Double Genetic Diagnosis Involving MECP2 and EPHB4 in a Child with Neurodevelopmental Delay and Vascular Anomalies: A Case Report. [PDF]
Mol SyndromolSanri A, Mutlu MB.
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Dysregulated DNA Methylation in <i>Abca4<sup>-/-</sup></i> Retinal Pigment Epithelium: Insights into Early Stage of Stargardt Disease. [PDF]
Int J Mol SciDave A +6 more
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Metformin Induces MeCP2 in the Hippocampus of Male Mice with Sex-Specific and Brain-Region-Dependent Molecular Impact [PDF]
Khatereh Saei Arezoumand +2 more
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Optimized clonal isolation and immortalization of Rett syndrome patient fibroblasts for in vitro modeling of MECP2 mutations. [PDF]
Sci RepSarne V +5 more
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MeCP2 inhibits cell functionality through FoxO3a and autophagy in endothelial progenitor cells
, 2019 Siyuan Zha +4 more
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miR-199a functions downstream of MeCP2 in neurons of <i>MECP2</i> duplication syndrome models. [PDF]
iScienceAkaba Y +20 more
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Transcriptional Consequences of MeCP2 Knockdown and Overexpression in Mouse Primary Cortical Neurons. [PDF]
Int J Mol SciRezapour M +3 more
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MECP2 Dysfunction in Rett Syndrome: Molecular Mechanisms, Multisystem Pathology, and Emerging Therapeutic Strategies. [PDF]
Int J Mol SciChoi G, Lee S, Yoo S, Do JT.
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