المؤلفون: Adhikari, Anna, Copping, Nycole A, Onaga, Beth, Pride, Michael C, Coulson, Rochelle L, Yang, Mu, Yasui, Dag H, LaSalle, Janine M, Silverman, Jill L

مصطلحات موضوعية: Biological Psychology, Psychology, Brain Disorders, Genetics, Pediatric, Behavioral and Social Science, Congenital Structural Anomalies, Basic Behavioral and Social Science, Mental Health, Obesity, Intellectual and Developmental Disabilities (IDD), Rare Diseases, Neurosciences, Clinical Research, Aetiology, 2.1 Biological and endogenous factors, Mental health, Animals, Cognitive Dysfunction, Disease Models, Animal, Gene Deletion, Humans, Mice, Prader-Willi Syndrome, RNA, Small Nucleolar, Behavior, Animal model, Neurodevelopment, Learning and memory, Prader-Willi, Snord116, Cognitive, Medical and Health Sciences, Psychology and Cognitive Sciences, Behavioral Science & Comparative Psychology, Biological psychology, Cognitive and computational psychology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/1kn8s3fj

المؤلفون: Copping, Nycole A, Berg, Elizabeth L, Foley, Gillian M, Schaffler, Melanie D, Onaga, Beth L, Buscher, Nathalie, Silverman, Jill L, Yang, Mu

مصطلحات موضوعية: Biological Psychology, Cognitive and Computational Psychology, Psychology, Behavioral and Social Science, Brain Disorders, Intellectual and Developmental Disabilities (IDD), Neurosciences, Mental Health, Autism, Pediatric, Basic Behavioral and Social Science, Neurological, Mental health, Animals, Association Learning, Autistic Disorder, Chromosome Deletion, Chromosome Disorders, Chromosomes, Human, Pair 22, Discrimination, Psychological, Disease Models, Animal, Learning Disabilities, Male, Mice, Transgenic, Microfilament Proteins, Motor Activity, Nerve Tissue Proteins, Neuropsychological Tests, Social Behavior, Visual Perception, SHANK3, Phelan-McDermid Syndrome, autism, touchscreen, mouse models, associative learning, Phelan–McDermid Syndrome, Cognitive Sciences, Neurology & Neurosurgery, Biological psychology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/1fj9p0sj

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المؤلفون: Adhikari A; MIND Institute, University of California, Davis School of Medicine, Department of Psychiatry and Behavioral Sciences, Sacramento, CA, USA., Copping NA; MIND Institute, University of California, Davis School of Medicine, Department of Psychiatry and Behavioral Sciences, Sacramento, CA, USA., Onaga B; MIND Institute, University of California, Davis School of Medicine, Department of Psychiatry and Behavioral Sciences, Sacramento, CA, USA., Pride MC; MIND Institute, University of California, Davis School of Medicine, Department of Psychiatry and Behavioral Sciences, Sacramento, CA, USA., Coulson RL; MIND Institute, Genome Center, UC Davis School of Medicine, Department of Medical Microbiology and Immunology, Davis, CA, USA., Yang M; Department of Psychiatry and Institute for Genomic Medicine, New York, NY, USA., Yasui DH; MIND Institute, Genome Center, UC Davis School of Medicine, Department of Medical Microbiology and Immunology, Davis, CA, USA., LaSalle JM; MIND Institute, Genome Center, UC Davis School of Medicine, Department of Medical Microbiology and Immunology, Davis, CA, USA., Silverman JL; MIND Institute, University of California, Davis School of Medicine, Department of Psychiatry and Behavioral Sciences, Sacramento, CA, USA. Electronic address: jsilverman@ucdavis.edu.

المصدر: Neurobiology of learning and memory [Neurobiol Learn Mem] 2019 Nov; Vol. 165, pp. 106874. Date of Electronic Publication: 2018 May 23.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Review

بيانات الدورية: Publisher: Academic Press Country of Publication: United States NLM ID: 9508166 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1095-9564 (Electronic) Linking ISSN: 10747427 NLM ISO Abbreviation: Neurobiol Learn Mem Subsets: MEDLINE

مواضيع طبية MeSH: Gene Deletion*, Cognitive Dysfunction/*genetics , Prader-Willi Syndrome/*genetics , RNA, Small Nucleolar/*genetics, Animals ; Cognitive Dysfunction/etiology ; Disease Models, Animal ; Humans ; Mice ; Prader-Willi Syndrome/complications