Efficient generation of all ESC-derived mice carrying a homozygous lethal mutation through eight-cell embryo injection
Xidi Yin(Chinese Academy of Sciences), Qing Li(Wenzhou University), Yanbo Cheng(South China Agricultural University), Yilai Shu(Fudan University), Yingyi Wang(Shanghai Jiao Tong University), Nan Liu(Hubei University of Medicine), Jinsong Li(ShanghaiTech University), Meng Yan(University of Chinese Academy of Sciences), Chong Cui(Fudan University), Zhoujie Li(Chinese Academy of Sciences)
Cited by 1
Related Papers
Cationic lipid-mediated delivery of proteins enables efficient protein-based genome editing in vitro and in vivo
|Nature Biotechnology|2014|1.5k
AAV1-hOTOF gene therapy for autosomal recessive deafness 9: a single-arm trial
|The Lancet|2024|323
GmWRKY16 Enhances Drought and Salt Tolerance Through an ABA-Mediated Pathway in Arabidopsis thaliana
|Frontiers in Plant Science|2019|226
One-step generation of complete gene knockout mice and monkeys by CRISPR/Cas9-mediated gene editing with multiple sgRNAs
|Cell Research|2017|218
AAV‐Mediated Gene Therapy Restores Hearing in Patients with DFNB9 Deafness
|Advanced Science|2024|176