(Q28138069)

2

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A Johannsmeyer

3

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K H Grzeschik

4

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E Schwinger

Random rapid amplification of cDNA ends (RRACE) allows for cloning of multiple novel human cDNA fragments containing (CAG)n repeats

5

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language of work or name

English

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publication date

1999

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published in

Mitochondrial DNA

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volume

10

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issue

1

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page(s)

1-6

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cites work

1 reference

https://api.crossref.org/works/10.3109%2F10425179909033929

Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F10425179909033929

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F10425179909033929

Characterization of four novel CAG repeat-containing cDNAs

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F10425179909033929

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F10425179909033929

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F10425179909033929

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F10425179909033929

Novel triplet repeat containing genes in human brain: cloning, expression, and length polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F10425179909033929

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/10.3109%2F10425179909033929

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F10425179909033929

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F10425179909033929

Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F10425179909033929

Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F10425179909033929

Human genes containing polymorphic trinucleotide repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F10425179909033929

Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F10425179909033929

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/10.3109%2F10425179909033929

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F10425179909033929