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http://purl.uniprot.org/citations/11830665http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/11830665http://www.w3.org/2000/01/rdf-schema#comment"Although the biochemical targets of most drugs are known, the biological consequences of their actions are typically less well understood. In this study, we have used two whole-genome technologies in Saccharomyces cerevisiae to determine the cellular impact of the proteasome inhibitor PS-341. By combining population genomics, the screening of a comprehensive panel of bar-coded mutant strains, and transcript profiling, we have identified the genes and pathways most affected by proteasome inhibition. Many of these function in regulated protein degradation or a subset of mitotic activities. In addition, we identified Rpn4p as the transcription factor most responsible for the cell's ability to compensate for proteasome inhibition. Used together, these complementary technologies provide a general and powerful means to elucidate the cellular ramifications of drug treatment."xsd:string
http://purl.uniprot.org/citations/11830665http://purl.org/dc/terms/identifier"doi:10.1073/pnas.032516399"xsd:string
http://purl.uniprot.org/citations/11830665http://purl.uniprot.org/core/author"Bulawa C.E."xsd:string
http://purl.uniprot.org/citations/11830665http://purl.uniprot.org/core/author"Sadis S."xsd:string
http://purl.uniprot.org/citations/11830665http://purl.uniprot.org/core/author"Blackman R.K."xsd:string
http://purl.uniprot.org/citations/11830665http://purl.uniprot.org/core/author"Fleming J.A."xsd:string
http://purl.uniprot.org/citations/11830665http://purl.uniprot.org/core/author"Lightcap E.S."xsd:string
http://purl.uniprot.org/citations/11830665http://purl.uniprot.org/core/author"Thoroddsen V."xsd:string
http://purl.uniprot.org/citations/11830665http://purl.uniprot.org/core/date"2002"xsd:gYear
http://purl.uniprot.org/citations/11830665http://purl.uniprot.org/core/name"Proc Natl Acad Sci U S A"xsd:string
http://purl.uniprot.org/citations/11830665http://purl.uniprot.org/core/pages"1461-1466"xsd:string
http://purl.uniprot.org/citations/11830665http://purl.uniprot.org/core/title"Complementary whole-genome technologies reveal the cellular response to proteasome inhibition by PS-341."xsd:string
http://purl.uniprot.org/citations/11830665http://purl.uniprot.org/core/volume"99"xsd:string
http://purl.uniprot.org/citations/11830665http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/11830665
http://purl.uniprot.org/citations/11830665http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/11830665
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http://purl.uniprot.org/uniprot/#_P34761-mappedCitation-11830665http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/11830665
http://purl.uniprot.org/uniprot/#_P39011-mappedCitation-11830665http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/11830665
http://purl.uniprot.org/uniprot/#_P40056-mappedCitation-11830665http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/11830665
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http://purl.uniprot.org/uniprot/#_Q06675-mappedCitation-11830665http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/11830665
http://purl.uniprot.org/uniprot/#_Q06708-mappedCitation-11830665http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/11830665
http://purl.uniprot.org/uniprot/#_P38200-mappedCitation-11830665http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/11830665
http://purl.uniprot.org/uniprot/#_P38265-mappedCitation-11830665http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/11830665