Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

Chen, Richard Z., Akbarian, Schahram, Tudor, Matthew, Jaenisch, Rudolf·2001·Nature Genetics
DOI 10.1038/85906

Cited by (1,001)

Items 301–400 of 1,001

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  2. A new animal model of infantile spasms with unprovoked persistent seizures
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  3. Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndrome
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  4. Olfactory biopsies demonstrate a defect in neuronal development in Rett's syndrome
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  5. MeCP2 and Rett syndrome: reversibility and potential avenues for therapy
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  6. Linking Epigenetics to Human Disease and Rett Syndrome: The Emerging Novel and Challenging Concepts in MeCP2 Research
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  7. An altered neonatal behavioral phenotype in Mecp2 mutant mice
    Jonathan D. Picker, Rebecca J. Yang, Laura Ricceri, Joanne E. Berger-Sweeney · 2006 · Neuroreport
  8. Environmental enrichment alters locomotor behaviour and ventricular volume in Mecp21lox mice
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  9. Methylation-Mediated Proviral Silencing Is Associated with MeCP2 Recruitment and Localized Histone H3 Deacetylation
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  10. Rett syndrome: the complex nature of a monogenic disease
    Alessandra Renieri, Ilaria Meloni, Ilaria Longo, Francesca Ariani, Francesca Mari, Chiara Pescucci, Franca Cambi · 2003 · Journal of Molecular Medicine
  11. The molecular basis of variable phenotypic severity among common missense mutations causing Rett syndrome
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  12. Role of DNA Methyl-CpG-Binding Protein MeCP2 in Rett Syndrome Pathobiology and Mechanism of Disease
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  13. Many paths to one goal? The proteins that recognize methylated DNA in eukaryotes
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  14. MeCP2: A Critical Regulator of Chromatin in Neurodevelopment and Adult Brain Function
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  15. Neuronal Nsun2 deficiency produces tRNA epitranscriptomic alterations and proteomic shifts impacting synaptic signaling and behavior
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  16. Neuronal differentiation of neural precursor cells is promoted by the methyl-CpG-binding protein MeCP2
    Keita Tsujimura, Masahiko Abematsu, Jun Kohyama, Masakazu Namihira, Kinichi Nakashima · 2009 · Experimental Neurology
  17. Postnatal inactivation reveals enhanced requirement for MeCP2 at distinct age windows
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  18. Evidence for abnormal early development in a mouse model of Rett syndrome
    Santos, M., Silva‐Fernandes, A., Oliveira, P., Sousa, Nuno, Maciel, Patrícia · 2007 · Genes, Brain and Behavior
  19. The role of oxidative stress in Rett syndrome: an overview
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  20. Phosphorylation of Distinct Sites in MeCP2 Modifies Cofactor Associations and the Dynamics of Transcriptional Regulation
    Michael L. Gonzales, Sarrita Adams, Keith W. Dunaway, Janine M. LaSalle · 2012 · Molecular and Cellular Biology
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  22. MECP2 regulates cortical plasticity underlying a learned behaviour in adult female mice
    Keerthi Krishnan, Billy Y. B. Lau, Gabrielle Ewall, Z. Josh Huang, Stephen D. Shea · 2017 · Nature Communications
  23. Dendritic spine dysgenesis in Rett syndrome
    Xin Xu, Eric C. Miller, Lucas D. Pozzo‐Miller · 2014 · Frontiers in Neuroanatomy
  24. Modelling brain diseases in mice: the challenges of design and analysis
    Kei Watase, Huda Yahya Zoghbi · 2003 · Nature Reviews Genetics
  25. DNA methylation in animal development
    Richard R. Meehan · 2003 · Seminars in Cell and Developmental Biology
  26. Synaptic Circuit Abnormalities of Motor-Frontal Layer 2/3 Pyramidal Neurons in an RNA Interference Model of Methyl-CpG-Binding Protein 2 Deficiency
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  27. Developmental maturation of astrocytes and pathogenesis of neurodevelopmental disorders
    Yongjie Yang, Haruki Higashimori, Lydie Morel · 2013 · Journal of Neurodevelopmental Disorders
  28. Emerging roles for MEF2 in brain development and mental disorders
    Assali, Ahlem, Harrington, Adam J, Cowan, Christopher W · 2019 · Current Opinion in Neurobiology
  29. Activity-dependent synaptic plasticity modulates the critical phase of brain development
    Sraboni Chaudhury, Vikram Sharma, Vivek Kumar, Tapas Chandra Nag, Shashi Wadhwa · 2015 · Brain and Development
  30. Targeted delivery of an Mecp2 transgene to forebrain neurons improves the behavior of female Mecp2-deficient mice
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  32. Plasticity of dendritic spines: Molecular function and dysfunction in neurodevelopmental disorders
    Jun Nishiyama · 2019 · Psychiatry and Clinical Neurosciences
  33. Heterogeneity in residual function of MeCP2 carrying missense mutations in the methyl CpG binding domain
    Shinichi Kudo, Y Nomura, M Segawa, N Fujita, Mitsuyoshi Nakao, C Schanen, M Tamura · 2003 · Journal of Medical Genetics
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  35. The short-time structural plasticity of dendritic spines is altered in a model of Rett syndrome
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  36. MECP2, a multi-talented modulator of chromatin architecture
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  43. MeCP2 functions largely cell-autonomously, but also non-cell-autonomously, in neuronal maturation and dendritic arborization of cortical pyramidal neurons
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  49. Recruitment of MBD1 to target genes requires sequence-specific interaction of the MBD domain with methylated DNA
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  66. DNA Methylation and Adult Neurogenesis
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  72. Rett syndrome
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  74. Alterations of cortical and hippocampal EEG activity in MeCP2-deficient mice
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  76. X‐linked mental retardation: vanishing boundaries between non‐specific (MRX) and syndromic (MRXS) forms
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  78. Rett syndrome
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  79. Airway mechanosensors
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  83. Increased dendritic complexity and axonal length in cultured mouse cortical neurons overexpressing methyl-CpG-binding protein MeCP2
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  84. Supportive evidence for the DYX3 dyslexia susceptibility gene in Canadian families
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  90. Physiological and Pathological Roles of CaMKII-PP1 Signaling in the Brain
    Norifumi Shioda, Kohji Fukunaga · 2017 · International Journal of Molecular Sciences
  91. Evidence for both neuronal cell autonomous and nonautonomous effects of methyl-CpG-binding protein 2 in the cerebral cortex of female mice with Mecp2 mutation
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  94. Heterogeneity in the modification and involvement of chromatin components of the CpG island of the silenced human CDH1 gene in cancer cells
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  95. MicroRNA-22 Regulates Smooth Muscle Cell Differentiation From Stem Cells by Targeting Methyl CpG–Binding Protein 2
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  97. Genetic modifiers of MeCP2 function in Drosophila
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  99. Differences in DNA methylation patterns between humans and chimpanzees
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  100. Rett Syndrome and the Impact of MeCP2 Associated Transcriptional Mechanisms on Neurotransmission
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