MeCP2 Controls Excitatory Synaptic Strength by Regulating Glutamatergic Synapse Number
暂无分享,去创建一个
Christian Rosenmund | Huda Y. Zoghbi | Hsiao-Tuan Chao | H. Zoghbi | Christian Rosenmund | Hsiao-Tuan Chao
[1] A. Bird,et al. Reversal of Neurological Defects in a Mouse Model of Rett Syndrome , 2007, Science.
[2] A. Dahlström,et al. Morphological study of neocortical areas in Rett syndrome , 1996, Acta Neuropathologica.
[3] Christian Rosenmund,et al. Nonuniform probability of glutamate release at a hippocampal synapse. , 1993, Science.
[4] S. Nelson,et al. Homeostatic plasticity in the developing nervous system , 2004, Nature Reviews Neuroscience.
[5] M. Kennedy,et al. The rat brain postsynaptic density fraction contains a homolog of the drosophila discs-large tumor suppressor protein , 1992, Neuron.
[6] 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.
[7] Jurgen Klingauf,et al. Synaptic vesicles recycling spontaneously and during activity belong to the same vesicle pool , 2007, Nature Neuroscience.
[8] G. Davis. Homeostatic control of neural activity: from phenomenology to molecular design. , 2006, Annual review of neuroscience.
[9] M. Cuccaro,et al. Identification of MeCP2 mutations in a series of females with autistic disorder. , 2003, Pediatric neurology.
[10] Juan I. Young,et al. Mice with Truncated MeCP2 Recapitulate Many Rett Syndrome Features and Display Hyperacetylation of Histone H3 , 2002, Neuron.
[11] R. Jaenisch,et al. Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2 , 2007, Proceedings of the National Academy of Sciences.
[12] H. Zoghbi,et al. Learning and Memory and Synaptic Plasticity Are Impaired in a Mouse Model of Rett Syndrome , 2006, The Journal of Neuroscience.
[13] James H. Eubanks,et al. Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndrome , 2006, Neurobiology of Disease.
[14] S. Sommer,et al. Detection of heterozygous deletions and duplications in the MECP2 gene in Rett syndrome by Robust Dosage PCR (RD‐PCR) , 2005, Human mutation.
[15] A Rett,et al. [On a unusual brain atrophy syndrome in hyperammonemia in childhood]. , 1966, Wiener medizinische Wochenschrift.
[16] J. Fryns,et al. A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males. , 2000, American journal of human genetics.
[17] H. Zoghbi,et al. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 , 1999, Nature Genetics.
[18] M. Sheng,et al. Interaction between the C terminus of NMDA receptor subunits and multiple members of the PSD-95 family of membrane-associated guanylate kinases , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[19] M. Sheng,et al. Heterogeneity in the Molecular Composition of Excitatory Postsynaptic Sites during Development of Hippocampal Neurons in Culture , 1998, The Journal of Neuroscience.
[20] P. Seeburg,et al. Domain interaction between NMDA receptor subunits and the postsynaptic density protein PSD-95. , 1995, Science.
[21] R. Stevenson,et al. Recurrent Infections, Hypotonia, and Mental Retardation Caused by Duplication of MECP2 and Adjacent Region in Xq28 , 2006, Pediatrics.
[22] A. Federico,et al. MECP2 mutation in male patients with non‐specific X‐linked mental retardation , 2000, FEBS letters.
[23] E. Kavalali,et al. MeCP2-Dependent Transcriptional Repression Regulates Excitatory Neurotransmission , 2006, Current Biology.
[24] Thomas Bourgeron,et al. Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders , 2007, Nature Genetics.
[25] W. Regehr,et al. Short-term synaptic plasticity. , 2002, Annual review of physiology.
[26] B. Voss,et al. SAP90, a rat presynaptic protein related to the product of the Drosophila tumor suppressor gene dlg-A. , 1993, The Journal of biological chemistry.
[27] 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.
[28] Ankita Patel,et al. Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males , 2006, Genetics in Medicine.
[29] 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.
[30] R. Malinow,et al. The probability of transmitter release at a mammalian central synapse , 1993, Nature.
[31] B. Antalffy,et al. Selective Dendritic Alterations in the Cortex of Rett Syndrome , 1995, Journal of neuropathology and experimental neurology.
[32] H. Zoghbi. Postnatal Neurodevelopmental Disorders: Meeting at the Synapse? , 2003, Science.
[33] Charles E. Schwartz,et al. High frequency of neurexin 1β signal peptide structural variants in patients with autism , 2006, Neuroscience Letters.
[34] A. Bird,et al. A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome , 2001, Nature Genetics.
[35] K. Harris,et al. Three-dimensional structure of dendritic spines and synapses in rat hippocampus (CA1) at postnatal day 15 and adult ages: implications for the maturation of synaptic physiology and long-term potentiation. , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[36] 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.
[37] H. Zoghbi,et al. Mild overexpression of MeCP2 causes a progressive neurological disorder in mice. , 2004, Human molecular genetics.
[38] H. Ropers,et al. MECP2 is highly mutated in X-linked mental retardation. , 2001, Human molecular genetics.
[39] C. Stevens,et al. Excitatory and inhibitory autaptic currents in isolated hippocampal neurons maintained in cell culture. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[40] A. C. Meyer,et al. Released Fraction and Total Size of a Pool of Immediately Available Transmitter Quanta at a Calyx Synapse , 1999, Neuron.
[41] Thomas Bourgeron,et al. Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism , 2003, Nature Genetics.
[42] Eric C. Griffith,et al. Brain-Specific Phosphorylation of MeCP2 Regulates Activity-Dependent Bdnf Transcription, Dendritic Growth, and Spine Maturation , 2006, Neuron.
[43] Christian Rosenmund,et al. The effects of temperature on vesicular supply and release in autaptic cultures of rat and mouse hippocampal neurons , 2002, The Journal of physiology.
[44] R. Fremeau,et al. Uptake of glutamate into synaptic vesicles by an inorganic phosphate transporter. , 2000, Science.