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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 & Hazard ratio. The organization has 6842 authors who have published 9512 publications receiving 171005 citations. The organization is also known as: FJU & Fu Jen.


Papers
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Journal ArticleDOI
TL;DR: In this article, the effects of international experience on multinational enterprises' ownership strategy across a range of developed and developing economies are examined, and the authors distinguish competence-building and partner selection effects of experience, which vary between general international experience and country-specific experience and across host contexts.

96 citations

Journal ArticleDOI
A. Vossen1, A. Vossen2, R. Seidl, I. Adachi, H. Aihara3, T. Aushev4, Vladislav Balagura, W. Bartel, M. Bischofberger5, A.E. Bondar6, A.E. Bondar7, M. Bračko8, T. E. Browder, M. C. Chang9, A. Chen10, Po-Hsun Chen11, B. G. Cheon12, K. Cho13, Y. Choi14, S.I. Eidelman7, S.I. Eidelman6, M. Feindt15, V. Gaur16, N. Gabyshev6, N. Gabyshev7, A. Garmash6, A. Garmash7, B. Golob17, M. Grosse Perdekamp2, J. Haba, K. Hayasaka18, Yasuyuki Horii19, Y. Hoshi20, W. S. Hou11, H. J. Hyun21, K. Inami18, A. Ishikawa22, M. Iwabuchi23, Y. Iwasaki, T. Iwashita5, N. J. Joshi16, H. Kichimi, H. O. Kim21, M. J. Kim21, B. R. Ko24, T. Kumita25, J. S. Lange26, M. J. Lee27, Sang Hoon Lee24, M. Leitgab2, Yang Li28, C. Liu29, D. Liventsev, R. Louvot4, S. McOnie30, H. Miyata31, Y. Miyazaki18, R. Mizuk, G. B. Mohanty16, E. Nakano32, S. Nishida, O. Nitoh33, A. Ogawa, T. Ohshima18, S. Okuno34, G. Pakhlova, H. Park21, H. K. Park21, Marko Petrič, L. E. Piilonen28, Sunmin Ryu27, H. Sahoo, Y. Sakai, O. Schneider4, C. Schwanda35, O. Seon18, M. Shapkin, V.E. Shebalin7, V.E. Shebalin6, T. A. Shibata36, J. G. Shiu11, P. Smerkol, Y. S. Sohn23, E. Solovieva, Samo Stanič37, M. Starič, M. Sumihama38, T. Sumiyoshi25, Y. Teramoto32, M. Uchida36, S. Uehara, T. Uglov, Y. Unno12, S. Uno, G. S. Varner, A. Vinokurova7, A. Vinokurova6, C. H. Wang39, M. Z. Wang11, P. Wang, Y. Watanabe34, E. Won, Bruce Yabsley30, Y. Yamashita, V.N. Zhilich6, V.N. Zhilich7, Ping Zhou40, Vladimir Zhulanov7, Vladimir Zhulanov6 
TL;DR: Nonzero asymmetries for pairs of charge-ordered π(+)π(-) pairs are reported, which indicate a significant interference fragmentation function in this channel.
Abstract: The interference fragmentation function translates the fragmentation of a quark with a transverse projection of the spin into an azimuthal asymmetry of two final-state hadrons. In e(+)e(-) annihilation the product of two interference fragmentation functions is measured. We report nonzero asymmetries for pairs of charge-ordered π(+)π(-) pairs, which indicate a significant interference fragmentation function in this channel. The results are obtained from a 672 fb(-1) data sample that contains 711 × 10(6) π(+)π(-) pairs and was collected at and near the Υ(4S) resonance, with the Belle detector at the KEKB asymmetric-energy e(+)e(-) collider.

96 citations

Journal ArticleDOI
TL;DR: The risk of ARF is significantly increased in patients with advanced liver cirrhosis presenting with marked hyperbilirubinemia, hyponatremia, elevated liver enzymes, infection, and GI bleeding, which leads to higher mortality rates in both viral and alcohol-induced liver Cirrhosis.
Abstract: BACKGROUND Acute renal failure (ARF) is a life-threatening entity that frequently complicates advanced liver disease. This study documents a number of factors that may predispose to or precipitate ARF and influence outcomes in patients with advanced liver disease. Comparisons are also made between subgroups of patients with viral and alcohol-induced liver cirrhosis in those with ARF. PATIENTS AND METHODS We conducted a retrospective chart review over one year of 127 consecutive hospital admissions in 82 patients who were diagnosed with advanced liver cirrhosis (Child-Pugh Class C) in a tertiary care center. A diagnosis of ARF was made in 29 admissions and another 98 admissions not complicated by ARF served as controls. This study evaluated different etiologies of ARF and developed a database which included clinical features, biochemical parameters, the etiology of cirrhosis, possible predisposing factors, and precipitating events. Version II of the Acute Physiology and Chronic Health Physiology Scoring system (APACHE II) was applied to predict short-term hospital mortality rates. RESULTS ARF occurred in 29 admissions over the one-year study period (23%). The mean age of these patients was 56.8 +/- 12.0 years, and 73% were men. The patients with ARF had significant hyponatremia and higher levels of serum bilirubin, aspartate aminotransferase (AST), alanine aminotransferase (ALT), and white cell counts on admission than the controls. Patients who developed ARF were more likely to have had infection, especially septicemia, and gastrointestinal (GI) bleeding. Mortality rate in the patients with ARF was much higher than in those patients without ARF (72% vs. 13%, p < 0.001). The patients with viral cirrhosis and ARF were found to have higher leukocyte counts, serum bilirubin levels, and more frequent incidence of infection, septicemia and GI bleeding compared to the patients with alcoholic liver cirrhosis and ARF. Those with viral hepatitis were also significantly older and had more frequent incidence of ascites, but had lower levels of gamma-glutamyl transpeptidase and less frequent incidence of encephalopathy. CONCLUSIONS The risk of ARF is significantly increased in patients with advanced liver cirrhosis presenting with marked hyperbilirubinemia, hyponatremia, elevated liver enzymes, infection, and GI bleeding. The presence of ARF leads to higher mortality rates in both viral and alcohol-induced liver cirrhosis.

96 citations

Journal ArticleDOI
11 Sep 2018-Toxins
TL;DR: Oral sorbent AST-120 reduces serum levels of uremic toxins in CKD patients by adsorbing the precursors of IS and PCS generated by amino acid metabolism in the intestine, and reduces the production of reactive oxygen species by endothelial cells, to impede the subsequent oxidative stress.
Abstract: Uremic toxins, such as indoxyl sulfate (IS) and p-cresol, or p-cresyl sulfate (PCS), are markedly accumulated in the organs of chronic kidney disease (CKD) patients These toxins can induce inflammatory reactions and enhance oxidative stress, prompting glomerular sclerosis and interstitial fibrosis, to aggravate the decline of renal function Consequently, uremic toxins play an important role in the worsening of renal and cardiovascular functions Furthermore, they destroy the quantity and quality of bone Oral sorbent AST-120 reduces serum levels of uremic toxins in CKD patients by adsorbing the precursors of IS and PCS generated by amino acid metabolism in the intestine Accordingly, AST-120 decreases the serum IS levels and reduces the production of reactive oxygen species by endothelial cells, to impede the subsequent oxidative stress This slows the progression of cardiovascular and renal diseases and improves bone metabolism in CKD patients Although large-scale studies showed no obvious benefits from adding AST-120 to the standard therapy for CKD patients, subsequent sporadic studies may support its use This article summarizes the mechanisms of the uremic toxins, IS, and PCS, and discusses the multiple effects of AST-120 in CKD patients

95 citations

Journal ArticleDOI
TL;DR: OSU-53 is a potent, orally bioavailable AMPK activator that acts through a broad spectrum of antitumor activities downstream of AMPK activation and modulated relevant intratumoral biomarkers of drug activity.

95 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