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  1. Article: Editorial: Zoonotic emerging viral infectious diseases.

    Chen, Ji-Ming / Ji, Yu-Fei / Duan, Zhao-Jun / Wei, Bin

    Frontiers in veterinary science

    2023  Volume 10, Page(s) 1194324

    Language English
    Publishing date 2023-04-11
    Publishing country Switzerland
    Document type Editorial
    ZDB-ID 2834243-4
    ISSN 2297-1769
    ISSN 2297-1769
    DOI 10.3389/fvets.2023.1194324
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: LncRNA PITPNA-AS1/miR-223-3p/PTN axis regulates malignant progression and stemness in lung squamous cell carcinoma.

    Peng, Bi-Hao / Ji, Yu-Fei / Qiu, Xiao-Jian

    Journal of clinical laboratory analysis

    2022  Volume 36, Issue 7, Page(s) e24506

    Abstract: Background: Long noncoding RNAs (lncRNAs) are a kind of molecule that cannot code proteins, and their expression is dysregulated in diversified cancers. LncRNA PITPNA-AS1 has been shown to act as a tumor promoter in a variety of malignancies, but its ... ...

    Abstract Background: Long noncoding RNAs (lncRNAs) are a kind of molecule that cannot code proteins, and their expression is dysregulated in diversified cancers. LncRNA PITPNA-AS1 has been shown to act as a tumor promoter in a variety of malignancies, but its function and regulatory mechanisms in lung squamous cell carcinoma (LUSC) are yet unknown.
    Methods: The mRNA and protein expression of genes were examined by RT-qPCR, western blot, and IHC assay. The cell proliferation, migration, invasion, and stemness were detected through CCK-8, colony formation, Transwell and spheroid formation assays. The CD44
    Results: The lncRNA PITPNA-AS1 had increased expression in LUSC and was linked to a poor prognosis. In LUSC, PITPNA-AS1 also enhanced cell proliferation, migration, invasion, and stemness. This mechanistic investigation showed that PITPNA-AS1 absorbed miR-223-3p and that miR-223-3p targeted PTN. MiR-223-3p inhibition or PTN overexpression might reverse the inhibitory effects of PITPNA-AS1 suppression on LUSC progression, as demonstrated by rescue experiments. In addition, the PITPNA-AS1/miR-223-3p/PTN axis accelerated tumor development in vivo.
    Conclusions: It is the first time we investigated the potential role and ceRNA regulatory mechanism of PITPNA-AS1 in LUSC. The data disclosed that PITPNA-AS1 upregulated PTN through sponging miR-223-3p to enhance the onset and progression of LUSC. These findings suggested the ceRNA axis may serve as a promising therapeutic biomarker for LUSC patients.
    MeSH term(s) Animals ; Carcinoma, Squamous Cell/genetics ; Carrier Proteins/genetics ; Cell Line, Tumor ; Cell Proliferation/genetics ; Cytokines/genetics ; Gene Expression Regulation, Neoplastic ; Humans ; Lung/metabolism ; Mice ; Mice, Nude ; MicroRNAs/genetics ; MicroRNAs/metabolism ; RNA, Long Noncoding/genetics ; RNA, Long Noncoding/metabolism
    Chemical Substances Carrier Proteins ; Cytokines ; MIRN223 microRNA, human ; MicroRNAs ; RNA, Long Noncoding ; pleiotrophin (134034-50-7)
    Language English
    Publishing date 2022-05-19
    Publishing country United States
    Document type Journal Article
    ZDB-ID 645095-7
    ISSN 1098-2825 ; 0887-8013
    ISSN (online) 1098-2825
    ISSN 0887-8013
    DOI 10.1002/jcla.24506
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Dual impacts of the COVID-19 nonpharmaceutical interventions on other infectious diseases.

    Chen, Yi-Qing / Ji, Yu-Fei / Chen, Ji-Ming

    Journal of medical virology

    2022  Volume 94, Issue 10, Page(s) 4588–4590

    MeSH term(s) COVID-19/prevention & control ; Communicable Diseases ; Disease Outbreaks ; Humans ; SARS-CoV-2
    Language English
    Publishing date 2022-06-16
    Publishing country United States
    Document type Letter ; Research Support, Non-U.S. Gov't
    ZDB-ID 752392-0
    ISSN 1096-9071 ; 0146-6615
    ISSN (online) 1096-9071
    ISSN 0146-6615
    DOI 10.1002/jmv.27922
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: A highly powerful nonspecific strategy to reduce COVID-19 deaths.

    Chen, Ji-Ming / Li, Guo-Hui / Ji, Yu-Fei / Sun, Ming-Hui / Gong, Huan-Yu / Chen, Rui-Xu / Chen, Ji-Wang

    Journal of medical virology

    2022  Volume 94, Issue 10, Page(s) 5051–5055

    Abstract: The coronavirus disease 2019 (COVID-19) pandemic caused by the coronavirus severe acute respiratory syndrome coronavirus 2 remains risky worldwide. We elucidate here that good IDM (isolation, disinfection, and maintenance of health) is powerful to reduce ...

    Abstract The coronavirus disease 2019 (COVID-19) pandemic caused by the coronavirus severe acute respiratory syndrome coronavirus 2 remains risky worldwide. We elucidate here that good IDM (isolation, disinfection, and maintenance of health) is powerful to reduce COVID-19 deaths based on the striking differences in COVID-19 case fatality rates among various scenarios. IDM means keeping COVID-19 cases away from each other and from other people, disinfecting their living environments, and maintaining their health through good nutrition, rest, and treatment of symptoms and pre-existing diseases (not through specific antiviral therapy). Good IDM could reduce COVID-19 deaths by more than 85% in 2020 and more than 99% in 2022. This is consistent with the fact that good IDM can minimize co-infections and maintain body functions and the fact that COVID-19 has become less pathogenic (this fact was supported with three novel data in this report). Although IDM has been frequently implemented worldwide to some degree, IDM has not been highlighted sufficiently. Good IDM is relative, nonspecific, flexible, and feasible in many countries, and can reduce deaths of some other relatively mild infectious diseases. IDM, vaccines, and antivirals aid each other to reduce COVID-19 deaths. The IDM concept and strategy can aid people to improve their health behavior and fight against COVID-19 and future pandemics worldwide.
    MeSH term(s) Antiviral Agents/therapeutic use ; COVID-19/drug therapy ; Humans ; Pandemics/prevention & control ; SARS-CoV-2
    Chemical Substances Antiviral Agents
    Language English
    Publishing date 2022-07-01
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 752392-0
    ISSN 1096-9071 ; 0146-6615
    ISSN (online) 1096-9071
    ISSN 0146-6615
    DOI 10.1002/jmv.27949
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Highly adaptive Phenuiviridae with biomedical importance in multiple fields.

    Sun, Ming-Hui / Ji, Yu-Fei / Li, Guo-Hui / Shao, Jian-Wei / Chen, Rui-Xu / Gong, Huan-Yu / Chen, Shou-Yi / Chen, Ji-Ming

    Journal of medical virology

    2022  Volume 94, Issue 6, Page(s) 2388–2401

    Abstract: The newly established virus family Phenuiviridae in Bunyavirales harbors viruses infecting three kingdoms of host organisms (animals, plants, and fungi), which is rare in known virus families. Many phenuiviruses are arboviruses and replicate in two ... ...

    Abstract The newly established virus family Phenuiviridae in Bunyavirales harbors viruses infecting three kingdoms of host organisms (animals, plants, and fungi), which is rare in known virus families. Many phenuiviruses are arboviruses and replicate in two distinct hosts (e.g., insects and humans or rice). Multiple phenuivirid species, such as Dabie bandavirus, Rift Valley fever phlebovirus, and Rice stripe tenuivirus, are highly pathogenic to humans, animals, or plants. They impose heavy global burdens on human health, livestock industry, and agriculture and are research hotspots. In recent years the taxonomy of Phenuiviridae has been expanded greatly, and research on phenuiviruses has made significant progress. With these advances, this review drew a novel panorama regarding the biomedical significance, distribution, morphology, genomics, taxonomy, evolution, replication, transmission, pathogenesis, and control of phenuiviruses, to aid researchers in various fields to recognize this highly adaptive and important virus family and conduct relevant risk analysis.
    MeSH term(s) Animals ; Arboviruses ; Genomics ; Humans ; Phlebovirus ; RNA Viruses
    Language English
    Publishing date 2022-02-02
    Publishing country United States
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 752392-0
    ISSN 1096-9071 ; 0146-6615
    ISSN (online) 1096-9071
    ISSN 0146-6615
    DOI 10.1002/jmv.27618
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Zoonotic

    Chen, Rui-Xu / Gong, Huan-Yu / Wang, Xiu / Sun, Ming-Hui / Ji, Yu-Fei / Tan, Su-Mei / Chen, Ji-Ming / Shao, Jian-Wei / Liao, Ming

    Viruses

    2023  Volume 15, Issue 8

    Abstract: ... ...

    Abstract Hantaviridae
    MeSH term(s) Animals ; Humans ; Public Health ; Chiroptera ; Shrews ; RNA Viruses ; Orthohantavirus/genetics
    Language English
    Publishing date 2023-08-08
    Publishing country Switzerland
    Document type Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 2516098-9
    ISSN 1999-4915 ; 1999-4915
    ISSN (online) 1999-4915
    ISSN 1999-4915
    DOI 10.3390/v15081705
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Bis[4-amino-3,5-bis-(pyridin-2-yl)-4H-1,2,4-triazole-κ(2)N(1),N(5)]diaqua-cobalt(II) bis-(perchlorate).

    Feng, Mi / Ji, Yu-Fei / Liang, Sheng-Li / Liu, Zhi-Liang

    Acta crystallographica. Section E, Structure reports online

    2012  Volume 68, Issue Pt 10, Page(s) m1272–3

    Abstract: In the title structure, [Co(C(12)H(10)N(6))(2)(H(2)O)(2)](ClO(4))(2), the Co(II) atom lies on an inversion centre and is coordinated in a slightly distorted octa-hedral geometry by four N atoms from two 4-amino-3,5-bis-(pyridin-2-yl)-4H-1,2,4-triazole ( ... ...

    Abstract In the title structure, [Co(C(12)H(10)N(6))(2)(H(2)O)(2)](ClO(4))(2), the Co(II) atom lies on an inversion centre and is coordinated in a slightly distorted octa-hedral geometry by four N atoms from two 4-amino-3,5-bis-(pyridin-2-yl)-4H-1,2,4-triazole (adpt) ligands in equatorial positions and two O atoms from two water mol-ecules in axial positions. An intra-molecular N-H⋯N inter-action stabilizes the mol-ecular conformation. Inter-molecular N-H⋯O and O-H⋯O inter-actions involving the perchlorate counter-anions extend the monomeric compound into a two-dimensional network parallel to the bc plane.
    Language English
    Publishing date 2012-09-15
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2041947-8
    ISSN 1600-5368 ; 1600-5368
    ISSN (online) 1600-5368
    ISSN 1600-5368
    DOI 10.1107/S1600536812038573
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Bis[3-(pyrazin-2-yl)-5-(pyridin-2-yl-κN)-1,2,4-triazol-1-ido-κN(1)]copper(II).

    Cong, Lin-Lin / Kang, Min-Yan / Ji, Yu-Fei / Liu, Zhi-Liang

    Acta crystallographica. Section E, Structure reports online

    2012  Volume 68, Issue Pt 5, Page(s) m669

    Abstract: In the mononuclear title complex, [Cu(C(11)H(7)N(6))(2)], the Cu(II) atom lies on a crystallographic inversion centre and is coordinated by four N atoms from two bidentate chelate monoanionic 3-(pyrazin-2-yl)-5-(pyridin-2-yl-1,2,4-triazol-1-ido ligands, ... ...

    Abstract In the mononuclear title complex, [Cu(C(11)H(7)N(6))(2)], the Cu(II) atom lies on a crystallographic inversion centre and is coordinated by four N atoms from two bidentate chelate monoanionic 3-(pyrazin-2-yl)-5-(pyridin-2-yl-1,2,4-triazol-1-ido ligands, two from the triazolide rings [Cu-N = 1.969 (2) Å] and two from the pyridine rings [Cu-N = 2.027 (2) Å], giving a slightly distorted square-planar geometry.
    Language English
    Publishing date 2012-04-25
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2041947-8
    ISSN 1600-5368 ; 1600-5368
    ISSN (online) 1600-5368
    ISSN 1600-5368
    DOI 10.1107/S1600536812016777
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Bis(2-amino-5-methyl-1,3,4-thia-diazole-κN(3))dichloridocobalt(II).

    Song, Ye / Ji, Yu-Fei / Kang, Min-Yan / Liu, Zhi-Liang

    Acta crystallographica. Section E, Structure reports online

    2012  Volume 68, Issue Pt 6, Page(s) m772

    Abstract: In the monomeric title complex, [CoCl(2)(C(3)H(5)N(3)S)(2)], the Co(II) atom is tetra-coordinated by two chloride anions and two N atoms from two monodentate 2-amino-5-methyl-1,3,4-thia-diazole ligands, giving a slightly distorted tetra-hedral ... ...

    Abstract In the monomeric title complex, [CoCl(2)(C(3)H(5)N(3)S)(2)], the Co(II) atom is tetra-coordinated by two chloride anions and two N atoms from two monodentate 2-amino-5-methyl-1,3,4-thia-diazole ligands, giving a slightly distorted tetra-hedral stereochemistry [bond angle range about Co = 105.16 (12)-112.50 (10)°]. In the complex, the dihedral angle between the 1,3,4-thia-diazole planes in the two ligands is 72.8 (1)°. There are two intra-molecular N-H⋯Cl inter-actions in the complex unit, while in the crystal, inter-molecular N-H⋯N and N-H⋯Cl hydrogen bonds link these units into a two-dimensional layered structure parallel to (011).
    Language English
    Publishing date 2012-05-16
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2041947-8
    ISSN 1600-5368 ; 1600-5368
    ISSN (online) 1600-5368
    ISSN 1600-5368
    DOI 10.1107/S1600536812020995
    Database MEDical Literature Analysis and Retrieval System OnLINE

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