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Yoshikazu Sugimoto

Researcher at Keio University

Publications -  314
Citations -  12957

Yoshikazu Sugimoto is an academic researcher from Keio University. The author has contributed to research in topics: Gene & Multiple drug resistance. The author has an hindex of 58, co-authored 304 publications receiving 12105 citations. Previous affiliations of Yoshikazu Sugimoto include Hokkaido University & Japanese Foundation for Cancer Research.

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The Genome Sequence of Taurine Cattle: A Window to Ruminant Biology and Evolution

Christine G. Elsik, +328 more
- 24 Apr 2009 - 
TL;DR: To understand the biology and evolution of ruminants, the cattle genome was sequenced to about sevenfold coverage and provides a resource for understanding mammalian evolution and accelerating livestock genetic improvement for milk and meat production.
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Calcium oxide as a solid base catalyst for transesterification of soybean oil and its application to biodiesel production

TL;DR: In this paper, solid base catalyst for biodiesel production with environmental benignity, transesterification of edible soybean oil with refluxing methanol was carried out in the presence of calcium oxide (CaO), -hydroxide (Ca(OH)2), or -carbonate (CaCO3).
Journal Article

C421A polymorphism in the human breast cancer resistance protein gene is associated with low expression of Q141K protein and low-level drug resistance.

TL;DR: People with C376T and/or C421A polymorphisms may express low amounts of BCRP, and this low BCRp expression might result in hypersensitivity of normal cells to such anticancer drugs as irinotecan and mitoxantrone.
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Evidence that the Rous sarcoma virus transforming gene product phosphorylates phosphatidylinositol and diacylglycerol

TL;DR: When serum-starved chicken embryo fibroblasts transformed by a virus mutant temperature-sensitive for transformation were shifted from the nonpermissive to permissive temperature, an increase of 50-100% in the labeling of phosphatidylinositol 4-phosphate, phosphatide 4,5-bisph phosphate, and phosph atidic acid was observed, as compared to uninfected cells.
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ABCG2 Transports Sulfated Conjugates of Steroids and Xenobiotics

TL;DR: It was suggested that ABCG2 preferentially transports sulfate conjugates and that E1S and DHEAS are the potential physiological substrates for this transporter.