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TranscriptomicsUbe3a-ATS characterization with strand-speicific microarray
This strand-specific array is performed to characterize expression features of Ube3a-ATS, including its imprinting status, its exon-intron structure, its transcriptional initiation and termination site as well as its polyadenylation status. The array contains reverse-complementary probes detecting t...
ORGANISM(S): Mus musculus 
2012-05-02 | E-GEOD-29254 | biostudies-arrayexpress
ProteomicsCoordinate control of endoplasmic reticulum chaperone biosynthesis and peptide hormone secretion revealed by a β-cell model of Prader-Willi syndrome
Prader-Willi syndrome (PWS) is a multisystem disorder caused by loss of expression of a cluster of paternally-expressed, imprinted genes. Neonatal failure to thrive is followed by childhood-onset hyperphagia, obesity, neurobehavioral abnormalities, and hormonal deficits. Prior evidence from a mouse ...
ORGANISM(S): Rattus norvegicus (Rat) 
2023-04-11 | PXD037875 | Pride
Crispr/cas9  genomic imprinting  hormone secretion  metabolic disease  pancreatic islet 
ProteomicsCoordinate control of endoplasmic reticulum chaperone biosynthesis and peptide hormone secretion revealed by a β-cell model of Prader-Willi syndrome
Prader-Willi syndrome (PWS) is a multisystem disorder caused by loss of expression of a cluster of paternally-expressed, imprinted genes. Neonatal failure to thrive is followed by childhood-onset hyperphagia, obesity, neurobehavioral abnormalities, and hormonal deficits. Prior evidence from a mouse ...
ORGANISM(S): Rattus norvegicus (Rat) 
2023-04-11 | PXD037874 | Pride
Crispr/cas9  genomic imprinting  hormone secretion  metabolic disease  pancreatic islet 
UnknownTime spent outside of target glucose range for young children with type 1 diabetes: a continuous glucose monitor study.
Not available
S-EPMC9065795 | biostudies-literature
UnknownSafety and tolerability of the treatment of youth-onset type 2 diabetes: the TODAY experience.
Not available
S-EPMC3661822 | biostudies-literature
UnknownSleep in children with type 1 diabetes and their parents in the T1D Exchange.
Not available
S-EPMC7650845 | biostudies-literature
UnknownTargeting fidelity of adenine and cytosine base editors in mouse embryos.
Not available
S-EPMC6238002 | biostudies-literature
TranscriptomicsExpression data from human skeletal muscle
Insulin is a potent pleiotropic hormone that affects processes such as cellular growth, differentiation, apoptosis, ion flux, energy expenditure, and carbohydrate, lipid, and protein metabolism. We used microarrays to detail the global programme of gene expression underlying the influence of insulin...
ORGANISM(S): Homo sapiens 
2010-07-08 | E-GEOD-22309 | biostudies-arrayexpress
TranscriptomicsMethylation profiling in individuals with uniparental disomy identifies novel differentially methylated regions on chromosome 15
Methylation profiles of chr12-16 were generated by meDIP and array hybridisation in 3 cases with maternal uniparental disomy of chromosome 15, and three cases of paternal uniparental disomy of chromosome 15. Comparison of these profiles reveals differentially methylated (imprinted) regions on chromo...
ORGANISM(S): Homo sapiens 
2010-06-12 | E-GEOD-22188 | biostudies-arrayexpress
UnknownEvaluation of ADA HbA1c criteria in the diagnosis of pre-diabetes and diabetes in a population of Chinese adolescents and young adults at high risk for diabetes: a cross-sectional study.
Not available
S-EPMC6089273 | biostudies-literature
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