Grants per year
Personal profile
Education/Academic qualification
PhD, University of Massachusetts
… → 2007
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Dive into the research topics where Kazuaki Homma is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Grants
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Defining the pathological mechanisms of hereditary hearing loss
National Institute on Deafness and Other Communication Disorders
12/1/18 → 11/30/23
Project: Research project
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Dynamic interaction among proteins in hair cells
National Institute on Deafness and Other Communication Disorders
8/1/17 → 7/31/19
Project: Research project
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Investigate The Effectiveness Of Salicylate In Preventing Hpβcd-Induced Ototoxicity In The NPC1 Mouse Model
Ara Parseghian Medical Research Foundation
9/1/16 → 8/30/17
Project: Research project
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Defining molecular mechanisms in the SLC26 family of proteins
National Institute on Deafness and Other Communication Disorders
4/1/15 → 6/30/18
Project: Research project
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Research Output
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Axodendritic versus axosomatic cochlear efferent termination is determined by afferent type in a hierarchical logic of circuit formation
Webber, J. L., Clancy, J. C., Zhou, Y., Yraola, N., Homma, K. & García-Añoveros, J., Jan 20 2021, In: Science Advances. 7, 4, eabd8637.Research output: Contribution to journal › Article › peer-review
Open Access -
Three-dimensional otic neuronal progenitor spheroids derived from human embryonic stem cells
Heuer, R. A., Nella, K. T., Chang, H. T., Coots, K. S., Oleksijew, A. M., Roque, C. B., Silva, L. H. A., McGuire, T. L., Homma, K. & Matsuoka, A. J., Feb 2021, In: Tissue Engineering - Part A. 27, 3-4, p. 256-269 14 p.Research output: Contribution to journal › Article › peer-review
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Systematic quantification of the anion transport function of pendrin (SLC26A4) and its disease-associated variants
Wasano, K., Takahashi, S., Rosenberg, S. K., Kojima, T., Mutai, H., Matsunaga, T., Ogawa, K. & Homma, K., Jan 1 2020, In: Human mutation. 41, 1, p. 316-331 16 p.Research output: Contribution to journal › Article › peer-review
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Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans
Mutai, H., Wasano, K., Momozawa, Y., Kamatani, Y., Miya, F., Masuda, S., Morimoto, N., Nara, K., Takahashi, S., Tsunoda, T., Homma, K., Kubo, M. & Matsunaga, T., Apr 2020, In: PLoS genetics. 16, 4, e1008643.Research output: Contribution to journal › Article › peer-review
Open Access2 Scopus citations -
Deletion of exons 17 and 18 in prestin’s STAS domain results in loss of function
Takahashi, S., Yamashita, T., Homma, K., Zhou, Y., Zuo, J., Zheng, J. & Cheatham, M. A., Dec 1 2019, In: Scientific reports. 9, 1, 6874.Research output: Contribution to journal › Article › peer-review
Open Access1 Scopus citations