20 research outputs found

    Effectiveness of conceptual inquiry instruction on the inquiry skills achievement of high school students in the biology class

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    ํ•™์œ„๋…ผ๋ฌธ(๋ฐ•์‚ฌ)--์„œ์šธๅคงๅญธๆ ก ๅคงๅญธ้™ข :็ง‘ๅญธๆ•Ž่‚ฒ็ง‘ ็”Ÿ็‰ฉๅฐˆๆ”ป,1996.Docto

    (A) genetic study on the dimension of dental arches in twins

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    ์˜ํ•™๊ณผ/์„์‚ฌ[ํ•œ๊ธ€] A Genetic study on the dimension of dental arches in twins. Nam Il Kim, D.D.S. Department of Medical Science, Graduate School, Yonsei University The purpose of this study is to evaluate the influence of genetics of the dimensions of dental arches in twins. Thirty-four pairs of Korean twins, of which twenty-three were monozygotic and eleven dizygotic, participated in the study. The twins ranged in age from 6 years to 12 years with mixed dentition. The results were as follows: 1) No significant differences were observed between male and female in mean interpair differences of monozygotic twins. 2) Mean interpair differences of monozygotic twins were lesser than those of dizygotic twins. 3) Highly significiant zygotic differences were observed in the mean interpair differences of the width of upper and lower dental arch. This suggest that there is a significant component of hereditary variability. [์˜๋ฌธ] The purpose of this study is to evaluate the influence of genetics of the dimensions of dental arches in twins. Thirty-four pairs of Korean twins, of which twenty-three were monozygotic and eleven dizygotic, participated in the study. The twins ranged in age from 6 years to 12 years with mixed dentition. The results were as follows: 1) No significant differences were observed between male and female in mean interpair differences of monozygotic twins. 2) Mean interpair differences of monozygotic twins were lesser than those of dizygotic twins. 3) Highly significiant zygotic differences were observed in the mean interpair differences of the width of upper and lower dental arch. This suggest that there is a significant component of hereditary variability.restrictio

    (A) study on experimental infection of Korean chipmunks (Eutamias sibiricus asiaticus) by candida albicans

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    ์˜ํ•™๊ณผ/๋ฐ•์‚ฌ[ํ•œ๊ธ€] 1751๋…„ John Hill์— ์˜ํ•˜์—ฌ Candids๊ฐ€ ์ตœ์ดˆ๋กœ ๊ด€์ฐฐ๋˜์—ˆ์œผ๋ฉฐ Berkhout(1923)์— ์˜ํ•˜์—ฌ C andida๋ผ ์žฌ๋ช…๋ช…๋œ ์ด๋ž˜ ํ˜„์žฌ๊นŒ์ง€ 100์—ฌ์ข…์ด ๋ณด๊ณ ๋˜์–ด ์žˆ๋‹ค. ์ด์ค‘Candida albicans๋งŒ์ด ๋ณ‘์›์„ฑ์„ ๋‚˜ํƒ€๋‚ธ๋‹ค๊ณ  ์•Œ๋ ค์ ธ ์™”์œผ๋‚˜ ๊ทผ๋ž˜์— ์™€์„œ ํƒ€Candida์ข…๋“ค๋„ ์งˆ๋ณ‘์„ ์•ผ๊ธฐํ•  ์ˆ˜ ์žˆ๋‹ค ๋Š” ๋ณด๊ณ ๊ฐ€ ์žˆ์œผ๋ฉฐ ๊ฐ์ข… ์ง„๊ท ์ฆ์˜ ๊ฐ์—ผ ์ฆ๊ฐ€์ถ”์„ธ์™€ ๋”๋ถˆ์–ด ์บ”๋””๋‹ค์ฆ ์—ญ์‹œ ์ฆ๊ฐ€ํ•˜๋Š” ํ˜„์ƒ์„ ๋‚˜ํƒ€๋‚ด๊ณ  ์žˆ๋‹ค. ์ด๋Ÿฌํ•œ ์ง„๊ท ์ฆ์˜ ์ฆ๊ฐ€์ถ”์„ธ๋Š” ํ•ญ์ƒ์ œ์˜ ๋‚จ์šฉ, ๋ฉด์—ญ์–ต์ œ์ œ์˜ ์‚ฌ์šฉ, ๊ฐ์ข… ์ข…์–‘ ๋ฐ ๋ฉด์—ญ๊ฒฐํ•์„ฑ ์งˆํ™˜ ๋“ฑ ์—ฌ๋Ÿฌ๊ฐ€์ง€ ์†Œ์ธ์— ์˜ํ•œ๋‹ค๊ณ  ๋ณด๊ณ ๋˜์–ด ์žˆ๋‹ค. ํ˜„์žฌ๊นŒ์ง€ ๊ฐ์ข… ์ง„๊ท ์ฆ์˜ ์›์ธ๊ท ์— ๋Œ€ํ•œ ์ ๋‹นํ•˜๊ณ  ์šฐ์ˆ˜ํ•œ ์‹คํ—˜๋™๋ฌผ์ด๋‚˜ Candida species ์— ๋Œ€ํ•œ ์‹คํ—˜๋™๋ฌผ์— ๊ด€ํ•œ ์—ฐ๊ตฌ๋Š” ๋ณ„๋กœ ์ฐพ์•„๋ณผ ์ˆ˜ ์—†์œผ๋ฉฐ ํ•™์ž๋“ค ๊ฐ„์—๋„ ์„œ๋กœ ๋‹ค๋ฅธ ์˜๊ฒฌ๋“ค ์ด ์žˆ๋Š” ์‹ค์ •์ด๋‹ค. ๋”ฐ๋ผ์„œ ๋ณธ ์—ฐ๊ตฌ์—์„œ๋Š” ์—ฐ์„ธ์˜๋Œ€ ๋ฏธ์ƒ๋ฌผํ•™๊ต์‹ค์—์„œ ์—ฐ๊ตฌ ๊ฐœ๋ฐœํ•˜์—ฌ ํ˜„์žฌ๊นŒ์ง€ ํ•ญ์‚ฐ๊ตฐ์ฆ์— ๋Œ€ํ•˜์—ฌ ์ข‹์€ ์‹คํ—˜๋™๋ฌผ๋กœ์„œ ๋ณด๊ณ ๋œ ํ•œ๊ตญ์‚ฐ ๋‹ค๋žŒ์ €(Eutamias sibiricus asiaticus)๋ฅผ ์‚ฌ์šฉ ํ•˜์—ฌ ์„ธ๊ณ„์ ์œผ๋กœ ๋„๋ฆฌ ๋ถ„ํฌ๋˜์–ด ์žˆ์œผ๋ฉฐ ์‹ฌ์žฌ์„ฑ ์ง„๊ท ์ฆ์„ ์•ผ๊ธฐํ•˜๋Š” ์ง„๊ท ์˜ ์ผ์ข…์ธ Candida albicans์— ๋Œ€ํ•œ ๊ฐ์ˆ˜์„ฑ ์—ฌ๋ถ€๋ฅผ ๊ทœ๋ช…ํ•˜๊ณ  ์‹คํ—˜๋™๋ฌผ๋กœ์„œ์˜ ์ด์šฉ๊ฐ€๋Šฅ์„ฑ ์—ฌ๋ถ€๋ฅผ ๊ทœ๋ช…ํ•  ๋ชฉ ์ ์œผ๋กœ ์‹คํ—˜์— ์ฐฉ์ˆ˜ํ•˜์—ฌ ๋‹ค์Œ๊ณผ ๊ฐ™์€ ๊ฒฐ๊ณผ๋ฅผ ์–ป์—ˆ๋‹ค. 1. ์ •๋งฅ์„ ํ†ตํ•˜์—ฌ ๋‹ค๋žŒ์ฅ์— Candida albicans๋ฅผ ๊ฐ์—ผ์‹œ์ผฐ์„ ๊ฒฝ์šฐ LD^^50 ๋Š” 1ml๋‹น 5.7 ร—10**4 cell ์ด์—ˆ์œผ๋ฉฐ ๋‹ค๋žŒ์ฅ์—์„œ 100% ์‚ฌ๋ง์œจ์„ ๋‚˜ํƒ€๋‚ธ 1ml๋‹น 3.2ร—10**5 cell์—์„œ์˜ ๋งˆ์šฐ์Šค์‚ฌ๋ง์œจ์€ 20%์ด์—ˆ๋‹ค. 2. ์ •๋งฅ๋‚ด๋กœ ์ฃผ์‚ฌํ•œ ๋‹ค๋žŒ์ฅ์˜ ์ง์ ‘๋„๋ง๊ฒ€๊ฒฝ ๋ฐ ๋ฐฐ์–‘์„ฑ์ ์—์„œ๋Š” ๊ท ์ ‘์ข… 4์ผ ํ›„๋ถ€ํ„ฐ๋Š” ์‹  ์žฅ์—์„œ๋งŒ ๊ท ๊ฒ€์ถœ์ด ๊ฐ€๋Šฅํ•˜์˜€๋‹ค. 3. ๊ฐ ์žฅ๊ธฐ์—์„œ์˜ ์ƒ๊ท ์ˆ˜์ธก์ • ๊ฒฐ๊ณผ๋Š” ์‹ ์žฅ์„ ์ œ์™ธํ•˜๊ณ ๋Š” ๊ท ์ ‘์ข… 1์ผ๋‚ด์ง€ 2์ผ ์ด๋‚ด์— ์ตœ ๊ณ ์— ๋‹ฌํ•˜์˜€๋‹ค๊ฐ€ ๊ธ‰์†ํžˆ ๊ฐ์†Œํ•˜์˜€์œผ๋‚˜ ์‹ ์žฅ์—์„œ๋Š” 31์ผ๊นŒ์ง€๋„ ๊ท ์˜ ๊ด€์ฐฐ์ด ๊ฐ€๋Šฅํ•˜์˜€๋‹ค. 4. ํ˜ˆ์•กํ•™์  ๊ฒ€์‚ฌ์„ฑ์ ์— ์žˆ์–ด์„œ ๋ฐฑํ˜ˆ๊ตฌ์˜ ์ˆ˜๋Š” ๊ท ์ ‘์ข…์ „์— ๋น„ํ•˜์—ฌ ๊ท ์ ‘์ฆ 4์ผ์— 4๋ฐฐ์˜ ์ค‘๊ฐ€๋ฅผ ๋ณด์˜€๋‹ค. 5. ๋ณ‘๋ฆฌ์กฐ์งํ•™์  ์†Œ๊ฒฌ์„ ๋ณด๋ฉด ์ ‘์ข… ์ดˆ๊ธฐ์—๋Š” ๊ฐ ์žฅ๊ธฐ์—์„œ ์กฐ์ง ๋ณ€ํ™”์—†์ด ๊ตฐ์ฒด์˜ ๊ด€์ฐฐ์ด ๊ฐ€๋Šฅํ•˜์˜€์œผ๋‚˜ ๊ท ์ ‘์ข… 31์ผ์—์„œ๋Š” ์‹ ์žฅ์—์„œ ์‹ฌํ•œ ๋‹ค๋ฐœ์„ฑ๊ตญ์†Œ ๋†์–‘ ๋ฐ ๊ดด์ €๋ฅผ ์ดˆ๋ž˜ํ•œ ํ˜„์ƒ ์„ ๊ด€์ฐฐํ•จ๊ณผ ๋™์‹œ์— ๋งŽ์€ ๊ท ์‚ฌ์ฒด๊ฐ€ ๋ฐœ๊ฒฌ๋˜์—ˆ๋‹ค. ์ด์ƒ์˜ ์‹คํ—˜๊ฒฐ๊ณผ๋ฅผ ์ข…ํ•ฉํ•˜์—ฌ ๋ณผ ๋•Œ ํ•œ๊ตญ์‚ฐ ๋‹ค๋žŒ์ฅ๋Š” Candida albicans์— ๋Œ€ํ•˜์—ฌ ๊ฐ์ˆ˜์„ฑ ์„ ๊ฐ€์ง€๊ณ  ์žˆ๋Š” ๋™์‹œ์— ์‹คํ—˜๋™๋ฌผ๋กœ์„œ์˜ ๊ฐ€๋Šฅ์„ฑ์„ ๋‚ดํฌํ•˜๊ณ  ์žˆ๋‹ค๊ณ  ์‚ฌ๋ฃŒ๋œ๋‹ค. [์˜๋ฌธ] Introduction In 1751, John Hill observed yeast-like organisms harvested from rotting vegetation, which he named Monilia. But, the genus Monilia was erected by Persoon in 1797 to encompass certain species of fungi isolated from rotting fruit. In 1923, Berkhout reclassified the genus Candida and this name was accepted as a "nomen conservandum'by the 8th Botanical Congress at Paris in 1954. It is generally recognized that Candida albicans is the only species of Candida known to be pathogenic to man and to a number of laboratory animals, but recently it has been found that all of the Candida species may be involved in any from of candidiasis. Presently, Candida albicans is one of the normal flora of the alimentary tract, mucous membrane, oral cavity and skin of many mammals. The incidence of human disease caused by this organism has increased steadily in recent years due to the wider use of immuno-suppressive drugs and broad spectrum antibiotics. The variety of predisposing factors, the range of the clinical disease, and the poor antibiotic chemotherapy now avilable have made candidasis a serious clinical problem. The need to understand the immunity, host-parasite relationship and pathogenesis involved in human diseases due to Candida albicans has made it desirable animal model for candidasis that mimics the systemic disease seen in human. Several animal models from disseminated candidiasis have been described. Baine et al. (1974) used the rabbit to study systemic candidiasis and estab1ished that the infection is of a chronic nature. Hurley and Winner (1963) described the histological picture of experimental Candida albicans infection in the tissue of mice. But up untill now, a properly susceptible and sensitive animal model for experimental systemic candidiasis has not been found. For this reason, the author has also studied the course of an experimental Candida albicans infection in the Korean chipmunks (Eutamias sibiricus asiaticus) in order to establish whether this animal can be used as an experimental animal model. Materials and Methods A. Materials 1. Experimental organism: Candida albicans ATCC 7491 was obtained from H. Miyazaki (Juntendo University, Tokyo, Japan). It was maintained in our laboratory by transfers on Sabouraud's glucose agar slant. The morphological and biochemical characteristics of Candida albicans were verified by microscopic observation and sugar fermentation reactions. 2. Animals: Wild chipmunks were obtained. They were maintained on a nutritional diet and their adaptability to caged life was observed for 2 months prior to inoculation with fungal suspension. Also, white ICR-mice were obtained from the Institute of Leprosy, Japan and were used in all of the control studies. B. Methods 1. Challenge Procedure: Aliquots of the stored Candida albicans suspension diluted in saline were prepared to obtain the proper dose of administration. 0.2 ml of the appropriate suspension were injected into the tail vein. Otherwise, 0.5 ml of the suspension were injected intraperitoneally. 2. Enumeration of the Candida albicans Viab1e Unit: Chimmunks were sacrificed, under aseptic condition. The appropriate organs were removed and weighed and placed in tissue homogenizers. Sterile saline was added. Each organ was homogenized and then number of Candida albicans viable units in the homogenate was determined by the pour plate dilution method, using Sabouraud's glucose agar. Colony forming units (CFU) were determined by counting the colonies used as a source of the organisms. 3. Histopathological Study: Experimental animals Were sacrificed at 24 hours, 48 hours and 31 days after intarvenous inoculation of approximately 3.2ร—10**3 cell/ml. Sections of brain, lung, heart, liver, spleen and kidney were studied after staining with hematoxylin eosin and Periodic acid-Schiff's reagent. 4. Hematological Study: Experimental chipmunks were infected with 3.2ร—10**3 cell/ml, and 0.5ml of whole blood were obtained daily for 5 days by cutting tail vein. Blood was placed in tubes containing 0.3% sodium citrate solution, and white blood cell(WBC), red blood cell (RBC) and hematocrit counts were determined with Hema-Count TM System Model MK-3 type. Results and Conclusions 1. Mortality Rate and Histopathological Study: In an attempt to produce a disseminated infection, up to 3.2ร—10**5 cell/ml of Candida albicans were given intravenously. With this inoculum, death of all animals was observed within 24 hours. The LD^^50 was determined as 5.7ร—10**4 cell/ml. Between the inocula of 2.0ร—10**4 cell/ml and 7.2ร—10**4 cell/ml mortality rose sharply, increasing from 10% to 90%. Autopsies of animals given lethal and sublethal doses of Candida albicans intravenous revealed disseminated microabscesses or inflammatory cell infiltrations throughout the kidney, heart, lung, liver and spleen. Also, Candida albicans could be cultured from these organs in the early stage of infection and cells in the mycelial phase were demonstrated histopathologically in the renal and myocardial abscesses after 31 days. 2. Course of Infection: For the study of the course of infection over time, a sublethal dose of Candida albicans was given (3.2ร—10**4 cel1/ml) and animals were autopsied at 24, 48, 72, 96, 120 hours and 31 days after injection, spleen, liver, lung, heart and kidney were cultured. Over the next 5 days, colony counts revealed a decreasing number of viable organisms in all tissues except the kidney. Between 24 hours and 48 hours the decline was rapid: between 96 hours and 120 hours all nonrenal organs became sterile. Although the initial renal colony counts was similar to colony counts in other organs, there was gradual increase in renal colony count over the first 2 days of infection, with maximal counts of viable organism of 7.0ร—10**5 CFU/gm tissue at 3 days. Subsequently, there was a gradual decline in colony count. By day 31, the colony counts was 4.8ร—10**3 CFU/gm tissue. 3. Hematological Study: Paralleling the inefection, leukocytosis was observed 24 hours after injection and continued to rise until 4 days, when the total count of (18.05ยฑ4.26)ร—10**3 WBC/cmm was seen. Blood cultures were positive for the infecting organism for the entire 5 days period of the blood collection. 4. In summary of the above results, the chipmunk appears to be one of the most susceptible to Candida albicans among all the experimental animals known to date. Therefore this animal can be adopted as an expermental animal model for candidiasis .restrictio

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    ํ•™์œ„๋…ผ๋ฌธ(์„์‚ฌ)--์„œ์šธ๋Œ€ํ•™๊ต ๋Œ€ํ•™์› :ํ† ๋ชฉ๊ณตํ•™๊ณผ ํ† ๋ชฉ๊ณตํ•™์ „๊ณต,1995.Maste
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