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Institution

Korea University

EducationSeoul, South Korea
About: Korea University is a education organization based out in Seoul, South Korea. It is known for research contribution in the topics: Population & Catalysis. The organization has 39756 authors who have published 82424 publications receiving 1860927 citations. The organization is also known as: Bosung College & Bosung Professional College.
Topics: Population, Catalysis, Thin film, Cancer, Medicine


Papers
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Journal ArticleDOI
Baizeng Fang1, Nitin K. Chaudhari1, Min-Sik Kim1, Jung Ho Kim1, Jong-Sung Yu1 
TL;DR: The Pt NPs deposited on Vulcan XC-72 (VC) carbon black by the HD-EG strategy show smaller size with more uniform dispersion, higher Pt utilization efficiency, and considerably improved fuel-cell polarization performance compared with the Pt NBP prepared by conventional sodium borohydride reduction or by a microwave-assisted polyol approach.
Abstract: A simple and efficient approach has been developed for synthesis of carbon-supported Pt nanoparticles (NPs) that combines homogeneous deposition (HD) of Pt complex species through a gradual increase of pH realized by in situ hydrolysis of urea and subsequent uniform reduction by ethylene glycol (EG) in a polyol process, giving control over the size and dispersion of Pt NPs. With increasing amount of urea in the starting Pt salt aqueous solution, the size of Pt complex species decreases and so does that of the metallic Pt NPs. The decrease in size of the Pt species is likely attributable to two determining factors: the steric contraction effect and the electrostatic charge effect. The excellent electrocatalysis ability of the Pt catalysts produced by HD-EG is demonstrated through the determination of electrochemical surface area and fuel-cell polarization performance. The Pt NPs deposited on Vulcan XC-72 (VC) carbon black by the HD-EG strategy show smaller size with more uniform dispersion, higher Pt utili...

277 citations

Journal ArticleDOI
A. Adare1, S. Afanasiev2, Christine Angela Aidala3, N. N. Ajitanand4  +442 moreInstitutions (49)
TL;DR: In this article, the e(+)e(-) pair continuum was measured in root s(NN) = 200 GeV Au+Au and p+p collisions over a wide range of mass and transverse momenta.
Abstract: PHENIX has measured the e(+)e(-) pair continuum in root s(NN) = 200 GeV Au+Au and p+p collisions over a wide range of mass and transverse momenta. The e(+)e(-) yield is compared to the expectations from hadronic sources, based on PHENIX measurements. In the intermediate-mass region, between the masses of the phi and the J/psi meson, the yield is consistent with expectations from correlated c (c) over bar production, although other mechanisms are not ruled out. In the low-mass region, below the phi, the p+p inclusive mass spectrum is well described by known contributions from light meson decays. In contrast, the Au+Au minimum bias inclusive mass spectrum in this region shows an enhancement by a factor of 4.7 +/- 0.4(stat) +/- 1.5(syst) +/- 0.9(model). At low mass (m(ee) < 0.3 GeV/c(2)) and high p(T) (1 < p(T) < 5 GeV/c) an enhanced e(+)e(-) pair yield is observed that is consistent with production of virtual direct photons. This excess is used to infer the yield of real direct photons. In central Au+Au collisions, the excess of the direct photon yield over the p+p is exponential in p(T), with inverse slope T = 221 +/- 19(stat) +/- 19(syst) MeV. Hydrodynamical models with initial temperatures ranging from T-init similar or equal to 300-600 MeV at times of 0.6-0.15 fm/c after the collision are in qualitative agreement with the direct photon data in Au+Au. For low p(T) < 1 GeV/c the low-mass region shows a further significant enhancement that increases with centrality and has an inverse slope of T similar or equal to 100 MeV. Theoretical models underpredict the low-mass, low-p(T) enhancement.

277 citations

Journal ArticleDOI
TL;DR: The possibility that MPTP and 6‐hydroxydopamine act on distinct cell death pathways in a murine dopaminergic neuronal cell line is examined, finding that cells treated with 6‐OHDA accompanied ultrastructural changes typical of apoptosis, whereas MPP+ treatment induced necrotic manifestations.
Abstract: In this study, we examined the possibility that MPTP and 6-hydroxydopamine (6-OHDA) act on distinct cell death pathways in a murine dopaminergic neuronal cell line, MN9D. First, we found that cells treated with 6-OHDA accompanied ultrastructural changes typical of apoptosis, whereas MPP+ treatment induced necrotic manifestations. Proteolytic cleavage of poly(ADP-ribose)polymerase by caspase was induced by 6-OHDA, whereas it remained uncleaved up to 32 h after MPP+ treatment and subsequently disappeared. Accordingly, 6-OHDA- but not MPP+-induced cell death was significantly attenuated in the presence of a broad-spectrum caspase inhibitor, N-benzyloxy-carbonyl-Val-Ala-Asp-fluomethylketone (Z-VAD-fmk). As measured by fluorometric probes, the level of reactive oxygen species (ROS) significantly increased after 6-OHDA treatment. In contrast, the level of dihydroethidium-sensitive ROS following MPP+ treatment remained unchanged while a slight increase in dichlorofluorescin-sentive ROS was temporarily observed. As demonstrated by immunoblot analysis, the level of superoxide dismutase was down-regulated following 6-OHDA treatment, whereas it remained unchanged after MPP+ treatment. Cotreatment of cells with antioxidants such as N-acetylcysteine or Mn(III)tetrakis(4-benzoic acid)porphyrin chloride (MnTBAP, cell-permeable superoxide dismutase mimetic) rescued 6-OHDA- but not MPP+-induced cell death, whereas inclusion of catalase or NG-nitro-l-arginine had no effect in both cases. In addition, 6-OHDA induced ROS-mediated c-Jun N-terminal kinase (JNK) activation that was attenuated in the presence of N-acetylcysteine or MnTBAP but not catalase or Z-VAD-fmk. In contrast, MPP+ has little effect on JNK activity, indicating that ROS and/or ROS-induced cell death signaling pathway seems to play an essential role in 6-OHDA–mediated apoptosis but not in MPP+-induced necrosis in a mesencephalon-derived, dopaminergic neuronal cell line. J. Neurosci. Res. 57:86–94, 1999. © 1999 Wiley-Liss, Inc.

277 citations

Journal ArticleDOI
TL;DR: In this paper, the effects of conjugated linoleic acid (CLA) on lipid composition and gene expression during the differentiation of mouse 3T3-L1 preadipocytes were investigated.
Abstract: Conjugated linoleic acids (CLA) are a group of positional and geometric conjugated dienoic isomers of linoleic acid. The objective of this study was to determine the effects of the cis-9,trans-11 and trans-10,cis-12 isomers of conjugated linoleic acid on lipid composition and gene expression during the differentiation of mouse 3T3-L1 preadipocytes. Treatment of differentiating 3T3-L1 preadipocytes with trans-10,cis-12 conjugated linoleic acid (CLA) resulted in a dose-dependent decrease in the expression of the stearoyl-CoA desaturase 1 gene (SCD1). The expression of other adipocyte genes such as adipose P2 (aP2), fatty acid synthase (FAS), SCD2 and the key adipogenic transcription factors, peroxisome proliferator-activated receptor gamma2 (PPARgamma2) and CCAAT enhancer binding protein alpha (C/EBPalpha), remained elevated. Cells treated with trans-10,cis-12 CLA exhibited smaller lipid droplets, with reduced levels of the major monounsaturated fatty acids, palmitoleate and oleate. By contrast, the cis-9,trans-11 isomer did not alter adipocyte gene expression. Repression of the stearoyl-CoA desaturase gene expression in adipocytes by the trans-10,cis-12 isomer may contribute to the mechanisms by which CLA reduces body fat in mice.

276 citations

Journal ArticleDOI
Yung-Gil Kim1, W.Y. Choi1, Joel Jang1, Ki-Pung Yoo2, Cherl-Ho Lee1 
TL;DR: In this article, the authors compared the group segment numbers and interaction energy parameters between groups for the group contribution non-random lattice-fluid equation of state for room temperature ionic liquids and carbon dioxide.

276 citations


Authors

Showing all 40083 results

NameH-indexPapersCitations
Anil K. Jain1831016192151
Hyun-Chul Kim1764076183227
Yongsun Kim1562588145619
Jongmin Lee1502257134772
Byung-Sik Hong1461557105696
Daniel S. Berman141136386136
Christof Koch141712105221
David Y. Graham138104780886
Suyong Choi135149597053
Rudolph E. Tanzi13563885376
Sung Keun Park133156796933
Tae Jeong Kim132142093959
Robert S. Brown130124365822
Mohammad Khaja Nazeeruddin12964685630
Klaus-Robert Müller12976479391
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023121
2022611
20216,359
20206,208
20195,608
20185,088