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  1. Article ; Online: Progress in understanding primary glomerular disease: insights from urinary proteomics and in-depth analyses of potential biomarkers based on bioinformatics.

    Ge, Lili / Liu, Jianhua / Lin, Baoxu / Qin, Xiaosong

    Critical reviews in clinical laboratory sciences

    2023  Volume 60, Issue 5, Page(s) 346–365

    Abstract: Chronic kidney disease (CKD) has become a global public health challenge. While primary glomerular disease (PGD) is one of the leading causes of CKD, the specific pathogenesis of PGD is still unclear. Accurate diagnosis relies largely on invasive renal ... ...

    Abstract Chronic kidney disease (CKD) has become a global public health challenge. While primary glomerular disease (PGD) is one of the leading causes of CKD, the specific pathogenesis of PGD is still unclear. Accurate diagnosis relies largely on invasive renal biopsy, which carries risks of bleeding, pain, infection and kidney vein thrombosis. Problems with the biopsy procedure include lack of glomeruli in the tissue obtained, and the sampling site not being reflective of the overall lesion in the kidney. Repeated renal biopsies to monitor disease progression cannot be performed because of the significant risks of bleeding and kidney vein thrombosis. On the other hand, urine collection, a noninvasive method, can be performed repeatedly, and urinary proteins can reflect pathological changes in the urinary system. Advancements in proteomics technologies, especially mass spectrometry, have facilitated the identification of candidate biomarkers in different pathological types of PGD. Such biomarkers not only provide insights into the pathogenesis of PGD but also are important for diagnosis, monitoring treatment, and prognosis. In this review, we summarize the findings from studies that have used urinary proteomics, among other omics screens, to identify potential biomarkers for different types of PGD. Moreover, we performed an in-depth bioinformatic analysis to gain a deeper understanding of the biological processes and protein-protein interaction networks in which these candidate biomarkers may participate. This review, including a description of an integrated analysis method, is intended to provide insights into the pathogenesis, noninvasive diagnosis, and personalized treatment efforts of PGD and other associated diseases.
    MeSH term(s) Humans ; Proteomics/methods ; Biomarkers ; Renal Insufficiency, Chronic/diagnosis ; Renal Insufficiency, Chronic/metabolism ; Computational Biology/methods ; Thrombosis
    Chemical Substances Biomarkers
    Language English
    Publishing date 2023-02-23
    Publishing country England
    Document type Review ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 280641-1
    ISSN 1549-781X ; 1040-8363 ; 0590-8191
    ISSN (online) 1549-781X
    ISSN 1040-8363 ; 0590-8191
    DOI 10.1080/10408363.2023.2178378
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Immunology of SARS-CoV-2 infection and vaccination.

    Lin, Baoxu / Cheng, Linlin / Zhang, Jin / Yang, Mei / Zhang, Yixiao / Liu, Jianhua / Qin, Xiaosong

    Clinica chimica acta; international journal of clinical chemistry

    2023  Volume 545, Page(s) 117390

    Abstract: Comprehensive elucidation of humoral immune responses to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and vaccination is critical for understanding coronavirus disease 2019 (COVID-19) pathogenesis in general and developing ... ...

    Abstract Comprehensive elucidation of humoral immune responses to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and vaccination is critical for understanding coronavirus disease 2019 (COVID-19) pathogenesis in general and developing antibody-based diagnostic and therapeutic strategies specifically. Following the emergence of SARS-CoV-2, significant scientific research has been conducted worldwide using omics, sequencing and immunologic approaches. These studies have been critical to the successful development of vaccines. Here, the current understanding of SARS-CoV-2 immunogenic epitopes, humoral immunity to SARS-CoV-2 structural proteins and non-structural proteins, SARS-CoV-2-specific antibodies, and T-cell responses in convalescents and vaccinated individuals are reviewed. Additionally, we explore the integrated analysis of proteomic and metabolomic data to examine mechanisms of organ injury and identify potential biomarkers. Insight into the immunologic diagnosis of COVID-19 and improvements of laboratory methods are highlighted.
    MeSH term(s) Humans ; COVID-19 ; SARS-CoV-2 ; Proteomics ; Vaccination ; Antibodies, Viral ; Immunity, Humoral
    Chemical Substances Antibodies, Viral
    Language English
    Publishing date 2023-05-13
    Publishing country Netherlands
    Document type Journal Article ; Review
    ZDB-ID 80228-1
    ISSN 1873-3492 ; 0009-8981
    ISSN (online) 1873-3492
    ISSN 0009-8981
    DOI 10.1016/j.cca.2023.117390
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Novel Biomarkers in Membranous Nephropathy.

    Liu, Qiuying / Liu, Jianhua / Lin, Baoxu / Zhang, Yue / Ma, Meichen / Yang, Mei / Qin, Xiaosong

    Frontiers in immunology

    2022  Volume 13, Page(s) 845767

    Abstract: Membranous nephropathy (MN) is the main cause of adult nephrotic syndrome (NS). The pathogenesis of MN is complex and involves subepithelial immune complex deposition. Approximately one-third of patients with MN develop end-stage renal disease (ESRD). ... ...

    Abstract Membranous nephropathy (MN) is the main cause of adult nephrotic syndrome (NS). The pathogenesis of MN is complex and involves subepithelial immune complex deposition. Approximately one-third of patients with MN develop end-stage renal disease (ESRD). Timely diagnosis and reasonable intervention are the keys to improving prognosis. In recent years, with the development of high-throughput technologies, such as mass spectrometry (MS), microarray, and sequencing technologies, the discovery of biomarkers for MN has become an important area of research. In this review, we summarize the significant progress in biomarker identification. For example, a variety of podocyte target antigens and their autoantibodies have been reported. Phospholipase A2 receptor (PLA2R) is the most well-established target antigen in MN. PLA2R and its autoantibodies have clinical significance, with both diagnostic and therapeutic value for MN. In addition, a variety of new biomarkers, including proteins, metabolites, noncoding RNAs (ncRNAs), and immune cells, have recently been found. These MN-related biomarkers have great significance in the diagnosis, progression, prognosis, and treatment response of MN.
    MeSH term(s) Adult ; Autoantibodies ; Biomarkers ; Female ; Glomerulonephritis, Membranous ; Humans ; Male ; Prognosis ; Receptors, Phospholipase A2
    Chemical Substances Autoantibodies ; Biomarkers ; Receptors, Phospholipase A2
    Language English
    Publishing date 2022-04-22
    Publishing country Switzerland
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2022.845767
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Progress in understanding COVID-19: insights from the omics approach.

    Lin, Baoxu / Liu, Jianhua / Liu, Yong / Qin, Xiaosong

    Critical reviews in clinical laboratory sciences

    2020  Volume 58, Issue 4, Page(s) 242–252

    Abstract: Sequencing the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) genome is a crucial task for controlling the ongoing coronavirus disease (COVID-19) pandemic. However, elucidating the pathological mechanisms of SARS-CoV-2 in humans has been ... ...

    Abstract Sequencing the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) genome is a crucial task for controlling the ongoing coronavirus disease (COVID-19) pandemic. However, elucidating the pathological mechanisms of SARS-CoV-2 in humans has been challenging. A comprehensive analysis of the molecular characteristics of SARS-CoV-2 and molecular changes in COVID-19 patients may have practical significance in developing assays for the detection of SARS-CoV-2 and formulating clinical treatment strategies against COVID-19. The omics approach for studying biochemical mechanisms can be used to elucidate the molecular characteristics and pathophysiology of SARS-CoV-2. The omics-scale research on COVID-19 has been carried out rapidly, bringing hope for developing a robust diagnostic assay, discovering reliable biomarkers to assess disease progression, and developing therapeutic drugs and vaccines. In this review, we summarize, from an omics perspective, the strategies for the detection of SARS-CoV-2 antigens and antibodies against the virus, the metabolomic and proteomic changes in COVID-19 patients, and the progress of research on anti-SARS-CoV-2 drugs with their potential clinical applications.
    MeSH term(s) Antibodies, Viral/immunology ; Antigens, Viral/immunology ; Antiviral Agents/pharmacology ; Antiviral Agents/therapeutic use ; COVID-19 ; Host-Pathogen Interactions/genetics ; Host-Pathogen Interactions/immunology ; Humans ; Metabolome ; Metabolomics ; Proteome ; Proteomics ; SARS-CoV-2
    Chemical Substances Antibodies, Viral ; Antigens, Viral ; Antiviral Agents ; Proteome
    Language English
    Publishing date 2020-12-29
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 280641-1
    ISSN 1549-781X ; 1040-8363 ; 0590-8191
    ISSN (online) 1549-781X
    ISSN 1040-8363 ; 0590-8191
    DOI 10.1080/10408363.2020.1851167
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: A prognostic model for SARS-CoV-2 breakthrough infection: Analyzing a prospective cellular immunity cohort.

    Yang, Mei / Meng, Yuan / Hao, Wudi / Zhang, Jin / Liu, Jianhua / Wu, Lina / Lin, Baoxu / Liu, Yong / Zhang, Yue / Yu, Xiaojun / Wang, Xiaoqian / Gong, Yu / Ge, Lili / Fan, Yan / Xie, Conghong / Xu, Yiyun / Chang, Qing / Zhang, Yixiao / Qin, Xiaosong

    International immunopharmacology

    2024  Volume 131, Page(s) 111829

    Abstract: Background: Following the COVID-19 pandemic, studies have identified several prevalent characteristics, especially related to lymphocyte subsets. However, limited research is available on the focus of this study, namely, the specific memory cell subsets ...

    Abstract Background: Following the COVID-19 pandemic, studies have identified several prevalent characteristics, especially related to lymphocyte subsets. However, limited research is available on the focus of this study, namely, the specific memory cell subsets among individuals who received COVID-19 vaccine boosters and subsequently experienced a SARS-CoV-2 breakthrough infection.
    Methods: Flow cytometry (FCM) was employed to investigate the early and longitudinal pattern changes of cellular immunity in patients with SARS-CoV-2 breakthrough infections following COVID-19 vaccine boosters. XGBoost (a machine learning algorithm) was employed to analyze cellular immunity prior to SARS-CoV-2 breakthrough, aiming to establish a prognostic model for SARS-CoV-2 breakthrough infections.
    Results: Following SARS-CoV-2 breakthrough infection, naïve T cells and T
    Conclusion: SARS-CoV-2 breakthrough infection leads to disturbances in cellular immunity. Assessing cellular immunity prior to breakthrough infection serves as a valuable prognostic tool for SARS-CoV-2 infection, which facilitates clinical decision-making.
    MeSH term(s) Humans ; COVID-19 Vaccines ; COVID-19 ; SARS-CoV-2 ; Breakthrough Infections ; Pandemics ; Prognosis ; Prospective Studies ; Tumor Necrosis Factor-alpha ; Immunity, Cellular ; Antibodies, Viral
    Chemical Substances COVID-19 Vaccines ; Tumor Necrosis Factor-alpha ; Antibodies, Viral
    Language English
    Publishing date 2024-03-14
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 2043785-7
    ISSN 1878-1705 ; 1567-5769
    ISSN (online) 1878-1705
    ISSN 1567-5769
    DOI 10.1016/j.intimp.2024.111829
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Metformin combined with rapamycin ameliorates podocyte injury in idiopathic membranous nephropathy through the AMPK/mTOR signaling pathway.

    Ma, Meichen / Pan, Yue / Zhang, Yue / Yang, Mei / Xi, Ying / Lin, Baoxu / Hao, Wudi / Liu, Jianhua / Wu, Lina / Liu, Yong / Qin, Xiaosong

    Journal of cell communication and signaling

    2023  Volume 17, Issue 4, Page(s) 1405–1415

    Abstract: Autophagy activation protects against podocyte injury in idiopathic membranous nephropathy (IMN). The AMPK/mTOR signaling pathway is a vital autophagy regulatory pathway. Metformin promotes autophagy, whereas rapamycin is an autophagy agonist. However, ... ...

    Abstract Autophagy activation protects against podocyte injury in idiopathic membranous nephropathy (IMN). The AMPK/mTOR signaling pathway is a vital autophagy regulatory pathway. Metformin promotes autophagy, whereas rapamycin is an autophagy agonist. However, the therapeutic mechanisms of metformin and rapamycin in IMN remain unclear. Thus, we examined the mechanisms of action of metformin and rapamycin in IMN by regulating the AMPK/mTOR autophagy signaling pathway. Female Sprague-Dawley (SD) rats were treated with cationic bovine serum albumin (C-BSA) to establish an IMN model and were randomly divided into IMN model, metformin, rapamycin, and metformin + rapamycin groups. A control group was also established. Metformin and rapamycin were used as treatments. Renal histological changes, urinary protein excretion, the protein expression levels of key AMPK/mTOR signaling pathway proteins, renal tissue cell apoptosis, and autophagy-associated proteins (Beclin 1 and LC3) were examined. In addition, a C5b-9 sublysis model using the MPC-5 mouse podocyte cell line was established to verify the effect of metformin combined with rapamycin on podocytes. Metformin combined with rapamycin improved urinary protein excretion in IMN rats. Metformin combined with rapamycin attenuated the inflammatory response, renal fibrosis, and podocyte foot process fusion. In addition, it improved autophagy in podocytes as demonstrated by the enhanced expression of Beclin-1, p-AMPK/AMPK, LC3-II/I, and autophagosomes in podocytes and decreased p-mTOR/mTOR expression. In conclusion, metformin combined with rapamycin decreased proteinuria, improved renal fibrosis and podocyte autophagy via AMPK/mTOR pathway in IMN rats. The metformin and rapamycin decreased proteinuria and inproved renal fibrosis in IMN model rats.
    Language English
    Publishing date 2023-09-13
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 2299380-0
    ISSN 1873-961X ; 1873-9601
    ISSN (online) 1873-961X
    ISSN 1873-9601
    DOI 10.1007/s12079-023-00781-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Urinary peptidomics reveals proteases involved in idiopathic membranous nephropathy.

    Lin, Baoxu / Liu, Jianhua / Zhang, Yue / Wu, Yabin / Chen, Shixiao / Bai, Yibo / Liu, Qiuying / Qin, Xiaosong

    BMC genomics

    2021  Volume 22, Issue 1, Page(s) 852

    Abstract: Background: Idiopathic membranous nephropathy (IMN) is a cause of nephrotic syndrome that is increasing in incidence but has unclear pathogenesis. Urinary peptidomics is a promising technology for elucidating molecular mechanisms underlying diseases. ... ...

    Abstract Background: Idiopathic membranous nephropathy (IMN) is a cause of nephrotic syndrome that is increasing in incidence but has unclear pathogenesis. Urinary peptidomics is a promising technology for elucidating molecular mechanisms underlying diseases. Dysregulation of the proteolytic system is implicated in various diseases. Here, we aimed to conduct urinary peptidomics to identify IMN-related proteases.
    Results: Peptide fingerprints indicated differences in naturally produced urinary peptide components among 20 healthy individuals, 22 patients with IMN, and 15 patients with other kidney diseases. In total, 1,080 peptide-matched proteins were identified, 279 proteins differentially expressed in the urine of IMN patients were screened, and 32 proteases were predicted; 55 of the matched proteins were also differentially expressed in the kidney tissues of IMN patients, and these were mainly involved in the regulation of proteasome-, lysosome-, and actin cytoskeleton-related signaling pathways. The 32 predicted proteases showed abnormal expression in the glomeruli of IMN patients based on Gene Expression Omnibus databases. Western blot revealed abnormal expression of calpain, matrix metalloproteinase 14, and cathepsin S in kidney tissues of patients with IMN.
    Conclusions: This work shown the calpain/matrix metalloproteinase/cathepsin axis might be dysregulated in IMN. Our study is the first to systematically explore the role of proteases in IMN by urinary peptidomics, which are expected to facilitate discovery of better biomarkers for IMN.
    MeSH term(s) Biomarkers ; Glomerulonephritis, Membranous/genetics ; Humans ; Peptide Hydrolases
    Chemical Substances Biomarkers ; Peptide Hydrolases (EC 3.4.-)
    Language English
    Publishing date 2021-11-24
    Publishing country England
    Document type Journal Article
    ZDB-ID 2041499-7
    ISSN 1471-2164 ; 1471-2164
    ISSN (online) 1471-2164
    ISSN 1471-2164
    DOI 10.1186/s12864-021-08155-3
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Reverse-transcription recombinase-aided amplification assay for H7 subtype avian influenza virus.

    Wang, Suchun / Huang, Baoxu / Ma, Xuejun / Liu, Ping / Wang, Yang / Zhang, Xiaoguang / Zhu, Lin / Fan, Qingying / Sun, Yawei / Wang, Kaicheng

    Transboundary and emerging diseases

    2019  Volume 67, Issue 2, Page(s) 877–883

    Abstract: H7 subtype avian influenza virus infection is an emerging zoonosis in some Asian countries and an important avian disease worldwide. A rapid and simple test is needed to confirm infection in suspected cases during disease outbreaks. In this study, we ... ...

    Abstract H7 subtype avian influenza virus infection is an emerging zoonosis in some Asian countries and an important avian disease worldwide. A rapid and simple test is needed to confirm infection in suspected cases during disease outbreaks. In this study, we developed a reverse-transcription recombinase-aided amplification assay for the detection of H7 subtype avian influenza virus. Assays were performed at a single temperature (39°C), and the results were obtained within 20 min. The assay showed no cross-detection with Newcastle disease virus or infectious bronchitis virus, which are the other main respiratory viruses affecting birds. The analytical sensitivity was 10
    MeSH term(s) Animals ; Birds ; Humans ; Influenza A virus/classification ; Influenza A virus/genetics ; Influenza in Birds/diagnosis ; Influenza in Birds/virology ; Influenza, Human/virology ; Nucleic Acid Amplification Techniques/veterinary ; Real-Time Polymerase Chain Reaction ; Recombinases/metabolism ; Reverse Transcriptase Polymerase Chain Reaction/veterinary ; Reverse Transcription ; Sensitivity and Specificity ; Zoonoses
    Chemical Substances Recombinases
    Keywords covid19
    Language English
    Publishing date 2019-12-04
    Publishing country Germany
    Document type Evaluation Study ; Journal Article
    ZDB-ID 2414822-2
    ISSN 1865-1682 ; 1865-1674
    ISSN (online) 1865-1682
    ISSN 1865-1674
    DOI 10.1111/tbed.13411
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Comprehensive Analyses of the Immunoglobulin Proteome for the Classification of Glomerular Diseases.

    Liu, Jianhua / Li, Yang / Dai, Jiayu / Lin, Baoxu / Xiao, Chunying / Zhang, Xinpeng / Luo, Lin / Wang, Tingting / Li, Xiaoying / Yu, Yao / Chen, Shixiao / Wu, Lina / Liu, Yong / Yu, Xiaobo / Qin, Xiaosong

    Journal of proteome research

    2020  Volume 19, Issue 4, Page(s) 1502–1512

    Abstract: Glomerular diseases, which are currently diagnosed using an invasive renal biopsy, encompass numerous disease subtypes that often display similar clinical manifestations even though they have different therapeutic regimes. Therefore, a noninvasive assay ... ...

    Abstract Glomerular diseases, which are currently diagnosed using an invasive renal biopsy, encompass numerous disease subtypes that often display similar clinical manifestations even though they have different therapeutic regimes. Therefore, a noninvasive assay is needed to classify and guide the treatment of glomerular diseases. Here, we develop and apply a high-throughput and quantitative microarray platform to characterize the immunoglobulin proteome in the serum from 419 healthy and diseased patients. The immunoglobulin proteome-clinical variable correlation network revealed novel pathological mechanisms of glomerular diseases. Furthermore, an immunoglobulin proteome-multivariate normal distribution (IP-MiND) mathematical model based on the correlation network classified healthy volunteers and patients with idiopathic membranous nephropathy with an average recall of 48% (23-80%) in the discovery cohort and 64% (63-65%) in an independent validation cohort. Our results demonstrate the translational utility of our microarray platform to glomerular diseases as well as its clinical potential in characterizing other human diseases.
    MeSH term(s) Cohort Studies ; Humans ; Immunoglobulins ; Proteome ; Proteomics
    Chemical Substances Immunoglobulins ; Proteome
    Language English
    Publishing date 2020-03-23
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2078618-9
    ISSN 1535-3907 ; 1535-3893
    ISSN (online) 1535-3907
    ISSN 1535-3893
    DOI 10.1021/acs.jproteome.9b00748
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Reverse‐transcription recombinase‐aided amplification assay for H7 subtype avian influenza virus

    Wang, Suchun / Huang, Baoxu / Ma, Xuejun / Liu, Ping / Wang, Yang / Zhang, Xiaoguang / Zhu, Lin / Fan, Qingying / Sun, Yawei / Wang, Kaicheng

    Transboundary and emerging diseases. 2020 Mar., v. 67, no. 2

    2020  

    Abstract: H7 subtype avian influenza virus infection is an emerging zoonosis in some Asian countries and an important avian disease worldwide. A rapid and simple test is needed to confirm infection in suspected cases during disease outbreaks. In this study, we ... ...

    Abstract H7 subtype avian influenza virus infection is an emerging zoonosis in some Asian countries and an important avian disease worldwide. A rapid and simple test is needed to confirm infection in suspected cases during disease outbreaks. In this study, we developed a reverse‐transcription recombinase‐aided amplification assay for the detection of H7 subtype avian influenza virus. Assays were performed at a single temperature (39°C), and the results were obtained within 20 min. The assay showed no cross‐detection with Newcastle disease virus or infectious bronchitis virus, which are the other main respiratory viruses affecting birds. The analytical sensitivity was 102 RNA copies per reaction at a 95% probability level according to probit regression analysis, with 100% specificity. Compared with published reverse‐transcription quantitative real‐time polymerase chain reaction assays, the κ value of the reverse‐transcription recombinase‐aided amplification assay in 342 avian clinical samples was 0.988 (p < .001). The sensitivity for avian clinical sample detection was 100% (95%CI, 90.40%–100%), and the specificity was 99.96% (95%CI, 97.83%–99.98%). These results indicated that our reverse‐transcription recombinase‐aided amplification assay may be a valuable tool for detecting avian influenza H7 subtype virus.
    Keywords Avian orthoavulavirus 1 ; Infectious bronchitis virus ; Influenza A virus ; RNA ; avian influenza ; birds ; detection limit ; disease outbreaks ; emerging diseases ; probability ; quantitative polymerase chain reaction ; regression analysis ; reverse transcription ; temperature ; viruses ; zoonoses ; Asia ; covid19
    Language English
    Dates of publication 2020-03
    Size p. 877-883.
    Publishing place John Wiley & Sons, Ltd
    Document type Article
    Note JOURNAL ARTICLE
    ZDB-ID 2414822-2
    ISSN 1865-1682 ; 1865-1674
    ISSN (online) 1865-1682
    ISSN 1865-1674
    DOI 10.1111/tbed.13411
    Database NAL-Catalogue (AGRICOLA)

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