Abnormal gene product identified in hereditary dentatorubral–pallidoluysian atrophy (DRPLA) brain (Q24324461)

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scientific article published on May 1, 1995

Language	Label	Description	Also known as
English	Abnormal gene product identified in hereditary dentatorubral–pallidoluysian atrophy (DRPLA) brain	scientific article published on May 1, 1995

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scholarly article

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Abnormal gene product identified in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) brain (English)

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Abnormal gene product identified in hereditary dentatorubral–pallidoluysian atrophy (DRPLA) brain (English)

1 reference

10.1038/NG0595-99

https://api.crossref.org/works/10.1038/NG0595-99

14 July 2024

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1 reference

GOA release 2020-03-11

central nervous system development

1 reference

GOA release 2020-03-11

dentatorubral-pallidoluysian atrophy

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based on heuristic

inferred from title

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7647802

14 July 2024

author name string

I. Yazawa

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7647802

14 July 2024

N. Nukina

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7647802

14 July 2024

H. Hashida

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7647802

14 July 2024

J. Goto

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7647802

14 July 2024

M. Yamada

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7647802

14 July 2024

I. Kanazawa

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7647802

14 July 2024

language of work or name

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publication date

May 1995

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full work available at URL

http://www.nature.com/articles/ng0595-99

1 reference

10.1038/NG0595-99

https://api.crossref.org/works/10.1038/NG0595-99

14 July 2024

http://www.nature.com/articles/ng0595-99.pdf

Portable Document Format

1 reference

10.1038/NG0595-99

https://api.crossref.org/works/10.1038/NG0595-99

14 July 2024

Nature Genetics

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10

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1

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99-103

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Unusual form of cerebellar ataxia; combined dentato-rubral and pallido-Luysian degeneration

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

21 January 2018

Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

21 January 2018

DNA analysis in hereditary dentatorubral-pallidoluysian atrophy: correlation between CAG repeat length and phenotypic variation and the molecular basis of anticipation

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

21 January 2018

Hereditary dentatorubral-pallidoluysian atrophy: Clinical and pathologic variants in a family

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

Anticipation in hereditary dentatorubral-pallidoluysian atrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American family

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

Exclusion mapping of the hereditary dentatorubropallidoluysian atrophy gene from the Huntington's disease locus

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

Novel triplet repeat containing genes in human brain: cloning, expression, and length polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

An unstable triplet repeat in a gene related to myotonic muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

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%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

Absence of expression of the FMR-1 gene in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

Characterization and localization of the FMR-1 gene product associated with fragile X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy.

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

Myotonic dystrophy kinase is a component of neuromuscular junctions

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

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%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

Characterization and localization of the Huntington disease gene product

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

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%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

Dynamic mutations hit double figures

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

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%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

A common RNA recognition motif identified within a defined U1 RNA binding domain of the 70K U1 snRNP protein

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

Androgen receptor abnormality in X-linked spinal and bulbar muscular atrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

FMR1 Protein: Conserved RNP Family Domains and Selective RNA Binding

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

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%2FNG0595-99

7 January 2021

based on heuristic

inferred from DOI database lookup

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10.1038/NG0595-99

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