Rchr
J-GLOBAL ID：200901076805895246
Update date: Aug. 31, 2024
Sakate Ryuichi
サカテ リュウイチ | Sakate Ryuichi
Affiliation and department：
Job title：
Deputy Director
Other affiliations (2)：
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National Institutes of Biomedical Innovation, Health and Nutrition
Laboratory of Rare Disease Information and Resource Library, Center for Intractable Diseases and ImmunoGenomics (CiDIG)
Project Leader
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National Institutes of Biomedical Innovation, Health and Nutrition
Platform of Therapeutics for Rare Disease, Center for Intractable Diseases and ImmunoGenomics (CiDIG)
Project Leader
Research field (1)：
Systems genomics
Research theme for competitive and other funds (2)：
- 2020 - 2023 Construction of Database of Drug Development for Intractable/Rare Diseases
- 2009 - 2011 Relations between characteristic features of biological dynamic pathway models and gene polymorphisms or gene functions
Papers (36)：
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Mao Tanabe, Makoto Hirata, Ryuichi Sakate. Trends in drug development for rare and intractable diseases based on the KEGG NETWORK. NAR Molecular Medicine. 2024
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Mao Tanabe, Ryuichi Sakate, Jun Nakabayashi, Kyosuke Tsumura, Shino Ohira, Kaoru Iwato, Tomonori Kimura. A novel in silico scaffold-hopping method for drug repositioning in rare and intractable diseases. Scientific Reports. 2023. 13. 1
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Naoki Nakagawa, Tomonori Kimura, Ryuichi Sakate, Takehiko Wada, Kengo Furuichi, Hirokazu Okada, Yoshitaka Isaka, Ichiei Narita. Demographics and treatment of patients with primary nephrotic syndrome in Japan using a national registry of clinical personal records. Scientific reports. 2023. 13. 1. 14771-14771
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Naoki Nakagawa, Tomonori Kimura, Ryuichi Sakate, Yoshitaka Isaka, Ichiei Narita. Demographics and treatment of patients with primary membranoproliferative glomerulonephritis in Japan using a national registry of clinical personal records. Clinical and experimental nephrology. 2023
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Yusuke Tsukamoto, Yumi Nakamura, Makoto Hirata, Daisuke Okuzaki, Ryuichi Sakate, Tomonori Kimura. GCN2 kinase-mediated upregulation of ubiquitin C maintains intracellular glutamine level and tRNAGln (CUG) charging under amino acid starvation. FEBS letters. 2023. 597. 12. 1638-1650
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MISC (33)：
Lectures and oral presentations (15)：
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難病創薬に向けた情報解析 〜難治性疾患研究開発・支援センターの取り組み〜
(第15回 霊長類医科学フォーラム 2019)
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難病・希少疾患の疾患オントロジー
(トーゴーの日シンポジウム2019 2019)
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DDrare -難病創薬と標的遺伝子・パスウェイのデータベース-
(トーゴーの日シンポジウム2019 2019)
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難病・希少疾患の創薬情報の解析
(大阪大学薬学研究科PRP/PharmaTrain教育コース 2018)
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DDrare: Database of Drug Development for Rare Diseases and Its Data Analysis - Multiple Drugs Tested in a Clinical Trial -
(The 41st Annual Meeting of the Molecular Biology Society of Japan 2018)
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Professional career (1)：
Association Membership(s) (2)：
THE MOLECULAR BIOLOGY SOCIETY OF JAPAN
, SOCIETY OF EVOLUTIONARY STUDIES
