The science of autism has seen tremendous breakthroughs in the past few decades. A multitude of relatively rare mutations have been identified to explain around 15 % of autism cases with many of these genetic causes systematically examined in animal models. This marriage of human genetics and basic neurobiology has led to major advances in our understanding of how these genetic mutations alter brain function and help to better understand the human disease.
These scientific approaches are leading to the identification of potential therapeutic targets for autism that can be tested in the very same genetic models and hopefully translated into novel, rational therapies. The Autisms: Molecules to Model Systems provides a roadmap to many of these genetic causes of autism and clarifies what is known at the molecular, cellular, and circuit levels. Focusing on tractable genetic findings in human autism and painstakingly dissecting the underlying neurobiology, the book explains, is the key to understanding the pathophysiology of autism and ultimately to identifying novel treatments.
Les informations fournies dans la section « Synopsis » peuvent faire référence à une autre édition de ce titre.
Craig M. Powell, M.D., Ph.D. is a Neurologist and Neuroscientist interested in the molecular, cellular, and circuit-level mechanisms underlying cognitive function and cognitive dysfunction in disorders such as autism and intellectual disability. Dr. Powell has been integrally involved in understanding brain abnormalities in genetic animal models of autism based on mutations in autism-associated genes such as SHANK3, neuroligins, neurexins, and PTEN. His work integrates multiple approaches to understanding how genetic mutations lead to altered neuronal function and altered circuit function to cause the behavioral symptoms of autism. His work has identified potential therapeutic targets for autism using such models.
Lisa M. Monteggia, PhD is the Ginny and John Eulich Professor in Autism Spectrum Disorders, and Associate Professor of Psychiatry, at University of Texas Southwestern Medical Center in Dallas. Dr. Monteggia's research interests focus on the molecular and cellular basis of neural plasticity as it pertains to psychiatric disorders. She utilizes molecular, cellular, behavioral, biochemical and electrophysiological approaches to elucidate how specific genes may contribute to psychiatric disorders in animal models, specifically focusing on better understanding Rett Syndrome/Autism and depression. Once these mechanisms are understood, treatments can be developed to target specific molecular pathways for therapeutic advances.
Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.
Vendeur : Research Ink, Takoma Park, MD, Etats-Unis
Hardback. Etat : As new. xii + 405 pp. Dust jacket. book. N° de réf. du vendeur 27696
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Vendeur : BIBLIOPE by Calvello Books, Oakland, CA, Etats-Unis
Hardcover. Etat : Near Fine(+). Large quarto in purple and yellow illus jacket; xii, 405 pages: illustrations; 27 cm; bibliographical references and index. Contents: Introduction / Craig M. Powell & Lisa M. Monteggia -- Autism and autism spectrum disorders: clinical overview / Lisa Joseph, Sarah Spence & Audrey -- Neuroimaging in autism spectrum disorders human imaging / Mikle South, John D. Herrington, Sarah J. Patterson -- An overview of the genetics of autism spectrum disorders / Joseph D. Buxbaum -- Rett syndrome: on clinical and genetic features, and experimental models based on Mecp2 dysfunction / Gaston Calfa, Alan K. Percy and Lucas Pozzo-Miller -- Mecp2 knockout in mouse models of Rett syndrome / Megumi Adachi and Lisa M. Monteggia -- Putting into perspective the use of the Fmr1 KO mouse as a model for autism spectrum disorder / Richard Paylor -- Molecular functions of the mammalian fragile X mental retardation protein: insights into mental retardation and synaptic plasticity / Claudia Bagni & Eric Klann -- Tuberous sclerosis and autism / Dan Ehninger and Alcino J. Silva -- PTEN and autism with macrocephaly / Craig M. Powell -- SHANK gene family and autism / Craig M. Powell -- Smith-Lemli-Opitz Syndrome and role of cholesterol in autism / Geeta Sarphare, Ryan Lee, and Elaine Tierney -- Angelman syndrome / Edwin J. Weeber -- Neuroligins and neurexins: bridging the synaptic cleft in autism / Craig M. Powell & Antony A. Boucard -- Alterations of the serotonin-melatonin pathway in autism spectrum disorders: biological evidence and clinical consequences / Cecile Pagan, Richard Delorme, Jean-Marie Launay, Thomas Bourgeron -- CNTNAP2 and autism spectrum disorders / Olga Penagarikano & Daniel H. Geschwind -- Chromosome 15q11.2q13.3 aneusomies and autism spectrum disorders / David J. Wu and Carolyn Schanen -- Oxytocin and vasopressin: mechanisms for potential sex differences observed in ASD / C. Sue Carter & Suma Jacob -- FOXP2: linking language and autism / Genevieve Konopka. / "The science of autism has seen tremendous breakthroughs in the past few decades. A multitude of relatively rare mutations have been identified to explain around 15 % of autism cases with many of these genetic causes systematically examined in animal models. This marriage of human genetics and basic neurobiology has led to major advances in our understanding of how these genetic mutations alter brain function and help to better understand the human disease. These scientific approaches are leading to the identification of potential therapeutic targets for autism that can be tested in the very same genetic models and hopefully translated into novel, rational therapies. Craig M. Powell and Lisa M. Monteggia provide a roadmap to many of these genetic causes of autism and clarifies what is known at the molecular, cellular, and circuit levels. Focusing on tractable genetic findings in human autism and painstakingly dissecting the underlying neurobiology, the book explains, is the key to understanding the pathophysiology of autism and ultimately to identifying novel treatments. Readership: Neuroscientists, Clinicians, Psychologists, Graduate Students, and Advanced Undergraduates." ? Publisher / Autism spectrum disorders -- Genetic aspects. Autism spectrum disorders -- Pathophysiology. Biological models. Child Development Disorders, Pervasive -- genetics Child Development Disorders, Pervasive -- physiopathology Models, Biological Troubles du spectre de l'autisme -- Aspect g?n?tique. Troubles du spectre de l'autisme -- Physiopathologie. Mod?les biologiques. Biological models. Autism spectrum disorders -- Genetic aspects. Autismus Physiologische Psychologie. Fine in near fine(+) jacket in near fine dust-jacket. N° de réf. du vendeur 94041
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Vendeur : Prior Books Ltd, Cheltenham, Royaume-Uni
Hardcover. Etat : New. Etat de la jaquette : New. First Edition. A new copy in a new dustjacket: firm, clean, square and tight with no underlining or splits. N° de réf. du vendeur 033504
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Vendeur : Revaluation Books, Exeter, Royaume-Uni
Hardcover. Etat : Brand New. 1st edition. 405 pages. 10.00x6.00x1.00 inches. In Stock. N° de réf. du vendeur zk0199744319
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Vendeur : Basi6 International, Irving, TX, Etats-Unis
Etat : Brand New. New. US edition. Expediting shipping for all USA and Europe orders excluding PO Box. Excellent Customer Service. N° de réf. du vendeur ABEOCT25-63884
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Vendeur : Romtrade Corp., STERLING HEIGHTS, MI, Etats-Unis
Etat : New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide. N° de réf. du vendeur ABNR-258858
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Vendeur : GoldBooks, Denver, CO, Etats-Unis
Etat : new. N° de réf. du vendeur 78X69_93_0199744319
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Vendeur : Books Puddle, New York, NY, Etats-Unis
Etat : New. pp. 416. N° de réf. du vendeur 2637466110
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Vendeur : Majestic Books, Hounslow, Royaume-Uni
Etat : New. pp. 416. N° de réf. du vendeur 38539297
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Vendeur : Biblios, Frankfurt am main, HESSE, Allemagne
Etat : New. pp. 416. N° de réf. du vendeur 1837466100
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