An in vitro model for Lewy body-like hyaline inclusion/astrocytic hyaline inclusion: induction by ER stress with an ALS-linked SOD1 mutation (Q33302125)

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

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scholarly article

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Europe PubMed Central

PubMed publication ID

25 July 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

amyotrophic lateral sclerosis

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based on heuristic

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author name string

Satoru Yamagishi

1

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Europe PubMed Central

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25 July 2017

Yoshihisa Koyama

2

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25 July 2017

Taiichi Katayama

3

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Europe PubMed Central

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25 July 2017

Manabu Taniguchi

4

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25 July 2017

Junichi Hitomi

5

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25 July 2017

Masaaki Kato

6

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

Masashi Aoki

7

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

Yasuto Itoyama

8

1 reference

Europe PubMed Central

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25 July 2017

Shinsuke Kato

9

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25 July 2017

Masaya Tohyama

10

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25 July 2017

language of work or name

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publication date

10 October 2007

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Europe PubMed Central

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25 July 2017

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Europe PubMed Central

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25 July 2017

2

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25 July 2017

10

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

e1030

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Europe PubMed Central

PubMed publication ID

25 July 2017

copyright license

Creative Commons Attribution 4.0 International

10 October 2007

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April 2022 Public Data File from Crossref

copyright status

0 references

Ubiquitin-proteasome-dependent degradation of mammalian ER stearoyl-CoA desaturase.

1 reference

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14 July 2018

Spinal cord endoplasmic reticulum stress associated with a microsomal accumulation of mutant superoxide dismutase-1 in an ALS model

1 reference

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14 July 2018

Unraveling the mechanisms involved in motor neuron degeneration in ALS

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2000355

14 July 2018

Involvement of caspase-4 in endoplasmic reticulum stress-induced apoptosis and Abeta-induced cell death

1 reference

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14 July 2018

Phosphorylation of BCL-2 regulates ER Ca2+ homeostasis and apoptosis.

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14 July 2018

Pael receptor, endoplasmic reticulum stress, and Parkinson?s disease

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14 July 2018

'Unfolding' pathways in neurodegenerative disease

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14 July 2018

Parkin and endoplasmic reticulum stress

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14 July 2018

Mutant SOD1 linked to familial amyotrophic lateral sclerosis, but not wild-type SOD1, induces ER stress in COS7 cells and transgenic mice.

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14 July 2018

Uncleaved BAP31 in association with A4 protein at the endoplasmic reticulum is an inhibitor of Fas-initiated release of cytochrome c from mitochondria

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14 July 2018

Orchestrating the unfolded protein response in health and disease

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14 July 2018

Dorfin ubiquitylates mutant SOD1 and prevents mutant SOD1-mediated neurotoxicity

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2000355

14 July 2018

Association of calnexin with mutant peripheral myelin protein-22 ex vivo: a basis for "gain-of-function" ER diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2000355

14 July 2018

Toxic proteins in neurodegenerative disease

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14 July 2018

ASK1 is essential for endoplasmic reticulum stress-induced neuronal cell death triggered by expanded polyglutamine repeats

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2000355

14 July 2018

Mutant Cu, Zn superoxide dismutase that causes motoneuron degeneration is present in mitochondria in the CNS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2000355

14 July 2018

From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2000355

14 July 2018

New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: inclusions containing SOD1 in neurons and astrocytes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2000355

14 July 2018

Amyotrophic lateral sclerosis

1 reference

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14 July 2018

Amyotrophic lateral sclerosis. unfolding the toxicity of the misfolded

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2000355

14 July 2018

Cross-talk between two cysteine protease families. Activation of caspase-12 by calpain in apoptosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2000355

14 July 2018

Functional and genomic analyses reveal an essential coordination between the unfolded protein response and ER-associated degradation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2000355

14 July 2018

What transgenic mice tell us about neurodegenerative disease

1 reference

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14 July 2018

Coupling of stress in the ER to activation of JNK protein kinases by transmembrane protein kinase IRE1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2000355

14 July 2018

Caspase-12 mediates endoplasmic-reticulum-specific apoptosis and cytotoxicity by amyloid-beta

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2000355

14 July 2018

Presenilin-1 mutations downregulate the signalling pathway of the unfolded-protein response

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2000355

14 July 2018

Recent advances in research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 gene mutations: neuronal Lewy body-like hyaline inclusions and astrocytic hyaline inclusions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2000355

14 July 2018

A stress response pathway from the endoplasmic reticulum to the nucleus requires a novel bifunctional protein kinase/endoribonuclease (Ire1p) in mammalian cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2000355

14 July 2018

Identification of the protein import components of the rat mitochondrial inner membrane, rTIM17, rTIM23, and rTIM44

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2000355

14 July 2018

ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2000355

14 July 2018

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2000355

14 July 2018

Familial amyotrophic lateral sclerosis. A subgroup characterized by posterior and spinocerebellar tract involvement and hyaline inclusions in the anterior horn cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2000355

14 July 2018

Disturbed activation of endoplasmic reticulum stress transducers by familial Alzheimer's disease-linked presenilin-1 mutations

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0001030

21 January 2018

Expression of an endoplasmic reticulum-resident chaperone, glucose-regulated stress protein 78, in the spinal cord of a mouse model of amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0001030

21 January 2018

CHIP promotes proteasomal degradation of familial ALS-linked mutant SOD1 by ubiquitinating Hsp/Hsc70.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0001030

21 January 2018

Proteasomal inhibition causes the formation of protein aggregates containing a wide range of proteins, including nitrated proteins

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0001030

21 January 2018

Histological evidence of redox system breakdown caused by superoxide dismutase 1 (SOD1) aggregation is common to SOD1-mutated motor neurons in humans and animal models

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0001030

21 January 2018

XIAP decreases caspase-12 cleavage and calpain activity in spinal cord of ALS transgenic mice.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0001030

21 January 2018

Caspase-12 cleavage and increased oxidative stress during motoneuron degeneration in transgenic mouse model of ALS.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0001030

21 January 2018

Characterization of the signal that directs Tom20 to the mitochondrial outer membrane

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0001030

21 January 2018

Intense superoxide dismutase-1 immunoreactivity in intracytoplasmic hyaline inclusions of familial amyotrophic lateral sclerosis with posterior column involvement

2 references

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0001030

21 January 2018

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2000355

31 October 2018

Variance of age at onset in a Japanese family with amyotrophic lateral sclerosis associated with a novel Cu/Zn superoxide dismutase mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17925878

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ubiquitin and the control of protein fate in the secretory and endocytic pathways

1 reference

https://pubmed.ncbi.nlm.nih.gov/17925878

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Astrocytic hyaline inclusions contain advanced glycation endproducts in familial amyotrophic lateral sclerosis with superoxide dismutase 1 gene mutation: immunohistochemical and immunoelectron microscopical analyses

1 reference

https://pubmed.ncbi.nlm.nih.gov/17925878

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impairment of axonal transport in the axon hillock and the initial segment of anterior horn neurons in transgenic mice with a G93A mutant SOD1 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/17925878

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Advanced glycation endproduct-modified superoxide dismutase-1 (SOD1)-positive inclusions are common to familial amyotrophic lateral sclerosis patients with SOD1 gene mutations and transgenic mice expressing human SOD1 with a G85R mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17925878

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Formation of advanced glycation end-product-modified superoxide dismutase-1 (SOD1) is one of the mechanisms responsible for inclusions common to familial amyotrophic lateral sclerosis patients with SOD1 gene mutation, and transgenic mice expressing

1 reference

https://pubmed.ncbi.nlm.nih.gov/17925878

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amyotrophic lateral sclerosis: pathogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17925878

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Copper chaperone for superoxide dismutase co-aggregates with superoxide dismutase 1 (SOD1) in neuronal Lewy body-like hyaline inclusions: an immunohistochemical study on familial amyotrophic lateral sclerosis with SOD1 gene mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17925878

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0001030

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

2007PLoSO...2.1030Y

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PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

ResearchGate publication ID

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