Cargando…
Premyogenic progenitors derived from human pluripotent stem cells expand in floating culture and differentiate into transplantable myogenic progenitors
Human induced pluripotent stem cells (hiPSCs) are a potential source for cell therapy of Duchenne muscular dystrophy. To reliably obtain skeletal muscle progenitors from hiPSCs, we treated hiPS cells with a Wnt activator, CHIR-99021 and a BMP receptor inhibitor, LDN-193189, and then induced skeletal...
Autores principales: | Sakai-Takemura, Fusako, Narita, Asako, Masuda, Satoru, Wakamatsu, Toshifumi, Watanabe, Nobuharu, Nishiyama, Takashi, Nogami, Ken’ichiro, Blanc, Matthias, Takeda, Shin’ichi, Miyagoe-Suzuki, Yuko |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920060/ https://www.ncbi.nlm.nih.gov/pubmed/29700358 http://dx.doi.org/10.1038/s41598-018-24959-y |
Ejemplares similares
-
Prostaglandin EP2 receptor downstream of Notch signaling inhibits differentiation of human skeletal muscle progenitors in differentiation conditions
por: Sakai-Takemura, Fusako, et al.
Publicado: (2020) -
Mesenchymal stem cells derived from human induced pluripotent stem cells improve the engraftment of myogenic cells by secreting urokinase-type plasminogen activator receptor (uPAR)
por: Elhussieny, Ahmed, et al.
Publicado: (2021) -
Induction of Pluripotent Stem Cells from a Manifesting Carrier of Duchenne Muscular Dystrophy and Characterization of Their X-Inactivation Status
por: Miyagoe-Suzuki, Yuko, et al.
Publicado: (2017) -
iNOS is not responsible for RyR1 S-nitrosylation in mdx mice with truncated dystrophin
por: Nogami, Ken’ichiro, et al.
Publicado: (2020) -
Antioxidants restore store‐operated Ca(2+) entry in patient‐iPSC‐derived myotubes with tubular aggregate myopathy‐associated Ile484ArgfsX21 STIM1 mutation via upregulation of binding immunoglobulin protein
por: Sakai‐Takemura, Fusako, et al.
Publicado: (2023)