Glutamine repeats and neurodegenerative diseases: molecular aspects (Q33546888)

27 July 2017

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title

Glutamine repeats and neurodegenerative diseases: molecular aspects (English)

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27 July 2017

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M F Perutz

1

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PubMed ID

10098399

27 July 2017

language of work or name

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1 February 1999

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27 July 2017

6

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Trends in Biochemical Sciences

inferred from page(s)

published in

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27 July 2017

24

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27 July 2017

58-63

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27 July 2017

2

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

27 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

Huntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansion

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

Partial characterisation of murine huntingtin and apparent variations in the subcellular localisation of huntingtin in human, mouse and rat brain.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

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%2FS0968-0004%2898%2901350-4

7 January 2021

SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel gene

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

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%2FS0968-0004%2898%2901350-4

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

Incorporation of glutamine repeats makes protein oligomerize: implications for neurodegenerative diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

Nuclear inclusions in oculopharyngeal dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

Transgenic models of Huntington's disease

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https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

Neural precursor cells: applications for the study and repair of the central nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

Huntingtin is ubiquitinated and interacts with a specific ubiquitin-conjugating enzyme

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https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

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%2FS0968-0004%2898%2901350-4

7 January 2021

Cleavage, aggregation and toxicity of the expanded androgen receptor in spinal and bulbar muscular atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

Characterization of an expanded glutamine repeat androgen receptor in a neuronal cell culture system

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

Identification of a self-association region within the SCA1 gene product, ataxin-1

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

Human genetic diseases due to codon reiteration: relationship to an evolutionary mechanism

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

Peptides containing glutamine repeats as substrates for transglutaminase-catalyzed cross-linking: relevance to diseases of the nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

Glutamine repeats and inherited neurodegenerative diseases: molecular aspects

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

The biostructural pathology of the serpins: critical function of sheet opening mechanism

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

Inhibiting transthyretin amyloid fibril formation via protein stabilization

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

alpha-Synuclein in filamentous inclusions of Lewy bodies from Parkinson's disease and dementia with lewy bodies

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0004%2898%2901350-4

7 January 2021

10.1016/S0968-0004(98)01350-4

Identifiers

DOI

1 reference

27 July 2017

1 reference

PubMed ID

10098399