Formation of polyglutamine inclusions in non-CNS tissue (Q45298039)

11 December 2017

Formation of polyglutamine inclusions in non-CNS tissue (English)

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11 December 2017

7

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11 December 2017

4

L Mangiarini

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11 December 2017

K Sathasivam

1

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11 December 2017

C Hobbs

2

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11 December 2017

M Turmaine

3

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11 December 2017

A Mahal

5

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11 December 2017

F Bertaux

6

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11 December 2017

P Doherty

8

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11 December 2017

S W Davies

9

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11 December 2017

G P Bates

10

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11 December 2017

1 May 1999

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11 December 2017

Human Molecular Genetics

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11 December 2017

8

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11 December 2017

5

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11 December 2017

813-822

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Transgenic mice in the study of polyglutamine repeat expansion diseases.

11 December 2017

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https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

Striking changes in anxiety in Huntington's disease transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

Neuronal distribution of intranuclear inclusions in Huntington's disease with adult onset.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

Aggregation of N-terminal huntingtin is dependent on the length of its glutamine repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

Truncated N-terminal fragments of huntingtin with expanded glutamine repeats form nuclear and cytoplasmic aggregates in cell culture.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

A cellular model that recapitulates major pathogenic steps of Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

Subcellular localization of the Huntington's disease gene product in cell lines by immunofluorescence and biochemical subcellular fractionation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

Altered brain neurotransmitter receptors in transgenic mice expressing a portion of an abnormal human huntington disease gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

Sporadic inclusion-body myositis and its similarities to Alzheimer disease brain. Recent approaches to diagnosis and pathogenesis, and relation to aging.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

Transgenic mice over-expressing the C-99 fragment of betaPP with an alpha-secretase site mutation develop a myopathy similar to human inclusion body myositis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

Amyloid-beta deposition in skeletal muscle of transgenic mice: possible model of inclusion body myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

Mice transgenic for an expanded CAG repeat in the Huntington's disease gene develop diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

Missense mutation of amylin gene (S20G) in Japanese NIDDM patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

Nonneural nuclear inclusions of androgen receptor protein in spinal and bulbar muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.813

21 January 2018

Identifiers

DOI

10.1093/HMG/8.5.813

1 reference

11 December 2017

1 reference