• 한국군사과학기술학회지
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• 제24권2호
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• pp.165-174
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• 2021

This study describes a method of measurement and verification of array manifold of uniform circular array antenna applicable to multistatic Passive Coherent Location(PCL) system using FM broadcasting. In an environment of outdoor test where FM broadcast signals are scattered, array manifold measurement methods using network analyzer and multi-channel digital receiver are introduced. Also, the descriptions and solutions for the test limits of each measurement method and the considerations affecting the measurement accuracy are presented. In addition, to verify the validity of the measured array manifold, the gain and phase difference were compared with the array manifold data obtained by EM simulation, and the effectiveness and accuracy of the measured array manifolds were compared and analyzed by estimating the direction of arrival of the FM broadcast signal received from the multistatic PCL system.

• 한국전자통신학회논문지
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• 제11권3호
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• pp.293-302
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• 2016

본 논문에서는 전이규칙이 모두 102인 Uniform CA(Uniform Cellular Automata, UCA) $\mathbb{C}_u$와 특성다항식이 $(x+1)^m$인 m-셀 90/150 hybrid CA $\mathbb{C}_h$를 합성한 CA의 특성을 분석한다. 먼저 $\mathbb{C}_u$로부터 유도된 여원 그룹 CA의 사이클 구조를 분석하고 이를 통해 모든 사이클의 길이가 같아지는 여원 CA의 조건을 제시한다. 그리고 $\mathbb{C}_u$와 $\mathbb{C}_h$를 합성한 CA $\mathbb{C}$의 최소다항식이 $(x+1)^q$일 때 $(T+I)^{q-1}F{\neq}0$을 만족하는 F를 여원벡터로 택하여 구성한 여원 그룹 CA $\mathbb{C}^{\prime}$의 사이클 구조를 분석한다.

• 대한의생명과학회지
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• 제13권3호
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• pp.239-244
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• 2007

Hoxc8 is one of the homeotic developmental control genes regulating the expression of many downstream target genes, through which animal body pattern is established during embryonic development. In previous proteomics analysis, proliferating cell nuclear antigen (PCNA) which is also known as cyclin, has been implied to be regulated by Hoxc8 in F9 murine embryonic teratocarcinoma cell. When the 5' upstream region of PCNA was analyzed, it turned out to contain 20 Hox core binding sites (ATTA) in about 1.17 kbp (kilo base pairs) region ($-520{\sim}-1690$). In order to test whether this region is responsible for Hoxc8 regulation, the upstream 2.3 kbp fragment of PCNA was amplified through PCR and then cloned into the pGL3 basic vector containing a luciferase gene as a reporter. When the luciferase activity was measured in the presence of effector plasmid (pcDNA : c8) expressing murine Hoxc8, the PCNA promoter driven reporter activity was reduced. To confirm whether this reduction is due to the Hoxc8 protein, the siRNA against Hoxc8 (5'-GUA UCA GAC CUU GGA ACU A-3' and 5'-UAG UUC CAA GGU CUG AUA C-3') was prepared. Interestingly enough, siRNA treatment up regulated the luciferase activity which was down regulated by Hoxc8, indicating that Hoxc8 indeed regulates the expression of PCNA, in particular, down regulation in NIN3T3 cells. These results altogether indicate that Hoxc8 might orchestrate the pattern formation by regulating PCNA which is one of the important proteins involved in several processes such as DNA replication and methylation, chromatin remodeling, cell cycle regulation, differentiation, as well as programmed cell death.

• 한국어병학회지
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• 제22권1호
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• pp.15-21
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• 2009

White spot syndrome virus (WSSV) is a strong causative agent for high mortality in cultured and wild shrimps. From this study, the WSSV prevalence in marine organisms around shrimp farm as well as live feed-mediated transmission of WSSV to farmed shrimps were investigated. Based on nested-PCR method, WSSV was detected in wide array of marine organisms including Perinereis aibuhitensis (81.3% of prevalence rate, 13/16), Enedrias fangi (100%, 16/16), Ruditapes philippinarum (20%, 2/10), crab larvae (100%, 10/10), copepoda (30%, 3/10), Periophthalmus modestus (50%, 5/10), Pachygrapsus crassipes (10%, 1/10), Helice tridens (20%, 2/10) and Neomysis sp. (70%, 7/10). On the other hand, WSSV was not detected in Bullacta exarata, Uca arcuata, and Reishia clavigera. The percent prevalence of WSSV in wild shrimps, Fenneropenaeus chinensis was only 6%, but markedly increased up to 56% after a feeding trial using polychaete worms for one month, indicating that the live feed is one of significant carriers of WSSV to shrimps under practical farming conditions.