Waseda University

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.

Electrochemical Synthesis of One‐Dimensional Mesoporous Pt Nanorods Using the Assembly of Surfactant Micelles in Confined Space

Abstract: of metals affords electrocatalystsshowing a superior performance because of their highporosity, large area per unit volume, and excellent activity–structure relationship. Therefore, the successful synthesis of1D mesoporous Pt motifs can be expected to be a newdirection in the fabrication of superior electrocatalysts. Thetraditional hard-templating method, which is widely used tosynthesize mesoporous carbon materials,

Postbounce evolution of core-collapse supernovae: Long-term effects of equation of state

Abstract: We study the evolution of supernova core from the beginning of gravitational collapse of a 15Msolar star up to 1 second after core bounce. We present results of spherically symmetric simulations of core-collapse supernovae by solving general relativistic neutrino-radiation-hydrodynamics in the implicit time-differencing. We aim to explore the evolution of shock wave in a long term and investigate the formation of protoneutron star together with supernova neutrino signatures. These studies are done to examine the influence of equation of state (EOS) on the postbounce evolution of shock wave in the late phase and the resulting thermal evolution of protoneutron star. We make a comparison of two sets of EOS, that is, by Lattimer and Swesty (LS-EOS) and by Shen et al.(SH-EOS). We found that, for both EOSs, the core does not explode and the shock wave stalls similarly in the first 100 milliseconds after bounce. The revival of shock wave does not occur even after a long period in either cases. However, the recession of shock wave appears different beyond 200 milliseconds after bounce, having different thermal evolution of central core. A more compact protoneutron star is found for LS-EOS than SH-EOS with a difference in the central density by a factor of ~2 and a difference of ~10 MeV in the peak temperature. Resulting spectra of supernova neutrinos are different to the extent that may be detectable by terrestrial neutrino detectors.

Measurement of Higgs boson production in the diphoton decay channel in pp collisions at center-of-mass energies of 7 and 8 TeV with the ATLAS detector

Abstract: A measurement of the production processes of the recently discovered Higgs boson is performed in the two-photon final state using 4.5 fb(-1) of proton-proton collisions data at root s = 7 TeV and 20.3 fb(-1) at root s = 8 TeV collected by the ATLAS detector at the Large Hadron Collider. The number of observed Higgs boson decays to diphotons divided by the corresponding Standard Model prediction, called the signal strength, is found to be mu = 1.17 +/- 0.27 at the value of the Higgs boson mass measured by ATLAS, m(H) = 125.4 GeV. The analysis is optimized to measure the signal strengths for individual Higgs boson production processes at this value of m(H). They are found to be mu(ggF) = 1.32 +/- 0.38, mu(VBF) = 0.8 +/- 0.7, mu(WH) = 1.0 +/- 1.6, mu(ZH) = 0.1(-0.1)(+3.7), and mu t (t) over barH = 1.6(-1.8)(+2.7), for Higgs boson production through gluon fusion, vector-boson fusion, and in association with a W or Z boson or a top-quark pair, respectively. Compared with the previously published ATLAS analysis, the results reported here also benefit from a new energy calibration procedure for photons and the subsequent reduction of the systematic uncertainty on the diphoton mass resolution. No significant deviations from the predictions of the Standard Model are found.

Induction of IRF-3/-7 kinase and NF-kappaB in response to double-stranded RNA and virus infection: common and unique pathways.

Abstract: Background Infection by virus or treatment with double-stranded RNA (dsRNA) results in the activation of transcription factors including IRF-3, IRF-7 and a pleiotropic regulator NF-kappaB by specific phosphorylation. These factors are important in triggering a cascade of antiviral responses. A protein kinase that is yet to be identified is responsible for the activation of these factors and plays a key role in the responses. Results The signal cascade was analysed using sensitive assays for the activation of IRF-3 and NF-kappaB, and various inhibitors. We found that the activation of IRF-3 and NF-kappaB by dsRNA or virus involves a process that is sensitive to Geldanamycin. Although the induction of NF-kappaB by dsRNA/virus and TNF-alpha involves common downstream pathways including IKK activation, the upstream, Geldanamycin-sensitive process was unique to the dsRNA/virus-induced signal. By an in vitro assay using cell extract, we found an inducible protein kinase activity with physiological specificity of IRF-3 phosphorylation. Furthermore, the same extract specifically phosphorylated IRF-7 in a similar manner. Conclusions Double-stranded RNA or virus triggers a specific signal cascade that results in the activation of the IRF-3/-7 kinase we detected, which corresponds to the long-sought signalling machinery that is responsible for triggering the early phase of innate response. The signal branches to a common NF-kappaB activation cascade, thus resulting in the activation of a set of critical transcription factors for the response.