Institution
Waseda University
Education•Tokyo, Japan•
About: Waseda University is a education organization based out in Tokyo, Japan. It is known for research contribution in the topics: Catalysis & Large Hadron Collider. The organization has 24220 authors who have published 46859 publications receiving 837855 citations. The organization is also known as: Waseda daigaku & Sōdai.
Topics: Catalysis, Large Hadron Collider, Robot, Computer science, Population
Papers published on a yearly basis
Papers
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TL;DR: It is found that mGluR1 agonist-induced currents and [Ca2+]i increases in PCs were enhanced following co-activation of GABAB receptors, and the interaction between the two types of metabotropic receptors provides a likely mechanism for regulating cerebellar synaptic plasticity.
Abstract: Metabotropic gamma-aminobutyric acid type B (GABAB) and glutamate receptors (mGluRs) are postsynaptically co-expressed at cerebellar parallel fiber (PF)-Purkinje cell (PC) excitatory synapses, but their functional interactions are unclear. We found that mGluR1 agonist-induced currents and [Ca2+]i increases in PCs were enhanced following co-activation of GABAB receptors. A GABAB antagonist and a G-protein uncoupler suppressed these effects. Low-concentration baclofen, a GABAB agonist, augmented mGluR1-mediated excitatory synaptic current produced by stimulating PFs. These results indicate that postsynaptic GABAB receptors functionally interact with mGluR1 and enhance mGluR1-mediated excitatory transmission at PF-PC synapses. The interaction between the two types of metabotropic receptors provides a likely mechanism for regulating cerebellar synaptic plasticity.
206 citations
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01 Jun 2005TL;DR: This paper proposes a new technique called spanning tree-based genetic algorithm (hst-GA) that is hybridized with the fuzzy logic controller (FLC) concept for auto-tuning the GA parameters and shows that the proposed method gives better results.
Abstract: In this paper, we deal with a production/distribution problem to determine an efficient integration of production, distribution and inventory system so that products are produced and distributed at the right quantities, to the right customers, and at the right time, in order to minimize system wide costs while satisfying all demand required. This problem can be viewed as an optimization model that integrates facility location decisions, distribution costs, and inventory management for multi-products and multi-time periods. To solve the problem, we propose a new technique called spanning tree-based genetic algorithm (hst-GA). In order to improve its efficiency, the proposed method is hybridized with the fuzzy logic controller (FLC) concept for auto-tuning the GA parameters. The proposed method is compared with traditional spanning tree-based genetic algorithm approach. This comparison shows that the proposed method gives better results.
206 citations
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TL;DR: Following application of ultrasounds to cells treated with BTNPs, fluorescence imaging of ion dynamics revealed that the synergic stimulation is able to elicit a significant cellular response in terms of calcium and sodium fluxes; moreover, tests with appropriate blockers demonstrated that voltage-gated membrane channels are activated.
Abstract: Tetragonal barium titanate nanoparticles (BTNPs) have been exploited as nanotransducers owing to their piezoelectric properties, in order to provide indirect electrical stimulation to SH-SY5Y neuron-like cells. Following application of ultrasounds to cells treated with BTNPs, fluorescence imaging of ion dynamics revealed that the synergic stimulation is able to elicit a significant cellular response in terms of calcium and sodium fluxes; moreover, tests with appropriate blockers demonstrated that voltage-gated membrane channels are activated. The hypothesis of piezoelectric stimulation of neuron-like cells was supported by lack of cellular response in the presence of cubic nonpiezoelectric BTNPs, and further corroborated by a simple electroelastic model of a BTNP subjected to ultrasounds, according to which the generated voltage is compatible with the values required for the activation of voltage-sensitive channels.
206 citations
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TL;DR: The circadian-immune connection is bidirectional, because in addition to this circadian control of immune functions, immune challenges and immune mediators were shown to have strong effects on circadian rhythms at the molecular, cellular, and behavioral levels.
Abstract: Various features, components, and functions of the immune system present daily variations. Immunocompetent cell counts and cytokine levels present variations according to the time of day and the sleep-wake cycle. Moreover, different immune cell types, such as macrophages, natural killer cells, and lymphocytes, contain a circadian molecular clockwork. The biological clocks intrinsic to immune cells and lymphoid organs, together with inputs from the central pacemaker of the suprachiasmatic nuclei via humoral and neural pathways, regulate the function of cells of the immune system, including their response to signals and their effector functions. Consequences of this include, for example, the daily variation in the response to an immune challenge (e.g., bacterial endotoxin injection) and the circadian control of allergic reactions. The circadian-immune connection is bidirectional, because in addition to this circadian control of immune functions, immune challenges and immune mediators (e.g., cytokines) were shown to have strong effects on circadian rhythms at the molecular, cellular, and behavioral levels. This tight crosstalk between the circadian and immune systems has wide-ranging implications for disease, as shown by the higher incidence of cancer and the exacerbation of autoimmune symptoms upon circadian disruption.
206 citations
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TL;DR: The findings reveal that diverse changes of miRNAs occur during liver development and, one of these, miR-500 is an oncofetal miRNA relevant to the diagnosis of human HCC.
Abstract: We identified that microRNA expression changed dynamically during liver development and found that miR-500 is an oncofetal miRNA in liver cancer. miR-500 was abundantly expressed in several human liver cancer cell lines and 45% of human hepatocellular carcinoma (HCC) tissue. Most importantly, an increased amount of miR-500 was found in the sera of the HCC patients. In fact, miR-500 levels in sera of the HCC patients returned to normal after the surgical treatment in three HCC patients. Our findings reveal that diverse changes of miRNAs occur during liver development and, one of these, miR-500 is an oncofetal miRNA relevant to the diagnosis of human HCC.
206 citations
Authors
Showing all 24378 results
Name | H-index | Papers | Citations |
---|---|---|---|
Yusuke Nakamura | 179 | 2076 | 160313 |
Yoshio Bando | 147 | 1234 | 80883 |
Charles Maguire | 142 | 1197 | 95026 |
Kazunori Kataoka | 138 | 908 | 70412 |
Senta Greene | 134 | 1346 | 90697 |
Intae Yu | 134 | 1372 | 89870 |
Kohei Yorita | 131 | 1389 | 91177 |
Wei Xie | 128 | 1281 | 77097 |
Susumu Kitagawa | 125 | 809 | 69594 |
Leon O. Chua | 122 | 824 | 71612 |
Jun Kataoka | 121 | 603 | 54274 |
S. Youssef | 120 | 683 | 65110 |
Katsuhiko Mikoshiba | 120 | 866 | 62394 |
Yusuke Yamauchi | 117 | 1000 | 51685 |
Teruo Okano | 117 | 476 | 47081 |