Rchr
J-GLOBAL ID:200901048725784520   Update date: Sep. 05, 2024

Yoshiura Koh'ichiro

ヨシウラ コウイチロウ | Yoshiura Koh'ichiro
Affiliation and department:
Job title: Associate Prefessor
Homepage URL  (1): https://www-sdc.med.nagasaki-u.ac.jp/dhge/
Research field  (2): Human pathology ,  Medical biochemistry
Research keywords  (4): Human Genetics ,  genetic disorder ,  分子遺伝学 ,  Molecular Genetics
Research theme for competitive and other funds  (70):
  • 2023 - 2026 Comprehensive disease-associated interactome and model mice elucidate diversity and periodicity of the autoinflammatory disease
  • 2022 - 2026 甲状腺濾胞性腫瘍の術前細胞診断を可能とする53BP1発現型の定量解析
  • 2022 - 2025 Elucidation of the pathophysiology of schizophrenia / autism spectrum disorder using EP400 gene transgenic mice
  • 2021 - 2025 HTLV-1の分子系統別疾患感受性の解明と層別化コホート研究の構築
  • 2020 - 2023 Study for the mechanism of onset for myelodysplastic syndromes among atomic bomb survivors through temporal axis
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Papers (355):
  • Yuji Kobayashi, Koji Ando, Yoshitaka Imaizumi, Hikaru Sakamoto, Hideaki Kitanosono, Masataka Taguchi, Hiroyuki Mishima, Akira Kinoshita, Shara Bekytbek, Maki Baba, et al. RUNX1 expression is regulated by a super-enhancer and is a therapeutic target in adult T-cell leukemia/lymphoma. Leukemia & lymphoma. 2024. 1-13
  • Masaki Ibe, Shinobu Tamura, Hideki Kosako, Yusuke Yamashita, Masamichi Ishii, Masaoh Tanaka, Hiroyuki Mishima, Akira Kinoshita, Sadahiro Iwabuchi, Shuhei Morita, et al. Familial schwannomatosis carrying LZTR1 variant p.R340X with brain tumor: A case report. Molecular genetics and metabolism reports. 2024. 40. 101107-101107
  • Daisuke Hatta, Shiho Makiya, Kaito Kanamoto, Kaori Watanabe, Yuki Fuchigami, Shigeru Kawakami, Akira Kinoshita, Koh-Ichiro Yoshiura, Naohiro Kurotaki, Keiro Shirotani, et al. Proline-rich transmembrane protein 2 regulates the magnitude and frequency of dopamine release by repetitive neuronal stimuli in the striatum of L-dopa-treated mice. Neuropsychopharmacology reports. 2024
  • Zheng Wang, Mitsuhiro Kometani, Leonid Zeitlin, Yael Wilnai, Akira Kinoshita, Koh-ichiro Yoshiura, Hiroko Ninomiya, Takeshi Imamura, Long Guo, Jingyi Xue, et al. Heterozygous mutations in the straitjacket region of the latency-associated peptide domain of TGFB2 cause Camurati-Engelmann disease type II. Journal of Human Genetics. 2024
  • Zheng Wang, Mitsuhiro Kometani, Leonid Zeitlin, Yael Wilnai, Akira Kinoshita, Koh-Ichiro Yoshiura, Hiroko Ninomiya, Takeshi Imamura, Long Guo, Jingyi Xue, et al. Heterozygous mutations in the straitjacket region of the latency-associated peptide domain of TGFB2 cause Camurati-Engelmann disease type II. Journal of human genetics. 2024
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MISC (201):
  • 北之園英明, 安東恒史, 今泉芳孝, 小林裕児, 三嶋博之, 木下晃, 田口正剛, 坂本光, 加藤丈晴, 佐藤信也, et al. Combination therapy of PRMT5 inhibitor and PHD2 inhibitor (IOX4) for adult T-cell leukemia/lymphoma. 日本血液学会学術集会抄録(Web). 2021. 83rd
  • 小林裕児, 安東恒史, 今泉芳孝, 北之園英明, 三嶋博之, 木下晃, 田口正剛, 坂本光, 加藤丈晴, 佐藤信也, et al. RUNX1 as a therapeutic target for adult T-cell leukemia/lymphoma. 日本血液学会学術集会抄録(Web). 2021. 83rd
  • 宮田 海香子, 長谷川 ゆり, 三浦 生子, 高尾 麻未, 松本 正, 吉浦 孝一郎, 三浦 清徳. IRUDにより腎尿細管形成不全症と確定した家族との関わり. 日本遺伝カウンセリング学会誌. 2019. 40. 2. 137-137
  • 高尾 真未, 長谷川 ゆり, 三浦 生子, 宮田 海香子, 松本 正, 吉浦 孝一郎, 三浦 清徳. IRUDにおける遺伝カウンセリングの検討. 日本遺伝カウンセリング学会誌. 2019. 40. 2. 159-159
  • 森田 修平, 竹島 健, 古川 安志, 浦木 進丞, 稲葉 秀文, 有安 宏之, 岩倉 浩, 古田 浩人, 西 理宏, 三嶋 博之, et al. 褐色細胞腫を合併したWaardenburg症候群の1例. 日本内分泌学会雑誌. 2019. 95. Suppl.Update. 149-150
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Books (5):
  • 遺伝医学への招待
    南江堂 2020 ISBN:9784524249312
  • Linkage Analysis
    2019
  • 全ゲノム関連解析研究(GWAS)の原理と考え方.
    メディカルドゥ 2019
  • Genetics and Genomics in Medicine
    2016
  • Color Atlas of Genetics
    2009
Lectures and oral presentations  (292):
  • Broad clinical spectrum and various diagnostic opportunities in patients with Coffin-Siris syndrome.
    (2023)
  • Investigating batch effects in whole genome sequencing: A study of paired samples from two sequencing project.
    (2023)
  • A first Japanese case with Bryant-Li-Bhoj neurodevelopmental syndrome associated with a novel variant in the H3-3A gene
    (2023)
  • Establishment of a mouse model of Sotos syndrome and its phenotypic analysis
    (2023)
  • Autoimmune disease in Kabuki syndrome
    (2023)
more...
Education (1):
  • 1990 - 1994 Nagasaki University
Professional career (3):
  • (BLANK) (Nagasaki University)
  • (BLANK) (Nagasaki University)
  • (BLANK)
Work history (11):
  • 2013/04 - 現在 Nagasaki University
  • 2008/04 - 2013/03 Nagasaki University Graduate School of Biomedical Sciences, Atomic Bomb Disease Institute
  • 2007/04 - 2008/03 Nagasaki University Graduate School of Biomedical Sciences
  • 2003/10 - 2007/03 Nagasaki University
  • 1998/04 - 2003/10 Nagasaki University School of Medicine
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Committee career (3):
  • 2014/01 - 現在 日本人類遺伝学会 Journal of Human Human Genetics 編集委員
  • 2003/08 - 現在 日本人類遺伝学会 評議員
  • 2005 - Japanese Society of Human Genetics councilor
Awards (2):
  • 2001 - 日本人類遺伝学会奨励賞
  • 2001 - Japan Society of Human Genetics, Encouraging prize
Association Membership(s) (3):
THE MOLECULAR BIOLOGY SOCIETY OF JAPAN ,  THE JAPAN SOCIETY OF HUMAN GENETICS ,  Japanese Society of Molecular Biology
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