http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
양영호,김창규,최동일,조동제,황동훈,허갑범,Yang, Young-Ho,Kim, Chang-Kyu,Choi, Dong-Il,Cho, Dong-Zae,Hwang, Dong-Whun,Huh, Gap-Bum 대한생식의학회 1986 Clinical and Experimental Reproductive Medicine Vol.13 No.2
The high rate of chromosomal abnormalities in patients with primary amenorrhea implies the need for routine screening for chromosomal abnormalities among such patients. This study was designed for the cytogenetic analysis of 236 patients with primary amenorrhea, which was referred to Yonsei University Medical Center, from January, 1, 1974 to December, 31, 1985. The results were as follows: 1. Of the 236 patients, 145 cases (61.4%) showed normal karyotype, and 91 cases (38.6%) showed chromosomal abnormalities. 2. Gonadal dysgenesis was found in 56 cases, consisting of 42 cases, Turner's syndrome, 12 cases, pure gonadal dysgenesis, and 2 cases mixed gonadal dysgenesis. a) Turner's syndrome was found in 42 cases, consisting of 18 cases of 45, X and 24 cases of mosaicism. b) Pure gonadal dysgenesis was found in 12 cases, consisting of 10 cases of 46, XX and 2 cases of 46, XY. c) Mixed gonadal dysgenesis was found in 2 cases, consisting of 1 case of 46, XY and 1 case of 45, X/46, XY. 3. Intersex was found in 80 cases, consisting of 35 cases of 46, XX, and 45 cases of 46, XY. 4. Congenital anomalies of reproductive system was found in 82 cases and all cases were normal karyotype.
전로(轉爐)슬래그를 활용(活用)한 완효성(緩效性) 칼리 비료(肥料)의 제조(製造) 특성(特性)
양영호,김영환,고인용,Yang, Yeong-Ho,Kim, Young-Hwan,Ko, In-Yong 한국자원리싸이클링학회 2007 資源 리싸이클링 Vol.16 No.4
As a basic study for reusing converter slag as slow-release potassium fertilizer by a sintering process, powdery converter slag and reagent grade $SiO_2\;and\;K_2CO_3$ were mixed with ball mill above 24 hours and sintered at $900^{\circ}C{\sim}1000^{\circ}C\;for\;10{\sim}60$ min. Basicity of the mixed powder was controlled to 0.7, 1.0 and 1.4 and content of $K_2O$ was fixed with 22 mass%. After sintering, property of the potassium fertilizer was investigated with X-ray diffraction pattern and ICP analysis. Also effects of basicity, sintering temperature and time on the making slow-release potassium fertilizer was investigated. Water solubility of KBO in sample were decreased with sintering time, temperature and decreased with basicity. Citric acid solubility of $K_2O$ were increased with basicity and decreased with sintering temperature. 전로슬래그를 완효성 칼리비료로 활용하기 위한 기초연구로, 전로슬래그 분말에 시약급 $SiO_2$와 $K_2CO_3$를 첨가하여 염기도를 각각 0.7, 1.0및 1.4로 조절하고, $K_2O$의 함량은 22mass%로 고정한 후 볼밀에서 24시간 이상 혼합하여 $900^{\circ}C{\sim}1000^{\circ}C$ 사이의 온도에서 10분${\sim}$60분 동안 소결하였다. 소결 후 X-선 회절과 ICP분석을 이용하여 제조된 칼리비료의 특성을 조사하고 또한 염기도, 소결온도 및 소결시간이 완효성 칼리비료의 제조 조건에 미치는 영향을 검토하였다. 소결체의 수용성 $K_2O$의 용출특성은 소결시간이 길어질수록, 소결온도가 높아질수록, 염기도가 감소할수록 용출율이 감소하였다. 한편 구용성 $K_2O$의 용출특성은 염기도가 증가할수록 증가하는 경향이 뚜렷하였으며, 소결온도가 높을수록 용출율은 완만하게 감소하였다.
유전질환 진단에 있어서의 Fluorescence in Situ Hybridization ( FISH ) 법의 임상적 유용성
양영호(Young Ho Yang),강지용(Ji Yong Kang),양은석(Eun Suk Yang),장시영(Si Young Jang),조재성(Jae Sung Cho),박용원(Yong Won Park),김인규(In Kyu Kim),김세광(Sei Kwang Kim),남명숙(Myung Sook Nam) 대한산부인과학회 2002 Obstetrics & Gynecology Science Vol.45 No.6
Introduction : The traditional cytogenetic analysis requires relatively long cell culture time, intensive labour and trained personnel. But, in clinical situations, rapid diagnosis of genetic disease is very important for urgent decision for future management. So we need more rapid and precise diagnostic tools for clinical genetic counselling. The fluorescence in situ hybridization (FISH) has been studied for detecting chromosomal aneuploidies because this method can get rapid and precise results of cytogenetic studies. Objective : To evaluate the clinical utility of fluorescence in situ hybridization technique as a diagnostic tool of chromosomal anomaly. Methods : Peripheral blood or gonadal tissue were obtained from the patients (n=63) clinically suspicious of genetic disease. Chorionic villi (n=6), amniotic fluid (n=9), and fetal cord blood (n=2) were obtained from 15 pregnancies undergoing fetal karyotyping at 9 to 30 weeks of gestation for prenatal genetic counselling. Karyotyping was performed by both traditional cytogenetics and FISH, using commercially available kits. After the procedures, the results of FISH were compared with the results of traditional cytogenetic studies. Results : In a blind series of 17 samples all, including trisomy 21 (1 case), trisomy 18 (1 case), monosomyX (1 case), 47,XYY (1 case), and 47,XXY (1 case), were correctly identified. FISH results were correspondent with conventional karyotyping results in 7 patients with intersex except one case of suspicious of mosaicism. In nine children of Turner syndrome, the results of two methods were correspondent too. There was a fluorescent signal defect in band 15 q11-q13 in one of chromosome 15 in 18 children of 29 patients, clinically suspicious of Prader-Willi syndrome, with FISH method and only four patients were diagnosed as Prader-Willi syndrome with G-banding microscope. It was impossible to identify the defect in chromosome 15 q11-q13 in 10 (34%) children by both methods. Two children of 11 patients, clinically suspicious of Angelman syndrome, were diagnosed as Angelman syndrome with both method respectively. And four children were diagnosed as Angelman syndrome only with FISH method. In 5 cases, we cannot detect the defect in chromosome 15 q11-q13 with both methods. In four cases of Williams syndrome, the results of both methods were as follows; 1 case (25%): diagnosed as Williams syndrome by both methods; 2 cases (50%): diagnosed as Williams syndrome by only FISH method; 1 cases (25%): negative in both methods. We could not detect microdeletion in the cases clinically suspicious of Digeorge syndrome and Miller-Dieker syndrome. Conclusion : FISH is a rapid and effective diagnostic method, which can be used as an adjunctive test to traditional cytogenetic analysis, for detection of chromosomal aneuploidies in clinical diagnosis for genetic disease.
모체의 말초 혈액에 존재하는 태아 세포 분리에 의한 새로운 기형아 진단 - Microdissection 에 의한 CGH 기법의 사용
양영호(Young Ho Yang),김성훈(Sung Hoon Kim),김세광(Sei Kwang Kim),박용원(Yong Won Park),조재성(Jae Sung Cho),김인규(In Kyu Kim),최종락(Jong Rak Choi),김미순(Mi Soon Kim) 대한산부인과학회 2002 Obstetrics & Gynecology Science Vol.45 No.2
Objective: The objective of this study was to determine the clinical use of CGH (comparative genomic hybridization) for detection of fetal aneuploidy from fetal cells (nucleated red blood cells, nRBCs) isolated Methods: Maternal peripheral venous blood sample was collected and treated by heparin. Triple density gradient centrifugation, and MACS (magnetic activated cell sorting) using CD45 and CD 71 were used to isolated the fetal nRBCs. With microdissection, DOP (degenerate oligonucleotide primed)-PCR (polymerase chain reaction), and nick translation, CGH was performed. Results: Fetal nRBCs were successfully isolated from maternal peripheral blood. After microdissection of fetal nRBCs, DOP-PCR. and nick translation, DNA size was suitable for hybridization. In CGH analysis, we can confirm normal female and trisomy 21 male fetus. Conclusion: Prenatal diagnosis from fetal cells in maternal peripheral blood by comparative genomic hybridization shows clinical promise in terms of speed, accuracy, and non-invasiveness. To enable widespread use of this method, further studies involving many cases are warrented.