Increased reactive oxygen species in familial amyotrophic lateral sclerosis with mutations in SOD1. (Q40863663)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10930589%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

title

Increased reactive oxygen species in familial amyotrophic lateral sclerosis with mutations in SOD1 (English)

1 reference

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amyotrophic lateral sclerosis

9 November 2019

main subject

0 references

reactive oxygen species

1 reference

4

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9 November 2019

Teepu Siddique

5

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9 November 2019

author name string

M Said Ahmed

1

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9 November 2019

W Y Hung

2

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9 November 2019

J S Zu

3

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9 November 2019

publication date

1 June 2000

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Journal of the Neurological Sciences

9 November 2019

published in

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9 November 2019

volume

176

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9 November 2019

issue

2

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9 November 2019

page(s)

88-94

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

9 November 2019

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Superoxide dismutase concentration and activity in familial amyotrophic lateral sclerosis

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Two novel SOD1 mutations in patients with familial amyotrophic lateral sclerosis

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

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

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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

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The familial amyotrophic lateral sclerosis-associated amino acid substitutions E100G, G93A, and G93R do not influence the rate of inactivation of copper- and zinc-containing superoxide dismutase by H2O2

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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.

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