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http://purl.uniprot.org/citations/18550052http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/18550052http://www.w3.org/2000/01/rdf-schema#comment"C6 glioma cells were treated with clinically relevant concentrations of valproic acid (0.5 or 1.0 mM) for 1-7 days and RT-PCR used to examine expression of the melatonin MT(1) receptor and selected epigenetic modulators. Valproic acid caused significant time-dependent changes in the mRNA expression of the melatonin MT(1) receptor, histone deacetylase (HDAC) 1, 2 and 3, and methyl CpG binding protein 2 (MeCP2). A structurally distinct HDAC inhibitor, trichostatin A, also caused a significant concentration-dependent induction of melatonin MT(1) receptor mRNA expression, suggesting involvement of an epigenetic mechanism. The ability of clinical concentrations of valproic acid to significantly alter melatonin MT(1) receptor expression, suggests a role for this receptor in the diverse neuropharmacological and oncostatic effects of this agent."xsd:string
http://purl.uniprot.org/citations/18550052http://purl.org/dc/terms/identifier"doi:10.1016/j.ejphar.2008.04.058"xsd:string
http://purl.uniprot.org/citations/18550052http://purl.uniprot.org/core/author"Kim B."xsd:string
http://purl.uniprot.org/citations/18550052http://purl.uniprot.org/core/author"Niles L.P."xsd:string
http://purl.uniprot.org/citations/18550052http://purl.uniprot.org/core/author"Jawed S."xsd:string
http://purl.uniprot.org/citations/18550052http://purl.uniprot.org/core/author"Rincon Castro L.M."xsd:string
http://purl.uniprot.org/citations/18550052http://purl.uniprot.org/core/date"2008"xsd:gYear
http://purl.uniprot.org/citations/18550052http://purl.uniprot.org/core/name"Eur J Pharmacol"xsd:string
http://purl.uniprot.org/citations/18550052http://purl.uniprot.org/core/pages"45-48"xsd:string
http://purl.uniprot.org/citations/18550052http://purl.uniprot.org/core/title"Clinically relevant concentrations of valproic acid modulate melatonin MT(1) receptor, HDAC and MeCP2 mRNA expression in C6 glioma cells."xsd:string
http://purl.uniprot.org/citations/18550052http://purl.uniprot.org/core/volume"589"xsd:string
http://purl.uniprot.org/citations/18550052http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/18550052
http://purl.uniprot.org/citations/18550052http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/18550052
http://purl.uniprot.org/uniprot/Q4QQW4#attribution-AE5D4BFBF6A0E40A55FE34735E2BAFD4http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/18550052
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http://purl.uniprot.org/uniprot/F7ENH8#attribution-AE5D4BFBF6A0E40A55FE34735E2BAFD4http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/18550052
http://purl.uniprot.org/uniprot/A0A8I6AP99#attribution-AE5D4BFBF6A0E40A55FE34735E2BAFD4http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/18550052
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http://purl.uniprot.org/uniprot/#_A0A0G2K814-mappedCitation-18550052http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18550052
http://purl.uniprot.org/uniprot/#_A0A0G2K1C8-mappedCitation-18550052http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18550052
http://purl.uniprot.org/uniprot/#_D4AEB0-mappedCitation-18550052http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18550052
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http://purl.uniprot.org/uniprot/#_A6J3D3-mappedCitation-18550052http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18550052