Altered proliferation and networks in neural cells derived from idiopathic autistic individuals - Marchetto, M C; Belinson, H; Tian, Y; Freitas, B C; Fu, C; Vadodaria, K C; Beltrao-Braga, P C; Trujillo, C A; Mendes, A P D; Padmanabhan, K; Nunez, Y; Ou, J; et al. (Molecular psychiatry, 2017)
Keywords: 13; 13/100; 13/106; 631/532; Adolescent; Autism; Autism Spectrum Disorder - metabolism; Autism Spectrum Disorder - physiopathology; Autistic Disorder - metabolism; Autistic Disorder - pathology; Autistic persons; Behavior; Behavioral Sciences; beta Catenin - metabolism; Biological Psychology; Brain - metabolism; Brain research; Cell culture; Cell cycle; Cell proliferation; Cell Proliferation - genetics; Cells, Cultured; Child; Child, Preschool; Children & youth; Clinical trials; Disease; Female; Fibroblasts; Fibroblasts - metabolism; Gene expression; Genetic aspects; Genetics; Genomes; Growth; Growth factors; Health aspects; Humans; Induced Pluripotent Stem Cells - metabolism; Insulin; Insulin-like growth factor I; Insulin-Like Growth Factor I - metabolism; Insulin-Like Growth Factor I - therapeutic use; Magnetic resonance imaging; Male; Medicine; Medicine & Public Health; Molecular modelling; Neural networks; Neural stem cells; Neural Stem Cells - metabolism; Neurodevelopmental disorders; Neurogenesis; Neuroimaging; Neurons; Neurons - metabolism; Neurons - physiology; Neurosciences; original-article; Pathogenesis; Pathophysiology; Pediatrics; Pharmacotherapy; Pluripotency; Progenitor cells; Psychiatry; Stem cells; Synaptogenesis; Tissue Culture Techniques - methods; Toddlers; Transcription; β-Catenin; La Jolla California; United States--US; California