Nuclear inclusions in glutamine repeat disorders: are they pernicious, coincidental, or beneficial? (Q77430975)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9778239%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

title

Nuclear inclusions in glutamine repeat disorders: are they pernicious, coincidental, or beneficial? (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9778239%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

author name string

S S Sisodia

series ordinal

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9778239%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

language of work or name

English

0 references

publication date

1 October 1998

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9778239%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9778239%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

volume

95

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5 December 2019

issue

1

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5 December 2019

page(s)

1-4

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SCA1 transgenic mice: A model for neurodegeneration caused by an expanded CAG trinucleotide repeat

5 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981743-2

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%2FS0092-8674%2800%2981743-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981743-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981743-2

7 January 2021

Inactivation of the mouse Huntington's disease gene homolog Hdh

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981743-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981743-2

7 January 2021

Polyglutamine-expanded human huntingtin transgenes induce degeneration of Drosophila photoreceptor neurons.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981743-2

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%2FS0092-8674%2800%2981743-2

7 January 2021

A huntingtin-associated protein enriched in brain with implications for pathology

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981743-2

7 January 2021

Mad cows meet psi-chotic yeast: the expansion of the prion hypothesis

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981743-2

7 January 2021

The cerebellar leucine-rich acidic nuclear protein interacts with ataxin-1

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981743-2

7 January 2021

Mice lacking ataxin-1 display learning deficits and decreased hippocampal paired-pulse facilitation

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981743-2

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%2FS0092-8674%2800%2981743-2

7 January 2021

Trinucleotide repeats in neurogenetic disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981743-2

7 January 2021

Transport routes through the nuclear pore complex

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981743-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981743-2

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%2FS0092-8674%2800%2981743-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981743-2

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%2FS0092-8674%2800%2981743-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981743-2

7 January 2021

10.1016/S0092-8674(00)81743-2

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9778239%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

1 reference