Wu Xiaoshan | 名古屋市立大学 生体高分子
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概要
関連著者
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OKADA Noriko
Department of Applied Physics, Nagoya University
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Wu Xiaoshan
Department Of Molecular Biology Nagoya City University School Of Medicine
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Wu Xiaoshan
名古屋市立大学 生体高分子
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OKADA HIDECHIKA
Department of Molecular Biology, Nagoya City University School of Medicine
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Okada N
Dep. Of Biodefence Medicine Nagoya City Univ. Graduate School Of Medicine
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Okada N
Department Of Biodefense Nagoya City University Graduate School Of Medical Sciences
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Okada Hidechika
Department Of Biodefence Nagoya City University Graduate School Of Medical Science
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Okada N
Nagoya City Univ. School Of Medicine Nagoya Jpn
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Okada H
Choju Medical Institute Fukushimura Hospital
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Okada H
Department Of Biodefense Medicine Nagoya City University Graduate School Of Medical Sciences
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Okada Noriko
Department Of Applied Physics Nagoya University
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Wu Xiaoshan
Department of Biodefense, Nagoya City University Graduate School of Medical Sciences
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Okada N
Choju Medical Institute Fukushimura Hospital
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Okada H
Department Of Biodefense Nagoya City University Graduate School Of Medical Sciences
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Okada Hidechika
Department Of Biodefense Medicine Nagoya City University Graduate School Of Medical Sciences
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Ogawa Norihiro
Choju Medical Inst. Fukushimura Hospital
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Okada Noriko
Department Of Molecular Biology Nagoya City University School Of Medicine
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Okada Hidechika
Choju Medical Inst. Fukushimura Hospital
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MIZOKAMI Masashi
Department of Clinical Molecular Informative Medicine, Nagoya City University Graduate School of Med
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Asai Suzuka
Department of Immunology, Nagoya City University Graduate School of Medical Sciences
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Kimbara Noriaki
Department of Immunology, Nagoya City University Graduate School of Medical Sciences
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IWAMOTO Aikichi
Department of Infectious Diseases, Institute of Medical Science, The University of Tokyo
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YIN Shuping
Department of Biodefense, Nagoya City University Graduate School of Medical Sciences
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DOHI Natsuki
Department of Biodefense, Nagoya City University Graduate School of Medical Sciences
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HOSOKAWA Masato
Department of Biodefense, Nagoya City University Graduate School of Medical Sciences
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GOTO Mieko
Department of Infectious Diseases, The Institute of Medical Science, The Univesity of Tokyo
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IRIE Reiko
Department of Biotechnology Sciences, john Wayne Cancer Institute
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IWAMORI Masao
Department of Biochemistry,Faculty of Medicine,University of Tokyo
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Goto Mieko
Department Of Infectious Diseases The Institute Of Medical Science The Univesity Of Tokyo
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Irie Reiko
Department Of Biotechnology Sciences John Wayne Cancer Institute
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Hosokawa Masato
Department Of Biodefense Nagoya City University Graduate School Of Medical Sciences
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Iwamoto Aikichi
Department Of Lnfectious Diseases Institute Of Medical Science University Of Tokyo
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Iwamoto Aikichi
Department Of Infectious Diseases And Applied Immunology Institute Of Medical Science University Of
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Iwamoto Aikichi
Department Of Infectious Diseases The Institute Of Medical Science The Univesity Of Tokyo
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Yin Shuping
Department Of Biodefense Nagoya City University Graduate School Of Medical Sciences
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Dohi Natsuki
Department Of Molecular Biology' Nagoya City University School Of Medicine
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Iwamori Masao
Department Of Biochemistry Faculty Of Medicine University Of Tokyo
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Mizokami Masashi
Department Of 2nd Internal Medicine Nagoya City University School Of Medicine
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Iwamoto Aikichi
Department Of Infectious Disease And Applied Immunology University Of Tokyo
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Asai Suzuka
Department of Biodefense Medicine, Nagoya City University Graduate School of Medical Sciences
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Dohi Natsuki
Department of Biodefense Medicine, Nagoya City University Graduate School of Medical Sciences
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Kimbara Noriaki
Department of Biodefense Medicine, Nagoya City University Graduate School of Medical Sciences
著作論文
- Human IgM Monoclonal Antibodies Reactive with HIV-1-Infected Cells Generated Using a Trans-Chromosome Mouse
- The IgM Antibody Level against Ganglioside GM2 Correlates to the Disease Status of HIV-1-Infected Patients
- Human IgM Monoclonal Antibody to Ganglioside GM2 and Complement Suppress Virus Propagation in Ex Vivo Cultures of Lymphocytes from HIV-1 Infected Patients
- Complement-mediated cytolysis and azidothymidine are synergistic in HIV-1 suppression
- Presence of IgM Antibodies Which Sensitize HIV-1-Infected Cells to Cytolysis by Homologous Complement in Long-Term Survivors of HIV Infection
- IgM natural antibody against an asiolo-oligosaccharide, gangliotetraose(Gg4),sensitizes HIV-I infgected cells for cytolysis by homologous complement