Publication:
Generation of an integration-free human induced pluripotent stem cell line MUSIi010-A from occipital scalp fibroblasts of a male patient with androgenetic alopecia

Issued Date

2019-07-01

Resource Type

Article

ISSN

18767753
18735061

DOI

10.1016/j.scr.2019.101486

Other identifier(s)

2-s2.0-85067454820

Rights

Mahidol University

Rights Holder(s)

SCOPUS

Bibliographic Citation

Stem Cell Research. Vol.38, (2019)

Suggested Citation

Nutnicha Tantarungsee, Zaukir Bostan Ali, Rungtip Soi-ampornkul, Chuda Rujitharanawong, Chanika Subchookul, Alisa Ritthaphai, Bootsakorn Boonkaew, Methichit Wattanapanitch, Kanchalit Thanomkitti, Daranporn Triwongwaranat, Chinnavuth Vatanashevanopakorn, Rattapon Thuangtong Generation of an integration-free human induced pluripotent stem cell line MUSIi010-A from occipital scalp fibroblasts of a male patient with androgenetic alopecia. Stem Cell Research. Vol.38, (2019). doi:10.1016/j.scr.2019.101486 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/50132

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Title

Generation of an integration-free human induced pluripotent stem cell line MUSIi010-A from occipital scalp fibroblasts of a male patient with androgenetic alopecia

Author(s)

Nutnicha Tantarungsee
 Zaukir Bostan Ali
 Rungtip Soi-ampornkul
 Chuda Rujitharanawong
 Chanika Subchookul
 Alisa Ritthaphai
 Bootsakorn Boonkaew
 Methichit Wattanapanitch
 Kanchalit Thanomkitti
 Daranporn Triwongwaranat
 Chinnavuth Vatanashevanopakorn
 Rattapon Thuangtong

Other Contributor(s)

Faculty of Medicine, Siriraj Hospital, Mahidol University

Abstract

© 2019 The Authors An induced pluripotent stem cell (iPSC) line, MUSIi010-A, was established by Sendai virus (SeV) transduction of scalp fibroblasts from a 59-year-old male with androgenetic alopecia (AGA). Pluripotency of the iPSC line was verified by immunofluorescence staining of pluripotent markers and by in vitro trilineage differentiation. The MUSIi010-A line was shown to retain normal karyotype and free of SeV vectors at passage 17. This iPSC line can be used for studying pathological mechanisms of AGA.

Keyword(s)

Biochemistry, Genetics and Molecular Biology

Availability

URI

https://repository.li.mahidol.ac.th/handle/20.500.14594/50132

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Scopus 2019