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      • KCI등재

        돼지 H-FABP 유전자의 다형성 및 경제 형질과의 연관성 구명

        최봉환,김태헌,이지웅,조용민,이혜영,조병욱,정일정 한국동물자원과학회 2003 한국축산학회지 Vol.45 No.5

        The purpose of this study was to detect association between genetic variation and economic trait in the porcine heart type fatty acid-binding protein gene as a candidate gene for the traits related with growth and meat quality in pigs. The H-FABP is a 15-kDa protein expressed in several tissues with high demand for fat metabolism such as cardiac and skeletal muscle and lactating mammary gland. H-FABP is small intracellular protein involved in fatty acid transport from the plasma membrane to the site of β-oxidation and/or triacylglycerol or phospholipid synthesis. In this study, H-FABP PCR-RFLP was performed in F_(2) population composed of 214 individuals form an intercross between Korean Native Boars and Landrace sows. PCR products form tow primer sets within H-FABP gene were amplified in 850bp and 700bp. Digestion of PCR products with the restriction digestion enzymes HaeⅢ and Hinf Ⅰ, revealed fragment length polymorphisms(RFL. Ps). The genotype frequencies from H-FABP/HaeⅢ was .29 for genotype DD, .53 for genotype Dd, and .15 for genotype dd, respectively. The genotype frequencies of HH, Hh, and hh from H-FABP(hinf Ⅰ was .38, .41, and .20, respectively, in the population.Relationships between their genotypes and economic traits were estimated. In H-FABP/HaeⅢ locus, there were specific genotypes(Dd and dd) associated with economic traits such as body weight. In H-FABP/Hinf Ⅰ Iocus, Genotypes of HH and Hh associated with growth traits such as body weights at 5, 12, and 30 week of age (p<.05 or p<.001) and back fat thickness, body fat including abdominal and trimmed fat (p<.001) and intramuscular fat(p<.05). The 'H'allele was positivecly associated with gaining of body weight and fatness deposition. In conclusion, a significant association of the H-FABP gene from its genetic variation was found on body weight, intramuscular fat and backfat thickness.

      • Supplementation of oil-based inactivated H9N2 vaccine with M2e antigen enhances resistance against heterologous H9N2 avian influenza virus infection

        Park, J.K.,Lee, D.H.,Cho, C.H.,Yuk, S.S.,To, E.O.,Kwon, J.H.,Noh, J.Y.,Kim, B.Y.,Choi, S.W.,Shim, B.S.,Song, M.K.,Lee, J.B.,Park, S.Y.,Choi, I.S.,Song, C.S. Elsevier Scientific Pub. Co 2014 Veterinary microbiology Vol.169 No.3

        Avian influenza virus (AIV) subtype H9N2 has been evolving rapidly and vaccine escape variants have been reported to cause circulation of infections and economic losses. In the present study, we developed and evaluated ectodomain of the AIV matrix 2 (M2e) protein as a supplementing antigen for oil-based inactivated H9N2 vaccine to increase resistance against vaccine escape variants. AIV H9N2 M2e antigen was expressed in Escherichia coli and supplemented to inactivated H9N2 oil emulsion vaccine. Specific pathogen-free chickens received a single injection of inactivated H9N2 oil emulsion vaccines with or without M2e supplementation. At three weeks post vaccination, hemagglutination inhibition tests and enzyme-linked immunosorbent assays were performed to determine serological immune responses. Challenge study using a vaccine escape H9N2 variant was performed to evaluate the efficacy of M2e supplementation. M2e antigen supplemented in oil emulsion vaccine was highly immunogenic, and a single M2e-supplemented vaccination reduced challenge virus replication and shedding more effectively than non-supplemented vaccination.

      • Enhanced PCR efficiency of high-fidelity DNA polymerase from Thermococcus waiotapuensis

        Cho, S.S.,Yu, M.,Kim, S.H.,Kwon, S.T. IPC Science and Technology Press ; Elsevier Scienc 2014 Enzyme and microbial technology Vol.63 No.-

        Twa DNA polymerase from hyperthermophilic archaeon Thermococcus waiotapuensis has exceedingly high fidelity among family B DNA polymerases. However, Twa DNA polymerase has significant shortcomings in terms of a low extension rate and poor processivity. To resolve these weaknesses, we focused on two amino acid residues (N565 and H633) in the palm and thumb subdomains of the Twa DNA polymerase. These two residues were replaced by site-directed mutagenesis and the enzymatic properties of the mutants were analyzed. Here, Twa H633R DNA polymerase showed significantly improved polymerase function compared to wild-type Twa DNA polymerase in terms of processivity (2-fold), extension rate (1.5-fold) and PCR efficiency. Kinetic analysis using DNA as a template revealed that the k<SUB>cat</SUB> value of the Twa H633R mutant was similar to that of wild-type, but the K<SUB>m</SUB> of the Twa H633R mutant was about 1.6-fold lower than that of the wild-type. These results showed that the Arg residue substitution at H633 located in the thumb subdomain has a positive effect on processivity, extension rate and PCR efficiency, suggesting that the Twa H633R mutant allows a conformational change for easy access of the primer-template to the binding site of the polymerase domain.

      • SCISCIESCOPUSKCI등재

        Aluminizing and Boroaluminizing Treatments of Mar-M247 and Their Effect on Hot Corrosion Resistance in Na₂SO₄-NaCl Molten Salt

        Cho, J.H.,Kim, T.W.,Son, K.S.,Yoon, J.H.,Kim, H.S.,Leisk, G.G.,Mitton, D.B.,Latanision, R.M. 대한금속재료학회 2003 METALS AND MATERIALS International Vol.9 No.3

        The effect of surface modifications of Mar-M247 superalloy on hot corrosion resistance was examined in Na₂SO₄-NaCl molten salt. The Mar-M247 was aluminized and boroaluminized by pack cementation in Ar and underwent a cyclic hot corrosion test in Na₂SO₄-NaCl molten salt. The XRD results showed that a Ni2Al3 phase was formed between the aluminized layer and the substrate when the surface modification temperature was below 1273 K. However, a NiAl phase formed when the temperature was above 1273 K. The intensity of the XRD peak in the NiAl phase increased after post heat treatment. Hot corrosion resistance increased for the specimens containing NiAl rather than Ni₂Al₃ phase. The ductile NiAl phase suppressed the potential for crack initiation during thermal cycling. Post heat treatment increased the corrosion resistance of the aluminized layer for Mar-M247, which underwent surface modification at 1273 K and above. In the boroaluminized Mar-M247 specimens, corrosion resistance decreased as a result of the blocking of outward diffusion of Cr by boron and decreased cohesion between the oxide scale and the aluminized layer during thermal cycling.

      • KCI우수등재

        돼지의 선발에 있어서 능력검정 방법에 따른 육종가 및 유전적 개량량의 변화

        조규호,김시동,김명직,이일주,전광주 한국동물자원과학회 2001 한국축산학회지 Vol.43 No.6

        본 연구에서는 이유시체중(㎏), 90㎏ 도달일령을 대상형질로 하여 폐쇄돈군에서 이유시 체중을 기초로 5가지의 선발방법에 따라 선발된 선발축의 산육 능력을 검정하여 검정이 완료된 개체들에 대해 유전능력 평가를 실시한후 검정대상 선발두수의 크기에 따른 유전적 개량량을 비교하여 이상적인 검정방법을 찾고자 실시하였다. 시뮬레이션 결과 90㎏ 도달일령에 대한 육종가 추정치의 변화는 Method Ⅴ그룹에서 -36.2일의 단축효과를 보였으며 세대당 유전적 개량량 또한 Method Ⅴ그룹에서 -7.5일로 가장 높은 개량을 보였다. 따라서 개량적인 측면에 있어서는 전수검정을 실시하는 것이 가장 좋을 것으로 사료되지만 농장의 검정능력이나 전수검정을 실시할 때 드는 초과비용에 대한 경제적인 분석은 더 연구되어져야 될 것으로 사료된다. This study was carried out to find the ideal testing method by comparing predicted breeding values, and genetic gain by the size of testing group. Tested traits were weaning weight and days to 90㎏. Five methods for selecting testing group were adopted: Method Ⅰ (MⅠ ; 30% selected based on litter weight at weaning for female, and 30% selected based on individual weight at weaning for mail), Method Ⅱ (MⅡ ; 30% selected based on individual weight at weaning for female and male, respectively), Method Ⅲ (MⅢ ; 50% selected based on individual weight at weaning for female and male, respectively), Method Ⅳ (MⅣ ; 70% selected based on individual weight at weaning for female and male, respectively), Method Ⅴ (MⅤ ; all piglets were tested). Genetic ability was evaluated by multiple trait animal model using MTDFREML package. Based on the predicted breeding values for days to 90㎏, the next generation was selected up to 5th generation. The above procedure were repeated and simulated by 4 times. The results obtained in the present study are summarized as follows; Phenotypic mean and predicted breeding values mean of days to 90㎏ was 114.3, -27.8, 113.7, -27.0, 107.5, -32.6, 105.7, -34.4, 103.7 and -36.2 days for MⅠ, MⅡ, MⅢ, MⅣ and MⅤ, respectively. Phenotypic and predicted breeding values variance of days to 90㎏ was 20.9, 4.1, 19.0, 3.4, 15.3, 1.8, 13.8, 1.7, 13.3 and 1.2 days for MⅠ, MⅡ, MⅢ, MⅣ and MⅤ, respectively. Genetic gain of days to 90㎏ was -6.2, -6.0, -7.1, -7.3 and -7.5 days for MⅠ, MⅡ, MⅢ, MⅣ and MⅤ, respectively. In all case, Method Ⅴ group, all piglets be tested, is the most efficient for improving the target economic traits.

      • SCISCIESCOPUS

        Attenuation of oxidative neuronal cell death by coffee phenolic phytochemicals

        Cho, E.S.,Jang, Y.J.,Hwang, M.K.,Kang, N.J.,Lee, K.W.,Lee, H.J. Elsevier 2009 Mutation research Vol.661 No.1

        Neurodegenerative disorders such as Alzheimer's disease (AD) are strongly associated with oxidative stress, which is induced by reactive oxygen species (ROS) including hydrogen peroxide (H<SUB>2</SUB>O<SUB>2</SUB>). Recent studies suggest that moderate coffee consumption may reduce the risk of neurodegenerative diseases such as AD, but the molecular mechanisms underlying this effect remain to be clarified. In this study, we investigated the protective effects of chlorogenic acid (5-O-caffeoylquinic acid; CGA), a major phenolic phytochemical found in instant decaffeinated coffee (IDC), and IDC against oxidative PC12 neuronal cell death. IDC (1 and 5μg/ml) or CGA (1 and 5μM) attenuated H<SUB>2</SUB>O<SUB>2</SUB>-induced PC12 cell death. H<SUB>2</SUB>O<SUB>2</SUB>-induced nuclear condensation and DNA fragmentation were strongly inhibited by pretreatment with IDC or CGA. Pretreatment with IDC or CGA also inhibited the H<SUB>2</SUB>O<SUB>2</SUB>-induced cleavage of poly(ADP-ribose) polymerase (PARP), and downregulation of Bcl-X<SUB>L</SUB> and caspase-3. The accumulation of intracellular ROS in H<SUB>2</SUB>O<SUB>2</SUB>-treated PC12 cells was dose-dependently diminished by IDC or CGA. The activation of c-Jun N-terminal protein kinase (JNK) and p38 mitogen-activated protein kinase (MAPK) by H<SUB>2</SUB>O<SUB>2</SUB> in PC12 cells was also inhibited by IDC or CGA. Collectively, these results indicate that IDC and CGA protect PC12 cells from H<SUB>2</SUB>O<SUB>2</SUB>-induced apoptosis by blocking the accumulation of intracellular ROS and the activation of MAPKs.

      • Evolution of carbides in cold-work tool steels

        Kim, H.,Kang, J.Y.,Son, D.,Lee, T.H.,Cho, K.M. Elsevier 2015 Materials characterization Vol.107 No.-

        This study aimed to present the complete history of carbide evolution in a cold-work tool steel along its full processing route for fabrication and application. A sequence of processes from cast to final hardening heat treatment was conducted on an 8% Cr-steel to reproduce a typical commercial processing route in a small scale. The carbides found at each process step were then identified by electron diffraction with energy dispersive spectroscopy in a scanning or transmission electron microscope. After solidification, MC, M<SUB>7</SUB>C<SUB>3</SUB> and M<SUB>2</SUB>C carbides were identified and the last one dissolved during hot compression at 1180<SUP>o</SUP>C. In a subsequent annealing at 870<SUP>o</SUP>C followed by slow cooling, M<SUB>6</SUB>C and M<SUB>23</SUB>C<SUB>6</SUB> were added, while they were dissolved in the following austenitization at 1030<SUP>o</SUP>C. After the final tempering at 520<SUP>o</SUP>C, fine M<SUB>23</SUB>C<SUB>6</SUB> precipitated again, thus the final microstructure was the tempered martensite with MC, M<SUB>7</SUB>C<SUB>3</SUB> and M<SUB>23</SUB>C<SUB>6</SUB> carbide. The transient M<SUB>2</SUB>C and M<SUB>6</SUB>C originated from the segregation of Mo and finally disappeared due to attenuated segregation and the consequent thermodynamic instability.

      • Divergences in morphological changes and antioxidant responses in salt-tolerant and salt-sensitive rice seedlings after salt stress

        Lee, M.H.,Cho, E.J.,Wi, S.G.,Bae, H.,Kim, J.E.,Cho, J.Y.,Lee, S.,Kim, J.H.,Chung, B.Y. Gauthier-Villars ; Elsevier Science Ltd 2013 Plant physiology and biochemistry Vol.70 No.-

        Salinization plays a primary role in soil degradation and reduced agricultural productivity. We observed that salt stress reversed photosynthesis and reactive oxygen scavenging responses in leaves or roots of two rice cultivars, a salt-tolerant cultivar Pokkali and a salt-sensitive cultivar IR-29. Salt treatment (100 mM NaCl) on IR-29 decreased the maximum photochemical efficiency (Fv/Fm) and the photochemical quenching coefficient (qP), thereby inhibiting photosynthetic activity. By contrast, the salt treatment on Pokkali had the converse effect on Fv/Fm and qP, while increasing the nonphotochemical quenching coefficient (NPQ), thereby favoring photosynthetic activity. Notably, chloroplast or root cells in Pokkali maintained their ultrastructures largely intact under the salt stress, but, IR-29 showed severe disintegration of existing grana stacks, increase of plastoglobuli, and swelling of thylakoidal membranes in addition to collapsed vascular region in adventitious roots. Pokkali is known to have higher hydrogen peroxide (H<SUB>2</SUB>O<SUB>2</SUB>)-scavenging enzyme activities in non-treated seedlings, including ascorbate peroxidase, catalase, and peroxidase activities. However, these enzymatic activities were induced to a greater extent in IR-29 by the salt stress. While the level of endogenous H<SUB>2</SUB>O<SUB>2</SUB> was lower in Pokkali than in IR-29, it was reversed upon the salt treatment. Nevertheless, the decreased amount of H<SUB>2</SUB>O<SUB>2</SUB> in IR-29 upon the salt stress didn't result in a high scavenging activity of total cell extracts for H<SUB>2</SUB>O<SUB>2</SUB>, as well as O<SUB>2</SUB>?<SUP>-</SUP> and ?OH species. The present study suggests that the tolerance to the moderate salinity in Pokkali derives largely from the constitutively maintained antioxidant enzymatic activities as well as the induced antioxidant enzyme system.

      • Oxidative degradation of endotoxin by advanced oxidation process (O<sub>3</sub>/H<sub>2</sub>O<sub>2</sub> & UV/H<sub>2</sub>O<sub>2</sub>)

        Oh, B.T.,Seo, Y.S.,Sudhakar, D.,Choe, J.H.,Lee, S.M.,Park, Y.J.,Cho, M. Elsevier Scientific Pub. Co 2014 Journal of hazardous materials Vol.279 No.-

        The presence of endotoxin in water environments may pose a serious public health hazard. We investigated the effectiveness of advanced oxidative processes (AOP: O<SUB>3</SUB>/H<SUB>2</SUB>O<SUB>2</SUB> and UV/H<SUB>2</SUB>O<SUB>2</SUB>) in the oxidative degradation of endotoxin. In addition, we measured the release of endotoxin from Escherichia coli following typical disinfection methods, such as chlorine, ozone alone and UV, and compared it with the use of AOPs. Finally, we tested the AOP-treated samples in their ability to induce tumor necrosis factor alpha (TNF-α) in mouse peritoneal macrophages. The production of hydroxyl radical in AOPs showed superior ability to degrade endotoxin in buffered solution, as well as water samples from Korean water treatment facilities, with the ozone/H<SUB>2</SUB>O<SUB>2</SUB> being more efficient compared to UV/H<SUB>2</SUB>O<SUB>2</SUB>. In addition, the AOPs proved effective not only in eliminating E. coli in the samples, but also in endotoxin degradation, while the standard disinfection methods lead to the release of endotoxin following the bacteria destruction. Furthermore, in the experiments with macrophages, the AOPs-deactivated endotoxin lead to the smallest induction of TNF-α, which shows the loss of inflammation activity, compared to ozone treatment alone. In conclusion, these results suggest that AOPs offer an effective and mild method for endotoxin degradation in the water systems.

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