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accession-icon GSE16158
Gene expression induced by trace fear conditioning in murine hippocampus
  • organism-icon Mus musculus
  • sample-icon 12 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Genome 430A 2.0 Array (mouse430a2)

Description

Gene expression profiling following different learning paradigms may help in defining the moleular pathways of memory formation. In this study we analyzed the gene expression pattern of murine hippocampus at different time points (0.5 h, 2h, 6h) after trace fear conditioning. We compared trained mice with naive mice that remained in their homecages.

Publication Title

Temporal gene expression profile of the hippocampus following trace fear conditioning.

Sample Metadata Fields

Sex, Specimen part

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accession-icon GSE32974
Cyclin-dependent kinases are regulators and effectors of oscillations driven by a transcription factor network
  • organism-icon Saccharomyces cerevisiae
  • sample-icon 33 Downloadable Samples
  • Technology Badge Icon Affymetrix Yeast Genome 2.0 Array (yeast2)

Description

Yeast cell cycle transcription dynamics in two S. cerevisae strains grown at 37C: BF264-15DU (MATa ade1 his2 leu2-3, 112 trp1-1 ura3Dns, bar1) (wild type) and a mutant of the wild type strain lacking all Cdk1 activity, cdc28-4.

Publication Title

Cyclin-dependent kinases are regulators and effectors of oscillations driven by a transcription factor network.

Sample Metadata Fields

Time

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accession-icon GSE58095
Dissecting the heterogeneity of skin gene expression patterns in systemic sclerosis.
  • organism-icon Homo sapiens
  • sample-icon 59 Downloadable Samples
  • Technology Badge IconIllumina HumanHT-12 V4.0 expression beadchip

Description

We identified fibro-inflammatory and keratin gene expression signatures in systemic sclerosis skin.

Publication Title

Dissecting the heterogeneity of skin gene expression patterns in systemic sclerosis.

Sample Metadata Fields

Age, Specimen part, Race, Subject, Time

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accession-icon GSE47162
Skin gene expression correlates of severity of interstitial lung disease in systemic sclerosis
  • organism-icon Homo sapiens
  • sample-icon 59 Downloadable Samples
  • Technology Badge IconIllumina HumanHT-12 V4.0 expression beadchip

Description

We identified eighty two skin transcripts significantly correlated with the severity of interstitial lung disease (ILD) in systemic sclerosis.

Publication Title

Skin gene expression correlates of severity of interstitial lung disease in systemic sclerosis.

Sample Metadata Fields

Age, Specimen part, Race, Subject

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accession-icon GSE86605
Brassinosteroids participate in the control of basal and acquired freezing tolerance of plants
  • organism-icon Arabidopsis thaliana
  • sample-icon 31 Downloadable Samples
  • Technology Badge Icon Arabidopsis Gene 1.1 ST Array (aragene11st)

Description

Brassinosteroids (BRs) are growth-promoting plant hormones that play a role in abiotic stress responses, but molecular modes that enable this activity remain largely unknown. Here we show that BRs participate in the regulation of freezing tolerance. BR signaling-defective mutants of Arabidopsis thaliana were hypersensitive to freezing before and after cold acclimation. The constitutive activation of BR signaling, in contrast, enhanced freezing resistance. Evidence is provided that the BR-controlled basic helixloophelix transcription factor CESTA (CES) can contribute to the constitutive expression of the C-REPEAT/DEHYDRATION-RESPONSIVE ELEMENT BINDING FACTOR (CBF) transcriptional regulators that control cold responsive (COR) gene expression. In addition, CBF-independent classes of BR-regulated COR genes are identified that are regulated in a BR- and CES-dependent manner during cold acclimation. A model is presented in which BRs govern different cold-responsive transcriptional cascades through the posttranslational modification of CES and redundantly acting factors. This contributes to the basal resistance against freezing stress, but also to the further improvement of this resistance through cold acclimation.

Publication Title

Brassinosteroids participate in the control of basal and acquired freezing tolerance of plants.

Sample Metadata Fields

Age, Specimen part, Treatment

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accession-icon SRP062555
Global analysis of pre-mRNA subcellular localization upon splicing inhibition by spliceostatin A
  • organism-icon Homo sapiens
  • sample-icon 12 Downloadable Samples
  • Technology Badge IconIlluminaHiSeq2000

Description

RNA-Seq analysis of SSA treated cells Overall design: HeLa cells, nuclear and cytoplasmic fractions, treated with SSA or MeOH

Publication Title

Global analysis of pre-mRNA subcellular localization following splicing inhibition by spliceostatin A.

Sample Metadata Fields

No sample metadata fields

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accession-icon GSE85756
BPTF Depletion Enhances NK Cell Mediated Antitumor Immunity
  • organism-icon Mus musculus
  • sample-icon 36 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Genome 430A 2.0 Array (mouse430a2)

Description

In mouse models, the bromodomain PHD finger transcription factor (BPTF) chromatin remodeling subunit in tumor cells suppresses natural killer (NK) cell antitumor activity.

Publication Title

BPTF Depletion Enhances T-cell-Mediated Antitumor Immunity.

Sample Metadata Fields

Specimen part, Cell line

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accession-icon GSE71864
Increased antigenicity of NURF-depleted tumors enhances CD8 T cell-mediated antitumor immunity
  • organism-icon Mus musculus
  • sample-icon 6 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Genome 430A 2.0 Array (mouse430a2)

Description

Depleting the NURF chromatin remodeling complex results in enhanced antitumor immunity using mouse tumor models syngenic to two strain backgrounds.

Publication Title

BPTF Depletion Enhances T-cell-Mediated Antitumor Immunity.

Sample Metadata Fields

Specimen part

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accession-icon SRP080962
Hepatic differentiation of liver organoids
  • organism-icon Homo sapiens
  • sample-icon 29 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2500

Description

We analyzed gene expression profiles of self-organizing, multi-cellular, 3D liver organoids derived by co-culture of induced Pluripotent Stem Cell and stromal progenitors. We report the RNA-seq results of liver organoid at day0, day2, day4, day6 of co-culture. We also report RNA-seq results of constituent of the liver organoid, which are human iPSC at hepatic specification stage, human Mesenchymal stem cells derived from bone marrow, human umbilical vein endothelial cell. As controls, we also report RNS-seq results of un-differentiated human iPSC, human iPSC at definitive endoderm stage, human liver tissue, and primary cultured human hepatocytes isolated from unused donor livers. Overall design: mRNA profiles of liver organoids and their constituents were generated by deep sequencing, in triplicate, using Illumina HiSeq 2500.

Publication Title

Paracrine signals regulate human liver organoid maturation from induced pluripotent stem cells.

Sample Metadata Fields

Subject, Time

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accession-icon GSE25557
Characterization of Definitive Endoderm formation from HESC and iPSC lines by Microarray analysis
  • organism-icon Homo sapiens
  • sample-icon 23 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Gene 1.0 ST Array (hugene10st)

Description

HESC-H9 and iPSC lines 3.5, 3.6 and 3.12 were analyzed using Affymetrix microarray before and after Definitive Endoderm (DE) formation. DE was induced using the ActivinA differentiation protocol described by D'Amour et al., 2006 (PMID: 16258519) Clustering analysis of transcripts that were differentially regulated during DE formation indicated that iPSC lines 3.5 and 3.12 differentiate in manner that is highly similar to HESC-H9 cells iPSC line 3.6 had a more divergent transcriptional profile.

Publication Title

Directed differentiation of human pluripotent stem cells into intestinal tissue in vitro.

Sample Metadata Fields

No sample metadata fields

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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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