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FUZZY $\gamma$-PRECONTINUOUS MAPS

  • Lee, Enu-Pyo;Lee, Seok-Jong
    • Proceedings of the Korean Institute of Intelligent Systems Conference
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    • 1997.10a
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    • pp.73-76
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    • 1997
  • We introduce new concepts of fuzzy $\gamma$-preopen($\gamma$-preclosed) sets and fuzzy $\gamma$-precontinuous($\gamma$-preopen, $\gamma$-preclosed) maps as generalizations of the concepts of fuzzy preopen and fuzzy precontinuous of Shahna [7].

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A Study of Gamma-ray Weapon (Gamma-ray 무기 연구)

  • Han, Dong Yoon
    • Journal of the Korea Institute of Military Science and Technology
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    • v.20 no.1
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    • pp.72-80
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    • 2017
  • Gamma-ray has some advantages as a weapon: it has the ability to transmutate matter, high penetrability through materials, and it is very harmful to living things. So it is worth to study the features of gamma-ray weapon in order to utilize it. Such abilities were simulated on the basis of Monte Carlo simulation program GEANT4. For the simulation conceptual design of gamma-ray weapon was conducted. High energy electrons, which were necessary for the high energy gamma-rays, were produced by linear electron accelerator, of which the parameters were derived from the Pohang Light Source(PLS-II). Gamma-rays were get by bremsstrahlung mechanism. The spectra of gamma-rays, that were measured at distances of 500 m, 1000 m, 1500 m and 2000 m, were gained by GEANT4.

ON DOMINATION NUMBERS OF GRAPH BUNDLES

  • Zmazek Blaz;Zerovnik Janez
    • Journal of applied mathematics & informatics
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    • v.22 no.1_2
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    • pp.39-48
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    • 2006
  • Let ${\gamma}$(G) be the domination number of a graph G. It is shown that for any $k {\ge} 0$ there exists a Cartesian graph bundle $B{\Box}_{\varphi}F$ such that ${\gamma}(B{\Box}_{\varphi}F) ={\gamma}(B){\gamma}(F)-2k$. The domination numbers of Cartesian bundles of two cycles are determined exactly when the fibre graph is a triangle or a square. A statement similar to Vizing's conjecture on strong graph bundles is shown not to be true by proving the inequality ${\gamma}(B{\bigotimes}_{\varphi}F){\le}{\gamma}(B){\gamma}(F)$ for strong graph bundles. Examples of graphs Band F with ${\gamma}(B{\bigotimes}_{\varphi}F) < {\gamma}(B){\gamma}(F)$ are given.

Chemically synthesized polyester for use as biodegradable polymers (생분해성 고분자 폴리에스테르의 합성)

  • Lee, Chan Woo
    • Textile Coloration and Finishing
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    • v.8 no.4
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    • pp.19-24
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    • 1996
  • Poly(3-hydroxybutylate) 및 그들 유도체의 화학적 합성을 위해 ${\gamma}$-butyrolactone(${\gamma}$BL)과 ${\gamma}$-valerolactone(${\gamma}$VL)을 사용 ${\gamma}$-butyrolactone($\beta$BL) 과의 개환중합을 시도했다. 공중합체는 5원황 락톤 단위를 포함한 코폴리에스테르를 $BF_{3}$. $OR_{t2}$ 촉매하에서 고상(bluk state)중합에 의해 얻었고, 이러한 방법으로 합성한 코폴리머의 구조를$^{1}H NMR$$^{13}C NMR$분석법으로 결정했다. 그결과 $\beta$BL, ${\gamma}$BL과 ${\gamma}$VL의 첨가비가 증가함에 따라 수율은 저하되었고, 또한 ${\gamma}$VL의 경우 4HV의 증가가 34~35%가 한계로써, ${\gamma}$VL의 첨가비가 0.5 (${\gamma}$VL/$\beta$VL=50/50)보다 증가 할지라도 안정상태를 유지하였다.

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A NOTE ON SINGULAR QUARTIC MOMENT PROBLEM

  • Li, Chun-Ji
    • Bulletin of the Korean Mathematical Society
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    • v.37 no.1
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    • pp.91-102
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    • 2000
  • Let ${\gamma}{\equiv}{\gamma}^{(2n)}$ denote a sequence of complex numbers ${\gamma}{00},{\gamma}{01},\cdots,{\gamma}0, 2n,...,{\gamma}{2n},0\;with\; {\gamma}{00}\;>\;0,{\gamma}{ji}={{\overline}{\gamma_{ij}}}$,and let K denote a closed subset of the complex plane C. The truncated K complex moment problem entails finding a positive Borel measure $\mu$ such that ${\gamma}{ij}={\int}{{\overline}{z}}^{i}z^{j}d{\mu}\;(0{\leq}\;i+j\;{\leq}\;2n)$ and supp ${\mu}{\subseteq}\;K$. If n=2, then is called the quartic moment problem. In this paper, we give partial solutions for the singular quartic moment problem with rank M(2)=5 and ${{\overline}{Z}}Z{\in}\;<1,Z,{{\overline}{Z}},Z^{2},{{\overline}{Z}}^2>$.

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Effects of IFN-γ on IL-18 Expression in Pregnant Rats and Pregnancy Outcomes

  • Si, Li-Fang;Zhang, Shou-Yan;Gao, Chun-Sheng;Chen, Shu-Lin;Zhao, Jin;Cheng, Xiang-Chao
    • Asian-Australasian Journal of Animal Sciences
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    • v.26 no.10
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    • pp.1399-1405
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    • 2013
  • The present study focused on establishing the effects of interferon-gamma (IFN-${\gamma}$) on interleukin-18 (IL-18) expression patterns and pregnancy outcomes in pregnant rats. Pregnant rats at the post-implantation stage were randomized into control, low IFN-${\gamma}$ (L-IFN-${\gamma}$) and high IFN-${\gamma}$ groups (H-IFN-${\gamma}$) that received normal saline, 100 IU/g of IFN-${\gamma}$ and 500 IU/g of IFN-${\gamma}$ vaginal muscular injection, respectively. The effects of IFN-${\gamma}$ on IL-18 expression and pregnancy outcomes were assessed systematically using several methods, including immunohistochemistry streptavidin-perosidase (SP), image pattern analysis, enzyme-linked immune-sorbent assay (ELISA), whole blood count (WBC) count, microscopy and visual observation. IL-18 was detected in the uteri of all pregnant rats, and mainly distributed in the endometrium, decidual cells, vascular endothelium and myometrium. Immunohistochemistry and image pattern analyses revealed significantly lower IL-18 expression in the H-IFN-${\gamma}$ group compared to the L-IFN-${\gamma}$ and control groups (p<0.01), indicating that high doses of IFN-${\gamma}$ induce downregulation of IL-18 in the uterus of pregnant rats. ELISA results disclosed that IL-18 expression in peripheral blood of the H-IFN-${\gamma}$ group was lower than that of the L-IFN-${\gamma}$ group (p<0.05), and significantly reduced compared to the control group (p<0.01). Moreover, the number of peripheral leukocytes in the H-IFN-${\gamma}$ group was significantly higher than those in the control and L-IFN-${\gamma}$ groups (p<0.01). Morphology analysis showed no evident differences between the L-IFN-${\gamma}$ and control groups. However, for the H-IFN-${\gamma}$ group, uterine mucosa bleeding, necrosis and excoriation were observed using microscopy. Visual observation revealed marroon, swelling, crassitude and no embryo in the uterus, which are obvious indicators of abortion. These results indicate that IFN-${\gamma}$ plays a regulatory role in IL-18 expression in the uterus and peripheral blood of pregnant rats at the post-implantation stage. Moreover, high levels (500 IU/g) of IFN-${\gamma}$ influence normal pregnancy at the early stages in rats by downregulating IL-18 expression in the uterus and peripheral blood and increasing the number of peripheral leukocytes, consequently triggering termination of pregnancy.

Effects of cytokines in the activation of peritoneal macrophages from mice infected with Toxopluma gondii (Cytokine이 Toxoplasma감염 마우스 복강대식세포의 활성화에 미치는 영향)

  • 이영하;신대환
    • Parasites, Hosts and Diseases
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    • v.32 no.3
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    • pp.185-194
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    • 1994
  • The present study was undertaken to assess the role of cytokines in the activation of peritoneal macrophages from Toxoplasma-infected mice. Peritoneal macrophages from Toxoplasma-infected mice (10 cysts of Beverley strain/mouse) were harvested 8 weeks after infection, and incubated with the mitogen-induced lymphokine, recombinant mouse $interferon-{\gamma}(IFN-{\gamma})$, recombinant mouse tumor necrosis $factor-{\alpha}{\;}(TNF-{\alpha})$ alone or in combination with 4$IFN-{\gamma}(IFN-{\gamma}/TNF-{\alpha})$ for 24hr at 37^{\circ}C$, 5% $CO_2$. Macrophage activation was measured by the amount of $H_20_2{\;}and{\;}N0_2^{-}$ production, and antiToxoplasma activities of macrophages. $IFN-{\gamma}{\;}or{\;}IFN-{\gamma}/TNF-{\alpha}-treated$ macrophages from Toxoplasma-infected mice revealed significantly higher $H_20_2$ production than resident macrophages from Toxoplasma-infected mice. The production of $N0_2^{-}{\;}by{\;}TNF-{\alpha}-,{\;}IFN-{\gamma}-{\;}or{\;}IFN-{\gamma}/TNF-{\alpha}-treated$ macrophages from Toxoplasma-infected mice were significantly higher than that by resident macrophages, whereas lymphokine-treated group produced similar amount as that produced by resident macrophages. Anti-Toxoplasma activities of cytokinetreated macrophages from Toxoplasma-infected mice were Significantly higher than those of resident macrophages. $IFN-{\gamma}-treated$ macrophages were significantly increased production of $H_20_2{\;}and{\;}N0_2^{-}$, and anti-Toxoplasma activities of macrophages between normal and Toxoplasma-infected mice, whereas the other cytokine-treated groups were not significant differences between them. These data suggested that IFN-{\gamma}was the only one of cytokines capable of significantly activating the peritoneal macrophages from Toxoplasmainfected mice.

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Development of Automatic Gamma Optimization System for Mobile TFT-LCD (DSP를 이용한 모바일 TFT-LCD의 자동 감마 최적화 시스템 개발)

  • Cho, Nae-Soo;Ryu, Jee-Youl;Park, Chul-Woo;Kwon, Woo-Hyen
    • Journal of Institute of Control, Robotics and Systems
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    • v.15 no.3
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    • pp.323-329
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    • 2009
  • This paper presents an automatic LCD gamma control system using gamma curve optimization. It controls automatically gamma adjustment registers in mobile LCD driver IC to reduce gamma correction error and adjusting time. The proposed gamma system contains Module-Under-Test (MUT, LCD module), PC installed with program, multimedia display tester for measuring luminance, and control board for interface between PC and LCD module. Proposed algorithm and program are applicable for most of the LCD modules. It is realized to calibrate gamma values of 1.8, 2.0, 2.2 and 3.0. The control board is designed with DSP and FPGA, and it supports various interfaces such as RGB and CPU. Developed automatic gamma control system showed significantly reduced gamma adjusting time of 240 sec. and much less average gamma error of 11% than 42h and 27% with conventional manual method. We believe that the proposed system is very useful to provide high-quality LCD and to improve production process.

THE CONNECTED SUBGRAPH OF THE TORSION GRAPH OF A MODULE

  • Ghalandarzadeh, Shaban;Rad, Parastoo Malakooti;Shirinkam, Sara
    • Journal of the Korean Mathematical Society
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    • v.49 no.5
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    • pp.1031-1051
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    • 2012
  • In this paper, we will investigate the concept of the torsion-graph of an R-module M, in which the set $T(M)^*$ makes up the vertices of the corresponding torsion graph, ${\Gamma}(M)$, with any two distinct vertices forming an edge if $[x:M][y:M]M=0$. We prove that, if ${\Gamma}(M)$ contains a cycle, then $gr({\Gamma}(M)){\leq}4$ and ${\Gamma}(M)$ has a connected induced subgraph ${\overline{\Gamma}}(M)$ with vertex set $\{m{\in}T(M)^*{\mid}Ann(m)M{\neq}0\}$ and diam$({\overline{\Gamma}}(M)){\leq}3$. Moreover, if M is a multiplication R-module, then ${\overline{\Gamma}}(M)$ is a maximal connected subgraph of ${\Gamma}(M)$. Also ${\overline{\Gamma}}(M)$ and ${\overline{\Gamma}}(S^{-1}M)$ are isomorphic graphs, where $S=R{\backslash}Z(M)$. Furthermore, we show that, if ${\overline{\Gamma}}(M)$ is uniquely complemented, then $S^{-1}M$ is a von Neumann regular module or ${\overline{\Gamma}}(M)$ is a star graph.

Gamma Irradiation-reduced IFN-γ Expression, STAT1 Signals, and Cell-mediated Immunity

  • Han, Seon-Kyu;Song, Jie-Young;Yun, Yeon-Sook;Yi, Seh-Yoon
    • BMB Reports
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    • v.35 no.6
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    • pp.583-589
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    • 2002
  • The signal transducer and activator of transcription (STAT)1 is a cytoplasmic-transcription factor that is phosphorylated by Janus kinases (Jak) in response to interferon $\gamma$ (IFN-$\gamma$). The phosphorylated STAT1 translocates to the nucleus, where it turns on specific sets of IFN-$\gamma$-inducible genes, such as the interferon regulatory factor (IRF)-1. We show here that gamma irradiation reduces the IFN-$\gamma$ mRNA expression. The inhibition of the STAT1 phosphorylation and the IRF-1 expression by gamma irradiation was also observed. In contrast, the mRNA levels of IL-5 and transcription factor GATA-3 were slightly induced by gamma irradiation when compared to the non-irradiated sample. Furthermore, we detected the inhibition of cell-mediated immunity by gamma irradiation in the allogenic-mixed lymphocytes' reaction (MLR). These results postulate that gamma irradiation induces the polarized-Th2 response and interferes with STAT1 signals, thereby causing the immunosuppression of the Th1 response.