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      • KCI등재

        The USP21/YY1/SNHG16 axis contributes to tumor proliferation, migration, and invasion of non-small-cell lung cancer

        Pei Xu,Haibo Xiao,Qi Yang,Rui Hu,Lianyong Jiang,Rui Bi,Xueyan Jiang,Lei Wang,Ju Mei,Fangbao Ding,Jianbing Huang 생화학분자생물학회 2020 Experimental and molecular medicine Vol.52 No.-

        Deubiquitinases (DUBs) and noncoding RNAs have been the subjects of recent extensive studies regarding their roles in lung cancer, but the mechanisms involved are largely unknown. In our study, we used The Cancer Genome Atlas data set and bioinformatics analyses and identified USP21, a DUB, as a potential contributor to oncogenesis in nonsmall-cell lung cancer (NSCLC). We further demonstrated that USP21 was highly expressed in NSCLCs. We then conducted a series of in vitro and in vivo assays to explore the effect of USP21 on NSCLC progression and the underlying mechanism involved. USP21 promoted NSCLC cell proliferation, migration, and invasion and in vivo tumor growth by stabilizing a well-known oncogene, Yin Yang-1 (YY1), via mediating its deubiquitination. Furthermore, YY1 transcriptionally regulates the expression of SNHG16. Moreover, StarBase bioinformatics analyses predicted that miR4500 targets SNHG16 and USP21. A series of in vitro experiments indicated that SNHG16 increased the expression of USP21 through miR-4500. In summary, the USP21/YY1/SNHG16 axis plays a role in promoting the progression of NSCLC. Therefore, the USP21/YY1/SNHG16/miR-4500 axis may be a potential therapeutic target in NSCLC treatment.

      • KCI등재

        Paritaprevir ameliorates experimental acute lung injury in vitro and in vivo

        Rui Ren,Xin Wang,Zehui Xu,Wanglin Jiang 대한약학회 2023 Archives of Pharmacal Research Vol.46 No.6

        Paritaprevir is a potent inhibitor of the NS3/4A protease used to treat chronic hepatitis C virus infection. However, its therapeutic effect on acute lung injury (ALI) remains to be elucidated. In this study, we investigated the effect of paritaprevir on a lipopolysaccharide (LPS)-induced two-hit rat ALI model. The anti-ALI mechanism of paritaprevir was also studied in human pulmonary microvascular endothelial (HM) cells following LPS-induced injury in vitro. Administration of 30 mg/kg paritaprevir for 3 days protected rats from LPS-induced ALI, as reflected by the changes in the lung coefficient (from 0.75 to 0.64) and lung pathology scores (from 5.17 to 5.20). Furthermore, the levels of the protective adhesion protein VE-cadherin and tight junction protein claudin-5 increased, and the cytoplasmic p-FOX-O1 and nuclear β-catenin and FOX-O1 levels decreased. Similar effects were observed in vitro with LPS-treated HM cells, including decreased nuclear β-catenin and FOX-O1 levels and higher VE-cadherin and claudin-5 levels. Moreover, β-catenin inhibition resulted in higher p-FOX-O1 levels in the cytoplasm. These results suggested that paritaprevir could alleviate experimental ALI via the β-catenin/p-Akt/ FOX-O1 signaling pathway.

      • Luciferase Assay to Screen Tumour-specific Promoters in Lung Cancer

        Xu, Rong,Guo, Long-Jiang,Xin, Jun,Li, Wen-Mao,Gao, Yan,Zheng, You-Xian,Guo, You-Hong,Lin, Yang-Jun,Xie, Yong-Hua,Wu, Ya-Qing,Xu, Rui-An Asian Pacific Journal of Cancer Prevention 2013 Asian Pacific journal of cancer prevention Vol.14 No.11

        Objective: Specific promoters could improve efficiency and ensure the safety of gene therapy. The aim of our study was to screen examples for lung cancer. Methods: The firefly luciferase gene was used as a reporter, and promoters based on serum markers of lung cancer were cloned. The activity and specificity of seven promoters, comprising CEACAM5 (carcinoembryonic antigen, CEA), GRP (Gastrin-Releasing Peptide), KRT19 (cytokeratin 19, KRT), SFTPB (surfactant protein B, SP-B), SERPINB3 (Squamous Cell Carcinoma Antigen, SCCA), SELP (Selectin P, Granule Membrane Protein 140kDa, Antigen CD62, GMP) and DKK1 (Dickkopf-1) promoters were compared in lung cancer cells to obtain cancer-specific examples with strong activity. Results: The CEACAM5, DKK1, GRP, SELP, KRT19, SERPINB3 and SFTPB promoters were cloned. Furthermore, we successfully constructed recombinant vector pGL-CEACAM5 (DKK1, GRP, SELP, KRT19, SERPINB3 and SFTPB) contained the target gene. After cells were transfectedwith recombinant plasmids, we found that the order of promoter activity from high to low was SERPINB3, DKK1, SFTPB, KRT19, CEACAM5, SELP and GRP and the order for promoters regarding specificity and high potential were SERPINB3, DKK1, SELP, SFTPB, CEACAM5, KRT19 and GRP. Conclusion: The approach adopted is feasible to screen for new tumour specific promoters with biomarkers. In addition, the screened lung-specific promoters might have potential for use in lung cancer targeted gene therapy research.

      • KCI등재

        Modified nonlinear force density method for form-finding of membrane SAR antenna

        Rui Xu,DongXu Li,Wang Liu,JianPing Jiang,YiHuan Liao,Jie Wang 국제구조공학회 2015 Structural Engineering and Mechanics, An Int'l Jou Vol.54 No.6

        Form-finding for cable-membrane structures is a delicate operation. During the last decades, the force density method (FDM) was considered to be an efficient method to address the problem. Many researchers were devoted to improving this method and proposed many methods such as natural force density method (NFDM), improved nonlinear force density method (INFDM), et al. In this paper, a modified nonlinear force density method (MNFDM) is proposed. In this method, the stresses of membrane elements were transformed to the force-densities of cable nets by an equivalent relationship, and then they can be used as initial conditions. By comparing with the forming finding results by using the FDM, NFDM, INFDM and MNFDM, it had demonstrated that the MNFDM presented in this paper is the most efficient and precise.

      • An Optimization of CORDIC Algorithm and FPGA Implementation

        Rui Xu,Zhanpeng Jiang,Hai Huang,Changchun Dong 보안공학연구지원센터 2015 International Journal of Hybrid Information Techno Vol.8 No.6

        ASIC and FPGA ASIC and FPGA are considered to be the ideal platform for special fast calculations because of the hardware structure, and how to achieve computational algorithm by is the hotpot of research. The CORDIC (Coordinate Rotational Digital Computer) can break the basis functions down to operations of shift and addition or subtraction, which can be used to lay the foundation for the realization of complex logic. But the functions selected by traditional CODIC for angle encoding are too complex, which will lead to some problems, such as too much of area consumption and large delay. In this paper, an optimization of CORDIC algorithm are proposed, which reduce the consumption of Adders and comparators, decrease the complexity and delay of the algorithm implement in hardware. The proposed algorithms are modeled in Verilog Hardware Description Language and implemented with FPGA. The simulation results show that the functions of sine and cosine are realized successfully, and the proposed algorithm not only improves the computation speed but also reduces the system hardware resources.

      • KCI등재

        Triterpenoids and Sterones from the Stem Bark of Ailanthus altissima

        Xiao-Jiang Zhou,Min Xu,Xue-Song Li,Yue-Hu Wang,Ye Gao,Rui Cai,Yong-Xian Cheng 대한화학회 2011 Bulletin of the Korean Chemical Society Vol.32 No.1

        One new tirucallane-type triterpenoid, alianthusaltinin A (1), one new C29 sterone, alianthaltone A (2), and 12 known compounds have been isolated from the stem bark of Ailanthus altissima. The structures of new compounds were identified by means of spectroscopic methods. Compound 3 was isolated from natural sources for the first time, and compounds 4, 5, and 9 were isolated from this plant for the first time.

      • Quantitative Assessment of the Association between ABC Polymorphisms and Osteosarcoma Response: a Meta-analysis

        Chen, Xu,Jiang, Min,Zhao, Rui-Ke,Gu, Guo-Hao Asian Pacific Journal of Cancer Prevention 2015 Asian Pacific journal of cancer prevention Vol.16 No.11

        Background: ABC proteins are one key type of transport superfamilies which undertake majority of drug transport, which affect the osteosarcoma response to chemotherapeutics. Previous studies have suggested the association between ABC polymorphisms and osteosarcoma response. However, the results of previous studies remain controversial. Therefore, we perform a meta-analysis to get a more precise estimation of this association. The association between ABC polymorphisms and osteosarcoma response was assessed by odds ratios (ORs) together with their 95% confidence intervals (CIs). Three polymorphisms of ABC including ABCB1 rs1128503, ABCC3 rs4148416 and ABCC2 rs717620 polymorphism were investigated. Overall, significant association was observed between ABCC3 rs4148416 polymorphism and osteosarcoma response under allele contrast (T vs. C: OR=1.73, 95%CI=1.09-2.74, P=0.019), homozygote comparison (TT vs. CC: OR=2.00, 95%CI=1.25-3.23, P=0.004), recessive genetic model (TT vs. TC/CC: OR=1.80, 95%CI=1.14-2.84, P=0.011) and dominant genetic model (TT/TC vs. CC: OR=1.70, 95%CI=1.20-2.42, P=0.003). Moreover, significant association was also observed in Caucasian population rather than Asian population for ABCB1 rs1128503 polymorphism. We conclude that ABCC3 rs4148416 polymorphism was significantly associated with poor osteosarcoma response and ABCB1 rs1128503 polymorphism was significantly associated with good osteosarcoma response in Caucasian population rather than Asian population.

      • Design of a ROM-Less Direct Digital Frequency Synthesizer on FPGA

        Zhanpeng Jiang,Rui Xu,Hai Huang,Changchun Dong 보안공학연구지원센터 2015 International Journal of Signal Processing, Image Vol.8 No.5

        DDFS (Direct Digital Frequency Synthesizer) is a new technique of frequency synthesizes which introduces the advanced digital processing theory into frequency synthesis. A direct digital frequency synthesizer is composed of a phase accumulator, an adder, an ROM for wave pattern saving, a D/A converter and a LPF (low pass filter). With the rapid development of VLSI, the speed of algorithm is required increasingly higher. This paper proposes a new frequency synthesizer by improving the structure of data storage which ensures the accuracy and speed. Rotation method was used to resolve the expected angle into many small rotation angles and sting wave symmetry principle was used to resolve the string wave. From point to area, the values in one quadrant were calculated and sampled and then the data was saved in ROM. Under the control of frequency, the data in ROM was read and then transferred to the D/A converter chip and the following low pass filter to achieve frequency synthesize. This algorithm could reduce the usage of ROM to increase the calculation efficiency.

      • KCI등재

        Contributed Mini Review : Role of Wnt signaling in fracture healing

        ( Hui Yun Xu ),( Jing Duan ),( Dan Dan Ning ),( Jing Bao Li ),( Ruo Fei Liu ),( Rui Xin Yang ),( Jean X Jiang ),( Peng Shang ) 생화학분자생물학회(구 한국생화학분자생물학회) 2014 BMB Reports Vol.47 No.12

        The Wnt signaling pathway is well known to play major roles in skeletal development and homeostasis. In certain aspects, fracture repair mimics the process of bone embryonic development. Thus, the importance of Wnt signaling in fracture healing has become more apparent in recent years. Here, we summarize recent research progress in the area, which may be conducive to the development of Wnt-based therapeutic strategies for bone repair.

      • SCOPUSKCI등재

        Triterpenoids and Sterones from the Stem Bark of Ailanthus altissima

        Zhou, Xiao-Jiang,Xu, Min,Li, Xue-Song,Wang, Yue-Hu,Gao, Ye,Cai, Rui,Cheng, Yong-Xian Korean Chemical Society 2011 Bulletin of the Korean Chemical Society Vol.32 No.1

        One new tirucallane-type triterpenoid, alianthusaltinin A (1), one new $C_{29}$ sterone, alianthaltone A (2), and 12 known compounds have been isolated from the stem bark of Ailanthus altissima. The structures of new compounds were identified by means of spectroscopic methods. Compound 3 was isolated from natural sources for the first time, and compounds 4, 5, and 9 were isolated from this plant for the first time.

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