Rchr
J-GLOBAL ID：201801018644714254
Update date: Mar. 22, 2024
Shibata Mami
シバタ マミ | Shibata Mami
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Affiliation and department：
Fukuoka University Faculty of Medicine, School of Medicine
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Detailed information
Research field (2)：
Genomics
, Genetics
Research theme for competitive and other funds (2)：
2022 - 2025 次世代シーケンシング解析による子宮内膜再生microRNAの同定と創薬基盤開発
2019 - 2022 mRNA-Seq analysis in KCNQ2-related epilepsy model mice and the exploration of novel therapeutic drug candidates for KCNQ2-EE
Papers (7)：
Eisuke Ichise, Tomohiro Chiyonobu, Mitsuru Ishikawa, Yasuyoshi Tanaka, Mami Shibata, Takenori Tozawa, Yoshihiro Taura, Satoshi Yamashita, Michiko Yoshida, Masafumi Morimoto, et al. Impaired neuronal activity and differential gene expression in
STXBP1
encephalopathy patient iPSC-derived GABAergic neurons. Human Molecular Genetics. 2021. 30. 14. 1337-1348
Mami Shibata, Atsushi Ishii, Ayako Goto, Shinichi Hirose. Comparative characterization of PCDH19 missense and truncating variants in PCDH19-related epilepsy. Journal of Human Genetics. 2020. 66. 6. 569-578
Shinichi Hirose, Yasuyoshi Tanaka, Mami Shibata, Yuichi Kimura, Mitsuru Ishikawa, Norimichi Higurashi, Toshiyuki Yamamoto, Eisuke Ichise, Tomohiro Chiyonobu, Atsushi Ishii. Application of induced pluripotent stem cells in epilepsy. Molecular and Cellular Neuroscience. 2020. 108. 103535-103535
Ayako Goto, Atsushi Ishii, Mami Shibata, Yukiko Ihara, Edward C. Cooper, Shinichi Hirose. Characteristics of
KCNQ2
variants causing either benign neonatal epilepsy or developmental and epileptic encephalopathy. Epilepsia. 2019. 60. 9. 1870-1880
Akihisa Okumura, Koichi Maruyama, Mami Shibata, Hirokazu Kurahashi, Atsushi Ishii, Shingo Numoto, Shinichi Hirose, Tomoko Kawai, Manami Iso, Shinsuke Kataoka, et al. A patient with a GNAO1 mutation with decreased spontaneous movements, hypotonia, and dystonic features. Brain & development. 2018. 40. 10. 926-930
ｍore...
Professional career (1)：
博士(農学) (九州大学)
Association Membership(s) (1)：
日本人類遺伝学会
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