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      • KCI등재

        Core/Shell Molecular Imprinting Microparticles Prepared Using RAFT Technology for Degradation of Paraoxon

        Yong Guo,Tian Ying Guo,Ying Yang,Lei Zhang 한국고분자학회 2011 Macromolecular Research Vol.19 No.11

        We have developed a uniform core-shell structured surface hydrogel imprinted molecular imprinting polymer (MIP). This was achieved by surface grafting on a disulfide ester modified polystyrene core, using reversible addition-fragmentation transfer polymerization (RAFT) with N-methacryloyl-histidine-Cu2^+ complex (MAHCu ^2+) as the functional monomer and methyl paraoxon as the template to simulate phosphotriesterase (PTE). Subsequently,we investigated the catalytic (hydrolytic) activities of MIP to the template methyl paraoxon and the template analogue ethyl paraoxon. The results showed that the catalytic (hydrolytic) activity of MIP to the template methyl paraoxon was the highest, and the value of k was 8.67×10^-5 mM·L^-1·min^-1, which was 3.89-fold higher than MIP to ethyl paraoxon and 2.79-fold higher than the non-imprinting polymer (NIP) to methyl paraoxon. The K_m and r_m of MIP were also determined: the K_m was 3.95×10-4 M and the r_m 2.12 μM/min. The MIP can be reused with only lose 7% of catalytic activity for four cycles.

      • SCIESCOPUSKCI등재
      • KCI등재

        SARSEvaluation of CRISPR-Based Assays for Rapid Detection of SARS-CoV-2: A Systematic Review and Meta-Analysis

        Pei-Ying Huang,Xin Yin,Yue-Ting Huang,Qi-Qing Ye,Si-Qing Chen,Xun-Jie Cao,Tian-Ao Xie,Xu-Guang Guo 연세대학교의과대학 2022 Yonsei medical journal Vol.63 No.5

        Purpose: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the pathogen of coronavirus disease 2019. Diagnosticmethods based on the clustered regularly interspaced short palindromic repeats (CRISPR) have been developed to detect SARSCoV-2 rapidly. Therefore, a systematic review and meta-analysis were performed to assess the diagnostic accuracy of CRISPR fordetecting SARS-CoV-2 infection. Materials and Methods: Studies published before August 2021 were retrieved from four databases, using the keywords “SARS-CoV-2”and “CRISPR.” Data were collected from these publications, and the sensitivity, specificity, negative likelihood ratio (NLR), positivelikelihood ratio (PLR), and diagnostic odds ratio (DOR) were calculated. The summary receiver operating characteristic curve wasplotted for analysis with MetaDiSc 1.4. The Stata 15.0 software was used to draw Deeks’ funnel plots to evaluate publication bias. Results: We performed a pooled analysis of 38 independent studies shown in 30 publications. The reference standard was reversetranscription-quantitative PCR. The results indicated that the sensitivity of CRISPR-based methods for diagnosis was 0.94 (95% CI0.93–0.95), the specificity was 0.98 (95% CI 0.97–0.99), the PLR was 34.03 (95% CI 20.81–55.66), the NLR was 0.08 (95% CI 0.06–0.10), and the DOR was 575.74 (95% CI 382.36–866.95). The area under the curve was 0.9894. Conclusion: Studies indicate that a diagnostic method based on CRISPR has high sensitivity and specificity. Therefore, this wouldbe a potential diagnostic tool to improve the accuracy of SARS-CoV-2 detection.

      • Plasma Post-operative miR-21 Expression in the Prognosis of Gastric Cancers

        Ma, Guo-Jian,Gu, Rong-Min,Zhu, Ming,Wen, Xu,Li, Jin-Tian,Zhang, Yuan-Ying,Zhang, Xiao-Mei,Chen, Sen-Qing Asian Pacific Journal of Cancer Prevention 2013 Asian Pacific journal of cancer prevention Vol.14 No.12

        Tumor-associated microRNAs have been detected in serum or plasma, but whether plasma microRNA-21 (miR-21) could be a potential circulating biomarker for gastric cancer (GC) prognosis in Chinese is still uncertain. Real-time quantitative reverse transcription PCR (qRT-PCR) was employed in this study to compare the relative expression of miR-21 between pre-operative and post-operative paired plasmas from 42 patients with primary GCs. The results showed that the expression levels of miR-21 in the post-operative plasmas were significantly reduced by an average of 18.2 times in all patients when compared to the pre-operative plasmas, and by 22.1 times in the subgroup of patients without family history, while only 1.76 times in the subgroup of patients with a family history. With respect of clinicopathological characteristics, the plasma miR-21 expression was highly associated with differentiation degree and lymph node metastasis rate. The results suggested plasma miR-21 could be a novel potential biomarker for GC prognosis and evaluation of surgery outcomes, especially in patients without a family history.

      • Apoptotic Effects of psiRNA-STAT3 on 4T1 Breast Cancer Cells in Vitro

        Zhou, Yue,Tian, Lin,Zhang, Ying-Chao,Guo, Bao-Feng,Zhou, Qing-Wei Asian Pacific Journal of Cancer Prevention 2014 Asian Pacific journal of cancer prevention Vol.15 No.16

        Background: The aim of this study was to investigate the effect of a Lipofectamine2000 (Life2000) Transfection Reagent transfected psiRNA-STAT3 plasmid on 4T1 breast cancer cells. Materials and Methods: MTT was used to detect the cell proliferation of breast cancer 4T1 cells at different periods (0h, 6h, 8h, 10h); the cell cycle was assessed by flow cytometry; variation of apoptosis and mitochondrial membrane potential was observed under a fluorescence microscope; immunohistochemical staining was used to determine the expression of caspase-3 and cyclin-D1 protein. Results: An obvious effect of inhibition to 4T1 cancer cells could be observed at 8h after the psiRNA-STAT3 was transfected. Typical alterations of apoptotic morphological features were visible in the psiRNA-STAT3 treatment group. Mitochondrial membrane potential decreased significantly, the number of cells was increased in G0/G1 phase, and the number of cells was decreased in S phase, and the data were statistically significant (p<0.05), compared with the Scramble and Mock groups. Expression of caspase-3 protein was increased significantly, while that of cyclin D1 was significantly decreased. Conclusions: Life2000 transfected psiRNA-STAT3 plasmid can inhibit 4T1 tumor cell proliferation and promote apoptosis of 4T1 tumor cells, which process depends on the regulation of expression of cyclin D1 and caspase-3 protein.

      • SCIESCOPUSKCI등재
      • KCI등재

        Differential metabolism of juvenile hormone III between diapause and non-diapause of Aspongopus chinensis Dallas (Hemiptera: Dinidoridae) revealed by transcriptome sequencing

        Wu Youfang,Tian Ying,Tan Jun,Zhao Shuai,Zhou Wenzhen,Luo Rui,Guo Jian-Jun 한국응용곤충학회 2021 Journal of Asia-Pacific Entomology Vol.24 No.2

        Aspongopus chinensis Dallas, 1851 is an important insect resource with a long utilization history as traditional Chinese medicine and food owing to its various health benefits, including anti-cancer, anti-bacteria, and anticlotting properties. However, the long period of reproductive diapause during the overwintering stage has limited the broad utilization and artificial cultivation of A. chinensis. Diapause is largely regulated by juvenile hormones. Therefore, understanding the relationship between juvenile hormone metabolism and A. chinensis diapause may provide useful insight for developing genetic engineering strategies to regulate diapause. We identified differentially expressed genes in diapause and non-diapause adults of A. chinensis by transcriptome sequencing. A total of 336,230,260 clean reads were assembled into 80,769 unigenes. Overall, 3,524 differen tially expressed genes were identified, including 2,174 down-regulated and 1,350 up-regulated genes in diapause adults. Among these differentially expressed genes, 22 were significantly enriched in the JH III metabolismrelated pathway based on Kyoto Encyclopedia of Genes and Genomes analysis. These results provide insight into the molecular-level mechanism of diapause regulation and highlight new targets for preventing diapause to improve A. chinensis cultivation and productivity.

      • KCI등재

        Identification of two putative phospholipid hydroperoxide glutathione peroxidase genes and the induction of three environmental stresses in Neoseiulus barkeri (Acari: Phytoseiidae)

        Chuan Bei Tian,Guo Hao Zhang,Ya Ying Li,Huai Liu 한국응용곤충학회 2017 Journal of Asia-Pacific Entomology Vol.20 No.1

        Phospholipid hydroperoxide glutathione peroxidase (PHGPX) is an antioxidant enzyme that plays a crucial role in metabolizing phospholipid hydroperoxides in membrane against oxidative damage. Here, two PHGPX genes fromthe predatory mite Neoseiulus barkeri were identified and characterized (NbPHGPX1 and NbPHGPX2). Alignment analysis of NbPHGPX1 and NbPHGPX2 showed a great deal of similarity with other known PHGPXs from databases. The well-conserved regions, NVASXCGXT, FPCNQFXXQEP, and IKWNFXKFLV, were surrounded by reactive cysteine, glutamine, and tryptophan residues, respectively. The results of quantitative polymerase chain reaction at different stages of the N. barkeri life cycle showed both NbPHGPX1 and NbPHGPX2 genes were highly expressed in male adults, and their levels of expression were determined upon challenge by different triggers. The data showed that the expression of NbPHGPX1 could be induced by low(4 °C) and high (42 °C) temperatures, UV-B, pyridaben and fenpropathrin,whereas NbPHGPX2 could be only up-regulated by high (42 °C) temperature and fenpropathrin. These results suggested that NbPHGPX1 and NbPHGPX2 genesmight participate in protection of the organism from the oxidative damage challenge by oxidative stresses.

      • KCI등재

        Physiological and transcriptome analysis of acclimatory response to cold stress in marine red alga Pyropia yezoensis

        Li-Hong Ma,Lin Tian,Yu-Qing Wang,Cong-Ying Xie,Guo-Ying Du 한국조류학회I 2024 ALGAE Vol.39 No.1

        Red macroalga Pyropia yezoensis is a high valuable cultivated marine crop. Its acclimation to cold stress is especially important for long cultivation period across winter in coasts of warm temperate zone in East Asia. In this study, the response of P. yezoensis thalli to low temperature was analyzed on physiology and transcriptome level, to explore its acclimation mechanism to cold stress. The results showed that the practical photosynthesis activity (indicated by ΦPSII and qP) was depressed and pigment allophycocyanin content was decreased during the cold stress of 48 h. However, the Fv/Fm and non-photochemical quenching increased significantly after 24 h, and the average growth rate of thalli also rebounded from 24 to 48 h, indicating a certain extent of acclimation to cold stress. On transcriptionally, the low temperature promoted the expression of differentially expressed genes (DEGs) related to carbohydrate metabolism and energy metabolism, while genes related to photosynthetic system were depressed. The increased expression of DEGs involved in ribosomal biogenesis and lipid metabolism which could accelerate protein synthesis and enhance the degree of fatty acid unsaturation, might help P. yezoensis thallus cells to cope with cold stress. Further co-expression network analysis revealed differential expression trends along with stress time, and corresponding hub genes play important roles in the systemic acquired acclimation to cold stress. This study provides basic mechanisms of P. yezoensis acclimation to cold temperature and may aid in exploration of functional genes for genetic breeding of economic macroalgae.

      • Screening of MicroRNA in Patients with Esophageal Cancer at Same Tumor Node Metastasis Stage with Different Prognoses

        Zhao, Bao-Sheng,Liu, Shang-Guo,Wang, Tian-Yun,Ji, Ying-Hua,Qi, Bo,Tao, Yi-Peng,Li, Han-Chen,Wu, Xiang-Nan Asian Pacific Journal of Cancer Prevention 2013 Asian Pacific journal of cancer prevention Vol.14 No.1

        Patients at the same pathological stage of esophageal cancer (EC) that received the same surgical therapy by the same surgeon may have distinct prognoses. The current study aimed to explore the possibility of differentially-expressed microRNAs (miRNAs) underlying this phenomenon. Samples were collected from EC patients at the same tumor node metastasis (TNM) stage but with different prognoses. Paracancerous normal tissues were taken as controls. The specimens were histopathologically analyzed. Differentially-expressed miRNAs were analyzed using real-time quantitative reverse transcription polymerase chain reaction. Compared with patients with poor prognosis, those with good prognosis exhibited 88 two-fold or more than two-fold increased miRNA fragments and 4 half-decreased miRNAs. The most noticeably up-regulated miRNAs included hsa-miR-31, hsa-miR-196b, hsa-miR-652, hsa-miR-125a-5p, hsa-miR-146b, hsa-miR-200c, hsa-miR-23b, hsa-miR-29a, hsa-miR-186, hsa-miR-205, hsa-miR-376a, hsa-miR-410, hsa-miR-532-3p, and hsa-miR-598, whereas the most significantly-downregulated miRNAs were hsa-let-7e, hsa-miR-130b, and hsa-miR-103. EC patients at same TNM stage but with different prognoses show differentially-expressed miRNAs.

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