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Displaying 20 of 25 results for "CREB3L3"
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  1. The transcription factor cyclic AMP–responsive elementbinding protein H regulates triglyceride metabolism BioProject

    ID: PRJNA141223

    Keywords: Transcriptome or Gene expression

    Access Type: download

  2. The transcription factor cyclic AMP–responsive elementbinding protein H regulates triglyceride metabolism ArrayExpress

    ID: E-GEOD-29643

    Description: report that the transcription factor cyclic AMP–responsive elementbinding protein H (CREB...

  3. The transcription factor cyclic AMP–responsive elementbinding protein H regulates triglyceride metabolism OmicsDI

    ID: E-GEOD-29643

    Date Released: 06-02-2014

    Description: report that the transcription factor cyclic AMP–responsive elementbinding protein H (CREB...

  4. Effects of CREB3L1 on gene expression BioProject

    ID: PRJNA224587

    Keywords: Transcriptome or Gene expression

    Access Type: download

    dataset.description: The unfolded protein response (UPR) is activated in response to hypoxia-induced stress such as in the tumor microenvironment. This study examin...
  5. Association of CREB3L1 with promoters in LN4D6 CREB3L1 cells BioProject

    ID: PRJNA225612

    Keywords: Epigenomics

    Access Type: download

    dataset.description: The unfolded protein response (UPR) is activated in response to hypoxia-induced stress such as in the tumor microenvironment. This study examin...
  6. Association of CREB3L1 with promoters in MDA-MB-435 cells BioProject

    ID: PRJNA225610

    Keywords: Epigenomics

    Access Type: download

    dataset.description: The unfolded protein response (UPR) is activated in response to hypoxia-induced stress such as in the tumor microenvironment. This study examin...
  7. Association of CREB3L1 with promoters in LN4D6 CREB3L1 cells OmicsDI

    ID: E-GEOD-51802

    Date Released: 06-03-2014

    Description: The unfolded protein response (UPR) is activated in response to hypoxia-induced stress such as in the tumor microenvironment. This study examin...

  8. Glucose upregulates a limited number of genes in human beta cells. BioProject

    ID: PRJNA385303

    Keywords: Transcriptome or Gene expression

    Access Type: download

    dataset.description: ng conversion of multipotent progenitors into the 3 main human pancreatic cell types (acinar, ductal and endocrine) in vivo. As such, the data pave the way to extend our understanding of the origin of mature human pancreatic cell types and how such lineage decisions are regulated. While the mechanisms by which glucose regulates insulin secretion from pancreatic beta cells are now well described, the way glucose modulates gene expression in such cells needs more understanding. Here, we demonstrate that MondoA, but not its paralogue ChREBP, is the predominant glucose-responsive transcription factor in human pancreatic beta EndoC-βH1 cells and in human islets. In high glucose conditions, MondoA shuttles to the nucleus where it is required for the induction of the glucose-responsive genes ARRDC4 and TXNIP, the latter being a protein strongly linked to beta-cell dysfunction and diabetes. Importantly, increasing cAMP signaling in human beta cells, using forskolin or the GLP-1 mimetic Exendin-4, inhibits the shuttling of MondoA and potently inhibits TXNIP and ARRDC4 expression. Furthermore, we demonstrate that modulating MondoA expression functionally affects glucose uptake. Th...
  9. Genes regulated by the processed form of AIbZIP/CREB3L4 in LNCaP prostate cancer cells BioProject

    ID: PRJNA98395

    Keywords: Transcriptome or Gene expression

    Access Type: download

    dataset.description: nscription factor that is encoded by the CREB3L4 (cAMP responsive element binding protein 3-like 4) gene. In humans, AIbZIP mRNA is mo...
  10. Transcription profiling of human and moise primary hepatocytes from 12 donors were treated with PPARI? agonist Wy14643 ArrayExpress

    ID: E-GEOD-17254

    Description: ere commonly regulated in both species, including CREB3L3, KLF10, KLF11 and MAP3K8. Our results suggest that PPARα activation has a major impact on gene regulation in human hepatocytes. Importantly, the role of PPARα as master regulator of hepatic lipid metabolism is generally well-conserved between mouse and human. Overall, however, PPARα regulates a mostly divergent set of genes in mouse and human hepatocytes. GSE17250: Comparative analysis of gene regulation by the transcription factor PPARα_mouse; GSE17251: Comparative analysis of gene regulation by the transcription factor PPARα_human Experiment Overall Design: Refer to individual Series...

  11. Striatal microRNA controls cocaine intake through CREB signalling BioProject

    ID: PRJNA126865

    Keywords: Transcriptome or Gene expression

    Access Type: download

  12. CREB_ASPCL UniProt:Swiss-Prot

    ID: A1CIL1

    Description: Probable ubiquitin carboxyl-terminal hydrolase creB USP Nucleophile Proton acceptor

  13. The integral membrane protein ITM2A, a transcriptional target of PKA-CREB, regulates autophagic flux via interaction with the vacuolar ATPase Figshare

    ID: doi:10.6084/M9.FIGSHARE.1407383

    Release Date: 03-11-2016

    Description:

  14. Comparative analysis of gene regulation by the transcription factor PPARα_human BioProject

    ID: PRJNA123587

    Keywords: Transcriptome or Gene expression

    Access Type: download

    dataset.description: ere commonly regulated in both species, including CREB3L3, KLF10, KLF11 and MAP3K8. Our results suggest that PPARα activation has a major impact on gene regulation in human hepatocytes. Importantly, the role of PPARα as master regulator of hepatic lipid metabolism is generally well-conserved between mouse and human. Overall, however, PPARα regulates a mostly divergent set of genes in mouse and human hepatocytes. Keywords: Analysis of target gene regulation by using microarrays Overall design: Primary hepatocytes from 6 human subjects were treated with the PPARα agonist Wy14643 for 6 and 24 hours, and gene expression profiling was performed using Affymetrix GeneChips. Human hepatocytes and Hepatocyte Culture Medium Bulletkit were purchased from Lonza Bioscience (Verviers, Belgium). Primary hepatocytes were isolated from surgical liver biopsies obtained from six individual donors who underwent surgery after informed consent was obtained for surgery with subsequent use of samples in experiments. Hepatocytes were isolated with two-step collagenase perfusion method and the viability of the cells was over 80%. Cells were plated on collagen-coated six-well plates and filled with maintenance medium. Upon arrival of the cells, the medium was discarded and was replaced by Hepatocyte Culture Medium (HCM) with additives. The additives included Gentamicin sulphate/Amphotercin-B, Bovine serum albumin (Fatty acid free), Transferrin, Ascorbic acid, Insulin, Epidermal growth factor, Hydrocortisone hemisuccinate. The next day, cells were incubated in fresh medium in the presence or absence of Wy14643 (50 microM) dissolved in DMSO for 6 a...
  15. Crystal structure of the bromodomain of human CREBBP bound to the benzodiazepinone G02778174 PDB

    ID: PDB:5I86

    Description: CREB-binding protein

  16. Comparative analysis of gene regulation by the transcription factor PPARalpha between mouse and human - Mus musculus GEMMA

    ID: 1516

    Keywords: functional genomics

    Description: ere commonly regulated in both species, including CREB3L3, KLF10, KLF11 and MAP3K8. Our results suggest that PPARalpha activation has a major impact on gene regulation in human hepatocytes. Importantly, the role of PPARalpha as master regulator of hepatic lipid metabolism is generally well-conserved between mouse and human. Overall, however, PPARalpha regulates a mostly divergent set of genes in mouse and human hepatocytes. GSE17254.2: Comparative analysis of gene regulation by the transcription factor PPARalpha_mouse GSE17254.1: Comparative analysis of gene regulation by the transcription factor PPARalpha_human Last Updated (by provider): Jan 15 2010 Contributers: Maryam Rakhshandehroo Michael Müller Sander Kersten Guido Hooiveld...

  17. C646, a Novel p300/CREB-Binding Protein-Specific Inhibitor of Histone Acetyltransferase, Attenuates Influenza A Virus Infection ArrayExpress

    ID: E-GEOD-72503

    Description: A549 cells were treated with C646 or DMSO for 10 h, and then were infected with A/WSN/33 virus (WSN; H1N1) at a multiplicity of infection (MOI) 2. A549 cells for microarray studies were collected at different times. The gene expression in A549 cells was compared between C646-treated group and DMSO-treated group....

  18. The integral membrane protein ITM2A, a transcriptional target of PKA-CREB, regulates autophagic flux via interaction with the vacuolar ATPase Figshare

    ID: doi:10.6084/M9.FIGSHARE.1407383.V1

    Release Date: 03-11-2016

    Description:

  19. The integral membrane protein ITM2A, a transcriptional target of PKA-CREB, regulates autophagic flux via interaction with the vacuolar ATPase Figshare

    ID: doi:10.6084/M9.FIGSHARE.1407383.V3

    Release Date: 03-11-2016

    Description:

  20. A role for nuclear factor interleukin-3 (NFIL3), a critical transcriptional repressor, in down-regulation of periovulatory gene expression BioProject

    ID: PRJNA136147

    Keywords: Transcriptome or Gene expression

    Access Type: download


Displaying 20 of 25 results for "CREB3L3"