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Modeling human neurodevelopmental diseases with brain organoids.

Xiaoxiang LuJiajie YangYangfei Xiang
Published in: Cell regeneration (London, England) (2022)
Studying the etiology of human neurodevelopmental diseases has long been a challenging task due to the brain's complexity and its limited accessibility. Human pluripotent stem cells (hPSCs)-derived brain organoids are capable of recapitulating various features and functionalities of the human brain, allowing the investigation of intricate pathogenesis of developmental abnormalities. Over the past years, brain organoids have facilitated identifying disease-associated phenotypes and underlying mechanisms for human neurodevelopmental diseases. Integrating with more cutting-edge technologies, particularly gene editing, brain organoids further empower human disease modeling. Here, we review the latest progress in modeling human neurodevelopmental disorders with brain organoids.
Keyphrases
  • pluripotent stem cells
  • induced pluripotent stem cells
  • endothelial cells
  • resting state
  • white matter
  • functional connectivity
  • cerebral ischemia
  • blood brain barrier
  • congenital heart disease