Rchr
J-GLOBAL ID:200901080575221965   Update date: Apr. 11, 2024

Katoh Yuko

フクイ ユウコ | Katoh Yuko
Affiliation and department:
Job title: Chief Scientist
Research field  (8): Medical biochemistry ,  Developmental biology ,  Molecular biology ,  Genetics ,  Molecular biochemistry ,  Systems genomics ,  Genomics ,  Laboratory animal science
Research keywords  (4): マウス組織発生と機能維持機構 ,  クロマチン構造 ,  老化制御 ,  Chromatin Gene Regulation Longivity Develomental Biology
Research theme for competitive and other funds  (16):
  • 2019 - 2022 Molecular basis research for personalized nutrition
  • 2018 - 2021 Establishment of the chromatin state in gonadal development
  • 2015 - 2018 性分化関連遺伝子におけるポリコーム標的ゲノム領域の機能解明
  • 2011 - 2013 骨芽細胞におけるクロマチン性差
  • 2011 - 2013 性差構築の分子基盤
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Papers (74):
  • Atsushi Hattori, Atsuhito Seki, Naoto Inaba, Kazuhiko Nakabayashi, Kazue Takeda, Kuniko Tatsusmi, Yasuhiro Naiki, Akie Nakamura, Keisuke Ishiwata, Kenji Matsumoto, et al. Expression levels and DNA methylation profiles of the growth gene SHOX in cartilage tissues and chondrocytes. Scientific reports. 2024. 14. 1. 8069-8069
  • Yuki Muranishi, Yoshitomo Kobori, Yuko Katoh-Fukui, Satoshi Tamaoka, Atsushi Hattori, Akiyoshi Osaka, Hiroshi Okada, Kazuhiko Nakabayashi, Kenichiro Hata, Tomoko Kawai, et al. Systematic molecular analyses for 115 karyotypically normal men with isolated non-obstructive azoospermia. Human reproduction (Oxford, England). 2024
  • Satoshi Tamaoka, Akinari Fukuda, Kazuhiko Nakabayashi, Keiko Matsubara, Hiroko Ogata-Kawata, Yuki Muranishi, Kenichiro Hata, Yuko Kato-Fukui, Seisuke Sakamoto, Mureo Kasahara, et al. Rare sequence variants associated with the risk of non-syndromic biliary atresia. Hepatology research : the official journal of the Japan Society of Hepatology. 2023
  • Yuko Katoh-Fukui, Atsushi Hattori, Ruogu Zhang, Miho Terao, Shuji Takada, Kazuhiko Nakabayashi, Kenichiro Hata, Yutaka Yamada, Nobuo Matsuura, Maki Fukami. Chromosomal microdeletion leading to pituitary gigantism through hormone-gene overexpression. Human Molecular Genetics. 2023. 32. 14. 2318-2325
  • Satoshi Tamaoka, Kazuki Saito, Tomoko Yoshida, Kazuhiko Nakabayashi, Kenichi Tatsumi, Toshihiro Kawamura, Toshiya Matsuzaki, Keiko Matsubara, Hiroko Ogata-Kawata, Kenichiro Hata, et al. Exome-based genome-wide screening of rare variants associated with the risk of polycystic ovary syndrome. Reproductive medicine and biology. 2023. 22. 1. e12504
more...
MISC (25):
  • 福井由宇子、齋藤大輔、服部淳、鳴海宏子、五十嵐麻希、上原絵理香、島彦仁、菅野潤子、長谷川行洋、堀川玲子、深見真紀. DHX37疾患原因バリアントを有する46,XY DSD患者が示す多様な臨床症状. 第56回 日本小児内分泌学会学術集会. 2023
  • 服部 淳, 関 敦仁, 内木 康博, 中村 明枝, 道上 敏美, 福井 由宇子, 緒方 勤, 鏡 雅代, 深見 真紀. 軟骨組織におけるSHOX発現性差: 成人身長性差における意義. 第56回 日本小児内分泌学会学術集会. 2023
  • 齋藤大輔, 福井由宇子, 村西雄貴, 今雅史, 三井貴彦, 室谷浩二, 深見真紀. 非症候群性尿道下裂患者においてDHX37病原性バリアントは稀である. 第56回 日本小児内分泌学会学術集会. 2023
  • Atsushi Hattori, Atsuhito Seki, Kazuhiko Nakabayashi, Yasuhiro Naiki, Akie Nakamura, Keisuke Ishiwata, Kenji Matsumoto, Kohji Okamura, Yuko Katoh-Fukui, Tsutomu Ogata, et al. Male-dominant SHOX expression in cartilage tissues: implications for sex differences in adult height. The 68th Annual Meeting of the Japan Society of Human Genetics. 2023
  • Yuko Katoh-Fukui, Daisuke Saito, Hiroko Narumi, Atsushi Hattori, Maki Igarashi, Erika Uehara, Hirohito Shima, Junko Kanno, Yukihiro Hasegawa, Reiko Horikawa, et al. Diverse clinical manifestations due to pathogenic DHX37 variants in 46,XY disorders of sex development. The 68th Annual Meeting of the Japan Society of Human Genetics. 2023
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Education (2):
  • Tokyo Metropolitan University Faculty of Science Department of Biology
  • Tokyo Metropolitan University Graduate School of Science
Professional career (1):
  • 理学博士 (東京都立大学)
Work history (3):
  • National Institutes of Natural Sciences
  • 三菱生命科学研究所・研究員
  • 国立長寿医療研究センター 室長
Association Membership(s) (4):
日本人類遺伝学会 ,  THE JAPANESE SOCIETY FOR PEDIATRIC ENDOCRINOLOGY ,  日本発生生物学会 ,  日本分子生物学会
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