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accession-icon GSE45747
Weight loss after gastric bypass surgery in human obesity induces promoter methylation
  • organism-icon Homo sapiens
  • sample-icon 16 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U219 Array (hgu219), Illumina Genome Analyzer IIx

Description

This SuperSeries is composed of the SubSeries listed below.

Publication Title

Weight loss after gastric bypass surgery in human obesity remodels promoter methylation.

Sample Metadata Fields

Sex, Specimen part

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accession-icon GSE45745
Gene expression profiling in skeletal muscle before and after GBP surgery
  • organism-icon Homo sapiens
  • sample-icon 16 Downloadable Samples
  • Technology Badge IconIllumina Genome Analyzer IIx, Affymetrix Human Genome U219 Array (hgu219)

Description

Profiling of gene expression in Vastus Lateralis from female patients before and after GBP surgery and from lean Control

Publication Title

Weight loss after gastric bypass surgery in human obesity remodels promoter methylation.

Sample Metadata Fields

Sex, Specimen part

View Samples
accession-icon GSE65058
Altered DNA methylation of glycolytic and lipogenic genes in liver from obese and type 2 diabetic patients
  • organism-icon Homo sapiens
  • sample-icon 21 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Gene 1.1 ST Array (hugene11st)

Description

This SuperSeries is composed of the SubSeries listed below.

Publication Title

Altered DNA methylation of glycolytic and lipogenic genes in liver from obese and type 2 diabetic patients.

Sample Metadata Fields

Sex, Specimen part, Disease stage

View Samples
accession-icon GSE64998
Altered DNA methylation of glycolytic and lipogenic genes in liver from obese and type 2 diabetic patients [transcriptome analysis]
  • organism-icon Homo sapiens
  • sample-icon 21 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Gene 1.1 ST Array (hugene11st)

Description

Type 2 diabetes is a complex disease associated with many underlying pathomechanisms. Epigenetic regulation of gene expression by DNA methylation has become increasingly recognized as an important component in the etiology of type 2 diabetes. We performed genome-wide methylome and transcriptome analysis in liver from severely obese patients with or without type 2 diabetes to discover aberrant pathways underlying the development of insulin resistance. We identified hypomethylation of five key genes involved in hepatic glycolysis, de novo lipogenesis and insulin resistance with concomitant increased mRNA expression and protein content. The CpG-site within the ATF-motif was hypomethylated in four of these genes in liver of non-diabetic and type 2 diabetic obese patients, suggesting epigenetic regulation of transcription by altered ATF-DNA binding. In conclusion, severely obese non-diabetic and type 2 diabetic patients have distinct alterations in the hepatic methylome and transcriptome and genes controlling glucose and lipid metabolism are hypomethylated at a regulatory site. Thus, obesity may epigenetically reprogram the liver towards increased lipid production and exacerbate the development of insulin resistance.

Publication Title

Altered DNA methylation of glycolytic and lipogenic genes in liver from obese and type 2 diabetic patients.

Sample Metadata Fields

Sex, Specimen part, Disease stage

View Samples
accession-icon GSE55934
Expression data from Mus musculus white adipose tissue
  • organism-icon Mus musculus
  • sample-icon 6 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Gene 2.0 ST Array (mogene20st)

Description

We used microarrays to detail the gene expression profile during WAT -beige transition by treatment of beta adrenergic receptor agonist .

Publication Title

Endothelial PDGF-CC regulates angiogenesis-dependent thermogenesis in beige fat.

Sample Metadata Fields

Specimen part

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refine.bio is a repository of uniformly processed and normalized, ready-to-use transcriptome data from publicly available sources. refine.bio is a project of the Childhood Cancer Data Lab (CCDL)

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Cite refine.bio

Casey S. Greene, Dongbo Hu, Richard W. W. Jones, Stephanie Liu, David S. Mejia, Rob Patro, Stephen R. Piccolo, Ariel Rodriguez Romero, Hirak Sarkar, Candace L. Savonen, Jaclyn N. Taroni, William E. Vauclain, Deepashree Venkatesh Prasad, Kurt G. Wheeler. refine.bio: a resource of uniformly processed publicly available gene expression datasets.
URL: https://www.refine.bio

Note that the contributor list is in alphabetical order as we prepare a manuscript for submission.

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