Rescue of Methyl-CpG Binding Protein 2 Dysfunction-induced Defects in Newborn Neurons by Pentobarbital
暂无分享,去创建一个
G. Ming | K. Hsu | G. Augustine | Guillaume Marcy | Chih-hao Yang | E. Goh | Dongliang Ma | Su-In Yoon | J. Han | W. Leong | N. Zhao | V. Ganapathy | A. M. Van Dongen | Vinu Ganapathy | A. M. V. Van Dongen | Na Zhao
[1] J. Roux,et al. GABA and Glutamate Pathways Are Spatially and Developmentally Affected in the Brain of Mecp2-Deficient Mice , 2014, PloS one.
[2] Erika D. Nelson,et al. GABAA Receptor Antagonism Ameliorates Behavioral and Synaptic Impairments Associated with MeCP2 Overexpression , 2014, Neuropsychopharmacology.
[3] Stephanie C. Licata,et al. Alterations in Brain-Derived Neurotrophic Factor in the Mouse Hippocampus Following Acute but Not Repeated Benzodiazepine Treatment , 2013, PloS one.
[4] Zhaolan Zhou,et al. Neuronal morphology in MeCP2 mouse models is intrinsically variable and depends on age, cell type, and Mecp2 mutation , 2013, Neurobiology of Disease.
[5] D. Fischer,et al. Erratum to “CXCL12/SDF-1 facilitates optic nerve regeneration” [Neurobiol. Dis. 55 (2013) 76–86] , 2013, Neurobiology of Disease.
[6] A. Bird,et al. Systemic Delivery of MeCP2 Rescues Behavioral and Cellular Deficits in Female Mouse Models of Rett Syndrome , 2013, The Journal of Neuroscience.
[7] A. Bird,et al. Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor , 2013, Nature Neuroscience.
[8] G. Ming,et al. Class 3 Semaphorin Mediates Dendrite Growth in Adult Newborn Neurons through Cdk5/FAK Pathway , 2013, PloS one.
[9] W. Löscher,et al. How theories evolved concerning the mechanism of action of barbiturates , 2012, Epilepsia.
[10] Guillaume Marcy,et al. Taurine Induces Proliferation of Neural Stem Cells and Synapse Development in the Developing Mouse Brain , 2012, PloS one.
[11] K. Delaney,et al. MeCP2 Mutation Results in Compartment-Specific Reductions in Dendritic Branching and Spine Density in Layer 5 Motor Cortical Neurons of YFP-H Mice , 2012, PloS one.
[12] J. Raber,et al. A role for glia in the progression of Rett’s syndrome , 2011, Nature.
[13] Rodney C. Samaco,et al. Adult Neural Function Requires MeCP2 , 2011, Science.
[14] G. Hilaire,et al. The benzodiazepine Midazolam mitigates the breathing defects of Mecp2-deficient mice , 2011, Respiratory Physiology & Neurobiology.
[15] N. Amariglio,et al. Ex Vivo Treatment with a Novel Synthetic Aminoglycoside NB54 in Primary Fibroblasts from Rett Syndrome Patients Suppresses MECP2 Nonsense Mutations , 2011, PloS one.
[16] J. Hablitz,et al. Network hyperexcitability in hippocampal slices from Mecp2 mutant mice revealed by voltage-sensitive dye imaging. , 2011, Journal of neurophysiology.
[17] P. Huppke,et al. Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model , 2010, Journal of Molecular Medicine.
[18] Fred H. Gage,et al. A Model for Neural Development and Treatment of Rett Syndrome Using Human Induced Pluripotent Stem Cells , 2010, Cell.
[19] J. Eubanks,et al. Aminoglycoside‐mediated partial suppression of MECP2 nonsense mutations responsible for Rett syndrome in vitro , 2010, Journal of neuroscience research.
[20] Izumi Maezawa,et al. Rett Syndrome Microglia Damage Dendrites and Synapses by the Elevated Release of Glutamate , 2010, The Journal of Neuroscience.
[21] E. Korpi,et al. Regulation of GABAA Receptor Subunit Expression by Pharmacological Agents , 2010, Pharmacological Reviews.
[22] J. D. Macklis,et al. MeCP2 functions largely cell-autonomously, but also non-cell-autonomously, in neuronal maturation and dendritic arborization of cortical pyramidal neurons , 2010, Experimental Neurology.
[23] Y. Zhang,et al. Altered synchrony and connectivity in neuronal networks expressing an autism-related mutation of neuroligin 3 , 2009, Neuroscience.
[24] S. Kudo,et al. Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations , 2009, Neurobiology of Disease.
[25] S. Kügler,et al. Remodelling of the respiratory network in a mouse model of Rett syndrome depends on brain‐derived neurotrophic factor regulated slow calcium buffering , 2009, The Journal of physiology.
[26] S. Kudo,et al. Bdnf overexpression in hippocampal neurons prevents dendritic atrophy caused by Rett-associated MECP2 mutations , 2009, Neurobiology of Disease.
[27] P. Huppke,et al. Suppression of Nonsense Mutations in Rett Syndrome by Aminoglycoside Antibiotics , 2009, Pediatric Research.
[28] D. Harvey,et al. Rett Syndrome Astrocytes Are Abnormal and Spread MeCP2 Deficiency through Gap Junctions , 2009, The Journal of Neuroscience.
[29] G. Mandel,et al. Non–cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology , 2009, Nature Neuroscience.
[30] Nathan R. Wilson,et al. Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice , 2009, Proceedings of the National Academy of Sciences.
[31] M. Jackson,et al. Distinct structural changes in the GABAA receptor elicited by pentobarbital and GABA. , 2009, Biophysical journal.
[32] G. Ming,et al. beta1-integrin mediates myelin-associated glycoprotein signaling in neuronal growth cones , 2008, Molecular Brain.
[33] J. Aimone,et al. Mecp2 deficiency leads to delayed maturation and altered gene expression in hippocampal neurons , 2007, Neurobiology of Disease.
[34] A. Bird,et al. Reversal of Neurological Defects in a Mouse Model of Rett Syndrome , 2007, Science.
[35] Eric C. Griffith,et al. Brain-Specific Phosphorylation of MeCP2 Regulates Activity-Dependent Bdnf Transcription, Dendritic Growth, and Spine Maturation , 2006, Neuron.
[36] E. Kavalali,et al. MeCP2-Dependent Transcriptional Repression Regulates Excitatory Neurotransmission , 2006, Current Biology.
[37] Hongjun Song,et al. GABA regulates synaptic integration of newly generated neurons in the adult brain , 2006, Nature.
[38] James H. Eubanks,et al. Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndrome , 2006, Neurobiology of Disease.
[39] H. Zoghbi,et al. Learning and Memory and Synaptic Plasticity Are Impaired in a Mouse Model of Rett Syndrome , 2006, The Journal of Neuroscience.
[40] G. Cheron,et al. Purkinje cell rhythmicity and synchronicity during modulation of fast cerebellar oscillation , 2005, Neuroscience.
[41] Juan I. Young,et al. Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[42] M. Bikson,et al. Neuronal aggregate formation underlies spatiotemporal dynamics of nonsynaptic seizure initiation. , 2003, Journal of neurophysiology.
[43] J. Steinbach,et al. Modulation of GABAA receptor channel gating by pentobarbital , 2001, The Journal of physiology.
[44] H. Zoghbi,et al. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 , 1999, Nature Genetics.
[45] E. Gruenstein,et al. Mechanism of synchronized Ca2+ oscillations in cortical neurons , 1997, Brain Research.
[46] A. Bird,et al. MeCP2 Is a Transcriptional Repressor with Abundant Binding Sites in Genomic Chromatin , 1997, Cell.
[47] Xavier Leinekugel,et al. Ca2+ Oscillations Mediated by the Synergistic Excitatory Actions of GABAA and NMDA Receptors in the Neonatal Hippocampus , 1997, Neuron.
[48] 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.
[49] M. Missler,et al. Early defects of GABAergic synapses in the brain stem of a MeCP2 mouse model of Rett syndrome. , 2008, Journal of neurophysiology.
[50] C. Christakos. Note on the estimation of the correlation function of neural spike trains , 2004, Biological Cybernetics.