(Q58992775)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020848%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

title

Hypermutable myotonic dystrophy CTG repeats in transgenic mice (English)

1 reference

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31 October 2019

1 reference

1 reference

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31 October 2019

Coolbaugh MI

1 reference

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31 October 2019

Ashizawa KT

series ordinal

1 reference

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31 October 2019

Siciliano MJ

series ordinal

1 reference

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31 October 2019

Caskey CT

series ordinal

1 reference

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31 October 2019

language of work or name

English

0 references

publication date

1 February 1997

1 reference

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31 October 2019

1 reference

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31 October 2019

volume

1 reference

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31 October 2019

issue

1 reference

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31 October 2019

page(s)

193-196

1 reference

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Unstable triplet repeat diseases.

31 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

Somatic mosaicism, germline expansions, germline reversions and intergenerational reductions in myotonic dystrophy males: small pool PCR analyses

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

An unstable triplet repeat in a gene related to myotonic muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

7 January 2021

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

https://api.crossref.org/works/10.1038%2FNG0297-193

7 January 2021

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

7 January 2021

Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeat

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

7 January 2021

SCA1 transgenic mice: A model for neurodegeneration caused by an expanded CAG trinucleotide repeat

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

7 January 2021

Stability of an expanded trinucleotide repeat in the androgen receptor gene in transgenic mice

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

7 January 2021

Absence of disease phenotype and intergenerational stability of the CAG repeat in transgenic mice expressing the human Huntington disease transcript

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

7 January 2021

Molecular features of the CAG repeats and clinical manifestation of Machado--Joseph disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

7 January 2021

Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

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/10.1038%2FNG0297-193

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

7 January 2021

Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

7 January 2021

Prenatal lethality in a transgenic mouse line is the result of a chromosomal translocation

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

7 January 2021

Spontaneous mutation at the hypervariable mouse minisatellite locus Ms6-hm: flanking DNA sequence and analysis of germline and early somatic mutation events

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

7 January 2021

A tetranucleotide repeat mouse minisatellite displaying substantial somatic instability during early preimplantation development

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

7 January 2021

Variable germline and embryonic instability of the human minisatellite MS32 (D1S8) in transgenic mice.

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

7 January 2021

Instability of long inverted repeats within mouse transgenes

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

7 January 2021

Mitotic stability of fragile X mutations in differentiated cells indicates early post-conceptional trinucleotide repeat expansion.

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

7 January 2021

Repeat unit sequence variation in minisatellites: a novel source of DNA polymorphism for studying variation and mutation by single molecule analysis

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

7 January 2021

Structure, sequence, and chromosomal location of the gene for USF2 transcription factors in mouse

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-193

7 January 2021

Identifiers

DOI

10.1038/NG0297-193

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020848%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020848%20AND%20SRC:MED&resulttype=core&format=json