(Q40847656)

24 September 2017

title

DMSO and glycerol reduce bacterial death induced by expression of truncated N-terminal huntingtin with expanded polyglutamine tracts (English)

1 reference

24 September 2017

Y Nagao

1

1 reference

24 September 2017

H Ishiguro

series ordinal

2

1 reference

24 September 2017

N Nukina

series ordinal

3

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24 September 2017

publication date

1 October 2000

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Biochimica et Biophysica Acta

24 September 2017

published in

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24 September 2017

volume

1502

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24 September 2017

issue

2

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24 September 2017

page(s)

247-256

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

24 September 2017

cites work

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900047-8

7 January 2021

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

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900047-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900047-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900047-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900047-8

7 January 2021

Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900047-8

7 January 2021

Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation

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7 January 2021

Spinocerebellar ataxia type 1 with multiple system degeneration and glial cytoplasmic inclusions

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7 January 2021

Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3.

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7 January 2021

Nuclear inclusions of the androgen receptor protein in spinal and bulbar muscular atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900047-8

7 January 2021

Intranuclear neuronal inclusions in Huntington's disease and dentatorubral and pallidoluysian atrophy: correlation between the density of inclusions and IT15 CAG triplet repeat length

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900047-8

7 January 2021

Spinocerebellar ataxia type 7 (SCA7): a neurodegenerative disorder with neuronal intranuclear inclusions

1 reference

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7 January 2021

Ectopically expressed CAG repeats cause intranuclear inclusions and a progressive late onset neurological phenotype in the mouse.

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7 January 2021

Expanded polyglutamine protein forms nuclear inclusions and causes neural degeneration in Drosophila

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7 January 2021

Toxicity of expanded polyglutamine-domain proteins in Escherichia coli.

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7 January 2021

Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900047-8

7 January 2021

SH3GL3 associates with the Huntingtin exon 1 protein and promotes the formation of polygln-containing protein aggregates

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900047-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900047-8

7 January 2021

The influence of huntingtin protein size on nuclear localization and cellular toxicity.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900047-8

7 January 2021

Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretch.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900047-8

7 January 2021

A trace amount of the human pro-apoptotic factor Bax induces bacterial death accompanied by damage of DNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4439%2800%2900047-8

7 January 2021

10.1016/S0925-4439(00)00047-8

Identifiers

DOI

1 reference

24 September 2017

1 reference