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Makiko Takagi

Researcher at University of Tokyo

Publications -  14
Citations -  249

Makiko Takagi is an academic researcher from University of Tokyo. The author has contributed to research in topics: Hepatitis C virus & Ribavirin. The author has an hindex of 8, co-authored 12 publications receiving 235 citations.

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Characterization of a broadly reactive monoclonal antibody against norovirus genogroups I and II: recognition of a novel conformational epitope.

TL;DR: This study is the first group to identify the GI and GII cross-reactive monoclonal antibody, which recognizes the novel conformational epitope and could be used further to develop immunochromatography.
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Development of a rapid immunochromatographic test for noroviruses genogroups I and II.

TL;DR: The result of the detection limit of viral load as small as approximately 10(6-7)copies/g of stool, the current immunochromatography test is justified for screening for NoV infection with simple laboratory support.
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Incidence of hepatocellular carcinoma in patients with chronic hepatitis B virus infection who have normal alanine aminotransferase values.

TL;DR: High HBV‐DNA levels and low platelet counts are associated with the development of HCC in patients infected with hepatitis B who have normal ALT values, and maintenance of low HBV-DNA levels is important for the prevention of H CC in patients with low platelets, particularly in patients whose ALTvalues fall within the current normal range.
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Fluctuation of endogenous cytokinin contents in rice during its life cycle ― quantification of cytokinins by selected ion monitoring using deuterium-labelled internal standards

TL;DR: In this article, the change in the levels of endogenous cytokinins in the shoot and grain of rice (Oryza sativa L. japonica cultivar Nihonbare) during its growth and development was followed by selected ion monitoring using deuterium-labeled internal standards.
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Quantitative changes of free-base, riboside, ribotide and glucoside cytokinins in developing rice grains

TL;DR: In this article, deuterium-labeled internal standards were used to identify endogenous free-base, riboside, ribotide and glucoside cytokinins on the basis of GC/MS and GC/SIM.