고온에서 HAN 계열 추진제 액적의 거동에 대한 연구

황창환(Chang Hwan Hwang),백승욱(Seung Wook Baek),한조영(Cho Young Han),김수겸(Su Kyum Kim),전형열(Hyung Yeol Jeon) 한국연소학회 2012 KOSCOSYMPOSIUM논문집 Vol.- No.45

The droplet behavior of 83.9 wt.% HAN water solution was investigated experimentally with various ambient temperature and nitrogen environment. At the initial stage of evaporation under thermal decomposition temperature of HAN, gradual decreasing of droplet diameter was observed. After that, the droplet started to expand due to the internal pressure build up by water nucleation inside the droplet. The micro explosion was observed at higher temperature than the decomposition temperature of HAN and the remaining droplet showed similar behavior of single composition droplet. The decreasing rate was augmented as the ambient temperature increasing.

서울의 Penicillinase Producing Neisseria gonorrhoeae 발생빈도(1998)

김재홍,김준호,반재용,이정우,황성주,정준규,정성태,강진문,조흔정,홍창의,정혜신,이한승,김이선,이봉길,이종호,선영우,한기덕,윤성필,이성훈,안종성,박석범,문승현,조항래,김형섭,류지호,황재영,박준홍,손상욱 한양대학교 의과대학 2001 한양의대 학술지 Vol.21 No.1

In recent years, gonorrhea has been pandemic and remains one of the most common STDs in the world, especially in developing countries. For the detection of a more effective therapeutic regimen and assessing the prevalence of Penicillinase Producing Neisseria gonorrhoeae(PPNG), we have been trying to study the patients who have visited the Venereal Disease Clinic of Choong-Ku Public Health Center in Seoul since 1980 by menas of the chromogenic cephalosporin method. In 1998, 93 strians of N. genorrhoeae were isolated, among which 60(64.5%) were PPNG. The prevalence of PPNG in Seoul, which had been decreased to 39% in 1996 after a peak of 74.3% in 1993, is increased to 64.5% in 1998.

영상분석 시스템 구현(Ⅰ)

김동욱,한한수,김석경,이중,하영호,김희수 內務部 國立科學搜査硏究所 2001 國立 科學 搜査 硏究所 年報 Vol.33 No.-

野生鳥獸의 分布와 捿息密度 및 食性에 關한 硏究 -第2報-

金甲德,禹漢貞,金泰旭 서울大學校 農科大學 1980 서울대농학연구지 Vol.5 No.1

1. Birds and Mammals census by line transect (Roadside census) and food plants for birds (plants birds like the most) was made at Mt. Baek Woon, No.4 No.5 No.6 and at Mt. Chi Ak, during 18 April 1978 to 11 February 1979. 2. The number per hour and percent dominance (for the total of all species) were calculated as indices for relative abundance of each species, (Table: 4,5,6,7). 3. Distance (per Km), width (per ha.), time (per hour) and relative abundance for each species in four census areas were observed. 4. 49 species of bird recorded, Great Tit, Parus major, Brandt's Jay, Garrulus glandarius, Crow Tit, Paradoxornis webbiana, Meadow Bunting, Emberiza cioides(resident) and Naumann's Thrush, Turdus naumanni, Brambling, Fringilla montifringilla, Rustic Bunting, Emberiza rustica(winter bird) were recorded as dominant species Mt.Baek Woon. Great Tit, Parus major, Blue Magpie, Cyanopica cyane, and Crow Tit, Paradoxornis webbiana were recorded as dominant species at Mt. ChiAK. 5. Blue Magpie, Cyanopica cyane is breeding at Mt. ChiAK but at Mt. Baek Woon it was not yet observed. 6. Korean Magpie, Pica pica is no distributed four census areas. 7. Mammalian fauna in four census area is relatively low and Korean Red Fox, Vulpes vulpes Chinese Wolf, Canis lupus and Siberian Leopard, Panthera pardus had exterminated since Korean War Table: 3) 8. A few number of Korean Flying Squirrel, Petaurista leucogenys hintoni is breeding at Mt. ChiAK.

한국인 집단에서 미토콘드리아 DNA의 'Asian-specific 9-bp결실'다형현상

김욱,진한준 단국대학교 1999 論文集 Vol.34 No.-

Length changes in mitochondrial DNA (mtDNA) offer a useful marker for the study of female aspects of human population history. One such length change is the intergenic COⅡ/tRNA^Lys 9-bp deletion, which the region usually contains two tandemly arranged copies of a 9-bp sequence (ccccctcta) in human mtDNA. This deletion has been reported at varying frequencies in populations from Asia. Polynesia, the New World, and sub-Saharan Africa. This genetic polymorphism of mtDNA was analyzed in samples from 171 unrelated individuals from the Korean population and compared the frequency and distribution of 9-bp deletion with other Asian population. The frequency of the 9-bp deletion was found to be 17.5% (30/171) in the Korean populations. Uncommonly, a new insertion allele of approximately 6-bp in the intergenic COⅡ/tRNA^Lys region in the Korean population (2/171) was first identified in this study. East Asian populations including Chinese. Japanese, and Koreans were relatively homogeneous in the frequency of 9-bp deletion. with the exception of the low frequency of this deletion in Mongolians. On the other hand, Indonesians and Malaysians of Southeast Asian populations were found to show relatively high frequencies of the 9-bp deletion. Based on results of the frequencies of the 9-bp deletion, the Japanese population appeared to have a closer genetic relationship to Koreans than to the other surveyed Asian populations. Therefore, the results of this study also supported the hypothesis that a large amount of the gene pool in mainland Japanese was derived from the continental gene flow after the Yayoi Age.

비침습적 검사를 이용한 수술후 하지 심부 정맥 혈전증의 감시

김영욱,정한준,윤봉호,김신윤,이상국,변경환,김태헌 경북대학교 병원 1997 경북대학교병원의학연구소논문집 Vol.1 No.1

Deep vein thrombosis is recognized as a common complication in surgical patients in western countries especially in patients with high risk factors. The purposes of this study were to detect leg DVTs in early postoperative period by non-invasive surveillance and to analyze the risk factors of DVT. One hundred seventy one patients who underwent major operations(67 curative resection of colorectal cancer, 64 total hip replacement, 38 femur operation for fracture, and 2 colon resections for benign colon disease) were included for the prospective surveillance of leg DVT within 2 weeks after the operations. For the surveillance of leg DVT, strain gauge plethysmography(SPG) and Duplex scanning of both legs were completed for all patients except 10 patients. These 10 patients were examined in only one leg. The patients with past history of leg DVT or under prophylactic anticoagulant therapy were excluded from this study. To determine the risk factors related with leg DVT formation, age and sex of the patients, indication of surgery or surgical procedures, duration of operation, position during the operation, duration of postoperative immobilization, and preoperative serum level of antithrombin III (AT- III) were analyzed using Chi-square test. After performing SPG of 342 legs, 38 legs, showed abnormal on venous outflow/venous capacitance discriminant line chart, and 13 legs of 12 patients showed the finding(s) suggesting DVT on duplex scanning. Among the patients with abnormal duplex findings, 7 limbs(53.8%) were symptomatic, but the remaining 6 legs were silent. In 6 (15.8%) patients of 36 femur operations, 3(4.7%) of 64 total hip replacements and 3(4.5%) of 67 curative resections of colorectal cancer developed DVT by duplex scanning in the iliac(5), femoral-popliteal(6), and isolated calf(2) veins. After analyzing the risk factors, we could not find any statistically significant(p<0.05) factor related with leg DVT.

XSL을 지원하는 XML문서 편집기 설계 및 구현

김동욱,최한석 木浦大學校 情報産業硏究所 1999 情報産業硏究誌 Vol.7 No.-

The Purpose of this thesis is to design and implementation of a XML document editor supporting XSL for user friendly. This Editor support edit of hierarchical architecture and various XML documents type. Also, an XSL stylesheet editor specifies the presentation of a class of XML documents by describing how an instance of the class is transformed into an XML document that uses the formatting vocabulary. This thesis implements an exclusive user friendly XML document editor supporting various function different from previous XML editor.

한국인 Fragile-X 증후군 환자의 분자 유전학적 진단

김경모,유한욱 울산대학교 의과대학 1994 울산의대학술지 Vol.3 No.2

Fragile-X syndrome (FXS) is the most common cause of inherited mental retardation. Until recently, the diagnosis of FXS has been made based on the cytogenetic expression of the fragile site at Xq27.3 (FRAXA) in the patients' cultured cells and on the results of linkage analysis with DNA markers surrounding the fragile X locus. The recent cloning of fragile-X gene(FMR-1) made it possible investigate the molecular defects in FMR-1 gene of individuals at risk. Vast majority of molecular defects of FXS has been known to be an abnormally amplified trinucleotide(cytosine guanine guanine) repeat. This study aims at establishing the molecular genetic diagnosis of FXS as well as correlating genotype-phenotype analyzing the increment of amplified CGG repeat number, clinical findings, and cytogenetic expression rate in two Korean families with FXS patients. The FXS patients are tested cytogenetically & molecular genetically. The fragile site at Xq27.3 was cytogenetically expressed in folate deficient medium by culturing lymphocytes for 4 days. Molecular diagnostic approaches utilize the genomic DNA Southern blot analysis using genomic probe FXA 241 (ONCOR) and radiolabelled PCR-denaturing polyacrylamide gelelcetrophoresis. Each patient expressed a FRAXA site in folate deficient medium with the expression rate of 38%, 16% respectively. The molecular genetic study showed that each patient had the CGG amplification 1.6kb, 0.7-0.8kb in the FMR-1 gene respectively. In addition, this study clarified the carrier status of each family members. In conclusion, molecular genetic studies employed in this study can be utilized for a confimatory diagnostic purpose in FXS patients.

음파 및 초음파기구를 이용한 근관형성법의 효율성에 관한 실험적 연구

김한욱,이정식 大韓齒科保存學會 1988 Restorative Dentistry & Endodontics Vol.13 No.1

傳染性單核球增加症 1例 報告

金相仁,高光昱,趙漢翊,崔玲姬,崔勇,李在英 대한의학협회 1972 대한의학협회지 Vol.15 No.6