(Q48011121)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12659845%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12659845%20AND%20SRC:MED&resulttype=core&format=json

amyotrophic lateral sclerosis

1 November 2019

main subject

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author

Manabu Wada

5

1 reference

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1 November 2019

author name string

Shinsuke Tobisawa

1

1 reference

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1 November 2019

Yasukazu Hozumi

2

1 reference

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1 November 2019

Shigeki Arawaka

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12659845%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Shingo Koyama

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12659845%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Makiko Nagai

6

1 reference

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1 November 2019

Masashi Aoki

7

1 reference

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1 November 2019

Yasuto Itoyama

8

1 reference

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1 November 2019

Kaoru Goto

9

1 reference

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1 November 2019

Takeo Kato

10

1 reference

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1 November 2019

language of work or name

English

0 references

publication date

1 April 2003

1 reference

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Biochemical and Biophysical Research Communications

1 November 2019

published in

1 reference

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1 November 2019

volume

303

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1 November 2019

issue

2

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1 November 2019

page(s)

496-503

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

1 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

Mutations in all five exons ofSOD-1 may cause ALS

7 January 2021

1 reference

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Mild ALS in Japan associated with novel SOD mutation

7 January 2021

1 reference

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A novel SOD mutant and ALS

7 January 2021

1 reference

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Superoxide dismutase activity, oxidative damage, and mitochondrial energy metabolism in familial and sporadic amyotrophic lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

Transgenic mice expressing an altered murine superoxide dismutase gene provide an animal model of amyotrophic lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

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

7 January 2021

1 reference

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Molecular genetic basis of familial ALS.

7 January 2021

1 reference

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Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

Toxic mutants in Charcot's sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

Aggregation and Motor Neuron Toxicity of an ALS-Linked SOD1 Mutant Independent from Wild-Type SOD1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

ALS, SOD and peroxynitrite

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

Altered reactivity of superoxide dismutase in familial amyotrophic lateral sclerosis

7 January 2021

1 reference

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Medicine: danger--misfolding proteins.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

Inherent toxicity of aggregates implies a common mechanism for protein misfolding diseases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

Naturally secreted oligomers of amyloid beta protein potently inhibit hippocampal long-term potentiation in vivo

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

Formation of high molecular weight complexes of mutant Cu, Zn-superoxide dismutase in a mouse model for familial amyotrophic lateral sclerosis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

pEF-BOS, a powerful mammalian expression vector

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

A 104-kDa diacylglycerol kinase containing ankyrin-like repeats localizes in the cell nucleus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

Galectin-1 Is a Component of Neurofilamentous Lesions in Sporadic and Familial Amyotrophic Lateral Sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

Aggregation of mutant Cu/Zn superoxide dismutase proteins in a culture model of ALS

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

Formation of granular cytoplasmic aggregates in COS7 cells expressing mutant Cu/Zn superoxide dismutase associated with familial amyotrophic lateral sclerosis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

Tripartite management of unfolded proteins in the endoplasmic reticulum

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

In vitro synthesis of superoxide dismutases of rat liver

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

Molecular immunocytochemistry of the CuZn superoxide dismutase in rat hepatocytes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

Subcellular distribution of superoxide dismutases (SOD) in rat liver: Cu,Zn-SOD in mitochondria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

Decreased levels of proteasome activity and proteasome expression in aging spinal cord

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

The Chaperone Protein BiP Binds to a Mutant Prion Protein and Mediates Its Degradation by the Proteasome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

An unfolded putative transmembrane polypeptide, which can lead to endoplasmic reticulum stress, is a substrate of Parkin

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900353-X

10.1016/S0006-291X(03)00353-X

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12659845%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

1 reference