(Q45300220)

11 December 2017

title

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

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11 December 2017

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Morton AJ

1

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11 December 2017

Leavens W

series ordinal

2

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11 December 2017

publication date

1 May 2000

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11 December 2017

published in

Brain Research Bulletin

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11 December 2017

volume

52

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11 December 2017

issue

1

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11 December 2017

page(s)

51-59

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Neurochemical and histologic characterization of striatal excitotoxic lesions produced by the mitochondrial toxin 3-nitropropionic acid

11 December 2017

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Intranuclear neuronal inclusions in Huntington's disease and dentatorubral and pallidoluysian atrophy: correlation between the density of inclusions and IT15 CAG triplet repeat length

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

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A YAC mouse model for Huntington's disease with full-length mutant huntingtin, cytoplasmic toxicity, and selective striatal neurodegeneration.

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

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7 January 2021

Clinical and neuropathologic assessment of severity in Huntington's disease

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Inhibition of caspase-1 slows disease progression in a mouse model of Huntington's disease

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7 January 2021

Dopamine modulates the susceptibility of striatal neurons to 3-nitropropionic acid in the rat model of Huntington's disease.

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Axonal transport of N-terminal huntingtin suggests early pathology of corticostriatal projections in Huntington disease

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7 January 2021

Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions.

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7 January 2021

Widespread patterns of neuronal damage following systemic or intracerebral injections of kainic acid: a histological study

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7 January 2021

A Huntington's disease CAG expansion at the murine Hdh locus is unstable and associated with behavioural abnormalities in mice

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7 January 2021

Nuclear inclusions in glutamine repeat disorders: are they pernicious, coincidental, or beneficial?

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7 January 2021

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7 January 2021

Neuronal loss in the hippocampus in Huntington's disease: a comparison with HIV infection

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7 January 2021

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

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7 January 2021

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7 January 2021

Expanded polyglutamine protein forms nuclear inclusions and causes neural degeneration in Drosophila

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7 January 2021

10.1016/S0361-9230(00)00238-0

Identifiers

DOI

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release_62pyjjekancmrjm66kiwmawr5u

11 December 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/62pyjjekancmrjm66kiwmawr5u

24 November 2022

mapped directly with Wikidata item

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