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  • American Scientific Publishers  (5)
  • 1
    Online Resource
    Online Resource
    American Scientific Publishers ; 2021
    In:  Journal of Medical Imaging and Health Informatics Vol. 11, No. 11 ( 2021-11-01), p. 2722-2732
    In: Journal of Medical Imaging and Health Informatics, American Scientific Publishers, Vol. 11, No. 11 ( 2021-11-01), p. 2722-2732
    Abstract: The outbreak of 2019 novel coronavirus (COVID-19) has caused more than 176 million confirmed cases by June 14, 2021, and this number will continue to grow. Automatic and accurate COVID-19 detection/evaluation from the computed tomography (CT) scans is of great significance for COVID-19 diagnosis and treatment. Due to individual variations of patients and the influx of a large number of patients, the current clinical practices remain subject to shortcomings of potential high-risk and time-consumption issues from radiologists. In this paper, we propose a computer aided detection system to relieve the clinical physicians from tediously reading the CT images of COVID-19 patients. Particularly, a COVID-19 detection network (COVIDNet) is proposed using deep convolutional neural networks (DCNNs) for patient-level COVID-19 detection to distinguish infected and non-infected patients. The underlying method complementarily and comprehensively extract multi-level interplane volumetric correlation features of typical ground glass opacities (GGOs) lesions using 3D multi-Scale Network (MSN). To cover more GGO lesion features and reduce intra-class differences, a Phase Ensemble (PE) is proposed for aggregation of different phases in one CT scan. The proposed method is evaluated on a clinically established COVID-19 database with five-fold cross-validation. Experimental results show that the proposed framework achieves classification performance with the specificity of 1.0000, sensitivity of 0.9700, accuracy of 0.9850, precision of 1.0000, and Area Under the Curve (AUC) of 0.9980. All of these indicate that our method enables an efficient, accurate and reliable patient-level COVID-19 detection for clinical diagnosis. This can significantly improve the work efficiency of clinical physicians on COVID-19 patient diagnosis and evaluation in hospitals and clinics. Impact statement —The proposed method can automatically and accurately distinguish the COVID-19 patients from patient-level CT scan images. On a clinically established large-scale COVID-19 database with five-fold cross-validation, the experimental results show that the proposed framework achieves a classification performance with the specificity of 1.0000, sensitivity of 0.9700, accuracy of 0.9850, precision of 1.0000, and Area Under the Curve (AUC) of 0.9980. It can relieve the clinical physicians from tediously reading the CT images of COVID-19 patients. Thus, it can significantly improve the work efficiency of clinical physicians on COVID-19 patient diagnosis and evaluation in hospitals and clinics, particularly in the pandemic period of COVID-19.
    Type of Medium: Online Resource
    ISSN: 2156-7018
    Language: English
    Publisher: American Scientific Publishers
    Publication Date: 2021
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  • 2
    In: Journal of Biomedical Nanotechnology, American Scientific Publishers, Vol. 19, No. 4 ( 2023-04-01), p. 658-666
    Abstract: The respiratory condition known as chronic obstructive pulmonary disease (COPD) is widespread, but its pathogenesis remains unclear. To investigate the mechanism by which dental pulp stem cells (DPSCs) and their exosomes inhibit cellular senescence, senescence was first induced in bronchial epithelial cells by treatment with 5% cigarette smoke extract (5% CSE). Our results revealed that the senescence of bronchial epithelial cells induced by 5% CSE was decreased when co-cultured with dental pulp stem cells or their exosomes. Fur thermore, this study identified that 5% CSE promoted cell senescence through the Nuclear factor kappa B (NF-kB) pathway. In addition, 5% CSE-induced cell senescence was limited when IKK β was knocked out in bronchial epithelial cells. Meanwhile, DPSCs inhibited cell senescence through exosomal-MALAT1. Contrastingly, this effect was reversed by MALAT1 knockout. In the mouse COPD model, it was found that DPSCs could effectively inhibit COPD progression via reducing cell senescence-related proteins in mouse lung tissues, such as p21 and GLB1, and upregulating the MALAT1 expression. TNF- α and p21 expression levels were considerably reduced after treatment with dental pulp stem cells, according to IHC staining. Finally, we validated that DPSCs and their exosomes inhibit cell senescence by regulating MALAT1 and the NF-kB pathway in vitro as well as in vivo , thereby exerting a therapeutic effect in COPD.
    Type of Medium: Online Resource
    ISSN: 1550-7033
    Language: English
    Publisher: American Scientific Publishers
    Publication Date: 2023
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  • 3
    Online Resource
    Online Resource
    American Scientific Publishers ; 2012
    In:  Advanced Science Letters Vol. 7, No. 1 ( 2012-03-30), p. 496-500
    In: Advanced Science Letters, American Scientific Publishers, Vol. 7, No. 1 ( 2012-03-30), p. 496-500
    Type of Medium: Online Resource
    ISSN: 1936-6612 , 1936-7317
    Language: English
    Publisher: American Scientific Publishers
    Publication Date: 2012
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  • 4
    Online Resource
    Online Resource
    American Scientific Publishers ; 2012
    In:  Advanced Science Letters Vol. 5, No. 1 ( 2012-01-01), p. 279-282
    In: Advanced Science Letters, American Scientific Publishers, Vol. 5, No. 1 ( 2012-01-01), p. 279-282
    Type of Medium: Online Resource
    ISSN: 1936-6612
    Language: English
    Publisher: American Scientific Publishers
    Publication Date: 2012
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  • 5
    Online Resource
    Online Resource
    American Scientific Publishers ; 2015
    In:  Journal of Nanoscience and Nanotechnology Vol. 15, No. 9 ( 2015-09-01), p. 7081-7086
    In: Journal of Nanoscience and Nanotechnology, American Scientific Publishers, Vol. 15, No. 9 ( 2015-09-01), p. 7081-7086
    Type of Medium: Online Resource
    ISSN: 1533-4880
    Language: English
    Publisher: American Scientific Publishers
    Publication Date: 2015
    SSG: 11
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