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Lee, K. H.,Kang, S. K.,Goo, J. M.,Lee, J. S.,Cheon, G. J.,Seo, S.,Hwang, E. J. INTERNATIONAL INSTITUTE OF ANTICANCER RESEARCH 2017 Anticancer research Vol.37 No.3
<P>Background/Aim: To compare the relationship between Ktrans from DCE-MRI and K1 from dynamic (NNH3)-N-13- PET, with simultaneous and separate MR/PET in the VX-2 rabbit carcinoma model. Materials and Methods: MR/PET was performed simultaneously and separately, 14 and 15 days after VX-2 tumor implantation at the paravertebral muscle. The Ktrans and K-1 values were estimated using an in-house software program. The relationships between Ktrans and K-1 were analyzed using Pearson's correlation coefficients and linear/non-linear regression function. Results: Assuming a linear relationship, Ktrans and K-1 exhibited a moderate positive correlations with both simultaneous ( r=0.54-0.57) and separate ( r=0.53-0.69) imaging. However, while the Ktrans and K-1 from separate imaging were linearly correlated, those from simultaneous imaging exhibited a non-linear relationship. The amount of change in K-1 associated with a unit increase in Ktrans varied depending on Ktrans values. Conclusion: The relationship between K-trans and K-1 may be mis-interpreted with separate MR and PET acquisition.</P>
K<sub>2</sub>WO<sub>4</sub> flux 에 의한 K<sub>2</sub>Oㆍ6TiO<sub>2</sub> whisker 의 합성
이진식 ( J. S. Lee ),이상문 ( S. M. Lee ),이철태 ( C. T. Lee ),권긍택 ( K. T. Kohn ),김영명 ( Y. M. Kim ) 한국공업화학회 1993 한국공업화학회 연구논문 초록집 Vol.1993 No.0
K<sub>2</sub>Oㆍ6TiO<sub>2</sub> whisker는 구조적인 특성 때문에 물리ㆍ화학적으로 매우 안정하며 보강재, 마찰재, 단열재 등의 많은 용도를 갖게된다. 특히 최근에는 석면이 발암물질로 인한 자동차 브레이크 마찰재료의 사용이 금지됨에 따라 K<sub>2</sub>Oㆍ6TiO<sub>2</sub> whisker는 이의 대체 섬유로서 주목을 받고 있다. 이러한 K<sub>2</sub>Oㆍ6TiO<sub>2</sub> whisker의 합성방법으로는 TiO<sub>2</sub>와 K<sub>2</sub>CO<sub>3</sub>의 화학양론적 조성의 혼합들을 설정온도에서 소성(calcination method)시키는 방법을 비롯하여 응용법(melting method), 수열법(hydrothermal method), 융제법(flux) 및 KDC법(kneading-drying-calcination method) 등의 방법이 있다. 그러나 수열법의 경우 양질의 whisker를 얻을 수 있으나 고압합성 이므로 위험하고 가격이 비싼 결점이 있으며 공업상 제조에 필요한 조건이 복잡하고 연속조작이 어려워 비현실적인 방법이다. 또한 서냉소성법의 경우 공정이 단순하며 공업화가 쉬우나 비교적 장섬유가 얻어지게 된다. 따라서 본 연구에서는 융제법을 이용하여 K<sub>2</sub>Oㆍ6TiO<sub>2</sub> whisker를 합성하였으며. 과거에 용제로 사용된 KC1-KF계. K<sub>2</sub>O-Na<sub>2</sub>O-B<sub>2</sub>O<sub>3</sub>계 등의 높은 volatility와 viscosity 그리고 낮은 solubility에 대한 문제점을 개선하기 위해 K<sub>2</sub>WO<sub>4</sub>를 flux로 선정하여 K<sub>2</sub>Oㆍ6TiO<sub>2</sub> whisker를 합성하였다.
Novel dentin phosphoprotein frameshift mutations in dentinogenesis imperfecta type II
Lee, K‐,E,Kang, H‐,Y,Lee, S‐,K,Yoo, S‐,H,Lee, J‐,C,Hwang, Y‐,H,Nam, KH,Kim, J‐,S,Park, J‐,C,Kim, J‐,W Blackwell Publishing Ltd 2011 Clinical genetics Vol.79 No.4
<P>Lee K‐E, Kang H‐Y, Lee S‐K, Yoo S‐H, Lee J‐C, Hwang Y‐H, Nam KH, Kim J‐S, Park J‐C, Kim J‐W. Novel dentin phosphoprotein frameshift mutations in dentinogenesis imperfecta type II.</P><P>The dentin sialophosphoprotein (<I>DSPP</I>) gene encodes the most abundant non‐collagenous protein in tooth dentin and DSPP protein is cleaved into several segments including the highly phosphorylated dentin phosphoprotein (DPP). Mutations in the <I>DSPP</I> gene have been solely related to non‐syndromic form of hereditary dentin defects. We recruited three Korean families with dentinogenesis imperfecta (DGI) type II and sequenced the exons and exon–intron boundaries of the <I>DSPP</I> gene based on the candidate gene approach. Direct sequencing of PCR products and allele‐specific cloning of the highly repetitive exon 5 revealed novel single base pair (bp) deletional mutations (c.2688delT and c.3560delG) introducing hydrophobic amino acids in the hydrophilic repeat domain of the DPP coding region. All affected members of the three families showed exceptionally rapid pulp chambers obliteration, even before tooth eruption. Individuals with the c.3560delG mutation showed only mild, yellowish tooth discoloration, in contrast to the affected individuals from two families with c.2688delT mutation. We believe that these results will help us to understand the molecular pathogenesis of DGI type II as well as the normal process of dentin biomineralization.</P>
Runx3 is required for the differentiation of lung epithelial cells and suppression of lung cancer
Lee, K-S,Lee, Y-S,Lee, J-M,Ito, K,Cinghu, S,Kim, J-H,Jang, J-W,Li, Y-H,Goh, Y-M,Chi, X-Z,Wee, H,Lee, H-W,Hosoya, A,Chung, J-H,Jang, J-J,Kundu, J K,Surh, Y-J,Kim, W-J,Ito, Y,Jung, H-S,Bae, S-C Macmillan Publishers Limited 2010 Oncogene Vol.29 No.23
Human lung adenocarcinoma, the most prevalent form of lung cancer, is characterized by many molecular abnormalities. K-ras mutations are associated with the initiation of lung adenocarcinomas, but K-ras-independent mechanisms may also initiate lung tumors. Here, we find that the runt-related transcription factor Runx3 is essential for normal murine lung development and is a tumor suppressor that prevents lung adenocarcinoma. Runx3−/− mice, which die soon after birth, exhibit alveolar hyperplasia. Importantly, Runx3−/− bronchioli exhibit impaired differentiation, as evidenced by the accumulation of epithelial cells containing specific markers for both alveolar (that is SP-B) and bronchiolar (that is CC10) lineages. Runx3−/− epithelial cells also express Bmi1, which supports self-renewal of stem cells. Lung adenomas spontaneously develop in aging Runx3+/− mice (∼18 months after birth) and invariably exhibit reduced levels of Runx3. As K-ras mutations are very rare in these adenomas, Runx3+/− mice provide an animal model for lung tumorigenesis that recapitulates the preneoplastic stage of human lung adenocarcinoma development, which is independent of K-Ras mutation. We conclude that Runx3 is essential for lung epithelial cell differentiation, and that downregulation of Runx3 is causally linked to the preneoplastic stage of lung adenocarcinoma.