(Q24324374)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647801%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647801%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

0 references

1 reference

GOA release 2020-03-11

spinocerebellar ataxia type 1

1 reference

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647801%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

Huda Zoghbi

6

1 reference

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22 October 2019

author name string

Servadio A

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647801%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

Koshy B

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647801%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

Armstrong D

3

1 reference

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22 October 2019

Antalffy B

4

1 reference

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22 October 2019

language of work or name

English

0 references

publication date

1 May 1995

1 reference

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22 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647801%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

volume

10

1 reference

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22 October 2019

issue

1

1 reference

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22 October 2019

page(s)

94-98

1 reference

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

22 October 2019

cites work

1 reference

7 January 2021

Identification and characterization of the gene causing type 1 spinocerebellar ataxia

1 reference

7 January 2021

Dynamic mutations hit double figures

1 reference

7 January 2021

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

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

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

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado-Joseph disease

1 reference

7 January 2021

Complete deletion of the androgen receptor gene: definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier status

1 reference

7 January 2021

The 56/58 kDa androgen-binding protein in male genital skin fibroblasts with a deleted androgen receptor gene.

1 reference

7 January 2021

Deletion of Huntington's disease-linked G8 (D4S10) locus in Wolf-Hirschhorn syndrome.

1 reference

7 January 2021

Homozygotes for Huntington's disease

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Characterization and localization of the Huntington disease gene product

1 reference

7 January 2021

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

1 reference

7 January 2021

Analysis of Sp1 in vivo reveals multiple transcriptional domains, including a novel glutamine-rich activation motif

1 reference

7 January 2021

Different activation domains of Sp1 govern formation of multimers and mediate transcriptional synergism

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1 reference

7 January 2021

Antigen unmasking on formalin-fixed, paraffin-embedded tissue sections

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG0595-94

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647801%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

22 October 2019

1029169187

0 references

1 reference

Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017