A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophy

por Sullivan, Lori S., Baylin, Eric B., Font, Ramon, Daiger, Stephen P., Pepose, Jay S., Clinch, Thomas E., Nakamura, Hisashi, Zhao, Xinping C., Yee, Richard W.
Publicado 2007

Generation and validation of APOE knockout human iPSC-derived cerebral organoids

por Martens, Yuka A., Xu, Siming, Tait, Richard, Li, Gary, Zhao, Xinping C., Lu, Wenyan, Liu, Chia-Chen, Kanekiyo, Takahisa, Bu, Guojun, Zhao, Jing
Publicado 2021