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FMR1 reactivating treatments in Fragile X iPSC-derived neural progenitors in-vitro and in-vivo
PubMed Similar studies Analyze with GEO2RSRA Run Selector
Rescue of Fragile X syndrome by DNA methylation editing of the FMR1
PubMed Full text in PMC Similar studies
Rescue of Fragile X syndrome neurons by DNA methylation editing of the FMR1 gene [RNA-seq]
PubMed Full text in PMC Similar studies Analyze with GEO2RSRA Run Selector
Rescue of Fragile X syndrome neurons by DNA methylation editing of the FMR1 gene [methylation]
PubMed Full text in PMC Similar studies SRA Run Selector
Rescue of Fragile X syndrome by DNA methylation editing of the FMR1 [ChIP-seq II]
Rescue of Fragile X syndrome by DNA methylation editing of the FMR1 [ChIP-seq]
Transcriptomic analysis of human iPS cells derived from fragile X syndrome patients during neural differentiation
Gene expression profile of FMR1-KO iPSCs-derived NPCs
PubMed Full text in PMC Similar studies Analyze with GEO2R
Cell-type-specific profiling of defects in translation and neurogenesis in a human iPSC model of fragile X syndrome
DNAseq analysis of a genome-wide loss-of-function CRISPR/Cas9 library in haploid human embryonic stem cells transfected with a methylated construct containing the FXS-related mutation upstream to an EGFP reporter gene
RNAseq analysis of CRISPR/Cas9-based perturbation of DNMT1 in FXS induced pluripotent stem cells
Sustainedcorrection of hippocampal neurogenic and cognitive deficits after a brief treatment by Nutlin-3 in a mousemodel of Fragile X Syndrome.
Identification of FMRP targets in human neural progenitors and neurons
Reprogramming of fibroblasts from Fragile-X patients to induced pluripotent stem cells (iPS) with defined factors
Reduced LYNX1 and epilepsy phenotype-related changes in transcriptome of human iPSC-derived neural progenitors modeling fragile X syndrome
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