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      • Linear Combination Analysis Using GPS Data

        Park, Woon-Yong,Lee, Dong-Rak,Back, Ki-Suk,Hong, Jung-Soo 東亞大學校 建設技術硏究所 2005 硏究論文集 Vol.28 No.2

        We can process and compute the position, velocity and time by satellite signals of GPS. The signals are used to compute positioning of three dimensions and timing offset of the receiver clock when we can track the tour satellite signals at least. One of the specified aims is to use less expensive single frequency code/carrier phase GPS receivers, which are typically around half the price of dual frequency receivers. In the study, the author analyzed the accuracy and applicability of frequence linear combination using triangulation points evaluated distance limitation.

      • 박막 크로멜-알루멜 열전퇴형 교류-직류 변환기

        정인식,김호운,김진섭,이정희,이종현,신장규,박세일,권성원 경북대학교 센서기술연구소 1998 센서技術學術大會論文集 Vol.9 No.1

        A planar chromel-alumel multijunction ac-dc converter was fabricated on a LPCVD Si_(3)N_(4)/SiO_(2)/Si_(3)N_(4)-diaphragm, prepared by silicon bulk micromachining, which thermally isolated a bifilar evanohm-heater and the hot junctions of a chromel-alumel thermopile from the silicon substrate. The voltage responsivity, the ac-dc transfer error, and the fluctuation of the output thermoelectric voltage of the converter were investigated. The respective voltage responsivities in air and in a vacuum of the converter were about 3.16 mV/mW and 9.41 mV/mW. The ac-dc voltage and the current transfer errors in air were about ±1.5 ppm and ±0.7 ppm in a frequency range from 10 Hz to 10 kHz, respectively. The fluctuation of the output thermoelectric voltage from 5 seconds to 120 seconds after preheating in air for 5 seconds was about 0.06 % for a heater input of dc 1 V.

      • 세균성 질환진단 검사기술 개발동향과 임상검사에의 적용

        정운원 청주대학교 보건의료과학연구소 2019 보건의료과학연구 Vol.7 No.2

        Conventional culture-based identification systems are well standardized and widely adopted to detect and identify infectious pathogens in the microbiological diagnostics. These traditional methods as gold standard have the advantages of high sensitivity, high specificity and low cost, whereas they shows the disadvantages on intensive labor, long test time and non-growing some microorganisms that not grow in artificial medium. A fast and reliable identification of pathogens is a keyfacts in clinical diagnostics. In order to meet these problems, the new technological methods has been applied on the identification of clinically important pathogens over the last decades. Although microbiological analysis is too complexed to automate because of the various reasons, automation of culture system is becoming a reality in recent years in microbiological laboratories. Revolutionary nucleic acid analysis such as polymerase chain reaction(PCR), hybridization, sequencing and others has been increasingly used and considered to compensate or replace traditional culture-based methods in the future. Another technique is the matrix-assisted laser desorption/ionisation time of flight mass spectrometry (MALDI-TOF/MS). These new methods do not need bacterial culture to confirm the pathogens and have fast, easy and high-throughput features. Along with the more advanced technologies to be able to identify pathogens accurately, the clinical applications of them in microbial laboratories will be sustainedly performed. The recent trend of microbial diagnostic technologies and their clinical applications in microbiological laboratories would be discussed in this review.

      • 임상 분자진단에서의 Digital PCR의 유용성

        정운원 청주대학교 보건의료과학연구소 2015 보건의료과학연구 Vol.4 No.1

        In molecular diagnostics, the methodological development and application of detecting and quantifying nucleic acid has been made over the past decades. Nucleic acid analysis based polymerase chain reaction(PCR) has been dominated among various techniques, such as PCR, sequencing, microarray and others. Detection and quantification of disease-related genes gives us a important information that may be used to predict disease progression, signs of infection and the efficacy of therapeutic agent. traditional PCR is based on exponential amplification and quantification of nucleic acids may be determined by comparing the number of amplification cycles and amount of PCR product to those of a reference specimen. However, many factors can complicate the calculation of quantification, resulting in uncertainties and inaccuracies. Digital PCR is considered to have overcome the critical problems of insufficient quantification in traditional PCR. The difference between dPCR and traditional PCR lies on the measuring method for nucleic acids amounts. Absolute quantification through clonal amplification is a key factor in digital PCR. It has many possible applications which include the detection and quantification of low-level pathogens, viral load, rare allele, copy number variation, and relative gene expression. Along with the more advanced development in technology of digital PCR, the clinical applications of digital PCR will be greatly expanded. Therefore, the present review describes the principle, technological types and clinical applications of digital PCR as useful molecular diagnostic tool.

      • 비부착 텐던을 갖는 원형 PSC 돔 구조물의 시간 의존적 해석

        김운학,최정호 한경대학교 2009 論文集 Vol.41 No.-

        This study presents analytical prediction of time-dependent characteristics and behaviors of the 1/4 prestressed concrete containment vessel with unbonded tendon considering time-dependent behavior. To represent the interaction between unbonded tendon and concrete, an unbonded tendon element based on the finite element method is developed using proposed unbonded tendon model. Some numerical examples of PSC structures with unbonded tendon are carried out using unbonded element and RC shell. The numerical results are verified by comparison with reliable experimental results. The crack and damage patterns also show good agreements with experiments

      • 비부착 PS콘크리트 구조의 시간의존적 특성을 고려한 비선형 해석에 관한 연구

        최정호;김운학;박재근 한경대학교 2008 論文集 Vol.40 No.-

        This paper presents a comparative study on nonlinear analysis of the unbonded PSC structure considering time-dependent effect. For developing a finite element analysis program, an unbonded PS tendon model which can represent straight or curved unbonded tendon is proposed. The F.E. analysis program, named RCAHEST(Reinforced Concrete Analysis in Higher Evaluation System Technology), is used. Material nonlinearities of cracked concrete are taken into account by tension, compression, and shear models. And nonlinear material models for reinforcing and prestressing steels are included. These models work with models for time-dependent effect such as aging, creep and shrinkage of concrete and stress relaxation of prestressing tendon. The developed finite element analysis program is verified by comparison with reliable experimental results.

      • 임상 분자진단검사의 진단기법 동향

        정운원 청주대학교 보건의료과학연구소 2014 보건의료과학연구 Vol.3 No.1

        Over the past decades, the development and application of molecular diagnostics has been made in all fields of laboratory medicine as in vitro diagnostics. Although conventional methods are mainly used, there is an increasing trend towards molecular diagnostics. These techniques are superior to conventional ones in rapid detection, higher sensitivity and specificity. Polymerase chain reaction(PCR)-based systems has dominated in various nucleic acid-based techniques, such as PCR, sequencing, DNA microarray, lab-on-a-chip(LOC) and etc. PCR-based systems can detect the etiologic agents through the amplification of disease-related gene directly from clinical samples and have been undergone various modification for more rapid, accurate and applicable to diagnostic tests. Sequencing analysis ensures exact identification and better characterization of the etiologic agents. Some like array-based systems offer the multiparameter results where many pathogen-related markers and gene mutations can be analysed simultaneously. The development of LOC chip should allow point-of-care testing for the revolutionary improvement of healthcare. Along with the development of proteomic or metabolomic-based tests, More advanced diagnostic tools will expand the applications of molecular diagnostic testing. The user-friendly automation about both the high throughput and the use of minimal quantity of sample makes these technologies more widely available.

      • DNA Microarray를 이용한 인유두종 바이러스(Human Papilloma Virus:HPV)의 진단

        정운원,이승관,이창규,조경진,김성욱 高麗大學校 倂設 保健大學 保健科學硏究所 2001 保健科學論集 Vol.27 No.1

        Human papillomavirus(HPV) has been known as one of the important pathogenic agent in uterine cervical carcinoma. The molecular works such as PCR enable the detection of large number of HPV genotypes obtained from viginal swab. Many of the PCR-based methods for HPV detection involve an amplification step followed by any of a number of methods for distinguishing different HPV types. In this study, we adopted the DNA chip technology enabling a HPV type-specific differentiation both low-risk group(type-6, 11, 34, 40, 42, 43, and 44) and high-risk group(type-16, 18, 31, 33, 35, 39, 45, 51,52,54, 56, and 58). MY09/MY11 and GP5+/GP6+primers covered LI region are used in nested PCR to improve PCR amplification. HPV type-specific probes for DNA chip were modified with NH2-C6, followed by spotting on silylated slides, washing slides and hybridization with each PCR products. Of 163 DNA samples chosen randomly, 42 samples were negative, 8 ones for low-risk group of HPV and 96 ones for high-risk group of HPV. Especially, co-infections with various HPVs were shown in 17 samples. A recent study found that multiple HPV is a factor in persistent HPV infection, resulting in the development of cervical dysplasia. This result emphasized the necessity to detect multiple HPV infection. The application of DNA-chip to determinate specific HPV typing will be a stronger candidate than any other PCR-based methods. Furthermore, the sequencing data of the positive PCR products were shown no discrepancy with DNA chip results. This means that DNA chip is very useful tool for both HPV detection and typing.

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