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한국인 다낭성 난소증후군 환자에서 $CYP11{alpha}$ 유전자 $(tttta)_n$ 다형성 양상 및 역할
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  • 한국인 다낭성 난소증후군 환자에서 $CYP11{alpha}$ 유전자 $(tttta)_n$ 다형성 양상 및 역할
  • $CYP11{alpha}$ $(tttta)_n$ Microsatellite Polymorphism in Korean Patients with Polycystic Ovary Syndrome
저자명
김진주,최영민,윤상호,정선하,최두석,구승엽,지병철,서창석,김석현,김정구,문신용,Kim. Jin-Ju,Choi. Young-Min,Yoon. Sang-Ho,Choung. Seon-Ha,Choi. Doo-Seok,Ku. Seung-Y
간행물명
대한불임학회지
권/호정보
2004년|31권 4호|pp.245-251 (7 pages)
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대한생식의학회
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
서지반출

기타언어초록

Objectives: To investigate the distribution and functional significance of $CYP11{alpha}$ $(tttta)_n$ microsatellite polymorphism in Korean patients with polycystic ovary syndrome Materials and Methods: Analysis of $CYP11{alpha}$ $(tttta)_n$ microsatellite polymorphism was carried out on DNA samples from 97 patients with polycystic ovary syndrome and 70 normal controls. Comparison were done between PCOS patients and controls concerning $CYP11{alpha}$ $(tttta)_n$ microsatellite polymorphism genotype or allele frequencies. Results: The most frequent allele observed in the controls was an allele with six repeats (60.7%). Significant difference in the frequency of genotype (4R (-) genotype) having no copy of four-repeatallele were observed between PCOS patients and controls (66.0% vs 34.0%, p=0.038, OR=1.939). But no significant difference was observed in the serum levels of total testosterone or free testosterone between 4R (+) genotype and 4R (-) genotype among PCOS patients. However, hyperandrogenic PCOS patients with 4R (+) genotype showed a higher serum testosterone levels compared to controls (mean $pm$ S.D: $0.49{pm}0.21;ng/ml$ vs $0.37{pm}0.18;ng/ml$, p=0.037). Conclusion: The alleleic distribution of $CYP11{alpha}$ $(tttta)_n$ microsatellite polymorphism in Korean subjects were different from those reported in Caucasians. $CYP11{alpha}$ $(tttta)_n$ microsatellite polymorphism was associated with polycystic ovary syndrome in the Korean population, and may play a role in the synthesis of androgens in patients with polycystic ovary syndrome.