Analysis of spinocerebellar ataxia type 2 in Gunma Prefecture in Japan: CAG trinucleotide expansion and clinical characteristics (Q43917868)

28 November 2017

title

Analysis of spinocerebellar ataxia type 2 in Gunma Prefecture in Japan: CAG trinucleotide expansion and clinical characteristics (English)

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spinocerebellar ataxia type 2

28 November 2017

main subject

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Mizushima K

1

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28 November 2017

Watanabe M

2

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28 November 2017

Abe K

3

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28 November 2017

Aoki M

4

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28 November 2017

Itoyama Y

5

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28 November 2017

Shizuka M

6

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28 November 2017

Okamoto K

7

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28 November 2017

Shoji M

8

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28 November 2017

publication date

1 April 1998

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Journal of the Neurological Sciences

28 November 2017

published in

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28 November 2017

volume

156

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28 November 2017

issue

2

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28 November 2017

page(s)

180-185

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Maternal anticipation of DRPLA

28 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

Reduction of CAG expansions in cerebellar cortex and spinal cord of DRPLA.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

Gametic and somatic tissue-specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

Has spinocerebellar ataxia type 2 a distinct phenotype? Genetic and clinical study of an Italian family.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

Analysis of spinocerebellar ataxia type 1 (SCA1)-related CAG trinucleotide expansion in Japan

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

Autosomal dominant cerebellar ataxia: clinical analysis of 263 patients from a homogeneous population in Holguín, Cuba

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

Central phenotype and related varieties of spinocerebellar ataxia 2 (SCA2): a clinical and genetic study with a pedigree in the Japanese

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

A clinical and pathologic study of a large Japanese family with Machado-Joseph disease tightly linked to the DNA markers on chromosome 14q

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

Spinocerebellar ataxia 1 (SCA1) in the Japanese in Hokkaido may derive from a single common ancestry

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

Analysis of CAG trinucleotide expansion associated with Machado-Joseph disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

Mitotic and meiotic stability of the CAG repeat in the X-linked spinal and bulbar muscular atrophy gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

A reproducible assay of polymerase chain reaction to detect trinucleotide repeat expansion of Huntington's disease and senile chorea

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900040-9

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0022-510X(98)00040-9

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28 November 2017

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