• Journal of the Korean Mathematical Society
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• v.51 no.2
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• pp.239-250
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• 2014

Let R be a commutative Noetherian (not necessarily local) ring, I an ideal of R and M a finitely generated R-module. In this paper, by computing the local cohomology modules and Ext-modules via the injective resolution of M, we proved that, if for an integer t > 0, dim$_RH_I^i(M){\leq}k$ for ${\forall}i$ < t, then $$\displaystyle\bigcup_{i=0}^{j}(Ass_RH_I^i(M))_{{\geq}k}=\displaystyle\bigcup_{i=0}^{j}(Ass_RExt_R^i(R/I^n,M))_{{\geq}k}$$ for ${\forall}j{\leq}t$ and ${\forall}n$ >0. This shows that${\bigcup}_{n>0}(Ass_RExt_R^i(R/I^n,M))_{{\geq}k}$ is a finite set for ${\forall}i{\leq}t$. Also, we prove that $\displaystyle\bigcup_{i=1}^{r}(Ass_RM/(x_1^{n_1},x_2^{n_2},{\ldots},x_i^{n_i})M)_{{\geq}k}=\displaystyle\bigcup_{i=1}^{r}(Ass_RM/(x_1,x_2,{\ldots},x_i)M)_{{\geq}k}$ if $x_1,x_2,{\ldots},x_r$ is M-sequences in dimension > k and $n_1,n_2,{\ldots},n_r$ are some positive integers. Here, for a subset T of Spec(R), set $T_{{\geq}i}=\{{p{\in}T{\mid}dimR/p{\geq}i}\}$.

• Journal of the Korean Mathematical Society
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• v.52 no.6
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• pp.1253-1270
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• 2015

Let (R, m) be a commutative Noetherian local domain, M a non-zero finitely generated R-module of dimension n > 0 and I be an ideal of R. In this paper it is shown that if $x_1,{\ldots },x_t$ ($1{\leq}t{\leq}n$) be a sub-set of a system of parameters for M, then the R-module $H^t_{(x_1,{\ldots },x_t)}$(R) is faithful, i.e., Ann $H^t_{(x_1,{\ldots },x_t)}$(R) = 0. Also, it is shown that, if $H^i_I$ (R) = 0 for all i > dim R - dim R/I, then the R-module $H^{dimR-dimR/I}_I(R)$ is faithful. These results provide some partially affirmative answers to the Lynch's conjecture in [10]. Moreover, for an ideal I of an arbitrary Noetherian ring R, we calculate the annihilator of the top local cohomology module $H^1_I(M)$, when $H^i_I(M)=0$ for all integers i > 1. Also, for such ideals we show that the finitely generated R-algebra $D_I(R)$ is a flat R-algebra.

• Bulletin of the Korean Mathematical Society
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• v.53 no.5
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• pp.1385-1394
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• 2016

Let (R, m) be a Noetherian local ring, I, J two ideals of R, and A an Artinian R-module. Let $k{\geq}0$ be an integer and $r=Width_{>k}(I,A)$ the supremum of lengths of A-cosequences in dimension > k in I defined by Nhan-Hoang [9]. It is first shown that for each $t{\leq}r$ and each sequence $x_1,{\cdots},x_t$ which is an A-cosequence in dimension > k, the set $$\Large(\bigcup^{t}_{i=0}Att_R(0:_A(x_1^{n_1},{\ldots},x_i^{n_i})))_{{\geq}k}$$ is independent of the choice of $n_1,{\ldots},n_t$. Let r be the eventual value of $Width_{>k}(0:_AJ^n)$. Then our second result says that for each $t{\leq}r$ the set $\large(\bigcup\limits_{i=0}^{t}Att_R(Tor_i^R(R/I,\;(0:_AJ^n))))_{{\geq}k}$ is stable for large n.

• Journal of the Korean Society for information Management
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• v.6 no.1
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• pp.3-14
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• 1989

The purpose of t h i s paper i s to i n v e s t i g a t e the development of academic magazines and i t s Charac t e r i s t ~ c s i n o r d e r to determine i t s function a s a means of p r e s e n t i n g t h e i r r e s u l t s of reasearch in Korea.

• 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 Society for information Management
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• v.6 no.1
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• pp.15-36
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• 1989

The r a p i d i n c r e a s e o f microcomputer technology has r e s u l t e d i n t h e broad a p p l i c a t i o n t o various f i e l d s . The purpose of t h l s paper 1s to design a computerized r e t r i e v a l system f o r nuclear information m a t e r i a l s using a microcomputer.

• Bulletin of the Korean Mathematical Society
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• v.51 no.3
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• pp.653-657
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• 2014

Let R be a commutative Noetherian ring, I and J two ideals of R, and M a finitely generated R-module. We prove that $$Ext^i{_R}(R/I,H^t{_{I,J}}(M))$$ is finitely generated for i = 0, 1 where t=inf{$i{\in}\mathbb{N}_0:H^2{_{I,J}}(M)$ is not finitely generated}. Also, we prove that $H^i{_{I+J}}(H^t{_{I,J}}(M))$ is Artinian when dim(R/I + J) = 0 and i = 0, 1.

• Journal of Plant Biology
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• v.29 no.1
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• pp.53-65
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• 1986

The montane forests of Ulreung Island, Korea, were investigated by the ZM school method. By comparing the montane forests of this island with those of Korean Peninsula and of Japan, a new order, F a g e t a l i a m u l t i n e r v i s, a new alliance, F a l g i o n m u l t i n e r v i s, a new association, H e p a t i c o-F a g e t u m m u l t i n e r v i s and Rhododendron brachycarpum-Pinus parviflora community were recognized. The H e p a t i c o - F a g e t u m m u l t i n e r v i s was further subdivided into four subassociations; Subass. of Sasa kurilensis, Subass. of Rumohra standishii, Subass. of Rhododendron brachycarpum and Subass. of typicum. Each community was described in terms of floristic, structural and environmental features.

• Bulletin of the Korean Mathematical Society
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• v.53 no.5
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• pp.1341-1352
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• 2016

Let R be a commutative Noetherian ring, ${\Phi}$ a system of ideals of R and $I{\in}{\Phi}$. In this paper among other things we prove that if M is finitely generated and $t{\in}\mathbb{N}$ such that the R-module $H^i_{\Phi}(M)$ is $FD_{{\leq}1}$ (or weakly Laskerian) for all i < t, then $H^i_{\Phi}(M)$ is ${\Phi}$-cofinite for all i < t and for any $FD_{{\leq}0}$ (or minimax) submodule N of $H^t_{\Phi}(M)$, the R-modules $Hom_R(R/I,H^t_{\Phi}(M)/N)$ and $Ext^1_R(R/I,H^t_{\Phi}(M)/N)$ are finitely generated. Also it is shown that if cd I = 1 or $dimM/IM{\leq}1$ (e.g., $dim\;R/I{\leq}1$) for all $I{\in}{\Phi}$, then the local cohomology module $H^i_{\Phi}(M)$ is ${\Phi}$-cofinite for all $i{\geq}0$. These generalize the main results of Aghapournahr and Bahmanpour [2], Bahmanpour and Naghipour [6, 7]. Also we study cominimaxness and weakly cofiniteness of local cohomology modules with respect to a system of ideals.

• Korean Journal of Microbiology
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• v.48 no.3
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• pp.180-186
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• 2012

Pseudomonas aeruginosa, a Gram-negative bacterium, is an ubiquitous and opportunistic human pathogen, which expresses many virulence factors through quorum sensing (QS) regulation. QscR, one of the QS signal receptors of P. aeruginosa, has unique features that make it possible to distinguish QscR from other QS receptors. In the present study, we focused on amino acid residues responsible for such a broad signal specificity of QscR. Thus we constructed mutant QscRs: $QscR_{T72I}$, $QscR_{R132M}$, and $QscR_{T140I}$ by substituting $72^{nd}$ threonine, $132^{nd}$ arginine, and $140^{th}$ threonine residues with isoleucine, methionine, and isoleucine, respectively by site-directed mutagenesis. When we examined the activity of these mutant QscRs, $QscR_{R132M}$ failed to respond to N-3-oxododecanoyl homoserine lactone (3OC12-HSL), but $QscR_{T72I}$ and $QscR_{T140I}$ remained the ability to respond to 3OC12-HSL despite much reduction of the sensitivity. When we treated a variety of acyl-HSLs with different structure, $QscR_{T72I}$ and $QscR_{T140I}$ showed better responsiveness to N-decanoyl HSL (C10-HSL) or N-dodecanoyl HSL (C12-HSL) that has no oxo-moiety at $3^{rd}$ carbon of acyl group than to 3OC12-HSL, and $QscR_{R132M}$ showed no responsiveness to any acyl-HSLs tested here. In addition, $QscR_{T72I}$ and $QscR_{T140I}$ were inhibited by 5f, a QscR inhibitor as similarly as wild type QscR was. These results suggest that while the $130^{th}$ arginine is crucial in both activity and acyl-HSL binding of QscR, the $72^{nd}$ and $140^{th}$ threonines are important in the activity, but they are little responsible for the discrimination of acyl-HSLs or competitive inhibitor.