3,183 research outputs found

    Two-stage Sampling on Additive Model for Quantitative Sensitive Question Survey and Its Application

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    Objective To explore scientific sampling methods and corresponding formulas for quantitative sensitive question survey on two-stage random sampling. To provide scientific data for the prevention and control of high risk AIDS population in Beijing. Methods Additive model for quantitative sensitive question survey, two-stage random sampling, properties of variance and mean were used. Results Formulas for the esti¬mation of the population proportions and its variance on additive model for quantitative sensitive question survey were deduced. The survey methods and formulas were employed successfully in the survey of the age of the first time when MSM having sex with men and the result was 21.9747. Conclusion The methods and corresponding formulas for two-stage sampling on additive model for quantitative sensitive question survey are feasible. Key words: Sensitive questions; Additive model for randomized response technique; Two-stage sampling; MS

    An Ultra-Wideband Circularly Polarized Asymmetric-S Antenna With Enhanced Bandwidth and Beamwidth Performance

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    This paper introduces an ultra-wideband circularly polarized (CP) asymmetric-S antenna with wide axial ratio beamwidth (ARBW) for C-band applications. The proposed antenna is realized by bending a linearly polarized dipole into asymmetric-S shape with variable trace width, which achieves CP radiation. Unlike the reported symmetric-S antenna, the proposed antenna is constituted with two unequal curved arms to enhance the bandwidth and beamwidth performances. Compared with the symmetric-S antenna, the proposed antenna demonstrates much wider AR bandwidth and wider ARBW over broader frequency range. A prototype is fabricated to verify the design principle. The measured and simulated results are very consistent and both indicate that the proposed antenna has a wide impedance bandwidth (VSWR <; 2) of 70.2% (3.58 to 7.46 GHz), and a wide 3-dB AR bandwidth of 84.8% (2.75 to 6.8 GHz). Moreover, maximum ARBW of 153° is achieved, and a 3-dB ARBW of more than 100° is maintained within a wide operation bandwidth of 46.3% (3.65-5.85 GHz)

    Induction of CCL8/MCP-2 by mycobacteria through the activation of TLR2/PI3K/Akt signaling pathway.

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    Pleural tuberculosis (TB), together with lymphatic TB, constitutes more than half of all extrapulmonary cases. Pleural effusions (PEs) in TB are representative of lymphocytic PEs which are dominated by T cells. However, the mechanism underlying T lymphocytes homing and accumulation in PEs is still incompletely understood. Here we performed a comparative analysis of cytokine abundance in PEs from TB patients and non-TB patients by protein array analysis and observed that MCP-2/CCL8 is highly expressed in the TB-PEs as compared to peripheral blood. Meanwhile, we observed that CCR5, the primary receptor used by MCP-2/CCL8, is mostly expressed on pleural CD4(+) T lymphocytes. Furthermore, we found that infection with either Mycobacterium bovis Bacillus Calmette-Guérin (BCG) or Mycobacterium tuberculosis H37Rv induced production of MCP-2/CCL8 at both transcriptional and protein level in Raw264.7 and THP-1 macrophage cells, mouse peritoneal macrophages as well as human PBMC monocyte-derived macrophages (MDMs). The induction of MCP-2/CCL8 by mycobacteria is dependent on the activation of TLR2/PI3K/Akt and p38 signaling pathway. We conclude that accumulation of MCP-2/CCL8 in TB-PEs may function as a biomarker for TB diagnosis

    [μ-1,4-Bis(1,2,4-triazol-1-ylmeth­yl)benzene]­bis­[aqua­(pyridine-2,6-dicarboxyl­ato)copper(II)] monohydrate

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    The title compound, [Cu2(C7H3NO4)2(C12H12N6)(H2O)2]·H2O, displays a discrete dinuclear structure, in which the central CuII atom is five-coordinated in a distorted square-based pyramidal coordination geometry and the flexible ligand 1,4-bis­(1,2,4-triazol-1-ylmeth­yl)benzene adopts a bis-monodentate bridging mode linking the CuII atoms. It is further assembled by O—H⋯O hydrogen-bond inter­actions involving both the coordinated and uncoordinated water molecules. The latter exhibits half-occupancy

    Expression of indoleamine 2,3-dioxygenase in nasopharyngeal carcinoma impairs the cytolytic function of peripheral blood lymphocytes

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    <p>Abstract</p> <p>Background</p> <p>Tumor-specific cytotoxic T cells and infiltrating lymphocytes are frequently found in tumor tissues in patients with nasopharyngeal carcinoma (NPC). Most patients with NPC, however, especially those with advanced stages, have a poor clinical prognosis despite conventional immunotherapy. The aim of this work was to examine the effect of indoleamine 2,3-dioxygenase (IDO), an immunosuppressive enzyme, on the lymphocyte function in NPC.</p> <p>Methods</p> <p>The NPC cell line CNE2 was treated by interferon-γ (IFNγ) and the levels of IDO expression was analyzed by Western blotting and reverse phase high-performance liquid chromatography (HPLC). Lymphocytes from health human exposed to the milieu created by IDO-positive CNE2 cells and the lymphocyte cytotoxicity to target tumor cells was analyzed by standard lactate dehydrogenase (LDH) release assay. Additionally, expression of IDO was determined by Immunohistochemical assay in the tumor tissues form clinically evaluated NPC.</p> <p>Results</p> <p>IDO expression was acutely induced in the NPC cell line CNE2 by low dose interferon-γ (IFNγ) or by co-incubation with activated lymphocytes. Exposure to the milieu created by IDO-positive CNE2 cells did not promote lymphocyte death, but lymphocyte cytotoxicity against target tumor cells was impaired. The suppression of lymphocyte cytotoxic function was fully restored when the conditioned medium was replaced by fresh medium for 24 h. In additionally, the IDO-positive cells were found scattered in the tumor tissues from patients with NPC.</p> <p>Conclusion</p> <p>Altogether, these findings suggest that IDO-mediated immunosuppression may be involved in the tumor immune evasion, and that blocking IDO activity in tumor cells may help to re-establish an effective anti-tumor T cell response in NPC.</p

    A versatile route to fabricate single atom catalysts with high chemoselectivity

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    Preparation of single atom catalysts (SACs) is of broad interest to materials scientists and chemists but remains a formidable challenge. Herein, we develop an efficient approach to synthesize SACs via a precursor-dilution strategy, in which metalloporphyrin (MTPP) with target metals are co-polymerized with diluents (tetraphenylporphyrin, TPP), followed by pyrolysis to N-doped porous carbon supported SACs (M1/N-C). Twenty-four different SACs, including noble metals and non-noble metals, are successfully prepared. In addition, the synthesis of a series of catalysts with different surface atom densities, bi-metallic sites, and metal aggregation states are achieved. This approach shows remarkable adjustability and generality, providing sufficient freedom to design catalysts at atomic-scale and explore the unique catalytic properties of SACs. As an example, we show that the prepared Pt1/N-C exhibits superior chemoselectivity and regioselectivity in hydrogenation. It only converts terminal alkynes to alkenes while keeping other reducible functional groups such as alkenyl, nitro group, and even internal alkyne intact

    Learning Enhanced Resolution-wise features for Human Pose Estimation

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    Recently, multi-resolution networks (such as Hourglass, CPN, HRNet, etc.) have achieved significant performance on pose estimation by combining feature maps of various resolutions. In this paper, we propose a Resolution-wise Attention Module (RAM) and Gradual Pyramid Refinement (GPR), to learn enhanced resolution-wise feature maps for precise pose estimation. Specifically, RAM learns a group of weights to represent the different importance of feature maps across resolutions, and the GPR gradually merges every two feature maps from low to high resolutions to regress final human keypoint heatmaps. With the enhanced resolution-wise features learnt by CNN, we obtain more accurate human keypoint locations. The efficacies of our proposed methods are demonstrated on MS-COCO dataset, achieving state-of-the-art performance with average precision of 77.7 on COCO val2017 set and 77.0 on test-dev2017 set without using extra human keypoint training dataset.Comment: Published on ICIP 202

    Table-GPT: Table-tuned GPT for Diverse Table Tasks

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    Language models, such as GPT-3.5 and ChatGPT, demonstrate remarkable abilities to follow diverse human instructions and perform a wide range of tasks. However, when probing language models using a range of basic table-understanding tasks, we observe that today's language models are still sub-optimal in many table-related tasks, likely because they are pre-trained predominantly on \emph{one-dimensional} natural-language texts, whereas relational tables are \emph{two-dimensional} objects. In this work, we propose a new "\emph{table-tuning}" paradigm, where we continue to train/fine-tune language models like GPT-3.5 and ChatGPT, using diverse table-tasks synthesized from real tables as training data, with the goal of enhancing language models' ability to understand tables and perform table tasks. We show that our resulting Table-GPT models demonstrate (1) better \emph{table-understanding} capabilities, by consistently outperforming the vanilla GPT-3.5 and ChatGPT, on a wide-range of table tasks, including holdout unseen tasks, and (2) strong \emph{generalizability}, in its ability to respond to diverse human instructions to perform new table-tasks, in a manner similar to GPT-3.5 and ChatGPT
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