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accession-icon GSE87030
Nipple fibroblast gene expression profile
  • organism-icon Mus musculus
  • sample-icon 6 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Gene 2.0 ST Array (mogene20st)

Description

The nipple is an example of specialized epidermis. The unique epidermal stratification and gene expression is induced and maintained by developmental distinct fibroblast populations.

Publication Title

Estrogen modulates mesenchyme-epidermis interactions in the adult nipple.

Sample Metadata Fields

Sex, Specimen part

View Samples
accession-icon GSE48334
The effect of Rapamycin on the transcriptome of old mouse liver
  • organism-icon Mus musculus
  • sample-icon 111 Downloadable Samples
  • Technology Badge IconIllumina MouseRef-8 v2.0 expression beadchip

Description

This SuperSeries is composed of the SubSeries listed below.

Publication Title

Mice fed rapamycin have an increase in lifespan associated with major changes in the liver transcriptome.

Sample Metadata Fields

Sex, Age, Specimen part, Treatment

View Samples
accession-icon GSE48333
The effect of chronic Rapamycin on the transcriptome of old mouse liver
  • organism-icon Mus musculus
  • sample-icon 69 Downloadable Samples
  • Technology Badge IconIllumina MouseRef-8 v2.0 expression beadchip

Description

Analysis of the effect of gene expression in the livers of old mice (25 months of age) fed rapamycin chronically (21 months) from 4 months of age.

Publication Title

Mice fed rapamycin have an increase in lifespan associated with major changes in the liver transcriptome.

Sample Metadata Fields

Sex, Age, Specimen part, Treatment

View Samples
accession-icon GSE48331
The effect of short term Rapamycin on the transcriptome of old mouse liver
  • organism-icon Mus musculus
  • sample-icon 42 Downloadable Samples
  • Technology Badge IconIllumina MouseRef-8 v2.0 expression beadchip

Description

Analysis of the effect of gene expression in the livers of old mice (25 months of age) fed rapamycin short term (6 months) Rapamycin from 19 months of age.

Publication Title

Mice fed rapamycin have an increase in lifespan associated with major changes in the liver transcriptome.

Sample Metadata Fields

Sex, Age, Specimen part, Treatment

View Samples
accession-icon GSE40972
EZH2 Inhibition as a Therapeutic Strategy for Lymphoma with EZH2 Activating Mutations
  • organism-icon Homo sapiens
  • sample-icon 43 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U133 Plus 2.0 Array (hgu133plus2)

Description

This SuperSeries is composed of the SubSeries listed below.

Publication Title

EZH2 inhibition as a therapeutic strategy for lymphoma with EZH2-activating mutations.

Sample Metadata Fields

Specimen part, Cell line, Treatment

View Samples
accession-icon GSE40971
Gene expression profiling of EZH2 mutant and wild type DLBCL cell lines treated with EZH2 inhibitor
  • organism-icon Homo sapiens
  • sample-icon 37 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U133 Plus 2.0 Array (hgu133plus2)

Description

We studied transcriptional changes by Affymetrix human microarrays in DLBCL cell lines as a result of treatment with GSK126, a potent, highly-selective, SAM-competitive, small molecule inhibitor of EZH2

Publication Title

EZH2 inhibition as a therapeutic strategy for lymphoma with EZH2-activating mutations.

Sample Metadata Fields

Specimen part, Cell line, Treatment

View Samples
accession-icon GSE41239
Gene expression profiling of two DLBCL cell lines upon shRNA mediated knockdown of EZH2
  • organism-icon Homo sapiens
  • sample-icon 6 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U133 Plus 2.0 Array (hgu133plus2)

Description

We studied transcriptional changes by Affymetrix human microarrays in 2 DLBCL cell lines as a result of shRNA mediated knockdown of EZH2.

Publication Title

EZH2 inhibition as a therapeutic strategy for lymphoma with EZH2-activating mutations.

Sample Metadata Fields

Specimen part, Cell line, Treatment

View Samples
accession-icon SRP055874
Defective structural RNA processing in relapsing-remitting multiple sclerosis
  • organism-icon Homo sapiens
  • sample-icon 14 Downloadable Samples
  • Technology Badge IconIlluminaHiSeq2500

Description

It is fundamentally unknown how normal cellular processes or responses to extracellular stimuli may invoke polyadenylation and degradation of ncRNA substrates or if human disease processes exhibit defects in polyadenylation of ncRNA substrates as part of their pathogenesis. Our results demonstrate that mononuclear cells from subjects with relapsing-remitting multiple sclerosis (RRMS) exhibit pervasive increases in levels of polyadenylated ncRNAs including Y1 RNA, 18S and 28S rRNA, and U1, U2, and U4 snRNAs and these defects are unique to RRMS. Defects in expression of both Ro60 and La proteins in RRMS appear to contribute to increased polyadenylation of ncRNAs. Further, IFN-ß1b, a common RRMS therapy, restores both Ro60 and La levels to normal as well as levels of polyadenylated Y1 RNA and U1 snRNA suggesting that aberrant polyadenylation of ncRNA substrates may have pathogenic consequences. Overall design: We extracted RNA from peripheral whole blood in healthy control subjects and patients with established relapsing-remitting multiple sclerosis using PaxGene tubes.

Publication Title

Defective structural RNA processing in relapsing-remitting multiple sclerosis.

Sample Metadata Fields

No sample metadata fields

View Samples
accession-icon SRP055474
Expression and functions of long noncoding RNAs during human T helper cell differentiation
  • organism-icon Homo sapiens
  • sample-icon 12 Downloadable Samples
  • Technology Badge IconIlluminaHiSeq2500

Description

To improve our understanding of lncRNA expression in T cells, we used whole genome sequencing (RNA-seq) to identify lncRNAs expressed in human T cells and those selectively expressed in T cells differentiated under TH1, TH2, or TH17 polarizing conditions. The majority of these lineage-specific lncRNAs are co-expressed with lineage-specific protein-coding genes. These lncRNAs are predominantly intragenic with co-expressed protein-coding genes and are transcribed in sense and antisense orientations with approximately equal frequencies. Further, genes encoding TH lineage specific mRNAs are not randomly distributed across the genome but are highly enriched in the genome in genomic regions also containing genes encoding TH lineage-specific lncRNAs. Our analyses also identify a cluster of antisense lncRNAs transcribed from the RAD50 locus that are selectively expressed under TH2 polarizing conditions and co-expressed with IL4, IL5 and IL13 genes. Depletion of these lncRNAs via selective siRNA treatment demonstrates the critical requirement of these lncRNAs for expression of the TH2 cytokines, IL-4, IL-5 and IL-13. Collectively, our analyses identify new lncRNAs expressed in a TH lineage specific manner and identify a critical role for a cluster of lncRNAs for expression of genes encoding TH2 cytokines. Overall design: Human peripheral blood mononuclear cells (PBMC) were cultured under TH1, TH2, and TH17 polarizing conditions. TH1, TH2, and TH17 primary and effector cultures were isolated and poly(A)+ and total RNA sequencing performed.

Publication Title

Expression and functions of long noncoding RNAs during human T helper cell differentiation.

Sample Metadata Fields

No sample metadata fields

View Samples
accession-icon GSE41220
Gene expression data from cultured cortical neurons.
  • organism-icon Mus musculus
  • sample-icon 6 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Gene 1.0 ST Array (mogene10st)

Description

We used Affymetrix DNA arrays to investigate the extent to which nuclear HDAC4 accumulation affects neuronal gene expression.

Publication Title

HDAC4 governs a transcriptional program essential for synaptic plasticity and memory.

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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