(Q44320440)

1 December 2017

title

Histone H3 is aberrantly phosphorylated in glutamine-repeat diseases (English)

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1 December 2017

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Ikuru Yazawa

1

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1 December 2017

Noriko Hazeki

2

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1 December 2017

Hirofumi Nakase

3

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1 December 2017

Ichiro Kanazawa

4

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1 December 2017

Masumi Tanaka

5

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1 December 2017

language of work or name

English

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publication date

1 February 2003

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Biochemical and Biophysical Research Communications

1 December 2017

published in

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1 December 2017

volume

302

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1 December 2017

issue

1

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1 December 2017

page(s)

144-149

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

1 December 2017

cites work

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain

7 January 2021

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

7 January 2021

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Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structures

7 January 2021

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

7 January 2021

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

7 January 2021

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Ataxin-1 nuclear localization and aggregation: role in polyglutamine-induced disease in SCA1 transgenic mice

7 January 2021

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Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human

7 January 2021

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

7 January 2021

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Expanded glutamine repeat enhances complex formation of dentatorubral-pallidoluysian atrophy (DRPLA) protein in human brains

7 January 2021

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Different complex formations of dentatorubral-pallidoluysian atrophy (DRPLA) protein in human and rat neurons

7 January 2021

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Abnormal dentatorubral-pallidoluysian atrophy (DRPLA) protein complex is pathologically ubiquitinated in DRPLA brains

7 January 2021

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Unique characteristics of ubiquitin-bonded complex play a pathological role in dentatorubral-pallidoluysian atrophy

7 January 2021

1 reference

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Expression of dentatorubral-pallidoluysian atrophy (DRPLA) proteins in patients.

7 January 2021

1 reference

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Ultrastructure of nuclear aggregates formed by expressing an expanded polyglutamine

7 January 2021

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Signaling to chromatin through histone modifications

7 January 2021

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Interference by huntingtin and atrophin-1 with cbp-mediated transcription leading to cellular toxicity

7 January 2021

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Expanded polyglutamine stretches interact with TAFII130, interfering with CREB-dependent transcription

7 January 2021

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10.1016/S0006-291X(03)00115-3

7 January 2021

Identifiers

DOI

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1 December 2017

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