(Q41025202)

25 September 2017

1 reference

title

Clinical implications of unstable DNA repeat sequences (English)

1 reference

25 September 2017

Lindblad K

1

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25 September 2017

Schalling M

series ordinal

2

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25 September 2017

language of work or name

English

0 references

publication date

1 March 1996

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25 September 2017

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25 September 2017

volume

85

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25 September 2017

issue

3

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25 September 2017

page(s)

265-271

1 reference

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

25 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Fragile X genotype characterized by an unstable region of DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Cloning of the essential myotonic dystrophy region and mapping of the putative defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Human genes containing polymorphic trinucleotide repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Prevalence of the fragile-X syndrome in mentally retarded boys in a Swedish county.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Further segregation analysis of the fragile X syndrome with special reference to transmitting males

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

DNA methylation represses FMR-1 transcription in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Translational suppression by trinucleotide repeat expansion at FMR1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

A point mutation in the FMR-1 gene associated with fragile X mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Chromosomal fragile sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Foci of trinucleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeat

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

DNA analysis in hereditary dentatorubral-pallidoluysian atrophy: correlation between CAG repeat length and phenotypic variation and the molecular basis of anticipation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Abnormal gene product identified in hereditary dentatorubral–pallidoluysian atrophy (DRPLA) brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Confidence intervals for predicted age of onset, given the size of (CAG)n repeat, in Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Direct detection of novel expanded trinucleotide repeats in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

CAG repeat expansions and schizophrenia: association with disease in females and with early age-at-onset.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Genetic anticipation in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

Expanded CAG repeats in schizophrenia and bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1996.TB14011.X

10.1111/J.1651-2227.1996.TB14011.X

21 January 2018

Identifiers

DOI

1 reference

25 September 2017

1 reference