(Q43764436)

26 November 2017

title

Glutamine synthetase activity and expression are not affected by the development of motor neuronopathy in the G93A SOD-1/ALS mouse (English)

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amyotrophic lateral sclerosis

26 November 2017

main subject

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5

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26 November 2017

A E Fray

1

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26 November 2017

S Dempster

series ordinal

2

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26 November 2017

R E Williams

series ordinal

3

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26 November 2017

M R Cookson

series ordinal

4

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26 November 2017

publication date

1 October 2001

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26 November 2017

published in

Molecular Brain Research

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26 November 2017

volume

94

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26 November 2017

issue

1-2

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26 November 2017

page(s)

131-136

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Astrocytosis in wobbler mouse spinal cord involves a population of astrocytes which is glutamine synthetase-negative.

26 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2801%2900228-5

7 January 2021

Glutamate uptake is decreased tardively in the spinal cord of FALS mice.

1 reference

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7 January 2021

Peroxynitrite and hydrogen peroxide induced cell death in the NSC34 neuroblastoma x spinal cord cell line: role of poly (ADP-ribose) polymerase.

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https://api.crossref.org/works/10.1016%2FS0169-328X%2801%2900228-5

7 January 2021

Oxidative Stress and Motor Neurone Disease

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https://api.crossref.org/works/10.1016%2FS0169-328X%2801%2900228-5

7 January 2021

Compartmentation of brain glutamate metabolism in neurons and glia

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https://api.crossref.org/works/10.1016%2FS0169-328X%2801%2900228-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0169-328X%2801%2900228-5

7 January 2021

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://api.crossref.org/works/10.1016%2FS0169-328X%2801%2900228-5

7 January 2021

Decreases in protective enzymes correlates with increased oxidative damage in the aging mouse brain.

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https://api.crossref.org/works/10.1016%2FS0169-328X%2801%2900228-5

7 January 2021

Oxidative damage to brain proteins, loss of glutamine synthetase activity, and production of free radicals during ischemia/reperfusion-induced injury to gerbil brain

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2801%2900228-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0169-328X%2801%2900228-5

7 January 2021

EAAT1 and EAAT2 immunoreactivity in transgenic mice with a G93A mutant SOD1 gene

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https://api.crossref.org/works/10.1016%2FS0169-328X%2801%2900228-5

7 January 2021

Early and transient increase in oxidative stress in the cerebral cortex of senescence-accelerated mouse.

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7 January 2021

Glutamate, excitotoxicity and amyotrophic lateral sclerosis

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7 January 2021

Excess brain protein oxidation and enzyme dysfunction in normal aging and in Alzheimer disease

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7 January 2021

Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2801%2900228-5

7 January 2021

SOD1 mutants linked to amyotrophic lateral sclerosis selectively inactivate a glial glutamate transporter.

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2801%2900228-5

7 January 2021

Cultured glial cells are resistant to the effects of motor neurone disease-associated SOD1 mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2801%2900228-5

7 January 2021

10.1016/S0169-328X(01)00228-5

Identifiers

DOI

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26 November 2017

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