Rchr
J-GLOBAL ID:201801015264071203   Update date: Mar. 07, 2024

Saito-Hakoda Akiko

Saito-Hakoda Akiko
Research field  (1): Other
Research theme for competitive and other funds  (6):
  • 2015 - 2018 Innovation of novel therapeutics against hypertension targeting CYP11B2 by RXR activation
  • 2014 - 2017 The elucidation of the molecular biologic pathology in the Osteogenesis imperfecta and new molecular target treatment by the Wnt signal pathway.
  • 2013 - 2016 Genetic analysis of HPMR syndrome
  • 2013 - 2016 An approach to identify novel therapeutics against diabetic nephropathy based on aldosterone synthase gene regulation
  • 2009 - 2011 Analysis of phosphate metabolism and treatment for hereditary hypophosphatemic rickets
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Papers (20):
  • Akiko Saito-Hakoda, Atsuo Kikuchi, Tadahisa Takahashi, Yu Yokoyama, Noriko Himori, Mika Adachi, Ryoukichi Ikeda, Yuri Nomura, Jun Takayama, Junko Kawashima, et al. Familial Paget's disease of bone with ocular manifestations and a novel TNFRSF11A duplication variant (72dup27). Journal of bone and mineral metabolism. 2022
  • 箱田 明子, 島 彦仁, 梅木 郁美, 鈴木 大, 上村 美季, 菅原 典子, 菅野 潤子, 藤原 幾磨. ACAN新規ヘテロ接合性ナンセンス変異を認めた低身長姉妹例. 日本内分泌学会雑誌. 2019. 95. 1. 427-427
  • Saito-Hakoda A, Kanno J, Suzuki D, Kawashima S, Kamimura M, Hirano K, Sakai K, Igarashi M, Fukami M, Fujiwara I. A Follow-Up from Infancy to Puberty in a Japanese Male with SRY-Negative 46,XX Testicular Disorder of Sex Development Carrying a p.Arg92Trp Mutation in NR5A1. Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation. 2019. 13. 2. 60-66
  • Rehana Parvin, Erika Noro, Akiko Saito-Hakoda, Hiroki Shimada, Susumu Suzuki, Kyoko Shimizu, Hiroyuki Miyachi, Atsushi Yokoyama, Akira Sugawara. Inhibitory Effects of a Novel PPAR-γ Agonist MEKT1 on Pomc Expression/ACTH Secretion in AtT20 Cells. PPAR Research. 2018. 2018. 1-16
  • Akiko Saito-Hakoda, Aki Nishii, Takashi Uchida, Atsuo Kikuchi, Junko Kanno, Ikuma Fujiwara, Shigeo Kure. A follow-up during puberty in a Japanese girl with type a insulin resistance due to a novel mutation in INSR. Clinical Pediatric Endocrinology. 2018. 27. 1. 53-57
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MISC (11):
  • 島 彦仁, 曽木 千純, 梅木 郁美, 鈴木 大, 上村 美季, 箱田 明子, 菅野 潤子, 呉 繁夫, 藤原 幾磨. 橋本病患者では低Caに対するPTHの分泌が低下する症例が存在する. 日本内分泌学会雑誌. 2019. 95. 1. 393-393
  • 菅野 潤子, 川嶋 明香, 島 彦仁, 曽木 千純, 梅木 郁美, 上村 美季, 鈴木 大, 箱田 明子, 呉 繁夫, 藤原 幾磨. 劇症1型糖尿病の2小児例. 日本内分泌学会雑誌. 2019. 95. 1. 485-485
  • 箱田明子, 島彦仁, 島彦仁, 梅木郁美, 鈴木大, 上村美季, 西井亜紀, 菅野潤子, 藤原幾磨, 藤原幾磨. 早発陰毛24症例における臨床的検討. 日本小児内分泌学会学術集会プログラム・抄録集. 2019. 53rd
  • 箱田明子, 箱田明子, 菅野潤子, 菅野潤子, 川嶋明香, 鈴木大, 上村美季, 平野浩次, 坂井清英, 五十嵐麻希, et al. 自然に思春期発来を認めたNR5A1変異を有するSRY陰性46,XX testicular DSDの1男性例. 日本小児内分泌学会学術集会プログラム・抄録集. 2018. 52nd
  • 箱田明子, 箱田明子, 川嶋明香, 鈴木大, 内田奈生, 上村美季, 熊谷直憲, 菅野潤子, 笹原洋二, 呉繁夫, et al. 精神症状の悪化と造血異常を認め,治療に難渋したROHHAD症候群の1女児例. 日本小児内分泌学会学術集会プログラム・抄録集. 2017. 51st
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