RNA sequencing data of Wild Type and Fmr1 KO hippocampal neuron
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https://www.ncbi.nlm.nih.gov/sra/SRP144498
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资源简介：
Fragile X syndrome (FXS), caused by mutations in fragile X mental retardation 1 gene (FMR1), is a prevailing genetic disorder of intellectual disability and autism. Analysis of transcriptome outcome (differentially expressed genes between WT and Fmr1 KO hippocampal neuron) associated with FXS reveal promising value of gene signature-based computation in repurposing drugs for potential practical treatment. Overall design: Primary DIV (Days in vitro) 14 Hippocampal neuron mRNA profiles of Wild Type (WT) and Fmr1 KO mice were generated in triplicate
创建时间：
2020-03-31
