(Q28594907)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12039035%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

title

Cloning and expression analysis of the murine homolog of the spinocerebellar ataxia type 7 (SCA7) gene (English)

2 references

1 February 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12039035%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

0 references

1 reference

GOA release 2020-03-11

spinocerebellar ataxia type 7

1 reference

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12039035%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

author name string

Anna Lena Ström

1

2 references

1 February 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12039035%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Jenni Jonasson

2

2 references

1 February 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12039035%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Thomas Brännström

4

2 references

1 February 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12039035%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Lars Forsgren

5

2 references

1 February 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12039035%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Monica Holmberg

6

2 references

1 February 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12039035%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

language of work or name

English

0 references

publication date

1 February 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12039035%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

2 references

1 February 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12039035%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

volume

285

2 references

1 February 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12039035%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

page(s)

91-99

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12039035%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

issue

1-2

2 references

1 February 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12039035%20AND%20SRC:MED&resulttype=core&format=json

Cloning and developmental expression analysis of the murine homolog of the spinocerebellar ataxia type 1 gene (Sca1).

9 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

Distribution of ataxin-7 in normal human brain and retina

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

1 reference

7 January 2021

Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

Ataxin-7 expression analysis in controls and spinocerebellar ataxia type 7 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

Molecular and clinical study of 18 families with ADCA type II: evidence for genetic heterogeneity and de novo mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

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/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

Expanded CAG repeats in Swedish spinocerebellar ataxia type 7 (SCA7) patients: effect of CAG repeat length on the clinical manifestation

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

Nuclear localization of the spinocerebellar ataxia type 7 protein, ataxin-7

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

Ataxin-7 interacts with a Cbl-associated protein that it recruits into neuronal intranuclear inclusions

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

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/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

Expression analysis of ataxin-7 mRNA and protein in human brain: evidence for a widespread distribution and focal protein accumulation

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

On an autosomal dominant form of retinal-cerebellar degeneration: an autopsy study of five patients in one family

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

Identification and localization of ataxin-7 in brain and retina of a patient with cerebellar ataxia type II using anti-peptide antibody.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

Conserved Phosphoprotein Interaction Motif Is Functionally Interchangeable between Ataxin-7 and Arrestins†

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

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/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

The mouse SCA2 gene: cDNA sequence, alternative splicing and protein expression

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

Identification of a ten-amino acid proline-rich SH3 binding site

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900399-2

7 January 2021

10.1016/S0378-1119(02)00399-2

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12039035%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

2 references

1 February 2017