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Epigenetic Characterization of the FMR1 Gene and Aberrant Neurodevelopment in Human Induced Pluripotent Stem Cell Models of Fragile X Syndrome Video | LabTube
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Missense mutation of Fmr1 results in impaired AMPAR-mediated plasticity and socio-cognitive deficits in mice | Nature Communications
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Frontiers | Long Noncoding RNA Can Be a Probable Mechanism and a Novel Target for Diagnosis and Therapy in Fragile X Syndrome
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Reversion of FMR1 Methylation and Silencing by Editing the Triplet Repeats in Fragile X iPSC-Derived Neurons - ScienceDirect
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Fragile X syndrome and the FMR1 gene Schematic representation of the... | Download Scientific Diagram
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What Mechanisms Induce Methylation of FMR1 Gene Full Mutation? A Still Unanswered Question | SpringerLink
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Gene therapy using human FMRP isoforms driven by the human FMR1 promoter rescues fragile X syndrome mouse deficits: Molecular Therapy - Methods & Clinical Development
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Differential increases of specific FMR1 mRNA isoforms in premutation carriers | Journal of Medical Genetics
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FMR1 gene enhances the translation of large autism-related proteins - Jane Coffin Childs Memorial Fund
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Genes | Free Full-Text | Transcriptional Reactivation of the FMR1 Gene. A Possible Approach to the Treatment of the Fragile X Syndrome
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