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accession-icon SRP124939
Adult functions for the Drosophila DHR78 nuclear receptor
  • organism-icon Drosophila melanogaster
  • sample-icon 8 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2000

Description

Here we study the adult functions of the single Drosophila member of this subfamily, DHR78, with the goal of defining its ancestral functions in the absence of genetic redundancy. We show that DHR78 mutants have a shortened lifespan and reduced motility. Mated DHR78 mutant females display reduced triglycerides along with a reduced feeding rate. Transcriptional profiling reveals a major role for DHR78 in promoting the expression of genes that are abundantly expressed in the midgut, suggesting that it contributes to nutrient uptake. We also identify roles for DHR78 in maintaining the expression of genes in the ecdysone and Notch signaling pathways. Overall design: Comparison of the transcriptional profile of DHR78-transheterozygote female mutants in a btl>DHR78 background with genetically matched controls

Publication Title

Adult functions for the Drosophila DHR78 nuclear receptor.

Alternate Accession IDs

GSE106866

Sample Metadata Fields

Sex, Age, Specimen part, Subject

View Samples
accession-icon SRP063610
Sir2 mutants versus Controls at 2 weeks of age
  • organism-icon Drosophila melanogaster
  • sample-icon 8 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2000

Description

Although SIRT1 plays a central role in maintaining metabolic homeostasis, the molecular mechanisms remain unclear. Here we show that loss of the Drosophila SIRT1 homolog sir2 leads to the progressive onset of diabetic phenotypes, similar to studies of SIRT1 in mice. Sir2 function is both necessary and sufficient in the fat body to maintain peripheral insulin sensitivity. This activity is mediated by the Drosophila HNF4 nuclear receptor, which is deacetylated and stabilized through protein interactions with Sir2. This study demonstrates that the key metabolic activities of SIRT1 have been conserved through evolution and establishes HNF4 as a critical downstream target. Overall design: 4 sir2 mutant, 4 control samples, independent biological replicates

Publication Title

Sir2 Acts through Hepatocyte Nuclear Factor 4 to maintain insulin Signaling and Metabolic Homeostasis in Drosophila.

Alternate Accession IDs

GSE72947

Sample Metadata Fields

Age, Subject

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accession-icon GSE63780
Increased Longevity in the Insulin-sensitive Syntaxin 4 Transgenic Mouse
  • organism-icon Mus musculus
  • sample-icon 2 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Gene 1.0 ST Array (mogene10st)

Description

There is a good deal of indirect evidence that improved insulin sensitivity may contribute to improved lifespan of mice in which aging has been slowed by mutations, drugs, or dietary means, even in stocks of mice that do not show signs of late-life diabetes. Peripheral responses to insulin can be augmented by over-expression of Syntaxin 4 (Syn4), a membrane SNARE protein. We show here that Syn4 transgenic (Tg) mice live approximately 33% longer than controls, and show increased peripheral insulin sensitivity, even at ages where controls show age-related insulin resistance. Hence, presumably Syn4 Tg mice spend more hours of each day under normoglycemic conditions, which may slow multiple aspects of aging and thereby extend lifespan, even in non-diabetic mice.

Publication Title

Syntaxin 4 Overexpression Ameliorates Effects of Aging and High-Fat Diet on Glucose Control and Extends Lifespan.

Alternate Accession IDs

E-GEOD-63780

Sample Metadata Fields

Sex, Specimen part

View Samples
accession-icon GSE3057
Temporal pattern of gene expression in the late third instar larvae and prepupae of Drosophila melanogaster
  • organism-icon Drosophila melanogaster
  • sample-icon 27 Downloadable Samples
  • Technology Badge Icon Affymetrix Drosophila Genome Array (drosgenome1)

Description

This study identifies genes that alter their expression in synchrony with the late third instar and prepupal pulses of 20E.

Publication Title

The genomic response to 20-hydroxyecdysone at the onset of Drosophila metamorphosis.

Alternate Accession IDs

E-GEOD-3057

Sample Metadata Fields

No sample metadata fields

View Samples
accession-icon GSE3069
Identification of genes dependent on the Ecdysone receptor (EcR) at the onset of metamorphosis in Drosophila
  • organism-icon Drosophila melanogaster
  • sample-icon 18 Downloadable Samples
  • Technology Badge Icon Affymetrix Drosophila Genome Array (drosgenome1)

Description

This study identifies those genes that are dependent on EcR for their proper regulation at the onset of metamorphosis in Drosophila melanogaster.

Publication Title

The genomic response to 20-hydroxyecdysone at the onset of Drosophila metamorphosis.

Alternate Accession IDs

E-GEOD-3069

Sample Metadata Fields

No sample metadata fields

View Samples
accession-icon GSE3060
Identification of 20E-regulated genes in Drosophila cultured larval organs
  • organism-icon Drosophila melanogaster
  • sample-icon 12 Downloadable Samples
  • Technology Badge Icon Affymetrix Drosophila Genome Array (drosgenome1)

Description

To identify 20E-regulated genes, wandering third instar larvae were dissected and their organs were cultured in the presence of either no hormone, 20E alone, cycloheximide alone, or 20E plus cycloheximide for six hours.

Publication Title

The genomic response to 20-hydroxyecdysone at the onset of Drosophila metamorphosis.

Alternate Accession IDs

E-GEOD-3060

Sample Metadata Fields

No sample metadata fields

View Samples
accession-icon GSE5096
Genomic responses to Phenobarbital in Drosophila melanogaster
  • organism-icon Drosophila melanogaster
  • sample-icon 12 Downloadable Samples
  • Technology Badge Icon Affymetrix Drosophila Genome 2.0 Array (drosophila2)

Description

Phenobarbital is a well studied xenobiotic compound. In this study, we describe the genomic responses in fruit flies and examine whether animals mutant for DHR96, an ortholog of xenobiotic nuclear receptors PXR and CAR, plays a role in mediating xenobiotic responses in Drosophila.

Publication Title

The DHR96 nuclear receptor regulates xenobiotic responses in Drosophila.

Alternate Accession IDs

E-GEOD-5096

Sample Metadata Fields

No sample metadata fields

View Samples
accession-icon SRP102705
AKHR F1 heterozygous progeny of obese parents and controls, 10-11 days old adults
  • organism-icon Drosophila melanogaster
  • sample-icon 12 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2000

Description

Transgenerational effects of parental metabolic state have been shown, but the mechanism is still unclear. Here we present transcriptome sequencing data from AKHR heterozygous F1 progeny, either from obese maternal or paternal parents, compared to genetically matched heterozygous controls or to wild-type controls Overall design: 3 AKHR heterozygous samples descended from obese maternal parents, 3 AKHR heterozygous samples descended from obese paternal parents, 3 AKHR heterozygous samples descended from non-obese parents, and 3 wild-type controls, independent biological replicates and independent experimental replicates (1 set of samples from each experimental replicate)

Publication Title

Parental obesity leads to metabolic changes in the F2 generation in <i>Drosophila</i>.

Alternate Accession IDs

GSE97201

Sample Metadata Fields

Specimen part, Subject

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accession-icon GSE5097
Genomic responses to ectopic expression of DHR96 in Drosophila melanogaster
  • organism-icon Drosophila melanogaster
  • sample-icon 6 Downloadable Samples
  • Technology Badge Icon Affymetrix Drosophila Genome 2.0 Array (drosophila2)

Description

DHR96 plays a role in regulating xenobiotic responses in Drosophila. Using a gain-of-function approach we test whether DHR96 is sufficient to affect detoxification genes in the absence of a xenobiotic insult.

Publication Title

The DHR96 nuclear receptor regulates xenobiotic responses in Drosophila.

Alternate Accession IDs

E-GEOD-5097

Sample Metadata Fields

No sample metadata fields

View Samples
accession-icon GSE19380
Gene expression from primary brain cell cultures and RNA mixtures.
  • organism-icon Rattus norvegicus
  • sample-icon 26 Downloadable Samples
  • Technology Badge Icon Affymetrix Rat Genome 230 2.0 Array (rat2302)

Description

Gene expression from primary neuronal, astrocytic, oligodendrocytic and microglial cultures, as well as from RNA mixtures thereof.

Publication Title

Population-specific expression analysis (PSEA) reveals molecular changes in diseased brain.

Alternate Accession IDs

E-GEOD-19380

Sample Metadata Fields

Specimen part

View Samples
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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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