检索结果 - Xu, Ranjie

High-Fidelity Modeling of Human Microglia with Pluripotent Stem Cells 由 Jiang, Peng, Turkalj, Luka, Xu, Ranjie

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Generating CNS organoids from human induced pluripotent stem cells for modeling neurological disorders 由 Brawner, Andrew T, Xu, Ranjie, Liu, Dingfeng, Jiang, Peng

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Three-Dimensional Hyaluronic Acid Hydrogel-Based Models for In Vitro Human iPSC-Derived NPC Culture and Differentiation 由 Wu, Shaohua, Xu, Ranjie, Duan, Bin, Jiang, Peng

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Hax-1 is rapidly degraded by the proteasome dependent on its PEST sequence 由 Li, Bin, Hu, Qingsong, Xu, Ranjie, Ren, Haigang, Fei, Erkang, Chen, Dong, Wang, Guanghui

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Pluripotent Stem Cell-Derived Cerebral Organoids Reveal Human Oligodendrogenesis with Dorsal and Ventral Origins 由 Kim, Hyosung, Xu, Ranjie, Padmashri, Ragunathan, Dunaevsky, Anna, Liu, Ying, Dreyfus, Cheryl F., Jiang, Peng

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Human iPSC-derived mature microglia retain their identity and functionally integrate in the chimeric mouse brain 由 Xu, Ranjie, Li, Xiaoxi, Boreland, Andrew J., Posyton, Anthony, Kwan, Kelvin, Hart, Ronald P., Jiang, Peng

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Developing human pluripotent stem cell-based cerebral organoids with a controllable microglia ratio for modeling brain development and pathology 由 Xu, Ranjie, Boreland, Andrew J., Li, Xiaoxi, Erickson, Caroline, Jin, Mengmeng, Atkins, Colm, Pang, Zhiping P., Daniels, Brian P., Jiang, Peng

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

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Type I Interferon Signaling Drives Microglial Dysfunction and Senescence in Human iPSC Models of Down Syndrome and Alzheimer’s Disease 由 Jin, Mengmeng, Xu, Ranjie, Wang, Le, Alam, Mahabub Maraj, Ma, Ziyuan, Zhu, Sining, Martini, Alessandra C., Jadali, Azadeh, Bernabucci, Matteo, Xie, Ping, Kwan, Kelvin Y., Pang, Zhiping P., Head, Elizabeth, Liu, Ying, Hart, Ronald P., Jiang, Peng

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