Ohrui Hiroshi | Yokohama Coll. Of Pharmacy
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概要
関連著者
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Ohrui Hiroshi
Yokohama Coll. Of Pharmacy
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Ohrui Hiroshi
Yokohama College Of Pharmacy
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大類 洋
横浜薬科大学
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大類 洋
東北大学農学部
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大類 洋
東北大・農
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Ohrui H
Department Of Applied Biological Chemistry Faculty Of Agriculture Tohoku University
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大類 洋
東北大学 農
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Ohrui Hiroshi
Department Of Biological Chemistry Faculty Of Agriculture Tohoku University
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Hamaguchi Motohiro
東北大学病院 血液･免疫科
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Mukai Hirofumi
国立がんセンター東病院 化学療法科血液
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Kuwahara Shigefumi
Laboratory Of Agricultural Chemicals Faculty Of Agriculture Ibaraki University
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MATSUOKA Masao
Institute for Virus Research, Kyoto University
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Matsuoka Masao
Institute For Virus Research Kyoto University
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KODAMA Eiichi
Institute for Virus Research, Kyoto University
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Mukai Hirofumi
National Cancer Center Hospital East Oncology/hematology
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Minami Hironobu
Oncology/hematology National Cancer Center Hospital East
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Hirano Masami
Department Of Hematology Fujita Health University School Of Medicine
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Kohgo Satoru
Yamasa Corporation
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Hayakawa Hiroyuki
Yamasa Corporation
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Mitsuya Hiroaki
National Cancer Institure
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Yoshida Mayumi
Laboratory Of Animal Biotechnology Interdisciplinary Graduate School Of Science And Technology Shins
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Kodama Eiichi
Institute For Virus Research Kyoto University
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Mitsuya Hiroaki
Department Of Hematology And Infectious Diseases Kumamoto University Graduate School Of Medical Scie
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Ohrui Hiroshi
Graduate School Of Life Sciences Tohoku Univ.
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Miyagi Takuho
Laboratory Of Applied Bioorganic Chemistry Graduate School Of Agricultural Science Tohoku University
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Nagasawa Tomohiro
Laboratory Of Applied Bioorganic Chemistry Graduate School Of Agricultural Science Tohoku University
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Kageyama Masayuki
Laboratory Of Applied Bioorganic Chemistry Graduate School Of Agricultural Science Tohoku University
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Yoshida Mayumi
Laboratory Of Applied Bioorganic Chemistry Graduate School Of Agricultural Science Tohoku University
著作論文
- P-39 2'-DEXY-4'-C-ETHYNYL-2-FLUOROADENOSINE, A NRTI THAT COULD BE AN IDEAL DRUG FOR BOTH HIV-AND HBV-INFECTIONS
- Development of modified nucleosides that have supremely high anti-HIV activity and low toxicity and prevent the emergence of resistant HIV mutants
- Development of Highly Potent Chiral Discrimination Methods That Solve the Problems of Diastereomer Method
- Development of highly potent chiral discrimination methods that solve the problems of the diastereomer method
- Concise Synthesis of the Anti-HIV Nucleoside EFdA