小型霊長類コモンマーモセットを用いた新規内耳研究プラットフォームの創生
Author:
Affiliation:
1. 慶應義塾大学医学部耳鼻咽喉科学教室
Publisher
Oto-Rhino-Laryngological Society of Japan, Inc.
Link
https://www.jstage.jst.go.jp/article/jibiinkotokeibu/125/12/125_1633/_pdf
Reference19 articles.
1. 1) Hosoya M, Fujioka M, Sone T, et al: Cochlear cell modeling using disease-specific iPSCs unveils a degenerative phenotype and suggests treatments for congenital progressive hearing loss. Cell Rep 2017; 18: 68-81.
2. 2) Hosoya M, Saeki T, Saegusa C, et al: Estimating the concentration of therapeutic range using disease-specific iPS cells: Low-dose rapamycin therapy for Pendred syndrome. Regen Ther 2019; 10: 54-63.
3. 3) Fujioka M, Akiyama T, Hosoya M, et al: A phase I/IIa double blind single institute trial of low dose sirolimus for Pendred syndrome/DFNB4. Medicine (Baltimore) 2020; 99: e19763.
4. 4) Marmoset Genome Sequencing and Analysis Consortium: The common marmoset genome provides insight into primate biology and evolution. Nat Genet 2014; 46: 850-857.
5. 5) Hosoya M, Fujioka M, Ogawa K, et al: Distinct expression patterns of causative genes responsible for hereditary progressive hearing loss in non-human primate cochlea. Sci Rep 2016; 6: 22250.
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