{"database":"GEO","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Other":["ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE329nnn/GSE329222/"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"omics_type":["Transcriptomics"],"species":["Mus musculus"],"gds_type":["Expression profiling by high throughput sequencing"],"full_dataset_link":["https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE329222"],"repository":["GEO"],"entry_type":["GSE"],"additional_accession":[]},"is_claimable":false,"name":"Transcriptional landscape of mouse adipose tissue transfected with LHX8 siRNA","description":"We have studied the role of LHX8 (Lim Homeobox 8) in adipocyte development. Mouse 3T3-L1 adipcoytes were used for our analyses. Cells were cultured in high glucose DMEM, supplemented with 10% FCS, 1% glutamine and 1% penicillin/streptomycin. Cells were grown to reach 70-80% confluence, and transfected with a siRNA silencer to decrease Lhx8 mRNA expression. Turbofectamine was used for cell transfection. Total RNA was isolated 48h post-transfection and used for subsequent NGS analysis.","dates":{"publication":"2026/05/21"},"accession":"GSE329222","cross_references":{"GSM":["GSM9699565","GSM9699564","GSM9699563","GSM9699562","GSM9699561","GSM9699560"],"GPL":["23479"],"GSE":["329222"],"taxon":["Mus musculus"]}}