(Q56909246)

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The expanding world of ataxins

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title

The expanding world of ataxins (English)

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1

Huda Y. Zoghbi

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language of work or name

English

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publication date

November 1996

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published in

Nature Genetics

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volume

14

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issue

3

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page(s)

237-238

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exact match

https://scigraph.springernature.com/pub.10.1038/ng1196-237

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cites work

Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.

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reference URL

https://api.crossref.org/works/10.1038%2FNG1196-237

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21 January 2018

Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.

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https://api.crossref.org/works/10.1038%2FNG1196-237

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21 January 2018

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats

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https://api.crossref.org/works/10.1038%2FNG1196-237

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21 January 2018

Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

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https://api.crossref.org/works/10.1038%2FNG1196-237

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21 January 2018

Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles.

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https://api.crossref.org/works/10.1038%2FNG1196-237

retrieved

21 January 2018

Morphometric studies in dominant olivopontocerebellar atrophy. Comparison of cell losses with amino acid decreases

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https://api.crossref.org/works/10.1038%2FNG1196-237

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21 January 2018

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

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https://api.crossref.org/works/10.1038%2FNG1196-237

retrieved

21 January 2018

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

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reference URL

https://api.crossref.org/works/10.1038%2FNG1196-237

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7 January 2021

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CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

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7 January 2021

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Dynamic mutations hit double figures

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7 January 2021

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Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.

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https://api.crossref.org/works/10.1038%2FNG1196-237

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7 January 2021

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The stabilization of repetitive tracts of DNA by variant repeats requires a functional DNA mismatch repair system

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reference URL

https://api.crossref.org/works/10.1038%2FNG1196-237

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7 January 2021

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Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies)

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https://api.crossref.org/works/10.1038%2FNG1196-237

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7 January 2021

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Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features.

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https://api.crossref.org/works/10.1038%2FNG1196-237

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7 January 2021

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Identifiers

DOI

10.1038/NG1196-237

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PubMed publication ID

8896544

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(Q56909246)

The expanding world of ataxins

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