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accession-icon GSE23845
Time course for bladder UCC development in UPII-SV40Tag mice
  • organism-icon Mus musculus
  • sample-icon 15 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Genome 430 2.0 Array (mouse4302)

Description

We have identified genes that are differentially expressed between the bladders of UPII-SV40Tag mice and their age-matched wild-type littermates at 3, 6, 20, and 30 weeks of age. These are ages that correspond to premalignant, carcinoma in situ, and early-stage and later stage invasive UCC, respectively

Publication Title

Identification of genes correlated with early-stage bladder cancer progression.

Sample Metadata Fields

Specimen part

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accession-icon SRP093643
Allelic expression in tibial growth plates from 21 day old C57BL/6J x CAST/EiJ F1s
  • organism-icon Mus musculus
  • sample-icon 28 Downloadable Samples
  • Technology Badge IconNextSeq 500

Description

We have identified candidate genes from the Feml2 QTL influencing femur length through allele specific expression analysis of growth plates in C57BL/6J x CAST/EiJ F1 hybrids. This work provides the foundation to identify novel genes affecting bone geometry. Overall design: total RNA sequencing in 7 male C57BL/6JxCAST F1s

Publication Title

Genetic Dissection of a QTL Affecting Bone Geometry.

Sample Metadata Fields

Sex, Age, Specimen part, Cell line, Subject

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accession-icon GSE41146
Expression data from uninfected and VSV-infected Drosophila cells at 4 hours post-infection
  • organism-icon Drosophila melanogaster
  • sample-icon 3 Downloadable Samples
  • Technology Badge Icon Affymetrix Drosophila Genome 2.0 Array (drosophila2)

Description

Expression profiling of rapidly-induced genes upon VSV infection at 4 hours post-infection in Drosophila cells

Publication Title

Transcriptional pausing controls a rapid antiviral innate immune response in Drosophila.

Sample Metadata Fields

Cell line

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accession-icon GSE41242
Global analysis of Cdk9-dependence for VSV-induced genes in Drosophila cells
  • organism-icon Drosophila melanogaster
  • sample-icon 3 Downloadable Samples
  • Technology Badge Icon Affymetrix Drosophila Genome 2.0 Array (drosophila2)

Description

To determine the Cdk9 targets of VSV-induced genes in Drosophila cells at 4 hours post-infection

Publication Title

Transcriptional pausing controls a rapid antiviral innate immune response in Drosophila.

Sample Metadata Fields

Cell line, Treatment

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accession-icon GSE31049
Circadian temporal profiling of MMH-D3 hepatocytes
  • organism-icon Mus musculus
  • sample-icon 22 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Genome 430 2.0 Array (mouse4302)

Description

The circadian clock generates daily rhythms in mammalian liver processes, such as glucose and lipid homeostasis, xenobiotic metabolism, and regeneration. The mechanisms governing these rhythms are not well understood, particularly the distinct contributions of the cell-autonomous clock and central pacemaker to rhythmic liver physiology. Through microarray expression profiling in MMH-D3 hepatocytes, we identified over 1,000 transcripts that exhibit circadian oscillations, demonstrating that many rhythms can be driven by the cell-autonomous clock and that MMH-D3 is a valid circadian model system. The genes represented by these circadian transcripts displayed both co-phasic and anti-phasic organization within a protein-protein interaction network, suggesting the existence of competition for binding sites or partners by genes of disparate transcriptional phases. Multiple pathways displayed enrichment in MMH-D3 circadian transcripts, including the polyamine synthesis module of the glutathione metabolic pathway. The polyamine synthesis module, which is highly associated with cell proliferation and whose products are required for initiation of liver regeneration, includes enzymes whose transcripts exhibit circadian oscillations, such as ornithine decarboxylase (Odc1) and spermidine synthase (Srm). Metabolic profiling revealed that the enzymatic product of SRM, spermidine, cycles as well. Thus, the cell-autonomous hepatocyte clock can drive a significant amount of transcriptional rhythms and orchestrate physiologically relevant modules such as polyamine synthesis.

Publication Title

Cell-autonomous circadian clock of hepatocytes drives rhythms in transcription and polyamine synthesis.

Sample Metadata Fields

Specimen part, Cell line

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accession-icon GSE32564
Genes affected upon dsRNA knockdown treatment for nbr/CG9247 in Drosophila DL1 cells and small RNA profiling in Drosophila wild-type and nbr[f02257] mutants
  • organism-icon Drosophila melanogaster
  • sample-icon 10 Downloadable Samples
  • Technology Badge Icon Affymetrix Drosophila Genome 2.0 Array (drosophila2)

Description

This SuperSeries is composed of the SubSeries listed below.

Publication Title

The exoribonuclease Nibbler controls 3' end processing of microRNAs in Drosophila.

Sample Metadata Fields

Sex, Specimen part

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accession-icon GSE32683
Genes affected upon dsRNA knockdown treatment for nbr/CG9247 in Drosophila DL1 cells
  • organism-icon Drosophila melanogaster
  • sample-icon 10 Downloadable Samples
  • Technology Badge Icon Affymetrix Drosophila Genome 2.0 Array (drosophila2)

Description

nbr/CG9247 gene function regulates the length of the 3'end of miRNAs.

Publication Title

The exoribonuclease Nibbler controls 3' end processing of microRNAs in Drosophila.

Sample Metadata Fields

No sample metadata fields

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accession-icon SRP008774
Small RNA profiling in Drosophila wild-type and nbr[f02257] mutants
  • organism-icon Drosophila melanogaster
  • sample-icon 2 Downloadable Samples
  • Technology Badge IconIllumina Genome Analyzer

Description

nbr/CG9247 gene regulates 3''end heterogeneity of a subset of miRNAs. It is not clear how broad this effect is on small RNA population. To address this, we compared small RNA population in wild-type and tmr[f02257] mutants. This approach identified more miRNAs whose 3''end heterogeneity was affected in nbr[f02257] mutants. Overall design: 2-3 day old control (w homogeneous strain Bloomington stock center 5905) and nbr[f02257] null mutant flies were collected. nbr[f02257] line was in the homogenous (Bloomington stock center stock 5905) background through a minimum of 5 backcrosses. Total RNA from whole flies was extracted using TRIzol reagent (Invitrogen). 40ug of total RNA from each genotype was used for small RNA library preparation with Small RNA Sample Prep kit (v1.5) (Illumina).

Publication Title

The exoribonuclease Nibbler controls 3' end processing of microRNAs in Drosophila.

Sample Metadata Fields

Sex, Specimen part, Subject

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accession-icon GSE14002
J82 human bladder cell line treated with frankincense oil
  • organism-icon Homo sapiens
  • sample-icon 5 Downloadable Samples
  • Technology Badge IconIllumina HumanRef-8 v3.0 expression beadchip

Description

Frankincense oil is prepared from aromatic hardened wood resin obtained by tapping Boswellia trees. For thousands of years, it has been important both socially and economically as an ingredient in incense and perfumes. Frankincense oil is a botanical oil distillate made from fermented plants that contains boswellic acid, a component known to have anti-neoplastic properties. We evaluated frankincense oil-induced cytotoxicity in bladder cancer cells. With a window of concentration, frankincense oil suppressed cell viability and induced cytotoxicity in bladder transitional carcinoma J82 cells but not normal bladder urothelial UROtsa cells immortalized with SV40 large T antigen. However, frankincense oil-induced J82 cell death did not result in DNA fragmentation. Microarray and bioinformatics analysis confirmed that frankincense oil activated cell cycle arrest, suppressed cell proliferation, and activated apoptosis in J82 cells through a series of potential pathways. These finding suggest that bladder cancer can be treated through intravesical administration of pharmaceutical agents similar to direct application on melanoma.

Publication Title

Frankincense oil derived from Boswellia carteri induces tumor cell specific cytotoxicity.

Sample Metadata Fields

No sample metadata fields

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accession-icon SRP017617
High throughput sequencing of small RNAs from Drosophila cells infected with a panel of viruses
  • organism-icon Drosophila melanogaster
  • sample-icon 25 Downloadable Samples
  • Technology Badge IconIllumina Genome Analyzer II

Description

We report the cloning and sequencing of both endogenous small RNAs and virus-derived siRNAs produced by the antiviral RNAi pathway in Drosophila. We find that a diverse panel of viruses are targeted by the RNAi pathway in Drosophila to produce abundant virus-derived siRNAs, and these siRNAs map to various locations within the viral genomes. Knockdown of various RNAi and miRNA pathway components alters the levels of these viral small RNAs. Overall design: Drosophila DL1 cells were treated with dsRNA for 3 days to deplete factors involved in the antiviral RNAi pathway and miRNA pathway, then were challenged with one of four viruses for 4 days. Total RNA was collected, and the small RNA populations from 15-29 nt were cloned and sequenced.

Publication Title

RNase III nucleases from diverse kingdoms serve as antiviral effectors.

Sample Metadata Fields

Cell line, 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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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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