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TranscriptomicsTranscription profiling of fat biopsies from monozygotic twins discordant for body mass index to elucidate the effects of acquired obesity
Elucidating the effects of acquired obesity by comparison of fat biopsies from monozygotic twins discordant for BMI.
ORGANISM(S): Homo sapiens 
2008-02-15 | E-MEXP-1425 | biostudies-arrayexpress
TranscriptomicsTranscription profiling of human spinal cord from fetuses suffering from Lethal Congenital Contracture Syndrome LCCS vs control comparison
Collection of data from mRNA obtained from the spinal cord of three human fetuses suffering from Lethal Congenital Contracture Syndrome and two age-matched human fetuses aborted to unrelated causes.
ORGANISM(S): Homo sapiens 
2008-06-11 | E-GEOD-1481 | biostudies-arrayexpress
TranscriptomicsTranscription profiling of mouse thymic stromal cells from 6-12 week old wild type (C57BL/6) and Aire knock-outs (mixed background)
Gene expression in different thymic stromal cells and subsets thereof was analyzed in 6-12 week old wild type (C57BL/6) and Aire knock-out (mixed background) mice. Thymic stromal cells were purified by sequential enzymatic digestion (collagenase, collagenase/dispase and trypsin) followed by gradient...
ORGANISM(S): Mus musculus 
2007-12-15 | E-GEOD-2585 | biostudies-arrayexpress
TranscriptomicsDap12-deficient mouse brain (1 month)
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL) is an inherited brain and bone disease. It manifests as dementia and bone fractures. The PLOSL phenotype is caused by loss-of-function mutations in one of the two genes encoding the components of the DAP12/TREM2 rec...
ORGANISM(S): Mus musculus 
2011-08-23 | E-GEOD-9061 | biostudies-arrayexpress
TranscriptomicsDap12 microglia
Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL) is an inherited brain and bone disease. It manifests as dementia and bone fractures. The PLOSL phenotype is caused by loss-of-function mutations in one of the two genes encoding the components of the DAP12/TREM2 rec...
ORGANISM(S): Mus musculus 
2011-08-23 | E-GEOD-9043 | biostudies-arrayexpress
GenomicSTAMPEED: Northern Finland Birth Cohort 1966 (NFBC1966)

The Northern Finland Birth Cohorts program (NFBC) was initiated in the 1960s in the two northernmost provinces of Finland to study risk factors involved in pre-term birth and intrauterine growth retardation, and the consequences of these early adverse events on subsequent morbidity and mortality....

phs000276 | dbGaP
TranscriptomicsTranscription profiling of human Familial combined hyperlipidemia individuals exhibiting the USF1 susceptibility haplotype and FCHL affected indiviuals carrying the protective haplotype
Comparison of gene expression for individuals affected with FCHL exhibiting the USF1 susceptibility haplotype and FCHL affected indiviuals carrying the protective haplotype
ORGANISM(S): Homo sapiens 
2007-09-28 | E-GEOD-590 | biostudies-arrayexpress
GenomicsTHL Biobank Data Access Committee
Data Access Committee EGAC00001000660
EGAC00001000660 | EGA
GenomicsThe Nordic Centre of Excellence Programme in Molecular Medicine Data Access Committee
Access to data generated by the NcOEDG is available by emailing application to the data access committee and will be granted to qualified investigators for appropriate use. For further guidelines, application form and data access agreement, please follow the link below
EGAC00000000006 | EGA
GenomicsGenomewide Association Study of Alcohol Use and Alcohol Use Disorder in Australian Twin-Families (OZ-ALC GWAS)

The Australian twin-family study of alcohol use disorder (OZALC study) derives from telephone diagnostic interview studies of two general population volunteer cohorts of Australian twins (cohort 1, mostly born 1940-1964; cohort 2, born 1964-71) and the spouses of the former cohort - a total of ov...

phs000181.v1.p1 | EGA
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