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English
Trinucleotide repeats and hereditary ataxias
scientific article published on 01 February 1997
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9018228
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9018228%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
title
Trinucleotide repeats and hereditary ataxias
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9018228
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9018228%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
author name string
T Klockgether
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9018228
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9018228%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
J Dichgans
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9018228
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9018228%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
publication date
1 February 1997
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9018228
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9018228%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
published in
Nature Medicine
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9018228
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9018228%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
volume
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9018228
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9018228%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9018228
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9018228%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
page(s)
149-150
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9018228
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9018228%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/nm0297-149
0 references
cites work
Trinucleotide repeat expansion in neurological disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNM0297-149
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNM0297-149
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNM0297-149
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNM0297-149
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNM0297-149
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNM0297-149
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Repeat length and disease progression in spinocerebellar ataxia type 3
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNM0297-149
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNM0297-149
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in vivo
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNM0297-149
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNM0297-149
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNM0297-149
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical and genetic abnormalities in patients with Friedreich's ataxia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNM0297-149
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Friedreich's ataxia gene encodes a novel phosphatidylinositol-4- phosphate 5-kinase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNM0297-149
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Late-onset Friedreich's ataxia. Molecular genetics, clinical neurophysiology, and magnetic resonance imaging.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNM0297-149
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NM0297-149
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9018228
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9018228%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
PubMed publication ID
9018228
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9018228
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9018228%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
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