(Q44219098)

30 November 2017

title

Huntington's disease transgenic mice are resistant to global cerebral ischemia (English)

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30 November 2017

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Johannes Schiefer

1

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30 November 2017

Anke Alberty

2

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30 November 2017

Tatjana Dose

3

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30 November 2017

Sabine Oliva

4

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30 November 2017

Johannes Noth

5

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30 November 2017

Christoph M Kosinski

6

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30 November 2017

language of work or name

English

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publication date

1 December 2002

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30 November 2017

number of pages

4

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inferred from page(s)

published in

Neuroscience Letters

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30 November 2017

volume

334

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30 November 2017

issue

2

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30 November 2017

page(s)

99-102

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Ischemic preconditioning and brain tolerance: temporal histological and functional outcomes, protein synthesis requirement, and interleukin-1 receptor antagonist and early gene expression

30 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901111-4

7 January 2021

Chronic quinolinic acid lesions in rats closely resemble Huntington's disease

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901111-4

7 January 2021

On the relationship of brain vasculature to production of neurological deficit and morphological changes following acute unilateral common carotid artery ligation in gerbils

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901111-4

7 January 2021

NMDA receptor function in mouse models of Huntington disease

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901111-4

7 January 2021

Are neuronal intranuclear inclusions the common neuropathology of triplet-repeat disorders with polyglutamine-repeat expansions?

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901111-4

7 January 2021

Resistance to NMDA toxicity correlates with appearance of nuclear inclusions, behavioural deficits and changes in calcium homeostasis in mice transgenic for exon 1 of the huntington gene

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901111-4

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901111-4

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901111-4

7 January 2021

Changes in cortical and striatal neurons predict behavioral and electrophysiological abnormalities in a transgenic murine model of Huntington's disease

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901111-4

7 January 2021

Impaired glutamate uptake in the R6 Huntington's disease transgenic mice.

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901111-4

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901111-4

7 January 2021

Mice transgenic for the human Huntington's disease mutation have reduced sensitivity to kainic acid toxicity

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901111-4

7 January 2021

Fluoro-Jade B: a high affinity fluorescent marker for the localization of neuronal degeneration

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7 January 2021

Neurobiology of Huntington's disease

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7 January 2021

Apolipoprotein E deficiency worsens outcome from global cerebral ischemia in the mouse

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901111-4

7 January 2021

Polyglutamine-expanded huntingtin promotes sensitization of N-methyl-D-aspartate receptors via post-synaptic density 95.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901111-4

7 January 2021

A comparison of strain-related susceptibility in two murine recovery models of global cerebral ischemia.

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https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901111-4

7 January 2021

Mutant huntingtin enhances excitotoxic cell death.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901111-4

7 January 2021

Increased sensitivity to N-methyl-D-aspartate receptor-mediated excitotoxicity in a mouse model of Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2901111-4

7 January 2021

10.1016/S0304-3940(02)01111-4

Identifiers

DOI

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30 November 2017

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