• 한국수자원학회:학술대회논문집
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• 한국수자원학회 2000년도 학술발표회 논문집
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• pp.37-47
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• 2000

The method of delays is widely used fur reconstructing chaotic attractors from experimental observations. Many studies have used a fixed delay time ${\tau}_d$ as the embedding dimension m is increased, but this is not necessarily the best choice for obtaining good convergence of the correlation dimension. Recently, some researchers have suggested that it is better to fix the delay time window ${\tau}_w$ instead. Unfortunately, ${\tau}_w$ cannot be estimated using either the autocorrelation function or the mutual information, and no standard procedure for estimating ${\tau}_w$has yet emerged. However, a new technique, called the C-C method, can be used to estimate either ${\tau}_d{\;}or{\;}{\tau}_w$. Using this method, we show that, for small data sets, fixing ${\tau}_w$, rather than ${\tau}_d$, does indeed lead to a more rapid convergence of the correlation dimension as the embedding dimension m is increased.

• 대한수학회논문집
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• 제16권4호
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• pp.585-594
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• 2001

Let η be the complex upper half plane, let h($\tau$) be a cusp form, and let $\tau$ be an imaginary quadratic in η. If h($\tau$)$\in$$\Omega$( $g_{2}$($\tau$)$^{m}$ $g_{3}$ ($\tau$)$^{ι}$with $\Omega$the field of algebraic numbers and m. l positive integers, then we show that h($\tau$) is integral over the ring Q[h/$\tau$/n/)…h($\tau$+n-1/n)] (No Abstract.see full/text)

• 한국응용약물학회:학술대회논문집
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• 한국응용약물학회 2003년도 Annual Meeting of KSAP : International Symposium on Pharmaceutical and Biomedical Sciences on Obesity
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• pp.87-87
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• 2003

Taurine (2-aminoethanesulfonic acid, $^{+}NH_3CH_2CH_2{SO_3}^{-}$) is endogenous $\beta$-amino acid which is essential in fetal nutrition and development and is present in abundant quantities in several tissues of fetus. In utero, taurine deficiency causes abnormal development and abnormal function of brain, retina, kidney and myocardium. Thus, transfer of taurine into fetus is important during embryonic development. Taurine transporter (TauT) has 12 hydrophobic membrane -spanning domains, which is typical of the $Na^{+}$- and $Cl^{-}$-dependent transporter gene family. Among the various biosynthetic enzymes of taurine, cysteine sulfinic acid decarboxylase (CSD) is the rate-limiting enzyme for biosynthesis of taurine. However, the enzyme activities of taurine biosynthesis are limited in early stage of embryonic development. To analyze the expression period of TauT and CSD during embryonic development, we have investigated the gene expression of TauT and CSD using reverse transcriptase polymerase chain reaction (RT-PCR) in mouse and chicken embryos. RT-PCR anaylsis revealed that both TauT and CSD mRNAs were already expressed at Day-4.5 in mouse embryo. In chicken whole embryo, TauT and CSD mRNAs began to appear on developing times of 48 hrs and 12 hrs, respectively. TauT mRNA was detected in the organs of heart, brain and eye of the day-3 chicken embryo. Our data show that TauT and CSD mRNAs were expressed in early stage of embryonic development.

• 대한수학회지
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• 제41권1호
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• pp.39-50
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• 2004

In [25] Taskinen shows that if $\{E_n\}_n\;and\;\{F_n\}_n$ are two sequences of Frechet spaces such that ($E_m,\;F_n$) has the BB-property for all m and n then (${\Pi}_m\;E_m,\;{\Pi}_n\;F_n$) also has the ΒΒ-property. Here we investigate when this result extends to (i) arbitrary products of Frechet spaces, (ii) countable products of DFN spaces, (iii) countable direct sums of Frechet nuclear spaces. We also look at topologies properties of ($H(U),\;\tau$) for U balanced open in a product of Frechet spaces and $\tau\;=\;{\tau}_o,\;{\tau}_{\omega}\;or\;{\tau}_{\delta}$.

• 한국데이터정보과학회:학술대회논문집
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• 한국데이터정보과학회 2005년도 춘계학술대회
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• pp.25-29
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• 2005

We analyze an M/G/1 queueing system under $P_{\lambda,\tau}^M$ service policy. By using the level crossing theory and solving the corresponding integral equations, we obtain the stationary distribution of the workload in the system explicitly.

• 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$(\frac{{X^\tau}_{u(m)}}{{X^s}_{u(n)}})$]

• Korean Journal of Mathematics
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• 제7권2호
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• pp.315-320
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• 1999

In this paper, we introduce the subsupratopology and the productsupratopology. In particular, we will show the class induced by a restricted supratopology contains the restricted class induced by the supratopology.

• Journal of applied mathematics & informatics
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• 제9권2호
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• pp.667-677
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• 2002

In this paper we obtain the matrix Tau Method representation of a general boundary value problem for Fredholm and Volterra integro-differential equations of order $\nu$. Some theoretical results are given that simplify the application of the Tau Method. The application of the Tau Method to the numerical solution of such problems is shown. Numerical results and details of the algorithm confirm the high accuracy and user-friendly structure of this numerical approach.

• Journal of the Korean Society for Industrial and Applied Mathematics
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• 제11권1호
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• pp.13-30
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• 2007

In this paper we study the numerical solutions of the stochastic functional differential equations of the following form $$du(x,\;t)\;=\;f(x,\;t,\;u_t)dt\;+\;g(x,\;t,\;u_t)dB(t),\;t\;>\;0$$ with initial data $u(x,\;0)\;=\;u_0(x)\;=\;{\xi}\;{\in}\;L^p_{F_0}\;([-{\tau},0];\;R^n)$. Here $x\;{\in}\;R^n$, ($R^n$ is the ${\nu}\;-\;dimenional$ Euclidean space), $f\;:\;C([-{\tau},\;0];\;R^n)\;{\times}\;R^{{\nu}+1}\;{\rightarrow}\;R^n,\;g\;:\;C([-{\tau},\;0];\;R^n)\;{\times}\;R^{{\nu}+1}\;{\rightarrow}\;R^{n{\times}m},\;u(x,\;t)\;{\in}\;R^n$ for each $t,\;u_t\;=\;u(x,\;t\;+\;{\theta})\;:\;-{\tau}\;{\leq}\;{\theta}\;{\leq}\;0\;{\in}\;C([-{\tau},\;0];\;R^n)$, and B(t) is an m-dimensional Brownian motion.

• 대한수학회보
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• 제46권5호
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• pp.867-871
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• 2009

A module M over a ring R is said to satisfy (P) if every generating set of M contains an independent generating set. The following results are proved; (1) Let $\tau$ = ($\mathbb{T}_\tau,\;\mathbb{F}_\tau$) be a hereditary torsion theory such that $\mathbb{T}_\tau$ $\neq$ Mod-R. Then every $\tau$-torsionfree R-module satisfies (P) if and only if S = R/$\tau$(R) is a division ring. (2) Let $\mathcal{K}$ be a hereditary pre-torsion class of modules. Then every module in $\mathcal{K}$ satisfies (P) if and only if either $\mathcal{K}$ = {0} or S = R/$Soc_\mathcal{K}$(R) is a division ring, where $Soc_\mathcal{K}$(R) = $\cap${I 4\leq$ $R_R$ : R/I$\in\mathcal{K}$}.