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전통목조건축에서 도리와 직접 결구되는 보 방향 긴결재에 관한 연구
김소미(Kim, So-Mi),전봉희(Jeon, Bong-Hee) 대한건축학회 2023 대한건축학회 학술발표대회 논문집 Vol.43 No.1
The purpose of this study is to classify the terminology used in Purlin-form tie which includes Chogong, Chobang, and Gyeryang. The Purlin-form tie is a member that connects two or more purlin columns, improving structural stability. In this paper, the Purlin-form tie is sorted by its function, position, and form properties then subdivided into support or connecting member, bracket or non-bracket member, and straight or curved member. As a result, the Chobang, Gyeryang, and Umiryang is reclassified based on the comparative analysis using preceding classification.
감귤의 고미제거 효소인 Limonoid UDP-glucosyltransferase의 대장균 내에서의 발현과 이의 분리
김소미 ( So Mi K. ),김영미 ( Young Mee Kim ),김민영 ( Min Young Kim ),이도승 ( Do Seung Lee ),김재훈 ( Jae Hoon Kim ),박세필 ( Se Pill Park ),류기중 ( Key Zung Riu ),이동선 ( Dong Sun Lee ) 한국식품저장유통학회(구 한국농산물저장유통학회) 2011 한국식품저장유통학회지 Vol.18 No.2
Limonoids are abundant as bitter taste in citrus fruit and other plants. Interestingly, limonoid UDP-glucosyltransferase (LUGT) effectively ameliorates the bitterness from limonoid. The high level of LUGT expression in Escherichia coli can result in the formation of insoluble aggregates known as inclusion bodies. We isolated the soluble LUGT protein when this inclusion body was renaturated with β-cyclidextrin treatment after protein denaturation by urea. Our present results suggest that the isolation of LUGT from inclusion body in cells leads to shed light to characterize the enzyme for food industry purposes.
문맥압 항진증을 동반한 간경변증 환자에서의 급성 신손상
김소미 ( So Mi Kim ),송일한 ( Il Han Song ) 대한소화기학회 2016 대한소화기학회지 Vol.68 No.5
Acute kidney injury (AKI) is one of the most common manifestations encountered in clinical practice. It is associated with high morbidity and mortality in cirrhotic pre- and post-transplantation patients. Hepatorenal syndrome (HRS), a special form of AKI in cirrhotic patients, was recognized as a consequence of renal vasoconstriction from systemic/renal hemodynamic alterations developed in advanced cirrhosis with portal hypertension. Recently, multiple factors-such as infection/inflammation, underlying glomerulonephritis, bile cast, or increased abdominal pressure-have been considered to contribute to renal dysfunction in cirrhotic patients, which were presumed to induce HRS. Moreover, in addition to changing the definition of AKI in the nephrologic guidelines, the new AKI definition for early diagnosis and intervention based on characteristics of liver cirrhosis has been proposed in an international meeting. This article provides a comprehensive and recent review of AKI definition, laying out the topics in accordance with the pathophysiologic mechanisms and therapeutic interventions of AKI in cirrhotic patients with portal hypertension. (Korean J Gastroenterol 2016;68:237-244)
고주파 자궁근종용해술 후 임신 15주1일에 발생한 자궁파열
김소미 ( So Mi Kim ),김근희 ( Geun Hee Kim ),정다운 ( Da Un Jeong ),서은주 ( Eun Ju Seo ),문지경 ( Ji Kyeung Moon ),송지은 ( Ji Eun Song ),이근영 ( Keun Young Lee ) 대한산부인과학회 2009 Obstetrics & Gynecology Science Vol.52 No.9
The development of myolysis has allowed number of gynecologic surgeons to treat myoma instead of hysterectomy or myomectomy. However not long time has passed since this operation started, little studies were conducted on this complication and side effect. Especially, there are not enough studies about complication and prognosis related pregnancy after myolysis. One of these complications, uterine rupture during pregnancy is not frequent, but fatal condition to both mother and fetus. We report a case of uterine rupture that occurred in early second-trimester who had been myolysis 22 months before pregnancy.
김소미 ( So Mi Kim ),유한욱 ( Han Wook Yoo ),김현우 ( Hyun Woo Kim ) 대한내과학회 2013 대한내과학회지 Vol.85 No.2
본 증례는 판코니-비켈 증후군으로 유전자 검사를 통해 진단되었으나 전형적인 임상양상과는 다른 경한 경과를 보여 유전자 돌연변이를 포함하여 문헌고찰과 함께 보고하는 바이다. Fanconi-Bickel syndrome is a rare autosomal recessive disorder caused by a mutation in the facilitative glucose transporter 2 gene (GLUT2 or SLC2A2 gene) that codes for the glucose transporter protein 2 expressed in hepatocytes, pancreatic beta-cells, enterocytes, and renal tubular cells. Mutation of this gene leads to defective carbohydrate metabolism, hepatomegaly, glucose intolerance, proximal renal tubular dysfunction, and hypophosphatemic rickets. We report a case of Fanconi Bickel syndrome in an 18-year-old man who presented due to renal glycosuria; a mutation was identified in the GLUT2 gene (c.482C > A + c.1556G > A). To the best of our knowledge, unlike previous reports of Fanconi-Bickel syndrome, this case was relatively unusual in that it caused only mild clinical signs. (Korean J Med 2013;85:210-213)