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Induction of Noonan syndrome-specific human-induced pluripotent stem cells under serum-, feeder-, and integration-free conditions

Noonan syndrome is an autosomal dominant developmental disorder. Although it is relatively common, and its phenotypical variability is well documented, its pathophysiology is not fully understood. Previously, with the aim of revealing the pathogenesis of genetic disorders, we reported the induction...

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Dettagli Bibliografici
Pubblicato in:In Vitro Cell Dev Biol Anim
Autori principali: Hamada, Atsuko, Akagi, Eri, Obayashi, Fumitaka, Yamasaki, Sachiko, Koizumi, Koichi, Ohtaka, Manami, Nishimura, Ken, Nakanishi, Mahito, Toratani, Shigeaki, Okamoto, Tetsuji
Natura: Artigo
Lingua:Inglês
Pubblicazione: Springer US 2020
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7723931/
https://ncbi.nlm.nih.gov/pubmed/33140329
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11626-020-00515-9
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