Heterozygous FOXJ1 Mutations Cause Incomplete Ependymal Cell Differentiation and Communicating Hydrocephalus

por Hou, Connie C., Li, Danielle, Berry, Bethany C., Zheng, Shaokuan, Carroll, Rona S., Johnson, Mark D., Yang, Hong Wei
Publicado 2023

Systematic decomposition of sequence determinants governing CRISPR/Cas9 specificity

por Fu, Rongjie, He, Wei, Dou, Jinzhuang, Villarreal, Oscar D., Bedford, Ella, Wang, Helen, Hou, Connie, Zhang, Liang, Wang, Yalong, Ma, Dacheng, Chen, Yiwen, Gao, Xue, Depken, Martin, Xu, Han
Publicado 2022