Structural investigation of Rett-inducing MeCP2 mutations
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Genetics(clinical),Molecular Biology,Biochemistry
Reference16 articles.
1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat Genet,1999
2. An AT-hook domain in MeCP2 determines the clinical course of Rett syndrome and related disorders;Baker;Cell,2013
3. MeCP2. A modulator of neuronal chromatin organization involved in Rett syndrome;Martínez de Paz;Adv Exp Med Biol,2017
4. Biophysical characterization of the basic cluster in the transcription repression domain of human MeCP2 with AT-rich DNA;Mushtaq;Biochem Biophys Res Commun,2018
5. The alphabet of intrinsic disorder: I. Act like a Pro: on the abundance and roles of proline residues in intrinsically disordered proteins;Theillet;Intrinsically Disord Proteins,2013
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1. MeCP2 is a naturally supercharged protein with cell membrane transduction capabilities;Protein Science;2024-09-14
2. Nuclease-free precise genome editing corrects MECP2 mutations associated with Rett syndrome;Frontiers in Genome Editing;2024-03-01
3. The Moonlighting Function of Soybean Disordered Methyl-CpG-Binding Domain 10c Protein;International Journal of Molecular Sciences;2023-05-12
4. Genetics behind Cerebral Disease with Ocular Comorbidity: Finding Parallels between the Brain and Eye Molecular Pathology;International Journal of Molecular Sciences;2022-08-26
5. MeCP2: The Genetic Driver of Rett Syndrome Epigenetics;Frontiers in Genetics;2021-01-21
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