<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/GSE329nnn/GSE329505/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE329505</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Evolution of leukemic stem cell states and transcriptional programs across serial xenotransplantation in acute myeloid leukemia</name><description>We performed bulk RNA-seq profiling of acute myeloid leukemia (AML) patient-derived xenograft models across serial transplantation passages (P0, P1, P2) to characterize transcriptional changes associated with leukemia propagation and stem cell activity.</description><dates><publication>2026/07/20</publication></dates><accession>GSE329505</accession><cross_references><GSM>GSM9705241</GSM><GSM>GSM9705240</GSM><GSM>GSM9705223</GSM><GSM>GSM9705245</GSM><GSM>GSM9705244</GSM><GSM>GSM9705222</GSM><GSM>GSM9705243</GSM><GSM>GSM9705221</GSM><GSM>GSM9705220</GSM><GSM>GSM9705242</GSM><GSM>GSM9705227</GSM><GSM>GSM9705226</GSM><GSM>GSM9705225</GSM><GSM>GSM9705224</GSM><GSM>GSM9705229</GSM><GSM>GSM9705228</GSM><GSM>GSM9705230</GSM><GSM>GSM9705234</GSM><GSM>GSM9705233</GSM><GSM>GSM9705232</GSM><GSM>GSM9705231</GSM><GSM>GSM9705238</GSM><GSM>GSM9705237</GSM><GSM>GSM9705236</GSM><GSM>GSM9705235</GSM><GSM>GSM9705219</GSM><GSM>GSM9705239</GSM><GPL>24676</GPL><GSE>329505</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>