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English
C-terminal deletion of the atrophin-1 protein results in growth retardation but not neurodegeneration in mice
scientific journal article
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instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
19681162
retrieved
31 January 2017
title
C-terminal deletion of the atrophin-1 protein results in growth retardation but not neurodegeneration in mice
(English)
1 reference
stated in
PubMed
PubMed ID
19681162
retrieved
31 January 2017
main subject
Atrophin 1
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stated in
GOA release 2020-03-11
neurodegeneration
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based on heuristic
inferred from title
author name string
Juehua Yu
series ordinal
1
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stated in
PubMed
PubMed ID
19681162
retrieved
31 January 2017
Mingyao Ying
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
19681162
retrieved
31 January 2017
Yuan Zhuang
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
19681162
retrieved
31 January 2017
Tian Xu
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
19681162
retrieved
31 January 2017
Min Han
series ordinal
5
1 reference
stated in
PubMed
PubMed ID
19681162
retrieved
31 January 2017
Xiaohui Wu
series ordinal
6
1 reference
stated in
PubMed
PubMed ID
19681162
retrieved
31 January 2017
Rener Xu
series ordinal
7
1 reference
stated in
PubMed
PubMed ID
19681162
retrieved
31 January 2017
publication date
1 October 2009
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stated in
PubMed
PubMed ID
19681162
retrieved
31 January 2017
published in
Developmental Dynamics
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stated in
PubMed
PubMed ID
19681162
retrieved
31 January 2017
volume
238
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stated in
PubMed
PubMed ID
19681162
retrieved
31 January 2017
issue
10
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stated in
PubMed
PubMed ID
19681162
retrieved
31 January 2017
page(s)
2471–2478
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stated in
PubMed
PubMed ID
19681162
retrieved
31 January 2017
cites work
Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
21 January 2018
Contribution of nuclear and extranuclear polyQ to neurological phenotypes in mouse models of Huntington's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of normal huntingtin function: new developments in Huntington's disease research
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
YAC transgenic mice carrying pathological alleles of the MJD1 locus exhibit a mild and slowly progressive cerebellar deficit.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Purkinje cell expression of a mutant allele of SCA1 in transgenic mice leads to disparate effects on motor behaviors, followed by a progressive cerebellar dysfunction and histological alterations.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inactivation of Hdh in the brain and testis results in progressive neurodegeneration and sterility in mice
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Flanking sequences profoundly alter polyglutamine toxicity in yeast
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretch.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
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7 January 2021
based on heuristic
inferred from DOI database lookup
Generation and characterization of Sca2 (ataxin-2) knockout mice
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA)
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nuclear localization of a non-caspase truncation product of atrophin-1, with an expanded polyglutamine repeat, increases cellular toxicity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dentatorubral-pallidoluysian atrophy protein interacts through a proline-rich region near polyglutamine with the SH3 domain of an insulin receptor tyrosine kinase substrate
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
When more is less: pathogenesis of glutamine repeat neurodegenerative diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pathogenesis of neurodegenerative diseases associated with expanded glutamine repeats: new answers, new questions.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transgenic mice harboring a full-length human mutant DRPLA gene exhibit age-dependent intergenerational and somatic instabilities of CAG repeats comparable with those in DRPLA patients.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nuclear accumulation of truncated atrophin-1 fragments in a transgenic mouse model of DRPLA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Distinct behavioral and neuropathological abnormalities in transgenic mouse models of HD and DRPLA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inactivation of the mouse Atxn3 (ataxin-3) gene increases protein ubiquitination
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional architecture of atrophins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Histone deacetylase-associating Atrophin proteins are nuclear receptor corepressors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Atrophin-1, the dentato-rubral and pallido-luysian atrophy gene product, interacts with ETO/MTG8 in the nuclear matrix and represses transcription
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Widespread occurrence of intranuclear atrophin-1 accumulation in the central nervous system neurons of patients with dentatorubral-pallidoluysian atrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Protein binding of a DRPLA family through arginine-glutamic acid dipeptide repeats is enhanced by extended polyglutamine
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormal gene product identified in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) brain
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of dentatorubral-pallidoluysian atrophy (DRPLA) proteins in patients.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sodium butyrate ameliorates histone hypoacetylation and neurodegenerative phenotypes in a mouse model for DRPLA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
SCA7 knockin mice model human SCA7 and reveal gradual accumulation of mutant ataxin-7 in neurons and abnormalities in short-term plasticity.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expanded polyglutamines induce neurodegeneration and trans-neuronal alterations in cerebellum and retina of SCA7 transgenic mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Drosophila atrophin homolog functions as a transcriptional corepressor in multiple developmental processes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Atrophin 2 recruits histone deacetylase and is required for the function of multiple signaling centers during mouse embryogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.22063
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1002/DVDY.22063
1 reference
stated in
PubMed
PubMed ID
19681162
retrieved
31 January 2017
PubMed ID
19681162
1 reference
stated in
PubMed
PubMed ID
19681162
retrieved
31 January 2017
ResearchGate publication ID
26742436
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