Institution
Tokyo University of Science
Education•Tokyo, Japan•
About: Tokyo University of Science is a education organization based out in Tokyo, Japan. It is known for research contribution in the topics: Thin film & Enantioselective synthesis. The organization has 15800 authors who have published 24147 publications receiving 438081 citations. The organization is also known as: Tōkyō Rika Daigaku & Science University of Tokyo.
Papers published on a yearly basis
Papers
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TL;DR: In this article, the effects of ultrasonic nanocrystalline surface modification (UNSM) technique on the tribological behavior of sintered Cu-based alloy prepared using a powder metallurgy (P/M) technique were investigated using a ball-on-disk reciprocating tribometer against a bearing steel ball under dry and oil-lubricated conditions.
101 citations
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TL;DR: Twenty isolates of Fusarium species were examined for their ability to produce trichothecene mycotoxins in shake culture and jar fermentation and none of the isolates produced significant amount of fusarenon-X in shake cultures.
Abstract: Twelve T-2 toxin-producing isolates and four fusarenon-X-producing isolates of Fusarium species were examined for their ability to produce trichothecene mycotoxins in shake culture and jar fermentation. T-2 toxin producers such as Fusarium solani, F. sporotrichioides, and F. tricinctum produced T-2 toxin and neosolaniol in semisynthetic medium. F. solani M-1-1 produced the largest amount of the mycotoxins in a nutrient medium consisting of 5% glucose (or sucrose), 0.1% peptone, and 0.1% yeast extract in either shake culture or jar fermentation at 24 to 27 C for 5 days. None of the isolates produced significant amounts of fusarenon-X in shake cultures.
101 citations
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TL;DR: Glutathione-protected Au25 clusters were used to load monodisperse gold nanoclusters onto BaLa4Ti4O15 to create photocatalysts for water splitting, and the photocatalyst activity was determined to be 2.6 times higher than that of catalysts loaded with larger gold nanoparticles via conventional photodeposition.
Abstract: Glutathione-protected Au25 clusters were used to load monodisperse gold nanoclusters (1.2 ± 0.3 nm) onto BaLa4Ti4O15 to create photocatalysts. The photocatalytic activity of the resulting material for water splitting was determined to be 2.6 times higher than that of catalysts loaded with larger gold nanoparticles (10-30 nm) via conventional photodeposition.
101 citations
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TL;DR: Aligned C60NWs could be transferred onto many different flat substrates, and, in this case, aligned C60 NWs on glass substrates were employed as a scaffold for cell culture, indicating their potential for use in biomedical applications.
Abstract: A versatile method for the rapid fabrication of aligned fullerene C60 nanowhiskers (C60NWs) at the air–water interface is presented. This method is based on the vortex motion of a subphase (water), which directs floating C60NWs to align on the water surface according to the direction of rotational flow. Aligned C60NWs could be transferred onto many different flat substrates, and, in this case, aligned C60NWs on glass substrates were employed as a scaffold for cell culture. Bone forming human osteoblast MG63 cells adhered well to the C60NWs, and their growth was found to be oriented with the axis of the aligned C60NWs. Cells grown on aligned C60NWs were more highly oriented with the axis of alignment than when grown on randomly oriented nanowhiskers. A study of cell proliferation on the C60NWs revealed their low toxicity, indicating their potential for use in biomedical applications.
101 citations
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TL;DR: Green tea polyphenol, (-)-epigallocatechin-3-gallate (EGCG) has potential as a novel therapeutic agent for myeloid leukemia via induction of apoptosis mediated by modification of the redox system.
Abstract: BACKGROUND AND OBJECTIVES: The aim of this study was to investigate the possibility of green tea polyphenol, (-)-epigallocatechin-3-gallate (EGCG) as a novel therapeutic agent for the patients with myeloid leukemia. DESIGN AND METHODS: We investigated the effects of EGCG on the induction of apoptosis in leukemic cells in vitro and in vivo. We further examined the molecular mechanisms of EGCG-induced apoptosis in myeloid leukemic cells. RESULTS: EGCG rapidly induced apoptotic cell death in retinoic acid (RA)-resistant acute promyelocytic leukemia (APL), UF-1 cells within 3 h. EGCG induced apoptosis in UF-1 cells was in association with the loss of mitochondrial transmembrane potentials (Deltapsim) and activation of caspase-3 and -9. Elevation of intracellular reactive oxygen species (ROS) production was also demonstrated during EGCG-induced apoptosis of UF-1 as well as fresh myeloid leukemic cells. In NOD/SCID mice transplanted with UF-1 cells, EGCG effectively inhibited tumor growth in vivo, and the number of mitoses among the cells significantly decreased in comparison to that of control mouse cells. INTERPRETATION AND CONCLUSIONS: In summary, EGCG has potential as a novel therapeutic agent for myeloid leukemia via induction of apoptosis mediated by modification of the redox system.
100 citations
Authors
Showing all 15878 results
Name | H-index | Papers | Citations |
---|---|---|---|
Kazunori Kataoka | 138 | 908 | 70412 |
Yoichiro Iwakura | 129 | 705 | 64041 |
Kouji Matsushima | 124 | 590 | 56995 |
Masaki Ishitsuka | 103 | 624 | 39383 |
Shinsuke Tanabe | 98 | 722 | 37445 |
Tatsumi Koi | 97 | 411 | 50222 |
Hirofumi Akagi | 94 | 618 | 43179 |
Clifford A. Lowell | 91 | 258 | 23538 |
Teruo Okano | 91 | 605 | 28346 |
László Á. Gergely | 89 | 426 | 60674 |
T. Sumiyoshi | 88 | 855 | 62277 |
Toshinori Nakayama | 86 | 405 | 25275 |
Akihiko Kudo | 86 | 328 | 39475 |
Hans-Joachim Gabius | 85 | 699 | 28085 |
Motohide Tamura | 85 | 1007 | 32725 |