Inagaki Hidehito

イナガキヒデヒト | Inagaki Hidehito

Affiliation and department：
Job title： Assistant Professor
Homepage URL (1)： https://www.fujita-hu.ac.jp/~genome/mg/

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 (12)：

2023 - 2026 染色体の核内配置編集による染色体転座の発生機序の解明
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

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Papers (132)：

Yuri Murase, Yui Shichiri, Hidehito Inagaki, Tatsuya Nakano, Yoshiharu Nakaoka, Yoshiharu Morimoto, Tomoko Ichikawa, Haruki Nishizawa, Eiji Sugihara, Hiroki Kurahashi. Comparative Analysis of Two NGS-Based Platforms for Product-of-Conception Karyotyping. Genes. 2024. 15. 8
Seiji Yamada, Motoki Tanikawa, Yuko Matsushita, Ryota Fujinami, Hiroshi Yamada, Kaishi Sakomi, Tomohiro Sakata, Hidehito Inagaki, Hideaki Yokoo, Koichi Ichimura, et al. SEGA-like circumscribed astrocytoma in a non-NF1 patient, harboring molecular profile of GBM. A case report. Neuropathology : official journal of the Japanese Society of Neuropathology. 2024. 44. 3. 190-199
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

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MISC (41)：

佐々木ひと美, 白木良一, 稲垣秀人, 倉橋浩紀. 日本人結節性硬化症患者における遺伝子変異と疾患重症度の関連性(Relevance of genetic mutations and disease severity in Japanese tuberous sclerosis). 日本泌尿器科学会総会. 2019. 107回. IS-29
池田真理子, 池田真理子, 堤真紀子, 内野俊平, 森岡一朗, 河合美紀, 加藤武馬, ENKHJARGAL Sarantuya, 稲垣秀人, 飯島一誠, et al. Severe mitochondrial neurogastrointestinal encephalomyopathy caused by DNA ligase enzyme deficiency. 日本人類遺伝学会大会プログラム・抄録集. 2019. 64th
別府秀彦, 稲垣秀人, 西井一宏, 新里昌功, 千原猛, 毛利彰宏, 齋藤邦明, 高橋久英, 倉橋浩樹. NGSを用いた小脳変性マウスのExome解析および原因遺伝子候補の神経栄養因子との関連脳機能改善素材開発試験の応用を目指して. 機能性食品と薬理栄養. 2018. 12. 3. 209-209
戸松瑛介, 加藤武馬, 富家由美, 植田佐保子, 垣田彩子, 高柳武志, 四馬田恵, 牧野真樹, 新海保子, 堤真紀子, et al. CDC73遺伝子の部分欠失を認めた副甲状腺癌の一例. 日本内分泌学会雑誌. 2018. 94. 1. 362-362
稲垣秀人, 杉本賢政, 堤真紀子, 井上義一, 田口佳広, 帽田仁子, 宮田昌史, 奥本隆行, 吉川哲史, 倉橋浩樹. 細胞培養モデルが明らかにしたX連鎖の疾患での女性重症化. 生命科学系学会合同年次大会. 2017. 2017年度. [2PT26-06(3P

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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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