Biblio

Author Title Type [ Year(Asc)]
Filters: First Letter Of Title is G and Author is Li, Xiaowei  [Clear All Filters]
2023
Sun W, Li X, Dong J, Zhou Y. Generation of a TAB2 knockout hESC line (WAe009-A-Z) derived from H9 using CRISPR/Cas9. Stem Cell Res. 2023;74:103284.
2021
Huang S, Fu W, Guo G, Tiana X, Zhao X, Dong J, Li X, Yang H. Generation of a hiPSC line ZZUNEUi017-A from a patient with dilated cardiomyopathy caused by mutation in TTN. Stem Cell Res. 2021;52:102248.
Tian X, Fu W, Guo G, Huang S, Dong Y, Li X, Dong J, Zhao X, Zhang Y. Generation of a human iPSC line ZZUNEUi015-A from a patient with hypertrophic cardiomyopathy caused by mutation in ALPK3. Stem Cell Res. 2021;52:102247.
Guo G, Fu W, Li X, Dong J, Zhao X, Zhang Y. Generation of an iPSC line (ZZUNEUi016-A) derived from a hypertrophic cardiomyopathy patient with the heterozygote mutation in MYH7 gene. Stem Cell Res. 2021;53:102262.
Dong Y, Li X, Fu W, Tian X, Guo G, Peng Y, Zhai Y, Zhao J, Ding Z, Zhao X, et al. Generation of an iPSC line (ZZUNEUi021-A) from a hypertrophic cardiomyopathy patient with TNNT2 mutation. Stem Cell Res. 2021;58:102622.
2020
Li X, Liu Y, Liu F, Wang X, Liu M, Du W, Zhao J, Wang M, Hu L, Wang C, et al. Generation of a hiPSC line ZZUNEUi007-A from a patient with hypertrophic cardiomyopathy caused by mutation in MYH7. Stem Cell Res. 2020;43:101699.
Wang M, Ruan Y, Tian X, Liu Y, Liu M, Fu W, Du W, Zhao J, Hu L, Li X, et al. Generation of a hiPSC line ZZUNEUi012-A from a healthy female individual. Stem Cell Res. 2020;50:102143.
Wu F, Li X, Bai R, Li Y'nan, Gao J, Lan F. Generation of a Junctophilin-2 homozygous knockout human embryonic stem cell line (WAe009-A-36) by an episomal vector-based CRISPR/Cas9 system. Stem Cell Res. 2020;48:101930.
Wang L, Li X, Fu W, Zhang S, Du W, Zhao J, Liu M, Wang M, Liu Y, Hu L, et al. Generation of an IPSC line from a patient with hypertrophic cardiomyopathy carrying a mutation in MYH6 gene. Stem Cell Res. 2020;50:102138.
2019
Li X, Dong T, Li Y'nan, Wu F, Lan F. Generation of a human iPSC line from a patient with Marfan syndrome caused by mutation in FBN1. Stem Cell Res. 2019;36:101414.