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Tetsutaro Sata

Researcher at National Institutes of Health

Publications -  328
Citations -  13513

Tetsutaro Sata is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Virus & Antigen. The author has an hindex of 60, co-authored 328 publications receiving 12582 citations. Previous affiliations of Tetsutaro Sata include Tokyo Medical and Dental University & Nagoya University.

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Modulation of TNF-α-converting enzyme by the spike protein of SARS-CoV and ACE2 induces TNF-α production and facilitates viral entry

TL;DR: It is found that the spike protein of SARS-CoV (SARS-S) induced TNF-α-converting enzyme (TACE)-dependent shedding of the ACE2 ectodomain, and this data suggest that cellular signals triggered by the interaction of Sars- coV with ACE2 are positively involved in viral entry but lead to tissue damage.
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Human APOBEC3F Is Another Host Factor That Blocks Human Immunodeficiency Virus Type 1 Replication

TL;DR: The human APOBEC3F protein is identified as another host factor that blocks human immunodeficiency virus type 1 (HIV-1) replication and induced G to A hypermutations in HIV genomic DNA, and the viral Vif protein counteracted its activity.
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Construction of an Excisable Bacterial Artificial Chromosome Containing a Full-Length Infectious Clone of Herpes Simplex Virus Type 1: Viruses Reconstituted from the Clone Exhibit Wild-Type Properties In Vitro and In Vivo

TL;DR: The infectious molecular clone pYEbac102 is in fact useful for mutagenesis of the HSV-1 genome by bacterial genetics, and a recombinant virus carrying amino acid substitutions in both copies of the α0 gene was generated.
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Naturally Acquired Plasmodium knowlesi Malaria in Human, Thailand

TL;DR: A case of naturally acquired infection with Plasmodium knowlesi in Thailand is described and diagnosis was confirmed by the small subunit ribosomal RNA and the mitochondrial cytochrome b sequences.
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Thymus-derived leukemia-lymphoma in mice transgenic for the Tax gene of human T-lymphotropic virus type I

TL;DR: The generation of HTLV-I Tax transgenic mice is described using the Lck proximal promoter to restrict transgene expression to developing thymocytes and this model accurately reproduces human disease and will provide a tool for analysis of the molecular events in transformation and for the development of new therapeutics.