Functions of synapse adhesion molecules neurexin/neuroligins and neurodevelopmental disorders
暂无分享,去创建一个
[1] Masahiko Watanabe,et al. Endocannabinoid-mediated control of synaptic transmission. , 2009, Physiological reviews.
[2] T. Südhof,et al. Mouse neurexin-1α deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments , 2009, Proceedings of the National Academy of Sciences.
[3] P. Scheiffele,et al. Control of Excitatory and Inhibitory Synapse Formation by Neuroligins , 2005, Science.
[4] A. Hannan,et al. Reduced susceptibility to induced seizures in the Neuroligin-3R451C mouse model of autism , 2015, Neuroscience Letters.
[5] Steven A. Connor,et al. The Specific α-Neurexin Interactor Calsyntenin-3 Promotes Excitatory and Inhibitory Synapse Development , 2013, Neuron.
[6] Thomas C. Südhof,et al. Presynaptic Neurexin-3 Alternative Splicing trans-Synaptically Controls Postsynaptic AMPA Receptor Trafficking , 2013, Cell.
[7] Giada Cellot,et al. Reduced inhibitory gate in the barrel cortex of Neuroligin3R451C knock‐in mice, an animal model of autism spectrum disorders , 2014, Physiological reports.
[8] T. Südhof,et al. α-Neurexins couple Ca2+ channels to synaptic vesicle exocytosis , 2003, Nature.
[9] Thomas C. Südhof,et al. Structures of Neuroligin-1 and the Neuroligin-1/Neurexin-1β Complex Reveal Specific Protein-Protein and Protein-Ca2+ Interactions , 2007, Neuron.
[10] T. Südhof,et al. Neuroligin 1 is a postsynaptic cell-adhesion molecule of excitatory synapses. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[11] T. Südhof,et al. β-Neurexins Control Neural Circuits by Regulating Synaptic Endocannabinoid Signaling , 2015, Cell.
[12] M. Yuzaki,et al. Cbln family proteins promote synapse formation by regulating distinct neurexin signaling pathways in various brain regions , 2011, The European journal of neuroscience.
[13] S. Jamain,et al. Neuroligin 2 is exclusively localized to inhibitory synapses. , 2004, European journal of cell biology.
[14] T. Südhof,et al. Activity-Dependent Validation of Excitatory versus Inhibitory Synapses by Neuroligin-1 versus Neuroligin-2 , 2007, Neuron.
[15] T. Südhof,et al. Pathogenic Mechanism of an Autism-Associated Neuroligin Mutation Involves Altered AMPA-Receptor Trafficking , 2015, Molecular Psychiatry.
[16] T. Südhof,et al. Neuroligin 1: A splice site-specific ligand for β-neurexins , 1995, Cell.
[17] T. Südhof,et al. A stoichiometric complex of neurexins and dystroglycan in brain , 2001, The Journal of cell biology.
[18] T. Südhof,et al. Neurexophilins Form a Conserved Family of Neuropeptide-Like Glycoproteins , 1998, The Journal of Neuroscience.
[19] T. Südhof,et al. Structure and evolution of neurexin genes: insight into the mechanism of alternative splicing. , 2002, Genomics.
[20] T. Südhof,et al. The Making of Neurexins , 1998, Journal of neurochemistry.
[21] J. Yates,et al. LRRTM2 Interacts with Neurexin1 and Regulates Excitatory Synapse Formation , 2009, Neuron.
[22] P. Jonas,et al. Perturbed Hippocampal Synaptic Inhibition and γ-Oscillations in a Neuroligin-4 Knockout Mouse Model of Autism , 2015, Cell reports.
[23] T. Südhof,et al. Neuroligin-1 Deletion Results in Impaired Spatial Memory and Increased Repetitive Behavior , 2010, The Journal of Neuroscience.
[24] M. Yuzaki,et al. Structural basis for integration of GluD receptors within synaptic organizer complexes , 2016, Science.
[25] M. Hoon,et al. Neuroligin 2 Drives Postsynaptic Assembly at Perisomatic Inhibitory Synapses through Gephyrin and Collybistin , 2009, Neuron.
[26] D. Collier,et al. Genetic targeting of NRXN2 in mice unveils role in excitatory cortical synapse function and social behaviors , 2015, Front. Synaptic Neurosci..
[27] R. Nicoll,et al. Autism-associated mutation inhibits protein kinase C-mediated neuroligin-4X enhancement of excitatory synapses , 2015, Proceedings of the National Academy of Sciences.
[28] Ann Marie Craig,et al. Neurexin–neuroligin signaling in synapse development , 2007, Current Opinion in Neurobiology.
[29] Igor Tsigelny,et al. The Arg451Cys-Neuroligin-3 Mutation Associated with Autism Reveals a Defect in Protein Processing , 2004, The Journal of Neuroscience.
[30] Thomas C. Südhof,et al. Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function , 2011, Proceedings of the National Academy of Sciences.
[31] T. Südhof,et al. Conditional ablation of neuroligin-1 in CA1 pyramidal neurons blocks LTP by a cell-autonomous NMDA receptor-independent mechanism , 2016, Molecular Psychiatry.
[32] P. Scheiffele,et al. Control of neuronal synapse specification by a highly dedicated alternative splicing program , 2016, Science.
[33] N. Craddock,et al. Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients , 2005, Molecular Psychiatry.
[34] Davide Comoletti,et al. Characterization of the Interaction of a Recombinant Soluble Neuroligin-1 with Neurexin-1β* , 2003, Journal of Biological Chemistry.
[35] Kenji F. Tanaka,et al. Shared Synaptic Pathophysiology in Syndromic and Nonsyndromic Rodent Models of Autism , 2012, Science.
[36] P. Somogyi,et al. Quantitative localisation of synaptic and extrasynaptic GABAA receptor subunits on hippocampal pyramidal cells by freeze‐fracture replica immunolabelling , 2010, The European journal of neuroscience.
[37] Thomas C. Südhof,et al. A Splice Code for trans-Synaptic Cell Adhesion Mediated by Binding of Neuroligin 1 to α- and β-Neurexins , 2005, Neuron.
[38] Ann Marie Craig,et al. Neurexins Induce Differentiation of GABA and Glutamate Postsynaptic Specializations via Neuroligins , 2004, Cell.
[39] J. Frahm,et al. Neuroligin‐3‐deficient mice: model of a monogenic heritable form of autism with an olfactory deficit , 2009, Genes, brain, and behavior.
[40] J. Gilbert,et al. Genomic screen and follow-up analysis for autistic disorder. , 2002, American journal of medical genetics.
[41] P. Scheiffele,et al. Disorder-associated mutations lead to functional inactivation of neuroligins. , 2004, Human molecular genetics.
[42] R. Fetter,et al. Neuroligin Expressed in Nonneuronal Cells Triggers Presynaptic Development in Contacting Axons , 2000, Cell.
[43] Kingkaew Pajareya,et al. A pilot randomized controlled trial of DIR/Floortime™ parent training intervention for pre-school children with autistic spectrum disorders , 2011, Autism : the international journal of research and practice.
[44] Jung Hoon Jung,et al. Neuroligin-1 controls synaptic abundance of NMDA-type glutamate receptors through extracellular coupling , 2012, Proceedings of the National Academy of Sciences.
[45] L. Peltonen,et al. A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27. , 2002, American journal of human genetics.
[46] Maureen S. Durkin,et al. Prevalence and Characteristics of Autism Spectrum Disorder Among Children Aged 8 Years — Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2012 , 2018, Morbidity and mortality weekly report. Surveillance summaries.
[47] Meghan T. Miller,et al. Structural Analysis of the Synaptic Protein Neuroligin and Its β-Neurexin Complex: Determinants for Folding and Cell Adhesion , 2007, Neuron.
[48] D. Skuse,et al. Xp deletions associated with autism in three females , 1999, Human Genetics.
[49] Mark J. Harris,et al. Developmental delays and reduced pup ultrasonic vocalizations but normal sociability in mice lacking the postsynaptic cell adhesion protein neuroligin2 , 2013, Behavioural Brain Research.
[50] T. Takeuchi,et al. Trans-Synaptic Interaction of GluRδ2 and Neurexin through Cbln1 Mediates Synapse Formation in the Cerebellum , 2010, Cell.
[51] S. Löwel,et al. Neuroligin-4 is localized to glycinergic postsynapses and regulates inhibition in the retina , 2011, Proceedings of the National Academy of Sciences.
[52] Jacqueline Blundell,et al. A Neuroligin-3 Mutation Implicated in Autism Increases Inhibitory Synaptic Transmission in Mice , 2007, Science.
[53] Jens Frahm,et al. Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism , 2008, Proceedings of the National Academy of Sciences.
[54] T. Südhof,et al. Increased anxiety‐like behavior in mice lacking the inhibitory synapse cell adhesion molecule neuroligin 2 , 2009, Genes, brain, and behavior.
[55] K. Tabuchi,et al. Enhanced synapse remodelling as a common phenotype in mouse models of autism , 2014, Nature Communications.
[56] T. Südhof,et al. Distinct circuit-dependent functions of presynaptic neurexin-3 at GABAergic and glutamatergic synapses , 2015, Nature Neuroscience.
[57] J. Gibson,et al. Increased Cortical Inhibition in Autism-Linked Neuroligin-3R451C Mice Is Due in Part to Loss of Endocannabinoid Signaling , 2015, PloS one.
[58] Thomas Bourgeron,et al. Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism , 2003, Nature Genetics.
[59] Thomas C. Südhof,et al. Cartography of neurexin alternative splicing mapped by single-molecule long-read mRNA sequencing , 2014, Proceedings of the National Academy of Sciences.
[60] T. Südhof,et al. An autism‐associated point mutation in the neuroligin cytoplasmic tail selectively impairs AMPA receptor‐mediated synaptic transmission in hippocampus , 2011, The EMBO journal.
[61] Seung-Hee Lee,et al. LRRTM3 Regulates Excitatory Synapse Development through Alternative Splicing and Neurexin Binding. , 2016, Cell reports.
[62] Jacob Ellegood,et al. Genetic Effects on Cerebellar Structure Across Mouse Models of Autism Using a Magnetic Resonance Imaging Atlas , 2014, Autism research : official journal of the International Society for Autism Research.
[63] Patrick E. Rothwell,et al. Autism-Associated Neuroligin-3 Mutations Commonly Impair Striatal Circuits to Boost Repetitive Behaviors , 2014, Cell.
[64] T. Südhof,et al. Neuroligin-2 Deletion Selectively Decreases Inhibitory Synaptic Transmission Originating from Fast-Spiking but Not from Somatostatin-Positive Interneurons , 2009, The Journal of Neuroscience.
[65] Masahiko Watanabe,et al. Presynaptically Released Cbln1 Induces Dynamic Axonal Structural Changes by Interacting with GluD2 during Cerebellar Synapse Formation , 2012, Neuron.
[66] T. Südhof,et al. Neurexins: synaptic cell surface proteins related to the alpha-latrotoxin receptor and laminin. , 1992, Science.
[67] Thomas C. Südhof,et al. LRRTM2 Functions as a Neurexin Ligand in Promoting Excitatory Synapse Formation , 2009, Neuron.
[68] M. Hoon,et al. Neuroligin 2 Controls the Maturation of GABAergic Synapses and Information Processing in the Retina , 2009, The Journal of Neuroscience.
[69] T. Südhof,et al. Autism-Associated Neuroligin-3 Mutations Commonly Disrupt Tonic Endocannabinoid Signaling , 2013, Neuron.
[70] T. Südhof,et al. Neurons generated by direct conversion of fibroblasts reproduce synaptic phenotype caused by autism-associated neuroligin-3 mutation , 2013, Proceedings of the National Academy of Sciences.
[71] N. Grishin,et al. Unusually rapid evolution of Neuroligin-4 in mice , 2008, Proceedings of the National Academy of Sciences.
[72] T. Bourgeron,et al. Development of an autism severity score for mice using Nlgn4 null mutants as a construct-valid model of heritable monogenic autism , 2013, Behavioural Brain Research.
[73] K. Hammerschmidt,et al. Juvenile manifestation of ultrasound communication deficits in the neuroligin-4 null mutant mouse model of autism , 2014, Behavioural Brain Research.
[74] J. Levinson,et al. A Crystal-Clear Interaction: Relating Neuroligin/Neurexin Complex Structure to Function at the Synapse , 2007, Neuron.
[75] Masahiko Watanabe,et al. Transsynaptic Modulation of Kainate Receptor Functions by C1q-like Proteins , 2016, Neuron.
[76] Bo Zhang,et al. Neuroligins Sculpt Cerebellar Purkinje-Cell Circuits by Differential Control of Distinct Classes of Synapses , 2015, Neuron.
[77] Elodie Ey,et al. The genetic landscapes of autism spectrum disorders. , 2013, Annual review of genomics and human genetics.