(Q45300303)

11 December 2017

title

Striatal oxidative damage parallels the expression of a neurological phenotype in mice transgenic for the mutation of Huntington's disease (English)

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11 December 2017

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Pérez-Severiano F

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11 December 2017

Ríos C

series ordinal

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11 December 2017

Segovia J

series ordinal

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11 December 2017

language of work or name

English

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publication date

1 April 2000

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11 December 2017

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11 December 2017

volume

862

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11 December 2017

issue

1-2

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11 December 2017

page(s)

234-237

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Mitochondrial dysfunction in neurodegenerative diseases

11 December 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0006-8993%2800%2902082-5

Characterization of progressive motor deficits in mice transgenic for the human Huntington's disease mutation.

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-8993%2800%2902082-5

Striatal transplantation in a transgenic mouse model of Huntington's disease

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-8993%2800%2902082-5

The measurement and mechanism of lipid peroxidation in biological systems

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-8993%2800%2902082-5

Transgenic mice expressing a Huntington's disease mutation are resistant to quinolinic acid-induced striatal excitotoxicity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2800%2902082-5

Mice transgenic for an expanded CAG repeat in the Huntington's disease gene develop diabetes

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-8993%2800%2902082-5

Selective discrimination learning impairments in mice expressing the human Huntington's disease mutation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2800%2902082-5

Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2800%2902082-5

Nitric oxide synthase inhibition prevents acute quinolinate-induced striatal neurotoxicity

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-8993%2800%2902082-5

Recent advances on the pathogenesis of Huntington's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2800%2902082-5

Oxidative damage to mitochondrial DNA in Huntington's disease parietal cortex

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-8993%2800%2902082-5

Behavioural abnormalities and selective neuronal loss in HD transgenic mice expressing mutated full-length HD cDNA.

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-8993%2800%2902082-5

Mitochondrial involvement in Parkinson's disease, Huntington's disease, hereditary spastic paraplegia and Friedreich's ataxia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2800%2902082-5

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2800%2902082-5

In vivo lipid peroxidation in rat brain following intracortical Fe2+ injection

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-8993%2800%2902082-5

Oxidative stress in Huntington's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2800%2902082-5

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0006-8993(00)02082-5

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11 December 2017

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