Impairment of the transition from proliferative stage to prehypertrophic stage in chondrogenic differentiation of human induced pluripotent stem cells harboring the causative mutation of achondroplasia in fibroblast growth factor receptor 3

INTRODUCTION: Achondroplasia (ACH) is a congenital disease which causes dwarfism and many symptoms resulting from skeletal dysplasia. Because present therapeutic strategies are mainly surgical procedures as symptomatic treatments, development of a radical treatment is desired. Clarification of the A...

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Detalles Bibliográficos
Autores principales: Horie, Naohiro, Hikita, Atsuhiko, Nishizawa, Satoru, Uto, Sakura, Takato, Tsuyoshi, Hoshi, Kazuto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society for Regenerative Medicine 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134919/
https://www.ncbi.nlm.nih.gov/pubmed/30271835
http://dx.doi.org/10.1016/j.reth.2016.11.002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134919/
https://www.ncbi.nlm.nih.gov/pubmed/30271835
http://dx.doi.org/10.1016/j.reth.2016.11.002

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