(Q41269608)

28 September 2017

title

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

1 reference

28 September 2017

0 references

Y Trottier

1

0 references

Geraldine Cancel-Tassin

G Cancel

6

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László Tora

L Tora

10

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Giovanni Stevanin

G Stevanin

3

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Didier Devys

D Devys

5

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author name string

Y Lutz

2

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28 September 2017

G Imbert

4

1 reference

28 September 2017

F Saudou

7

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28 September 2017

C Weber

8

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28 September 2017

G David

9

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28 September 2017

language of work or name

English

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publication date

1 November 1995

1 reference

28 September 2017

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28 September 2017

volume

378

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28 September 2017

issue

6555

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28 September 2017

page(s)

403-406

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Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

28 September 2017

cites work

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

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

1 reference

7 January 2021

Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)

1 reference

7 January 2021

Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p

1 reference

7 January 2021

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

1 reference

7 January 2021

Gain of glutamines, gain of function?

1 reference

7 January 2021

Genetics and molecular biology of Huntington's disease

1 reference

7 January 2021

The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1

1 reference

7 January 2021

Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3p.

1 reference

7 January 2021

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1

1 reference

7 January 2021

Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus

1 reference

7 January 2021

Anticipation in spinocerebellar ataxia type 2

1 reference

7 January 2021

Transcriptional activation modulated by homopolymeric glutamine and proline stretches

1 reference

7 January 2021

The gene for the TATA binding protein (TBP) that contains a highly polymorphic protein coding CAG repeat maps to 6q27.

1 reference

7 January 2021

Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form

1 reference

7 January 2021

HIV or zidovudine myopathy?

1 reference

7 January 2021

Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11.

1 reference

7 January 2021

Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p

1 reference

7 January 2021

Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q

1 reference

7 January 2021

Genes with triplet repeats: candidate mediators of neuropsychiatric disorders

1 reference

7 January 2021

Incorporation of glutamine repeats makes protein oligomerize: implications for neurodegenerative diseases

1 reference

7 January 2021

Instability of CAG repeats in Huntington's disease: relation to parental transmission and age of onset

1 reference

7 January 2021

Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals

1 reference

7 January 2021

A small-scale procedure for preparation of nuclear extracts that support efficient transcription and pre-mRNA splicing

1 reference

7 January 2021

Identifiers

DOI

10.1038/378403A0

1 reference

Dimensions Publication ID

28 September 2017

1011102548

0 references

1 reference