所属
医歯学域医学系 医歯学総合研究科 健康科学専攻 社会・行動医学講座 特任研究員
職名
特任研究員
ヒワタシ ハナエ
樋渡 英恵
HIWATASHI Hanae
学位
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修士（農学） （ 2003年3月 九州大学 ）
経歴
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鹿児島大学 医歯学域医学系 医歯学総合研究科 健康科学専攻 社会・行動医学講座 特任研究員
2015年11月 - 現在
論文
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Terasaki A. . DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion in TNRC6A . Journal of Human Genetics66 ( 4 ) 419 - 429 2021年4月
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Terasaki Akane, Nakamura Masayuki, Urata Yuka, Hiwatashi Hanae, Yokoyama Izumi, Yasuda Takeshi, Onuma Teiichi, Wada Kazumaru, Kaneko Sunao, Kan Rumiko, Niwa Shin-ichi, Hashimoto Ohiko, Komure Osamu, Goto Yu-ichi, Yamagishi Yuko, Nakano Misa, Furusawa Yoshihiko, Sano Akira . DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion in TNRC6A(和訳中) . Journal of Human Genetics66 ( 4 ) 419 - 429 2021年4月
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Akane Terasaki, Masayuki Nakamura, Yuka Urata, Hanae Hiwatashi, Izumi Yokoyama, Takeshi Yasuda, Teiichi Onuma, Kazumaru Wada, Sunao Kaneko, Rumiko Kan, Shin-ichi Niwa, Ohiko Hashimoto, Osamu Komure, Yu-ichi Goto, Yuko Yamagishi, Misa Nakano, Yoshihiko Furusawa & Akira Sano . DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion in TNRC6A . Journal of Human Genetics 2020年11月
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Nishida Y. . Novel pathogenic VPS13A gene mutations in Japanese patients with chorea-acanthocytosis . Neurology: Genetics5 ( 3 ) e332 2019年6月
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Urata Y. . Novel pathogenic XK mutations in McLeod syndrome and interaction between XK protein and chorein . Neurology: Genetics5 ( 3 ) e328 2019年6月
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Yuka Urata, Masayuki Nakamura, Natsuki Sasaki, Nari Shiokawa, Yoshiaki Nishida, Kaoru Arai, Hanae Hiwatashi, Izumi Yokoyama, Shinsuke Narumi, Yasuo Terayama, Takenobu Murakami, Yoshikazu Ugawa, Hiroki Sakamoto, Satoshi Kaneko, Yusuke Nakazawa, Ryo Yamasaki, Shoko Sadashima, Toshiaki Sakai, Hiroaki Arai, Akira Sano . Novel pathogenic XK mutations in McLeod syndrome and interaction between XK protein and chorein . Neurology: Genetics 2019年6月
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Yoshiaki Nishida, Masayuki Nakamura, Yuka Urata, Kei Kasamo, Hanae Hiwatashi, Izumi Yokoyama, Masahiro Mizobuchi, Kotaro Sakurai, Yasushi Osaki, Yukari Morita, Masako Watanabe, Kenji Yoshida, Kiyomi Yamane, Natsuki Miyakoshi, Ryouichi Okiyama, Takehiro Ueda, Noritaka Wakasugi, Yuji Saitoh, Takashi Sakamoto, Yuji Takahashi, Ken Shibano, Hideki Tokuoka, Atsushi Hara, Kazunari Monma, Katsuhisa Ogata, Keita Kakuda, Hideki Mochizuki, Takeo Arai, Manabu Araki, Takeshi Fujii, Kazuto Tsukita, Haruhi Sakamaki-Tsukita, Akira Sano . Novel pathogenic VPS13A gene mutations in Japanese patients with chorea-acanthocytosis . Neurology Genetics 2019年6月
MISC
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Terasaki A.
Journal of Human Genetics 66 ( 4 ) 449 - 450 2021年4月