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accession-icon GSE40404
Expression data from normal human fibroblasts expressing prelamin A or progerin, untreated or treated with farnesyltransferase inhibitor (FTI)
  • organism-icon Homo sapiens
  • sample-icon 7 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U133 Plus 2.0 Array (hgu133plus2)

Description

We compared the transcriptomes of isogenic diploid fibroblasts expressing progerin or elevated levels of wild-type prelamin A with that of wild-type fibroblasts. We subsequently used the reversion towards normal of two phenotypes, reduced cell growth and dismorphic nuclei, by treatment with farnesyltransferase inhibitor (FTI) or overexpression of ZMPSTE24, as a filtering strategy to identify genes linked to the onset of these two phenotypes.

Publication Title

A filtering strategy identifies FOXQ1 as a potential effector of lamin A dysfunction.

Alternate Accession IDs

E-GEOD-40404

Sample Metadata Fields

Specimen part, Cell line, Treatment

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accession-icon GSE66989
The effect of short-chain fatty acids (SCFAs) on human monocyte-derived dendritic cells (DCs)
  • organism-icon Homo sapiens
  • sample-icon 8 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Transcriptome Array 2.0 (hta20)

Description

We investigated the influence of SCFAs on human, monocyte derived DCs that represent a reliable in vitro model to study circulating DCs, one of the key regulators of our immune system. We studied the individual effect exerted by SCFA, the main metabolic end-products of fermentation by anaerobic bacteria in the gut, on the gene expression of immature and mature DC, exploring the potential of circulating bacterial metabolites to directly influence immune system cells. We found that SCFAs have little effect on the transcriptome of immature DC, whereas the transcriptome of mature DC was highly perturbed especially by butyrate and propionate. Our findings show an overall down-regulation of LPS-induced inflammatory responses and provide new insights into host-microbiome interactions.

Publication Title

The effect of short-chain fatty acids on human monocyte-derived dendritic cells.

Alternate Accession IDs

E-GEOD-66989

Sample Metadata Fields

Specimen part, Treatment

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accession-icon E-TABM-566
Transcription profiling by array of Arabidopsis mutant for ron1
  • organism-icon Arabidopsis thaliana
  • sample-icon 6 Downloadable Samples
  • Technology Badge Icon Affymetrix Arabidopsis ATH1 Genome Array (ath1121501)

Description

Transcription profiling of Arabidopsis mutant ron1-1 vs the wild type Ler

Publication Title

The RON1/FRY1/SAL1 gene is required for leaf morphogenesis and venation patterning in Arabidopsis.

Alternate Accession IDs

None

Sample Metadata Fields

Specimen part

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accession-icon E-MEXP-822
Transcription profiling by array of diploid and tetraploid S. cerevisiae cultures
  • organism-icon Saccharomyces cerevisiae
  • sample-icon 6 Downloadable Samples
  • Technology Badge Icon Affymetrix Yeast Genome S98 Array (ygs98)

Description

Diploid and tetraploid budding yeast cell cultures were grown in YPD, at 30C, to O.D. approx. 0.5.

Publication Title

Genome-wide genetic analysis of polyploidy in yeast.

Alternate Accession IDs

None

Sample Metadata Fields

Sex

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accession-icon GSE72046
Transcriptome profiles of mice intestine and liver upon infection with Salmonella typhimurium (MC71-TT and MC71-DcdtB)
  • organism-icon Mus musculus
  • sample-icon 12 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Gene 2.0 ST Array (mogene20st)

Description

Bacterial genotoxins, produced by several Gram-negative bacteria, induce DNA damage in the target cells. While the responses induced in the host cells have been extensively studied in vitro, the role of the genotoxins as effectors during the course of acute and chronic infections remains poorly characterized.To address this issue, we assessed the effects of the Salmonella enterica genotoxin, known as typhoid toxin, in in vivo models of murine chronic infections. Immunocompetent mice were chronically infected with isogenic S. enterica, serovar Typhimurium (S. Typhimurium) strains, encoding either a functional (MC71-TT) or an inactive (MC71-DcdtB) typhoid toxin.

Publication Title

The Typhoid Toxin Promotes Host Survival and the Establishment of a Persistent Asymptomatic Infection.

Alternate Accession IDs

E-GEOD-72046

Sample Metadata Fields

No sample metadata fields

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accession-icon GSE7676
Changes in gene expression following Protocadherin 12 knockout
  • organism-icon Mus musculus
  • sample-icon 10 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Genome 430 2.0 Array (mouse4302)

Description

Protocadherin 12 (Pcdh12) is a transmembrane adhesive protein with homophilic adhesive properties and expressed in endothelial cells, the glycogen trophoblast cells of the placenta, and the mesangial cells of kidney glomeruli. Pcdh12-deficient mice are alive although they show alterations in placenta development.

Publication Title

Protocadherin 12 deficiency alters morphogenesis and transcriptional profile of the placenta.

Alternate Accession IDs

E-GEOD-7676

Sample Metadata Fields

Sex

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accession-icon GSE40130
Regulation of epidermal growth factor receptor signaling and erlotinib sensitivity in head and neck cancer cells by miR-7
  • organism-icon Homo sapiens
  • sample-icon 10 Downloadable Samples
  • Technology Badge IconIllumina HumanWG-6 v3.0 expression beadchip

Description

Elevated expression and activity of the epidermal growth factor receptor (EGFR)/protein kinase B (Akt) signaling pathway is associated with development, progression and treatment resistance of head and neck cancer (HNC). Several studies have demonstrated that microRNA-7 (miR-7) regulates EGFR expression and Akt activity in a range of cancer cell types via its specific interaction with the EGFR mRNA 3 untranslated region (3-UTR). In the present study, we found that miR-7 regulated EGFR expression and Akt activity in HNC cell lines, and that this was associated with reduced growth in vitro and in vivo of cells (HN5) that were sensitive to the EGFR tyrosine kinase inhibitor (TKI) erlotinib (Tarceva). miR-7 acted synergistically with erlotinib to inhibit growth of erlotinib-resistant FaDu cells, an effect associated with increased inhibition of Akt activity. Microarray analysis of HN5 and FaDu cell lines transfected with miR-7 identified a common set of downregulated miR-7 target genes, providing insight into the tumor suppressor function of miR-7. Furthermore, we identified several target miR-7 mRNAs with a putative role in the sensitization of FaDu cells to erlotinib. Together, these data support the coordinate regulation of Akt signaling by miR-7 in HNC cells and suggest the therapeutic potential of miR-7 alone or in combination with EGFR TKIs in this disease.

Publication Title

Regulation of epidermal growth factor receptor signaling and erlotinib sensitivity in head and neck cancer cells by miR-7.

Alternate Accession IDs

E-GEOD-40130

Sample Metadata Fields

Specimen part, Cell line

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accession-icon GSE77461
R-spondin 1 and noggin facilitate expansion of resident stem cells from non-damaged gallbladders.
  • organism-icon Mus musculus
  • sample-icon 14 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Gene 1.0 ST Array (mogene10st)

Description

Pioneering studies within the last few years have allowed the in vitro expansion of tissue-specific adult stem cells from a variety of endoderm-derived organs, including the stomach, small intestine and colon. Here we derived organoids from mouse gallbladder tissue (gallbladder organoids), from mouse liver (including the extrahepatic biliary ducts and gallbladder; liver organoids) and from mouse small intestine tissue (intestinal organoids). RNA was prepared from these organoids and used to assay expression of 21,258 genes using Affymetrix gene expression arrays. RNA was also prepared from mouse gallbladder, liver and small intestine tissues and used to assay gene expression in these tissues. Finally, gallbladder organoids were induced to differentiate by removing R-spondin 1 and noggin from the culture media and subjected to gene expression array analysis.

Publication Title

R-spondin 1 and noggin facilitate expansion of resident stem cells from non-damaged gallbladders.

Alternate Accession IDs

E-GEOD-77461

Sample Metadata Fields

Specimen part

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accession-icon SRP151779
Gene expression in WT and Thpok-deficient LCMV-specific memory T cells
  • organism-icon Mus musculus
  • sample-icon 77 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2500

Description

Gene expression of memory CD4+ and CD8+ T cells determined by RNAseq 30 days after LCMV Armstrong infection Overall design: 30 days post-infection with LCMV Arm spleen GP66:I-Ab+ T cells from Zbtb7bAD (CD4 Zbtb7bAD) or Tnfrsf4-Cre– (CD4 Ctrl) mice and of spleen GP33:H-2Db+ T cells from Tnfrsf4-Cre– animals (CD8 Ctrl) were sorted and gene expression was determined by RNAseq

Publication Title

The Emergence and Functional Fitness of Memory CD4<sup>+</sup> T Cells Require the Transcription Factor Thpok.

Alternate Accession IDs

GSE116519

Sample Metadata Fields

Subject

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accession-icon SRP164943
Single-cell gene expression of anti-viral WT and Thpok-deficient effector and memory T cells
  • organism-icon Mus musculus
  • sample-icon 38 Downloadable Samples
  • Technology Badge IconNextSeq 500

Description

Single-cell gene expression of effector and memory CD4+ and CD8+ T cells from WT or Thppok-deficient animals was determined by sRNAseq after LCMV Armstrong infection Overall design: 7 and 30 days post-infection with LCMV Arm spleen T cells were sorted and gene expression was determined by scRNAseq

Publication Title

The Emergence and Functional Fitness of Memory CD4<sup>+</sup> T Cells Require the Transcription Factor Thpok.

Alternate Accession IDs

GSE121002

Sample Metadata Fields

Specimen part, Subject

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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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Developed by the Childhood Cancer Data Lab

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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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