(Q45296558)

11 December 2017

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

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11 December 2017

P H Reddy

1

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11 December 2017

M Williams

2

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11 December 2017

V Charles

3

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11 December 2017

L Garrett

4

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11 December 2017

L Pike-Buchanan

5

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11 December 2017

W O Whetsell

6

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11 December 2017

G Miller

7

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11 December 2017

D A Tagle

8

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11 December 2017

language of work or name

English

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publication date

1 October 1998

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11 December 2017

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11 December 2017

20

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11 December 2017

2

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11 December 2017

198-202

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https://scigraph.springernature.com/pub.10.1038/2510

11 December 2017

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cites work

Neuropathological classification of Huntington's disease

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7 January 2021

Neuronal loss in layers V and VI of cerebral cortex in Huntington's disease

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7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease

1 reference

7 January 2021

Trinucleotide repeat length instability and age of onset in Huntington's disease

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7 January 2021

Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15.

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7 January 2021

Huntington's disease gene (IT15) is widely expressed in human and rat tissues

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7 January 2021

Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues

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7 January 2021

Widespread expression of Huntington's disease gene (IT15) protein product

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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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7 January 2021

Ectopically expressed CAG repeats cause intranuclear inclusions and a progressive late onset neurological phenotype in the mouse.

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7 January 2021

Partial characterisation of murine huntingtin and apparent variations in the subcellular localisation of huntingtin in human, mouse and rat brain.

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7 January 2021

Huntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansion

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7 January 2021

Evidence for apoptotic cell death in Huntington disease and excitotoxic animal models.

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7 January 2021

DNA end labeling (TUNEL) in Huntington's disease and other neuropathological conditions

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7 January 2021

Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation

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7 January 2021

Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain

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7 January 2021

Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3.

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7 January 2021

Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structures

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7 January 2021

3-Nitropropionic acid animal model and Huntington's disease

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7 January 2021

Huntingtin immunoreactivity in the rat neostriatum: differential accumulation in projection and interneurons.

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7 January 2021

The complex pathology of trinucleotide repeats

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7 January 2021

The cerebellar leucine-rich acidic nuclear protein interacts with ataxin-1

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7 January 2021

Evidence from antibody studies that the CAG repeat in the Huntington disease gene is expressed in the protein

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7 January 2021

SH3 domain-dependent association of huntingtin with epidermal growth factor receptor signaling complexes

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7 January 2021

Identifiers

DOI

10.1038/2510

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Dimensions Publication ID

11 December 2017

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