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UnknownCiliary dyslexia candidate genes DYX1C1 and DCDC2 are regulated by Regulatory Factor X (RFX) transcription factors through X-box promoter motifs.
Not available
S-EPMC5024701 | biostudies-literature
UnknownEpigenome-Wide Meta-Analysis of Methylation in Children Related to Prenatal NO2 Air Pollution Exposure.
Not available
S-EPMC5226705 | biostudies-literature
TranscriptomicsTranscription profiling of human adenocarcinoma cell line A549 over-expressing ELMOD2
ELMOD2 cDNA from the IMAGE clone 3897166 was cloned into the pDsRed-Monomer-N1 expression vector. ELMOD2 was overexpressed in the A549(adenomcarcinoma)cell line and cells transfected with empty vector were considered controls. Transcript profiles were compared with the Affymetrix Hgu133plus2 arrays....
ORGANISM(S): Homo sapiens 
2009-12-07 | E-MEXP-1838 | biostudies-arrayexpress
TranscriptomicsTranscription profiling of Neuropeptide S Receptor 1-A (NPSR1-A) transfected human epithelial kidney cells stimulated with neuropeptide S to identify downstream targets
The purpose of this study was to identify downstream gene targets regulated by Neuropeptide S Receptor 1 (NPSR1) upon NPS stimulation. To do this we used human epithelial kidney (HEK)-293H cell lines stable transfected with NPSR1-A and stimulated with NPS for 6 hours. Two controls were used: NPS sti...
ORGANISM(S): Homo sapiens 
2006-08-24 | E-MEXP-829 | biostudies-arrayexpress
UnknownA common haplotype in the G-protein-coupled receptor gene GPR74 is associated with leanness and increased lipolysis.
Not available
S-EPMC1867099 | biostudies-literature
TranscriptomicsIntracellular signalling pathways and cytoskeletal functions converge on the psoriasis candidate gene CCHCR1 expressed at P-bodies and centrosomes
CCHCR1 (Coiled-Coil alpha-Helical Rod protein 1) is a putative psoriasis candidate gene with the risk alleles CCHCR1*WWCC and *Iso3, the latter inhibiting the translation of isoform 1. CCHCR1 was recently shown to be a centrosomal protein, as well as a component of cytoplasmic processing bodies (P-b...
ORGANISM(S): Homo sapiens 
2018-06-04 | E-MTAB-6848 | biostudies-arrayexpress
UnknownThe Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains.
Not available
S-EPMC24264 | biostudies-literature
UnknownMapping and identifying genes for asthma and psoriasis.
Not available
S-EPMC1569524 | biostudies-literature
UnknownTranscriptomic differences between human 8-cell-like cells reprogrammed with different methods.
Not available
S-EPMC10444576 | biostudies-literature
TranscriptomicsDifferential DNA Methylation in Purified Human Blood Cells
Methylation of cytosines at CpG sites is a common epigenetic DNA modification that can be measured by a large number of methods, now even in a genome-wide manner for hundreds of thousands of sites. The application of DNA methylation analysis is becoming widely popular in complex disorders, for examp...
ORGANISM(S): Homo sapiens 
2012-08-02 | E-GEOD-35069 | biostudies-arrayexpress
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