分子生物学部
研究業績
  1. Takechi F, Kato K, Makiyama T, Ohno S, Kabasawa M, Morishima H, Kawasoe Y, Okajima Y, Matsuo K, Horie M, Tateno S. Ventricular Fibrillation in a Family with Short QT Syndrome Type 2 Carrying a Heterozygous KCNQ1-V141M Variant. Journal of Pediatric Cardiology and Cardiac Surgery. 6, 31-36, 2022.
  2. Nagata Y, Watanabe R, Eichhorn C, Ohno S, Aiba T, Ishikawa T, Nakano Y, Aizawa Y, Hayashi K, Murakoshi N, Nakajima T, Yagihara N, Mishima H, Sudo T, Higuchi C, Takahashi A, Sekine A, Makiyama T, Tanaka Y, Watanabe A, Tachibana M, Morita H, Yoshiura KI, Tsunoda T, Watanabe H, Kurabayashi M, Nogami A, Kihara Y, Horie M, Shimizu W, Makita N, Tanaka T. Targeted deep sequencing analyses of long QT syndrome in a Japanese population. PLOS ONE. 17, e0277242, 2022.
  3. Horie M, Ohno S, Ai T. Pandora will never regret having opened her box: reappraisal of genes associated with CPVT and SQTS. European Heart Journal. 43, 1511-1513, 2022.
  4. 大野 聖子. 遺伝子に刻まれた旅の記憶. 心電図. 42, 201-202, 2022.
  5. 大野 聖子. 不整脈原性右室心筋症（ARVC）. 循環器ジャーナル. 70, 157-162, 2022.
  6. 大野 聖子. 不整脈原性心筋症（ACM）における遺伝子診断の重要性. 循環器内科. 91, 356-361, 2022.