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Institution

Yonsei University

EducationSeoul, South Korea
About: Yonsei University is a education organization based out in Seoul, South Korea. It is known for research contribution in the topics: Population & Cancer. The organization has 50162 authors who have published 106172 publications receiving 2279044 citations. The organization is also known as: Yonsei.
Topics: Population, Cancer, Medicine, Thin film, Breast cancer


Papers
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Journal ArticleDOI
Tareq Abu-Zayyad1, R. Aida2, Mark Allen1, Ross Anderson1, R. Azuma3, Elliott Barcikowski1, John Belz1, Douglas Bergman1, Samuel Blake1, R. Cady1, ByongGu Cheon4, Jyunsei Chiba5, Michiyuki Chikawa6, E. J. Cho4, W. R. Cho7, H. Fujii, T. Fujii8, T. Fukuda3, Masaki Fukushima9, William Hanlon1, K. Hayashi3, Y. Hayashi8, Naoaki Hayashida9, K. Hibino10, K. Hiyama9, Ken Honda2, T. Iguchi3, Daisuke Ikeda9, K. Ikuta2, Naoya Inoue11, Takaaki Ishii2, R. Ishimori3, Dmitri Ivanov12, Dmitri Ivanov1, S. Iwamoto2, C. C. H. Jui1, Kenichi Kadota13, Fumio Kakimoto3, Oleg Kalashev, T. Kanbe2, Katsuaki Kasahara14, H. Kawai15, S. Kawakami8, S. Kawana11, Eiji Kido9, HangBae Kim4, Hyun-Il Kim7, J. H. Kim1, K. Kitamoto6, S. Kitamura3, Yasunori Kitamura3, K. Kobayashi5, Yoji Kobayashi3, Y. Kondo9, Kiyoshi Kuramoto8, V.A. Kuzmin, Younghoon Kwon7, J. Lan1, S. I. Lim16, S. Machida3, K. Martens9, Tomohiro Matsuda, T. Matsuura3, Toshio Matsuyama8, John N. Matthews1, Mayuko Minamino8, K. Miyata5, Y. Murano3, Isaac Myers1, K. Nagasawa11, S. Nagataki17, Tomoyuki Nakamura18, S. W. Nam16, Toshiyuki Nonaka9, Shoichi Ogio8, M. Ohnishi9, H. Ohoka9, K. Oki9, D. Oku2, T. Okuda19, Akitoshi Oshima8, Shunsuke Ozawa14, Inkyu Park16, Maxim Pshirkov20, D. Rodriguez1, S. Y. Roh21, Grigory Rubtsov, Dongsu Ryu21, Hiroyuki Sagawa9, Nobuyuki Sakurai8, A. L. Sampson1, L. M. Scott12, Priti Shah1, Fumiya Shibata2, Tatsunobu Shibata9, H. Shimodaira9, B. K. Shin4, J. I. Shin7, T. Shirahama11, J. D. Smith1, Pierre Sokolsky1, B. T. Stokes1, S. R. Stratton1, S. R. Stratton12, Thomas Stroman1, S. Suzuki, Yukio Takahashi9, Masahiro Takeda9, Akimichi Taketa9, Masato Takita9, Yuichiro Tameda9, H. Tanaka8, Kenichi Tanaka22, M. Tanaka8, S. B. Thomas1, Gordon Thomson1, Peter Tinyakov20, Igor Tkachev, H. Tokuno3, Takayuki Tomida, Sergey Troitsky, Yoshiki Tsunesada3, K. Tsutsumi3, Y. Tsuyuguchi2, Yukio Uchihori23, S. Udo10, H. Ukai2, G. Vasiloff1, Y. Wada11, Tiffany Wong1, M. Wood1, Y. Yamakawa9, R. Yamane8, H. Yamaoka, K. Yamazaki8, J. Yang16, Y. Yoneda8, S. Yoshida15, H. Yoshii24, X. Zhou6, R. Zollinger1, Zach Zundel1 
TL;DR: The Telescope Array experiment is supported by the Japan Society for the Promotion of Science through Grants-in-Aids for Scientific Research on Specially Promoted Research (21000002) "Extreme Phenomena in the Universe Explored by Highest Energy Cosmic Rays" and for scientific research (S) (19104006), and the Inter-University Research Program of the Institute for Cosmic Ray Research.
Abstract: The Telescope Array experiment is supported by the Japan Society for the Promotion of Science through Grants-in-Aids for Scientific Research on Specially Promoted Research (21000002) "Extreme Phenomena in the Universe Explored by Highest Energy Cosmic Rays" and for Scientific Research (S) (19104006), and the Inter-University Research Program of the Institute for Cosmic Ray Research; by the U.S. National Science Foundation awards PHY-0307098, PHY-0601915, PHY-0703893, PHY-0758342, and PHY-0848320 (Utah), and PHY-0649681 (Rutgers); by the National Research Foundation of Korea (2006-0050031, 2007-0056005, 2007-0093860, 2010-0011378, 2010-0028071, R32-10130, 2011-0002617); by the Russian Academy of Sciences, RFBR grants 10-02-01406a and 11-02-01528a (INR), IISN project No. 4.4509.10 and Belgian Science Policy under IUAP VI/11 (ULB). The foundations of Dr. Ezekiel R. and Edna Wattis Dumke, Willard L. Eccles and the George S. and Dolores Dore Eccles all helped with generous donations. The State of Utah supported the project through its Economic Development Board, and the University of Utah through the Office of the Vice President for Research. The experimental site became available through the cooperation of the Utah School and Institutional Trust Lands Administration (SITLA), U. S. Bureau of Land Management, and the U. S. Air Force. We also thank the people and the officials of Millard County, Utah for their steadfast and warm support. We gratefully acknowledge the contributions from the technical staffs of our home institutions. An allocation of computer time from the Center for High Performance Computing at the University of Utah is gratefully acknowledged.

272 citations

Journal ArticleDOI
TL;DR: It is reported that Mtb Eis plays essential roles in modulating macrophage autophagy, inflammatory responses, and cell death via a reactive oxygen species (ROS)-dependent pathway and suppresses host innate immune defenses by modulating autophagic activation and cytokine production.
Abstract: The “enhanced intracellular survival” (eis) gene of Mycobacterium tuberculosis (Mtb) is involved in the intracellular survival of M. smegmatis. However, its exact effects on host cell function remain elusive. We herein report that Mtb Eis plays essential roles in modulating macrophage autophagy, inflammatory responses, and cell death via a reactive oxygen species (ROS)-dependent pathway. Macrophages infected with an Mtb eis-deletion mutant H37Rv (Mtb-Δeis) displayed markedly increased accumulation of massive autophagic vacuoles and formation of autophagosomes in vitro and in vivo. Infection of macrophages with Mtb-Δeis increased the production of tumor necrosis factor-α and interleukin-6 over the levels produced by infection with wild-type or complemented strains. Elevated ROS generation in macrophages infected with Mtb-Δeis (for which NADPH oxidase and mitochondria were largely responsible) rendered the cells highly sensitive to autophagy activation and cytokine production. Despite considerable activation of autophagy and proinflammatory responses, macrophages infected with Mtb-Δeis underwent caspase-independent cell death. This cell death was significantly inhibited by blockade of autophagy and c-Jun N-terminal kinase-ROS signaling, suggesting that excessive autophagy and oxidative stress are detrimental to cell survival. Finally, artificial over-expression of Eis or pretreatment with recombinant Eis abrogated production of both ROS and proinflammatory cytokines, which depends on the N-acetyltransferase domain of the Eis protein. Collectively, these data indicate that Mtb Eis suppresses host innate immune defenses by modulating autophagy, inflammation, and cell death in a redox-dependent manner.

272 citations

Journal ArticleDOI
TL;DR: Asymptomatic patients may be contagious and thus a potential source of transmission of COVID-19, and more than half of the patients without any symptoms present with CT abnormalities.

272 citations

Journal ArticleDOI
TL;DR: The IMDC prognostic model in the second-line targeted therapy setting has an improved prognostic performance and is applicable to a more contemporary patient cohort than that of the three-factor MSKCC model.
Abstract: Summary Background Previous prognostic models for second-line systemic therapy in patients with metastatic renal cell carcinoma have not been studied in the setting of targeted therapy. We sought to validate the International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) model in patients with metastatic renal cell carcinoma receiving next-line targeted therapy after progression on first-line targeted therapy. Methods In this population-based study, we analysed patients who received second-line targeted therapy for metastatic renal cell carcinoma at 19 centres in Canada, USA, Greece, Japan, Singapore, South Korea, and Denmark. The primary endpoint was overall survival since the initiation of second-line therapy. We compared the prognostic performance of the IMDC model with the three-factor MSKCC model used for previously treated patients for overall survival since the start of second-line targeted therapy. Findings Between Jan 1, 2005, and Nov 30, 2012, we included 1021 patients treated with second-line targeted therapy. Median overall survival since the start of second-line targeted therapy was 12·5 months (95% CI 11·3–14·3). Five of six predefined factors in the IMDC model (anaemia, thrombocytosis, neutrophilia, Karnofsky performance status [KPS] Interpretation The IMDC prognostic model can be applied to patients previously treated with targeted therapy, in addition to previously validated populations in first-line targeted therapy. The IMDC prognostic model in the second-line targeted therapy setting has an improved prognostic performance and is applicable to a more contemporary patient cohort than that of the three-factor MSKCC model. Funding DF/HCC Kidney Cancer SPORE P50 CA101942-01, Kidney Cancer Research Network of Canada, Canadian Institute for Health Research, Trust Family, Loker Pinard, Michael Brigham, and Gerald DeWulf.

271 citations

Journal ArticleDOI
Betty Abelev1, Jaroslav Adam2, Dagmar Adamová3, Andrew Marshall Adare4  +969 moreInstitutions (88)
11 Jul 2013
TL;DR: In this paper, the ALICE detector was used to measure the long-range correlations between trigger particles and various species of charged associated particles (unidentified particles, pions, kaons, protons and antiprotons).
Abstract: Angular correlations between unidentified charged trigger particles and various species of charged associated particles (unidentified particles, pions, kaons, protons and antiprotons) are measured by the ALICE detector in p-Pb collisions at a nucleon-nucleon centre-of-mass energy of 5.02 TeV in the transverse-momentum range 0.3 < p(T) < 4 GeV/c. The correlations expressed as associated yield per trigger particle are obtained in the pseudorapidity range vertical bar n(lab)vertical bar < 0.8. Fourier coefficients are extracted from the long-range correlations projected onto the azimuthal angle difference and studied as a function of p(T) and in intervals of event multiplicity. In high-multiplicity events, the second-order coefficient for protons, 4, is observed to be smaller than that for pions, v(2)(pi), up to about p(T) = 2 GeV/c. To reduce correlations due to jets, the per-trigger yield measured in low-multiplicity events is subtracted from that in high-multiplicity events. A two-ridge structure is obtained for all particle species. The Fourier decomposition of this structure shows that the second-order coefficients for pions and kaons are similar. The v(2)(p) is found to be smaller at low P-T and larger at higher p(T) than v(2)(pi), with a crossing occurring at about 2 GeV/c. This is qualitatively similar to the elliptic-flow pattern observed in heavy-ion collisions. A mass ordering effect at low transverse momenta is consistent with expectations from hydrodynamic model calculations assuming a collectively expanding system. (C) 2013 CERN. Published by Elsevier B.V. All rights reserved.

271 citations


Authors

Showing all 50632 results

NameH-indexPapersCitations
Younan Xia216943175757
Peer Bork206697245427
Ralph Weissleder1841160142508
Hyun-Chul Kim1764076183227
Gregory Y.H. Lip1693159171742
Yongsun Kim1562588145619
Jongmin Lee1502257134772
James M. Tiedje150688102287
Guanrong Chen141165292218
Kazunori Kataoka13890870412
Herbert Y. Meltzer137114881371
Peter M. Rothwell13477967382
Tae Jeong Kim132142093959
Shih-Chang Lee12878761350
Ming-Hsuan Yang12763575091
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023203
2022753
20217,800
20207,310
20196,827
20186,298