(Q33865534)

29 July 2017

title

No benefit of dietary restriction on disease onset or progression in amyotrophic lateral sclerosis Cu/Zn-superoxide dismutase mutant mice (English)

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amyotrophic lateral sclerosis

29 July 2017

main subject

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author name string

Pedersen WA

series ordinal

1

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29 July 2017

Mattson MP

series ordinal

2

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29 July 2017

language of work or name

English

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publication date

1 June 1999

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29 July 2017

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29 July 2017

volume

833

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29 July 2017

issue

1

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29 July 2017

page(s)

117-120

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Increased 3-nitrotyrosine in both sporadic and familial amyotrophic lateral sclerosis

29 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2901471-7

Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2901471-7

Increased 3-nitrotyrosine and oxidative damage in mice with a human copper/zinc superoxide dismutase mutation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2901471-7

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%2FS0006-8993%2899%2901471-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2901471-7

Dietary restriction benefits learning and motor performance of aged mice.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2901471-7

Massive mitochondrial degeneration in motor neurons triggers the onset of amyotrophic lateral sclerosis in mice expressing a mutant SOD1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2901471-7

Protein modification by the lipid peroxidation product 4-hydroxynonenal in the spinal cords of amyotrophic lateral sclerosis patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2901471-7

Presence of 4-hydroxynonenal in cerebrospinal fluid of patients with sporadic amyotrophic lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2901471-7

Oxidative damage, mitochondrial oxidant generation and antioxidant defenses during aging and in response to food restriction in the mouse

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2901471-7

Oxidative stress, caloric restriction, and aging

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2901471-7

The retardation of aging in mice by dietary restriction: longevity, cancer, immunity and lifetime energy intake

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2901471-7

Altered reactivity of superoxide dismutase in familial amyotrophic lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2901471-7

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%2FS0006-8993%2899%2901471-7

A familial amyotrophic lateral sclerosis-associated A4V Cu, Zn-superoxide dismutase mutant has a lower Km for hydrogen peroxide. Correlation between clinical severity and the Km value.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2901471-7

Evidence of increased oxidative damage in both sporadic and familial amyotrophic lateral sclerosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2901471-7

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0006-8993(99)01471-7

1 reference

29 July 2017

1 reference