Research theme for competitive and other funds (10)：
2021 - 2025 Methylation of genes related to cardiovascular and chronic kidney diseases in preterm low birth weight infants born to mothers with hypertensive disorders of pregnancy
2015 - 2019 The effects of the GPR37-mutation in autism spectrum disorder on the signal transduction by prosaponin
2015 - 2018 Molecular Pathogenesis of the abnormal spine morphology and 5-HTR complex induced by ASD-related mutated Mupp1
2014 - 2018 DNA methylation of human glucocorticoid receptor gene (NR3C1) and stress response in low birth weight infants
2012 - 2016 Studies on the influence of brain and neurons of mutation of synaptic cell adhesion molecule protein, Cadm1 using autism mouse models.
2011 - 2014 Analysis for the pathogenesis and the target molecules of treatment for autism focusing on G-protein coupled receptors and synaptic molecules
2009 - 2011 The regulation of mouse ultrasonic vocalization and behavior by Foxp2
2009 - 2011 The mechanisms of language acquisition and evolution of mouse brain in Foxp2-KI mice
1997 - 1999 Taste active components of fish sauces
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Papers (70)：
Akihiko Miyauchi, Chika Watanabe, Naoya Yamada, Eriko F Jimbo, Mizuki Kobayashi, Natsumi Ohishi, Atsuko Nagayoshi, Shiho Aoki, Yoshihito Kishita, Akira Ohtake, et al. Apomorphine is a potent inhibitor of ferroptosis independent of dopaminergic receptors. Scientific reports. 2024. 14. 1. 4820-4820
Kiri Koshu, Kazuhiro Muramatsu, Tomomi Maru, Yoshie Kurokawa, Yoshitaka Mizobe, Hirokazu Yamagishi, Daisuke Matsubara, Koji Yokoyama, Eriko Jimbo, Hideki Kumagai, et al. Neonatal onset of Niemann-Pick disease type C in a patient with cholesterol re-accumulation in the transplanted liver and inflammatory bowel disease. Brain & development. 2023. 45. 9. 517-522
Chika Watanabe, Hitoshi Osaka, Miyuki Watanabe, Akihiko Miyauchi, Eriko F Jimbo, Takeshi Tokuyama, Hideki Uosaki, Yoshihito Kishita, Yasushi Okazaki, Takanori Onuki, et al. Total and reduced/oxidized forms of coenzyme Q10 in fibroblasts of patients with mitochondrial disease. Molecular genetics and metabolism reports. 2023. 34. 100951-100951
Mari Kuwajima, Karin Kojima, Hitoshi Osaka, Yusuke Hamada, Eriko Jimbo, Miyuki Watanabe, Shiho Aoki, Ikuko Sato-Shirai, Keiko Ichimoto, Takuya Fushimi, et al. Valine metabolites analysis in ECHS1 deficiency. Molecular genetics and metabolism reports. 2021. 29. 100809-100809
Sachie Nakamura, Hitoshi Osaka, Shin-Ichi Muramatsu, Naomi Takino, Mika Ito, Eriko F Jimbo, Chika Watanabe, Shuji Hishikawa, Takeshi Nakajima, Takanori Yamagata. Intra-cisterna magna delivery of an AAV vector with the GLUT1 promoter in a pig recapitulates the physiological expression of SLC2A1. Gene therapy. 2021. 28. 6. 329-338
