(Q43488914)

23 November 2017

title

Characterization of the Asian myopathy patients with VCP mutations (English)

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23 November 2017

14

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23 November 2017

Z Shi

1

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23 November 2017

Y K Hayashi

2

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23 November 2017

S Mitsuhashi

3

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23 November 2017

K Goto

4

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23 November 2017

D Kaneda

5

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23 November 2017

Y-C Choi

6

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23 November 2017

C Toyoda

7

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23 November 2017

S Hieda

8

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23 November 2017

T Kamiyama

9

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23 November 2017

H Sato

10

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23 November 2017

M Wada

11

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23 November 2017

S Noguchi

12

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23 November 2017

I Nonaka

13

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23 November 2017

publication date

31 October 2011

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European Journal of Neurology

23 November 2017

published in

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23 November 2017

volume

19

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23 November 2017

issue

3

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23 November 2017

page(s)

501-509

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

23 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

Exome sequencing reveals VCP mutations as a cause of familial ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

Inclusion body myopathy with Paget disease of bone and frontotemporal dementia linked to VCP p.Arg155Cys in a Korean family

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

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/10.1111%2FJ.1468-1331.2011.03575.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

Distal myopathy with rimmed vacuoles and hereditary inclusion body myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

Inclusion body myopathy, Paget's disease of the bone and fronto-temporal dementia: a disorder of autophagy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

HDAC6-p97/VCP controlled polyubiquitin chain turnover

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

HDAC6 controls autophagosome maturation essential for ubiquitin-selective quality-control autophagy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

Autoantibodies from primary biliary cirrhosis patients with anti-p95c antibodies bind to recombinant p97/VCP and inhibit in vitro nuclear envelope assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

TDP-43 regulates retinoblastoma protein phosphorylation through the repression of cyclin-dependent kinase 6 expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

Crucial mitochondrial impairment upon CDC48 mutation in apoptotic yeast.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

A stress-responsive system for mitochondrial protein degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

Wild-type human TDP-43 expression causes TDP-43 phosphorylation, mitochondrial aggregation, motor deficits, and early mortality in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

Neurotoxic 43-kDa TAR DNA-binding protein (TDP-43) triggers mitochondrion-dependent programmed cell death in yeast

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

Valosin-containing protein and the pathogenesis of frontotemporal dementia associated with inclusion body myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2011.03575.X

10.1111/J.1468-1331.2011.03575.X

21 January 2018

Identifiers

DOI

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23 November 2017

1 reference