OLIG2 Drives Abnormal Neurodevelopmental Phenotypes in Human iPSC-Based Organoid and Chimeric Mouse Models of Down Syndrome Article

Xu, Ranjie, Brawner, Andrew T, Li, Shenglan et al. (2019). OLIG2 Drives Abnormal Neurodevelopmental Phenotypes in Human iPSC-Based Organoid and Chimeric Mouse Models of Down Syndrome . 24(6), 908-+. 10.1016/j.stem.2019.04.014

Open Access

cited authors

  • Xu, Ranjie; Brawner, Andrew T; Li, Shenglan; Liu, Jing-Jing; Kim, Hyosung; Xue, Haipeng; Pang, Zhiping P; Kim, Woo-Yang; Hart, Ronald P; Liu, Ying; Jiang, Peng

sustainable development goals

authors

publication date

  • June 6, 2019

webpage

keywords

  • CORTICAL DEVELOPMENT
  • CRITICAL REGION
  • Cell & Tissue Engineering
  • Cell Biology
  • HUMAN BRAIN
  • LONG-TERM POTENTIATION
  • Life Sciences & Biomedicine
  • OBJECT RECOGNITION
  • PLURIPOTENT STEM-CELLS
  • PROGENITOR CELLS
  • REGULATES NEUROGENESIS
  • SYNAPTIC PLASTICITY
  • Science & Technology
  • TS65DN MOUSE

Digital Object Identifier (DOI)

publisher

  • CELL PRESS

start page

  • 908

end page

  • +

volume

  • 24

issue

  • 6