(Q40975834)

English

Up-regulation of protein chaperones preserves viability of cells expressing toxic Cu/Zn-superoxide dismutase mutants associated with amyotrophic lateral sclerosis

scientific article published on February 1999

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

Up-regulation of protein chaperones preserves viability of cells expressing toxic Cu/Zn-superoxide dismutase mutants associated with amyotrophic lateral sclerosis (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

amyotrophic lateral sclerosis

0 references

molecular chaperones

0 references

author name string

Bruening W

1

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

Roy J

2

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

Giasson B

3

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

Figlewicz DA

4

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

Mushynski WE

5

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

Durham HD

6

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

language of work or name

0 references

publication date

1 February 1999

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

Journal of Neurochemistry

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

72

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

693-699

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720693.X

21 January 2018

Elevated free nitrotyrosine levels, but not protein-bound nitrotyrosine or hydroxyl radicals, throughout amyotrophic lateral sclerosis (ALS)-like disease implicate tyrosine nitration as an aberrant in vivo property of one familial ALS-linked superox

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720693.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720693.X

21 January 2018

Neuropathological changes in two lines of mice carrying a transgene for mutant human Cu,Zn SOD, and in mice overexpressing wild type human SOD: a model of familial amyotrophic lateral sclerosis (FALS).

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720693.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720693.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720693.X

21 January 2018

Benefit of vitamin E, riluzole, and gabapentin in a transgenic model of familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720693.X

21 January 2018

Subunit asymmetry in the three-dimensional structure of a human CuZnSOD mutant found in familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720693.X

21 January 2018

Proteasome inhibition enhances the stability of mouse Cu/Zn superoxide dismutase with mutations linked to familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720693.X

21 January 2018

Mutations in copper-zinc superoxide dismutase that cause amyotrophic lateral sclerosis alter the zinc binding site and the redox behavior of the protein

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720693.X

21 January 2018

Expression of heat shock genes (hsp70) in the rabbit spinal cord: localization of constitutive and hyperthermia-inducible mRNA species

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720693.X

21 January 2018

Instability of mutant Cu/Zn superoxide dismutase (Ala4Thr) associated with familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720693.X

21 January 2018

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/10.1046%2FJ.1471-4159.1999.0720693.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720693.X

21 January 2018

Reexamination of the mechanism of hydroxyl radical adducts formed from the reaction between familial amyotrophic lateral sclerosis-associated Cu,Zn superoxide dismutase mutants and H2O2.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720693.X

21 January 2018

Altered reactivity of superoxide dismutase in familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720693.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720693.X

21 January 2018

A gain-of-function of an amyotrophic lateral sclerosis-associated Cu,Zn-superoxide dismutase mutant: An enhancement of free radical formation due to a decrease in Km for hydrogen peroxide

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720693.X

21 January 2018

Increased sensitivity of fibroblasts from amyotrophic lateral sclerosis patients to oxidative stress

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720693.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720693.X

21 January 2018

Mutations in all five exons ofSOD-1 may cause ALS

1 reference

https://api.crossref.org/works/10.1046%2FJ.1471-4159.1999.0720693.X

21 January 2018

Identifiers

10.1046/J.1471-4159.1999.0720693.X

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 September 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q40975834&oldid=2092786355"