Institute of Science Tokyo · Graduate School of Medical and Dental Sciences · 教授

Research keywords先制医療・神経内科学・神経難病・遺伝子診療・分子病態・脊髄小脳変性症・RNA病態

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• Wang D, Honda S, Shin MK, Watase K, Mizusawa H, Ishikawa K, Shimizu S. Subcellular localization and ER-mediated cytotoxic function of α1A and α1ACT in spinocerebellar ataxia type 6. Biochemical and biophysical research communications. 2024.02; 695 149481. ( PubMed , DOI )2024
• Takahashi S, Ono D, Shintaku H, Oyama J, Nishida Y, Ishikawa K, Yokota T. Cryptogenic New-onset Refractory Status Epilepticus with Hyperintensity of T1-weighted Magnetic Resonance Imaging in the Bilateral Basal Ganglia: An Autopsy Report. Internal medicine (Tokyo, Japan). 2024.09; ( PubMed , DOI )2024
• Rayle Mamuti, Sato Nozomu, Ozaki Kokoro, Higashi Miwa, Okita Michi, Yajima Reiko, Amano Akiko, Mizusawa Hidehiro, Yokota Takanori, Ishikawa Kinya. Degenerative ataxiaの日本人患者167名のコホートを対象とした、多型性を示すSCA37遺伝子座の解析(Analysis of the polymorphic SCA37 locus in a cohort of 167 Japanese patients with degenerative ataxia) Journal of Medical and Dental Sciences. 2024; 71 11-17. ( 医中誌 )2024
• Honda T, Matsumura K, Hashimoto Y, Yokota T, Mizusawa H, Nagao S, Ishikawa K. Temporal Relationship between Impairment of Cerebellar Motor Learning and Deterioration of Ataxia in Patients with Cerebellar Degeneration. Cerebellum (London, England). 2024.08; 23 (4): 1280-1292. ( PubMed , DOI )2024

• 本邦に高頻度存在する脊髄小脳変性症に対する画期的免疫療法の開発
• 優性遺伝型脊髄小脳変性症のハイスループット遺伝子変異探索
• 脊髄小脳失調症6型および31型の分子病態に基づく治療法開発研究
• 第16番染色体長腕に連鎖する優性遺伝性小脳変性症関連遺伝子の機能解析

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