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  1. Article ; Online: First Case of Covid-19 in the United States.

    Zhang, Yue-Miao

    The New England journal of medicine

    2020  Volume 382, Issue 21, Page(s) e53

    MeSH term(s) Betacoronavirus ; COVID-19 ; Coronavirus ; Coronavirus Infections ; Humans ; Pandemics ; Pneumonia, Viral ; SARS-CoV-2 ; United States
    Keywords covid19
    Language English
    Publishing date 2020-04-22
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 207154-x
    ISSN 1533-4406 ; 0028-4793
    ISSN (online) 1533-4406
    ISSN 0028-4793
    DOI 10.1056/NEJMc2004794
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Glucocorticoids for IgA nephropathy-pro.

    Zhang, Yue-Miao / Lv, Ji-Cheng / Wong, Muh Geot / Zhang, Hong / Perkovic, Vlado

    Kidney international

    2023  Volume 103, Issue 4, Page(s) 666–669

    MeSH term(s) Humans ; Glucocorticoids/therapeutic use ; Glomerulonephritis, IGA/drug therapy
    Chemical Substances Glucocorticoids
    Language English
    Publishing date 2023-03-22
    Publishing country United States
    Document type Journal Article
    ZDB-ID 120573-0
    ISSN 1523-1755 ; 0085-2538
    ISSN (online) 1523-1755
    ISSN 0085-2538
    DOI 10.1016/j.kint.2023.01.018
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Genetic Roadmap for Kidney Involvement of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection.

    Zhang, Yue-Miao / Zhang, Hong

    Clinical journal of the American Society of Nephrology : CJASN

    2020  Volume 15, Issue 7, Page(s) 1044–1046

    MeSH term(s) Angiotensin-Converting Enzyme 2 ; Betacoronavirus ; COVID-19 ; Coronavirus Infections/complications ; Gene Expression ; Genetic Predisposition to Disease/genetics ; Humans ; Kidney Diseases/genetics ; Kidney Diseases/metabolism ; Kidney Diseases/virology ; Kidney Tubules/metabolism ; Pandemics ; Peptidyl-Dipeptidase A/genetics ; Peptidyl-Dipeptidase A/metabolism ; Pneumonia, Viral/complications ; Quantitative Trait Loci ; RNA, Messenger/metabolism ; SARS-CoV-2
    Chemical Substances RNA, Messenger ; Peptidyl-Dipeptidase A (EC 3.4.15.1) ; ACE2 protein, human (EC 3.4.17.23) ; Angiotensin-Converting Enzyme 2 (EC 3.4.17.23)
    Keywords covid19
    Language English
    Publishing date 2020-04-23
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2226665-3
    ISSN 1555-905X ; 1555-9041
    ISSN (online) 1555-905X
    ISSN 1555-9041
    DOI 10.2215/CJN.04370420
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Insights into the Role of Mucosal Immunity in IgA Nephropathy.

    Zhang, Yue-Miao / Zhang, Hong

    Clinical journal of the American Society of Nephrology : CJASN

    2018  Volume 13, Issue 10, Page(s) 1584–1586

    MeSH term(s) Glomerulonephritis, IGA/immunology ; Humans ; Immunity, Mucosal
    Language English
    Publishing date 2018-07-31
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2226665-3
    ISSN 1555-905X ; 1555-9041
    ISSN (online) 1555-905X
    ISSN 1555-9041
    DOI 10.2215/CJN.04370418
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Editorial: Multi-Omics Study in Revealing Underlying Pathogenesis of Complex Diseases: A Translational Perspective.

    Zhang, Yue-Miao / Wang, Yong-Fei / Rasheed, Humaira / Ott, Jurg

    Frontiers in genetics

    2021  Volume 12, Page(s) 789294

    Language English
    Publishing date 2021-10-22
    Publishing country Switzerland
    Document type Editorial
    ZDB-ID 2606823-0
    ISSN 1664-8021
    ISSN 1664-8021
    DOI 10.3389/fgene.2021.789294
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Update on treatment of immunoglobulin A nephropathy.

    Zhang, Yue-Miao / Zhang, Hong

    Nephrology (Carlton, Vic.)

    2018  Volume 23 Suppl 4, Page(s) 62–67

    Abstract: Immunoglobulin A nephropathy (IgAN) is the most common form of primary glomerulonephritis worldwide and the most common cause of end-stage renal disease in young adults. However, there are still no specific therapies capable of targeting key pathways ... ...

    Abstract Immunoglobulin A nephropathy (IgAN) is the most common form of primary glomerulonephritis worldwide and the most common cause of end-stage renal disease in young adults. However, there are still no specific therapies capable of targeting key pathways involved in disease pathogenesis. Recently, many large randomized controlled trials have been reported, such as Supportive Versus Immunosuppressive Therapy for the Treatment of Progressive IgA Nephropathy, Targeted-release Budesonide Versus Placebo in Patients with IgA Nephropathy and Therapeutic Evaluation of Steroids in IgA Nephropathy Global, which are considered to update the 2012 Kidney Disease: Improving Global Outcomes Guideline. More importantly, with a deeper understanding of the roles of mucosal immunity, B-cell activation and complement activation in IgAN, the studies of targeting pathogenic pathways are ongoing. In this review, by systemically searching the clinical trials in IgAN on ClinicalTrials.gov (https://clinicaltrials.gov/), we update the evidence for corticosteroids/immunosuppressive therapy in IgAN and explore the promising targeting pathogenic pathway therapeutic options. With better understanding of pathogenesis of IgAN, emerging therapies will soon become a reality in future.
    MeSH term(s) Adrenal Cortex Hormones/adverse effects ; Adrenal Cortex Hormones/therapeutic use ; Glomerulonephritis, IGA/diagnosis ; Glomerulonephritis, IGA/drug therapy ; Glomerulonephritis, IGA/immunology ; Humans ; Immunoglobulin A/immunology ; Immunosuppressive Agents/adverse effects ; Immunosuppressive Agents/therapeutic use ; Kidney Glomerulus/drug effects ; Kidney Glomerulus/immunology ; Kidney Glomerulus/pathology ; Treatment Outcome
    Chemical Substances Adrenal Cortex Hormones ; Immunoglobulin A ; Immunosuppressive Agents
    Language English
    Publishing date 2018-10-24
    Publishing country Australia
    Document type Journal Article ; Review
    ZDB-ID 1303661-0
    ISSN 1440-1797 ; 1320-5358
    ISSN (online) 1440-1797
    ISSN 1320-5358
    DOI 10.1111/nep.13453
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: A cluster of type I interferon-regulated genes associates with disease activity and prognosis in patients with IgA nephropathy.

    Qu, Shu / Gan, Ting / Wang, Yan-Na / Qi, Yuan-Yuan / Zhang, Yue-Miao / Berthier, Celine C / Liu, Li-Jun / Shi, Su-Fang / Lv, Ji-Cheng / Zhang, Hong / Zhou, Xu-Jie

    International immunopharmacology

    2024  Volume 131, Page(s) 111920

    Abstract: The exact pathogenesis of IgA nephropathy (IgAN) is complex and so far, not well defined. Since it has been shown that microbial infections could induce high levels of type I interferon (IFN-I) and there is an evident link between mucosal infection and ... ...

    Abstract The exact pathogenesis of IgA nephropathy (IgAN) is complex and so far, not well defined. Since it has been shown that microbial infections could induce high levels of type I interferon (IFN-I) and there is an evident link between mucosal infection and gross hematuria in IgAN, we hypothesized that IFN-I may play a role in the pathogenic process. In this study, we investigated the type I interferon status in IgAN based on the expression of 17 IFN-regulated genes (IRGs) in whole blood from 59 IgAN patients in a cross-sectional study, of which 34 patients followed longitudinally. Analysis of the IFN-score showed that there was a significant elevated IFN-score in the IgAN patients compared with healthy controls (n = 28, p = 9.80 × 10
    MeSH term(s) Humans ; Glomerulonephritis, IGA/genetics ; Glomerulonephritis, IGA/drug therapy ; Interferon Type I/genetics ; Interferon Type I/therapeutic use ; Cross-Sectional Studies ; Prognosis ; Kidney/pathology
    Chemical Substances Interferon Type I
    Language English
    Publishing date 2024-03-23
    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.2024.111920
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Unveiling biomarkers and therapeutic targets in IgA nephropathy through large-scale blood transcriptome analysis.

    Gan, Ting / Qu, Lu-Xi / Qu, Shu / Qi, Yuan-Yuan / Zhang, Yue-Miao / Wang, Yan-Na / Li, Yang / Liu, Li-Jun / Shi, Su-Fang / Lv, Ji-Cheng / Zhang, Hong / Peng, Yi-Jie / Zhou, Xu-Jie

    International immunopharmacology

    2024  Volume 132, Page(s) 111905

    Abstract: Introduction: IgA nephropathy (IgAN) is the most prevalent form of glomerulonephritis. Unfortunately, molecular biomarkers for IgAN derived from omics studies are still lacking. This research aims to identify critical genes associated with IgAN through ... ...

    Abstract Introduction: IgA nephropathy (IgAN) is the most prevalent form of glomerulonephritis. Unfortunately, molecular biomarkers for IgAN derived from omics studies are still lacking. This research aims to identify critical genes associated with IgAN through large-scale blood transcriptome analysis.
    Methods: We constructed novel blood transcriptome profiles from peripheral blood mononuclear cells (PBMCs) of 53 Chinese IgAN patients and 28 healthy individuals. Our analysis included GO, KEGG, and GSEA for biological pathways. We analyzed immune cell profiles with CIBERSORT and constructed PPI networks with STRING, visualized in Cytoscape. Key differentially expressed genes (DEGs) were identified using CytoHubba and MCODE. We assessed the correlation between gene expressions and clinical data to evaluate clinical significance and identified hub genes through machine learning, validated with an open-access dataset. Potential drugs were explored using the CMap database.
    Results: We identified 333 DEGs between IgAN patients and healthy controls, mainly related to immune response and inflammation. Key pathways included NK cell mediated cytotoxicity, complement and coagulation cascades, antigen processing, and B cell receptor signaling. Cytoscape revealed 16 clinically significant genes (including KIR2DL1, KIR2DL3, VISIG4, C1QB, and C1QC, associated with sub-phenotype and prognosis). Machine learning identified two hub genes (KLRC1 and C1QB) for a diagnostic model of IgAN with 0.92 accuracy, validated at 1.00 against the GSE125818 dataset. Sirolimus, calcifediol, and efaproxiral were suggested as potential therapeutic agents.
    Conclusion: Key DEGs, particularly VISIG4, KLRC1, and C1QB, emerge as potential specific markers for IgAN, paving the way for future targeted personalized treatment options.
    MeSH term(s) Humans ; Glomerulonephritis, IGA/genetics ; Glomerulonephritis, IGA/blood ; Glomerulonephritis, IGA/drug therapy ; Glomerulonephritis, IGA/immunology ; Gene Expression Profiling ; Transcriptome ; Biomarkers/blood ; Male ; Female ; Adult ; Protein Interaction Maps ; Leukocytes, Mononuclear/metabolism ; Leukocytes, Mononuclear/immunology ; Machine Learning ; Gene Regulatory Networks ; Middle Aged
    Chemical Substances Biomarkers
    Language English
    Publishing date 2024-03-28
    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.2024.111905
    Database MEDical Literature Analysis and Retrieval System OnLINE

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