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Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes.
scientific article published in July 2004
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15188443
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15188443%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
title
Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15188443
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15188443%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
main subject
Down syndrome
1 reference
based on heuristic
inferred from title
author
Lisa E Olson
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15188443
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15188443%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
Randall J. Roper
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15188443
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15188443%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
Laura L Baxter
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15188443
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15188443%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
author name string
Carlson EJ
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15188443
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15188443%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
Epstein CJ
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15188443
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15188443%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
Reeves RH
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15188443
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15188443%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
publication date
1 July 2004
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15188443
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15188443%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
published in
Developmental Dynamics
1 reference
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Europe PubMed Central
PubMed publication ID
15188443
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15188443%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
volume
230
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15188443
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15188443%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15188443
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15188443%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
page(s)
581-589
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15188443
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15188443%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
cites work
Cerebellar volume in adults with Down syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.20079
retrieved
21 January 2018
Anomalous brain morphology on magnetic resonance images in Williams syndrome and Down syndrome.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.20079
retrieved
21 January 2018
Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouse.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.20079
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Failed retrograde transport of NGF in a mouse model of Down's syndrome: reversal of cholinergic neurodegenerative phenotypes following NGF infusion
1 reference
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Crossref
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7 January 2021
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An improved method for preparing G-banded chromosomes from mouse peripheral blood
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7 January 2021
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Molecular mapping of twenty-four features of Down syndrome on chromosome 21.
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7 January 2021
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Cerebellar granule cell neurogenesis is regulated by cell-cell interactions in vitro.
1 reference
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Crossref
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7 January 2021
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Mouse models of Down syndrome: how useful can they be? Comparison of the gene content of human chromosome 21 with orthologous mouse genomic regions
1 reference
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Crossref
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https://api.crossref.org/works/10.1002%2FDVDY.20079
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7 January 2021
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A gene expression map of human chromosome 21 orthologues in the mouse
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Crossref
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7 January 2021
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inferred from DOI database lookup
The DNA sequence of human chromosome 21
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.20079
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7 January 2021
based on heuristic
inferred from DOI database lookup
Motor learning in Ts65Dn mice, a model for Down syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.20079
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The cerebellum and event timing
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.20079
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Down syndrome phenotypes: the consequences of chromosomal imbalance
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.20079
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel mutations in an otherwise strictly conserved domain of CuZn superoxide dismutase
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.20079
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7 January 2021
based on heuristic
inferred from DOI database lookup
A comparison of whole-genome shotgun-derived mouse chromosome 16 and the human genome.
1 reference
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Crossref
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https://api.crossref.org/works/10.1002%2FDVDY.20079
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7 January 2021
based on heuristic
inferred from DOI database lookup
Use of comparative physical and sequence mapping to annotate mouse chromosome 16 and human chromosome 21
1 reference
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Crossref
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https://api.crossref.org/works/10.1002%2FDVDY.20079
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7 January 2021
based on heuristic
inferred from DOI database lookup
Selective neuroanatomic abnormalities in Down's syndrome and their cognitive correlates: evidence from MRI morphometry.
1 reference
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Crossref
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https://api.crossref.org/works/10.1002%2FDVDY.20079
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7 January 2021
based on heuristic
inferred from DOI database lookup
A mouse model for Down syndrome exhibits learning and behaviour deficits.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.20079
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Too much of a good thing: mechanisms of gene action in Down syndrome.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.20079
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7 January 2021
based on heuristic
inferred from DOI database lookup
Nineteen additional unpredicted transcripts from human chromosome 21
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.20079
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7 January 2021
based on heuristic
inferred from DOI database lookup
Parallels of craniofacial maldevelopment in Down syndrome and Ts65Dn mice.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.20079
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.20079
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7 January 2021
based on heuristic
inferred from DOI database lookup
Stereotaxic display of brain lesions
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.20079
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ts1Cje, a partial trisomy 16 mouse model for Down syndrome, exhibits learning and behavioral abnormalities
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.20079
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic dissection of region associated with behavioral abnormalities in mouse models for Down syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.20079
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7 January 2021
based on heuristic
inferred from DOI database lookup
The pathogenesis of aneuploid phenotypes: the fallacy of explanatory reductionism
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.20079
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Whither Down syndrome critical regions?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.20079
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional screening of 2 Mb of human chromosome 21q22.2 in transgenic mice implicates minibrain in learning defects associated with Down syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FDVDY.20079
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1002/DVDY.20079
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15188443
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15188443%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
PubMed publication ID
15188443
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15188443
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15188443%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
ResearchGate publication ID
8519538
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