• Communications of the Korean Mathematical Society
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• v.12 no.3
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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 $G_n(F) \oplus \pi_n(B)$.

• Journal of the Chungcheong Mathematical Society
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• v.8 no.1
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• pp.111-117
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• 1995

A function $f:{\Omega}{\rightarrow}X$ is called intrinsically-separable valued if there exists $E{\in}{\Sigma}$ with ${\mu}(E)=0$ such that $f({\Omega}-E)$ is a separable in X. For a given Dunford integrable function $f:{\Omega}{\rightarrow}X$ and a weakly compact operator T, we show that if f is intrinsically-separable valued, then f is Pettis integrable, and if there exists a sequence ($f_n$) of Dunford integrable and intrinsically-separable valued functions from ${\Omega}$ into X such that for each $x^*{\in}X^*$, $x^*f_n{\rightarrow}x^*f$ a.e., then f is Pettis integrable. We show that a function f is Pettis integrable if and only if for each $E{\in}{\Sigma}$, F(E) is $weak^*$-continuous on $B_{X*}$ if and only if for each $E{\in}{\Sigma}$, $M=\{x^*{\in}X^*:F(E)(x^*)=O\}$ is $weak^*$-closed.

• ALGAE
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• v.27 no.4
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• pp.235-247
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• 2012

Regardless of continuous researches, recent researches on the genus Eucampia (Bacillariophyceae) have focused mainly on E. zodiacus f. zodiacus In the present study, species of the genus Eucampia have been studied based on their morphological characteristics. Eucampia species were collected at 24 sites from July 2008 to June 2011 in Korean coastal waters. Species were mainly identified based on the shape of valve, ocellus, and aperture, along with the length and shape of the bipolar elevations. As a result, five Eucampia species were identified: Eucampia cornuta, E. groenlandica, E. zodiacus f. zodiacus, E. zodiacus f. cylindrocornis, and E. zodiacus var. cornigera. E. cornuta and E. groenlandica have long pervalvar axis length, but the others display short or moderate length. Ocellus shape of E. cornuta, E. groenlandica and E. zodiacus f. cylindrocornis are linear ribs, whereas E. zodiacus f. zodiacus and E. zodiacus var. cornigera have radial ribs with central area. E. cornuta and E. zodiacus f. cylindrocornis have long and narrow cylindrical elevations. E. groenlandica and E. zodiacus f. zodiacus have short and broad elevations with blunt tips. E. zodiacus var. cornigera has long and broad conical elevations. In terms of aperture shape, E. cornuta has large elliptical form, E. groenlandica has almost circular to rounded rectangular form, E. zodiacus f. zodiacus has narrow and elliptical rounded rectangular to a narrow lanceolate form, E. zodiacus f. cylindrocornis has almost rectangular form, and E. zodiacus var. cornigera has rounded rhombic form. On the basis of elevations in broad girdle view, 5 Eucampia taxa could be divided into 3 types: 'narrow H type', E. cornuta and E. groenlandica; 'regular H type', E. zodiacus f. cylindrocornis and E. zodiacus var. cornigera (partial); 'wide H type', E. zodiacus f. zodiacus (almost).

• Journal of Microbiology and Biotechnology
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• v.24 no.2
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• pp.287-294
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• 2014

The transcription factor E2F1 is active during G1 to S transition and is involved in the cell cycle and progression. A recent study reported that increased E2F1 is associated with DNA damage and tumor development in several tissues using transgenic models. Here, we show that E2F1 expression is regulated by tristetraprolin (TTP) in prostate cancer. Overexpression of TTP decreased the stability of E2F1 mRNA and the expression level of E2F1. In contrast, inhibition of TTP using siRNA increased the E2F1 expression. E2F1 mRNA contains three AREs within the 3'UTR, and TTP destabilized a luciferase mRNA that contained the E2F1 mRNA 3'UTR. Analyses of point mutants of the E2F1 mRNA 3'UTR demonstrated that ARE2 was mostly responsible for the TTP-mediated destabilization of E2F1 mRNA. RNA EMSA revealed that TTP binds directly to the E2F1 mRNA 3'UTR of ARE2. Moreover, treatment with siRNA against TTP increased the proliferation of PC3 human prostate cancer cells. Taken together, these results demonstrate that E2F1 mRNA is a physiological target of TTP and suggests that TTP controls proliferation as well as migration and invasion through the regulation of E2F1 mRNA stability.

• The Korean Journal of Physiology and Pharmacology
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• v.14 no.6
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• pp.391-397
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• 2010

E2F transcription factors and their target genes have been known to play an important role in cell growth control. We found that curcumin, a polyphenolic phytochemical isolated from the plant Curcuma longa, markedly suppressed E2F4 expression in HCT116 colon cancer cells. Hydrogen peroxide was also found to decrease E2F4 protein level, indicating the involvement of reactive oxygen species (ROS) in curucmin-induced downregulation of E2F4 expression. Involvement of ROS in E2F4 downregulation in response to curcumin was confirmed by the result that pretreatment of cells with N-acetylcystein (NAC) before exposure of curcumin almost completely blocked the reduction of E2F4 expression at the protein as well as mRNA level. Anti-proliferative effect of curcumin was also suppressed by NAC which is consistent to previous reports showing curcumin-superoxide production and induction of poly (ADP-ribose) polymerase (PARP) cleavage as well as apoptosis. Expression of several genes, cyclin A, p21, and p27, which has been shown to be regulated in E2F4-dependent manner and involved in the cell cycle progression was also affected by curcumin. Moreover, decreased (cyclin A) and increased (p21 and p27) expression of these E2F4 downstream genes by curcumin was restored by pretreatment of cells with NAC and E2F4 overexpression which is induced by doxycycline. In addition, E2F4 overexpression was observed to partially ameliorate curcumin-induced growth inhibition by cell viability assay. Taken together, we found curcumin-induced ROS down-regulation of E2F4 expression and modulation of E2F4 target genes which finally lead to the apoptotic cell death in HCT116 colon cancer cells, suggesting that E2F4 appears to be a novel determinant of curcumin-induced cytotoxicity.

• Kyungpook Mathematical Journal
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• v.45 no.2
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• pp.293-299
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• 2005

Let ${\cal{L}}$ be a commutative subspace lattice on a Hilbert space ${\cal{H}}$ and X and Y be operators on ${\cal{H}}$. Let $${\cal{M}}_X=\{{\sum}{\limits_{i=1}^n}E_{i}Xf_{i}:n{\in}{\mathbb{N}},f_{i}{\in}{\cal{H}}\;and\;E_{i}{\in}{\cal{L}}\}$$ and $${\cal{M}}_Y=\{{\sum}{\limits_{i=1}^n}E_{i}Yf_{i}:n{\in}{\mathbb{N}},f_{i}{\in}{\cal{H}}\;and\;E_{i}{\in}{\cal{L}}\}.$$ Then the following are equivalent. (i) There is an operator A in $Alg{\cal{L}}$ such that AX = Y, Ag = 0 for all g in ${\overline{{\cal{M}}_X}}^{\bot},A^*A=AA^*$ and every E in ${\cal{L}}$ reduces A. (ii) ${\sup}\;\{K(E, f)\;:\;n\;{\in}\;{\mathbb{N}},f_i\;{\in}\;{\cal{H}}\;and\;E_i\;{\in}\;{\cal{L}}\}\;<\;\infty,\;{\overline{{\cal{M}}_Y}}\;{\subset}\;{\overline{{\cal{M}}_X}}$and there is an operator T acting on ${\cal{H}}$ such that ${\langle}EX\;f,Tg{\rangle}={\langle}EY\;f,Xg{\rangle}$ and ${\langle}ET\;f,Tg{\rangle}={\langle}EY\;f,Yg{\rangle}$ for all f, g in ${\cal{H}}$ and E in ${\cal{L}}$, where $K(E,\;f)\;=\;{\parallel}{\sum{\array}{n\\i=1}}\;E_{i}Y\;f_{i}{\parallel}/{\parallel}{\sum{\array}{n\\i=1}}\;E_{i}Xf_{i}{\parallel}$.

• Journal of Integrative Natural Science
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• v.6 no.1
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• pp.46-52
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• 2013

In this thesis, we consider isoparametric curves of quadratic F-B$\acute{e}$zier curves. F-B$\acute{e}$zier curves unify C-B$\acute{e}$zier curves whose basis is {sint, cos t, t, 1} and H-B$\acute{e}$zier curves whose basis is {sinht, cosh t, t,1}. Thus F-B$\acute{e}$zier curves are more useful in Geometric Modeling or CAGD(Computer Aided Geometric Design). We derive the relation between the quadratic F-B$\acute{e}$zier curves and the quadratic rational B$\acute{e}$zier curves. We also obtain the geometric properties of isoparametric curve of the quadratic F-B$\acute{e}$zier curves at both end points and prove the continuity of the isoparametric curve.

• Journal of the Chungcheong Mathematical Society
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• v.23 no.4
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• pp.679-689
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• 2010

By developing and using certain operators like those initiated by Burchnall-Chaundy, the authors aim at investigating several decomposition formulas associated with the $Kamp{\acute{e}}$ de $F{\acute{e}}riet$ function $F_{2:0;0}^{0:3;3}$ [x, y]. For this purpose, many operator identities involving inverse pairs of symbolic operators are constructed. By employing their decomposition formulas, they also present a new group of integral representations of Eulerian type for the $Kamp{\acute{e}}$ de $F{\acute{e}}riet$ function $F_{2:0;0}^{0:3;3}$ [x, y], some of which include several hypergeometric functions such as $_2F_1$, $_3F_2$, an Appell function $F_3$, and the $Kamp{\acute{e}}$ de $F{\acute{e}}riet$ functions $F_{2:0;0}^{0:3;3}$ and $F_{1:0;1}^{0:2;3}$.

• Molecules and Cells
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• v.21 no.3
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• pp.356-359
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• 2006

The transcription factor E2F1 coordinates cell cycle progression and induces apoptosis in response to DNA damage stress. Aside from DNA damage, the role of E2F1 in the endoplasmic reticulum (ER) stress signaling pathways is unclear. We found that $E2F1^{-/-}$ murine embryonic fibroblasts (MEFs) are resistant to apoptosis triggered by the ER stress inducer thapsigargin. In addition, E2F1 deficiency results in enhanced phosphorylation of eukaryotic translation initiation factor $2{\alpha}$ ($elF2{\alpha}$). These results therefore indicate that E2F1 deficiency increases phosphorylation of $elF2{\alpha}$ in response to ER stress triggered by thapsigargin, and suggest that the reduction in ER stress-induced apoptosis in E2F1-deficient cells is related to the high level of $elF2{\alpha}$ phosphorylation.

• Journal of the Korean Society of Safety
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• v.18 no.3
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• pp.46-53
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• 2003

For the tensile tests of the F.E.M., microvoids are created by the boundary separation process at the martensite boundary or neighborhood and at inclusions within the fracture. to grow to the ductile dimple fracture. For the case of the M.E.F., microvoids created at the discontinuities of the martensite phase which exists at the grain boundary of the primary ferrite are grown to coalescence with the cleavage cracks induced at the interior of the ferrite, which as a result show the discontinuous brittle fracture behavior. In spite of their similar tensile strengths, the fatigue limit and the notch sensitivity of the M. E.F. is superior to those of the F.E.M., The M.E.F. is much more insensitive to notch than F.E.M. from the stress concentration factor($\alpha$).