• 한국항공운항학회지
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• 제16권4호
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• pp.12-19
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• 2008

GIOVE-B is the second experimental Galileo satellite for the Galileo In-Orbit Validation, which was launched by a Soyuz/Fregat rocket departing from the Baikonur cosmodrome in Kazakhstan on 27 April and now operated successfully. This paper presents the results obtained from processing of the E5a signal transmitted from the GIOVE-B. The acquisition and tracking of the data and pilot channels are performed by the E5a software receiver implemented by ETRI. Moreover, the paper suggests the GIOVE-B E5a-I/E5a-Q secondary code, which is determined by analyzing the correlation output of the primary correlator using the primary code.

• 대한원격탐사학회:학술대회논문집
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• 대한원격탐사학회 2004년도 Proceedings of ISRS 2004
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• pp.457-459
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• 2004

The Channel Coding Unit (CCU) is an integral component of Payload Data Transmission System (PDTS) for the Multi-Spectral Camera (MSC) data. The main function of the CCU is channel coding and encryption. CCU has two channels (I & Q) for data processing. The input of CCU is the output of DCSU (Data Compression & Storage Unit). The output of CCU is the input of QTX which modulate data for RF communication. In this paper, there are the overview, short H/W description and operation concept of CCU.

• 한국항해항만학회:학술대회논문집
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• 한국항해항만학회 2006년도 International Symposium on GPS/GNSS Vol.2
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• pp.395-398
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• 2006

In this paper, for implementing a real-time software GNSS receiver we propose the highly efficient and fast algorithms such as partial down-conversion, phase rotator, composite I&Q accumulation, Virtual DCO technique, and parallel acquisition using FFT. When the proposed algorithms are used, more 30 tracking channels with 3 tracking arm(early-prompt-late) is operated real-time on Intel 2.8GHz personal computer. Also, the partial down-conversion reduces the FFT size, for parallel acquisition, to 1/8 of conventional FFT-size and the program size includes map is not exceed 1Mbyte. Finally, the proposed real-time software GNSS receiver using the proposed algorithms provides the navigation solution with below 10 meter rms error.

• 고려인삼학회:학술대회논문집
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• 고려인삼학회 2002년도 학술대회지
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• pp.66-83
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• 2002

Recently, we have provided evidence that ginsenosides, the active components of Panax ginseng, utilize pertussis toxin (PTX)-insensitive $G{\alpha}_{q/11}-phospholipase\;C-{\beta}3(PLC-{\beta}3)$ signal transduction pathway for the enhancement of $Ca^{2+}-activated\;Cl^{-}$ current in the Xenopus oocyte (British J. Pharmacol. 132, 641-647, 2001; JBC 276, 48797-48802, 2001). Other investigators have shown that stimulation of receptors linked to $G{\alpha}-PLC$ pathway inhibits the activity of G proteincoupled inwardly rectifying $K^+$ (GIRK) channel. In the present study, we sought to determine whether ginsenosides influenced the activity of GIRK 1 and GIRK 4 (GIRK 1/4) channels expressed in the Xenopus oocyte, and if so, the underlying signal transduction mechanism. In oocyte injected with GIRK 1/4 channel cRNAs, bath-applied ginsenosides inhibited high potassium (HK) solution-elicited GIRK current $(EC_{50}:4.9{\pm}4.3\;{\mu}g/ml).$ Pretreatment of the oocyte with PTX reduced the HK solution-elicited GIRK current by $49\%,$ but it did not alter the inhibitory ginsenoside effect on GIRK current. Prior intraoocyte injection of cRNA(s) coding $G{\alpha}_q,\;G{\alpha}_{11}\;or\;G{\alpha}_q/G{\alpha}_{11},\;but\;not\;G{\alpha}_{i2}\;or\;G{\alpha}_{oA}$ attenuated the inhibitory ginsenoside effect. Injection of cRNAs coding $G{\beta}_{1{\gamma}2}$ also attenuated the ginsenoside effect. Similarly, injection of the cRNAs coding regulators of G protein signaling 1, 2 and 4 (RGS1, RGS2 and RGS4), which interact with $G{\alpha}_i\;and/or\;G{\alpha}_{q/11}$ and stimulates the hydrolysis of GTP to GDP in active GTP-bound $G{\alpha}$ subunit, resulted in a significant reduction of ginsenoside effect on GIRK current. Preincubation of GIRK channel-expressing oocyte in PLC inhibitor (U73122) or protein kinase C (PKC) inhibitor (staurosporine or chelerythrine) blocked the inhibitory ginsenoside effect on GIRK current. On the other hand, intraoocyte injection of BAPTA, a free $Ca^{2+}$ chelator, had no significant effect on the ginsenoside action. Taken together, these results suggest that ginsenosides inhibit the activity of GIRK 1/4 channel expressed in the Xenopus oocyte through a PTX-insensitive and $G{\alpha}_{q/11}$-,PLC-and PKC-mediated signal transduction pathway.

• Molecules and Cells
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• 제38권7호
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• pp.616-623
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• 2015

P2 receptors are membrane-bound receptors for extracellular nucleotides such as ATP and UTP. P2 receptors have been classified as ligand-gated ion channels or P2X receptors and G protein-coupled P2Y receptors. Recently, purinergic signaling has begun to attract attention as a potential therapeutic target for a variety of diseases especially associated with gastroenterology. This study determined the ATP and UTP-induced receptor signaling mechanism in feline esophageal contraction. Contraction of dispersed feline esophageal smooth muscle cells was measured by scanning micrometry. Phosphorylation of $MLC_{20}$ was determined by western blot analysis. ATP and UTP elicited maximum esophageal contraction at 30 s and $10{\mu}M$ concentration. Contraction of dispersed cells treated with $10{\mu}M$ ATP was inhibited by nifedipine. However, contraction induced by $0.1{\mu}M$ ATP, $0.1{\mu}M$ UTP and $10{\mu}M$ UTP was decreased by U73122, chelerythrine, ML-9, PTX and $GDP{\beta}S$. Contraction induced by $0.1{\mu}M$ ATP and UTP was inhibited by $G{\alpha}i_3$ or $G{\alpha}q$ antibodies and by $PLC{\beta}_1$ or $PLC{\beta}_3$ antibodies. Phosphorylated $MLC_{20}$ was increased by ATP and UTP treatment. In conclusion, esophageal contraction induced by ATP and UTP was preferentially mediated by P2Y receptors coupled to $G{\alpha}i_3$ and $G{\alpha}q$ proteins, which activate $PLC{\beta}_1$ and $PLC{\beta}_3$. Subsequently, increased intracellular $Ca^{2+}$ and activated PKC triggered stimulation of MLC kinase and inhibition of MLC phosphatase. Finally, increased $pMLC_{20}$ generated esophageal contraction.

• 융합정보논문지
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• 제9권8호
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• pp.134-139
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• 2019

본 논문은 직교방식(quadrature) 디지털 고주파기억장치의 다중신호 재생성 효과를 기술하였다. 대부분의 고주파기억장치는 단일 신호를 저장한 후 재생성을 잘하지만 다중신호를 저장한 후 재생성할 경우에는 스프리어스 신호가 크게 나타난다. 직교방식 디지털 고주파기억장치는 I채널과 Q채널로 구성되어 있으며 다중신호 재생성시 스프리어스 신호를 크게 줄일 수 있다. 스프리어스 신호크기는 고주파기억장치에서 저장하는 데이터의 비트 수에 따라 달라지며, 본 논문에서는 다중신호에 대해서 고주파기억장치의 저장데이터의 비트 수에 따라 스프리어스 신호의 크기를 구해서 고주파기억장치의 용도에 따른 신호 재생성 비트 수를 구하였다. 본 연구 결과 4 비트 직교방식 디지털 고주파 기억장치는 -20dB 이하의 스프리어스 출력을 얻을 수 있어서 전자전 장비의 신호분석과 재밍장치 개발에 크게 기할 것으로 판단된다.

• 정보보호학회논문지
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• 제6권4호
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• pp.3-38
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• 1996

The mobile station shall convolutionally encode the data transmitted on the reverse traffic channel and the access channel prior to interleaving. Code symbols output from the convolutional encoder are repeated before being interleaved except the 9600 bps data rate. All the symbols are then interleaved, 64-ary orthogonal modulation, direct-sequence spreading, quadrature spreading, baseband filtering and QPSK transmission. The sync, paging, and forward traffic channel except the pilot channel in the forward CDMA channel are convolutionally encoded, block interleaved, spread with Walsh function at a fixed chip rate of 1.2288 Mcps to provide orthogonal channelization among all code channels. Following the spreading operation, the I and Q impulses are applied to respective baseband filters. After that, these impulses shall be transmitted by QPSK. Authentication in the CDMA system is the process for confirming the identity of the mobile station by exchanging information between a mobile station and the base station. The authentication scheme is to generate a 18-bit hash code from the 152-bit message length appended with 24-bit or 40-bit padding. Several techniques are proposed for the authentication data computation in this paper. To protect sensitive subscriber information, it shall be required enciphering ceratin fields of selected traffic channel signaling messages. The message encryption can be accomplished in two ways, i.e., external encryption and internal encryption.

• 한국전자파학회논문지
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• 제21권7호
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• pp.761-768
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• 2010

본 논문에서는 주파수 체배 방식을 이용하여 고해상도 영상 레이더의 광대역 파형 생성을 위한 효율적인 기법에 대한 연구를 수행하였다. 또한 직교 변조기와 주파수 체배기를 사용한 첩 변조 파형의 대역폭 확장시 발생되는 3차 혼변조 성분에 의한 스펙트럴 재성장에 대한 근본적인 원인을 분석하였다. 또한 직교 변조기의 진폭 및 위상 불균형 오차에 대한 요구 조건을 시뮬레이션을 통하여 정의하였다. 이와 같은 해석을 통하여 임펄스 응답 특성인 거리 방향 해상도, PSLR(Peak Sidelobe Ratio) 및 ISLR(Integrated Sidelobe Ratio) 특성이 악화되는 것을 최소화시킬 수 있었다. 주파수 체배기와 메모리 맵 방식을 사용한 광대역 파형 발생장치가 제작되었으며, 진폭과 위상 오차를 최소화시킴으로써 생성된 SAR 파형의 부엽에서 발생되는 스펙트럴 재성장 성분을 최소화 시키는 보상 기법이 제시되었다. 직교 변조기의 I 및 Q 채널간의 불균형 특성을 조절함으로써, 반송파 레벨을 －28.7 dBm에서 －53.4 dBm으로 억압할 수 있었으며, S-대역에서 150 MHz 대역폭의 첩 변조 파형을 X-대역에서 600 MHz 대역폭으로 성공적으로 확장시켰다. 또한 부엽에서 발생한 스펙트럴 재성장 성분들을 대략 8~9 dB 정도 줄일 수 있었다.

• 한국통신학회논문지
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• 제24권6B호
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• pp.1156-1164
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• 1999

본 논문은 최근 지상파 디지털TV 표준 방식으로 정해진 8VSB(8 Levels Vestigial Side Band) 방식의 변조기에 관련된 내용이다. 디지털TV 시스템 개발에 있어서 가장 어려운 문제점 중 하나는 위상오차를 해결하여 얼마나 디지털 신호를 왜곡 없이 사용자에게 전송할 수 있느냐\ulcorner 이다. 그러나 설계상의 문제, 환경변화, 부품의 열화등의 원인에 의해 발생될 수 있는 위상오차는 VSB 방식의 변조기에서의 I, Q 데이터에 왜곡을 일으키게 하거나, 1KW 이상의 송신을 하는 방송 장비에 유지되어 타 인접 채널에 심각한 영향을 일으키기도 한다. 이와 관련하여 본 논문에서는 위상오차 원인 중의 하나인 8레벨의 디지털 신호에서 IF(Intermediate Frequency) 주파수대로 변환될 때에 발생되는 위상오차를 분석하였고, 이에 대한 보상 알고리듬을 제안하였고, 이를 적용한 결과를 논하였다.

• Archives of Pharmacal Research
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• 제29권11호
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• pp.977-983
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• 2006

The objective was to devise an animal model of myocardial infarction (MI) against which cardioprotective drugs might be tested. We describe the effects of nimesulide, a COX experience with development and validation of such a model. The rabbit was chosen in preference to rodents because its heart and cardiac circulation more closely resemble those of human. Thus, the cardiovascular system of anaesthetized male rabbits, 1 to 1.5 kg (n=11), was stressed by a single bolus intravenous injection of isoprenaline (ISP), 65 mg/kg. The effects of the injection were followed for sixteen days and were evaluated in four ways: 1) measurements of creatinine kinase isozyme and troponin-I (TPI) in serum 2) Electrocardiographic (ECG) changes (ST elevation and Q wave development) 3) Cardiac histopathology observed in tissue sections of the isolated of the heart. The histopathological analysis showed that rabbit heart on 2nd day after ISP injection showed changes of coagulation necrosis. Day 4 total coagulation with the loss of nuclear and striation associated with heavy interstitial infiltrate of neutrophils was found. Day 8 after infarction showed collagen deposition with capillary channels in between the remaining islands of myocytes in the infarcted area. On the 16th day scarring was complete. Coronary perfusion rates (CPR) and heart rate (HR) of the infarcted and nimesulide (a COX-2 inhibitor) treated rabbits displayed significant improvement (n=11) on each corresponding day after infarction as compared to the infarcted and saline treated rabbits (P<0.05). All four indices revealed similarities with effects commonly associated with MI in humans.