• Journal of the Korean Mathematical Society
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• v.48 no.1
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• pp.105-115
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• 2011

Let f be a function which assigns a positive integer f(v) to each vertex v $\in$ V (G), let r, s and t be non-negative integers. An f-coloring of G is an edge-coloring of G such that each vertex v $\in$ V (G) has at most f(v) incident edges colored with the same color. The minimum number of colors needed to f-color G is called the f-chromatic index of G and denoted by ${\chi}'_f$(G). An [r, s, t; f]-coloring of a graph G is a mapping c from V(G) $\bigcup$ E(G) to the color set C = {0, 1, $\ldots$; k - 1} such that |c($v_i$) - c($v_j$ )| $\geq$ r for every two adjacent vertices $v_i$ and $v_j$, |c($e_i$ - c($e_j$)| $\geq$ s and ${\alpha}(v_i)$ $\leq$ f($v_i$) for all $v_i$ $\in$ V (G), ${\alpha}$ $\in$ C where ${\alpha}(v_i)$ denotes the number of ${\alpha}$-edges incident with the vertex $v_i$ and $e_i$, $e_j$ are edges which are incident with $v_i$ but colored with different colors, |c($e_i$)-c($v_j$)| $\geq$ t for all pairs of incident vertices and edges. The minimum k such that G has an [r, s, t; f]-coloring with k colors is defined as the [r, s, t; f]-chromatic number and denoted by ${\chi}_{r,s,t;f}$ (G). In this paper, we present some general bounds for [r, s, t; f]-coloring firstly. After that, we obtain some important properties under the restriction min{r, s, t} = 0 or min{r, s, t} = 1. Finally, we present some problems for further research.

• Journal of the Korean Mathematical Society
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• v.37 no.4
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• pp.521-530
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• 2000

We find the values of numerical invariants col(R) and row (R) for R=k[te, te+1, t(e-1)e-1] where k is a field and e$\geq$4. We also show that col(R) = crs (R) and row (R) = drs(R), but they are strictly less than the reduction number of R plus 1.

• Journal of Animal Environmental Science
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• v.14 no.2
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• pp.81-90
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• 2008

This study was carried out to investigate the effects of the organic feed on weight gain, feed conversion rate, and carcass characteristics of Hanwoo steers. Three feeding treatments(T1 : rice straw and commercial concentrates, T2 : organic hay and concentrates, T3 : organic corn silage and concentrates) for 22 months (from 6 to 28 months) were used. As a result, weight gain was not significantly different among treatments throughout this study. Also T1 tended to improve weight gain and daily weight gain without significance. The percentage of meat quality grade over the first grads ($1,\;1^+,\;1^{++}$) were 50% in the carcass of Hanwoo steers fed T1 and T2, and 70% fed T3, respectively. T2 and T3 tended to improve marbling score and oleic acid content.

• The Pure and Applied Mathematics
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• v.2 no.2
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• pp.173-181
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• 1995

Our objective is to investigate approximate controllability of a class of partial integrodifferential systems. This work continuous the investigations of [8]. As a model for this class one may take the equation $\frac{\partialy(t,\;\xi)}{\partialt}\;=\;\frac{\partial}{\partial\xi}(a(t,\;\xi\frac{\partialy(t,\;\xi)}{\partial\xi})\;+\;F(t,\;y(t\;-\;r,\;\xi),\;{{\int_0}^t}\;k(t,\;s,\;y(s\;-\;r,\;\xi))ds)\;+\;b(\xi)u(t),\;0\;\leq\;\xi\;\leq\;1,\;\leq\;t\;\leq\;T$ with initial-boundary conditions y(t,\;0)\;=\;y(t,\;1)\;=\;0,\;0\;\leq\;t\;\leq\;T,\;y(t,\;\xi)\;=\;\phi(t,\;\xi),\;0\;\leq\;1,\;-r\;\leq\;t\;\leq\;0$.(omitted)

• Kyungpook Mathematical Journal
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• v.52 no.4
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• pp.413-431
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• 2012

Let $C^r[0,t]$ be the function space of the vector-valued continuous paths $x:[0,t]{\rightarrow}\mathbb{R}^r$ and define $X_t:C^r[0,t]{\rightarrow}\mathbb{R}^{(n+1)r}$ and $Y_t:C^r[0,t]{\rightarrow}\mathbb{R}^{nr}$ by $X_t(x)=(x(t_0),\;x(t_1),\;{\cdots},\;x(t_{n-1}),\;x(t_n))$ and $Y_t(x)=(x(t_0),\;x(t_1),\;{\cdots},\;x(t_{n-1}))$, respectively, where $0=t_0$ < $t_1$ < ${\cdots}$ < $t_n=t$. In the present paper, using two simple formulas for the conditional expectations over $C^r[0,t]$ with the conditioning functions $X_t$ and $Y_t$, we establish evaluation formulas for the analogue of the conditional analytic Fourier-Feynman transform for the function of the form $${\exp}\{{\int_o}^t{\theta}(s,\;x(s))\;d{\eta}(s)\}{\psi}(x(t)),\;x{\in}C^r[0,t]$$ where ${\eta}$ is a complex Borel measure on [0, t] and both ${\theta}(s,{\cdot})$ and ${\psi}$ are the Fourier-Stieltjes transforms of the complex Borel measures on $\mathbb{R}^r$.

• Communications of the Korean Mathematical Society
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• v.12 no.2
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• pp.393-401
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• 1997

Let $A_1,A_2,\cdots,A_m$ and $B_1,B_2,\cdots,B_n$ be two sequences of events on a given probability space. Let $X_m$ and $Y_n$, respectively, be the number of those $A_i$ and $B_j$, which occur we establish new upper and lower bounds on the probability $P(X=r, Y=t)$ which improve upper bounds and classical lower bounds in terms of the bivariate binomial moment $S_{r,t},S_{r+1,t},S_{r,t+1}$ and $S_{r+1,t+1}$.

• Journal of the Korean Mathematical Society
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• v.48 no.1
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• pp.191-205
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• 2011

It is well known that for a Krull domain R, the divisor class group of R is a torsion group if and only if every subintersection of R is a ring of quotients. Thus a natural question is that under what conditions, for a non-Krull domain R, every (t-)subintersection (resp., t-linked overring) of R is a ring of quotients or every (t-)subintersection (resp., t-linked overring) of R is at. To address this question, we introduce the notions of *-compact packedness and *-coprime packedness of (an ideal of) an integral domain R for a star operation * of finite character, mainly t or w. We also investigate the t-theoretic analogues of related results in the literature.

• Korean Journal of Mathematics
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• v.7 no.2
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• pp.167-169
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• 1999

Let R be a Noetherian domain. It is proved that $t$-dimR = 1 if and only if each (proper if R is not a valuation domain) $t$-linked overring D of R is of $t$-dimD = 1 if and only if each integrally closed $t$-linked overring of R is a Krull domain.

• Parasites, Hosts and Diseases
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• v.38 no.2
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• pp.107-110
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• 2000

We investigated the role of recombinant Toxoplasma gondii heat shock protein (rT.g.HSP) 70-full length, rT.g. HSP70-NH2-terminal region, or rT.g. HSP70-carboxy-terminal region in prophylactic immunity in C57BL/6 mice perorally infected with Fukaya cysts of T. gondii. At 3, 4, 5, and 6 weeks after infection, the number of T gondii in the brain tissue of each mouse was measured by quantitative competitive-polymerase chain reaction (QC-PCR) targeting the surface antigen (SAG) 1 gene. Immunization with rT.g.HSP70-full length or rT.g.HSP70-carboxy-terminal region increased the number of T. gondii in the brain tissue after T. gondii infection, whereas immunization with rT.g.HSP70-NHa-terminal region did not. These results suggest that T.g. HSP70-carboxy-terminal region as well as T.g.HSP70-full length may induce deleterious effects on the protective immunity of mice infected with a cyst-forming T. gondii strain, Fukaya.

• Bulletin of the Korean Mathematical Society
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• v.52 no.2
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• pp.531-540
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• 2015

Let (R, m) be a Noetherian local ring, I an ideal of R, and A an Artinian R-module. Let $k{\geq}0$ be an integer and $r=Width_{&gt;k}(I,A)$ the supremum of length of A-cosequence in dimension > k in I defined by Nhan-Hoang [8]. It is shown that for all $t{\leq}r$ the sets $$(\bigcup_{i=0}^{t}Att_R(Tor_i^R(R/I^n,A)))_{{\geq}k}\;and\\(\bigcup_{i=0}^{t}Att_R(Tor_i^R(R/(a_1^{n_1},{\cdots},a_l^{n_l}),A)))_{{\geq}k}$$ are independent of the choice of $n,n_1,{\cdots},n_l$ for any system of generators ($a_1,{\cdots},a_l$) of I.