• Korean journal of applied entomology
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• v.32 no.1
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• pp.1-23
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• 1993

A taxonomical revision of the Korean species of family Belonolaimidae has been undertaken. Twenty three species belonging to four different genera under two subfamily were reported from Korea hiteroto. Among them Tylenchorhynchus martini to T. annulatus. Merlinius acuminatus, M. brevidens, M. joctus, M. lenorus, M. nothus and M. koreanus to genus Geocenamus. M. clavicaudatus, M. macrurus, M. socialis to genus Amplimerlinius and Quinisulcius capitatus to Tylenchorhynchus capitatus were synonymized respectively. The keys of the each genera were proposed for identification. Distribution, host plants and photograps were included.

• Microbiology and Biotechnology Letters
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• v.23 no.1
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• pp.24-30
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• 1995

The effects of amino acids in growth media on the biosynthesis of Serratia marcescens biodegradative threonine dehydratase activity were examined. The enzyme activity was decreased by 44 and 34% by 10 mM isoleucine and valine, respectively, whereas it was increased approximately by 20% by 10 mM threonine. Among several metabolites tested, pyruvate increased the enzyme activity by 60% at 5 mM, but decreased the enzyme activity approximately by 20 to 70% above 20 mM. The enzyme activity was increased by 64% by 5 mM glyoxylate, whereas it decreased the enzyme activity approximately by 40 to 70% above 20 mM glyoxylate. The thiamine, monopyrrole derivative, also increased the enzyme activity by 84% at 50 $\mu $g/ml, but did not affected the enzyme activity above 300 $\mu $g/ml. cAMP increased the enzyme activity by 58% at 0.5 mM, but decreased the enzyme activity by 15% at 2 mM. These data suggested that the biosynthesis of Serratia marcescens biodegradative threonine dehydratase is regulated by concentrations of pyruvate, glyoxylate and cAMP.

• Proceedings of the Korean Information Science Society Conference
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• 2012.06d
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• pp.230-232
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• 2012

M2M 서비스는 센서 네트워크의 데이터 수집 및 제어를 넘어서는 새로운 타입의 서비스이다. M2M 서비스는 홈 네트워크 디바이스, 사용자의 스마트 디바이스, 개인 컴퓨터 등을 이용하여 스마트 환경의 감시, 관리, 그리고 제어 등을 제공하는 새로운 서비스 타입이다. 오늘날 M2M 서비스를 제공하기 위한 연구들이 진행되고 있는데, 이를 제공하기 위한 플랫폼 연구는 아직 많이 부족한 현실이다. 따라서 본 논문은 서비스 오버레이 네트워크를 이용하여 M2M 서비스를 제공하기 위한 플랫폼 구조를 제안한다. 또한 다양한 M2M 서비스들을 조합하여 새로운 서비스를 사용자에게 제공할 수 있는 서비스 컴포지션 방법 및 절차를 제안한다. 서비스 오버레이 네트워크 플랫폼을 이용한 M2M 서비스 플랫폼은 사용자에게 향상된 서비스 기능, 범용성, 호환성, 그리고 지능화 및 능동적 기능을 제공할 수 있다.

• Proceedings of the Korean Society of Precision Engineering Conference
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• 2006.05a
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• pp.345-346
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• 2006

In the future, a machine will be more improved in the form of advanced concept with collaborative ability in M2M(Machine to Machine, Mobile to Machine) environment for u-Manufacturing system. This paper tried to standardize M2M and design advanced concept machine. The M2M is front-end system for implementing autonomous ubiquitous environment. The advanced machine in M2M will be a collaborative machine with knowledge-evolutionary ability such as u-Machine(Ubiquitous machine), Vortal(Vertical Portal) machine and P2P(Peer to Peer) machine. Such advanced concept machines will be the key subject for M2M cooperation.

• Analytical Science and Technology
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• v.17 no.6
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• pp.464-469
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• 2004

Cyclic voltammetry was used for elucidating the electrochemical behavior of Ru-cupferron complex in 1 mM phosphate buffer. The optimal conditions of ruthenium were found to be 1 mM phosphate buffer solution (pH 6.0) containing 0.1 mM cupferron, scan rate of 100 mV/s. By using the plot on the reduction peak currents of linear scan voltammograms vs. ruthenium concentration, the detection limit ($3{\sigma}$) was $1.2{\times}10^{-7}M$.

• Honam Mathematical Journal
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• v.45 no.1
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• pp.123-129
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• 2023

In this paper, we introduce the reverse of the operator Davis-Choi-Jensen's inequality. Our results are employed to establish a new bound for the Furuta inequality. More precisely, we prove that, if $A,\;B{\in}{\mathcal{B}}({\mathcal{H}})$ are self-adjoint operators with the spectra contained in the interval [m, M] with m < M and A ≤ B, then for any $r{\geq}{\frac{1}{t}}>1,\,t{\in}(0,\,1)$ $A^r{\leq}({\frac{M1_{\mathcal{H}}-A}{M-m}}m^{rt}+{\frac{A-m1_{\mathcal{H}}}{M-m}}M^{rt}){^{\frac{1}{t}}}{\leq}K(m,\;M,\;r)B^r,$ where K (m, M, r) is the generalized Kantorovich constant.

• Journal of KIISE:Computer Systems and Theory
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• v.29 no.12
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• pp.665-679
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• 2002

The fault diameter of a graph G is the maximum of lengths of the shortest paths between all two vertices when there are $\chi$(G) - 1 or less faulty vertices, where $\chi$(G) is connectivity of G. In this paper, we analyze the fault diameter of recursive circulant $G(2^m,2^k)$ with $k{\geq}3$. Let $ dia_{m.k}$ denote the diameter of $G(2^m,2^k)$. We show that if $2{\leq}m,2{\leq}k, the fault diameter of $G(2{\leq}m,2{\leq}k)$ is equal to $2^m-2$, and if m=k+1, it is equal to $2^k-1$. It is also shown that for m>k+1, the fault diameter is equal to di a_$m{\neq}1$(mod 2k); otherwise, it is less than or equal to$dia_{m.k+2}$.

• Bulletin of the Korean Chemical Society
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• v.13 no.2
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• pp.158-162
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• 1992

Hydrocarbon solution of $(PPh_3)_2(CO)MOSO_2CF_3(M=Rh$, Ir)reacts rapidly with Pyrazine or 4,4'-bipyridyl to yield dinuclear metal complexes $[(PPh_3)_3(CO)M({\mu}-pyrazine)M(CO)(PPh_3)_2](SO_3CF_3)_2$ (I: M= RhH; III: M=Ir) or [$(PPh_3)_2$(CO)M(${\mu}$-44'-bipyridyl)M(CO)$(PPh_3)_2](SO_3CF_3)_2$, (II: M=Rh; IV: M=Ir), respectively. Compounds, I, II, III, and IV were characterized by $^1H-NMR$, $^{13}C-NMR$, $^{31}P-NMR$, and infrared spectrum. Ethanol solution of $(PPh_3)_2(CO)MOSO_2CF_3$ (M=Rh, Ir) also reacts with $(TBA)_2$M'$(CN)_4$ (M'=Pd, Pt) to yield trinuclear metal complexes [$(PPh_3)_2$(CO)dM-NCM'$(CN)_2$CN-M(CO)$(PPh_3)_2]$ (V : M=Rh, M'=Pd; VI : M=Rh, M'=Pt; VII: M=Ir, M'=Pd; VIII: M=Ir, M'=Pt). The trinuclear metal complexes V, VI, VII, and VIII are bridged by the cyanide groups. The infrared spectrum of V, VI, VII, and VIII supports the presence of the bridged cyanide and terminal cyanide group.

• Journal of Life Science
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• v.20 no.2
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• pp.298-303
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• 2010

In this work, the effects of $Cs^+$ on root growth of 2-day-old maize seedlings were scrutinized. CsCl (5 mM - 30 mM) decreased the fresh weight of the primary root and of the shoot above the coleoptilar node. The elongation growth of the primary root was also inhibited by CsCl. The CsCl-inhibited growth was partially restored by 60 mM KCl. Lineweaver-Burk plot of the reaction in the presence and absence of 60 mM KCl displayed competitive interaction of CsCl (at higher than 10 mM). However, the Reversal of the inhibition by 60 mM KCl did not follow the competitive relationship with 5 mM CsCl, indicating the presence of differential mechanisms of $K^+$ influence depending on the concentration of CsCl. The differential effects of CsCl dependent on the concentrations were also observed in the CsCl-evoked radial expansion of the subapical region of the root. In spite of the decrease in length of the root, shrinkage of the root apical meristem was not observed. CsCl above 10 mM induced the expression of ZmKUP1, indicating functional deficiency of $K^+$ due to competition with Cs. However, the expression of ZmKUP1 by 5 mM CsCl was unclear. Conclusively, exogenously applied $Cs^+$ decreased root elongation and fresh weight and caused radial expansion of the subapical region of the primary root in 2-day-old maize seedlings by complex mechanisms including competitive and noncompetitive interactions with $K^+$. Because the shrinkage of the root apical meristem was not observed, it is concluded that the effects of CsCl on maize root growth was mainly related to cell expansion.

• Korean Journal of Veterinary Research
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• v.14 no.2
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• pp.135-150
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• 1974

한국재내산양(韓國在來山羊) 11마리의 전지근(前肢筋)을 절개하여 관찰하였던 바 다음과 같은 결과를 얻었다. 1. 한국재내산양(韓國在來山羊)의 전지(前肢)에서는 다음과 같은 근(筋)들을 관찰할 수 있었다. 승모근(僧帽筋) M. trapezus, 릉형근(菱形筋) M. rhomboideus, 완두근(腕頭筋) M. brachiocephalicus, 쇄골하근(鎖骨下筋) M. subclavius, 견갑횡구근(肩甲橫究筋) M. omotransv-ersarius, 란배근(瀾背筋) M. latissimus dorsi, 천흉근(淺胸筋) M. pectoralis guperficialis, 탐흉근(探胸筋) M. pectorlis profundus, 복거근(腹鋸筋) M. serratus ventralis, 삼각근(三角筋) M. deltoideus, 극하근(棘下筋) M. infraspinatus, 극상근(棘上筋) M. supraspinatus, 견갑하근(肩甲下筋) M. subscapularis, 대원근(大圓筋) M. teres major, 소원근(小圓筋) M. theres minor, 전완근막장근(前腕筋膜張筋) M. tensor fascia antebrachii, 삼두완근(三頭腕筋) M. triceps brachii, 주근 M. anconeus, 이두완근(二頭腕筋) M. biceps brachii, 상완근(上腕筋) M. brachialis, 조훼완근(鳥喙腕筋) M. coracobrachialis, 요완신근(橈腕伸筋) M. extensor carpi radialis, 고유제삼지신근(固有第三指伸筋) M. extensor digiti tertii proprius, 총지신근(總指伸筋) M. extensor digitorum cemmunis 고유제사지신근(固有第四指伸筋) M. extensor digiti quartii proprius, 척완신근(尺腕伸筋) M. extensor carpi ulnaris, 장모지외전근(長母指外轉筋) M. abductor pollicis longus, 척완굴근(尺腕屈筋) M. flexor carpi ulnaris, 요완굴근(橈腕屈筋) M. flexor carpi radialis, 원회내근(圓回內筋) M. pronator teres, 천지굴근(淺指屈筋) M. flexor digitorum suprficialis, 탐지굴근(探指屈筋) M. flexor digitorum profundus, 골간근(骨間筋) M. interosseus medius. 2. 천흉근(淺胸筋)과 심흉근(深胸筋)은 각각 전부(前部)와 후부(後部)로 명확히 분리(分離)되어있으며 특히 심흉근(深胸筋)의 전부(前部)와 후부(後部)는 서로 떨어져서 기시(起始)를 하고있어 그 사이에는 흉골(胸骨)이 노출되어 있었다. 3. 쇄골하근(鎖骨下筋)은 전예(全例)에서 관찰할 수 있었다. 4. 조탁흉근(鳥啄胸筋)은 소나 양에 비하여 매우 발달하였으며 특히 3예(例)에서는 더욱 발달하여 3개의 부분(部分)으로 되어있어 상완골 내측면 거의 전체를 덮고 있었다. 5. 주근, 소원근(小圓筋) 등 소동물(小動物)에서는 작은 근(筋)들이 매우 발달하였으나 장모지외전근(長母指外轉筋)은 엷고 작았다. 6. 반추류(反芻類)에서 가끔 볼 수 있는 M. extensor pollicis는 관찰할 수 없었다.