• The Journal of Korean Institute of Electromagnetic Engineering and Science
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• v.23 no.12
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• pp.1380-1387
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• 2012

The transmit/receive(T/R) module is a key component in the active phased array system. The brick-type T/R module has been widely used and the miniaturization has been an important factor to get the flexibility of the system configuration. For the miniaturization, multi-function chips(MFC) having a common leg configuration are suitable to reduce the number of required MMICs and a high isolation between transmit and receive paths is necessary for the high gain T/R modules. In this work, we propose a bias timing scheme for the compact T/R module and show the optimum timing based on measurements, in order to improve the feed-back path loop problem and the consequent isolation problem of the common leg configuration. We have implemented high power(7 W/channel) and high T/R gain(35 dB transmit and 30 dB receive gains) within the half size($140{\times}80{\times}16mm^3$) of the conventional T/R modules.

• 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.

• Experimental and Molecular Medicine
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• v.50 no.12
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• pp.13.1-13.12
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• 2018

We aimed to explore whether changes in circulating levels of miRNAs according to type 2 diabetes mellitus (T2DM) or prediabetes status could be used as biomarkers to evaluate the risk of developing the disease. The study included 462 patients without T2DM at baseline from the CORDIOPREV trial. After a median follow-up of 60 months, 107 of the subjects developed T2DM, 30 developed prediabetes, 223 maintained prediabetes and 78 remained disease-free. Plasma levels of four miRNAs related to insulin signaling and beta-cell function were measured by RT-PCR. We analyzed the relationship between miRNAs levels and insulin signaling and release indexes at baseline and after the follow-up period. The risk of developing disease based on tertiles (T1-T2-T3) of baseline miRNAs levels was evaluated by COX analysis. Thus, we observed higher miR-150 and miR-30a-5p and lower miR-15a and miR-375 baseline levels in subjects with T2DM than in disease-free subjects. Patients with high miR-150 and miR-30a-5p baseline levels had lower disposition index (p = 0.047 and p = 0.007, respectively). The higher risk of disease was associated with high levels (T3) of miR-150 and miR-30a-5p ($HR_{T3-T1}=4.218$ and $HR_{T3-T1}=2.527$, respectively) and low levels (T1) of miR-15a and miR-375 ($HR_{T1-T3}=3.269$ and $HR_{T1-T3}=1.604$, respectively). In conclusion, our study showed that deregulated plasma levels of miR-150, miR-30a-5p, miR-15a, and miR-375 were observed years before the onset of T2DM and pre-DM and could be used to evaluate the risk of developing the disease, which may improve prediction and prevention among individuals at high risk for T2DM.

• 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.

• Bulletin of the Korean Mathematical Society
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• v.45 no.4
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• pp.663-670
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• 2008

In this paper, the aim is to solve the neutral delay differential equations in the following form using multiquadric approximation scheme, (1) $$\{_{\;y(t)\;=\;{\phi}(t),\;\;\;\;\;t\;{\leq}\;{t_1},}^{\;y'(t)\;=\;f(t,\;y(t),\;y(t\;-\;{\tau}(t,\;y(t))),\;y'(t\;-\;{\sigma}(t,\;y(t)))),\;{t_1}\;{\leq}\;t\;{\leq}\;{t_f},}$$ where f : $[t_1,\;t_f]\;{\times}\;R\;{\times}\;R\;{\times}\;R\;{\rightarrow}\;R$ is a smooth function, $\tau(t,\;y(t))$ and $\sigma(t,\;y(t))$ are continuous functions on $[t_1,\;t_f]{\times}R$ such that t-$\tau(t,\;y(t))$ < $t_f$ and t - $\sigma(t,\;y(t))$ < $t_f$. Also $\phi(t)$ represents the initial function or the initial data. Hence, we present the advantage of using the multiquadric approximation scheme. In the sequel, presented numerical solutions of some experiments, illustrate the high accuracy and the efficiency of the proposed method even where the data points are scattered.

• Communications of the Korean Mathematical Society
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• v.16 no.4
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• pp.621-626
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• 2001

Let { $A_{>o}$ t= exp(M log t)} $_{t}$ be a dilation group where M is a real n$\times$n matrix whose eigenvalues has strictly positive real part, and let $\rho$be an $A_{t}$ -homogeneous distance function defined on ( $R^{n}$ ). Suppose that K is a function defined on ( $R^{n}$ ) such that /K(x)/$\leq$ (No Abstract.see full/text) for a decreasing function defined on (t) on R+ satisfying where wo(x)=│log│log (x)ll. For f$\in$ $L_{1}$ ( $R^{n}$ ), define f(x)=sup t>0 Kt*f(x)=t-v K(Al/tx) and v is the trace of M. Then we show that \ulcorner is a bounded operator of $L_{-{1}( $R^{n}$ ) into $L^1$,$\infty$( $R^{n}$).

• Journal of the Korean Mathematical Society
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• v.37 no.4
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• pp.521-530
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• 2000

We find the values of numerical invariants col(R) and row (R) for R=k[te, te+1, t(e-1)e-1] where k is a field and e$\geq$4. We also show that col(R) = crs (R) and row (R) = drs(R), but they are strictly less than the reduction number of R plus 1.

• Journal of Aquaculture
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• v.4 no.1
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• pp.13-18
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• 1991

In order to obtain basic biological data for effective seed production of the red sea bream, Pargus major, the influence of water temperature on egg development was investigated. The time of egg development was shorter with higher water temperature. The relationships between the water temperature($T\;:\;^{\circ}C$) and the required time(t : hour) from egg to each developmental stage were given as follows : 8-cell 1/t=0.0618T-0.5877(r=0.9899) Morula : 1/t=0.0284T-0.2556(r=0.9948) Kupffer's : 1/t=0.0076T-0.0829(r=0.9902) vesicle Hatching : 1/t=0.0031T-0.0350(r=0.9985) Biological minimium temperature for the egg development was estimated to be $10.2^{\circ}C$ in average.

• Journal of Aquaculture
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• v.10 no.3
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• pp.357-362
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• 1997

In order to obtain the basic information for seedling production of flatfish, Limanda herzensteini, the influence of water temperature and salinity on egg development was investigated. The desirable water temperature for egg hatching was9~$15^\circC$. The time of egg development was shorter with higher water temperature. The relationships between the water temperature (T:$^\circC$) and the required time (t:hour) from egg to each development stage were given as follows ; 8-cell : 1/t=0.0284T-0.0554 (r=0.9999) Morula : 1/t=0.0137T-0.0527 (r=0.9998) Kupffer's vesicle : 1/t=0.0035T-0.0133 (r=0.9762) Hatching : 1/t=0.0012T-0.0007 (r=0.9981) Biological mimimum temperature for the egg development was estimated to the be $2.6^\circC$ in average. The salinity which showed over 50% survival rate from fertilized egg to hatching was 35~$38\textperthousand$.