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Genetics and Microbiology, Duke University School of Medicinehttps://www.ebi.ac.uk/ena/browser/view/PRJNA838490Mus musculusTo identify DDX3X-dependent translation targets in the developing mouse cortex, we used E11.5 cortices from both sexes of wildtype and conditional Ddx3x knockout mice (driven by Emx1-Cre). We performed RNAseq and Riboseq on these samples in parallel. Overall design: Comparative gene expression profiling analysis of RNA-seq and Ribo-seq data for wildtype and Ddx3x conditional knockout mouse E11.5 cortex. The following are biological replicates: Female controls: F2, F3; Male controls: M1, M2, M3; cKO females: F1, F2, F3; cKO mals: M1, M2, M3ENAcortex, protein translation, CAP-Rf, DDX3, protein anabolism, DDX14, Fin14, HLP2, An3, protein biosynthetic process, protein synthesis, Mus, mice, pl10, protein formation, mouse, protein biosynthesis, Mouse, cortex of organ., house mouse, DBX, Ddx3, D1Pas1-rs2cortex, protein translation, CAP-Rf, DDX3, protein anabolism, DDX14, Fin14, HLP2, An3, protein biosynthetic process, protein synthesis, Mus, mice, pl10, protein formation, mouse, protein biosynthesis, Mouse, cortex of organ., house mouse, DBX, Ddx3, D1Pas1-rs20.00.00.00.00.0falseIdentification of DDX3X-dependent translation targets in the E11.5 mouse cortexIdentification of DDX3X-dependent translation targets in the E11.5 mouse cortex2022-07-072022-05-19PRJNA838490GSE20307810090