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TranscriptomicsCpG Island methylation variation in placentae of Intra-Uterine Growth Restricted (IUGR) fetuses versus controls
Methylation profiling of CpG Island Methylation of genomic DNA samples extracted from placentae of Intra-Uterine Growth Restricted newborns and gestational age matched controls. These data can be used for methylation comparisons between these two types of samples. The results of such comparisons can...
ORGANISM(S): Homo sapiens 
2011-04-11 | E-GEOD-22326 | biostudies-arrayexpress
TranscriptomicsEpigenetic profiling in CD4 and CD8 T cells from Graves’ disease patients reveals changes in genes associated with T cell receptor signaling [methylation]
In Graves’ disease (GD), a combination of genetic, epigenetic and environmental factors causes an autoimmune response to the thyroid gland, characterized by lymphocytic infiltrations and autoantibodies targeting the thyroid stimulating hormone receptor (TSHR) and other thyroid antigens. To identif...
ORGANISM(S): Homo sapiens 
2015-11-06 | E-GEOD-71955 | biostudies-arrayexpress
TranscriptomicsDNA-METHYLATION - Integrative multi-omics survey of effects carbon-based engineered nanomaterials on lung derived cell-lines
In this study we exposed three human lung derived cell lines to sublethal dosages of nanomaterials for a limited amount of time. For the first time, we assessed the simultaneous effects of nanomaterials exposure on three distinct molecular layers along with their interactions in the determination of...
ORGANISM(S): Homo sapiens 
2018-05-19 | E-MTAB-6397 | biostudies-arrayexpress
UnknownANKRD11 pathogenic variants and 16q24.3 microdeletions share an altered DNA methylation signature in patients with KBG syndrome.
Not available
S-EPMC10117159 | biostudies-literature
TranscriptomicsEpigenetic profiling in CD4 and CD8 T cells from Graves disease patients reveals changes in genes associated with T cell receptor signaling
This SuperSeries is composed of the SubSeries listed below. Refer to individual Series
ORGANISM(S): Homo sapiens 
2015-11-06 | E-GEOD-71957 | biostudies-arrayexpress
TranscriptomicsNSD1 Mutations Generate a Genome-Wide DNA Methylation Signature
Sotos syndrome (SS) represents an important human model system for the study of epigenetic regulation; it is an overgrowth/intellectual disability syndrome caused by mutations in a histone methyltransferase, NSD1. As layered epigenetic modifications are often interdependent, we propose that pathogen...
ORGANISM(S): Homo sapiens 
2015-12-16 | E-GEOD-74432 | biostudies-arrayexpress
UnknownGenome-Wide DNA Methylation Analysis Reveals Epigenetic Dysregulation of MicroRNA-34A in TP53-Associated Cancer Susceptibility.
Not available
S-EPMC6366343 | biostudies-literature
UnknownDon't brush off buccal data heterogeneity.
Not available
S-EPMC6557604 | biostudies-literature
UnknownSocial Location and Decision-Making Among Women Living with HIV in the Southern United States: An Intersectional Approach
Not available
S-EPMC11675124 | biostudies-literature
UnknownPaternal Uniparental Disomy of the Entire Chromosome 20 in a Child with Beckwith-Wiedemann Syndrome.
Not available
S-EPMC7911624 | biostudies-literature
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