 October 2017

1 reference

6 October 2017

79

1 reference

6 October 2017

10

1 reference

6 October 2017

1186-1189

1 reference

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

6 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586594

Pathological consequences of VCP mutations on human striated muscle

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586594

Sporadic inclusion body myositis--diagnosis, pathogenesis and therapeutic strategies

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586594

Inclusion-body myositis: a myodegenerative conformational disorder associated with Abeta, protein misfolding, and proteasome inhibition

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586594

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

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586594

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

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586594

Nuclear inclusions in oculopharyngeal muscular dystrophy consist of poly(A) binding protein 2 aggregates which sequester poly(A) RNA

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586594

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586594

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

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586594

Rimmed vacuoles and the added value of SMI-31 staining in diagnosing sporadic inclusion body myositis.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586594

Twisted tubulofilaments of inclusion body myositis muscle resemble paired helical filaments of Alzheimer brain and contain hyperphosphorylated tau.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586594

β‐Amyloid precursor epitopes in muscle fibers of inclusion body myositis

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586594

TDP-43 in amyotrophic lateral sclerosis: pathophysiology or patho-babel?

18 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18796596

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18796596

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JNNP.2007.131334

1 reference

6 October 2017

1 reference

6 October 2017

PubMed publication ID

18796596

1 reference