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http://purl.uniprot.org/citations/23871667http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/23871667http://www.w3.org/2000/01/rdf-schema#comment"Female human pluripotent stem cells show vast heterogeneity regarding the status of X chromosome inactivation. By comparing the gene expression profile of cells with two active X chromosomes (XaXa cells) to that of cells with only one active X chromosome (XaXi cells), a set of autosomal genes was shown to be overexpressed in the XaXa cells. Among these genes, we found significant enrichment for genes regulated by the X-linked transcription factor ELK-1. Comparison of the phenotype of XaXa and XaXi cells demonstrated differences in programmed cell death and differentiation, implying some growth disadvantage of the XaXa cells. Interestingly, ELK-1-overexpressing cells mimicked the phenotype of XaXa cells, whereas knockdown of ELK-1 with small hairpin RNA mimicked the phenotype of XaXi cells. When cultured at low oxygen levels, these cellular differences were considerably weakened. Our analysis implies a role of ELK-1 in the differences between pluripotent stem cells with distinct X chromosome inactivation statuses."xsd:string
http://purl.uniprot.org/citations/23871667http://purl.org/dc/terms/identifier"doi:10.1016/j.celrep.2013.06.026"xsd:string
http://purl.uniprot.org/citations/23871667http://purl.uniprot.org/core/author"Benvenisty N."xsd:string
http://purl.uniprot.org/citations/23871667http://purl.uniprot.org/core/author"Yanuka O."xsd:string
http://purl.uniprot.org/citations/23871667http://purl.uniprot.org/core/author"Bruck T."xsd:string
http://purl.uniprot.org/citations/23871667http://purl.uniprot.org/core/date"2013"xsd:gYear
http://purl.uniprot.org/citations/23871667http://purl.uniprot.org/core/name"Cell Rep"xsd:string
http://purl.uniprot.org/citations/23871667http://purl.uniprot.org/core/pages"262-270"xsd:string
http://purl.uniprot.org/citations/23871667http://purl.uniprot.org/core/title"Human pluripotent stem cells with distinct X inactivation status show molecular and cellular differences controlled by the X-Linked ELK-1 gene."xsd:string
http://purl.uniprot.org/citations/23871667http://purl.uniprot.org/core/volume"4"xsd:string
http://purl.uniprot.org/citations/23871667http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/23871667
http://purl.uniprot.org/citations/23871667http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/23871667
http://purl.uniprot.org/uniprot/#_Q86SR6-mappedCitation-23871667http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23871667
http://purl.uniprot.org/uniprot/#_P19419-mappedCitation-23871667http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23871667
http://purl.uniprot.org/uniprot/#_Q6FG56-mappedCitation-23871667http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23871667
http://purl.uniprot.org/uniprot/#_Q59GR2-mappedCitation-23871667http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23871667
http://purl.uniprot.org/uniprot/#_Q8N9S0-mappedCitation-23871667http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23871667
http://purl.uniprot.org/uniprot/P19419http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/23871667
http://purl.uniprot.org/uniprot/Q59GR2http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/23871667
http://purl.uniprot.org/uniprot/Q8N9S0http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/23871667
http://purl.uniprot.org/uniprot/Q6FG56http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/23871667
http://purl.uniprot.org/uniprot/Q86SR6http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/23871667