Rescue of Methyl-CpG Binding Protein 2 Dysfunction-induced Defects in Newborn Neurons by Pentobarbital

[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]  J. Jefferys,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.