(Q58125527)

ORCID Public Data File 2021

author name string

Yasuyuki Honjo

1

0 references

Satoshi Kaneko

2

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Hidefumi Ito

3

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Tomohisa Horibe

4

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Masato Nagashima

5

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Kengo Fujita

7

0 references

Ryosuke Takahashi

8

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Hirofumi Kusaka

9

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Koji Kawakami

Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders

10

0 references

publication date

11 July 2011

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published in

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volume

12

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issue

6

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page(s)

444-450

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cites work

Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2011.594055

Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2011.594055

TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2011.594055

Cell death: protein misfolding and neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2011.594055

Protein Disulfide Isomerase Acts as a Redox-Dependent Chaperone to Unfold Cholera Toxin

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2011.594055

Protein disulphide isomerase protects against protein aggregation and is S-nitrosylated in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2011.594055

Protein disulfide isomerase-immunopositive inclusions in patients with Alzheimer disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2011.594055

Accumulation of Hsc70 and Hsp70 in glial cytoplasmic inclusions in patients with multiple system atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2011.594055

Functional differences between human and yeast protein disulfide isomerase family proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2011.594055

Evidence for mitochondrial localization of P5, a member of the protein disulphide isomerase family

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2011.594055

Functional analysis of the CXXC motif using phage antibodies that cross-react with protein disulphide-isomerase family proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2011.594055

An in vitro model for Lewy body-like hyaline inclusion/astrocytic hyaline inclusion: induction by ER stress with an ALS-linked SOD1 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2011.594055

ALS-linked mutant SOD1 induces ER stress- and ASK1-dependent motor neuron death by targeting Derlin-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2011.594055

Derlin-1 overexpression ameliorates mutant SOD1-induced endoplasmic reticulum stress by reducing mutant SOD1 accumulation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2011.594055

Chromogranin-mediated secretion of mutant superoxide dismutase proteins linked to amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2011.594055

Endoplasmic reticulum stress and induction of the unfolded protein response in human sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2011.594055

Slowing of axonal transport is a very early event in the toxicity of ALS-linked SOD1 mutants to motor neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2011.594055