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Dynamic dysregulation of the transcriptome upon deletion of Mecp2 in adult mice

GSE246119 Mus musculus Expression profiling by high throughput sequencing 144 samples 2024/12/16 GPL17021
Summary
Loss of function mutations in methyl Cpg binding protein 2 (MECP2) cause Rett syndrome. Loss of MeCP2 causes global transcriptional dysregulation, but it was unknown whether this transcriptional dysregulation was proximal to Mecp2 function. We deleted Mecp2 from adult mice and performed a time-series RNA-seq experiment to identif what transcripts were altered immediately upon loss of MeCP2.
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NCBI GEO page ↗ Paper (PMID 39689710) ↗ {# Names what the click gives you. "Open in finder" meant nothing to a visitor who arrived from a search engine and has never seen the tool. #} Find more mouse RNA-seq datasets →
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