Institution
Kyungpook National University
Education•Daegu, South Korea•
About: Kyungpook National University is a education organization based out in Daegu, South Korea. It is known for research contribution in the topics: Population & Catalysis. The organization has 20497 authors who have published 42107 publications receiving 834608 citations.
Topics: Population, Catalysis, Large Hadron Collider, Adsorption, Medicine
Papers published on a yearly basis
Papers
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TL;DR: An enhancement to Chien et al.'s scheme enables users to change their passwords freely and securely without the help of a remote server, while also providing secure mutual authentication.
Abstract: Recently, Ku-Chen proposed an improvement to Chien et al.'s scheme to prevent from some weaknesses. However, the improved scheme is not only still susceptible to parallel session attack, but also insecure for changing the user's password in password change phase. Accordingly, the current paper presents an enhancement to resolve such problems. As a result, the proposed scheme enables users to change their passwords freely and securely without the help of a remote server, while also providing secure mutual authentication.
175 citations
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Vardan Khachatryan, Albert M. Sirunyan, Armen Tumasyan, Wolfgang Adam1 +2184 more•Institutions (152)
TL;DR: In this article, the production of J/psi mesons from b-hadron decays at the LHC was studied in pp collisions at 6.5 to 30 GeV/c and in three rapidity ranges.
Abstract: The production of J/psi mesons is studied in pp collisions at sqrt(s)=7 TeV with the CMS experiment at the LHC. The measurement is based on a dimuon sample corresponding to an integrated luminosity of 314 inverse nanobarns. The J/psi differential cross section is determined, as a function of the J/psi transverse momentum, in three rapidity ranges. A fit to the decay length distribution is used to separate the prompt from the non-prompt (b hadron to J/psi) component. Integrated over J/psi transverse momentum from 6.5 to 30 GeV/c and over rapidity in the range |y| < 2.4, the measured cross sections, times the dimuon decay branching fraction, are 70.9 \pm 2.1 (stat.) \pm 3.0 (syst.) \pm 7.8(luminosity) nb for prompt J/psi mesons assuming unpolarized production and 26.0 \pm 1.4 (stat.) \pm 1.6 (syst.) \pm 2.9 (luminosity) nb for J/psi mesons from b-hadron decays.
175 citations
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TL;DR: The superior mechanical properties of the PI/GO nanocomposites were attributed to the good dispersion and effective stress transfer between the polymer and GO sheets, as evidenced by the results from X-ray diffraction (XRD) and morphological studies.
Abstract: Chemically modified graphene sheets were dispersed in a high-performance polyimide (PI) matrix using polyamic acid (PAA)/graphene nanocomposite as a precursor. PI nanocomposite films with different loadings of graphene sheets were prepared by thermal imidization of the as-prepared PAA/graphene nanocomposites. Graphene oxide (GO) synthesized by Hummer’s method was chemically reduced with various reducing agents to produce reduced GOs (rGOs). The incorporation of only 5 wt % GO resulted in an ∼12-fold and ∼18-fold increase in the tensile strength and tensile modulus of PI, respectively, while the PI/rGO nanocomposites were found to have relatively inferior tensile properties. The superior mechanical properties of the PI/GO nanocomposites were attributed to the good dispersion and effective stress transfer between the polymer and GO sheets, as evidenced by the results from X-ray diffraction (XRD) and morphological studies. Furthermore, the PI/GO nanocomposites exhibited higher loading capacity than PI/rGO. T...
175 citations
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TL;DR: To facilitate the understanding of vascular calcification, across any number of bioscientific disciplines, this review of a detailed updated molecular mechanism of VC encompasses a vascular smooth muscle phenotypic of osteogenic differentiation, and multiple signaling pathways of VC induction, including the roles of inflammation and cellular microorganelle genesis.
Abstract: Vascular calcification (VC), which is categorized by intimal and medial calcification, depending on the site(s) involved within the vessel, is closely related to cardiovascular disease. Specifically, medial calcification is prevalent in certain medical situations, including chronic kidney disease and diabetes. The past few decades have seen extensive research into VC, revealing that the mechanism of VC is not merely a consequence of a high-phosphorous and -calcium milieu, but also occurs via delicate and well-organized biologic processes, including an imbalance between osteochondrogenic signaling and anticalcific events. In addition to traditionally established osteogenic signaling, dysfunctional calcium homeostasis is prerequisite in the development of VC. Moreover, loss of defensive mechanisms, by microorganelle dysfunction, including hyper-fragmented mitochondria, mitochondrial oxidative stress, defective autophagy or mitophagy, and endoplasmic reticulum (ER) stress, may all contribute to VC. To facilitate the understanding of vascular calcification, across any number of bioscientific disciplines, we provide this review of a detailed updated molecular mechanism of VC. This encompasses a vascular smooth muscle phenotypic of osteogenic differentiation, and multiple signaling pathways of VC induction, including the roles of inflammation and cellular microorganelle genesis.
175 citations
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TL;DR: A recently identified claudin-low breast cancer subtype that is characterized by the enrichment of EMT and stem cell-like features is significantly associated with disease recurrence, underscoring the importance of claudins as predictors of tumor recurrence.
Abstract: Claudins are major integral membrane proteins of tight junctions. Altered expression of several claudin proteins, in particular claudin-1, -3, -4 and -7, has been linked to the development of various cancers. Although their dysregulation in cancer suggests that claudins play a role in tumorigenesis, the exact underlying mechanism remains unclear. The involvement of claudins in tumor progression was suggested by their important role in the migration, invasion and metastasis of cancer cells in a tissue-dependent manner. Recent studies have shown that they play a role in epithelial to mesenchymal transition (EMT), the formation of cancer stem cells or tumor-initiating cells (CSCs/TICs), and chemoresistance, suggesting that claudins are promising targets for the treatment of chemoresistant and recurrent tumors. A recently identified claudin-low breast cancer subtype that is characterized by the enrichment of EMT and stem cell-like features is significantly associated with disease recurrence, underscoring the importance of claudins as predictors of tumor recurrence. The critical role of epigenetic mechanisms in the regulation of claudin expression indicates the possible application of epigenetic therapy to target claudins. A better understanding of the emerging role of claudins in CSC/TICs and chemoresistance may help to develop therapies against recurrent cancers.
174 citations
Authors
Showing all 20671 results
Name | H-index | Papers | Citations |
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Hyun-Chul Kim | 176 | 4076 | 183227 |
David R. Jacobs | 165 | 1262 | 113892 |
Yang Yang | 164 | 2704 | 144071 |
Yongsun Kim | 156 | 2588 | 145619 |
Jongmin Lee | 150 | 2257 | 134772 |
Inkyu Park | 144 | 1767 | 109433 |
Christopher George Tully | 142 | 1843 | 111669 |
Teruki Kamon | 142 | 2034 | 115633 |
Manfred Paulini | 141 | 1791 | 110930 |
Kazuhiko Hara | 141 | 1956 | 107697 |
Luca Lista | 140 | 2044 | 110645 |
Dong-Chul Son | 138 | 1370 | 98686 |
Christoph Paus | 137 | 1585 | 100801 |
Frank Filthaut | 135 | 1684 | 103590 |
Andreas Warburton | 135 | 1578 | 97496 |