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English
Trinucleotide diseases on the rise
scientific article published on 01 August 1994
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7951310
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7951310%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
title
Trinucleotide diseases on the rise
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7951310
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7951310%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
author name string
Mandel JL
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7951310
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7951310%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
publication date
1 August 1994
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7951310
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7951310%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7951310
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7951310%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
volume
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7951310
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7951310%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7951310
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7951310%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
page(s)
453-455
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7951310
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7951310%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ng0894-453
0 references
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Questions of expansion
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
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Trinucleotide repeat instability: when and where?
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
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Simple repeat DNA is not replicated simply
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Trinucleotide repeat expansions and human genetic disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Studying human mutations by sperm typing: instability of CAG trinucleotide repeats in the human androgen receptor gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence of founder chromosomes in fragile X syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
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%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expansion of unstable DNA region in Japanese myotonic dystrophy patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fragile X founder effect?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Striking founder effect for the fragile X syndrome in Finland.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Origin of the expansion mutation in myotonic dystrophy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Absence of myotonic dystrophy in southern African Negroids is associated with a significantly lower number of CTG trinucleotide repeats
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
De novo expansion of a (CAG)n repeat in sporadic Huntington's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Triplet repeat genes raise questions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Huntington's disease candidate region exhibits many different haplotypes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Meiotic drive at the myotonic dystrophy locus?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gametic but not somatic instability of CAG repeat length in Huntington's disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0894-453
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0894-453
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7951310
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7951310%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
PubMed publication ID
7951310
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7951310
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7951310%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
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