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accession-icon GSE54852
Inferring causal metabolic signals that regulate the dynamic TORC1-dependent transcriptome
  • organism-icon Saccharomyces cerevisiae
  • sample-icon 41 Downloadable Samples
  • Technology Badge Icon Affymetrix Yeast Genome 2.0 Array (yeast2)

Description

This SuperSeries is composed of the SubSeries listed below.

Publication Title

Inferring causal metabolic signals that regulate the dynamic TORC1-dependent transcriptome.

Sample Metadata Fields

Treatment

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accession-icon GSE54850
Dynamic mRNA gene expression during a nutritional downshift from glutamine to proline
  • organism-icon Saccharomyces cerevisiae
  • sample-icon 14 Downloadable Samples
  • Technology Badge Icon Affymetrix Yeast Genome 2.0 Array (yeast2)

Description

Dynamic mRNA gene expression from the wildtype YSBN6 during a nutritional downshift from glutamine to proline. Glutamine and proline were initially together in the media, with cells consuming exlusively glutamine (proline utilization inhibited due to nitrogen catabolite repression). The concentration of glutamine was frequently evaluated at-line, and the moment at which glutamine was not detected anymore is referred to as the time of the shift.

Publication Title

Inferring causal metabolic signals that regulate the dynamic TORC1-dependent transcriptome.

Sample Metadata Fields

Treatment

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accession-icon GSE54851
Dynamic mRNA gene expression following a rapamycin treatment
  • organism-icon Saccharomyces cerevisiae
  • sample-icon 14 Downloadable Samples
  • Technology Badge Icon Affymetrix Yeast Genome 2.0 Array (yeast2)

Description

Dynamic mRNA gene expression from the wildtype YSBN6 during a rapamycin treatment (rapamycin-induced downshift). Rapamycin was added to yeast cells growing exponentially on glutamine as sole nitrogen source.

Publication Title

Inferring causal metabolic signals that regulate the dynamic TORC1-dependent transcriptome.

Sample Metadata Fields

Treatment

View Samples
accession-icon GSE54844
Dynamic mRNA gene expression during a nutritional upshift from proline to glutamine
  • organism-icon Saccharomyces cerevisiae
  • sample-icon 13 Downloadable Samples
  • Technology Badge Icon Affymetrix Yeast Genome 2.0 Array (yeast2)

Description

Dynamic mRNA gene expression from the wildtype YSBN6 during a nutritional upshift from proline to glutamine. Glutamine was added to yeast cells growing exponentially on proline as the sole nitrogen source.

Publication Title

Inferring causal metabolic signals that regulate the dynamic TORC1-dependent transcriptome.

Sample Metadata Fields

Treatment

View Samples
accession-icon GSE37605
Expression Data of Treg and Tconv Cells from FoxP3-GFP Chimeric and FoxP3-ires-GFP B6 and NOD Mice
  • organism-icon Mus musculus
  • sample-icon 16 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Gene 1.0 ST Array (mogene10st)

Description

The aim of this study was to quantify the impact of chimeric Foxp3-GFP protein on the Treg cell transcriptional program.

Publication Title

An N-terminal mutation of the Foxp3 transcription factor alleviates arthritis but exacerbates diabetes.

Sample Metadata Fields

Sex, Age, Specimen part

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accession-icon GSE39864
Treg specific Gata3 knock out array
  • organism-icon Mus musculus
  • sample-icon 6 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Genome 430A 2.0 Array (mouse430a2)

Description

The transcription factor Foxp3 is indispensible for the differentiation and function of regulatory T cells (Treg cells). To gain insights into the molecular mechanisms of Foxp3 mediated gene expression we purified Foxp3 complexes and explored their composition. Biochemical and mass-spectrometric analyses revealed that Foxp3 forms multi-protein complexes of 400-800 kDa or larger and identified 361 associated proteins ~30% of which are transcription-related. Foxp3 directly regulates expression of a large proportion of the genes encoding its co-factors. Reciprocally, some transcription factor partners of Foxp3 facilitate its expression. Functional analysis of Foxp3 cooperation with one such partner, Gata3, provided further evidence for a network of transcriptional regulation afforded by Foxp3 and its associates to control distinct aspects of Treg cell biology.

Publication Title

Transcription factor Foxp3 and its protein partners form a complex regulatory network.

Sample Metadata Fields

Specimen part

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accession-icon GSE60148
Role of milk fat globule membrane (MFGM) in modulating gene expression in humans
  • organism-icon Homo sapiens
  • sample-icon 49 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Gene 2.1 ST Array (hugene21st)

Description

The aim of this study was to investigate if milk fat globule membrane (MFGM) enclosing the dairy fat influence peripheral blood mononuclear cells (PBMC) gene expression. This study was a 8-week single-blind, randomized, controlled isocaloric trial with two parallel groups including overweight (mean BMI: 28) adult women (n=30). All subjects consumed 40 g dairy fat per day either as cream (MFGM diet) or as butter oil (control diet).

Publication Title

Potential role of milk fat globule membrane in modulating plasma lipoproteins, gene expression, and cholesterol metabolism in humans: a randomized study.

Sample Metadata Fields

Age, Specimen part, Time

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accession-icon SRP124496
ETS1 acts as a tumor suppressor in breast cancer by inhibiting growth-related factors
  • organism-icon Homo sapiens
  • sample-icon 12 Downloadable Samples
  • Technology Badge IconNextSeq 500

Description

To characterize the effect of Core regulatory element (CRE) deletion in breast cancer cell line (MDA-MB-231 cells), we performed gene expression RNA-seq analysis for WT and KO (Core Regulatory Element deleted) MDA-MB-231 cells after 0h, 6h and 24h of P/I treatment. Overall design: Total RNA was extracted from WT and KO (CRE deleted) MDA-MB-231 cells of mock and PMA/Ionomycin treated group.

Publication Title

ETS1 Suppresses Tumorigenesis of Human Breast Cancer via Trans-Activation of Canonical Tumor Suppressor Genes.

Sample Metadata Fields

Cell line, Subject

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accession-icon SRP170017
Ets1 suppresses atopic dermatitis by suppressing pathogenic T cell responses
  • organism-icon Mus musculus
  • sample-icon 6 Downloadable Samples
  • Technology Badge IconNextSeq 500

Description

To identify the molecular mechanisms responsible for enhanced atopic dermatitis (AD) pathogenesis upon Ets1 deficiency in CD4+ T cells, we compared transcriptome profile between CD4+ T cells from littermate control (LMC) and Ets1?dLck mice at the peak of AD progression by performing RNA-seq. Overall design: Skin-draining lymph nodes near sites of inflammation under AD were excised from LMC and Ets1?dLck mice and prepared into single cell suspensions. CD4+ T cells were purified by CD4+ negative selection method.

Publication Title

Ets1 suppresses atopic dermatitis by suppressing pathogenic T cell responses.

Sample Metadata Fields

Cell line, Subject

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accession-icon GSE36279
Expression data from murine liver tissue upon depletion of regulatory T cells
  • organism-icon Mus musculus
  • sample-icon 11 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Gene 1.0 ST Array (mogene10st)

Description

Regulatory T cells (Treg) play a pivotal role in modulating immune responses and were shown to decrease atherosclerosis in murine models. How this effect is brought about remains elusive.

Publication Title

Depletion of FOXP3+ regulatory T cells promotes hypercholesterolemia and atherosclerosis.

Sample Metadata Fields

Specimen part, Treatment

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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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