Mutation of orthologous prickle genes causes a similar epilepsy syndrome in flies and humans
暂无分享,去创建一个
J. Robert Manak | Alexander G. Bassuk | T. Kitamoto | A. Bassuk | J. Manak | Anthony J. Lilienthal | Atulya S R Iyengar | Haley Koerselman | S. N. Ehaideb | Elizabeth Wignall | J. Kasuya | W. H. Evans | Junko Kasuya | Toshihiro Kitamoto | Salleh N. Ehaideb | Elizabeth A. Wignall | William H. Evans | Atulya Iyengar | Haley L. Koerselman | S. Ehaideb
[1] B. Dickson,et al. A genome-wide transgenic RNAi library for conditional gene inactivation in Drosophila , 2007, Nature.
[2] M. Tanouye,et al. Action potentials in normal and Shaker mutant Drosophila. , 1985, Journal of neurogenetics.
[3] Frank Hirth,et al. The Dopaminergic System in the Aging Brain of Drosophila , 2010, Front. Neurosci..
[4] J. Rosenfeld,et al. Mutations in prickle orthologs cause seizures in flies, mice, and humans. , 2011, American journal of human genetics.
[5] Jisue Lee,et al. Mutation of Drosophila focal adhesion kinase induces bang‐sensitive behavior and disrupts glial function, axonal conduction and synaptic transmission , 2008, The European journal of neuroscience.
[6] Barry J. Dickson,et al. Neuronal Control of Drosophila Walking Direction , 2014, Science.
[7] M. Tanouye,et al. The Drosophila slamdance gene: a mutation in an aminopeptidase can cause seizure, paralysis and neuronal failure. , 2002, Genetics.
[8] D. O'Dowd,et al. Model systems for studying cellular mechanisms of SCN1A-related epilepsy. , 2016, Journal of neurophysiology.
[9] A. Hilliker,et al. A Novel Leg-Shaking Drosophila Mutant Defective in a Voltage-Gated K+ Current and Hypersensitive to Reactive Oxygen Species , 2000, The Journal of Neuroscience.
[10] B. Ganetzky,et al. Indirect Suppression Involving Behavioral Mutants with Altered Nerve Excitability in DROSOPHILA MELANOGASTER. , 1982, Genetics.
[11] Giorgio F. Gilestro,et al. pySolo: a complete suite for sleep analysis in Drosophila , 2009, Bioinform..
[12] S. Morato,et al. The role of vision and proprioception in the aversion of rats to the open arms of an elevated plus-maze , 2002, Behavioural Processes.
[13] Y. Jan,et al. Cloning of genomic and complementary DNA from Shaker, a putative potassium channel gene from Drosophila. , 1987, Science.
[14] M. Tanouye,et al. Drosophila sodium channel mutations: Contributions to seizure-susceptibility , 2015, Experimental Neurology.
[15] S. Morato,et al. Effects of floor surface and environmental illumination on exploratory activity in the elevated plus-maze. , 1989, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.
[16] Jisue Lee,et al. Electroconvulsive Seizure Behavior in Drosophila: Analysis of the Physiological Repertoire Underlying a Stereotyped Action Pattern in Bang-Sensitive Mutants , 2002, The Journal of Neuroscience.
[17] S. Leal,et al. A distinct autosomal recessive ataxia maps to chromosome 12in an inbred family from Jordan , 2006, Brain and Development.
[18] A. Sharma,et al. Transcriptomic Analysis in a Drosophila Model Identifies Previously Implicated and Novel Pathways in the Therapeutic Mechanism in Neuropsychiatric Disorders , 2011, Front. Neurosci..
[19] Jean-René Martin,et al. Centrophobism/thigmotaxis, a new role for the mushroom bodies in Drosophila. , 2005, Journal of neurobiology.
[20] M. Picciotto,et al. Decreased Synaptic Vesicle Recycling Efficiency and Cognitive Deficits in Amphiphysin 1 Knockout Mice , 2002, Neuron.
[21] M. Meisler,et al. Sodium channel mutations in epilepsy and other neurological disorders. , 2005, The Journal of clinical investigation.
[22] D. Tree,et al. The balance between isoforms of the prickle LIM domain protein is critical for planar polarity in Drosophila imaginal discs. , 1999, Genes & development.
[23] L. Salkoff,et al. Temperature-induced seizure and frequency-dependent neuromuscular block in a ts mutant of Drosophila , 1978, Nature.
[24] K. Shianna,et al. Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy. , 2012, American journal of human genetics.
[25] D R Soll,et al. A computer-assisted system for reconstructing and interpreting the dynamic three-dimensional relationships of the outer surface, nucleus and pseudopods of crawling cells. , 1998, Cell motility and the cytoskeleton.
[26] J. J. Shepherd,et al. Northern epilepsy syndrome: an inherited childhood onset epilepsy with associated mental deterioration. , 1994, Journal of medical genetics.
[27] A. Bassuk,et al. Mechanisms of prickle1a function in zebrafish epilepsy and retinal neurogenesis , 2013, Disease Models & Mechanisms.
[28] A. Spradling,et al. The Drosophila Gene Disruption Project: Progress Using Transposons With Distinctive Site Specificities , 2011, Genetics.
[29] D. Treit,et al. Thigmotaxis as a test for anxiolytic activity in rats , 1988, Pharmacology Biochemistry and Behavior.
[30] Atulya S R Iyengar,et al. Flight and Seizure Motor Patterns in Drosophila Mutants: Simultaneous Acoustic and Electrophysiological Recordings of Wing Beats and Flight Muscle Activity , 2014, Journal of neurogenetics.
[31] C. Mahaffey,et al. A Missense Mutation in a Highly Conserved Alternate Exon of Dynamin-1 Causes Epilepsy in Fitful Mice , 2010, PLoS genetics.
[32] Michael R. Johnson,et al. De novo mutations in the classic epileptic encephalopathies , 2013, Nature.
[33] K. Nocka,et al. The synaptic vesicle protein SV2A is the binding site for the antiepileptic drug levetiracetam. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[34] M. Tanouye,et al. Seizures and failures in the giant fiber pathway of Drosophila bang- sensitive paralytic mutants , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[35] D. Suzuki,et al. Temperature-sensitive mutations in Drosophila melanogaster. VII. A mutation (para-ts) causing reversible adult paralysis. , 1971, Proceedings of the National Academy of Sciences of the United States of America.
[36] M. Tanouye,et al. The Drosophila easily shocked gene: A mutation in a phospholipid synthetic pathway causes seizure, neuronal failure, and paralysis , 1994, Cell.
[37] G. Carvill,et al. Seizures Are Regulated by Ubiquitin-specific Peptidase 9 X-linked (USP9X), a De-Ubiquitinase , 2015, PLoS genetics.
[38] M. Tanouye,et al. Seizure and epilepsy: studies of seizure disorders in Drosophila. , 2011, International review of neurobiology.
[39] R. Strauss,et al. Coordination of legs during straight walking and turning in Drosophila melanogaster , 1990, Journal of Comparative Physiology A.
[40] J. Wessnitzer,et al. Open Source Tracking and Analysis of Adult Drosophila Locomotion in Buridan's Paradigm with and without Visual Targets , 2012, PloS one.
[41] M. Tanouye,et al. Mutations of the Calcium Channel Gene cacophony Suppress Seizures in Drosophila , 2016, PLoS genetics.
[42] S. Morato,et al. Vibrissal sense is not the main sensory modality in rat exploratory behavior in the elevated plus-maze , 2001, Behavioural Brain Research.
[43] Steven Petrou,et al. SCN1A mutations and epilepsy , 2005, Human mutation.
[44] J. Axelrod,et al. prickle modulates microtubule polarity and axonal transport to ameliorate seizures in flies , 2014, Proceedings of the National Academy of Sciences.
[45] W. D. Kaplan,et al. The behavior of four neurological mutants of Drosophila. , 1969, Genetics.
[46] Jisue Lee,et al. Genetic modifications of seizure susceptibility and expression by altered excitability in Drosophila Na(+) and K(+) channel mutants. , 2006, Journal of neurophysiology.
[47] M. Dickinson,et al. A New Chamber for Studying the Behavior of Drosophila , 2010, PloS one.
[48] M. Tanouye,et al. Drosophila as a Model for Intractable Epilepsy: Gilgamesh Suppresses Seizures in parabss1 Heterozygote Flies , 2013, G3: Genes, Genomes, Genetics.
[49] Yiannis A. Savva,et al. Knock-in model of Dravet syndrome reveals a constitutive and conditional reduction in sodium current. , 2014, Journal of neurophysiology.
[50] De novo mutations in epileptic encephalopathies , 2013 .
[51] D. Gubb,et al. Molecular dissection of Drosophila Prickle isoforms distinguishes their essential and overlapping roles in planar cell polarity. , 2009, Developmental biology.
[52] P. Mitra,et al. Analysis of the Trajectory of Drosophila melanogaster in a Circular Open Field Arena , 2007, PloS one.
[53] Chad A Shaw,et al. Molecular Diagnostic Experience of Whole-Exome Sequencing in Adult Patients , 2015, Genetics in Medicine.
[54] Juan Song,et al. From bench to drug: Human seizure modeling using Drosophila , 2008, Progress in Neurobiology.
[55] B. Ganetzky,et al. Molecular analysis of the para locus, a sodium channel gene in Drosophila , 1989, Cell.
[56] Vivian Nguyen,et al. A Knock-In Model of Human Epilepsy in Drosophila Reveals a Novel Cellular Mechanism Associated with Heat-Induced Seizure , 2012, The Journal of Neuroscience.
[57] Ke Dong,et al. Drosophila as a Model for Epilepsy: bss Is a Gain-of-Function Mutation in the Para Sodium Channel Gene That Leads to Seizures , 2011, Genetics.
[58] M. Scott,et al. A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome. , 2008, American journal of human genetics.
[59] Vinit B. Mahajan,et al. PRICKLE1 Interaction with SYNAPSIN I Reveals a Role in Autism Spectrum Disorders , 2013, PloS one.