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accession-icon GSE6795
Expression data from C57BL6 tissues and 3T3-L1 fibroblasts
  • organism-icon Mus musculus
  • sample-icon 28 Downloadable Samples
  • Technology Badge Icon Affymetrix Murine 11K SubA Array (mu11ksuba)

Description

This SuperSeries is composed of the SubSeries listed below.

Publication Title

Xanthine oxidoreductase is a regulator of adipogenesis and PPARgamma activity.

Sample Metadata Fields

No sample metadata fields

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accession-icon GSE6794
Expression data from 3T3-L1 adipogenesis
  • organism-icon Mus musculus
  • sample-icon 18 Downloadable Samples
  • Technology Badge Icon Affymetrix Murine 11K SubA Array (mu11ksuba)

Description

3T3-L1 fibroblasts are a commonly used in vitro model for adipogenesis. When induced with hormones, they differentiate into mature fat cells. Here, microarrays were used to study 3T3-L1 adipose differentiation through time.

Publication Title

Xanthine oxidoreductase is a regulator of adipogenesis and PPARgamma activity.

Sample Metadata Fields

No sample metadata fields

View Samples
accession-icon GSE6793
Expression data from select tissues harvested from C57BL6 mice
  • organism-icon Mus musculus
  • sample-icon 10 Downloadable Samples
  • Technology Badge Icon Affymetrix Murine 11K SubA Array (mu11ksuba)

Description

Gene expression was studied from different mouse tissues

Publication Title

Xanthine oxidoreductase is a regulator of adipogenesis and PPARgamma activity.

Sample Metadata Fields

No sample metadata fields

View Samples
accession-icon SRP083760
Genetic vs Dietary Models of Iron Overload in the Mouse Liver
  • organism-icon Mus musculus
  • sample-icon 9 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2500

Description

Iron overload causes the generation of reactive oxygen species, which can lead to lasting damage to the liver and other organs. We studied the effects of iron deficiency and iron overload on the hepatic transcriptional and metabolomic profile in mouse models. Overall design: We studied effect of different iron overloads (High, medium and Low) on liver transcriptome using whole genome transcriptome profiling.

Publication Title

Nicotinamide N-methyltransferase expression decreases in iron overload, exacerbating toxicity in mouse hepatocytes.

Sample Metadata Fields

Cell line, Subject

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accession-icon SRP083889
Genetic Model of iron deficiency in the Mouse Liver
  • organism-icon Mus musculus
  • sample-icon 4 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2500

Description

Iron overload causes the generation of reactive oxygen species, which can lead to lasting damage to the liver and other organs. We studied the effects of iron deficiency and iron overload on the hepatic transcriptional and metabolomic profile in mouse models. Overall design: We studied effect of different iron deficiency by HJV gene knockout mice on liver transcriptome using whole genome transcriptome profiling.

Publication Title

Nicotinamide N-methyltransferase expression decreases in iron overload, exacerbating toxicity in mouse hepatocytes.

Sample Metadata Fields

Specimen part, Subject

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accession-icon SRP158524
Ewing sarcoma resistance to SP-2509 is not mediated through KDM1A/LSD1 mutation I
  • organism-icon Homo sapiens
  • sample-icon 24 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2000

Description

The transcriptional profile of A673 parental and SP-2509 Drug resistant cells treated with DMSO and SP-2509 (2uM 48hrs) Overall design: A673 parental and SP-2509 Drug resistant cells treated with DMSO and SP-2509 (2uM 48hrs)

Publication Title

Ewing sarcoma resistance to SP-2509 is not mediated through KDM1A/LSD1 mutation.

Sample Metadata Fields

Treatment, Subject

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accession-icon SRP158525
Ewing sarcoma resistance to SP-2509 is not mediated through KDM1A/LSD1 mutation II
  • organism-icon Homo sapiens
  • sample-icon 9 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2000

Description

The transcriptional profile of A673 parental, and SP-2509 drug resistant washout cells (4 and 6 months) Overall design: Following generation of A673 SP-2509 drug resistant cells (chronic exposure for 7 months), drug was withdrawn with cell pellets collected 4 and 6 months after removal.

Publication Title

Ewing sarcoma resistance to SP-2509 is not mediated through KDM1A/LSD1 mutation.

Sample Metadata Fields

Disease, Treatment, Subject

View Samples
accession-icon GSE7891
Trancriptome profiling of rat inner medullary collecting duct
  • organism-icon Rattus norvegicus
  • sample-icon 6 Downloadable Samples
  • Technology Badge Icon Affymetrix Rat Genome 230 2.0 Array (rat2302)

Description

Identification of gene expressed in the enriched inner medullary collecting duct cells in rat.

Publication Title

Transcriptional profiling of native inner medullary collecting duct cells from rat kidney.

Sample Metadata Fields

Sex, Age, Specimen part

View Samples
accession-icon GSE54501
Gene expression profiles in the colon of APC and Olfm4 double mutant mice
  • organism-icon Mus musculus
  • sample-icon 15 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Genome 430 2.0 Array (mouse4302)

Description

APC mutant mice develop polys in the intestine, but not carcinoma. We found that additional deletion of Olfm4 gene induced carcinoma formation in the distal colon. To explore the molecular mechanism, we performed cDNA microarray to understand the gene expression files in the tumor tissues compared with WT, APC mutant and Olfm4 mutant mice.

Publication Title

Olfactomedin 4 deletion induces colon adenocarcinoma in Apc<sup>Min/+</sup> mice.

Sample Metadata Fields

Sex, Age, Specimen part

View Samples
accession-icon SRP044099
The contribution of cohesin-SA1 to chromatin architecture and gene expression in two murine tissues
  • organism-icon Mus musculus
  • sample-icon 8 Downloadable Samples
  • Technology Badge Icon

Description

Cohesin, which consists of SMC1, SMC3, Rad21 and either SA1 or SA2, topologically embraces the chromatin fibers to hold sister chromatids together and to stabilize chromatin loops. Increasing evidence indicates that these loops are the organizing principle of higher-order chromatin architecture, which in turn is critical for gene expression. To determine how cohesin contributes to the establishment of tissue-specific transcriptional programs, we compared genome-wide cohesin distribution, gene expression and chromatin architecture in cerebral cortex and pancreas from adult mice. More than one third of cohesin binding sites differ between the two tissues and these are enriched at the regulatory regions of tissue-specific genes. Cohesin colocalizes extensively with the CCCTC-binding factor (CTCF). Cohesin/CTCF sites at active enhancers and promoters contain, at least, cohesin-SA1 whereas either cohesin-SA1 or cohesin-SA2 are present at active promoters independently of CTCF. Analyses of chromatin contacts at the Protocadherin gene cluster and the Regenerating islet-derived (Reg) gene cluster, mostly expressed in brain and pancreas respectively, revealed remarkable differences in the architecture of these loci in the two tissues that correlate with the presence of cohesin. Moreover, we found decreased binding of cohesin and reduced transcription of the Reg genes in the pancreas of SA1 heterozygous mice. Given that Reg proteins are involved in the control of inflammation in pancreas, such reduction may contribute to the increased incidence of pancreatic cancer reported in these animals. Overall design: Examination of the relationship between gene expression, genome wide cohesin distribution and chromatin structure

Publication Title

The contribution of cohesin-SA1 to gene expression and chromatin architecture in two murine tissues.

Sample Metadata Fields

No sample metadata fields

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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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