(Q28509836)

24 January 2017

title

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

1 reference

24 January 2017

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1 reference

GOA release 2020-03-11

Y. Trottier

1

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Didier Devys

object named as

D. Devys

2

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Yves Agid

8

object named as

Y. Agid

1 reference

24 January 2017

G. Imbert

3

1 reference

24 January 2017

F. Saudou

4

1 reference

24 January 2017

I. An

5

1 reference

24 January 2017

Y. Lutz

6

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24 January 2017

C. Weber

7

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24 January 2017

E. C. Hirsch

9

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24 January 2017

J. L. Mandel

10

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24 January 2017

language of work or name

English

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publication date

1 May 1995

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24 January 2017

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24 January 2017

volume

10

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24 January 2017

issue

1

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24 January 2017

page(s)

104–110

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Huntington's disease. Pathogenesis and management

24 January 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

Huntington's disease and repeating trinucleotides

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

Genetics and molecular biology of Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

Melanized dopaminergic neurons are differentially susceptible to degeneration in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

The epidemiology of Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

Neuropathological classification of Huntington's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

Selective sparing of a class of striatal neurons in Huntington's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

Identification and characterization of the gene causing type 1 spinocerebellar ataxia

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA)

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

Glutamine repeats as polar zippers: their possible role in inherited neurodegenerative diseases

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

Characterization and localization of the Huntington disease gene product

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

Transcriptional activation modulated by homopolymeric glutamine and proline stretches

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

Reduced transcriptional regulatory competence of the androgen receptor in X-linked spinal and bulbar muscular atrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

The length and location of CAG trinucleotide repeats in the androgen receptor N-terminal domain affect transactivation function

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

Human genetic diseases due to codon reiteration: relationship to an evolutionary mechanism

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

Seeding "one-dimensional crystallization" of amyloid: a pathogenic mechanism in Alzheimer's disease and scrapie?

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

Mouse Huntington's disease gene homolog (Hdh).

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

Sequence of the murine Huntington disease gene: evidence for conservation, alternate splicing and polymorphism in a triplet (CCG) repeat [corrected]

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

Human oestrogen receptor cDNA: sequence, expression and homology to v-erb-A

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

High efficiency gene transfer into mammalian cells

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021

Differences in tyrosine hydroxylase-like immunoreactivity characterize the mesostriatal innervation of striosomes and extrastriosomal matrix at maturity

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-104

7 January 2021