已收录 268921 条政策
 政策提纲
  • 暂无提纲
Generation of a transgene-free induced pluripotent stem cell line (SMBCi011-A) from a patient with Prader–Willi syndrome
[摘要] Prader–Willi syndrome (PWS) is a neurodevelopmental disorder caused by deficiency of paternal gene expression in the 15q11.2-q13 chromosome imprinted region. Hyperphagia and dysgnosia are typical clinical features in the early-childhood of patient. We generated an induced pluripotent stem cell (iPSC) line SMBCi011-A from a 6 years old male PWS patient, the line expressed pluripotent signs and had ability to differentiate into three germ layers in vivo.
[发布日期]  [发布机构] 
[效力级别]  [学科分类] 生理学
[关键词]  [时效性] 
   浏览次数:1      统一登录查看全文      激活码登录查看全文