Mice with mutations in Trpm1, a gene in the locus of 15q13.3 microdeletion syndrome, display pronounced hyperactivity and decreased anxiety-like behavior
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[1] M. Ptito,et al. Neural Networks Mediating Perceptual Learning in Congenital Blindness , 2020, Scientific Reports.
[2] R. Dalrymple,et al. NICE guideline review: Attention deficit hyperactivity disorder: diagnosis and management (NG87) , 2019, Archives of Disease in Childhood.
[3] M. Piché,et al. Pain Hypersensitivity is Associated with Increased Amygdala Volume and c-Fos Immunoreactivity in Anophthalmic Mice. , 2019, Neuroscience.
[4] R. Fick,et al. Homozygous 15q13.3 microdeletion in a child with hypotonia and impaired vision: A new report and review of the literature , 2019, Clinical case reports.
[5] Y. Yanagawa,et al. Feedback inhibition derived from the posterior parietal cortex regulates the neural properties of the mouse visual cortex , 2019, The European journal of neuroscience.
[6] N. Kaya,et al. First report of two successive deletions on chromosome 15q13 cytogenetic bands in a boy and girl: additional data to 15q13.3 syndrome with a report of high IQ patient , 2019, Molecular Cytogenetics.
[7] Fabrice de Chaumont,et al. Shank2 Mutant Mice Display Hyperactivity Insensitive to Methylphenidate and Reduced Flexibility in Social Motivation, but Normal Social Recognition , 2018, Front. Mol. Neurosci..
[8] Nathalie L Rochefort,et al. Action and learning shape the activity of neuronal circuits in the visual cortex , 2018, Current Opinion in Neurobiology.
[9] Rodney C. Samaco,et al. Otud7a Knockout Mice Recapitulate Many Neurological Features of 15q13.3 Microdeletion Syndrome. , 2018, American journal of human genetics.
[10] Y. Saalmann,et al. Feedback from human posterior parietal cortex enables visuospatial category representations as early as primary visual cortex , 2017, Brain and behavior.
[11] L. Xiong,et al. Deficiency of tumor suppressor NDRG2 leads to attention deficit and hyperactive behavior , 2017, The Journal of clinical investigation.
[12] Georg B. Keller,et al. A Sensorimotor Circuit in Mouse Cortex for Visual Flow Predictions , 2017, Neuron.
[13] M. Tachibana,et al. Different Activity Patterns in Retinal Ganglion Cells of TRPM1 and mGluR6 Knockout Mice , 2017, BioMed research international.
[14] J. Cheong,et al. Exploring the Validity of Proposed Transgenic Animal Models of Attention-Deficit Hyperactivity Disorder (ADHD) , 2017, Molecular Neurobiology.
[15] H. Okano,et al. In vivo microscopic voxel-based morphometry with a brain template to characterize strain-specific structures in the mouse brain , 2017, Scientific Reports.
[16] C. Schaaf,et al. Chrna7 deficient mice manifest no consistent neuropsychiatric and behavioral phenotypes , 2017, Scientific Reports.
[17] O. Halbach,et al. A novel form of capsaicin-modified amygdala LTD mediated by TRPM1 , 2016, Neurobiology of Learning and Memory.
[18] T. Werge,et al. 15q13.3 homozygous knockout mouse model display epilepsy-, autism- and schizophrenia-related phenotypes , 2016, Translational Psychiatry.
[19] M. Ptito,et al. Congenital blindness affects diencephalic but not mesencephalic structures in the human brain , 2016, Brain Structure and Function.
[20] A. Yamanaka,et al. TRPV4 activation at the physiological temperature is a critical determinant of neuronal excitability and behavior , 2015, Pflügers Archiv - European Journal of Physiology.
[21] C. C. Wrenn,et al. Effects of clonidine and methylphenidate on motor activity in Fmr1 knockout mice , 2015, Neuroscience Letters.
[22] M. Ptito,et al. Pain Perception Is Increased in Congenital but Not Late Onset Blindness , 2014, PloS one.
[23] Christian R. Marshall,et al. Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature , 2014, Genetics in Medicine.
[24] L. Vallée,et al. Further delineation of eye manifestations in homozygous 15q13.3 microdeletions including TRPM1: A differential diagnosis of ceroid lipofuscinosis , 2014, American journal of medical genetics. Part A.
[25] I. Ito,et al. Comprehensive behavioral study of mGluR3 knockout mice: implication in schizophrenia related endophenotypes , 2014, Molecular Brain.
[26] M. Ptito,et al. Compensatory plasticity and cross-modal reorganization following early visual deprivation , 2014, Neuroscience & Biobehavioral Reviews.
[27] T. Miyakawa,et al. Comprehensive Behavioral Analysis of Cluster of Differentiation 47 Knockout Mice , 2014, PloS one.
[28] Emily Petrus,et al. Crossmodal Induction of Thalamocortical Potentiation Leads to Enhanced Information Processing in the Auditory Cortex , 2014, Neuron.
[29] Y. Goshima,et al. Mice lacking collapsin response mediator protein 1 manifest hyperactivity, impaired learning and memory, and impaired prepulse inhibition , 2013, Front. Behav. Neurosci..
[30] Bung-Nyun Kim,et al. Baseline severity of parent-perceived inattentiveness is predictive of the difference between subjective and objective methylphenidate responses in children with attention-deficit/hyperactivity disorder. , 2013, Journal of child and adolescent psychopharmacology.
[31] T. Miyakawa,et al. Chronic overload of SEPT4, a parkin substrate that aggregates in Parkinson’s disease, causes behavioral alterations but not neurodegeneration in mice , 2013, Molecular Brain.
[32] N. Philip,et al. Mosaic 15q13.3 deletion including CHRNA7 gene in monozygotic twins. , 2013, European journal of medical genetics.
[33] K. Wain,et al. Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype , 2013, Clinical genetics.
[34] Hui Zhao,et al. The Rd8 mutation of the Crb1 gene is present in vendor lines of C57BL/6N mice and embryonic stem cells, and confounds ocular induced mutant phenotypes. , 2012, Investigative ophthalmology & visual science.
[35] N. Vardi,et al. mGluR6 deletion renders the TRPM1 channel in retina inactive. , 2012, Journal of neurophysiology.
[36] U. Surti,et al. A small homozygous microdeletion of 15q13.3 including the CHRNA7 gene in a girl with a spectrum of severe neurodevelopmental features , 2011, American journal of medical genetics. Part A.
[37] M. Kamermans,et al. Ultrastructural localization and expression of TRPM1 in the human retina. , 2011, Investigative ophthalmology & visual science.
[38] D. Horn,et al. Homozygous deletion of chromosome 15q13.3 including CHRNA7 causes severe mental retardation, seizures, muscular hypotonia, and the loss of KLF13 and TRPM1 potentially cause macrocytosis and congenital retinal dysfunction in siblings. , 2011, European journal of medical genetics.
[39] T. Takumi,et al. Decreased Exploratory Activity in a Mouse Model of 15q Duplication Syndrome; Implications for Disturbance of Serotonin Signaling , 2010, PloS one.
[40] C. Büchel,et al. Corticocortical Connections Mediate Primary Visual Cortex Responses to Auditory Stimulation in the Blind , 2010, The Journal of Neuroscience.
[41] Hiroshi Ueda,et al. TRPM1: a vertebrate TRP channel responsible for retinal ON bipolar function. , 2010, Cell calcium.
[42] M. Holder,et al. Delineation of 15q13.3 microdeletions , 2010, Clinical genetics.
[43] T. Miyakawa,et al. Behavioral profiles of three C57BL/6 substrains , 2010, Neuroscience Research.
[44] D. Bittel,et al. A 15q13.3 homozygous microdeletion associated with a severe neurodevelopmental disorder suggests putative functions of the TRPM1, CHRNA7, and other homozygously deleted genes , 2010, American journal of medical genetics. Part A.
[45] Makoto Nakamura,et al. TRPM1 mutations are associated with the complete form of congenital stationary night blindness , 2010, Molecular vision.
[46] M. Tachibana,et al. TRPM1 is a component of the retinal ON bipolar cell transduction channel in the mGluR6 cascade , 2009, Proceedings of the National Academy of Sciences of the United States of America.
[47] G. Holder,et al. Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans. , 2009, American journal of human genetics.
[48] R. Duvoisin,et al. TRPM1 is required for the depolarizing light response in retinal ON-bipolar cells , 2009, Proceedings of the National Academy of Sciences.
[49] Marie E. Burns,et al. What are the Effects of Severe Visual Impairment on the Cortical Organization and Connectivity of Primary Visual Cortex? , 2009, Front. Neuroanat..
[50] D. Clapham,et al. TRPM1 Forms Ion Channels Associated with Melanin Content in Melanocytes , 2009, Science Signaling.
[51] Jiannis Ragoussis,et al. A 15q13.3 microdeletion segregating with autism , 2009, European Journal of Human Genetics.
[52] B. V. van Bon,et al. Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome , 2009, Journal of Medical Genetics.
[53] M. Daly,et al. Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders , 2008, Journal of Medical Genetics.
[54] Yu Wang,et al. A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures , 2008, Nature Genetics.
[55] M. Ptito,et al. Alterations of the visual pathways in congenital blindness , 2008, Experimental Brain Research.
[56] U. Noppeney. The effects of visual deprivation on functional and structural organization of the human brain , 2007, Neuroscience & Biobehavioral Reviews.
[57] Z. Mei,et al. Reduced Anxiety and Depression-Like Behaviors in Mice Lacking GABA Transporter Subtype 1 , 2007, Neuropsychopharmacology.
[58] T. Miyakawa,et al. Light/dark Transition Test for Mice , 2006, Journal of visualized experiments : JoVE.
[59] T. Miyakawa,et al. Investigating Gene‐to‐Behavior Pathways in Psychiatric Disorders , 2006, Annals of the New York Academy of Sciences.
[60] Y. Shichida,et al. Recovery of rod-mediated a-wave during light-adaptation in mGluR6-deficient mice , 2006, Vision Research.
[61] G. Wittenberg,et al. Functional connectivity between somatosensory and visual cortex in early blind humans , 2004, The European journal of neuroscience.
[62] G. Koob,et al. Corticotropin Releasing Factor Receptor 1–Deficient Mice Display Decreased Anxiety, Impaired Stress Response, and Aberrant Neuroendocrine Development , 1998, Neuron.
[63] S. Nakanishi,et al. Impairment of Pupillary Responses and Optokinetic Nystagmus in the mGluR6-deficient Mouse , 1997, Neuropharmacology.
[64] Tomomitsu Miyoshi,et al. Specific deficit of the ON response in visual transmission by targeted disruption of the mGIuR6 gene , 1995, Cell.
[65] C. Njiokiktjien,et al. Methylphenidate and information processing. Part 1: Differentiation between responders and nonresponders; Part 2: Efficacy in responders. , 1994, Journal of clinical and experimental neuropsychology.
[66] J. Rauschecker,et al. Crossmodal changes in the somatosensory vibrissa/barrel system of visually deprived animals. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[67] Hilde van der Togt,et al. Publisher's Note , 2003, J. Netw. Comput. Appl..