Molecular investigation of TBP allele length: a SCA17 cellular model and population study (Q40646395)

22 September 2017

title

Molecular investigation of TBP allele length: a SCA17 cellular model and population study (English)

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spinocerebellar ataxia type 17

22 September 2017

main subject

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1

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2

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5

Marcy E MacDonald

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6

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8

Richard L M Faull

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11

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22 September 2017

author name string

Willeke M C van Roon-Mom

3

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22 September 2017

A Lesley Jones

4

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22 September 2017

Matthew J During

7

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22 September 2017

Michael J Owen

9

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22 September 2017

Mike Dragunow

10

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22 September 2017

publication date

1 June 2003

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22 September 2017

number of pages

9

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inferred from page(s)

published in

Neurobiology of Disease

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22 September 2017

volume

13

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22 September 2017

issue

1

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22 September 2017

page(s)

37-45

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Biochemistry and structural biology of transcription factor IID (TFIID)

22 September 2017

cites work

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CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia

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Evolution of sequence repetition and gene duplications in the TATA-binding protein TBP (TFIID).

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Amyloid formation by mutant huntingtin: threshold, progressivity and recruitment of normal polyglutamine proteins

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

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

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Prolonged survival and decreased abnormal movements in transgenic model of Huntington disease, with administration of the transglutaminase inhibitor cystamine

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

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Polyglutamine protein aggregates are dynamic

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

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A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease?

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

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7 January 2021

Length of huntingtin and its polyglutamine tract influences localization and frequency of intracellular aggregates

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7 January 2021

CREB-binding protein sequestration by expanded polyglutamine

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7 January 2021

SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein

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7 January 2021

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

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7 January 2021

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

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Recruitment and the role of nuclear localization in polyglutamine-mediated aggregation

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Glutamine repeats as polar zippers: their possible role in inherited neurodegenerative diseases

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7 January 2021

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

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7 January 2021

Autosome search for schizophrenia susceptibility genes in multiply affected families

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7 January 2021

When more is less: pathogenesis of glutamine repeat neurodegenerative diseases

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7 January 2021

Analysis of polyglutamine-coding repeats in the TATA-binding protein in different human populations and in patients with schizophrenia and bipolar affective disorder

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7 January 2021

Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vitro and in vivo

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7 January 2021

Basal components of the transcription apparatus (RNA polymerase II, TATA-binding protein) contain activation domains: is the repetitive C-terminal domain (CTD) of RNA polymerase II a "portable enhancer domain"?

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Insoluble TATA-binding protein accumulation in Huntington's disease cortex.

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7 January 2021

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

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7 January 2021

Different types of repeat expansion in the TATA-binding protein gene are associated with a new form of inherited ataxia

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7 January 2021

10.1016/S0969-9961(03)00014-7

Identifiers

DOI

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22 September 2017

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