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최철준(Choul-Jun Choi),고가진(Jia-Chen Gao),김재열(Jae-Yeol Kim),정윤수(Yoon-Soo Jung) 한국기계가공학회 2016 한국기계가공학회지 Vol.15 No.4
From the first application of a thermoelectric module to nowtoday, it has been more than half a century. The application of a thermoelectric module is becoming more and more widely accepted since, people"s requirement rely more and more on the efficiency of thermoelectric modules and their reliability become higher and higher. So people pay more and more attention to the thermoelectric module. In Around the world, the more research for into improving the efficiency of thermoelectric modules is focused on the current materials. at present. However, the research of into available materials had has some limitations, and the research of materials had reached a bottleneckthere are limits to current applications. On the other hand, from the production process, if we assembled by materials withoutmodules without any damages and achieve the ideal state of a joint, we can make the a product to maximize performance and have a longer service life. SoTherefore, in this study we will prove the relationship between the any defects inside and the efficiency of a thermoelectric module to improve the quality management and performance of modern thermoelectric modules at present.
21 - Hydroxylase 결핍 선천성 부신 증식증 가계에서 ACTH Stimulation Test
최철준(Cheul Joon Choi),주영실(Young Sil Ju),이기영(Gi Young Yi),김성운(Sung Woon Kim),양인명(In Myung Yang),김진우(Jin Woo Kim),김영설(Young Seoul Kim),최영길(Young Kil Choi),오보훈(Bo Hoon Oh) 대한내과학회 1987 대한내과학회지 Vol.33 No.2
N/A CAH (congenital adrenal hyperplasia) due to 21-hydroxylase (2l-OH) deficiency is a autosomal recessive disorder in which affected homozygotes present with virilization, hirsutism and short stature. For the detection of heterozygote carrier, we measured 17-hydroxy progesterone (17-OHP), progesterone, cortisol and aldosterone after ACTH stimulation to the patient, her family members and controls. The following results were obtained. 1) ACTH stimulation test was a goad test for the confirm diagnosis of homozygotes and the detection of heterozygote carriers in 21-OH deficiency CAH. 2) The patient and two siblings were homozygotes. The mother and one sibling were heterozygotes, and her father was suggested to be a heterozygote without biochemical expression. 3) 21-hydroxylase deficiency of zona glomerulosa was Not deficient in all homozygotes.