(Q33890266)

29 July 2017

title

Nuclear accumulation of truncated atrophin-1 fragments in a transgenic mouse model of DRPLA. (English)

1 reference

29 July 2017

Schilling G

1

1 reference

29 July 2017

Wood JD

2

1 reference

29 July 2017

Duan K

3

1 reference

29 July 2017

Slunt HH

4

1 reference

29 July 2017

Gonzales V

5

1 reference

29 July 2017

Yamada M

6

1 reference

29 July 2017

Cooper JK

7

1 reference

29 July 2017

Margolis RL

8

1 reference

29 July 2017

Jenkins NA

9

1 reference

29 July 2017

Copeland NG

10

1 reference

29 July 2017

Takahashi H

11

1 reference

29 July 2017

Tsuji S

12

1 reference

29 July 2017

Price DL

13

1 reference

29 July 2017

Borchelt DR

14

1 reference

29 July 2017

Ross CA

15

1 reference

29 July 2017

language of work or name

English

0 references

publication date

1 September 1999

1 reference

29 July 2017

1 reference

29 July 2017

volume

24

1 reference

29 July 2017

issue

1

1 reference

29 July 2017

page(s)

275-286

1 reference

Identification and characterization of the gene causing type 1 spinocerebellar ataxia

29 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Dentatorubral and pallidoluysian atrophy (DRPLA). Clinical and neuropathological findings in genetically confirmed North American and European pedigrees

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

A vector for expressing foreign genes in the brains and hearts of transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Evidence for proteasome involvement in polyglutamine disease: localization to nuclear inclusions in SCA3/MJD and suppression of polyglutamine aggregation in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

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%2FS0896-6273%2800%2980839-9

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%2FS0896-6273%2800%2980839-9

7 January 2021

Are neuronal intranuclear inclusions the common neuropathology of triplet-repeat disorders with polyglutamine-repeat expansions?

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Kennedy's disease: caspase cleavage of the androgen receptor is a crucial event in cytotoxicity

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Cleavage of atrophin-1 at caspase site aspartic acid 109 modulates cytotoxicity

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Trinucleotide instability: a repeating theme in human inherited disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Nuclear and neuropil aggregates in Huntington's disease: relationship to neuropathology.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Hereditary dentatorubral-pallidoluysian atrophy: detection of widespread ubiquitinated neuronal and glial intranuclear inclusions in the brain

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

A YAC mouse model for Huntington's disease with full-length mutant huntingtin, cytoplasmic toxicity, and selective striatal neurodegeneration.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

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%2FS0896-6273%2800%2980839-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Dentato-rubro-pallido-luysian atrophy: a clinico-pathological study

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in vivo

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Dentatorubral-pallidoluysian atrophy: clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Transglutaminase action imitates Huntington's disease: selective polymerization of Huntingtin containing expanded polyglutamine.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

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%2FS0896-6273%2800%2980839-9

7 January 2021

Expression and distribution of the dentatorubral-pallidoluysian atrophy gene product (atrophin-1/drplap) in neuronal and non-neuronal tissues.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

DNA analysis in hereditary dentatorubral-pallidoluysian atrophy: correlation between CAG repeat length and phenotypic variation and the molecular basis of anticipation

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Novel triplet repeat containing genes in human brain: cloning, expression, and length polymorphisms

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

DRPLA gene (atrophin-1) sequence and mRNA expression in human brain

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

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%2FS0896-6273%2800%2980839-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Dentatorubral pallidoluysian atrophy (DRPLA) protein is cleaved by caspase-3 during apoptosis

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Intracellular aggregate formation of dentatorubral-pallidoluysian atrophy (DRPLA) protein with the extended polyglutamine

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA)

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Trinucleotide repeats in neurogenetic disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Behavioural abnormalities and selective neuronal loss in HD transgenic mice expressing mutated full-length HD cDNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Intranuclear neuronal inclusions: a common pathogenic mechanism for glutamine-repeat neurodegenerative diseases?

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Huntington's disease and dentatorubral-pallidoluysian atrophy: proteins, pathogenesis and pathology

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Huntington disease and the related disorder, dentatorubral-pallidoluysian atrophy (DRPLA).

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Caspase-8 is required for cell death induced by expanded polyglutamine repeats.

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

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%2FS0896-6273%2800%2980839-9

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%2FS0896-6273%2800%2980839-9

7 January 2021

Intranuclear inclusions and neuritic aggregates in transgenic mice expressing a mutant N-terminal fragment of huntingtin

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Unusual form of cerebellar ataxia; combined dentato-rubral and pallido-Luysian degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Polyglutamine-expanded androgen receptors form aggregates that sequester heat shock proteins, proteasome components and SRC-1, and are suppressed by the HDJ-2 chaperone

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Ataxin-3 is transported into the nucleus and associates with the nuclear matrix

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Hereditary dentatorubral-pallidoluysian atrophy: Clinical and pathologic variants in a family

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Caspase cleavage of gene products associated with triplet expansion disorders generates truncated fragments containing the polyglutamine tract

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

Atrophin-1, the DRPLA gene product, interacts with two families of WW domain-containing proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980839-9

7 January 2021

10.1016/S0896-6273(00)80839-9

Identifiers

DOI

1 reference

29 July 2017

1 reference