Research Output per year
Fingerprint Dive into the research topics where Makoto Hosoya is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 8 Similar Profiles
Cochlea
Medicine & Life Sciences
Hearing Loss
Medicine & Life Sciences
Callithrix
Medicine & Life Sciences
Primates
Medicine & Life Sciences
Deafness
Medicine & Life Sciences
Hearing
Medicine & Life Sciences
Genes
Medicine & Life Sciences
Mutation
Medicine & Life Sciences
Network
Recent external collaboration on country level. Dive into details by clicking on the dots.
Research Output 2011 2019
A new training method for velopharyngeal dysfunction: Self-inhalation for hypernasality
Kobayashi, R., Tsunoda, K., Takazawa, M., Ueha, R., Hosoya, M., Fujimaki, Y., Nito, T. & Yamasoba, T., 2019 Jan 1, (Accepted/In press) In : Auris Nasus Larynx.Research output: Contribution to journal › Article
Nose
Inhalation
Surgical Instruments
Rehabilitation
Dysarthria
2
Citations
(Scopus)
ClinGen expert clinical validity curation of 164 hearing loss gene–disease pairs
on behalf of the ClinGen Hearing Loss Clinical Domain Working Group, 2019 Jan 1, In : Genetics in Medicine.Research output: Contribution to journal › Article
Hearing Loss
Genome
Genes
Genetic Testing
Registries
Correction: ClinGen expert clinical validity curation of 164 hearing loss gene–disease pairs (Genetics in Medicine, (2019), 10.1038/s41436-019-0487-0)
on behalf of the ClinGen Hearing Loss Clinical Domain Working Group, 2019 Jan 1, In : Genetics in Medicine.Research output: Contribution to journal › Comment/debate
Open Access
Hearing Loss
Medicine
Estimating the concentration of therapeutic range using disease-specific iPS cells: Low-dose rapamycin therapy for Pendred syndrome
Hosoya, M., Saeki, T., Saegusa, C., Matsunaga, T., Okano, H., Fujioka, M. & Ogawa, K., 2019 Jun 1, In : Regenerative Therapy. 10, p. 54-63 10 p.Research output: Contribution to journal › Article
Audition
Sirolimus
Cell death
Cells
Stem cells
Generation of a human iPS cell line (CGMH.SLC26A4919-2) from a Pendred syndrome patient carrying SLC26A4 c.919-2A>G splice-site mutation
Cheng, Y. F., Chan, Y. H., Hu, C. J., Lu, Y. C., Saeki, T., Hosoya, M., Saegusa, C., Fujioka, M., Okano, H., Weng, S. M., Hsu, C. J., Chang, K. H. & Wu, C. C., 2019 Oct 1, In : Stem Cell Research. 40, 101524.Research output: Contribution to journal › Article
Open Access
Induced Pluripotent Stem Cells
Cell Line
Mutation
Genes
Germ Layers