Rchr
J-GLOBAL ID:200901031126879629
Update date: Nov. 05, 2024
Ohara Osamu
オハラ オサム | Ohara Osamu
Affiliation and department:
Job title:
Department Head
Other affiliations (1):
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Chiba University
Group director
Homepage URL (1):
http://www.kazusa.or.jp
Research field (1):
Molecular biochemistry
Research keywords (4):
Technology development of multiomics analysis
, Clinical proteomics
, ゲノミクス
, 1細胞生物学
Research theme for competitive and other funds (35):
- 2022 - 2025 Long-read sequencing analysis for difficult to diagnose cases of primary immunodeficiency
- 2022 - 2025 Characterization of molecular pathogenesis of primary immunodeficiency focusing on host susceptibility to viruses
- 2022 - 2025 遺伝性血栓症の病因(オミックス解析)と病態の解明
- 2019 - 2022 Characterization of etiology of primary immunodeficiency by focusing on host susceptibility to specific pathogens
- 2019 - 2022 Pathophysiological Study on Aortopathy towards Prevention
- 2018 - 2021 Multi-OMICS approaches to investigate molecular pathogenesis of primary immune deficiency
- 2017 - 2019 Roles of TET family in dynamic epigenomic alteration induced by EB virus infection
- 2016 - 2019 Investigation of molecular mechanism and therapeutic target of Chronic Mucocutaneous Candidiasis
- 2016 - 2019 Elucidating the mechanism of NLRP3 inflammasome activation using fluorescence and light emission protein-interaction sensors
- 2015 - 2018 Exploration of the causative genes and elucidation of the pathophysiology on immune dysregulatory diseases with intractable inflammation
- 2015 - 2018 Development of personalized lung cancer vaccine targeting neoantigens
- 2015 - 2018 Function of APOBEC3 in EBV-positive T or NK-cell lymphoproliferative diseases
- 2014 - 2017 Establishing a platform for molecular analysis and drug innovation of auto-inflammatory disorders
- 2014 - 2017 Elucidation of molecular mechanism of cytopenia associated with immunodeficiency/immune disorder
- 2014 - 2017 Establishment of novel diagnosis and analysis of pathogenesis of herediatry lymphoproliferative disorders
- 2014 - 2017 Establishing an innovative platform for the analysis of hemophagocytic lymphohistiocytosis
- 2014 - 2016 Investigation of pathology and development of specific medial care system and treatment associated with FLNA deficiency
- 2013 - 2016 Elucidation of cold-induced gene induction mechanism by analyzing Mendelian-inherited diseases with cold-induced inflammation
- 2013 - 2015 The study to clarify the molecular mechanism of fate decision of activated CD4 T cells
- 2013 - 2015 Establishment of mouse model of chronic mucocutaneous candidiasis disease and use them to find therapeutic target
- 2012 - 2015 Exploration of the responsible gene and the pathophysiology for unidentified fever syndromes by whole genome analysis and cell-based engineering
- 2011 - 2014 Analysis and development of medical treatment for autoinflammatory diseases
- 2011 - 2014 Research on molecular mechanisms of break in immunological tolerance in disorders caused by single-gene defect
- 2011 - 2014 Molecular mechanism on granuloma formation based on the analysis with cellular and molecular biology
- 2011 - 2012 A study to establish system to evaluate diversities of cell populations of melanoma
- 2010 - 2012 Research for developing of a screening method for the congenital immunodeficiency by KREC/TREC to apply the method to the pathologic analysis
- 2009 - 2011 Development of CINCA syndrome therapy based upon the pathophysiology of CINCA syndrome elucidated by cytoengineering.
- 2009 - 2011 Comprehensive analysis of splicing variants characteristic of acute myelogenous leukemia stem cells
- 2009 - 2010 遺伝子制御ネットワークの動的挙動の解明:制御論的理論解析と実験による検証
- 2009 - 2010 Development of easy and cost-effective mass-screening of severe combined immunodeficiency using neonatal guthrie cards.
- 2004 - 2006 Memory B cell commitment, maintenance and terminal differentiation
- 2001 - 2002 ヒト脳内長鎖cDNA解析データベースを基盤としたマウス扁桃体の情動神経機構の解明
- 1992 - 1994 Studies on neurofilament-deficient quails-an animal model for neuropathology
- 1994 - 免疫ゲノミクス
- Immunogenomics
Show all
Papers (676):
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Hirofumi Shibata, Daisuke Nakajima, Ryo Konno, Atsushi Hijikata, Motoko Higashiguchi, Hiroshi Nihira, Saeko Shimodera, Takayuki Miyamoto, Masahiko Nishitani-Isa, Eitaro Hiejima, et al. A Non-targeted Proteomics Newborn Screening Platform for Inborn Errors of Immunity. Journal of clinical immunology. 2024. 45. 1. 33-33
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Takashi Watanabe, Hikaru Hata, Yoshiki Mochizuki, Fumie Yokoyama, Tomoko Hasegawa, Naveen Kumar, Tomohiro Kurosaki, Osamu Ohara, Hidehiro Fukuyama. Development of a new genotype-phenotype linked antibody screening system. 2024
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Yohei Kirino, Ayaka Maeda, Tomoyuki Asano, Kiyoshi Migita, Yukiko Hidaka, Hiroaki Ida, Daisuke Kobayashi, Nobuhiro Oda, Ryo Rokutanda, Yuichiro Fujieda, et al. Low remission rates and high incidence of adverse events in a prospective VEXAS syndrome registry. Rheumatology (Oxford, England). 2024
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Atsushi Sakamoto, Toru Uchiyama, Ryohei Futatsugi, Osamu Ohara, Akihiro Iguchi, Tadashi Kaname, Makoto Hikosaka, Hiroshi Ono, Shinji Kunishima, Shuichi Ito, et al. Platelet changes and bleeding symptoms in children, adolescents, and adults with 22q11.2 deletion syndrome. Pediatric blood & cancer. 2024. e31292
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Yoshihiko Shitara, Ryo Konno, Masahito Yoshihara, Kohei Kashima, Atsushi Ito, Takeo Mukai, Goh Kimoto, Satsuki Kakiuchi, Masaki Ishikawa, Tomo Kakihara, et al. Host-derived protein profiles of human neonatal meconium across gestational ages. Nature communications. 2024. 15. 1. 5543-5543
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MISC (363):
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石川将己, 中島大輔, 紺野亮, 菅野敏生, 遠藤裕介, 小原收, 川島裕介. Glycosphingolipid-Binding Proteome Analysis by Affinity Purification-Mass Spectrometry. 日本プロテオーム学会大会プログラム・抄録集. 2024. 2024 (Web)
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紺野亮, 石川将己, 中島大輔, 遠藤裕介, 小原收, 川島祐介. Development of low-input sample preparation method using lauryl maltose neopentyl glycol. 日本プロテオーム学会大会プログラム・抄録集. 2024. 2024 (Web)
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中島大輔, 紺野亮, 石川将己, 宮下靖臣, 宮下靖臣, 小原收, 川島祐介. Development of an ultra-deep serum/plasma proteome analysis system using lectins. 日本プロテオーム学会大会プログラム・抄録集. 2024. 2024 (Web)
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佐藤 裕範, 伊藤 ありさ, 早田 衣里, 山本 健, 中野 泰至, 山出 史也, 井上 祐三朗, 冨板 美奈子, 川島 祐介, 小原 收, et al. 統合プロテオミクスを用いた小児期シェーグレン症候群の疾患モニタリングとバイオマーカー探索. 日本小児リウマチ学会総会・学術集会プログラム・抄録集. 2023. 32回. 118-118
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佐倉 文祥, 野々山 恵章, 今井 耕輔, 大西 秀典, 八角 高裕, 金兼 弘和, 小原 收, 岡田 賢. プロテオゲノミクス解析を用いた先天性免疫異常症の遺伝子診断. 日本臨床免疫学会総会プログラム・抄録集. 2023. 51回. 81-81
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Patents (145):
Books (3):
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外来で見つける先天代謝異常症
中山書店 2023 ISBN:9784521749242
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ヒトマイクロバイオーム
NTS(エヌ・ティー・エス) 2020 ISBN:9784860436599
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バイオ高性能機器・新技術利用マニュアル
共立出版 2004 ISBN:4320056264
Lectures and oral presentations (47):
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Establishment of a diagnosis system for somatic mosaicism in autoinflammation: From research to genetic testing
(2024)
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PCRアンプリコンによるロングリードシーケンシング:様変わりしつつあるロングPCR
(東洋紡xオックスフォード・ナノポアテクノロジーズ共催ウェビナー 2024)
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次世代シーケンシング(NGS)と難病の遺伝学的検査
(イルミナユーザーグループミーティング 2024)
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プロテオゲノミクス研究の現状と将来展望
(第73回日本電気泳動学会シンポジウム 2023)
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何のための「オミックス解析」?:その必要性と今後の展望
(第46回日本分子生物学会年会ランチオンセミナー 2023)
more...
Professional career (1):
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