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Items: 3

1.

Opposite phenotypic effects and genetic dosage in mouse models of 16p11.2 deletion and duplication syndromes

(Submitter supplied) The 16p11.2 deletion and duplication syndromes have been associated with developmental delay and autism spectrum disorders, and a reciprocal effect on body mass index. Here we explored these links with new engineered mouse models carrying a deletion (Del/+) and duplication (Dup/+) of the whole 16p11.2 homologous Sult1a1-Spn region. On a pure genetic background, compared to wild-types, Del/+ mice carrying the deletion showed weight and adipogenesis deficits, hyperactivity, repetitive behaviors, and recognition memory deficits, whereas Dup/+ mice showed the opposite phenotypes and Del/Dup individuals displayed no changes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17400
56 Samples
Download data: CEL
Series
Accession:
GSE66468
ID:
200066468
2.

[MoGene-2_1-st] Affymetrix Mouse Gene 2.1 ST Array [transcript (gene) version]

(Submitter supplied) Affymetrix submissions are typically submitted to GEO using the GEOarchive method described at http://www.ncbi.nlm.nih.gov/projects/geo/info/geo_affy.html MoGene-2_1-st-v1.na33.2.mm10.transcript.csv #%create_date=Thu Mar 28 17:33:46 2013 PDT #%chip_type=MoGene-2_1-st-v1 #%lib_set_name=MoGene-2_1-st #%lib_set_version=v1 #%genome-species=Mus musculus #%genome-version=mm10 #%genome-version-ucsc=mm10 #%genome-version-ncbi=38 #%genome-version-create_date=2011-12-00 #%genome-lifted-method=liftOver #%genome-lifted_from-species=Mus musculus #%genome-lifted_from-version-ucsc=mm10 #%genome-lifted_from-version-ncbi=38 #%netaffx-annotation-date=2012-09-30 #%netaffx-annotation-netaffx-build=33 Protocol: see manufacturer's web site
Organism:
Mus musculus
214 Series
6 Related Platforms
3551 Samples
Download data
Platform
Accession:
GPL17400
ID:
100017400
3.

Liver wildtype, A888_54_L49

Organism:
Mus musculus
Source name:
Liver, wildtype
Platform:
GPL17400
Series:
GSE66468
Download data: CEL
Sample
Accession:
GSM1623051
ID:
301623051
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