(Q45303594)

11 December 2017

title

Age-dependent and tissue-specific CAG repeat instability occurs in mouse knock-in for a mutant Huntington's disease gene (English)

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11 December 2017

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Ishiguro H

1

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11 December 2017

Yamada K

2

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11 December 2017

Sawada H

3

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11 December 2017

Nishii K

4

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11 December 2017

Ichino N

5

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11 December 2017

Sawada M

6

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Kurosawa Y

7

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Matsushita N

8

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11 December 2017

Kobayashi K

9

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11 December 2017

Goto J

10

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Hashida H

11

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Masuda N

12

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11 December 2017

Kanazawa I

13

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11 December 2017

Nagatsu T

14

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11 December 2017

publication date

1 August 2001

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Journal of Neuroscience Research

11 December 2017

published in

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11 December 2017

volume

65

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11 December 2017

issue

4

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11 December 2017

page(s)

289-297

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

11 December 2017

cites work

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SCA1 transgenic mice: A model for neurodegeneration caused by an expanded CAG trinucleotide repeat

21 January 2018

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

21 January 2018

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Inactivation of the mouse Huntington's disease gene homolog Hdh

21 January 2018

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

21 January 2018

1 reference

Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in vivo

21 January 2018

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Dramatic mutation instability in HD mouse striatum: does polyglutamine load contribute to cell-specific vulnerability in Huntington's disease?

21 January 2018

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Neurological abnormalities in a knock-in mouse model of Huntington's disease

21 January 2018

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

21 January 2018

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Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation.

21 January 2018

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Targeted disruption of the Huntington's disease gene results in embryonic lethality and behavioral and morphological changes in heterozygotes

21 January 2018

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

21 January 2018

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When more is less: pathogenesis of glutamine repeat neurodegenerative diseases

21 January 2018

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Intranuclear neuronal inclusions: a common pathogenic mechanism for glutamine-repeat neurodegenerative diseases?

21 January 2018

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Transgenic mice harboring a full-length human mutant DRPLA gene exhibit age-dependent intergenerational and somatic instabilities of CAG repeats comparable with those in DRPLA patients.

21 January 2018

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Intranuclear inclusions and neuritic aggregates in transgenic mice expressing a mutant N-terminal fragment of huntingtin

21 January 2018

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

21 January 2018

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

21 January 2018

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Expanded polyglutamine stretches interact with TAFII130, interfering with CREB-dependent transcription

21 January 2018

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Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

21 January 2018

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

21 January 2018

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Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm.

21 January 2018

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

21 January 2018

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Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouse

21 January 2018

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

21 January 2018

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Reversal of neuropathology and motor dysfunction in a conditional model of Huntington's disease

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/JNR.1153

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11 December 2017

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