日本大学 · 薬学科/薬学部

研究关键词hereditary hearing loss・GJB2 mutation・cochlear base editing・gap junction restoration・CDH23 mutation・USH2A iPSC・high-frequency hearing loss

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• Microtubule-associated protein 2 (MAP2) deficiency causes high-frequency hearing loss2025 · Frontiers in Audiology and Otology, 2025年10月, 査読有り
• AAV-mediated base editing restores cochlear gap junction in GJB2 dominant-negative mutation-associated syndromic hearing loss model2025 · JCI Insight, 2025年03月, 査読有り, 通常論文
• Generation of an induced pluripotent stem cell line from a late-onset, progressive high frequency hearing loss patient due to mutation in CDH232024 · Stem Cell Research, 2024年09月
• Generation and characterization of a human iPSC line (JUFMDOi007-A) from a patient with Usher syndrome due to mutation in USH2A.2023 · Stem cell research, 2023年06月, 査読有り

• アデノ随伴ウイルスによる遺伝子導入技術を用いた加齢性難聴に対する治療標的の探索2024

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