wakisaka tsuji keiko

わきさか(つじ) けいこ | wakisaka tsuji keiko

Affiliation and department：
Job title：研究員
Research theme for competitive and other funds (1)：

2021 - 2023 Roles of PINK1-Parkin on the differentiation of astrocytes in development of midbrain

Papers (27)：

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)：

Splicing errors in heart diseases. 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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