Biblio

Author Title Type [ Year(Asc)]
Filters: Author is Lai, Xingqiang  [Clear All Filters]
2023
Xia K, Wang F, Tan Z, Zhang S, Lai X, Ou W, Yang C, Chen H, Peng H, Luo P, et al. Precise Correction of Lhcgr Mutation in Stem Leydig Cells by Prime Editing Rescues Hereditary Primary Hypogonadism in Mice. Adv Sci (Weinh). 2023:e2300993.
2022
Xia K, Wang F, Lai X, Dong L, Luo P, Zhang S, Yang C, Chen H, Ma Y, Huang W, et al. AAV-mediated gene therapy produces fertile offspring in the Lhcgr-deficient mouse model of Leydig cell failure. Cell Rep Med. 2022:100792.
Liang C, Ke Q, Liu Z, Ren J, Zhang W, Hu J, Wang Z, Chen H, Xia K, Lai X, et al. BMAL1 moonlighting as a gatekeeper for LINE1 repression and cellular senescence in primates. Nucleic Acids Res. 2022.
Liu H, Huang S, Wang W, Wang H, Huang W, Zhai Z, Wang D, Fan Y, Sun J, Li D, et al. Migration deficits of the neural crest caused by CXADR triplication in a human Down syndrome stem cell model. Cell Death Dis. 2022;13(12):1018.
2019
Lai X, Jiang B, Liu J, Wang Y, Wu G. Generation of an induced pluripotent stem cell line (SYSUi002-A) from a patient with coronary slow flow phenomenon. Stem Cell Res. 2019;41:101646.
2018
Wang Y, Lai X, Huang L, Liu G, Zai Z, Zhu D, Zhang Y, Liang Z, Yao Z, Chen Y, et al. Establishment of an induced pluripotent stem cell model of Hirschsrpung disease, a congenital condition of the enteric nervous system, from a patient carrying a novel RET mutation. Neuroreport. 2018.