<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/GSE306nnn/GSE306304/</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=GSE306304</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Transcriptomic profiling of mouse hematopoietic stem cells after myelosuppressive injury</name><description>Hematopoietic stem cell (HSCs) were isolated from the bone marrow of a mouse model of irradiation-induced myelosuppressive injury at 1 day post irradiation. To investigate the role of itaconate metabolism in HSC maintenance after myelosuppressive injury, both Irg1-KO mice and exogenous OI treatment were empolyed in this study.</description><dates><publication>2026/08/24</publication></dates><accession>GSE306304</accession><cross_references><GSM>GSM9197108</GSM><GSM>GSM9197109</GSM><GSM>GSM9197106</GSM><GSM>GSM9197107</GSM><GSM>GSM9197104</GSM><GSM>GSM9197115</GSM><GSM>GSM9197105</GSM><GSM>GSM9197113</GSM><GSM>GSM9197102</GSM><GSM>GSM9197114</GSM><GSM>GSM9197103</GSM><GSM>GSM9197111</GSM><GSM>GSM9197101</GSM><GSM>GSM9197112</GSM><GSM>GSM9197110</GSM><GPL>24247</GPL><GSE>306304</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>