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1دورية أكاديمية
المؤلفون: Variants, Commission on Novel Technologies for Neurodevelopmental Copy Number, Buttermore, Elizabeth, Chamberlain, Stormy, Cody, Jannine, Costain, Gregory, Dang, Louis, DeWoody, Andrew, DeWoody, Yssa, Dies, Kira, Eichler, Evan, Girirajan, Santhosh, Gramm, Marie, Halladay, Alycia, Lal, Dennis, Lalli, Matthew, Levy, Tess, Logsdon, Glennis, Lowenstein, Daniel, Mefford, Heather, Mulle, Jennifer, Muotri, Alysson, Murphy, Melissa, Palma, Eduardo Perez, Pinter, Stefan, Pollak, Rebecca, Purcell, Ryan, Samaco, Rodney, Shah, Bina, Singh, Karun, So, Joyce, Sundberg, Maria, Veeraragavan, Surabi, Vogel-Farley, Vanessa, Wynshaw-Boris, Anthony
المصدر: American Journal of Human Genetics. 109(8)
مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Human Genome, Intellectual and Developmental Disabilities (IDD), Neurosciences, Brain Disorders, DNA Copy Number Variations, Genome, Humans, Neurodevelopmental Disorders, Patient Advocacy, Phenotype, Commission on Novel Technologies for Neurodevelopmental Copy Number Variants, CNVs, biobank, community engagement, copy-number variants, genomic disorders, iPSCs, inclusion, infrastructure, long-read sequencing, neurodevelopment, neurological, patient centered, patient led, structural variants, systematic phenotyping, team science, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/3tc3h13fTest
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2دورية أكاديمية
المؤلفون: Marchetto, Maria C, Belinson, Haim, Tian, Yuan, Freitas, Beatriz C, Fu, Chen, Vadodaria, Krishna, Beltrao-Braga, Patricia, Trujillo, Cleber A, Mendes, Ana PD, Padmanabhan, Krishnan, Nunez, Yanelli, Ou, Jing, Ghosh, Himanish, Wright, Rebecca, Brennand, Kristen, Pierce, Karen, Eichenfield, Lawrence, Pramparo, Tiziano, Eyler, Lisa, Barnes, Cynthia C, Courchesne, Eric, Geschwind, Daniel H, Gage, Fred H, Wynshaw-Boris, Anthony, Muotri, Alysson R
المصدر: Molecular psychiatry. 22(6)
مصطلحات موضوعية: Brain, Neurons, Cells, Cultured, Fibroblasts, Humans, Insulin-Like Growth Factor I, Tissue Culture Techniques, Autistic Disorder, Cell Proliferation, Adolescent, Child, Child, Preschool, Female, Male, beta Catenin, Neurogenesis, Induced Pluripotent Stem Cells, Neural Stem Cells, Autism Spectrum Disorder, Genetics, Stem Cell Research, Stem Cell Research - Induced Pluripotent Stem Cell - Human, Pediatric, Clinical Research, Stem Cell Research - Induced Pluripotent Stem Cell, Stem Cell Research - Nonembryonic - Human, Autism, Intellectual and Developmental Disabilities (IDD), Mental Health, Regenerative Medicine, Neurosciences, Brain Disorders, Stem Cell Research - Nonembryonic - Non-Human, 2.1 Biological and endogenous factors, Neurological, Mental health, Psychiatry, Biological Sciences, Medical and Health Sciences, Psychology and Cognitive Sciences
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/5f29t1rdTest
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3دورية أكاديمية
المؤلفون: Bershteyn, Marina, Nowakowski, Tomasz J, Pollen, Alex A, Di Lullo, Elizabeth, Nene, Aishwarya, Wynshaw-Boris, Anthony, Kriegstein, Arnold R
المصدر: Cell Stem Cell. 20(4)
مصطلحات موضوعية: Medical Biotechnology, Biomedical and Clinical Sciences, Intellectual and Developmental Disabilities (IDD), Stem Cell Research - Nonembryonic - Human, Clinical Research, Stem Cell Research, Brain Disorders, Stem Cell Research - Induced Pluripotent Stem Cell - Human, Stem Cell Research - Embryonic - Human, Stem Cell Research - Induced Pluripotent Stem Cell, Regenerative Medicine, Neurosciences, 2.1 Biological and endogenous factors, Aetiology, Neurological, Adult, Apoptosis, Cell Movement, Cerebrum, Chromosome Duplication, Classical Lissencephalies and Subcortical Band Heterotopias, Cytokinesis, Epithelium, Female, Humans, Induced Pluripotent Stem Cells, Infant, Infant, Newborn, Lissencephaly, Male, Middle Aged, Mitosis, Neuroglia, Neurons, Organoids, cerebral organoids, human lissencephaly, migration, outer radial glia, spindle orientation, Biological Sciences, Medical and Health Sciences, Developmental Biology, Biological sciences, Biomedical and clinical sciences
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/1sd77400Test
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4دورية أكاديمية
المؤلفون: Moon, Hyang Mi, Youn, Yong Ha, Pemble, Hayley, Yingling, Jessica, Wittmann, Torsten, Wynshaw-Boris, Anthony
المصدر: Human Molecular Genetics. 23(2)
مصطلحات موضوعية: Biochemistry and Cell Biology, Biological Sciences, Genetics, 1.1 Normal biological development and functioning, Underpinning research, Generic health relevance, 1-Alkyl-2-acetylglycerophosphocholine Esterase, Animals, Carrier Proteins, Cells, Cultured, Centrosome, Cerebral Cortex, Chromosome Segregation, Dyneins, HEK293 Cells, Humans, Lissencephaly, Mice, Microtubule-Associated Proteins, Microtubules, Mitosis, Mutation, Neurons, Protein Stability, Spindle Apparatus, Medical and Health Sciences, Genetics & Heredity
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/7sj2s0wxTest
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5دورية أكاديمية
المؤلفون: Chow, Maggie L, Pramparo, Tiziano, Winn, Mary E, Barnes, Cynthia Carter, Li, Hai-Ri, Weiss, Lauren, Fan, Jian-Bing, Murray, Sarah, April, Craig, Belinson, Haim, Fu, Xiang-Dong, Wynshaw-Boris, Anthony, Schork, Nicholas J, Courchesne, Eric
المصدر: PLOS Genetics. 8(3)
مصطلحات موضوعية: Biological Sciences, Genetics, Human Genome, Intellectual and Developmental Disabilities (IDD), Pediatric, Autism, Brain Disorders, Clinical Research, Mental Health, Biotechnology, Neurosciences, 2.1 Biological and endogenous factors, 1.1 Normal biological development and functioning, Aetiology, Underpinning research, Mental health, Neurological, Adolescent, Adult, Age Factors, Autistic Disorder, Autopsy, Cell Cycle Proteins, Cell Differentiation, Child, Child, Preschool, DNA Copy Number Variations, Female, Gene Deletion, Gene Expression Regulation, Gene Regulatory Networks, Genome, Human, Humans, Male, Middle Aged, Neurons, Prefrontal Cortex, Signal Transduction, Developmental Biology
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/172879gxTest