• 대한수학회지
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• 제42권1호
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• pp.53-63
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• 2005

Let R be a ring R and ${\sigma}$ be an endomorphism of R. R is called ${\sigma}$-rigid (resp. reduced) if $a{\sigma}r(a) = 0 (resp{\cdot}a^2 = 0)$ for any $a{\in}R$ implies a = 0. An ideal I of R is called a ${\sigma}$-ideal if ${\sigma}(I){\subseteq}I$. R is called ${\sigma}$-quasi-Baer (resp. right (or left) ${\sigma}$-p.q.-Baer) if the right annihilator of every ${\sigma}$-ideal (resp. right (or left) principal ${\sigma}$-ideal) of R is generated by an idempotent of R. In this paper, a skew polynomial ring A = R[$x;{\sigma}$] of a ring R is investigated as follows: For a ${\sigma}$-rigid ring R, (1) R is ${\sigma}$-quasi-Baer if and only if A is quasi-Baer if and only if A is $\={\sigma}$-quasi-Baer for every extended endomorphism $\={\sigma}$ on A of ${\sigma}$ (2) R is right ${\sigma}$-p.q.-Baer if and only if R is ${\sigma}$-p.q.-Baer if and only if A is right p.q.-Baer if and only if A is p.q.-Baer if and only if A is $\={\sigma}$-p.q.-Baer if and only if A is right $\={\sigma}$-p.q.-Baer for every extended endomorphism $\={\sigma}$ on A of ${\sigma}$.

• Asian Pacific Journal of Cancer Prevention
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• 제14권1호
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• pp.139-143
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• 2013

Patients at the same pathological stage of esophageal cancer (EC) that received the same surgical therapy by the same surgeon may have distinct prognoses. The current study aimed to explore the possibility of differentially-expressed microRNAs (miRNAs) underlying this phenomenon. Samples were collected from EC patients at the same tumor node metastasis (TNM) stage but with different prognoses. Paracancerous normal tissues were taken as controls. The specimens were histopathologically analyzed. Differentially-expressed miRNAs were analyzed using real-time quantitative reverse transcription polymerase chain reaction. Compared with patients with poor prognosis, those with good prognosis exhibited 88 two-fold or more than two-fold increased miRNA fragments and 4 half-decreased miRNAs. The most noticeably up-regulated miRNAs included hsa-miR-31, hsa-miR-196b, hsa-miR-652, hsa-miR-125a-5p, hsa-miR-146b, hsa-miR-200c, hsa-miR-23b, hsa-miR-29a, hsa-miR-186, hsa-miR-205, hsa-miR-376a, hsa-miR-410, hsa-miR-532-3p, and hsa-miR-598, whereas the most significantly-downregulated miRNAs were hsa-let-7e, hsa-miR-130b, and hsa-miR-103. EC patients at same TNM stage but with different prognoses show differentially-expressed miRNAs.

• 대한수학회보
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• 제57권1호
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• pp.167-177
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• 2020

Let I be an ideal of Noetherian local ring (R, m) and M an artinian R-module. In this paper, we study colocalization of local homology modules. In fact we give Colocal-global Principle for the artinianness and minimaxness of local homology modules, which is a dual case of Local-global Principle for the finiteness of local cohomology modules. We define the representation dimension r^I (M) of M and the artinianness dimension a^I (M) of M relative to I by r^I (M) = inf{i ∈ ℕ₀ : H^I_i (M) is not representable}, and a^I (M) = inf{i ∈ ℕ₀ : H^I_i (M) is not artinian} and we will prove that i) a^I (M) = r^I (M) = inf{r^IR_𝖕 (_𝖕M) : 𝖕 ∈ Spec(R)} ≥ inf{a^IR_𝖕 (_𝖕M) : 𝖕 ∈ Spec(R)}, ii) inf{i ∈ ℕ₀ : H^I_i (M) is not minimax} = inf{r^IR_𝖕 (_𝖕M) : 𝖕 ∈ Spec(R) ∖ {𝔪}}. Also, we define the upper representation dimension R^I (M) of M relative to I by R^I (M) = sup{i ∈ ℕ₀ : H^I_i (M) is not representable}, and we will show that i) sup{i ∈ ℕ₀ : H^I_i (M) ≠ 0} = sup{i ∈ ℕ₀ : H^I_i (M) is not artinian} = sup{R^IR_𝖕 (_𝖕M) : 𝖕 ∈ Spec(R)}, ii) sup{i ∈ ℕ₀ : H^I_i (M) is not finitely generated} = sup{i ∈ ℕ₀ : H^I_i (M) is not minimax} = sup{R^IR_𝖕 (_𝖕M) : 𝖕 ∈ Spec(R) ∖ {𝔪}}.

• 대한수학회보
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• 제56권2호
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• pp.439-450
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• 2019

Let R be a ring with unity. Given modules $M_R$ and $_RN$, $M_R$ is said to be absolutely $_RN$-pure if $M{\otimes}N{\rightarrow}L{\otimes}N$ is a monomorphism for every extension $L_R$ of $M_R$. For a module $M_R$, the subpurity domain of $M_R$ is defined to be the collection of all modules $_RN$ such that $M_R$ is absolutely $_RN$-pure. Clearly $M_R$ is absolutely $_RF$-pure for every flat module $_RF$, and that $M_R$ is FP-injective if the subpurity domain of M is the entire class of left modules. As an opposite of FP-injective modules, $M_R$ is said to be a test for flatness by subpurity (or t.f.b.s. for short) if its subpurity domain is as small as possible, namely, consisting of exactly the flat left modules. Every ring has a right t.f.b.s. module. $R_R$ is t.f.b.s. and every finitely generated right ideal is finitely presented if and only if R is right semihereditary. A domain R is $Pr{\ddot{u}}fer$ if and only if R is t.f.b.s. The rings whose simple right modules are t.f.b.s. or injective are completely characterized. Some necessary conditions for the rings whose right modules are t.f.b.s. or injective are obtained.

• 대한수학회보
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• 제53권4호
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• pp.1071-1085
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• 2016

For $b{\in}L^1_{loc}({\mathbb{R}}^n)$, let ${\mathcal{I}}_{\alpha}$ be the bilinear fractional integral operator, and $[b,{\mathcal{I}}_{\alpha}]_i$ be the commutator of ${\mathcal{I}}_{\alpha}$ with pointwise multiplication b (i = 1, 2). This paper shows that if the commutator $[b,{\mathcal{I}}_{\alpha}]_i$ for i = 1 or 2 is bounded from the product Morrey spaces $L^{p_1,{\lambda}_1}({\mathbb{R}}^n){\times}L^{p_2,{\lambda}_2}({\mathbb{R}}^n)$ to the Morrey space $L^{q,{\lambda}}({\mathbb{R}}^n)$ for some suitable indexes ${\lambda}$, ${\lambda}_1$, ${\lambda}_2$ and $p_1$, $p_2$, q, then $b{\in}BMO({\mathbb{R}}^n)$, as well as that the compactness of $[b,{\mathcal{I}}_{\alpha}]_i$ for i = 1 or 2 from $L^{p_1,{\lambda}_1}({\mathbb{R}}^n){\times}L^{p_2,{\lambda}_2}({\mathbb{R}}^n)$ to $L^{q,{\lambda}}({\mathbb{R}}^n)$ implies that $b{\in}CMO({\mathbb{R}}^n)$ (the closure in $BMO({\mathbb{R}}^n)$of the space of $C^{\infty}({\mathbb{R}}^n)$ functions with compact support). These results together with some previous ones give a new characterization of $BMO({\mathbb{R}}^n)$ functions or $CMO({\mathbb{R}}^n)$ functions in essential ways.

• 대한수학회보
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• 제21권1호
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• pp.1-5
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• 1984

The notion of linear 2-normed spaces was introduced by S. Gahler ([8,9,10,11]), and these space have been extensively studied by C. Diminnie, R. Ehret, S. Gahler, K. Iseki, A. White, Jr, and others. For nonzero vectors x,y in X, let V(x,y) denote the subspace of X generated by x and y. A linear 2-normed space (X,v) is said to be strictly convex ([3]) if v(x+y,z)=v(x,z)+v(y+z) and z not.mem.V(x,y) imply that y=ax for some a>0. Some characterizations of strict convexity for linear 2-normed spaces are given in [1,3,4,5,12]. Also, a linear 2-normed space (X,v) is said to be strictly 2-convex ([6]) if v(x,y)=v(x,z)=v(y,z)=1/3v(x+z, y+z)=1 implies that z=x+y. These space have been studied in [2,4,6,13]. It is easy to see that every strictly convex linear 2-normed space is always strictly 2-convex but the converse is not necessarily true. Throughout this paper, let (X,v) denote a linear 2-normed space.

• Kyungpook Mathematical Journal
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• 제46권4호
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• pp.553-563
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• 2006

Let A be a bounded linear operator acting on a Hilbert space H. The B-Weyl spectrum of A is the set ${\sigma}_{B{\omega}}(A)$ of all ${\lambda}{\in}\mathbb{C}$ such that $A-{\lambda}I$ is not a B-Fredholm operator of index 0. Let E(A) be the set of all isolated eigenvalues of A. Recently in [6] Berkani showed that if A is a hyponormal operator, then A satisfies generalized Weyl's theorem ${\sigma}_{B{\omega}}(A)={\sigma}(A)$\E(A), and the B-Weyl spectrum ${\sigma}_{B{\omega}}(A)$ of A satisfies the spectral mapping theorem. In [51], H. Weyl proved that weyl's theorem holds for hermitian operators. Weyl's theorem has been extended from hermitian operators to hyponormal and Toeplitz operators [12], and to several classes of operators including semi-normal operators ([9], [10]). Recently W. Y. Lee [35] showed that Weyl's theorem holds for algebraically hyponormal operators. R. Curto and Y. M. Han [14] have extended Lee's results to algebraically paranormal operators. In [19] the authors showed that Weyl's theorem holds for algebraically p-hyponormal operators. As Berkani has shown in [5], if the generalized Weyl's theorem holds for A, then so does Weyl's theorem. In this paper all the above results are generalized by proving that generalizedWeyl's theorem holds for the case where A is an algebraically ($p,\;k$)-quasihyponormal or an algebarically paranormal operator which includes all the above mentioned operators.

• Genomics & Informatics
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• 제19권2호
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• pp.17.1-17.13
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• 2021

Breast cancer is one of the leading causes of cancer in women all over the world and accounts for ~25% of newly observed cancers in women. Epigenetic modifications influence differential expression of genes through non-coding RNA and play a crucial role in cancer regulation. In the present study, epigenetic regulation of gene expression by in-silico analysis of histone modifications using chromatin immunoprecipitation sequencing (ChIP-Seq) has been carried out. Histone modification data of H3K4me3 from one normal-like and four breast cancer cell lines were used to predict miRNA expression at the promoter level. Predicted miRNA promoters (based on ChIP-Seq) were used as a probe to identify gene targets. Five triple-negative breast cancer (TNBC)-specific miRNAs (miR153-1, miR4767, miR4487, miR6720, and miR-LET7I) were identified and corresponding 13 gene targets were predicted. Eight miRNA promoter peaks were predicted to be differentially expressed in at least three breast cancer cell lines (miR4512, miR6791, miR330, miR3180-3, miR6080, miR5787, miR6733, and miR3613). A total of 44 gene targets were identified based on the 3'-untranslated regions of downregulated mRNA genes that contain putative binding targets to these eight miRNAs. These include 17 and 15 genes in luminal-A type and TNBC respectively, that have been reported to be associated with breast cancer regulation. Of the remaining 12 genes, seven (A4GALT, C2ORF74, HRCT1, ZC4H2, ZNF512, ZNF655, and ZNF608) show similar relative expression profiles in large patient samples and other breast cancer cell lines thereby giving insight into predicted role of H3K4me3 mediated gene regulation via the miRNA-mRNA axis.

• 한국수학교육학회지시리즈B:순수및응용수학
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• 제11권1호
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• pp.97-102
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• 2004

In this paper we establish some recurrence relations satisfied by quotient moments of upper record values from the Pareto distribution. Let ｛$X_n,n\qeq1$｝be a sequence of independent and identically distributed random variables with a common continuous distribution function(cdf) F($chi$) and probability density function(pdf) f($chi$). Let $Y_n\;=\;mas{X_1,X_2,...,X_n}$ for $ngeq1$. We say $X_{j}$ is an upper record value of {$X_{n},n\geq1$}, if $Y_{j}$＞$Y_{j-1}$,j＞1. The indices at which the upper record values occur are given by the record times ${u( n)}n,\geq1$, where u(n) = min{j｜j ＞u(n-l), $X_{j}$＞$X_{u(n-1)}$,n\qeq2$ and u(l) = 1. Suppose $X{\epsilon}PAR(\frac{1}{\beta},\frac{1}{\beta}$ then E$(\frac{{X^\tau}}_{u(m)}}{{X^{s+1}}_{u(n)})\;=\;\frac{1}{s}E$ E$(\frac{{X^\tau}}_{u(m)}{{X^s}_{u(n-1)}})$ - $\frac{(1+\betas)}{s}E(\frac{{X^\tau}_{u(m)}}{{X^s}_{u(n)}}$ and E$(\frac{{X^{\tau+1}}_{u(m)}}{{X^s}_{u(n)}})$ = $\frac{1}{(r+1)\beta}$ [E$(\frac{{X^{\tau+1}}}_u(m)}{{X^s}_{u(n-1)}})$ - E$(\frac{{X^{\tau+1}}_u(m)}}{{X^s}_{u(n-1)}})$ - (r+1)E$(\frac{{X^\tau}_{u(m)}}{{X^s}_{u(n)}})$]

• Journal of Periodontal and Implant Science
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• 제50권5호
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• pp.281-290
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• 2020

Purpose: The aim of this study was to compare microRNA (miRNA) gene expression in saliva using miRNA polymerase chain reaction (PCR) arrays in healthy and aggressive periodontitis (AP) patients. Methods: PCR arrays of 84 miRNAs related to the human inflammatory response and autoimmunity from the saliva samples of 4 patients with AP and 4 healthy controls were performed. The functions and diseases related to the miRNAs were obtained using TAM 2.0. Experimentally validated targets of differentially expressed miRNAs were obtained from mirTarBase. Gene ontology terms and pathways were analyzed using ConsensusPathDB. Results: Four downregulated miRNAs (hsa-let-7a-5p, hsa-let-7f-5p, hsa-miR-181b-5p, and hsa-miR-23b-3p) were identified in patients with AP. These miRNAs are associated with cell death and innate immunity, and they target genes associated with osteoclast development and function. Conclusions: This study is the first analysis of miRNAs in the saliva of patients with AP. Identifying discriminatory human salivary miRNA biomarkers reflective of periodontal disease in a non-invasive screening assay is crucial for the development of salivary diagnostics. These data provide a first step towards the discovery of key salivary miRNA biomarkers for AP.