M. Fujiwara

发表

Discovery of anti-influenza A virus activity of a corynanthe-type indole alkaloid, hirsutine, in vitro and the structure-activity relationship of natural and synthetic analogs

H. Inoue, H. Takayama, T. Yokota, 1997 .

Different Properties of Wild Type and Drug‐Resistant Mutants of Human Immunodeficiency Virus Type 1 Reverse Transcriptase In Vitro

M. Baba, T. Yokota, K. Konno, 1996, Microbiology and immunology.

Antisense therapy of influenza.

T. Abe, N. Miyano-Kurosaki, H. Takaku, 2001, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Inhibitory effects of an antisense oligonucleotide in an experimentally infected mouse model of influenza A virus.

T. Abe, N. Miyano-Kurosaki, H. Takaku, 2000, Biochemical and biophysical research communications.

Anti-HIV-1 activity of thiadiazole derivatives: structure-activity relationship, reverse transcriptase inhibition, and lipophilicity.

M. Matsushima, M. Baba, H. Takayama, 1996, Antiviral research.

Potent and specific inhibition of human immunodeficiency virus type 1 replication by 4-(2,6-dichlorophenyl)-1,2,5-thiadiazol-3-Y1 N,N-dialkylcarbamate derivatives

H. Takayama, K. Konno, M. Fujiwara, 1995, Antimicrobial agents and chemotherapy.

Ingenol Derivatives are Highly Potent and Selective Inhibitors of HIV Replication in Vitro

M. Baba, T. Yokota, K. Konno, 1996 .

Antiviral activities of nucleotide heterodimers against human immunodeficiency virus type 1 in vitro.

M. Baba, T. Yokota, K. Konno, 1996, Antiviral research.

Mechanism of selective inhibition of human immunodeficiency virus by ingenol triacetate

M. Baba, T. Yokota, K. Konno, 1996, Antimicrobial agents and chemotherapy.

Antisense oligonucleotides directed against the viral RNA polymerase gene enhance survival of mice infected with influenza A

T. Abe, N. Miyano-Kurosaki, H. Takaku, 1999, Nature Biotechnology.

Novel hepatitis C virus protease inhibitors: thiazolidine derivatives.

K. Shimotohno, M. Matsushima, K. Sudo, 1997, Biochemical and biophysical research communications.

RD6-2198, a novel betain-type fluoroalkylated oligomer, inhibits the replications of human immunodeficiency virus type 1 and other enveloped viruses.

M. Baba, H. Sawada, M. Okamoto, 1998, Antiviral research.

Studies of non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 2: synthesis and structure-activity relationships of 2-cyano and 2-hydroxy thiazolidenebenzenesulfonamide derivatives.

M. Matsuoka, M. Baba, H. Inoue, 2005, Bioorganic & medicinal chemistry.

Studies of nonnucleoside HIV-1 reverse transcriptase inhibitors. Part 1: Design and synthesis of thiazolidenebenzenesulfonamides.

M. Matsuoka, M. Baba, H. Inoue, 2004, Bioorganic & medicinal chemistry.

Inhibitory effect of hirsutine on influenza virus replication in vitro

H. Takayama, T. Yokota, K. Konno, 1997 .

Thiadiazole Derivatives: Highly Potent and Selective Inhibitors of Human Immunodeficiency Virus Type 1 (HIV‐1) Replications In Vitro

M. Baba, H. Takayama, T. Yokota, 1997, Microbiology and immunology.

Acridone derivatives are selective inhibitors of HIV-1 replication in chronically infected cells.

M. Baba, M. Okamoto, T. Yokota, 1999, Antiviral research.

Human Follicular Dendritic Cells Remain Uninfected and Capture Human Immunodeficiency Virus Type 1 through CD54-CD11a Interaction

M. Baba, T. Yokota, M. Fujiwara, 1999, Journal of Virology.

Thiadiazole derivatives: highly potent and specific HIV-1 reverse transcriptase inhibitors.

H. Takayama, K. Konno, S Sakai, 1995, Journal of medicinal chemistry.

Inhibition of Human Immunodeficiency Virus Replication by RD6-Y664, a Novel Benzylhydroxylamine Derivative

H. Mitsuya, M. Baba, E. Kodama, 1999, Antiviral chemistry & chemotherapy.

Upregulation of HIV-1 replication in chronically infected cells by ingenol derivatives

M. Baba, M. Okamoto, T. Yokota, 1998, Archives of Virology.

Thiadiazole derivatives as highly potent inhibitor of human immunodeficiency virus type 1 (HIV-1)

M. Baba, H. Takayama, T. Yokota, 1995 .

Characterization of Human Immunodeficiency Virus Type 1 Strains Resistant to the Non-Nucleoside Reverse Transcriptase Inhibitor RD4–2217

H. Mitsuya, M. Baba, E. Kodama, 1999, Antiviral chemistry & chemotherapy.

Utilization of wieland furoxan synthesis for preparation of 4-aryl-1,2,5-oxadiazole-3-yl carbamate derivatives having potent anti-HIV activity

M. Baba, H. Takayama, T. Yokota, 1996 .

Utilization of Wieland Furoxan Synthesis for Preparation of 4-Aryl-1,2, 5-oxadiazole-3-yl Carbamate Derivatives Having Potent Anti-HIV Activity.

M. Baba, H. Takayama, T. Yokota, 1996 .