• Journal of the Korean Statistical Society
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• v.21 no.2
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• pp.167-177
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• 1992

In this paper, we investigate the limiting distribution of $M_n = max (X_1, X-2, \cdots, X_n)$ in the infinite moving average process ${X_t = \sum c_i Z_{t-i}}$ generated from i.i.d. negative binomial variables $Z_i$'s. While no limit result is possible, nonetheless asymptotic bounds are derived. We also present the tail behavior of $X_t$, i.e., weighted sum of i.i.d. random variables. This continues a study made by Rootzen (1986) for discrete innovation sequences.

• Structural Engineering and Mechanics
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• v.6 no.5
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• pp.529-542
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• 1998

Generalised plane strain solution is presented for simply supported, angle-ply laminated hybrid plate under cylindrical bending. The arbitrary constants in the general solution of the governing differential equations are obtained from the boundary and interface conditions. The response of hybrid plates to sinusoidal loads is obtained to illustrate the effect of the thickness parameter and the ply-angle. The classical lamination theory and the first order shear deformation theory are also assessed.

• Honam Mathematical Journal
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• v.34 no.2
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• pp.161-169
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• 2012

Let R be a commutative Noetherian ring and I, J be ideals of R. We introduced the notion of (I; J)-cominimax R-modules. For an integer $n$ and an R-module M, let $H^i_{I,J}(M)$ be an (I; J)-cominimax R-module for all $i<n$. The J-minimaxness of some Ext modules of $H^n_{I,J}(M)$ is investigated. Among of the obtaining results, there is a generalization of the main result of [1].

• Bulletin of the Korean Mathematical Society
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• v.42 no.2
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• pp.231-244
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• 2005

We derive a comparison theorem for solutions of the following stochastic partial differential equations in a Hilbert space H. $$Lu^i=\alpha(u^i)M(t,\; x)+\beta^i(u^i),\;for\;i=1,\;2,$$ $where\;Lu^i=\;\frac{\partial u^i}{\partial t}\;-\;Au^{i}$, A is a linear closed operator on Hand M(t, x) is a spatially homogeneous Gaussian noise with covariance of a certain form. We are going to show that if $\beta^1\leq\beta^2\;then\;u^1{\leq}u^2$ under some conditions.

• Journal of applied mathematics & informatics
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• v.39 no.3_4
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• pp.277-294
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• 2021

In this paper, we introduce the notions of Wijsman regularly invariant convergence types, Wijsman regularly (${\mathcal{I}}_{\sigma}$, ${\mathcal{I}}^{\sigma}_2$)-convergence, Wijsman regularly (${\mathcal{I}}^*_{\sigma}$, ${\mathcal{I}}^{{\sigma}*}_2$)-convergence, Wijsman regularly (${\mathcal{I}}_{\sigma}$, ${\mathcal{I}}^{\sigma}_2$) -Cauchy double sequence and Wijsman regularly (${\mathcal{I}}^*_{\sigma}$, ${\mathcal{I}}^{{\sigma}*}_2$)-Cauchy double sequence of sets. Also, we investigate the relationships among this new notions.

• Korean Journal of Veterinary Research
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• v.40 no.3
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• pp.489-496
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• 2000

This study was conducted to investigate the effects of streptozotocin-induced (STZ) diabetes on insulin-like growth factor-I (IGF-I), insulin-like growth factor binding proteins (IGFBPs), and IGF-I carrier proteins in serum, liver, and kidney. The levels of total and free IGF-I were measured by radioimmunoassay (RIA). The patterns of IGFBPs were determined by western ligand blotting (WLB) analysis. The profiles of IGF-I carrier proteins in serum were determined by column chromatography. The levels of total and free IGF-I in serum were lower in STZ-induced diabetic rat than normal rat (p<0.01). Similarly, the levels of total IGF-I in liver was lowered in STZ-induced diabetic rats. On the other hand, the levels of total IGF-I in kidney were increased in STZ-induced diabetic rats compared with normal rats (p<0.01). In serum and liver from STZ-induced diabetic rats, the amount of IGFBP-3 was decreased and the amount of IGFBP-2 was increased compared with normal rats. There was a not difference in amount of IGFBP-4 in serum between STZ-induced diabetic rats and normal rats. The serums of normal rats have higher 150kDa carrier proteins than in STZ-induced diabetic rats, whereas, most of 50kDa carrier proteins were found in STZ-induced diabetic rats. These results demonstrate that in STZ-induced diabetic rats, IGF-I/IGFBPs system that included functional bioactivity was changed in serum as well as tissues, and these changes may play an important role in pathogenesis of diabetes.

• Journal of KIISE:Computer Systems and Theory
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• v.26 no.11
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• pp.1318-1332
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• 1999

본 논문에서는 입출력 응용을 위해 collective I/O 기법을 기반으로 한 실행시간 시스템의 설계, 구현 그리고 그 성능평가를 기술한다. 여기서는 모든 프로세서가 동시에 I/O 요구에 따라 스케쥴링하며 I/O를 수행하는 collective I/O 방안과 프로세서들이 여러 그룹으로 묶이어, 다음 그룹이 데이터를 재배열하는 통신을 수행하는 동안 오직 한 그룹만이 동시에 I/O를 수행하는 pipelined collective I/O 등의 두 가지 설계방안을 살펴본다. Pipelined collective I/O의 전체 과정은 I/O 노드 충돌을 동적으로 줄이기 위해 파이프라인된다. 이상의 설계 부분에서는 동적으로 충돌 관리를 위한 지원을 제공한다. 본 논문에서는 다른 노드의 메모리 영역에 이미 존재하는 데이터를 재 사용하여 I/O 비용을 줄이기 위해 collective I/O 방안에서의 소프트웨어 캐슁 방안과 두 가지 모형에서의 chunking과 온라인 압축방안을 기술한다. 그리고 이상에서 기술한 방안들이 입출력을 위해 높은 성능을 보임을 기술하는데, 이 성능결과는 Intel Paragon과 ASCI/Red teraflops 기계 상에서 실험한 것이다. 그 결과 응용 레벨에서의 bandwidth는 peak point가 55%까지 측정되었다.Abstract In this paper we present the design, implementation and evaluation of a runtime system based on collective I/O techniques for irregular applications. We present two designs, namely, "Collective I/O" and "Pipelined Collective I/O". In the first scheme, all processors participate in the I/O simultaneously, making scheduling of I/O requests simpler but creating a possibility of contention at the I/O nodes. In the second approach, processors are grouped into several groups, so that only one group performs I/O simultaneously, while the next group performs communication to rearrange data, and this entire process is pipelined to reduce I/O node contention dynamically. In other words, the design provides support for dynamic contention management. Then we present a software caching method using collective I/O to reduce I/O cost by reusing data already present in the memory of other nodes. Finally, chunking and on-line compression mechanisms are included in both models. We demonstrate that we can obtain significantly high-performance for I/O above what has been possible so far. The performance results are presented on an Intel Paragon and on the ASCI/Red teraflops machine. Application level I/O bandwidth up to 55% of the peak is observed.he peak is observed.

• Communications of the Korean Mathematical Society
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• v.31 no.2
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• pp.217-227
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• 2016

Let X be a nonempty set, and let $\mathfrak{F}=\{Y_i:i{\in}I\}$ be a family of nonempty subsets of X with the properties that $X={\bigcup}_{i{\in}I}Y_i$, and $Y_i{\cap}Y_j={\emptyset}$ for all $i,j{\in}I$ with $i{\neq}j$. Let ${\emptyset}{\neq}J{\subseteq}I$, and let $T^{(J)}_{\mathfrak{F}}(X)=\{{\alpha}{\in}T(X):{\forall}i{\in}I{\exists}_j{\in}J,Y_i{\alpha}{\subseteq}Y_j\}$. Then $T^{(J)}_{\mathfrak{F}}(X)$ is a subsemigroup of the semigroup $T(X,Y^{(J)})$ of functions on X having ranges contained in $Y^{(J)}$, where $Y^{(J)}:={\bigcup}_{i{\in}J}Y_i$. For each ${\alpha}{\in}T^{(J)}_{\mathfrak{F}}(X)$, let ${\chi}^{({\alpha})}:I{\rightarrow}J$ be defined by $i{\chi}^{({\alpha})}=j{\Leftrightarrow}Y_i{\alpha}{\subseteq}Y_j$. Next, we define two congruence relations ${\chi}$ and $\widetilde{\chi}$ on $T^{(J)}_{\mathfrak{F}}(X)$ as follows: $({\alpha},{\beta}){\in}{\chi}{\Leftrightarrow}{\chi}^{({\alpha})}={\chi}^{({\beta})}$ and $({\alpha},{\beta}){\in}\widetilde{\chi}{\Leftrightarrow}{\chi}^{({\alpha})}{\mid}_J={\chi}^{({\alpha})}{\mid}_J$. We begin this paper by studying the regularity of the quotient semigroups $T^{(J)}_{\mathfrak{F}}(X)/{\chi}$ and $T^{(J)}_{\mathfrak{F}}(X)/{\widetilde{\chi}}$, and the semigroup $T^{(J)}_{\mathfrak{F}}(X)$. For each ${\alpha}{\in}T_{\mathfrak{F}}(X):=T^{(I)}_{\mathfrak{F}}(X)$, we see that the equivalence class [${\alpha}$] of ${\alpha}$ under ${\chi}$ is a subsemigroup of $T_{\mathfrak{F}}(X)$ if and only if ${\chi}^{({\alpha})}$ is an idempotent element in the full transformation semigroup T(I). Let $I_{\mathfrak{F}}(X)$, $S_{\mathfrak{F}}(X)$ and $B_{\mathfrak{F}}(X)$ be the sets of functions in $T_{\mathfrak{F}}(X)$ such that ${\chi}^{({\alpha})}$ is injective, surjective and bijective respectively. We end this paper by investigating the regularity of the subsemigroups [${\alpha}$], $I_{\mathfrak{F}}(X)$, $S_{\mathfrak{F}}(X)$ and $B_{\mathfrak{F}}(X)$ of $T_{\mathfrak{F}}(X)$.

• The KIPS Transactions:PartC
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• v.11C no.6 s.95
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• pp.843-850
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• 2004

As mobile devices prevail, requests for various services using mobile devices have increased. Requests for application services that require large data space such as multimedia, game and database [1] specifically have greatly increased. However, mobile appliances have difficulty in applying various services like a wire environment, because the storage capacity of one is not enough. Therefore, research (5) which provides remote storage service for mobile appliances using iSCSI is being conducted to overcome storage space limitations in mobile appliances. But, when iSCSI is applied to mobile appliances, iSCSI I/O performance drops rapidly if a iSCSI client moves from the server to a far away position. In the case of write operation, $28\%$ reduction of I/O performance occurred when the latency of network is 64ms. This is because the iSCSI has a structural quality that is very .sensitive to delay time. In this paper, we will introduce an intermediate target server and localize iSCSI target to improve the shortcomings of iSCSI performance dropping sharply as latency increases when mobile appliances recede from a storage server.

• Food Science of Animal Resources
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• v.24 no.2
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• pp.171-175
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• 2004

Insulin-like growth factor-I (IGF-I) rich fraction, which was obtained molecules ranged between 30 kDa and 1 kDa, was fractionated by ultrafiltration from bovine colostral whey with 30 kDa and 1 kDa membrane. IGF-I included in fractionated IGF-I rich fraction was confirmed by SDS-PAGE and western blotting and then the quantity of IGF-I was measured by ELISA. IGF-I concentration in IGF-I rich fraction was 10ng/mg protein. Effect of IGF-I rich fraction on in vitro proliferation of several cells was tested. IEC-6 cell proliferation rate was increased 60％. 53％, 30％, and 20％ at l0ng, 1ng, 0.1ng and IGF-I of IGF-I, respectively, compared to control group which was not supplemented by IGF-I rich fraction. IGF-I rich fraction stimulated in vitro proliferation of IEC-6 cell in a dose dependent manner by increasing cell number. Detroit 551 cell proliferation was enhanced 56％ and 26％ at 10ng and 1ng level of IGF-I, respectively, compared to control group. EL-4 cell and L6 cell proliferation was increased 53％ and 46％ at 10ng of IGF-I, respectively, compared to control group.