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Lee, K.H.,Choi, E.Y.,Hyun, M.S.,Jang, B.I.,Kim, T.N.,Kim, S.W.,Song, S.K.,Kim, J.H.,Kim, J.-R. S. Karger AG 2007 European surgical research Vol.39 No.4
<P><I>Background:</I> Proteolytic shedding of the ectodomain of a variety of transmembrane proteins, including cell-to-cell adhesion molecules, has been observed in solid cancers. We have investigated whether extracellular cleavage of E-cadherin mediated by matrix metalloproteinase-7 (MMP-7) is involved in hepatocyte growth factor (HGF) induced in vitro invasion in stomach cancer cells. <I>Methods:</I> The effects of HGF on the expression of E-cadherin/β-catenin and MMP-7 at both the protein and mRNA levels were assessed in stomach cancer cells, NUGC-3 and MKN-28, and in cells in which the expression of MMP-7 was downregulated by transfection with a MMP-7 short hairpin RNA plasmid. <I>Results:</I> Treatment with HGF increased the extracellular cleavage of E-cadherin and the release of MMP-7 and reduced the level of E-cadherin in a dose- and time-dependent manner. HGF treatment repressed the phosphorylation of β-catenin in a Triton-soluble fraction, but enhanced this phosphorylation in a Triton-insoluble fraction. The association of E-cadherin with β-catenin was decreased by HGF treatment in the Triton-soluble fraction. In addition, treatment of MMP-7 short hairpin RNA transfected NUGC-3 cells with HGF resulted in no extracellular cleavage of E-cadherin and also decreased the in vitro cell invasion. <I>Conclusions:</I> These results suggest that incubation with HGF mediated the release of MMP-7, resulting in extracellular cleavage of E-cadherin from stomach cancer cells. This might be a key mechanism in HGF-induced in vitro invasion and metastasis.</P><P>Copyright © 2007 S. Karger AG, Basel</P>
Direct analysis of site-specific N-glycopeptides of serological proteins in dried blood spot samples
Choi, N. Y.,Hwang, H.,Ji, E. S.,Park, G. W.,Lee, J. Y.,Lee, H. K.,Kim, J. Y.,Yoo, J. S. Springer Science + Business Media 2017 Analytical and Bioanalytical Chemistry Vol.409 No.21
<P>Dried blood spot (DBS) samples have a number of advantages, especially with respect to ease of collection, transportation, and storage and to reduce biohazard risk. N-glycosylation is a major post-translational modification of proteins in human blood that is related to a variety of biological functions, including metastasis, cell-cell interactions, inflammation, and immunization. Here, we directly analyzed tryptic N-glycopeptides from glycoproteins in DBS samples using liquid chromatography-tandem mass spectrometry (LC-MS/MS) without centrifugation of blood samples, depletion of major proteins, desalting of tryptic peptides, and enrichment of N-glycopeptides. Using this simple method, we identified a total of 41 site-specific N-glycopeptides from 16 glycoproteins in the DBS samples, from immunoglobulin gamma 1 (IgG-1, 10 mg/mL) down to complement component C7 (50 mu g/mL). Of these, 32 N-glycopeptides from 14 glycoproteins were consistently quantified over 180 days stored at room temperature. The major abundant glycoproteins in the DBS samples were IgG-1 and IgG-2, which contain nine asialo-fucosylated complex types of 16 different N-glycopeptide isoforms. Sialo-non-fucosylated complex types were primarily detected in the other glycoproteins such as alpha-1-acid glycoprotein 1, 2, alpha-1-antitypsin, alpha-2-macroglobulin, haptoglobin, hemopexin, Ig alpha 1, 2 chain C region, kininogen-1, prothrombin, and serotransferrin. We first report the characterization of site-specific N-glycoproteins in DBS samples by LC-MS/MS with minimal sample preparation.</P>
Ji, E. S.,Hwang, H.,Park, G. W.,Lee, J. Y.,Lee, H. K.,Choi, N. Y.,Jeong, H. K.,Kim, K. H.,Kim, J. Y.,Lee, S. Springer Science + Business Media 2016 Analytical and Bioanalytical Chemistry Vol.408 No.27
<P>Fucosylation of N-glycoproteins has been implicated in various diseases, such as hepatocellular carcinoma (HCC). However, few studies have performed site-specific analysis of fucosylation in liver-secreted proteins. In this study, we characterized the fucosylation patterns of liver-secreted proteins in HCC plasma using a workflow to identify site-specific N-glycoproteins, where characteristic B- and/or Y-ion series with and without fucose in collision-induced dissociation were used in tandem mass spectrometry. In total, 71 fucosylated N-glycopeptides from 13 major liver-secreted proteins in human plasma were globally identified by LC-MS/MS. Additionally, 37 fucosylated N-glycopeptides were newly identified from nine liver-secreted proteins, including alpha-1-antichymotrypsin, alpha-1-antitrypsin, alpha-2-HS-glycoprotein, ceruloplasmin, alpha-1-acid glycoprotein 1/2, alpha-2-macroglobulin, serotransferrin, and beta-2-glycoprotein 1. Of the fucosylated N-glycopeptides, bi- and tri-antennary glycoforms were the most common ones identified in liver-secreted proteins from HCC plasma. Therefore, we suggest that this analytical method is effective for characterizing fucosylation in liver-secreted proteins.</P>
Lee, J-H,Lee, J-H,Lim, S-N,Kim, D-Y,Kim, S H,Lee, Y-S,Kang, Y-A,Kang, S-I,Jeon, M J,Seol, M,Seo, E-J,Chi, H S,Park, C J,Jang, S,Yun, S-C,Lee, K-H Macmillan Publishers Limited 2010 BONE MARROW TRANSPLANTATION -BASINGSTOKE- Vol.45 No.3
We analyzed the clinical significance of pre-transplant International Prognostic Scoring System (IPSS) score and comorbidity in 68 patients who underwent allogeneic hematopoietic cell transplantation (HCT) for myelodysplastic syndrome (MDS) (n=48) or acute myeloid leukemia evolved from MDS (n=20) between December 1995 and January 2008 in a single institute. During a median follow-up period of 41.0 months (range, 3.2–132.0 months), 27 patients died, and 7 relapsed. The 5-year probabilities of overall survival (OS) and event-free survival (EFS) were 60.0 and 57.4%, respectively, and the 5-year cumulative incidences of non-relapse mortality (CINRM) and relapse were 32.7 and 9.9%, respectively. OS, EFS, and CINRM were significantly different according to pre-transplant IPSS score and presence of pre-transplant comorbidity, which were independent risk factors along with Karnofsky performance score in multivariate analyses. In conclusion, pre-transplant IPSS score and comorbidity may stratify the risk of post transplant outcomes in MDS.
Lee, K.H.,Lee, J.H.,Lee, J.H.,Kim, D.Y.,Park, H.S.,Choi, E.J.,Ko, S.H.,Seol, M.,Lee, Y.S.,Kang, Y.A.,Jeon, M.,Baek, S.,Kang, Y.L.,Kim, S.H.,Yun, S.C.,Kim, H.,Jo, J.C.,Choi, Y.,Joo, Y.D.,Lim, S.N. Kluge Carden Jennings Pub. Co 2017 BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION Vol.23 No.9
To investigate the role of antithymocyte globulin (ATG)-containing reduced-intensity conditioning (RIC) in hematopoietic cell transplantation (HCT) from unrelated (UD) or haploidentical family donors (HFD), we conducted a phase 2 trial of 237 patients (age range, 16 to 69 years) with acute myeloid leukemia (AML) in remission. Patients undergoing UD-HCT (n@?=@?93) or HFD-HCT (n@?=@?59) received RIC comprising busulfan, fludarabine, and ATG, 9@?mg/kg, whereas those undergoing HCT from matched sibling donors (MSD, n@?=@?85) received myeloablative busulfan and cyclophosphamide conditioning or aforementioned RIC with ATG, 4.5@?mg/kg. For graft-versus-host disease (GVHD) prophylaxis, cyclosporine and methotrexate were administered. The median follow-up period was 44.7 months after HCT for 161 survivors. For UD-HCT versus HFD-HCT, there were no significant differences in leukemia recurrence, nonrelapse mortality, relapse-free survival, grades 2 to 4 acute GVHD, and moderate-to-severe chronic GVHD. Furthermore, when the outcomes of UD-HCT and HFD-HCT were combined and compared with those of MSD-HCT, there were no significant differences in leukemia recurrence (3-year cumulative incidence, 30% versus 29%), nonrelapse mortality (3-year cumulative incidence, 7% versus 8%), relapse-free survival (3-year estimate, 63% versus 63%), and grades 2 to 4 acute GVHD (120-day cumulative incidence, 16% versus 13%). Moderate-to-severe chronic GVHD, however, occurred less frequently in UD/HFD-HCT (2-year cumulative incidence, 22% versus 40%; P@?=@?.006). The addition of ATG to conditioning regimen was a significant predictor for less chronic GVHD (subdistribution hazard ratio, .59). In AML in remission, UD/HFD-HCT after ATG-containing RIC achieved leukemia control equivalent to that of MSD-HCT. Despite HLA disparity in UD/HFD-HCT, chronic GVHD occurred less frequently after ATG-containing RIC, suggesting a strong GVHD-modulating effect of ATG.
Neutral-point clamped n-level multilevel converter without dead time and shoot-through problem
Lee, E.,Choi, N.,Kim, H. IET 2017 Electronics letters Vol.53 No.15
<P>A generalised n-level multilevel converter that has no shoot-through problem and thus is operated without dead time at each commutation is proposed. It is obtained by modifying the traditional neutral-point clamped multilevel converter topology based on dual-buck converter concept. The m-phase n-level converter can be readily constructed by using the proposed multilevel converter topology. The half-bridge five-level inverter, as an example case, is presented along with the operating principle and modulation and control methods. Experimental results show the feasibility and validity of the proposed converter.</P>
돼지 대장에서 분리한 E.coli의 중금속 내성에 관한 연구
조창현,정욱진,이영수,최인실,강희옥,박남규,김명화,변미경,이현숙 경상대학교 환경보전연구소 1993 環境保全硏究所報 Vol.1 No.1
돼지의 대장에서 서식하는 466개의 대장균 균주들을 분리하여, 중금속인 Ag, Cd, Cu, Hg, Ni 및Pb에 대한 저항성을 조사 하였다. 거의 대부분의 균주들이 이들 여섯가지 중금속 모두에 강한 저항성을 보였다. 이것은 우리 주위환경의 중금속 오염 정도가 심각하다는 것을 간접적으로 나타내는 것이다. Ag, Pb 및 Hg를 함유하고 있는 고체 배지에서 균주를 성장시켰을때, colony 색깔이 중금속 자체의 광택과 같은 색깔을 나타내는 점으로 보아, 이들 중금속에 대한 저항기작은 유해한 중금속 이온을 세포내 에서 무해한 금속 형태로 전환시켜 세포내에 축적시키는 기작임을 시사하였다. 그 중 가장 높은 저항성을 나타내는 isolate 385를 Ag와 Pb를 함유한 액체배지에서 각각 배양한 뒤 세포내 Ag와 Pb 축적량을 조사한 결과, 건조세포 무게당 0.72g Ag 및 0.23g Pb를 세포내에 축적하고 있었다. 따라서, 이 균주를 유전자 조작 등의 방법으로 개발 한다면 산업 폐수내에 존재하는 이 중금속들의 제거에 효율적으로 사용할 수 있을 것이라 사료된다. We isolated E.coli from porcine intestines and examined the resistances to various heavy-metals, Ag, Cd, Cu, Hg, Ni, and Pb. The 466 isolates were resistant to the heavy-metals. Among them, 72.1% was survived in 1 mM AgNO₃, 9.3% in 80 mM AgNO₃, 95.9% in 0.6 mM Cd(NO₃)₂, 5.6% in 3 mN Cd(NO₃)₂. 95.9% in Cu(NO₃)₂, 48.5% in 0.2 mM HgCl₂, 3.4% in 0.6 mM HgCl₂, 64.4% in 5 mM NiCl₂ and 67.4% in 10 mM Pb(NO₃)₂. The isolate 385 was most resistant to silver and lead ions and the MICs of the ions were 80 mM and 11 mM, respectively. These resistances were inducible by Ag^+ and Pb^2+ ions. When isolate 385 grew in LB-agar plates containing AgNO₃ or Pb(NO₃)₂, the colony colors were changed from light yellow to deep brown. This change to brown color suggests that the resistances of 385 cells to Ag^+ and Pb^2+ ions were due to the reducing mechanism which converted them into the elementary metals(Ag^0, Pb^0) after the uptake of the ions into the cells. The resistant cells accumulated 0.72gr of Ag^0 and 0.23gr of Pb^0 per cells dry wt.
Electrical properties and radiation detector performance of free-standing bulk n-GaN
Lee, I.-H.,Polyakov, A.Y.,Smirnov, N.B.,Govorkov, A.V.,Kozhukhova, E.A.,Zaletin, V.M.,Gazizov, I.M.,Kolin, N.G.,Pearton, S.J. American Vacuum Society 2012 Journal of vacuum science and technology. material Vol.30 No.2