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• W2186309023 startingPage "52" @default.
• W2186309023 abstract "Schizophrenia (SCZ) and autism spectrum disorder (ASD) are genetically and phenotypically complex disorders of neural development. Human genetic studies, as well as studies examining structural changes at the cellular level, have converged on glutamatergic synapse formation, function, and maintenance as common pathophysiologic substrates involved in both disorders. Synapses as basic functional units of the brain are continuously modified by experience throughout life, therefore they are particularly attractive candidates for targeted therapy. Until recently we lacked a system to evaluate dynamic changes that lead to synaptic abnormalities. With the development of techniques to generate induced pluripotent stem cells (iPSCs) from patients, we are now able to study neuronal and synaptic development in cells from individual patients in the context of genetic changes conferring disease susceptibility. In this review, we discuss recent studies focusing on neural cells differentiated from SCZ and ASD patient iPSCs. These studies support a central role for glutamatergic synapse formation and function in both disorders and demonstrate that iPSC derived neurons offer a potential system for further evaluation of processes leading to synaptic dysregulation and for the design and screening of future therapies." @default.
• W2186309023 created "2016-06-24" @default.
• W2186309023 creator A5004329894 @default.
• W2186309023 creator A5009183873 @default.
• W2186309023 creator A5062886170 @default.
• W2186309023 date "2016-06-01" @default.
• W2186309023 modified "2023-10-17" @default.
• W2186309023 title "Modeling synaptogenesis in schizophrenia and autism using human iPSC derived neurons" @default.
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