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Human embryonic stem cell models of Huntington disease.
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1 reference
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Europe PubMed Central
PubMed publication ID
19573298
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19573298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
title
Human embryonic stem cell models of Huntington disease
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19573298
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19573298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
main subject
Huntington's disease
0 references
human embryonic stem cell
1 reference
based on heuristic
inferred from title
author
Jonathan C Niclis
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19573298
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19573298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
Alan Trounson
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19573298
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19573298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
Mirella Dottori
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3
1 reference
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Europe PubMed Central
PubMed publication ID
19573298
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19573298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
Andrew M Ellisdon
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4
1 reference
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Europe PubMed Central
PubMed publication ID
19573298
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19573298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
Yury Verlinsky
series ordinal
6
object named as
Y Verlinsky
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19573298
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19573298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
Stephen P Bottomley
series ordinal
5
object named as
Stephen P Bottomley
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19573298
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19573298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
author name string
David S Cram
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19573298
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19573298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
publication date
1 July 2009
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19573298
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19573298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
published in
Reproductive BioMedicine Online
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19573298
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19573298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
volume
19
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19573298
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19573298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19573298
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19573298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
page(s)
106-113
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19573298
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19573298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
cites work
Intranuclear neuronal inclusions in Huntington's disease and dentatorubral and pallidoluysian atrophy: correlation between the density of inclusions and IT15 CAG triplet repeat length
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Decreased association of the transcription factor Sp1 with genes downregulated in Huntington's disease
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Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation
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7 January 2021
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Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain
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7 January 2021
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Recurrent gain of chromosomes 17q and 12 in cultured human embryonic stem cells
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7 January 2021
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Sp1 and TAFII130 transcriptional activity disrupted in early Huntington's disease
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7 January 2021
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Proliferative and degenerative changes in striatal spiny neurons in Huntington's disease: a combined study using the section-Golgi method and calbindin D28k immunocytochemistry
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Cleavage at the caspase-6 site is required for neuronal dysfunction and degeneration due to mutant huntingtin
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Crossref
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7 January 2021
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Nuclear and neuropil aggregates in Huntington's disease: relationship to neuropathology.
1 reference
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Crossref
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7 January 2021
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Amyloid formation by mutant huntingtin: threshold, progressivity and recruitment of normal polyglutamine proteins
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7 January 2021
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Dramatic tissue-specific mutation length increases are an early molecular event in Huntington disease pathogenesis
1 reference
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Crossref
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7 January 2021
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Single sperm analysis of the trinucleotide repeats in the Huntington's disease gene: quantification of the mutation frequency spectrum
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7 January 2021
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Proteases acting on mutant huntingtin generate cleaved products that differentially build up cytoplasmic and nuclear inclusions
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7 January 2021
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Derivation of human embryonic stem cell lines from embryos obtained after IVF and after PGD for monogenic disorders.
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Reduced penetrance of the Huntington's disease mutation
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Apoptotic cascades as possible targets for inhibiting cell death in Huntington's disease
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7 January 2021
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Regulation of human embryonic stem cell differentiation by BMP-2 and its antagonist noggin
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Analysis of cell-differentiation lineage in human teratomas using new monoclonal antibodies to cytostructural antigens of embryonal carcinoma cells.
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7 January 2021
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Generation of a human embryonic stem cell line encoding the cystic fibrosis mutation deltaF508, using preimplantation genetic diagnosis
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Neural progenitors from human embryonic stem cells.
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Embryonic stem cell lines from human blastocysts: somatic differentiation in vitro
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inferred from DOI database lookup
Formation of polyglutamine inclusions in non-CNS tissue
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1472-6483%2810%2960053-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vitro and in vivo
1 reference
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
Preimplantation diagnosis for Huntington's disease (HD): clinical application and analysis of the HD expansion in affected embryos.
1 reference
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of mutant huntingtin in glial cells contributes to neuronal excitotoxicity
1 reference
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Crossref
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7 January 2021
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inferred from DOI database lookup
Modeling Huntington's disease in cells, flies, and mice
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1472-6483%2810%2960053-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm.
1 reference
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parent.
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS1472-6483%2810%2960053-3
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7 January 2021
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inferred from DOI database lookup
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1472-6483%2810%2960053-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Striatal specificity of gene expression dysregulation in Huntington's disease
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1472-6483%2810%2960053-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Repository of human embryonic stem cell lines and development of individual specific lines using stembrid technology
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1472-6483%2810%2960053-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human embryonic stem cell lines with genetic disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1472-6483%2810%2960053-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuropathological classification of Huntington's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1472-6483%2810%2960053-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Caspase cleavage of mutant huntingtin precedes neurodegeneration in Huntington's disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1472-6483%2810%2960053-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Towards a transgenic model of Huntington's disease in a non-human primate
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1472-6483%2810%2960053-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Integrative genomic and functional analyses reveal neuronal subtype differentiation bias in human embryonic stem cell lines
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1472-6483%2810%2960053-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S1472-6483(10)60053-3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19573298
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19573298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
PubMed publication ID
19573298
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19573298
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19573298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 February 2020
ResearchGate publication ID
26336816
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