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

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amyotrophic lateral sclerosis

24 February 2020

main subject

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author

Hiroyuki Morino

11

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24 February 2020

Masafumi Ihara

15

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24 February 2020

Riki Matsumoto

16

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24 February 2020

Makoto Urushitani

18

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24 February 2020

Hideshi Kawakami

19

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24 February 2020

5

Takayuki Kondo

1 reference

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24 February 2020

author name string

Takashi Ayaki

1

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24 February 2020

Hidefumi Ito

2

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24 February 2020

Hiroko Fukushima

3

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24 February 2020

Takeshi Inoue

4

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24 February 2020

Akito Ikemoto

6

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24 February 2020

Takeshi Asano

7

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24 February 2020

Akemi Shodai

8

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24 February 2020

Takuji Fujita

9

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24 February 2020

Satoshi Fukui

10

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24 February 2020

Satoshi Nakano

12

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24 February 2020

Hirofumi Kusaka

13

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24 February 2020

Hirofumi Yamashita

14

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24 February 2020

Jun Kawamata

17

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24 February 2020

Ryosuke Takahashi

20

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24 February 2020

language of work or name

1 reference

10 December 2014

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Acta Neuropathologica Communications

24 February 2020

published in

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24 February 2020

volume

2

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24 February 2020

page(s)

172

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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

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21 January 2018

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

21 January 2018

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21 January 2018

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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Oxidative and endoplasmic reticulum stress interplay in sporadic amyotrophic lateral sclerosis

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12 December 2020

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

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

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12 December 2020

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Identifiers

DOI

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

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24 February 2020

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24 February 2020

PubMed publication ID

25492614

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