• The Journal of the Institute of Internet, Broadcasting and Communication
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• v.14 no.5
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• pp.87-93
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• 2014

For n/m=qm+r, there is no simple divisibility rule for simple m=7 such that is the n multiply by m? This problem can be more complex for two or more digits of m. The Dunkels method has been known for generalized divisibility test method, but this method can not compute very large digits number that can not processed by computer. This paper suggests simple and exact divisibility method for m completely irrelevant n and m of digits. The proposed method sets $r_1=n_1n_2{\cdots}n_l(mod m)$ for $n=n_1n_2n_3{\cdots}n_k$, $m=m_1m_2{\cdots}m_l$. Then this method computes $r_i=r_{i-1}{\times}10+n_i(mod m)$, $i=2,3,{\cdots}k-l+1$ and reduces the digits of n one-by-one. The proposed method can be get the quotient and remainder with easy, fast and correct for various n,m experimental data.

• Kyungpook Mathematical Journal
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• v.56 no.1
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• pp.83-94
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• 2016

Let M and N be modules over a ring R. The purpose of this paper is to study modules M, N for which the bi-module [M, N] is regular or pi. It is proved that the bi-module [M, N] is regular if and only if a module N is semi M-projective and $Im({\alpha}){\subseteq}^{\oplus}N$ for all ${\alpha}{\in}[M,N]$, if and only if a module M is semi N-injective and $Ker({\alpha}){\subseteq}^{\oplus}N$ for all ${\alpha}{\in}[M,N]$. Also, it is proved that the bi-module [M, N] is pi if and only if a module N is direct M-projective and for any ${\alpha}{\in}[M,N]$ there exists ${\beta}{\in}[M,N]$ such that $Im({\alpha}{\beta}){\subseteq}^{\oplus}N$, if and only if a module M is direct N-injective and for any ${\alpha}{\in}[M,N]$ there exists ${\beta}{\in}[M,N]$ such that $Ker({\beta}{\alpha}){\subseteq}^{\oplus}M$. The relationship between the Jacobson radical and the (co)singular ideal of [M, N] is described.

• Communications of the Korean Mathematical Society
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• v.38 no.4
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• pp.1075-1090
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• 2023

In this paper, we study new classes of operators k-quasi (m, n)-paranormal operator, k-quasi (m, n)^*-paranormal operator, k-quasi (m, n)-class 𝒬 operator and k-quasi (m, n)-class 𝒬^* operator which are the generalization of (m, n)-paranormal and (m, n)^*-paranormal operators. We give matrix characterizations for k-quasi (m, n)-paranormal and k-quasi (m, n)^*-paranormal operators. Also we study some properties of k-quasi (m, n)-class 𝒬 operator and k-quasi (m, n)-class 𝒬^* operators. Moreover, these classes of composition operators on L² spaces are characterized.

• Bulletin of the Korean Mathematical Society
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• v.61 no.1
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• pp.1-12
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• 2024

In this paper, we introduce the notion of Gorenstein (m, n)-flat modules as an extension of (m, n)-flat left R-modules over a ring R, where m and n are two fixed positive integers. We demonstrate that the class of all Gorenstein (m, n)-flat modules forms a Kaplansky class and establish that (𝓖𝓕_m,n(R),𝓖𝓒_m,n(R)) constitutes a hereditary perfect cotorsion pair (where 𝓖𝓕_m,n(R) denotes the class of Gorenstein (m, n)-flat modules and 𝓖𝓒_m,n(R) refers to the class of Gorenstein (m, n)-cotorsion modules) over slightly (m, n)-coherent rings.

• Journal of the Korean Mathematical Society
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• v.56 no.6
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• pp.1599-1611
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• 2019

Let $m,n{\in}{\mathbb{N}}$. We represent the additive subgroups of the ring ${\mathbb{Z}}_m{\times}{\mathbb{Z}}_n$, which are also (unital) subrings, and deduce explicit formulas for $N^{(s)}(m,n)$ and $N^{(us)}(m,n)$, denoting the number of subrings of the ring ${\mathbb{Z}}_m{\times}{\mathbb{Z}}_n$ and its unital subrings, respectively. We show that the functions $(m,n){\mapsto}N^{u,s}(m,n)$ and $(m,n){\mapsto}N^{(us)}(m,n)$ are multiplicative, viewed as functions of two variables, and their Dirichlet series can be expressed in terms of the Riemann zeta function. We also establish an asymptotic formula for the sum $\sum_{m,n{\leq}x}N^{(s)}(m,n)$, the error term of which is closely related to the Dirichlet divisor problem.

• Journal of the Korean Mathematical Society
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• v.33 no.3
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• pp.669-677
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• 1996

Let $M_n$ be the $C^*$-algebra of all $n \times n$ matrices over the complex field, and $P[M_m, M_n]$ the convex cone of all positive linear maps from $M_m$ into $M_n$ that is, the maps which send the set of positive semidefinite matrices in $M_m$ into the set of positive semi-definite matrices in $M_n$. The convex structures of $P[M_m, M_n]$ are highly complicated even in low dimensions, and several authors [CL, KK, LW, O, R, S, W]have considered the possibility of decomposition of $P[M_m, M_n] into subcones.

• Bulletin of the Korean Mathematical Society
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• v.36 no.4
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• pp.799-808
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• 1999

We investigate when the .product of two smooth manifolds admits a weakly Lagrangian embedding. Assume M, N are oriented smooth manifolds of dimension m and n,. respectively, which admit weakly Lagrangian immersions into $C^m$ and $C^n$. If m and n are odd, then $M\;{\times}\;N$ admits a weakly Lagrangian embedding into $C^{m+n}$ In the case when m is odd and n is even, we assume further that $\chi$(N) is an even integer. Then $M\;{\times}\;N$ admits a weakly Lagrangian embedding into $C^{m+n}$. As a corollary, we obtain the result that $S^n_1\;{\times}\;S^n_2\;{\times}\;...{\times}\;S^n_k$, $\kappa$>1, admits a weakly Lagrang.ian embedding into $C^n_1+^n_2+...+^n_k$ if and only if some ni is odd.

• Journal of applied mathematics & informatics
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• v.42 no.2
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• pp.353-366
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• 2024

A total coloring of a graph G is an assignment of colors to both the vertices and edges of G, such that no two adjacent or incident vertices and edges of G are assigned the same colors. In this paper, we have discussed the total coloring of M(T_n), M(D_n), M(DT_n), M(AT_n), M(DA(T_n)), M(Q_n), M(AQ_n) and also obtained the total chromatic number of M(T_n), M(D_n), M(DT_n), M(AT_n), M(DA(T_n)), M(Q_n), M(AQ_n).

• Communications of the Korean Mathematical Society
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• v.17 no.4
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• pp.719-729
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• 2002

Consider the random n $\times$ m assignment problem with m $\geq$ $_{i,j}$ Let $u_{i,j}$ be iid uniform random variables on [0, 1] and exponential random variables with mean 1, respectively, and let $U_{n, m}$ and $T_{n, m}$ denote the optimal assignment costs corresponding to $u_{i, j}$ and $t_{i, j}$. In this paper we first give a comparison result about the discrepancy E $T_{n, m}$ -E $U_{n, m}$. Using this comparison result with a known lower bound for Var( $T_{n, m}$) we obtains a lower bound for Var( $U_{n, m}$). Finally, we study the way that E $U_{n, m}$ and E $T_{n, m}$ vary as m does. It turns out that only when m - n is large enough, the cost decreases significantly.tly.

• Journal of Acupuncture Research
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• v.22 no.3
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• pp.169-183
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• 2005

Objective : The purpose of this study was to investigate the anti-caner effect of cobrotoxin on the prostatic cancer cell line (PC-3).The goal of study is to ascertain whether cobrotoxin inhibits tile cell growth and cell cycle of PC-3, or the expression of relative genes and whether the regression of PC-3 cell growth is due to cell death or the expression of gene related to apoptosis. Methods : After the treatment of Pc-3 cells with cobrotoxin, we performed 형광현미경, MTT assay, Western blotting, Flow cytometry, PAGE electrophoresis and Surface plasmon resonance analysis to identify the cell viability, cell death, apoptosis, the changes of cell cycle and the related protein, Adk, MAP kinase. Results : 1. Compared with normal cell, the inhibition of cell growth reduced in proportion with the dose of cobrotoxin(0-16nM) in PC-3. 2. Cell viabilities of 0.1, 1, 4nM cobrotoxin treatment were decreased and those of 8, 16nM were decreased significantly. 3. S phase of cell cycle was decreased at the group of 1, 2, 4, 8, 16nM cobrotoxin, but M phase was increased at 0.1, 1, 2, 4, 8, 16nM cobrotoxin. 4. Cox-2 expression after cobrotoxin was peaked at 12hours and was decreased significantly after 6, 12, 24 hours. 5. The expression of Cdk4 was decreased dose-dependently at 1, 2, 4, 8nM cobrotoxin and was decreased siginificantly at 4, 8nM Cyclin D1 was decreased at 1, 2, 4, 8nM and Cycline E was not changed. Cycline B was decreased at 1, 2, 4, 8nM dose-dependently and was decreased siginificanlty at 2, 4, 8nM. 6. The expression of Akt was decreased at 1, 2, 4, 8nM dose-dependently and was decreased significantly at 2, 4, 8nM. 7. ERK was increased at 1, 2nM and decreased at 4, 8nM, p-ERK was increased at 1, 2, 4 nM, but decreased at 8nM. JNK and p-JNK were increased at 1, 4, 8 nM. p38 was increased at 2nM p-p38 was increased at lnM but decreased significantly at 2, 4, 8nM. 8. The nucli of normal cells were stained round and homogenous in DAPI staining, but those of PC-3 were stained condense and splitted. Apoptosis was increased dose-dependently at 2, 4, 8, 16nM and increased significantly at 2, 4, 8, 16nM. 9. Bax wasn`t changed at 1, 2, 4, 8nM and Bcl-2 was decreased significantly at 1, 2, 4, 8nM. Caspase 3 and 9 weren`t changed at 1, 2, 4nM but were decreased significantly at 8nM. Conclusions : These results indicate that cobrotoxin inhibits the growth of prostate Cancer cells, has anti-cancer effects by inducing apoptosis.