RETRACTED: A Mutant Form of MeCP2 Protein Associated with Human Rett Syndrome Cannot Be Displaced from Methylated DNA by Notch in Xenopus Embryos
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology
Reference33 articles.
1. Rett syndrome;Amir;Am. J. Med. Genet.,2000
2. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat. Genet.,1999
3. DNA methylation patterns and epigenetic memory;Bird;Genes Dev.,2002
4. Intrinsic differences between the superficial and deep layers of the Xenopus ectoderm control primary neuronal differentiation;Chalmers;Dev. Cell,2002
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1. Emerging physiological and pathological roles of MeCP2 in non-neurological systems;Archives of Biochemistry and Biophysics;2021-03
2. Tapping-lips aggravated interictal bilateral discharges in EEG in the patients with Rett syndrome: a case report;BMC Neurology;2019-05-01
3. Retraction Notice to: A Mutant Form of MeCP2 Protein Associated with Human Rett Syndrome Cannot Be Displaced from Methylated DNA by Notch in Xenopus Embryos;Molecular Cell;2019-03
4. Regulatory non-coding RNAs in nervous system development and disease;Frontiers in Bioscience;2019
5. MicroRNA-197 controls ADAM10 expression to mediate MeCP2’s role in the differentiation of neuronal progenitors;Cell Death & Differentiation;2018-12-18
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