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accession-icon GSE41930
Genome-wide analysis of gene expression in response to bortezomib treatment
  • organism-icon Mus musculus, Homo sapiens
  • sample-icon 44 Downloadable Samples
  • Technology Badge IconIllumina MouseWG-6 v2.0 expression beadchip

Description

This SuperSeries is composed of the SubSeries listed below.

Publication Title

Profiling bortezomib resistance identifies secondary therapies in a mouse myeloma model.

Sample Metadata Fields

Specimen part, Cell line, Time

View Samples
accession-icon GSE41927
Genome-wide analysis of gene expression in response to bortezomib treatment [mouse cell lines I]
  • organism-icon Mus musculus
  • sample-icon 24 Downloadable Samples
  • Technology Badge IconIllumina MouseWG-6 v2.0 expression beadchip

Description

Genome-wide analysis of gene expression in response to bortezomib treatment (33 nM) in cell lines before and after selection for resistance.

Publication Title

Profiling bortezomib resistance identifies secondary therapies in a mouse myeloma model.

Sample Metadata Fields

Specimen part, Cell line, Time

View Samples
accession-icon GSE41928
Genome-wide analysis of gene expression in response to bortezomib treatment [mouse cell lines II]
  • organism-icon Mus musculus
  • sample-icon 20 Downloadable Samples
  • Technology Badge IconIllumina MouseWG-6 v2.0 expression beadchip

Description

Genome-wide analysis of gene expression in response to bortezomib treatment(33 nM) in cell lines before and after selection for resistance.

Publication Title

Profiling bortezomib resistance identifies secondary therapies in a mouse myeloma model.

Sample Metadata Fields

Specimen part, Cell line, Time

View Samples
accession-icon GSE134026
Establishing hematopoietic stem cell gene therapy for breast cancer brain metastases using intratumoral myeloid cell-specific gene promoters
  • organism-icon Mus musculus
  • sample-icon 14 Downloadable Samples
  • Technology Badge IconIllumina MouseWG-6 v2.0 expression beadchip

Description

The goal was to identify genes that are differentially expressed between the bone marrow-derived CD11b+ myeloid cells infiltrating intracranial tumors and the peripheral myeloid cells (e.g. infiltrating the spleen and bone marrow).

Publication Title

Hematopoietic Stem Cell Gene Therapy for Brain Metastases Using Myeloid Cell-Specific Gene Promoters.

Sample Metadata Fields

Age, Specimen part

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accession-icon GSE23895
Selenium toxicity but not deficient or super-nutritional selenium status vastly alters the transcriptome in rodents
  • organism-icon Mus musculus, Rattus norvegicus
  • sample-icon 36 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Genome 430 2.0 Array (mouse4302)

Description

Protein and mRNA levels for several selenoproteins, such as glutathione peroxidase-1 (Gpx1), are down-regulated dramatically by selenium (Se) deficiency.

Publication Title

Selenium toxicity but not deficient or super-nutritional selenium status vastly alters the transcriptome in rodents.

Sample Metadata Fields

Specimen part, Treatment

View Samples
accession-icon SRP045088
RNAseq analysis of the global bovine retinal transcriptome
  • organism-icon Bos taurus
  • sample-icon 3 Downloadable Samples
  • Technology Badge IconIllumina HiScanSQ

Description

We report RNAseq analysis of the transcriptome of 3 biological replicates of bovine retina Overall design: Examine retinal transcriptome of 3 biological replicates with tissue collected between 7:00 - 10:00AM

Publication Title

Argonaute high-throughput sequencing of RNAs isolated by cross-linking immunoprecipitation reveals a snapshot of miRNA gene regulation in the mammalian retina.

Sample Metadata Fields

Specimen part, Cell line, Subject

View Samples
accession-icon GSE54011
C. Elegans expression: toxic vs. adequate vs. low selenium
  • organism-icon Caenorhabditis elegans
  • sample-icon 5 Downloadable Samples
  • Technology Badge Icon Affymetrix C. elegans Genome Array (celegans)

Description

Genome-wide expression analysis in C. Elegans grown in axenic media with low to toxic selenium concentrations

Publication Title

Toxic-selenium and low-selenium transcriptomes in Caenorhabditis elegans: toxic selenium up-regulates oxidoreductase and down-regulates cuticle-associated genes.

Sample Metadata Fields

No sample metadata fields

View Samples
accession-icon GSE85987
Inhibition of endothelial Notch signaling attenuates inflammation
  • organism-icon Mus musculus, Homo sapiens
  • sample-icon 44 Downloadable Samples
  • Technology Badge IconIllumina HumanHT-12 V4.0 expression beadchip, Affymetrix Mouse Gene 2.1 ST Array (mogene21st)

Description

This SuperSeries is composed of the SubSeries listed below.

Publication Title

Inhibition of Endothelial NOTCH1 Signaling Attenuates Inflammation by Reducing Cytokine-Mediated Histone Acetylation at Inflammatory Enhancers.

Sample Metadata Fields

Specimen part

View Samples
accession-icon GSE85992
Gene expression data from endothelial cells isolated from DNFB-treated ears of mice with inducible endothelial-specific overexpression of constitutively active Notch1 intracellular domain
  • organism-icon Mus musculus
  • sample-icon 20 Downloadable Samples
  • Technology Badge IconIllumina HumanHT-12 V4.0 expression beadchip, Affymetrix Mouse Gene 2.1 ST Array (mogene21st)

Description

Notch1 is a key regulator of endothelial cell behaviour. This experiment was designed to identify genes regulated by Notch1 signaling in inflammatory activated mouse endothelial cells.

Publication Title

Inhibition of Endothelial NOTCH1 Signaling Attenuates Inflammation by Reducing Cytokine-Mediated Histone Acetylation at Inflammatory Enhancers.

Sample Metadata Fields

Specimen part

View Samples
accession-icon GSE39180
Genes regulated/modulated by jagged1 in endothelial cells during inflammation
  • organism-icon Homo sapiens
  • sample-icon 12 Downloadable Samples
  • Technology Badge IconIllumina HumanHT-12 V4.0 expression beadchip

Description

Proinflammatory activation of endothelial cells leads to recruitment of leukocytes by upregulation of adhesion molecules and presentation of chemoattractants. In response to such activation there is also a strong shift in the endothelial expression of Notch ligands, with downregulation of Dll4 and a upregulation of JAG1. To assess whether Jagged1 would affect the endothelial activation profile, we suppressed JAG1 expression during IL-1-induced activation by means of siRNA and performed a genome-wide transcriptome analysis. Our results show for the first time that Jagged1 modulates the transcription profile of activated endothelial cells and describe data that imply a role for Jagged1 in sharpening the inflammatory profile of the vasculature, giving it an edge towards leukocyte recruitment. These findings imply that Jagged1 might be a potential therapeutic target to attenuate inflammation and reduce tissue damage in inflammatory diseases.

Publication Title

Inhibition of Endothelial NOTCH1 Signaling Attenuates Inflammation by Reducing Cytokine-Mediated Histone Acetylation at Inflammatory Enhancers.

Sample Metadata Fields

Specimen part

View Samples
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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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