• 대한한방부인과학회지
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• 제21권2호
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• pp.59-75
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• 2008

Purpose: This study was performed to determine the inhibitory effect of Polygonum multiflorum(PM) on melanin synthesis in B16F10. Methods: The Inhibitory effects of Polygonum multiflorum(PM) on melanin synthesis were determined by in-vitro assay. To elucidate inhibitory effects of Polygonum multiflorum on melanin synthesis, we determined the melanin release and melanin production in B16F10. And to investigate the action mechanism, we assessed the gene expression of tyrosinase, TRP-1, TRP-2, MMP-2, PKA, PKC, ERK-1 ERK-2, AKT-1, MITF in B16F10. Results: 1. PM inhibited melanin-release, melanin production in B16F10. 2. PM inhibited tyrosinase activity in vitro and in B16F10. 3. PM suppressed the expression of tyrosinase, TRP-1 in B16F10. 4. PM suppressed the expression of PKA in B16F10. 5. PM suppressed the expression of ERK-1, ERK-2, AKT-1 in B16F10. 6. PM suppressed the expression of MITF in B16F10. Conclusion: From these results, it may be concluded that PM possesses the antimelanogenetic effects.

• 한방안이비인후피부과학회지
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• 제20권3호
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• pp.1-13
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• 2007

Objective : This study was performed to assess the whitening effect of Bombysis Corpus on melanin synthesis. Methods : The whitening effects of Bombysis Corpus were examined by in vitro melanin production assay. We assessed inhibitory effects of Bombysis Corpus on melanin-release from B16F10, on melanin production in B16F10, on mushroom tyrosinase activity in vitro, on tyrosinase activity in B16F10, effect of Bombysis Corpus on the expression tyrosinase, TRP-1, PKA, ERK-1 ERK-2, AKT-1, MITF in B16F10. Results : 1. Bombysis Corpus inhibited melanin-release, melanin production in B16F10. 2. Bombysis Corpus inhibited tyrosinase activity in vitro and in B16F10. 3. Bombysis Corpus suppressed the expression of tyrosinase, TRP-1 in B16F10. 4. Bombysis Corpus suppressed the expression of PKA in B16F10. 5. Bombysis Corpus suppressed the expression of ERK-1, ERK-2, AKT-1 in B16F10. 6. Bombysis Corpus suppressed the expression of MITF in B16F10. Conclusion : The study shows that Bombysis Corpus inhibited melanin production on the melanogenesis.

• 한국통신학회논문지
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• 제7권4호
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• pp.156-160
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• 1982

A Comb Filter(C.F.) is constucted with a N-stages one-dimensional B.B.D.(Bucket-Brigade Device) delay line. One channel of the B.P.F. (Band Pass Filter) Bank is experimented, which includes a R.F.(Recursie Filter) using S/H circuits cascaded to the C.F. This algorithm of the C.F.B.(Comb Filter Bank) becomes the parallel spectrum analyzer circuit. The algorithm has less number of multiplication than that of FFT and improves the SNR.

• Korean Journal of Mathematics
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• 제30권3호
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• pp.467-474
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• 2022

In this article, we consider the integral operator 𝓒^b,c, which is defined as follows: $${\mathcal{C}}^{b,c}(f)(z)={\displaystyle\smashmargin{2}{\int\nolimits_{0}}^z}{\frac{f(w)*F(1,1;c;w)}{w(1-w)^{b+1-c}}}dw,$$ where * denotes the Hadamard/ convolution product of power series, F(a, b; c; z) is the classical hypergeometric function with b, c > 0, b + 1 > c and f(0) = 0. We investigate the boundedness of the 𝓒^b,c operators on Bloch spaces.

• 대한수학회보
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• 제40권3호
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• pp.457-464
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• 2003

Given a Riemannian manifold (M, $\alpha$) with an almost Hermitian structure f and a non-vanishing covariant vector field b, consider the generalized Randers metric $L\;=\;{\alpha}+{\beta}$, where $\beta$ is a special singular Riemannian metric defined by b and f. This metric L is called an (a, b, f)-metric. We compute the inverse and the determinant of the fundamental tensor ($g_{ij}$) of an (a, b, f)-metric. Then we determine the maximal domain D of $TM{\backslash}O$ for an (a, b, f)-manifold where a y-local Finsler structure L is defined. And then we show that any (a, b, f)-manifold is quasi-C-reducible and find a condition under which an (a, b, f)-manifold is C-reducible.

• 충청수학회지
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• 제31권1호
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• pp.29-42
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• 2018

In this paper, we investigate the stability of two functional equations f(ax+by + cz) - abf(x + y) - bcf(y + z) - acf(x + z) + bcf(y) - a(a - b - c)f(x) - b(b - a)f(-y) - c(c - a - b)f(z) = 0, f(ax+by + cz) + abf(x - y) + bcf(y - z) + acf(x - z) - a(a + b + c)f(x) - b(a + b + c)f(y) - c(a + b + c)f(z) = 0 by applying the direct method in the sense of Hyers and Ulam.

• Journal of applied mathematics & informatics
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• 제25권1_2호
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• pp.383-388
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• 2007

A (g, f)-factor F of a graph G is Called a Hamiltonian (g, f)-factor if F contains a Hamiltonian cycle. The binding number of G is defined by $bind(G)\;=\;{min}\;\{\;{\frac{{\mid}N_GX{\mid}}{{\mid}X{\mid}}}\;{\mid}\;{\emptyset}\;{\neq}\;X\;{\subset}\;V(G)},\;{N_G(X)\;{\neq}\;V(G)}\;\}$. Let G be a connected graph, and let a and b be integers such that $4\;{\leq}\;a\;<\;b$. Let g, f be positive integer-valued functions defined on V(G) such that $a\;{\leq}\;g(x)\;<\;f(x)\;{\leq}\;b$ for every $x\;{\in}\;V(G)$. In this paper, it is proved that if $bind(G)\;{\geq}\;{\frac{(a+b-5)(n-1)}{(a-2)n-3(a+b-5)},}\;{\nu}(G)\;{\geq}\;{\frac{(a+b-5)^2}{a-2}}$ and for any nonempty independent subset X of V(G), ${\mid}\;N_{G}(X)\;{\mid}\;{\geq}\;{\frac{(b-3)n+(2a+2b-9){\mid}X{\mid}}{a+b-5}}$, then G has a Hamiltonian (g, f)-factor.

• 대한가정학회지
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• 제26권2호
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• pp.1-13
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• 1988

The purpose of this study was to classify somatotype of males, to show changes of the body skin surface by the somatotype. The size of sample was 156 males between age 20 and 24. Somatotype classified into Bending somatotype, Standard somatotype, Turning over somatotype. And according to the somatotype, changing of the upper part of the body by the arm movements analyzed through gypsum experiment. The result obtained from this study were as follows; 1. the variation of the upper part of the body form by changing the am movements, by the increasing of movements, shoulder-point ws moved to be inside or upside, the anterior armpit point & armpit point were moved to the upside. 2. As a result of investigating into the rate of the expansion and contraction of the basic lines and body surface area by the arm movements, the rate of expansion and contraction of the basic lines by the arm movements, the side sea length showed the maximum rate of extension in 135 degrees, the shoulder length showed the maximum rate of contraction in 135 degrees. The rate of expansion and contraction on the body surface area by the arm movements showed the phenomenon of contraction, of items F1, F6, B1, B9 showed the phenomenon of extension, of items F3, F4, F8, F9, B8, B9. 3. According to somatotypes, items which show the significant difference were, of items f3, f8, b3, b8, F2, F7, F8, B3, B7, in all movements.

• Journal of applied mathematics & informatics
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• 제22권1_2호
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• pp.39-48
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• 2006

Let ${\gamma}$(G) be the domination number of a graph G. It is shown that for any $k {\ge} 0$ there exists a Cartesian graph bundle $B{\Box}_{\varphi}F$ such that ${\gamma}(B{\Box}_{\varphi}F) ={\gamma}(B){\gamma}(F)-2k$. The domination numbers of Cartesian bundles of two cycles are determined exactly when the fibre graph is a triangle or a square. A statement similar to Vizing's conjecture on strong graph bundles is shown not to be true by proving the inequality ${\gamma}(B{\bigotimes}_{\varphi}F){\le}{\gamma}(B){\gamma}(F)$ for strong graph bundles. Examples of graphs Band F with ${\gamma}(B{\bigotimes}_{\varphi}F) < {\gamma}(B){\gamma}(F)$ are given.

• 대한수학회논문집
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• 제12권3호
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• pp.709-715
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• 1997

For a fibration (E,B,p) with fiber F and a fiber map f, we show that if the inclusion $i : F \to E$ has a left homotopy inverse, then $G^f_n(E,F)$ is isomorphic to $G^f_n(F,E) \oplus \pi_n(B)$. In particular, by taking f as the identity map on E we have $G_n(E,F)$ is isomorphic to $G_n(F) \oplus \pi_n(B)$.