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 (77)：

Hibiki Doi, Ikuko Kageyama, Yuko Katoh-Fukui, Atsushi Hattori, Maki Fukami, Naoto Shimura. Homozygous 6-bp deletion of IGFALS in a prepubertal boy with short stature. Human genome variation. 2024. 11. 1. 27-27
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
Yuki Muranishi, Tomoyo Itonaga, Kenji Ihara, Yuko Katoh-Fukui, Satoshi Tamaoka, Atsushi Hattori, Masafumi Kon, Nobuo Shinohara, Maki Fukami. PTPN11 and FLNA variants in a boy with ambiguous genitalia, short stature, and non-specific dysmorphic features. Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology. 2024. 33. 3. 169-173
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

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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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