MeCP2 regulates cell-type-specific functions of depressive-like symptoms in the nucleus accumbens. [PDF]
Exp Mol MedBae J +8 more
europepmc +1 more source
RNA-Based Therapeutics in Genetic Neurodevelopmental Disorders: Bridging Molecular Genetics and Precision Medicine. [PDF]
Int J Mol SciFocșa IO +11 more
europepmc +1 more source
Current insights into PHF14: molecular features and functional roles. [PDF]
Front Mol BiosciGopalakrishnan V +3 more
europepmc +1 more source
MECP2 mutations disrupt pluripotent stem cell fate through remodeling of the three-dimensional genome. [PDF]
Cell Death DisZhou J +13 more
europepmc +1 more source
New insights into Rett syndrome pathogenesis: defining the role of MEPC2 in DNA damage. [PDF]
Front NeurolMansooralavi N, Lowry WE.
europepmc +1 more source
MeCP2 gene dosage-dependent neurodevelopmentally restricted defects arise by aberrant activation of cell fate-determining bivalent genes. [PDF]
Nat CommunLuoni M +10 more
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When Neurodevelopment Meets Autoimmunity: Pemphigus Foliaceus in Rett Syndrome Expands the Clinical Spectrum-A Case Report. [PDF]
Int J Mol SciSingh J +8 more
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Leptin antagonism improves Rett syndrome phenotype in symptomatic Mecp2-deficient mice. [PDF]
NeurotherapeuticsBelaïdouni Y +9 more
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Erratum: Erratum: Pubertal development is unaffected in female <i>Mecp2</i> -heterozygous mice. [PDF]
MicroPubl Bioleuropepmc +1 more source