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남지우,김동욱,배미영,박강순,김정현,노상률,최영일,김희종,장동욱,최소명,권영준,Hikita, S.,Yu, C.,Yoshimura, Y.,Kichimi, H. 성균관대학교 기초과학연구소 1998 論文集 Vol.49 No.-
We investigated the properties of BELLE Time Of Flight(TOF) counter using the data taken in Jan 98 beam test at Pi2 beam line at KEK 12 GeV proton synchrotron. Charge distributions from readout PMT were analysed in comparison with dE/dx distributions predicted by GEANT full simulation. Experimental setup of the beam test is described, then procedures of data analysis, Monte Carlo simulation and analysis results are also described.
Genome-wide gene expression analysis in the fetal trisomy 21 placenta
( Yj Han ),( Ej Choi ),( Jm Lee ),( Dw Kwak ),( Sw Lee ),( Mh Kim ),( Jh Chung ),( Hk Ahn ),( Js Choi ),( Jy Han ),( My Kim ),( Jh Lim ),( Hyun Mee Ryu ) 대한산부인과학회 2016 대한산부인과학회 학술대회 Vol.102 No.-
목적: To gain new insight of gene expression into the pathogenesis of trisomy 21 (T21) placenta, we performed whole human genome expression analysis in placenta tissue (normal and T21) samples. 방법: We profiled whole human genome expression of placenta samples from normal and T21 fetuses using GeneChip Human Genome U133 plus 2.0 array and predicted the functions of differentially expressed genes using bioinformatics tools. 결과: One hundred-ten genes were significantly differentially expressed in the T21 placenta compared with the normal placenta (33 down-regulated and 77 up-regulated). Among them, some genes were significantly associated with focal adhesion, Alzheimer's disease, and Parkinson's disease pathway. The down-regulated genes in the T21 placenta were distributed on various chromosomes. The down-regulated genes were significantly associated with cystitis, metaplasia, pathologic neovascularization, airway obstruction, and diabetes mellitus type 2. None of down-regulated genes were on chromosome 21 causing T21, whereas over half (59.7%) of up-regulated genes were located on chromosome 21. The up-regulated genes were significantly associated with T21 and T21-related disorders, such as mental retardation, neurobehavioral manifestations, and congenital abnormalities. 결론: Our findings provide a broad overview of whole human genome expression in the placentas of fetuses with T21 and could contribute to future research efforts concerning genes involvement in disease pathogenesis.
최영중(YJ Choi),최영균(YK Choi),이영혜(YH Lee),한의정(EJ Han) 대한산부인과학회 1977 Obstetrics & Gynecology Science Vol.20 No.1
최근 실질적으로 나타난 선천성 부신피질증식증에 의한 여성반음양을 경험하기에 문헌과함께 보고하는 바이다. Patient. Kim. S.R, was examined together with her younger sister (kim. J.R) because of enlargement of clitoris, fusion of labioscrotal folds and musculine configuration. The child has been brought up as a girl. The patient developed in a way similar to her younger sister. Sex chromatin in oral mucosa smear: positive. Chromosome study: cytogenenetically normal 46/XY, female. Baseline urinary 17 KS was 37.3㎎/24hours. After three day`s treatment with dexamethasone, the output oh 17KS was 4. 55㎎/24 hours. Retroperitoneal pneumogram including tomography revealed to marked enlargement bilateral adrenal gland. Vaginogram showed uterus measured 3×2 ㎝ and distended vagina 6㎝ in length. Two case of female pseudohermaphroditism with virilization delveloped in sisters is presented a brief review of the concerned literatures.
산전 초음파검사에서 본 제대탈추 및 횡경막결손을 동반한 심장이소증의 1 예
최영주(YJ Choi),백경돈(KD Baik),이흥섭(HS Lee),하부수(BS Ha),김상갑(SK Kim),지정희(CH Chi) 대한산부인과학회 1992 Obstetrics & Gynecology Science Vol.35 No.7
Omphalocele is a defect in the umbilical ring from which protrudes a sac, and into which abdominal contents have typically herniated. Ectopic cordis was first reported in 1671 by Stensen, which means that the heart is partially or totally outside the thorax. We have experienced a case of omphalocele and ectopia cordis with diaphragmatic defect. We report the case and review with literature briefly.
최영주(YJ Choi),이용미(YM Lee),정규호(KH Chung),박상철(SC Park),최규홍(KH Choi) 대한산부인과학회 1992 Obstetrics & Gynecology Science Vol.35 No.8
Thoracopagus is very rare congenital anomalies. We have diagnosed a case of it by ultrasonography and X-ray at intrauterine pregnancy for 25th weeks. We present it with brief review of literatures.
Testicular feminization syndrome 1례
최영균(YK Choi),이영혜(YH Lee),최영중(YJ Choi),정신호(SH Chung) 대한산부인과학회 1978 Obstetrics & Gynecology Science Vol.21 No.1
저자들은 최근 전주예수병원 산부인과에서 testicular feminization syndrome 1예를 경험하였기에 간단한 문헌적 고찰과 함께 그 증례를 보고하는 바이다. Testicular Feminization is a hereditary syndrome characterized by in dividuals with testes who present a female phenotype. We presented a case of testicular feminization syndrome with nearly normal size of blind vagina associated with bilateral inguinal gonads, who received laparatomy with resection of tsetes, with brief review of literatures.