<HashMap><database>ENA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR159/058/SRR15913358/SRR15913358_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR159/061/SRR15913361/SRR15913361_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR159/058/SRR15913358/SRR15913358_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR159/059/SRR15913359/SRR15913359_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR159/060/SRR15913360/SRR15913360_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR159/061/SRR15913361/SRR15913361_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR159/057/SRR15913357/SRR15913357_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR159/062/SRR15913362/SRR15913362_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR159/057/SRR15913357/SRR15913357_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR159/062/SRR15913362/SRR15913362_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR159/059/SRR15913359/SRR15913359_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR159/060/SRR15913360/SRR15913360_2.fastq.gz</Fastqsanger.gz></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>Huazhong Agricultural University</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA763827</full_dataset_link><scientific_name>Mus musculus</scientific_name><long_description>Our current study overexpressed Vdbp stably in DC to explore the function of this gene. CKK-8 results revealed Vdbp successfully inhibited viability of DC. Besides, we found overexpressing this gene greatly promoted apoptosis and obviously altered cell cycle distribution in DC. Moreover, RNA sequencing (RNA-seq) was carried out and numerous differently expressed genes (DEGs) were obtained. The results indicated that Vdbp globally mediated expression of mRNAs, which might translate into its potential functions. Finally, bio-informatics analysis illustrated that most DEGs were more uniformly enriched in immunity-related pathways. We believe that Vdbp regulates the function of DC by altering its cellular immunity. Overall design: Examination the overexpression of Vdbp in DCs.</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Transcriptomic Analysis Reveals the Responses of Dendritic Cells to Vdbp</name><description>Transcriptomic Analysis Reveals the Responses of Dendritic Cells to Vdbp</description><dates><last_updated>2025-09-24</last_updated><first_public>2024-08-02</first_public></dates><accession>PRJNA763827</accession><cross_references><GEO>GSE184258</GEO><taxon>10090</taxon></cross_references></HashMap>