Akagi Masao | Osaka University Of Pharmaceutical Sciences
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概要
関連著者
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Akagi Masao
Osaka University Of Pharmaceutical Sciences
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Urata Hidehito
Osaka University of Pharmaceutical Sciences
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Urata Hidehito
Osaka College Of Pharmacy
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Akagi M
Osaka University Of Pharmaceutical Sciences
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Otake Toru
Prefectural Institute Of Public Health
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Hara Hisafumi
Osaka University of Pharmaceutical Sciences
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Hirata Yoshihiro
Osaka University of Pharmaceutical Sciences
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AONO Chie
Osaka University of Pharmaceutical Sciences
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OHMOTO Norihiko
Osaka University of Pharmaceutical Sciences
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SHIMAMOTO Yuko
Osaka University of Pharmaceutical Sciences
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KOBAYASHI Yoshiko
Osaka University of Pharmaceutical Sciences
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MIYAGOSHI Hidetaka
Osaka University of Pharmaceutical Sciences
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KAKUYA Hitoshi
Osaka University of Pharmaceutical Sciences
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TOKUMOTO Hideki
Osaka University of Pharmaceutical Sciences
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KAWAHATA Takuya
Prefectural Institute of Public Health
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OMAE Daichi
Osaka University of Pharmaceutical Sciences
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TAMURA Yoshinori
Osaka University of Pharmaceutical Sciences
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UEDA Tetsujiro
Osaka University of Pharmaceutical Sciences
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KUMASHIRO Tetsuya
Osaka University of Pharmaceutical Sciences
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Urata H
Osaka University Of Pharmaceutical Sciences
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MORI Itsuo
Osaka College of Pharmacy
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Tamura Y
Osaka University Of Pharmaceutical Sciences
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Kato Keiji
Osaka University of Pharmaceutical Sciences
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Toyoda Minako
Osaka University of Pharmaceutical Sciences
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Fujita Yoshikazu
Osaka College of Pharmaceutical Sciences
著作論文
- EFFECTS OF CHIRAL MODIFICATION ON THE HELICAL STRUCTURE OF ADENYLYL(3'-5')ADENYLYL(3'-5')ADENOSINE(Chiral Homogeneity and D-Amino Acids, International Symposium on Origins of Life and Astrobiology)
- Efficient and Homochiral Selective Oligomerization of Racemic Ribonucleotides on Mineral Surface
- Design and Racemic Synthesis of Conformationally Restricted Carbocyclic Pyrimidine Nucleoside Analogs Based on the Structure of the L-Nucleoside Residue in Heterochiral DNA
- A Practical Synthesis of L-Ribose
- The application of diarylamine compounds in analytical chemistry. 1. Fluorescence reactions among 4-(4-methyl-2-quinolyl)aminosalicylic acid, cobalt(II) and hydrogen peroxide, and the fluorimetry of cobalt(II) by using its fluorescence reaction.