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English
Triplet repeats strike again
scientific article published on 01 January 1994
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8136830
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8136830%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
title
Triplet repeats strike again
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8136830
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8136830%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
author name string
Miwa S
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8136830
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8136830%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
publication date
1 January 1994
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8136830
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8136830%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8136830
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8136830%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
volume
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8136830
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8136830%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8136830
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8136830%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
page(s)
3-4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8136830
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8136830%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
cites work
Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary dentatorubral-pallidoluysian atrophy: Clinical and pathologic variants in a family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Trinucleotide repeat length instability and age of onset in Huntington's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Unusual form of cerebellar ataxia; combined dentato-rubral and pallido-Luysian degeneration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
'Haw River Syndrome' or Dentato-Rubro-Pallido-Luysian Atrophy?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ataxia, chorea, seizures, and dementia. Pathologic features of a newly defined familial disorder.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dentatorubro-pallidoluysian atrophy of the myoclonus epilepsy type with posterior column degeneration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The gene for Machado-Joseph disease maps to human chromosome 14q
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary spastic paraparesis. Clinical and genetic data from a large Dutch family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0194-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0194-3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8136830
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8136830%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
PubMed publication ID
8136830
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8136830
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8136830%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 October 2019
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