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Institution

Fu Jen Catholic University

EducationTaipei, Taiwan
About: Fu Jen Catholic University is a education organization based out in Taipei, Taiwan. It is known for research contribution in the topics: Population & Medicine. The organization has 6842 authors who have published 9512 publications receiving 171005 citations. The organization is also known as: FJU & Fu Jen.
Topics: Population, Medicine, Cancer, Hazard ratio, Apoptosis


Papers
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Journal ArticleDOI
Goodarz Danaei1, Saman Fahimi1, Yuan Lu1, Bin Zhou2  +427 moreInstitutions (134)
TL;DR: The effect of different diagnostic definitions on both the population prevalence of diabetes and the classification of previously undiagnosed individuals as having diabetes versus not having diabetes in a pooled analysis of data from population-based health examination surveys in different regions is assessed.

126 citations

Journal ArticleDOI
TL;DR: Most of the research about the hypoglycemic action effects of polysaccharides, proteoglycans, proteins and tritrerpenoids from G. lucidum are summarized to serve as a guide for future research.

125 citations

Journal ArticleDOI
TL;DR: It is hypothesized that the inhibitory mechanisms of emodin on activated T cells proliferation are related to the impairment of cytokine production, IL-2 mRNA level and [Ca2+]i in the cells.
Abstract: Objective and Design: This study was designed to elucidate action mechanisms of four anthraquinones identified from Polygonum hypoleucum Ohwi (P. hypoleucum Ohwi) on primary human T lymphocytes.¶Material and methods: The cells were isolated from peripheral blood.¶Treatment: T cells were treated with 5 to 60 μM of four anthraquinones with or without phytohemagglutinin (PHA; 5 μg/ml) for 3 days. Effects of 4 anthraquinones on T lymphocyte proliferation, production and gene expression of inflammatory cytokines and intracellular free Ca2+ concentration ([Ca2+]i) were determined. Data were assessed with Student's t-test.¶Results: On a percentage basis, emodin had the highest suppressing activity on T lymphocyte proliferation with an IC50 of 11.2 ± 0.6 μM. Emodin decreased cytokine production, IL-2 mRNA expression, and [Ca2+]i in activated T cells.¶Conclusions: We hypothesize that the inhibitory mechanisms of emodin on activated T cells proliferation are related to the impairment of cytokine production, IL-2 mRNA level and [Ca2+]i in the cells.¶

125 citations

Journal ArticleDOI
R. Mizuk, I. Adachi, H. Aihara1, K. Arinstein2, K. Arinstein3, T. Aushev4, A. M. Bakich5, Vladislav Balagura, E. L. Barberio6, A. Bay4, K. Belous, V. Bhardwaj7, A. Bozek8, M. Bračko9, T. E. Browder, M. C. Chang10, A. Chen11, B. G. Cheon12, C. C. Chiang13, R. Chistov, I. S. Cho14, S. K. Choi15, Y. Choi16, J. Dalseno, M. Danilov, S.I. Eidelman2, S.I. Eidelman3, N. Gabyshev3, N. Gabyshev2, P. Goldenzweig17, P. Goldenzweig18, B. Golob19, H. Ha20, J. Haba, B. Y. Han20, T. Hara, Yoji Hasegawa21, K. Hayasaka22, Y. Hoshi23, W. S. Hou13, H. J. Hyun24, T. Iijima22, K. Inami22, A. Ishikawa25, Hirokazu Ishino26, R. Itoh, Motoki Iwasaki1, Y. Iwasaki, N. J. Joshi27, D. H. Kah24, J. H. Kang14, P. Kapusta8, H. Kawai28, T. Kawasaki29, H. J. Kim24, H. O. Kim24, Jung-Hyun Kim16, Y. I. Kim24, Y. J. Kim30, K. Kinoshita17, B. R. Ko20, S. Korpar9, P. Križan19, P. Krokovny, A. Kuzmin3, A. Kuzmin2, Y. J. Kwon14, S. H. Kyeong14, J. S. Lange31, M. J. Lee32, S. E. Lee32, T. Lesiak8, C. Liu33, Yang Liu22, D. Liventsev, R. Louvot4, Daniel Robert Marlow34, A. Matyja8, S. McOnie5, K. Miyabayashi35, H. Miyata29, Y. Miyazaki22, T. Mori22, E. Nakano36, M. Nakao, H. Nakazawa11, Z. Natkaniec8, S. Nishida, O. Nitoh37, T. Ohshima22, S. Okuno38, S. L. Olsen, P. Pakhlov, G. Pakhlova, C. W. Park16, H. Park24, H. K. Park24, R. Pestotnik, L. E. Piilonen39, H. Sahoo, K. Sakai29, Y. Sakai, O. Schneider4, C. Schwanda40, A. Sekiya35, K. Senyo22, M. Shapkin, V.E. Shebalin3, V.E. Shebalin2, J. G. Shiu13, B.A. Shwartz2, B.A. Shwartz3, Samo Stanič41, M. Starič, T. Sumiyoshi42, Y. Teramoto36, I. Tikhomirov, K. Trabelsi, S. Uehara, T. Uglov, Y. Unno12, Phillip Urquijo6, G. S. Varner, Kevin Varvell5, K. Vervink4, C. H. Wang43, M. Z. Wang13, P. Wang, X. L. Wang, Y. Watanabe38, Robin Wedd6, E. Won20, Bruce Yabsley5, Y. Yamashita, C. Z. Yuan, C. C. Zhang, Z. P. Zhang33, Vladimir Zhulanov2, Vladimir Zhulanov3, T. Zivko, A. Zupanc, O. Zyukova2, O. Zyukova3 
TL;DR: In this paper, a Dalitz plot analysis of B→Kπ+ψ′ decays was performed on a 605fb-1 data sample that contains 657×106 BB pairs collected near the Υ(4S) resonance with the Belle detector at the KEKB asymmetric energy e+e-collider.
Abstract: From a Dalitz plot analysis of B→Kπ+ψ′ decays, we find a signal for Z(4430)+→π+ψ′ with a mass M=(4443-12-13+15+19)MeV/ c2, width Γ=(107-43-56+86+74)MeV, product branching fraction B(B0→K-Z(4430)+)×B(Z(4430)+→π+ψ′)=(3.2-0.9-1. 6+1.8+5.3)×10-5, and significance of 6.4σ that agrees with previous Belle measurements based on the same data sample. In addition, we determine the branching fraction B(B0→K*(892)0ψ′)=(5.52-0.32-0.58+0.35+0. 53)×10-4 and the fraction of K*(892)0 mesons that are longitudinally polarized fL=(44.8-2.7-5.3+4.0+4.0)%. These results are obtained from a 605fb-1 data sample that contains 657×106 BB pairs collected near the Υ(4S) resonance with the Belle detector at the KEKB asymmetric-energy e+e- collider. © 2009 The American Physical Society.

125 citations

Journal ArticleDOI
TL;DR: Compound 10 showed a significant inhibitory effect on the release of beta-glucuronidase from rat neutrophils stimulated with formyl-Met-Leu-Phe (fMLP)/cytochalasin B (CB) whereas compound 9 significantly inhibited superoxide anion formation in fMLP/CB-stimulated rat neutrophic cells.

125 citations


Authors

Showing all 6861 results

NameH-indexPapersCitations
P. Chang1702154151783
Christian Guilleminault13389768844
Pan-Chyr Yang10278646731
Po-Ren Hsueh92103038811
Shyi-Ming Chen9042522172
Peter J. Rossky7428021183
Chong-Jen Yu7257722940
Shuu Jiun Wang7150224800
Jaw-Town Lin6743415482
Lung Chi Chen6326713929
Ronald E. Taam5929012383
Jiann T. Lin5819010801
Yueh-Hsiung Kuo5761812204
San Lin You5517816572
Liang-Gee Chen5458212073
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202313
202233
2021726
2020666
2019571
2018528