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accession-icon GSE109007
LincK promotes proliferation and epithelial-to-mesenchymal transition and contributes to tumorigenesis and growth in breast cancer I
  • organism-icon Homo sapiens
  • sample-icon 5 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Gene 2.0 ST Array (hugene20st)

Description

In this study, we aimed to identify potential lncRNA deregulations associated with breast cancer malignancy instigated by MSCs-MCF7 co-culture. We profiled expression changes of lncRNAs in MCF-7 cells during EMT induced by coculture with hAD-MSCs, and found an intergenic lncRNA with proviouly unknown function (KB-1732A1.1, we termed it LincK), which was significantly elevated. Depletion of LincK decreased the growth, migration, invasion, and EMT in breast cancer cells, while overexpression of LincK exerted the opposite effects. Moreover, knockdown of LincK repressed tumorigenesis, and ectopic expression of LincK promoted tumor growth in MCF-7 xenograft model. LincKs can act as a sponge of mirR-200b, which inhibits its function in proliferation and metastasis. Thus we reported, for the rst time, the role of LincK in control of EMT and proliferation in breast cancer.

Publication Title

LincK contributes to breast tumorigenesis by promoting proliferation and epithelial-to-mesenchymal transition.

Alternate Accession IDs

E-GEOD-109007

Sample Metadata Fields

Cell line

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accession-icon GSE148456
Analysis of differentially expressed genes between circZbtb20+/+ and circZbtb20-/- ILC3s or between Nr4a1+/+ and Nr4a1-/- ILC3s
  • organism-icon Mus musculus
  • sample-icon 4 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Clariom S Array (clariomsmouse)

Description

Investigation of differentially expressed genes in circZbtb20 or Nr4a1 deficient ILC3s

Publication Title

No associated publication

Alternate Accession IDs

E-GEOD-148456

Sample Metadata Fields

No sample metadata fields

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accession-icon GSE106809
Expression analysis of control and Ccp6-depleted D3 ESCs
  • organism-icon Mus musculus
  • sample-icon 2 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Gene 2.0 ST Array (mogene20st)

Description

Investigation of differentially expressed genes in Ccp6-depleted D3 ESCs

Publication Title

No associated publication

Alternate Accession IDs

E-GEOD-106809

Sample Metadata Fields

No sample metadata fields

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accession-icon GSE97487
Expression analysis of Wild-type and Ccp2-deficient CHILPs
  • organism-icon Mus musculus
  • sample-icon 2 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Gene 2.0 ST Array (mogene20st)

Description

Investigation of differentially expressed genes in Ccp2-deficient CHILPs

Publication Title

IL-7Rα glutamylation and activation of transcription factor Sall3 promote group 3 ILC development.

Alternate Accession IDs

E-GEOD-97487

Sample Metadata Fields

No sample metadata fields

View Samples
accession-icon GSE142766
Expression analysis of Wild-type and circKcnt2-deficient ILC3s from DSS-treated mice
  • organism-icon Mus musculus
  • sample-icon 2 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Clariom S Array (clariomsmouse)

Description

Investigation of differentially expressed genes in circKcnt2-deficient ILC3s

Publication Title

No associated publication

Alternate Accession IDs

E-GEOD-142766

Sample Metadata Fields

No sample metadata fields

View Samples
accession-icon GSE59867
Gene expression profiling reveals potential prognostic biomarkers associated with the progression of heart failure
  • organism-icon Homo sapiens
  • sample-icon 436 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Gene 1.0 ST Array (hugene10st)

Description

Heart failure (HF) is the most common cause of morbidity and mortality in the developed countries, especially considering the present demographic tendencies in those populations.

Publication Title

Gene expression profiling reveals potential prognostic biomarkers associated with the progression of heart failure.

Alternate Accession IDs

E-GEOD-59867

Sample Metadata Fields

Specimen part

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accession-icon GSE62646
Altered gene expression pattern in peripheral blood mononuclear cells in patients with acute myocardial infarction
  • organism-icon Homo sapiens
  • sample-icon 97 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Gene 1.0 ST Array (hugene10st)

Description

Despite a substantial progress in diagnosis and therapy, acute myocardial infarction (MI) is a major cause of mortality in the general population. A novel insight into the pathophysiology of myocardial infarction obtained by studying gene expression should help to discover novel biomarkers of MI and to suggest novel strategies of therapy. The aim of our study was to establish gene expression patterns in leukocytes from acute myocardial infarction patients.

Publication Title

Altered gene expression pattern in peripheral blood mononuclear cells in patients with acute myocardial infarction.

Alternate Accession IDs

E-GEOD-62646

Sample Metadata Fields

Specimen part, Subject

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accession-icon GSE147124
Arabidopsis thaliana KO1 and KO3 deletion lines of the selective autophagy receptor AtNBR1
  • organism-icon Arabidopsis thaliana
  • sample-icon 17 Downloadable Samples
  • Technology Badge Icon Arabidopsis Gene 1.1 ST Array (aragene11st)

Description

We used the CRISPR/Cas9 technique to construct nbr1-KO lines (KO1 and KO3) in order to test the effects of AtNBR1 depletion. Reduced expression of several ABA-up regulated genes were observed in shoots of the two KO lines.

Publication Title

A selective autophagy cargo receptor NBR1 modulates abscisic acid signalling in Arabidopsis thaliana.

Alternate Accession IDs

E-GEOD-147124

Sample Metadata Fields

Age, Specimen part

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accession-icon ERP005383
mRNA sequencing of PyMT primary tumor cells with and without E-cadherin
  • organism-icon Mus musculus
  • sample-icon 2 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2000

Description

mRNA sequencing of PyMT primary tumor cells with and without E-cadherin were isolated using FACS, based on expression of tumor cell-specific YFP expression, and sorted into an E-cadherin-positive and E-cadherin-negative population based on the expression of endogenous E-cadherin-mCFP.

Publication Title

No associated publication

Alternate Accession IDs

None

Sample Metadata Fields

No sample metadata fields

View Samples
accession-icon GSE101747
Spleen transcriptional profiling of Mus musculus BALB/c strain after DNA vaccination against influenza H5N1
  • organism-icon Mus musculus
  • sample-icon 13 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Gene 2.1 ST Array (mogene21st)

Description

Hemagglutinin of the influenza virus is the main external glycoprotein. This very immunogenic protein is the target of the most anti-influenza vaccines. DNA vaccines are new alternative to conventional inactivated ones. Four DNA vaccines were tested. Each tested variant was based on the pCI vector with nucleotide sequence encoding hemagglutinin from A/swan/Poland/305-135V08/2006 (H5N1, clade 2.2). In K3/pCI, GK/pCI and HAneo/pCI the different optimization algorithms of hemagglutinin encoding sequence without amino acids change were tested. In 3NF/pCI the NFkappaB binding sites flanking the expression cassette were included in order to improve the nuclear transfer. Comparative transcriptome analysis of mice vaccinated the following vaccine HAneo/pCI,K3/pCI, GK/pCI or 3NF/pCI versus empty vector demonstrated minor changes in genes expression pattern. Most genes were expressed on the similar level in the vaccinated individuals and in the control mice. Small number of genes in particular variants showed the expression different than in the control mice. In general, the identified genes with the changed expression included some genes involved in metabolic processes and none of them seem to induce any undesirable pathways nor disease.

Publication Title

Immunogenicity of DNA Vaccine against H5N1 Containing Extended Kappa B Site: <i>In Vivo</i> Study in Mice and Chickens.

Alternate Accession IDs

E-GEOD-101747

Sample Metadata Fields

Sex, Specimen part, Treatment

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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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