<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/GSE326nnn/GSE326233/</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=GSE326233</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Transcriptomic effects of intermittent parathyroid hormone treatment and osteoprotegrin-Fc on Ebf3-lineage skeletal stem/progenitors</name><description>We employed 10X Genomics single cell RNA-sequencing to study the bone anabolic effects of intermittent parathyroid hormone treatment (iPTH) and osteoprotegerin-Fc (OPG-Fc) on subsets of bone marrow Cxcl12-abundant reticular (CAR) cells. CAR cells, marked by the expression of the transcription factor Early B-cell Factor 3 (Ebf3), are a critical class of osteoblast progenitors participating in bone remodeling during adulthood. Using lineage tracing approach with Ebf3-CreERT2 crossed with Ai9 tdTomato reporter mice, we traced Ebf3-expressing CAR cells and their descendants following 10 days of vehicle or iPTH treatment. This study represents a single cell atlas of bone marrow Ebf3-lineage CAR cells following 10 days of iPTH treatment.</description><dates><publication>2026/09/20</publication></dates><accession>GSE326233</accession><cross_references><GSM>GSM9625633</GSM><GPL>30172</GPL><GSE>326233</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>