• 한국환경과학회지
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• 제25권5호
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• pp.683-694
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• 2016

Sensitivity analysis of the WRF model according to the impact of nudging (e.g., nudging techniques and application domains) was conducted during high nocturnal ozone episode to improve the prediction of the regional ozone concentration in the southeastern coastal area of the Korean peninsula. The analysis was performed by six simulation experiments: (1) without nudging (e.g., CNTL case), (2) with observation nudging (ONE case) to all domains (domain 1~4), (3) with grid nudging (GNE case) to all domains, (4)~(6) with grid nudging to domain 1, domain 1~2 and domain 1~3, respectively (GNE-1, GNE-2, GNE-3 case). The results for nudging techniques showed that the GNE case was in very good agreement with those observed during all analysis periods (e.g., daytime, nighttime, and total), as compared to the ONE case. In particular, the large effect of grid nudging on the near-surface meteorological factors (temperature, relative humidity, and wind fields) was predicted at the coastline and nearby sea during daytime. The results for application domains showed that the effects of nudging were distinguished between the meteorological factors and between the time periods. When applied grid nudging until subdomain, the improvement effects of temperature and relative humidity had differential tendencies. Temperature was increased for all time, but relative humidity was increased in daytime and was decreased in nighttime. Thus, GNE case showed better result than other cases.

• 월간양계
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• 제15권통권162호
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• pp.48-50
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• 1983

• 생명과학회지
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• 제24권3호
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• pp.311-317
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• 2014

Rimed vacuole을 가진 원위 근육병(distal myopathy with rimmed vacuoles, DMRV)은 제2형 유전성 봉입체 근육병으로도 불리며 초기 성인기에 발병하여 원위부의 근력약화를 보이는 임상양상과 rimmed vacuole의 근육병리소견을 특징으로 하는 상염색체 열성의 근육병이다. 이러한 DMRV의 원인은 UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) 유전자의 돌연변이임이 밝혀져 있다. 저자들은 원위부 근력약화를 호소하는 환자에서 전체 엑솜 염기서열분석을 이용하여 GNE 유전자의 복합 이형접합성 돌연변이(p.Asp176Val 및 p.Val572Leu)를 확인하여 DMRV를 진단할 수 있었다. 본 연구는 근육병의 정확한 분자진단에 있어서 전체 엑솜 염기서열분석의 유용성을 보여주었기에 이를 보고하는 바이다.

• Coupled systems mechanics
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• 제8권2호
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• pp.95-98
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• 2019

This special issue contains selected papers first presented in a short format at the Congress CILAMCE 2018 ($39^{th}$ Ibero-Latin American Congress on Computational Methods in Engineering) held in Paris and in $Compi{\grave{e}}gne$, France, from 11 to 14 November 2018.

• Annals of Clinical Neurophysiology
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• 제21권2호
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• pp.79-86
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• 2019

Background: Magnetic resonance (MR) images are useful for diagnosing myopathy. The purpose of this study was to determine the usefulness of lower-limb MR images in Korean patients with distal myopathy. Methods: We reviewed medical records in the myopathy database from January 2002 to October 2016. We selected 21 patients from 91 unrelated families with distal myopathy: four with GNE myopathy, 11 with dysferlinopathy, and six with ADSSL1 myopathy. Results: Ten (48%) of the 21 patients were men. The ages of the participants at symptom onset and imaging were $19.2{\pm}9.5$ and $30.4{\pm}9.0$ years (mean${\pm}$standard deviation), respectively. Their grade on the modified Gardner-Medwin and Walton grade was $3.3{\pm}1.7$. The strength grade of the knee extensors was not correlated with the Mercuri scale for the quadriceps (r = -0.247, p = 0.115). However, the Medical Research Council grades of the knee flexors, ankle dorsiflexors, and ankle plantar flexors were significantly correlated with the Mercuri scale ratings of the knee flexors (r = -0.497, p = 0.001), tibialis anterior (r = -0.727, p < 0.001), and ankle plantar flexors (r = -0.620, p < 0.001), respectively. T1-weighted MR images showed characteristic fatty replacement patterns that were consistent with the causative genes. Unsupervised hierarchical clustering of the Mercuri scale showed that the main factors contributing to the dichotomy were the causative gene and the clinical severity. Conclusions: This study is the first to reveal the usefulness of lower-limb MR images in the differential diagnosis of distal myopathy in Korea.

• 대한치과의사협회지
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• 제12권5호
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• pp.327-332
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• 1974

The effects of enamel solubility by the varying concentration of fluoride and phosphate as well as pH of the acid fluoride-phosphate solutions were tested and compared with th 7% stannous fluoride solution. The smooth surface of the sound permanent 1st premolars were demineralized by the Buttner's method. And the phosphorus extracted from the 1st premolars were analyzed by the Fiske and Subbarow's method. Enamel smooth surfaces treated with the acid fluoride-phosphate solution and the 8% stannous fluoride solution were obserbed electron-microscopically by the Filmy Replica method. The results of this study were summarized as follows: !. The least enamel dissolution rate was observed at the acid fluoride-phosphate solution contained 1.25% fluorine, 0.5% phosphate, and pH 4. 2. The anti-cariogenic effects comparison between the acid fluoride-phosphate solution and 8% stannous fluoride, the former was higher.

• 한국동물학회지
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• 제38권2호
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• pp.196-203
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• 1995

The c-myc proto-oncogene, one of the immediately earlY genes, is expressed in various mammalian cell types and heavily involved in the regulation of cell proliferation and differentiation. To determine endogeneous expression pattern of c-myc gene in preimpBantation mouse embwos, we employed a reverse transcription coupled to polvrnerase chain reaction (RT-PCR). Transcript of c-myc was detected at fertilized embryos as a maternal transcript. At the early two-cell stave, transcript of c-myc gene was hardly detected, bu, appeared at late two-cell embryos as a zygotic transcript. The level of c-myc expresion was increased at later stases and peaked at blastocvst stage. To examine the functional role of promoter region for c-myc gene transcription, we fused the 5'upstream region (1.8 kb) including econ 1 of c-myc genomic DNA with E. coli lacE gene fnamed as pcMYC-laczl. pcMYC-lacZ was microiniected into the pronscleus of mouse one-cell embryovs, and p·salactosidase activity was determined tv histochemical staining with X-gal at different stases. f-galactosidase activity was detected only at blastocyst, but not at the earlier stage embryos. This result indicates that c-myc gene is transcriptionallv active during mouse preimplantation development.

• Tuberculosis and Respiratory Diseases
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• 제43권1호
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• pp.8-13
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• 1996

연구배경: 결핵균 katG유전자내 463 codon의 돌연변이는 INH 내성과 관련이 있을 것으로 보고되고 있어서 INH 감수성 균주를 대상으로 katG 유전자내 463 codon의 돌연변이 발생빈도를 관찰하여 INH 내성과의 관련성을 밝히고자 하였다. 방법: INH 감수성 균주(MIC${\geq}\;0.2{\mu}g/ml$) 28주를 선정하여 DNA를 추출하여 katG 유전자내 463 codon을 포함하는 지역을 PCR로 증폭 합성하였다. PCR산물을 제한효소인 Msp I으로 처리하여 절단 여부를 관찰하였고 그리고 SSCP로 표준균주와 차이를 관찰하였다. 결과: INH 감수성 균주 28주 중에서 7주(25%)만이 제한효소 Msp I에 의해 절단 되었다. 절단되지 않은 21주(75%)는 SSCP에서도 표준균주와 다른 양상을 나타내었다. 제한 효소로 절단되지 않은 균주의 katG 유전자를 염기서열 분석한 결과 463 codon Arg(CGG)이 Leu(CTG)으로 치환 되어있었다. 결론: INH내성에 영향을 줄 것으로 추정 되고있던 katG 유전자 463 codon 돌연변이는 INH 내성과 무관한 것으로 판명되었다.

• Molecules and Cells
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• 제22권3호
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• pp.343-352
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• 2006

Sialic acid is a sugar typically found at the N-glycan termini of glycoproteins in mammalian cells. Lec3 CHO cell mutants are deficient in epimerase activity, due to a defect in the gene that encodes a bifunctional UDP-GlcNAc 2-epimerase/ManNAc kinase (GNE). Sialic acid modification on the cell surface is partially affected in these cells. We have mutagenized Lec3 CHO cells and isolated six mutants (termed C2m) deficient in the cell surface expression of polysialic acid (PSA). Mutant C2m9 was partially defective in expression of cell-surface PSA and wheat germ agglutinin (WGA) binding, while in the other five mutants, both cell-surface PSA and WGA binding were undetectable. PSA expression was restored by complementation with the gene encoding the CMP-sialic acid transporter (CST), indicating that CST mutations were responsible for the phenotypes of the C2m cells. We characterized the CST mutations in these cells by Northern blotting and RT-PCR. C2m9 and C2m45 carried missense mutations resulting in glycine to glutamate substitutions at amino acids 217 (G217E) and 256 (G256E), respectively. C2m13, C2m39 and C2m31 had nonsense mutations that resulted in decreased CST mRNA stability, and C2m34 carried a putative splice site mutation. PSA and CD15s expression in CST-deficient Lec2 cells were partially rescued by G217E CST, but not by G256E CST, although both proteins were expressed at similar levels, and localized to the Golgi. These results indicate that the novel missense mutations isolated in this study affect CST activity.

• 공연문화연구
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• 제18호
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• pp.257-282
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• 2009

현재 국내에는 크게 세 종류의 뮤지컬이 공연되고 있다. 대본이나 음악을 순수하게 창작하여 공연하는 창작 뮤지컬, 외국 작품이 그대로 수입되어 공연되는 오리지널 뮤지컬 그리고 외국의 공연을 국내에서 라이선스를 취득하여 무대화하는 라이선스 뮤지컬. 모두 중요한 공연이고 필요한 공연일 것이다. 그러나 특히 라이선스 공연의 경우 다소간 문제가 있다고 볼 수 있다. 왜냐하면 세계적으로 알려진 작품들의 경우, 그 공연을 국내에서 제작함에 있어 국내의 작품성이나 아이덴티티는 완전히 무시되고 원작을 있는 그대로 복사할 것을 요구받기 때문이다. 완전히 서로 다른 문화적인 배경을 무시한 채 외국의 공연을 시청각적인 모든 면에서, 연기와 행동의 모든 면에서 동일하게 재생산을 요구하는 것은 그 공연이 무대에 오르는 사회에서 보다 강력하게 흡수되고 예술적인 영향력을 강하게 끼칠 수 있는 기회를 포기하는 것이라 볼 수 있다. 문화란 시공간을 초월하여 어느 곳에서나 동일하지 않기 때문이다. 이는 매우 주의 깊게 관찰되고 경계되어야 하는 일일 것이다. 왜냐하면 이런 공연들로 인하여 국내의 문화적인 지형이 파괴되거나 변형될 수 있기 때문이다. 그러므로 문화적인 정체성을 보다 확고히 확립하고 문화에 근거를 둔 예술교육을 진행함과 동시에 문화적인 작품들의 제작에 관심을 기울여야 할 것이다.