Autor: |
Ronghua Liu, Guoxing Weng, Fuzhen Zheng, Jinyan Chen, Kun Wang, Junyong Han, Jie Huang, Licheng Yan, Jingjun Jin |
Jazyk: |
angličtina |
Rok vydání: |
2024 |
Předmět: |
|
Zdroj: |
Stem Cell Research, Vol 81, Iss , Pp 103591- (2024) |
Druh dokumentu: |
article |
ISSN: |
1873-5061 |
DOI: |
10.1016/j.scr.2024.103591 |
Popis: |
Marfan syndrome (MFS) is a heritable dominant disorder of fibrous connective tissue, caused by mutations in the gene encoding fibrillin-1 on chromosome 15. Here, we report an induced pluripotent stem cell (iPSC) line generated from a patient with MFS who carries a heterozygous mutation of c.2777G > A(p.Cys926Tyr) in the FBN1 gene using an episomal method. The hiPS-MFS cell line has normal karyotype, expresses pluripotency markers, and has the ability to form three germ layers in vivo.This MFS-specific iPSC line can be used as a cell disease model to study the pathogenesis of Marfan syndrome. |
Databáze: |
Directory of Open Access Journals |
Externí odkaz: |
|