Your browser doesn't support javascript.
loading
Generation of an induced pluripotent stem cell line (SYSUSCi001-A) from a congenital cataract patient carrying heterozygous mutations in BFSP1 and RHO.
Chen, Fangyuan; Wang, Tao; Yang, Yuanting; Huang, Ziqing; Dong, Yuying; Zhang, Rijia; Chen, Jian; Zhou, Qing.
Afiliação
  • Chen F; The Department of Ophthalmology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
  • Wang T; Center for Stem Cell Biology and Tissue Engineering, Key Laboratory for Stem Cells and Tissue Engineering, Ministry of Education, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou, Guangdong, China; Department of Biochemistry, Zhongshan Medical School, Sun Yat-Sen University, Guangzhou
  • Yang Y; The Department of Ophthalmology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
  • Huang Z; The Department of Ophthalmology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
  • Dong Y; The Department of Ophthalmology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
  • Zhang R; The Department of Ophthalmology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China.
  • Chen J; The Department of Ophthalmology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China. Electronic address: drchenj@163.com.
  • Zhou Q; The Department of Ophthalmology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong, China. Electronic address: kerryzh@163.com.
Stem Cell Res ; 59: 102644, 2022 Mar.
Article em En | MEDLINE | ID: mdl-34995847
The human induced pluripotent stem cell (hiPSC) line was generated from peripheral blood mononuclear cells (PBMCs) isolated from a 1-year-old boy who suffering from congenital cataract (CC), carrying heterozygous mutations in BFSP1 and RHO. PBMCs from this patient were reprogrammed into hiPSCs using non-integrative Sendai viral vectors expressing OCT4, SOX2, KLF4 and C-MYC. CC-hiPSCs had normal karyotype and showed pluripotency both in vitro and in vivo. The CC-hiPSCs would supply an important cell model for studying the pathogenesis of CC.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Stem Cell Res Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Stem Cell Res Ano de publicação: 2022 Tipo de documento: Article