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Kazuaki Homma

  • 1294 Citations
20002020

Research output per year

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Personal profile

Education/Academic qualification

PhD, University of Massachusetts

… → 2007

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Grants

Defining the pathological mechanisms of hereditary hearing loss

Homma, K.

National Institute on Deafness and Other Communication Disorders

12/1/18 → 11/30/23

Project: Research project

    • Dynamic interaction among proteins in hair cells

    Cheatham, M. A., Homma, K. & Zheng, J.

    National Institute on Deafness and Other Communication Disorders

    8/1/17 → 7/31/19

    Project: Research project

    • Investigate The Effectiveness Of Salicylate In Preventing Hpβcd-Induced Ototoxicity In The NPC1 Mouse Model

    Homma, K. & Zheng, J.

    Ara Parseghian Medical Research Foundation

    9/1/16 → 8/30/17

    Project: Research project

    • Defining molecular mechanisms in the SLC26 family of proteins

    Homma, K.

    National Institute on Deafness and Other Communication Disorders

    4/1/15 → 6/30/18

    Project: Research project

    • Investigating prestin's role in outer hair cell survival

    Homma, K.

    Capita Foundation

    2/3/14 → 2/2/16

    Project: Research project

    • Research Output

    • 1294 Citations
    • 35 Article
    • 2 Comment/debate
    • 2 Letter

    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

    • 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

    Open Access

    • 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

    Open Access
    • 1 Scopus citations

    Prestin contributes to membrane compartmentalization and is required for normal innervation of outer hair cells

    Takahashi, S., Sun, W., Zhou, Y., Homma, K., Kachar, B., Cheatham, M. A. & Zheng, J., Jul 20 2018, In : Frontiers in Cellular Neuroscience. 12, 211.

    Research output: Contribution to journal › Article

    • 1 Scopus citations

    The extracellular loop of pendrin and prestin modulates their voltage-sensing property

    Kuwabara, M. F., Wasano, K., Takahashi, S., Bodner, J., Komori, T., Uemura, S., Zheng, J., Shima, T. & Homma, K., Jan 1 2018, In : Journal of Biological Chemistry. 293, 26, p. 9970-9980 11 p.

    Research output: Contribution to journal › Article

    • 4 Scopus citations