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  1. Article ; Online: The spectrum of rare monogenic diseases in patients with premature coronary artery disease.

    Teng, Yaqun / Du, Tian / Feng, Siqin / Tian, Ran / Liu, Yaping / Guo, Jian / Wang, Lei / Zhang, Zhiyu / Luan, Xiaodong / He, Shan / Zhuang, Shengsheng / Wang, Yifei / Zhang, Shuyuan / Chen, Shi / Liu, Zhenyu / Zhang, Shuyang

    Chinese medical journal

    2024  

    Language English
    Publishing date 2024-02-01
    Publishing country China
    Document type Journal Article
    ZDB-ID 127089-8
    ISSN 2542-5641 ; 0366-6999 ; 1002-0187
    ISSN (online) 2542-5641
    ISSN 0366-6999 ; 1002-0187
    DOI 10.1097/CM9.0000000000002996
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Mendelian randomization in COVID-19

    Yaqun Teng / Jiuyang Xu / Yang Zhang / Zhenyu Liu / Shuyang Zhang

    EBioMedicine, Vol 57, Iss , Pp 102847- (2020)

    Applications for cardiovascular comorbidities and beyond

    2020  

    Keywords Medicine ; R ; Medicine (General) ; R5-920
    Language English
    Publishing date 2020-07-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: Mendelian randomization in COVID-19: Applications for cardiovascular comorbidities and beyond.

    Teng, Yaqun / Xu, Jiuyang / Zhang, Yang / Liu, Zhenyu / Zhang, Shuyang

    EBioMedicine

    2020  Volume 57, Page(s) 102847

    MeSH term(s) Betacoronavirus ; COVID-19 ; Cardiovascular Diseases/complications ; Comorbidity ; Coronary Artery Disease/complications ; Coronavirus Infections/epidemiology ; Diabetes Mellitus/pathology ; Genetic Predisposition to Disease/genetics ; Genetic Variation/genetics ; Humans ; Mendelian Randomization Analysis ; Pandemics ; Pneumonia, Viral/epidemiology ; Risk Factors ; SARS-CoV-2
    Keywords covid19
    Language English
    Publishing date 2020-06-20
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 2851331-9
    ISSN 2352-3964
    ISSN (online) 2352-3964
    DOI 10.1016/j.ebiom.2020.102847
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Mendelian randomization in COVID-19

    Teng, Yaqun / Xu, Jiuyang / Zhang, Yang / Liu, Zhenyu / Zhang, Shuyang

    EBioMedicine

    Applications for cardiovascular comorbidities and beyond

    2020  Volume 57, Page(s) 102847

    Keywords covid19
    Language English
    Publisher Elsevier BV
    Publishing country us
    Document type Article ; Online
    ZDB-ID 2851331-9
    ISSN 2352-3964
    ISSN (online) 2352-3964
    DOI 10.1016/j.ebiom.2020.102847
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  5. Article ; Online: The FANCI/FANCD2 complex links DNA damage response to R-loop regulation through SRSF1-mediated mRNA export

    Anne Olazabal-Herrero / Boxue He / Youngho Kwon / Abhishek K. Gupta / Arijit Dutta / Yuxin Huang / Prajwal Boddu / Zhuobin Liang / Fengshan Liang / Yaqun Teng / Li Lan / Xiaoyong Chen / Huadong Pei / Manoj M. Pillai / Patrick Sung / Gary M. Kupfer

    Cell Reports, Vol 43, Iss 1, Pp 113610- (2024)

    2024  

    Abstract: Summary: Fanconi anemia (FA) is characterized by congenital abnormalities, bone marrow failure, and cancer susceptibility. The central FA protein complex FANCI/FANCD2 (ID2) is activated by monoubiquitination and recruits DNA repair proteins for ... ...

    Abstract Summary: Fanconi anemia (FA) is characterized by congenital abnormalities, bone marrow failure, and cancer susceptibility. The central FA protein complex FANCI/FANCD2 (ID2) is activated by monoubiquitination and recruits DNA repair proteins for interstrand crosslink (ICL) repair and replication fork protection. Defects in the FA pathway lead to R-loop accumulation, which contributes to genomic instability. Here, we report that the splicing factor SRSF1 and FANCD2 interact physically and act together to suppress R-loop formation via mRNA export regulation. We show that SRSF1 stimulates FANCD2 monoubiquitination in an RNA-dependent fashion. In turn, FANCD2 monoubiquitination proves crucial for the assembly of the SRSF1-NXF1 nuclear export complex and mRNA export. Importantly, several SRSF1 cancer-associated mutants fail to interact with FANCD2, leading to inefficient FANCD2 monoubiquitination, decreased mRNA export, and R-loop accumulation. We propose a model wherein SRSF1 and FANCD2 interaction links DNA damage response to the avoidance of pathogenic R-loops via regulation of mRNA export.
    Keywords CP: Molecular biology ; Biology (General) ; QH301-705.5
    Language English
    Publishing date 2024-01-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  6. Article ; Online: The FANCI/FANCD2 complex links DNA damage response to R-loop regulation through SRSF1-mediated mRNA export.

    Olazabal-Herrero, Anne / He, Boxue / Kwon, Youngho / Gupta, Abhishek K / Dutta, Arijit / Huang, Yuxin / Boddu, Prajwal / Liang, Zhuobin / Liang, Fengshan / Teng, Yaqun / Lan, Li / Chen, Xiaoyong / Pei, Huadong / Pillai, Manoj M / Sung, Patrick / Kupfer, Gary M

    Cell reports

    2024  Volume 43, Issue 1, Page(s) 113610

    Abstract: Fanconi anemia (FA) is characterized by congenital abnormalities, bone marrow failure, and cancer susceptibility. The central FA protein complex FANCI/FANCD2 (ID2) is activated by monoubiquitination and recruits DNA repair proteins for interstrand ... ...

    Abstract Fanconi anemia (FA) is characterized by congenital abnormalities, bone marrow failure, and cancer susceptibility. The central FA protein complex FANCI/FANCD2 (ID2) is activated by monoubiquitination and recruits DNA repair proteins for interstrand crosslink (ICL) repair and replication fork protection. Defects in the FA pathway lead to R-loop accumulation, which contributes to genomic instability. Here, we report that the splicing factor SRSF1 and FANCD2 interact physically and act together to suppress R-loop formation via mRNA export regulation. We show that SRSF1 stimulates FANCD2 monoubiquitination in an RNA-dependent fashion. In turn, FANCD2 monoubiquitination proves crucial for the assembly of the SRSF1-NXF1 nuclear export complex and mRNA export. Importantly, several SRSF1 cancer-associated mutants fail to interact with FANCD2, leading to inefficient FANCD2 monoubiquitination, decreased mRNA export, and R-loop accumulation. We propose a model wherein SRSF1 and FANCD2 interaction links DNA damage response to the avoidance of pathogenic R-loops via regulation of mRNA export.
    MeSH term(s) Humans ; R-Loop Structures ; Active Transport, Cell Nucleus ; Fanconi Anemia/metabolism ; Fanconi Anemia Complementation Group Proteins/metabolism ; Fanconi Anemia Complementation Group D2 Protein/genetics ; Fanconi Anemia Complementation Group D2 Protein/metabolism ; Ubiquitination ; DNA Repair ; Neoplasms ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; DNA Damage ; Serine-Arginine Splicing Factors/genetics ; Serine-Arginine Splicing Factors/metabolism
    Chemical Substances Fanconi Anemia Complementation Group Proteins ; Fanconi Anemia Complementation Group D2 Protein ; RNA, Messenger ; FANCD2 protein, human ; FANCI protein, human ; SRSF1 protein, human ; Serine-Arginine Splicing Factors (170974-22-8)
    Language English
    Publishing date 2024-01-01
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural
    ZDB-ID 2649101-1
    ISSN 2211-1247 ; 2211-1247
    ISSN (online) 2211-1247
    ISSN 2211-1247
    DOI 10.1016/j.celrep.2023.113610
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: The Effect of Prior Angiotensin-Converting Enzyme Inhibitor and Angiotensin Receptor Blocker Treatment on Coronavirus Disease 2019 (COVID-19) Susceptibility and Outcome: A Systematic Review and Meta-analysis.

    Xu, Jiuyang / Teng, Yaqun / Shang, Lianhan / Gu, Xiaoying / Fan, Guohui / Chen, Yijun / Tian, Ran / Zhang, Shuyang / Cao, Bin

    Clinical infectious diseases : an official publication of the Infectious Diseases Society of America

    2020  Volume 72, Issue 11, Page(s) e901–e913

    Abstract: There have been arguments on whether angiotensin-converting enzyme inhibitor (ACEI) and angiotensin receptor blocker (ARB) treatment alters the risk of coronavirus disease 2019 (COVID-19) susceptibility and disease severity. We identified a total of 102 ... ...

    Abstract There have been arguments on whether angiotensin-converting enzyme inhibitor (ACEI) and angiotensin receptor blocker (ARB) treatment alters the risk of coronavirus disease 2019 (COVID-19) susceptibility and disease severity. We identified a total of 102 eligible studies for systematic review, in which 49 studies adjusting for confounders were included in the meta-analysis. We found no association between prior ACEI/ARB use and risk of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in the general population (adjusted odds ratio [aOR], 1.00; 95% confidence interval [CI], .94-1.05). The risk of mortality (aOR, .87; 95% CI, .66-1.04) and severe outcomes (aOR, .95; 95% CI, .73-1.24) were also unchanged among COVID-19 patients taking ACEIs/ARBs. These findings remained consistent in subgroup analyses stratified by populations, drug exposures, and other secondary outcomes. This systematic review provides evidence-based support to current medical guidelines and position statements that ACEIs/ARBs should not be discontinued. Additionally, there has been no evidence for initiating ACEI/ARB regimen as prevention or treatment of COVID-19.
    MeSH term(s) Angiotensin Receptor Antagonists/therapeutic use ; Angiotensin-Converting Enzyme Inhibitors/therapeutic use ; COVID-19 ; Humans ; Hypertension ; SARS-CoV-2
    Chemical Substances Angiotensin Receptor Antagonists ; Angiotensin-Converting Enzyme Inhibitors
    Keywords covid19
    Language English
    Publishing date 2020-10-20
    Publishing country United States
    Document type Journal Article ; Meta-Analysis ; Research Support, Non-U.S. Gov't ; Systematic Review
    ZDB-ID 1099781-7
    ISSN 1537-6591 ; 1058-4838
    ISSN (online) 1537-6591
    ISSN 1058-4838
    DOI 10.1093/cid/ciaa1592
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: The Effect of Prior ACEI/ARB Treatment on COVID-19 Susceptibility and Outcome: A Systematic Review and Meta-Analysis

    Xu, Jiuyang / Teng, Yaqun / Shang, Lianhan / Gu, Xiaoying / Fan, Guohui / Chen, Yijun / Tian, Ran / Zhang, Shuyang / Cao, Bin

    Clin. infect. dis

    Abstract: There have been arguments on whether angiotensin-converting enzyme inhibitors (ACEI) and angiotensin receptor blockers (ARB) treatment alters the risk of COVID-19 susceptibility and disease severity. We identified a total of 102 eligible studies for ... ...

    Abstract There have been arguments on whether angiotensin-converting enzyme inhibitors (ACEI) and angiotensin receptor blockers (ARB) treatment alters the risk of COVID-19 susceptibility and disease severity. We identified a total of 102 eligible studies for systematic review, in which 49 studies adjusting for confounders were included in the meta-analysis. We found no association between prior ACEI/ARB use and risk of SARS-CoV-2 infection in general population (adjusted OR [aOR] 1.00, 95% confidence interval [CI] 0.94-1.05). The risk of mortality (aOR 0.87, 95%CI 0.66-1.04) and severe outcomes (aOR 0.95, 95%CI 0.73-1.24) are also unchanged among COVID-19 patients taking ACEI/ARB. These findings remain consistent in subgroup analyses stratified by populations, drug exposures and in other secondary outcomes. This systematic review provides evidence-based support to current medical guidelines and position statements that ACEI/ARB should not be discontinued. Additionally, there has been no evidence for initiating ACEI/ARB regimen as prevention or treatment of COVID-19.
    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #880793
    Database COVID19

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  9. Article ; Online: The Effect of Prior ACEI/ARB Treatment on COVID-19 Susceptibility and Outcome

    Xu, Jiuyang / Teng, Yaqun / Shang, Lianhan / Gu, Xiaoying / Fan, Guohui / Chen, Yijun / Tian, Ran / Zhang, Shuyang / Cao, Bin

    Clinical Infectious Diseases ; ISSN 1058-4838 1537-6591

    A Systematic Review and Meta-Analysis

    2020  

    Abstract: Abstract There have been arguments on whether angiotensin-converting enzyme inhibitors (ACEI) and angiotensin receptor blockers (ARB) treatment alters the risk of COVID-19 susceptibility and disease severity. We identified a total of 102 eligible studies ...

    Abstract Abstract There have been arguments on whether angiotensin-converting enzyme inhibitors (ACEI) and angiotensin receptor blockers (ARB) treatment alters the risk of COVID-19 susceptibility and disease severity. We identified a total of 102 eligible studies for systematic review, in which 49 studies adjusting for confounders were included in the meta-analysis. We found no association between prior ACEI/ARB use and risk of SARS-CoV-2 infection in general population (adjusted OR [aOR] 1.00, 95% confidence interval [CI] 0.94-1.05). The risk of mortality (aOR 0.87, 95%CI 0.66-1.04) and severe outcomes (aOR 0.95, 95%CI 0.73-1.24) are also unchanged among COVID-19 patients taking ACEI/ARB. These findings remain consistent in subgroup analyses stratified by populations, drug exposures and in other secondary outcomes. This systematic review provides evidence-based support to current medical guidelines and position statements that ACEI/ARB should not be discontinued. Additionally, there has been no evidence for initiating ACEI/ARB regimen as prevention or treatment of COVID-19.
    Keywords Microbiology (medical) ; Infectious Diseases ; covid19
    Language English
    Publisher Oxford University Press (OUP)
    Publishing country uk
    Document type Article ; Online
    DOI 10.1093/cid/ciaa1592
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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