<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE11nnn/GSE11561/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Saccharomyces cerevisiae</species><gds_type>Expression profiling by array</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE11561</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>MPA and NQO studies (Sevilla)</name><description>RNA polymerases deal with obstacles during transcription elongation that need to be removed. One important type of hindrance consists of DNA lesions, which are removed by transcription-coupled repair (TCR). To improve our knowledge of transcription elongation and its coupling to TCR, we performed DNA microarray experiments and used the yeast library of nonessential knock-out mutations to screen for genes conferring resistance to the transcription-elongation inhibitor micophenolic acid and the DNA-damaging agent 4- nitroquinoline-N-oxide.</description><dates><publication>2008/12/30</publication></dates><accession>GSE11561</accession><cross_references><GSM>GSM289019</GSM><GSM>GSM289029</GSM><GPL>4069</GPL><GSE>11561</GSE><taxon>Saccharomyces cerevisiae</taxon><PMID>[19197357]</PMID></cross_references></HashMap>