Brain-Specific Phosphorylation of MeCP2 Regulates Activity-Dependent Bdnf Transcription, Dendritic Growth, and Spine Maturation
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Eric C. Griffith | Wen G. Chen | M. Greenberg | J. Steen | Wen-Ning Zhao | C. Weitz | Yingxi Lin | Linda S. Hu | Elizabeth J. Hong | Zhaolan Zhou | Sonia Cohen | Erin M. Savner | H. H. Ho | L. Schmidt
[1] T. Soderling,et al. Activity-Dependent Dendritic Arborization Mediated by CaM-Kinase I Activation and Enhanced CREB-Dependent Transcription of Wnt-2 , 2006, Neuron.
[2] H. Zoghbi,et al. MeCP2 dysfunction in Rett syndrome and related disorders. , 2006, Current opinion in genetics & development.
[3] E. Kavalali,et al. MeCP2-Dependent Transcriptional Repression Regulates Excitatory Neurotransmission , 2006, Current Biology.
[4] P. Tam,et al. Mecp2 deficiency is associated with learning and cognitive deficits and altered gene activity in the hippocampal region of mice. , 2006, Brain : a journal of neurology.
[5] S. Nelson,et al. The Disease Progression of Mecp2 Mutant Mice Is Affected by the Level of BDNF Expression , 2006, Neuron.
[6] A. Bird,et al. Genomic DNA methylation: the mark and its mediators. , 2006, Trends in biochemical sciences.
[7] James H. Eubanks,et al. Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndrome , 2006, Neurobiology of Disease.
[8] H. Zoghbi,et al. Learning and Memory and Synaptic Plasticity Are Impaired in a Mouse Model of Rett Syndrome , 2006, The Journal of Neuroscience.
[9] B. D. de Vries,et al. Chromosomal copy number changes in patients with non-syndromic X linked mental retardation detected by array CGH , 2005, Journal of Medical Genetics.
[10] J. Gécz,et al. Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males. , 2005, American journal of human genetics.
[11] Rudolf Jaenisch,et al. Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett syndrome. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[12] G. Mandel,et al. REST and Its Corepressors Mediate Plasticity of Neuronal Gene Chromatin throughout Neurogenesis , 2005, Cell.
[13] M. Greenberg,et al. Transcriptional control of cognitive development , 2005, Current Opinion in Neurobiology.
[14] K. Hameister,et al. Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome , 2005, Journal of Medical Genetics.
[15] H. Zoghbi,et al. Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome. , 2005, Human molecular genetics.
[16] Noriyuki Kishi,et al. MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decisions , 2004, Molecular and Cellular Neuroscience.
[17] H. Zoghbi,et al. Mild overexpression of MeCP2 causes a progressive neurological disorder in mice. , 2004, Human molecular genetics.
[18] R. Rocchi,et al. Real‐time quantitative PCR as a routine method for screening large rearrangements in Rett syndrome: Report of one case of MECP2 deletion and one case of MECP2 duplication , 2004, Human mutation.
[19] T. Soderling,et al. Calcium Activation of ERK Mediated by Calmodulin Kinase I* , 2004, Journal of Biological Chemistry.
[20] R. Jaenisch,et al. Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[21] T. Soderling,et al. Regulation of Axonal Extension and Growth Cone Motility by Calmodulin-Dependent Protein Kinase I , 2004, The Journal of Neuroscience.
[22] Azad Bonni,et al. A CaMKII-NeuroD Signaling Pathway Specifies Dendritic Morphogenesis , 2004, Neuron.
[23] H. Zoghbi. Postnatal Neurodevelopmental Disorders: Meeting at the Synapse? , 2003, Science.
[24] Daisuke Hattori,et al. DNA Methylation-Related Chromatin Remodeling in Activity-Dependent Bdnf Gene Regulation , 2003, Science.
[25] Eric C. Griffith,et al. Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2 , 2003, Science.
[26] A. Bird,et al. DNA methylation and Rett syndrome. , 2003, Human molecular genetics.
[27] Eric C. Griffith,et al. Regulation of transcription factors by neuronal activity , 2002, Nature Reviews Neuroscience.
[28] Juan I. Young,et al. Mice with Truncated MeCP2 Recapitulate Many Rett Syndrome Features and Display Hyperacetylation of Histone H3 , 2002, Neuron.
[29] Anirvan Ghosh,et al. Calcium Regulation of Dendritic Growth via CaM Kinase IV and CREB-Mediated Transcription , 2002, Neuron.
[30] H. Bading,et al. Extrasynaptic NMDARs oppose synaptic NMDARs by triggering CREB shut-off and cell death pathways , 2002, Nature Neuroscience.
[31] Eric C. Griffith,et al. CREB Transcriptional Activity in Neurons Is Regulated by Multiple, Calcium-Specific Phosphorylation Events , 2002, Neuron.
[32] J. Lisman,et al. The molecular basis of CaMKII function in synaptic and behavioural memory , 2002, Nature Reviews Neuroscience.
[33] David Baltimore,et al. Germline Transmission and Tissue-Specific Expression of Transgenes Delivered by Lentiviral Vectors , 2002, Science.
[34] R. Jaenisch,et al. Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice , 2001, Nature Genetics.
[35] B. Lom,et al. Brain-Derived Neurotrophic Factor Differentially Regulates Retinal Ganglion Cell Dendritic and Axonal Arborization In Vivo , 1999, The Journal of Neuroscience.
[36] H. Zoghbi,et al. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 , 1999, Nature Genetics.
[37] A. Wolffe,et al. The methyl-CpG binding transcriptional repressor MeCP2 stably associates with nucleosomal DNA. , 1999, Biochemistry.
[38] M. Greenberg,et al. Akt Promotes Cell Survival by Phosphorylating and Inhibiting a Forkhead Transcription Factor , 1999, Cell.
[39] T. Soderling,et al. Characterization of a calmodulin kinase II inhibitor protein in brain. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[40] Tobias Meyer,et al. CaMKIIβ Functions As an F-Actin Targeting Module that Localizes CaMKIIα/β Heterooligomers to Dendritic Spines , 1998, Neuron.
[41] P. Worley,et al. Immediate-Early Genes and Synaptic Function , 1998, Neurobiology of Learning and Memory.
[42] C. Shatz,et al. Synaptic Activity and the Construction of Cortical Circuits , 1996, Science.
[43] M. Greenberg,et al. Calcium Influx via the NMDA Receptor Induces Immediate Early Gene Transcription by a MAP Kinase/ERK-Dependent Mechanism , 1996, The Journal of Neuroscience.
[44] Ted Abel,et al. Recombinant BDNF Rescues Deficits in Basal Synaptic Transmission and Hippocampal LTP in BDNF Knockout Mice , 1996, Neuron.
[45] J. Kornhauser,et al. Light, immediate-early genes, and circadian rhythms , 1996, Behavior genetics.
[46] Lawrence C. Katz,et al. Neurotrophins regulate dendritic growth in developing visual cortex , 1995, Neuron.
[47] T Bonhoeffer,et al. Hippocampal long-term potentiation is impaired in mice lacking brain-derived neurotrophic factor. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[48] H. Enslen,et al. Differential activation of CREB by Ca2+/calmodulin-dependent protein kinases type II and type IV involves phosphorylation of a site that negatively regulates activity. , 1994, Genes & development.
[49] A. Bird,et al. Purification, sequence, and cellular localization of a novel chromosomal protein that binds to Methylated DNA , 1992, Cell.
[50] D. Muller,et al. A simple method for organotypic cultures of nervous tissue , 1991, Journal of Neuroscience Methods.
[51] Jean Aicardi,et al. A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: Report of 35 cases , 1983, Annals of neurology.
[52] A Rett,et al. [On a unusual brain atrophy syndrome in hyperammonemia in childhood]. , 1966, Wiener medizinische Wochenschrift.
[53] J. Chelly,et al. Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized , 2006, Nature Reviews Genetics.
[54] K. Svoboda,et al. Structure and function of dendritic spines. , 2002, Annual review of physiology.
[55] S. Reppert,et al. Molecular analysis of mammalian circadian rhythms. , 2001, Annual review of physiology.
[56] A. Bird,et al. A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome , 2001, Nature Genetics.
[57] Mu-ming Poo,et al. Neurotrophins as synaptic modulators , 2001, Nature Reviews Neuroscience.
[58] S. Zeiler,et al. Development/Plasticity/Repair Brain-Derived Neurotrophic Factor Is Required for the Maintenance of Cortical Dendrites , 2022 .