Autor: |
Hangdi Wu, Gang Wang, Erzhi Gao, Jing Zhao, Li Zhang, Lang Chen, Yuqing Zhu, Jin Zhang, Zhihong Liu |
Jazyk: |
angličtina |
Rok vydání: |
2021 |
Předmět: |
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Zdroj: |
Stem Cell Research, Vol 53, Iss , Pp 102293- (2021) |
Druh dokumentu: |
article |
ISSN: |
1873-5061 |
DOI: |
10.1016/j.scr.2021.102293 |
Popis: |
Focal Segmental Glomerular Sclerosis (FSGS) is a glomerular disease which can be classified into primary, secondary, genetic, and unknown forms. WT1 mutation has been shown to be associated with this disorder. Recently, we identified a mutation in the Zinc finger C2H2 domain of WT1 gene in a patient with FSGS who also carried a family history of end-stage renal disease (ESRD). The Peripheral Blood Mononuclear Cells (PBMCs) of the patient were obtained and a line of induced pluripotent stem cells (iPSCs) was successfully generated. The iPSC line will be useful for further study of the pathogenesis and drug screening for FSGS. |
Databáze: |
Directory of Open Access Journals |
Externí odkaz: |
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