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This book contains a compendium of induced pluripotent stem cells (iPSCs) articles and reviews concerning state of the art technologies and how they are being applied to human neurodevelopmental disorders. With the establishment of effective technologies to produce iPSCs and their derivatives, like neural precursors, neurons, and glia, researchers have new platforms to study neurodevelopmental disorders. iPSC technology enables researchers to study how human neurons develop in individuals with neurodevelopmental disorders, providing an unparalleled opportunity to investigate their etiology. In turn, researchers have now begun to understand the underlying molecular and cellular pathways that contribute to human diseases. iPSCs technologies also provide an emerging tool for future translational studies and disease classification. The chapters will emphasize how among the diverse idiopathic and genetic disorders, there are common clinical as well as cellular and molecular phenotypes.

Pediatric neurology --- Brain --- Neurosciences. --- Diagnosis. --- Diseases. --- Neural sciences --- Neurological sciences --- Neuroscience --- Medical sciences --- Nervous system --- Brain diseases --- Psychology, Pathological --- Diagnosis --- Malalties neurodegeneratives --- Degeneració axònica --- Degeneració de Nissl --- Degeneració del sistema nerviós --- Degeneració nerviosa --- Degeneració neuronal --- Degeneració retrògrada --- Reacció axònica --- Reacció primària de Nissl --- Degeneració (Patologia) --- Malalties del sistema nerviós --- Malaltia d'Alzheimer --- Malaltia de Parkinson --- Regeneració del sistema nerviós

Choose an application

• Reference Manager
• EndNote
• RefWorks (Direct export to RefWorks)

This book contains a compendium of induced pluripotent stem cells (iPSCs) articles and reviews concerning state of the art technologies and how they are being applied to human neurodevelopmental disorders. With the establishment of effective technologies to produce iPSCs and their derivatives, like neural precursors, neurons, and glia, researchers have new platforms to study neurodevelopmental disorders. iPSC technology enables researchers to study how human neurons develop in individuals with neurodevelopmental disorders, providing an unparalleled opportunity to investigate their etiology. In turn, researchers have now begun to understand the underlying molecular and cellular pathways that contribute to human diseases. iPSCs technologies also provide an emerging tool for future translational studies and disease classification. The chapters will emphasize how among the diverse idiopathic and genetic disorders, there are common clinical as well as cellular and molecular phenotypes.

Neuropathology --- neurologie