(Q34405231)

2 August 2017

title

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

1 reference

spinocerebellar ataxia type 2

2 August 2017

main subject

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Sanpei K

1

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2 August 2017

Takano H

2

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2 August 2017

Igarashi S

3

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2 August 2017

Sato T

4

1 reference

2 August 2017

Oyake M

5

1 reference

2 August 2017

Sasaki H

6

1 reference

2 August 2017

Wakisaka A

7

1 reference

2 August 2017

Tashiro K

8

1 reference

2 August 2017

Ishida Y

9

1 reference

2 August 2017

Ikeuchi T

10

1 reference

2 August 2017

Koide R

11

1 reference

2 August 2017

Saito M

12

1 reference

2 August 2017

Sato A

13

1 reference

2 August 2017

Tanaka T

14

1 reference

2 August 2017

Hanyu S

15

1 reference

2 August 2017

Takiyama Y

16

1 reference

2 August 2017

Nishizawa M

17

1 reference

2 August 2017

Shimizu N

18

1 reference

2 August 2017

Nomura Y

19

1 reference

2 August 2017

Segawa M

20

1 reference

2 August 2017

Iwabuchi K

21

1 reference

2 August 2017

Eguchi I

22

1 reference

2 August 2017

Tanaka H

23

1 reference

2 August 2017

Takahashi H

24

1 reference

2 August 2017

Tsuji S

25

1 reference

2 August 2017

language of work or name

English

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publication date

1 November 1996

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2 August 2017

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2 August 2017

volume

14

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2 August 2017

issue

3

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2 August 2017

page(s)

277-284

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

2 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

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/10.1038%2FNG1196-277

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

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/10.1038%2FNG1196-277

The C. elegans cell death gene ced-3 encodes a protein similar to mammalian interleukin-1 beta-converting enzyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

Identification and inhibition of the ICE/CED-3 protease necessary for mammalian apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

Cleavage of huntingtin by apopain, a proapoptotic cysteine protease, is modulated by the polyglutamine tract

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

Mammalian subtilisins: the long-sought dibasic processing endoproteases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

Expansion and deletion of CTG repeats from human disease genes are determined by the direction of replication in E. coli

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

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/10.1038%2FNG1196-277

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

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%2FNG1196-277

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%2FNG1196-277

7 January 2021

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

7 January 2021

Anticipation in spinocerebellar ataxia type 2

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

7 January 2021

Autosomal dominant cerebellar ataxia with retinal degeneration: clinical, neuropathologic, and genetic analysis of a large kindred

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

7 January 2021

Direct detection of expanded (CAG/CTG) repeats in the myotonin-protein kinase genes of myotonic dystrophy patients using a high-stringency hybridization method

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

7 January 2021

Genetic heterogeneity of dominantly inherited olivopontocerebellar atrophy (OPCA) in the Japanese: linkage study of two pedigrees and evidence for the disease locus on chromosome 12q (SCA2)

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

7 January 2021

Radiation hybrid mapping: a somatic cell genetic method for constructing high-resolution maps of mammalian chromosomes

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

7 January 2021

An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

7 January 2021

Direct detection of novel expanded trinucleotide repeats in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

7 January 2021

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

7 January 2021

Genetic heterogeneity in type 1 Gaucher disease: multiple genotypes in Ashkenazic and non-Ashkenazic individuals

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

7 January 2021

Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

7 January 2021

Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

7 January 2021

DNA sequencing with chain-terminating inhibitors

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

7 January 2021

Supercoil sequencing: a fast and simple method for sequencing plasmid DNA

1 reference

https://api.crossref.org/works/10.1038%2FNG1196-277

7 January 2021

Identifiers

DOI

10.1038/NG1196-277

1 reference

Dimensions Publication ID

2 August 2017

1042064811

0 references

1 reference