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accession-icon GSE68454
Systems analysis of uterine and tumor microenvironments
  • organism-icon Mus musculus
  • sample-icon 63 Downloadable Samples
  • Technology Badge IconIllumina MouseWG-6 v2.0 expression beadchip

Description

This SuperSeries is composed of the SubSeries listed below.

Publication Title

Regulatory T Cells Orchestrate Similar Immune Evasion of Fetuses and Tumors in Mice.

Sample Metadata Fields

Age, Specimen part

View Samples
accession-icon GSE68433
Systems analysis of uterine microenvironment 4, 6, 8, 10, 11 or 12 days after fertilization
  • organism-icon Mus musculus
  • sample-icon 33 Downloadable Samples
  • Technology Badge IconIllumina MouseWG-6 v2.0 expression beadchip

Description

Analysis of uterine microenvironment at gene expression level. The hypothesis tested in the present study was that Tregs orchestrated the immune reponse triggered in presence of embryo

Publication Title

Regulatory T Cells Orchestrate Similar Immune Evasion of Fetuses and Tumors in Mice.

Sample Metadata Fields

Age, Specimen part

View Samples
accession-icon GSE68434
Systems analysis of B16 tumor microenvironment 4 or 14 days after tumor inoculation
  • organism-icon Mus musculus
  • sample-icon 16 Downloadable Samples
  • Technology Badge IconIllumina MouseWG-6 v2.0 expression beadchip

Description

Analysis of B16 tumor microenvironment at gene expression level. The hypothesis tested in the present study was that Tregs orchastrated the immune reponse triggered in presence of tumors

Publication Title

Regulatory T Cells Orchestrate Similar Immune Evasion of Fetuses and Tumors in Mice.

Sample Metadata Fields

Age, Specimen part

View Samples
accession-icon GSE68432
Systems analysis of uterine microenvironment in Treg depleted pregnant mice at 12 days after fertilization
  • organism-icon Mus musculus
  • sample-icon 14 Downloadable Samples
  • Technology Badge IconIllumina MouseWG-6 v2.0 expression beadchip

Description

Analysis of uterine microenvironment at gene expression level. The hypothesis tested in the present study was that Tregs orchestrated the immune reponse triggered in presence of embryo.

Publication Title

Regulatory T Cells Orchestrate Similar Immune Evasion of Fetuses and Tumors in Mice.

Sample Metadata Fields

Age, Specimen part

View Samples
accession-icon GSE67088
Vemurafenib resistance selects for highly malignant brain and lung-metastasizing melanoma cells
  • organism-icon Homo sapiens
  • sample-icon 6 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Transcriptome Array 2.0 (hta20)

Description

V600E being the most common mutation in BRAF, leads to constitutive activation of the MAPK signaling pathway. The majority of V600E BRAF positive melanoma patients treated with the BRAF inhibitor vemurafenib showed initial good clinical responses but relapsed due to acquired resistance to the drug. The aim of the present study was to identify possible biomarkers associated with the emergence of drug resistant melanoma cells. To this end we analyzed the differential gene expression of vemurafenib-sensitive and vemurafenib resistant brain and lung metastasizing melanoma cells.

Publication Title

Vemurafenib resistance selects for highly malignant brain and lung-metastasizing melanoma cells.

Sample Metadata Fields

Specimen part, Treatment

View Samples
accession-icon GSE83716
Interferon protects primary macrophages against HIV infection
  • organism-icon Homo sapiens
  • sample-icon 6 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Gene 2.0 ST Array (hugene20st)

Description

Interferon (IFN) is a unique type I IFN that is not induced by pattern-recognition response elements. IFN is constitutively expressed in mucosal tissues including the female genital mucosa. We show here that IFN induces an antiviral state in human macrophages that blocks HIV-1 replication.

Publication Title

IFN-<b>ε</b> protects primary macrophages against HIV infection.

Sample Metadata Fields

Specimen part, Treatment, Time

View Samples
accession-icon GSE64420
Multi-level omics analysis of dystrophin loss and therapeutic restoration in a murine model
  • organism-icon Mus musculus
  • sample-icon 22 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Gene 1.1 ST Array (mogene11st)

Description

This SuperSeries is composed of the SubSeries listed below.

Publication Title

Multi-level omics analysis in a murine model of dystrophin loss and therapeutic restoration.

Sample Metadata Fields

Specimen part, Treatment

View Samples
accession-icon GSE64418
Multi-level omics analysis of gene expression in a murine model of dystrophin loss and therapeutic restoration [mRNA]
  • organism-icon Mus musculus
  • sample-icon 11 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Gene 1.1 ST Array (mogene11st)

Description

Duchenne muscular dystrophy (DMD) is a classical monogenic disorder, a model disease for genomic studies and a priority candidate for regenerative medicine and gene therapy. Although the genetic cause of DMD is well known, the molecular pathogenesis of disease and the response to therapy are incompletely understood. Here,we describe analyses of protein, mRNA and microRNA expression in the tibialis anterior of the mdx mouse model of DMD. Notably, 3272 proteins were quantifiable and 525 identified as differentially expressed in mdx muscle (P < 0.01). Therapeutic restoration of dystrophin by exon skipping induced widespread shifts in protein and mRNA expression towards wild-type expression levels, whereas the miRNome was largely unaffected. Comparison analyses between datasets showed that protein and mRNA ratios were only weakly correlated (r = 0.405), and identified a multitude of differentially affected cellular pathways, upstream regulators and predicted miRNAtarget interactions. This study provides fundamental new insights into gene expression and regulation in dystrophic muscle.

Publication Title

Multi-level omics analysis in a murine model of dystrophin loss and therapeutic restoration.

Sample Metadata Fields

Specimen part, Treatment

View Samples
accession-icon GSE16838
Expression data from MDA-MB-231 reference and in vitro-derived subpopulations with distinct invasive potentials
  • organism-icon Homo sapiens
  • sample-icon 8 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Gene 1.0 ST Array (hugene10st)

Description

To understand the link between invasion behavior and the steps of metastasis formation, we isolated invasive subpopulations from MDA-MB-231 cells in vitro using matrigel coated boyden chambers. Whole genome transcriptional profiling was used to characterize the expression changes uniquely related to invasive abilities of these cells.

Publication Title

Invading basement membrane matrix is sufficient for MDA-MB-231 breast cancer cells to develop a stable in vivo metastatic phenotype.

Sample Metadata Fields

Cell line

View Samples
accession-icon GSE2196
PDGF induction of immediate early genes in NIH3T3 cells
  • organism-icon Mus musculus
  • sample-icon 17 Downloadable Samples
  • Technology Badge Icon Affymetrix Murine Genome U74A Version 2 Array (mgu74av2)

Description

This experiment was performed to identify immediate early genes that were induced by PDGF specifically through Src family kinases (SFKs), MEK1/2, or PI 3-K.

Publication Title

Platelet-derived growth factor stimulates Src-dependent mRNA stabilization of specific early genes in fibroblasts.

Sample Metadata Fields

No sample metadata fields

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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