Engraftment of Human Pluripotent Stem Cell-derived Progenitors in the Inner Ear of Prenatal Mice

There is, at present, no curative treatment for genetic hearing loss. We have previously reported that transuterine gene transfer of wild type CONNEXIN30 (CX30) genes into otocysts in CX30-deleted mice could restore hearing. Cell transplantation therapy might be another therapeutic option, although...

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Detalles Bibliográficos
Autores principales: Takeda, Hiroki, Hosoya, Makoto, Fujioka, Masato, Saegusa, Chika, Saeki, Tsubasa, Miwa, Toru, Okano, Hideyuki, Minoda, Ryosei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5792596/
https://www.ncbi.nlm.nih.gov/pubmed/29386634
http://dx.doi.org/10.1038/s41598-018-20277-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5792596/
https://www.ncbi.nlm.nih.gov/pubmed/29386634
http://dx.doi.org/10.1038/s41598-018-20277-5

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