研究者
J-GLOBAL ID:202001014754810863   更新日: 2024年01月30日

脇坂 啓子

わきさか(つじ) けいこ | wakisaka tsuji keiko
所属機関・部署:
職名: 研究員
競争的資金等の研究課題 (1件):
  • 2021 - 2023 胎生期のアストロサイト発生におけるPINK1, Parkinの新たな役割
論文 (27件):
  • Keiko Tsuji Wakisaka, Yuuka Muraoka, Jo Shimizu, Mizuki Yamaguchi, Ibuki Ueoka, Ikuko Mizuta, Hideki Yoshida, Masamitsu Yamaguchi. Drosophila Alpha-ketoglutarate-dependent dioxygenase AlkB is involved in repair from neuronal disorders induced by ultraviolet damage. Neuroreport. 2019. 30. 15. 1039-1047
  • Keiko Tsuji Wakisaka, Yuzuru Imai. The dawn of pirna research in various neuronal disorders. Frontiers in bioscience (Landmark edition). 2019. 24. 1440-1451
  • Jie Wu, Tomoko Sakaguchi, Kotoe Takenaka, Futoshi Toyoda, Keiko Tsuji, Hiroshi Matsuura, Minoru Horie. A trafficking-deficient KCNQ1 mutation, T587M, causes a severe phenotype of long QT syndrome by interfering with intracellular hERG transport. Journal of cardiology. 2019. 73. 5. 343-350
  • Keiko Tsuji Wakisaka, Ryo Tanaka, Tomoki Hirashima, Yuuka Muraoka, Yumiko Azuma, Hideki Yoshida, Takahiko Tokuda, Satoshi Asada, Kojiro Suda, Kenji Ichiyanagi, et al. Novel roles of Drosophila FUS and Aub responsible for piRNA biogenesis in neuronal disorders. Brain research. 2019. 1708. 207-219
  • Keiko Tsuji Wakisaka, Kenji Ichiyanagi, Seiko Ohno, Masanobu Itoh. Association of zygotic piRNAs derived from paternal P elements with hybrid dysgenesis in Drosophila melanogaster. Mobile DNA. 2018. 9. 7-7
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MISC (5件):
  • 脇坂 啓子, 堀江 稔. スプライシング異常と循環器疾患. 循環器内科. 2011. 70. 5. 523-529
  • Takeru Maklyama, Masaharu Akao, Satoshi Shizuta, Takahiro Doi, Seiko Ohno, Yukko Nishio, Keiko Tsuji, Hideki Itoh, Toru Kita, Minoru Horie. 3CN5A and Lamin A/C Gone Mutations are Highly Prevalent In Patients with Familial Bradyarrhythmic Disorders. CIRCULATION. 2008. 118. 18. S873-S873
  • Tomoko Sakaguchi, Wataru Shimizu, Hideki Ito, Takashi Noda, Yoshihiro Miyamoto, Iori Nagaoka, Takashi Ashihara, Makoto Ito, Keiko Tsuji, Seiko Ohno, et al. Age-related triggers for life-threatning arrhythmia in the genotyped long QT syndrome. CIRCULATION. 2007. 116. 16. 584-584
  • Hideki Itoh, Tomoko Sakaguchi, Wei-Guang Ding, Keiko Tsuji, Takashi Ashihara, Yuko Nakazawa, Hikari Jo, Takenori Yao, Makoto Ito, Hiroshi Matsuura, et al. A novel KCNH2 mutation associated with the short QT interval of Brugada syndrome: Impaired deactivation for the I-Kr channel. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY. 2007. 49. 9. 30A-30A
  • Hidetada Yoshida, Minoru Horie, Hideo Otani, Makoto Takano, Keiko Tsuji, Tomoyuki Kubota, Masatake Fukunami, Shigetake Sasayama. Characterization of a novel missense mutation in the pore of HERG in a patient with long QT syndrome. Journal of Cardiovascular Electrophysiology. 1999. 10. 9. 1262-1270
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