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accession-icon GSE37305
Age and Fasting in C. elegans
  • organism-icon Caenorhabditis elegans
  • sample-icon 12 Downloadable Samples
  • Technology Badge Icon Affymetrix C. elegans Genome Array (celegans)

Description

This SuperSeries is composed of the SubSeries listed below.

Publication Title

The Sexual Dimorphism of Dietary Restriction Responsiveness in Caenorhabditis elegans.

Sample Metadata Fields

Sex, Specimen part, Treatment

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accession-icon GSE37303
Fasting induced changes in gene expression profiles of C. elegans
  • organism-icon Caenorhabditis elegans
  • sample-icon 4 Downloadable Samples
  • Technology Badge Icon

Description

Many species undergo sexual reproduction to distribute the parental genomes and increase the genomic diversity of the progeny. Among such species, sexual dimorphism is often displayed through morphology, size, behavior, and life-span, depending on the survival and reproduction strategies of the species. The nematode Caenorhabditis elegans has two sexes, hermaphrodite and male, and only the hermaphrodites, which produce both oocytes and sperm, are essential for the perpetuation of the species. In this study, we found that dietary restriction, which is the most reproducible way to retard aging in many species, extends the life-span of C. elegans hermaphrodites but not that of males. Our analysis revealed that fasting induces male-enriched genes in hermaphrodites and that the sex determination pathway affects life-span regulation, even after the completion of development, and is regulated by food availability. Furthermore, fasting activates the entire X-chromosome only in hermaphrodites. Our tiling array analysis identified a fasting-inducible, X-linked non-coding RNA for which expression positively correlated with the activation level of the X-chromosome and longevity. These links between the sex determination mechanism and dietary restriction at multiple levels may give priority to the survival of hermaphrodites during food shortages in C. elegans.

Publication Title

The Sexual Dimorphism of Dietary Restriction Responsiveness in Caenorhabditis elegans.

Sample Metadata Fields

No sample metadata fields

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accession-icon GSE143985
Clinical significance of gene signature generated from the grade of tumor budding in colorectal cancer
  • organism-icon Homo sapiens
  • sample-icon 91 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U133 Plus 2.0 Array (hgu133plus2)

Description

Tumor budding is a definite prognostic marker, but does not always show favorable reproducibility.

Publication Title

Clinical Significance of a Gene Signature Generated from Tumor Budding Grade in Colon Cancer.

Sample Metadata Fields

Specimen part

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accession-icon GSE34771
Expression data from primary central nervous system lymphoma (PCNSL) patients
  • organism-icon Homo sapiens
  • sample-icon 28 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U133 Plus 2.0 Array (hgu133plus2)

Description

This study aimed to define the genes associated with PCNSL patient survival. Expression profiling was performed on 34 PCNSLs. A gene classifier was developed.

Publication Title

Gene expression signature-based prognostic risk score in patients with primary central nervous system lymphoma.

Sample Metadata Fields

Sex, Age, Specimen part, Disease, Disease stage

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accession-icon E-TABM-544
Transcription profiling of yeast mutants to determine gene regulation by sterol and sphingolipid composition
  • organism-icon Saccharomyces cerevisiae
  • sample-icon 31 Downloadable Samples
  • Technology Badge Icon Affymetrix Yeast Genome 2.0 Array (yeast2)

Description

determination of gene regulation by sterol and sphingolipid composition

Publication Title

Functional interactions between sphingolipids and sterols in biological membranes regulating cell physiology.

Sample Metadata Fields

Sex

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accession-icon GSE84422
Molecular Signatures Underlying Selective Regional Vulnerability to Alzheimer's Disease
  • organism-icon Homo sapiens
  • sample-icon 2001 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U133A Array (hgu133a)

Description

Alzheimer's disease (AD) is the most common form of dementia, characterized by progressive cognitive impairment and neurodegeneration as a result of abnormal neuronal loss. To elucidate the molecular systems associated with AD, we characterized the gene expression changes associated with multiple clinical and neuropathological traits in 1,053 postmortem brain samples across 19 brain regions from 125 persons dying with varying severities of dementia and variable AD-neuropathology severities.

Publication Title

Integrative network analysis of nineteen brain regions identifies molecular signatures and networks underlying selective regional vulnerability to Alzheimer's disease.

Sample Metadata Fields

Sex, Age, Specimen part, Race, Subject

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accession-icon GSE37841
Expression data from Prkch-/-Apoe-/- mouse
  • organism-icon Mus musculus
  • sample-icon 12 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Gene 1.0 ST Array (mogene10st)

Description

To examine function of PKCh for atherosclerosis, we compared the gene expression profiles of control Apoe-/- and Prkch-/-Apoe-/- mice by microarray analysis.

Publication Title

PKCη deficiency improves lipid metabolism and atherosclerosis in apolipoprotein E-deficient mice.

Sample Metadata Fields

Sex, Age, Specimen part, Treatment

View Samples
accession-icon GSE35011
PPARg agonists induce a white-to-brown fat conversion through stabilization of PRDM16 protein
  • organism-icon Mus musculus
  • sample-icon 8 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Genome 430A 2.0 Array (mouse430a2)

Description

Brown adipose tissue dissipates energy through heat and functions as a defense against cold and obesity. PPAR ligands have been shown to induce the browning of white adipocytes; however, the underlying mechanisms remain unclear. Here we show that PPAR ligands require full agonism to induce a brown fat gene program preferentially in subcutaneous white adipose. These effects require expression of PRDM16, a factor that controls the development of classical brown fat. Depletion of PRDM16 blunts the effects of the PPAR agonist rosiglitazone on the induced brown fat gene program. Conversely, PRDM16 and rosiglitazone synergistically activate the brown fat gene program in vivo. This synergy is tightly associated with an increased accumulation of PRDM16 protein, due in large measure to an increase in the half-life of the protein in agonist treated cells. Identifying compounds that stabilize PRDM16 protein may represent a novel therapeutic pathway for the treatment of obesity and diabetes.

Publication Title

PPARγ agonists induce a white-to-brown fat conversion through stabilization of PRDM16 protein.

Sample Metadata Fields

Sex

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accession-icon GSE3595
Identification of potential KLF7 target genes in olfactory sensory neurons
  • organism-icon Mus musculus
  • sample-icon 6 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Genome 430 2.0 Array (mouse4302)

Description

KLF7 null mice show profound axonal growth defects in the olfactory epithelium. The goal of this study was the identification of potential KLF7 target genes in olfactory sensory neurons.

Publication Title

Identification of genes regulated by transcription factor KLF7 in differentiating olfactory sensory neurons.

Sample Metadata Fields

No sample metadata fields

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accession-icon GSE27867
Expression data from C. elegans (wild type vs. tag-24)
  • organism-icon Caenorhabditis elegans
  • sample-icon 6 Downloadable Samples
  • Technology Badge Icon Affymetrix C. elegans Genome Array (celegans)

Description

To provide insights into the mechanism underlying the enhanced immunity of tag-24/octr-1 animals, we used genome microarrays to find clusters of genes commonly misregulated in tag-24 relative to wild-type animals grown on live P. aeruginosa.

Publication Title

Neuronal GPCR controls innate immunity by regulating noncanonical unfolded protein response genes.

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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