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Early activation of microglia and astrocytes in mouse models of spinocerebellar ataxia type 1.
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4344857
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25595967%20AND%20SRC:MED&resulttype=core&format=json
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28 February 2020
title
Early activation of microglia and astrocytes in mouse models of spinocerebellar ataxia type 1
(English)
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4344857
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25595967%20AND%20SRC:MED&resulttype=core&format=json
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28 February 2020
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microglia
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astrocyte
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spinocerebellar ataxia
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Harry T. Orr
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3
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Europe PubMed Central
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4344857
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28 February 2020
author name string
M Cvetanovic
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1
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4344857
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25595967%20AND%20SRC:MED&resulttype=core&format=json
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28 February 2020
M Ingram
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2
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4344857
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25595967%20AND%20SRC:MED&resulttype=core&format=json
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28 February 2020
P Opal
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4
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4344857
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28 February 2020
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English
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14 January 2015
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4344857
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28 February 2020
published in
Neuroscience
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Europe PubMed Central
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4344857
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25595967%20AND%20SRC:MED&resulttype=core&format=json
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28 February 2020
volume
289
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4344857
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28 February 2020
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289-299
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4344857
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25595967%20AND%20SRC:MED&resulttype=core&format=json
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28 February 2020
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11 June 2022
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Spinocerebellar ataxia type 7 cerebellar disease requires the coordinated action of mutant ataxin-7 in neurons and glia, and displays non-cell-autonomous bergmann glia degeneration.
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Vascular endothelial growth factor ameliorates the ataxic phenotype in a mouse model of spinocerebellar ataxia type 1.
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Suppression of the novel ER protein Maxer by mutant ataxin-1 in Bergman glia contributes to non-cell-autonomous toxicity
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Neurochemical alterations in spinocerebellar ataxia type 1 and their correlations with clinical status.
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Mutant huntingtin in glial cells exacerbates neurological symptoms of Huntington disease mice
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The role of LANP and ataxin 1 in E4F-mediated transcriptional repression
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Trinucleotide Repeat Disorders
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Expression of mutant huntingtin in glial cells contributes to neuronal excitotoxicity
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Neurologic disease induced in transgenic mice by cerebral overexpression of interleukin 6
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27 September 2018
Clinical features, neurogenetics and neuropathology of the polyglutamine spinocerebellar ataxias type 1, 2, 3, 6 and 7.
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27 September 2018
SCA1-like disease in mice expressing wild-type ataxin-1 with a serine to aspartic acid replacement at residue 776.
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344857
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27 September 2018
Reactive astrocytosis and glial glutamate transporter clustering are early changes in a spinocerebellar ataxia type 1 transgenic mouse model
1 reference
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PubMed Central
reference URL
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27 September 2018
Bergmann glia expression of polyglutamine-expanded ataxin-7 produces neurodegeneration by impairing glutamate transport.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344857
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27 September 2018
Serine 776 of ataxin-1 is critical for polyglutamine-induced disease in SCA1 transgenic mice
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344857
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27 September 2018
A long CAG repeat in the mouse Sca1 locus replicates SCA1 features and reveals the impact of protein solubility on selective neurodegeneration.
1 reference
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reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344857
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27 September 2018
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
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344857
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27 September 2018
SCA1 transgenic mice: A model for neurodegeneration caused by an expanded CAG trinucleotide repeat
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/25595967
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Dynamic transformation of Bergmann glial fibers proceeds in correlation with dendritic outgrowth and synapse formation of cerebellar Purkinje cells
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/25595967
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Clinical, neuropathologic, and genetic studies of a large spinocerebellar ataxia type 1 (SCA1) kindred
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/25595967
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A family with hereditary ataxia: HLA typing
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/25595967
retrieved
12 December 2020
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inferred from PubMed ID database lookup
Identifiers
DOI
10.1016/J.NEUROSCIENCE.2015.01.003
1 reference
stated in
Europe PubMed Central
PMCID
4344857
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25595967%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 February 2020
PMCID
4344857
1 reference
stated in
Europe PubMed Central
PMCID
4344857
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25595967%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 February 2020
PubMed ID
25595967
1 reference
stated in
Europe PubMed Central
PMCID
4344857
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25595967%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 February 2020
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