260 research outputs found

    Hierarchical-level rain image generative model based on GAN

    Full text link
    Autonomous vehicles are exposed to various weather during operation, which is likely to trigger the performance limitations of the perception system, leading to the safety of the intended functionality (SOTIF) problems. To efficiently generate data for testing the performance of visual perception algorithms under various weather conditions, a hierarchical-level rain image generative model, rain conditional CycleGAN (RCCycleGAN), is constructed. RCCycleGAN is based on the generative adversarial network (GAN) and can generate images of light, medium, and heavy rain. Different rain intensities are introduced as labels in conditional GAN (CGAN). Meanwhile, the model structure is optimized and the training strategy is adjusted to alleviate the problem of mode collapse. In addition, natural rain images of different intensities are collected and processed for model training and validation. Compared with the two baseline models, CycleGAN and DerainCycleGAN, the peak signal-to-noise ratio (PSNR) of RCCycleGAN on the test dataset is improved by 2.58 dB and 0.74 dB, and the structural similarity (SSIM) is improved by 18% and 8%, respectively. The ablation experiments are also carried out to validate the effectiveness of the model tuning

    Continuous and complete conversion of high concentration p-nitrophenol in a flow-through membrane reactor

    Get PDF
    Here, we report on a green and effective method for the continuous and complete conversion of high concentrations of p-nitrophenol (PNP) using a flow-through membrane reactor and less NaBH4. The catalytic membrane was successfully fabricated by loading Pd nanoparticles onto the surface of a branched TiO2 nanorod-functionalized ceramic membrane. The modification with branched TiO2 nanorods can significantly improve the loading amount of Pd nanoparticles onto ceramic membranes, resulting in enhanced catalytic performance. With 6 mg of Pd, 93 L mβˆ’2 hrβˆ’1 of flux density and 8.04 cm2 of membrane surface area in the flow-through membrane reactor, PNP at a concentration of 4,000 ppm can be converted to high-value p-aminophenol using less NaBH4 (using a molar ratio of NaBH4:PNP of 9.6) within 24 s at 30Β°C. More importantly, the conversion can be continuously and stably performed for 240 min

    Vektor Malaria Baru di Kabupaten Kotabaru, Provinsi Kalimantan Selatan, Indonesia

    Full text link
    Nyamuk Anopheles merupakan vektor dari Malaria. Dari sekitar 400 spesies nyamuk Anopheles telah ditemukan 67 spesies dapat menularkan malaria dan 24 diantaranya ditemukan di Indonesia. Kabupaten Kotabaru merupakan kabupaten endemis malaria di Kalimantan Selatan. Data mengenai spesies vektor malaria spesifik pada suatu daerah sangat berperan penting sebagai salah satu bahan rekomendasi bagi tindak lanjut kebijakan pengendalian malaria. Penelitian bertujuan untuk mengetahui data vektor malaria di Kabupaten Kotabaru melalui uji PCR. Penelitian deskriptif dengan desain cross sectional. Penangkapan nyamuk dilakukan di Desa Siayuh Trans dan Magalau Hulu, tambang emas Kura-Kura dan Desa Muara Uri dengan metode penangkapan UOL, UOD, dinding dan kandang. Uji PCR dilaksanakan di laboratorium biomolekuler BBPPVRP Salatiga pada bulan Februari-April 2015. Hasil penangkapan nyamuk didapatkan 345 ekor nyamuk Anopheles yang terdiri dari 9 spesies: An. barbirostris, An. tesselatus, An. balabacensis, An. vagus, An. hyrcanus group, An. peditaeniatus, An. kochi, An. flavirostris, An. umbrosus. Seluruh nyamuk Anopheles yang didapatkan dibuat 56 pool sampel Anopheles sp untuk diuji PCR yang telah diklasifikasikan berdasarkan spesies, tanggal dan metode penangkapan. Hasil PCR terindentifikasi 3 spesies vektor malaria di Desa Siayuh Trans yaitu An. vagus, An. peditaeniatus dan An. tesselatus yang merupakan vektor malaria baru di Propinsi Kalimantan Selatan

    Plexin-B1 silencing inhibits ovarian cancer cell migration and invasion

    Get PDF
    BACKGROUND: Elevated Plexin-B1 expression has been found in diverse human cancers and in non-neoplastic tissues, and it mediates diverse biological and pathological activities. However, whether or not Plexin-B1 expression is involved in human ovarian tumors remains unclear. In the present study, Plexin-B1 expression was explored in benign and malignant human ovarian tumor tissues. In addition, the impact of Plexin-B1 expression on ovarian cancer cell proliferation, migration and invasion were investigated in vitro. METHODS: Plexin-B1 expression was analyzed in normal and benign ovarian tissues and serous ovarian tumors (both borderline and malignant) by immunohistochemical staining, as well as in four human ovarian cancer cell lines (A2780, C13*, SKOV3, and OV2008) by RT-PCR and western blot analyses. Furthermore, endogenous Plexin-B1 expression was suppressed by Plexin-B1 siRNA in SKOV3 cells, which overexpress Plexin-B1. Protein levels of Plexin-B1, AKT and AKT(Ser473 )were examined by western blot analysis. Cell proliferation, migration and invasion were measured with MTT, wound healing and boyden chamber assays, respectively, and the cytoskeleton was monitored via F-actin staining. RESULTS: Expression levels of Plexin-B1 protein were significantly higher in serous ovarian carcinomas than in normal ovaries or benign ovarian neoplasms, and in the former, Plexin-B1 expression was positively correlated with lymphatic metastasis, and the membrane and cytoplasm of cancer cells stained positively. SKOV3 cells displayed the highest Plexin-B1 expression at both the mRNA and protein levels among the four tested human ovarian cancer cell lines and was selected as a cell model for further in vitro experiments. Plexin-B1 siRNA significantly suppressed phosphorylation of AKT at Ser473 in SKOV3 cells, but it did not alter total AKT expression. In addition, silencing of Plexin-B1 in SKOV3 cells inhibited cell migration and invasion and reorganized the cytoskeleton, whereas cell proliferation was not affected. CONCLUSION: Plexin-B1 expression correlates with malignant phenotypes of serous ovarian tumors, probably via phosphorylation of AKT at Ser473, suggesting that Plexin-B1 might be a useful biomarker and/or a novel therapeutic target

    Longer screen time utilization is associated with the polygenic risk for Attention-deficit/hyperactivity disorder with mediation by brain white matter microstructure

    Get PDF
    Attention-deficit/hyperactivity disorder (ADHD) has been reported to be associated with longer screen time utilization (STU) at the behavioral level. However, whether there are shared neural links between ADHD symptoms and prolonged STU is not clear and has not been explored in a single large-scale dataset. Leveraging the genetics, neuroimaging and behavioral data of 11,000+ children aged 9-11 from the Adolescent Brain Cognitive Development cohort, this study investigates the associations between the polygenic risk and trait for ADHD, STU, and white matter microstructure through cross-sectionally and longitudinal analyses. Children with higher polygenic risk scores for ADHD tend to have longer STU and more severe ADHD symptoms. Fractional anisotropy (FA) values in several white matter tracts are negatively correlated with both the ADHD polygenic risk score and STU, including the inferior frontal-striatal tract, inferior frontal-occipital fasciculus, superior longitudinal fasciculus and corpus callosum. Most of these tracts are linked to visual-related functions. Longitudinal analyses indicate a directional effect of white matter microstructure on the ADHD scale, and a bi-directional effect between the ADHD scale and STU. Furthermore, reduction of FA in several white matter tracts mediates the association between the ADHD polygenic risk score and STU. These findings shed new light on the shared neural overlaps between ADHD symptoms and prolonged STU, and provide evidence that the polygenic risk for ADHD is related, via white matter microstructure and the ADHD trait, to STU. This study was mainly supported by NSFC and National Key R&D Program of China. [Abstract copyright: Copyright Β© 2022 The Author(s). Published by Elsevier B.V. All rights reserved.
    • …
    corecore