<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/GSE240nnn/GSE240024/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</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=GSE240024</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>PI3K signaling is essential for leukemic transformation of Tet2 mutated pre-leukemic hematopoietic stem cells</name><description>Inhibition of PI3K rescues Tet2 loss driven leukemia. The signaling pathways by which Tet2 mutations contribute to myeloid transformation are poorly understood. We investigated that loss of Tet2 in HSC/Ps results in myeloproliferation, which is associated with hyperactivation of the PI3Kinase pathway.</description><dates><publication>2026/04/01</publication></dates><accession>GSE240024</accession><cross_references><GSM>GSM7679988</GSM><GSM>GSM7679987</GSM><GSM>GSM7679986</GSM><GSM>GSM7679985</GSM><GSM>GSM7679984</GSM><GSM>GSM7679983</GSM><GSM>GSM7679982</GSM><GSM>GSM7679981</GSM><GSM>GSM7679980</GSM><GSM>GSM7679979</GSM><GSM>GSM7679978</GSM><GSM>GSM7679989</GSM><GPL>21103</GPL><GSE>240024</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>