Rchr
J-GLOBAL ID：200901090324953857   Update date: Apr. 11, 2024

Inagaki Hidehito

イナガキヒデヒト | Inagaki Hidehito
Affiliation and department：
Fujita Health University Division of Molecular Genetics, Center for Medical Science

About Fujita Health University Division of Molecular Genetics, Center for Medical Science


Job title： Assistant Professor
Homepage URL  (1)： http://hp.fujita-hu.ac.jp/ICMS/
Research field  (4)： Tumor biology ,  Neuroscience - general ,  Molecular biology ,  Medical biochemistry
Research keywords  (11)： DNA高次構造 ,  DNA二重鎖切断 ,  DNAの高次構造 ,  発生・分化 ,  相同組み換え ,  染色体転座 ,  核酸 ,  遺伝子導入 ,  パリンドローム ,  染色体 ,  ゲノム
Research theme for competitive and other funds  (11)：
  • 2021 - 2024 Production of chromosomal structural abnormalities using cultured cell system
  • 2019 - 2023 網羅的遺伝子解析と三次元タンパク構造解析を用いたウエスト症候群の基礎病態解析
  • 2019 - 2023 ゲノム編集による過剰マーカー染色体の病因解明
  • 2013 - 2017 The study trains rehabilitation training to perform to spino- cerebellar degeneration patient to a cerebellar degenerative mouse
  • 2015 - 2017 体細胞モザイクがもたらす病態のモデル細胞系の構築
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Papers (130)：
  • Mamiko Yamada, Seiji Mizuno, Mie Inaba, Tomoko Uehara, Hidehito Inagaki, Hisato Suzuki, Fuyuki Miya, Toshiki Takenouchi, Hiroki Kurahashi, Kenjiro Kosaki. Truncating variants of the sterol recognition region of SHH cause hypertelorism phenotype rather than hypotelorism-holoprosencephaly. American journal of medical genetics. Part A. 2024. e63614
  • Takeshi Sugimoto, Hidehito Inagaki, Tasuku Mariya, Rie Kawamura, Mariko Taniguchi-Ikeda, Seiji Mizuno, Yukako Muramatsu, Ikuya Tsuge, Hirofumi Ohashi, Nakamichi Saito, et al. Breakpoints in complex chromosomal rearrangements correspond to transposase-accessible regions of DNA from mature sperm. Human genetics. 2023
  • Yusuke Kawano, Atsuhito Seki, Takashi Kuroiwa, Atsushi Maeda, Takuya Funahashi, Kanae Shizu, Katsuji Suzuki, Hidehito Inagaki, Hiroki Kurahashi, Nobuyuki Fujita. A case of bilateral elbow dislocation in a patient with Rubinstein-Taybi syndrome. JSES international. 2023. 7. 4. 714-718
  • Tasuku Mariya, Yui Shichiri, Takeshi Sugimoto, Rie Kawamura, Syunsuke Miyai, Hidehito Inagaki, Eiji Sugihara, Keiko Ikeda, Tsuyoshi Baba, Aki Ishikawa, et al. Clinical application of long-read nanopore sequencing in a preimplantation genetic testing pre-clinical workup to identify the junction for complex Xq chromosome rearrangement-related disease. Prenatal diagnosis. 2023. 43. 3. 304-313
  • Katsuyuki Yokoi, Yoko Nakajima, Yoshihisa Takahashi, Takashi Hamajima, Go Tajima, Kazuyoshi Saito, Shunsuke Miyai, Hidehito Inagaki, Tetsushi Yoshikawa, Hiroki Kurahashi, et al. Transport and Golgi organization 2 deficiency with a prominent elevation of C14:1 during a metabolic crisis: A case report. JIMD reports. 2023. 64. 1. 3-9
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MISC (41)：
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Education (2)：
  • 1993 - 1998 Nagoya University Graduate School of Science Department of Biology
  • 1989 - 1993 Nagoya University School of Science Department of Biology
Professional career (1)：
  • 理学博士 (名古屋大学大学院)
Work history (9)：
  • 2022/04 - 現在 Fujita Health University Division of Molecular Genetics, Center for Medical Science
  • 2018/10 - 2022/03 Fujita Health University Institute for Comprehensive Medical Science
  • 2015/02 - 2018/10 Fujita Health University Div Mol Genet, ICMS Assistant Professor
  • 2007/04 - 2015/01 藤田保健衛生大学 総合医科学研究所分子遺伝学 助教
  • 2003/04 - 2007/03 藤田保健衛生大学 総合医科学研究所分子遺伝学 助手
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Association Membership(s) (4)：
The Japan Society of Human Genetics ,  The Molecular Biology Society of Japan ,  日本人類遺伝学会 ,  日本分子生物学会
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