Výsledky vyhľadávania - "Viral Nonstructural Proteins/genetics"

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    Zdroj: Arch Virol
    Archives of Virology, Vol. 166, No 11 (2021) pp. 2999-3012

    Predmety: Puumala virus/isolation, Chlorocebus aethiops [MeSH], Viral Nonstructural Proteins/genetics [MeSH], Interferon Type I/genetics [MeSH], Virology, Virus Replication [MeSH], Gene Expression Regulation, Viral [MeSH], Infectious Diseases, Original Article, Interferon-beta/genetics [MeSH], Interferon Type I/metabolism [MeSH], Puumala virus/physiology [MeSH], Viral Nonstructural Proteins/metabolism [MeSH], Vero Cells [MeSH], Interferon-beta/metabolism [MeSH], A549 Cells [MeSH], Puumala virus/pathogenicity [MeSH], Mutation [MeSH], Humans [MeSH], Host-Pathogen Interactions/physiology [MeSH], Medical Microbiology, Animals [MeSH], Viral Nonstructural Proteins/chemistry [MeSH], Germany [MeSH], HEK293 Cells [MeSH], Hemorrhagic Fever with Renal Syndrome [MeSH], Adaptation, Physiological [MeSH], Promoter Regions, Genetic [MeSH], Puumala virus / pathogenicity, Gene Expression Regulation, Viral, 0301 basic medicine, Interferon Type I / metabolism, Physiological, Viral Nonstructural Proteins / genetics, Viral Nonstructural Proteins, Viral Nonstructural Proteins / metabolism, Virus Replication, Puumala virus, Promoter Regions, 03 medical and health sciences, Genetic, Germany, Host-Pathogen Interactions / physiology, Chlorocebus aethiops, Animals, Humans, Puumala virus / physiology, Viral, Adaptation, Promoter Regions, Genetic, Puumala virus / isolation & purification, Vero Cells, ddc:616, 0303 health sciences, Interferon-beta, Adaptation, Physiological, Interferon-beta / metabolism, 3. Good health, HEK293 Cells, Gene Expression Regulation, A549 Cells, Hemorrhagic Fever with Renal Syndrome, Host-Pathogen Interactions, Interferon Type I, Mutation, Interferon-beta / genetics, Viral Nonstructural Proteins / chemistry, Interferon Type I / genetics

    Popis súboru: application/pdf; pdf

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    Zdroj: Can J Gastroenterol Hepatol
    Canadian Journal of Gastroenterology and Hepatology, Vol 2019 (2019)

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    Zdroj: Popping, S, Cento, V, Seguin-Devaux, C, Boucher, C A B, de Salazar, A, Heger, E, Mor, O, Sayan, M, Salmon-Ceron, D, Weis, N, Krarup, H B, de Knegt, R J, Săndulescu, O, Chulanov, V, van de Vijver, D A M C, García, F, Ceccherini-Silberstein, F & on behalf of the HepCare as Part of the European Society for Translational Antiviral Research (ESAR) 2022, 'The european prevalence of resistance associated substitutions among direct acting antiviral failures', Viruses, vol. 14, no. 1, 16. https://doi.org/10.3390/v14010016

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    Relation: info:eu-repo/semantics/altIdentifier/pmid/35062220; info:eu-repo/semantics/altIdentifier/pissn/1999-4915

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    Prispievatelia: Marta Grandal Berta Pernas Andrés Tabernilla a ďalší

    Zdroj: RUC. Repositorio da Universidade da Coruña
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    Autori: Zeuzem, S Mizokami, M Pianko, S a ďalší

    Prispievatelia: Zeuzem, S Mizokami, M Pianko, S a ďalší

    Zdroj: Journal of Hepatology. 66:910-918

    Popis súboru: application/pdf

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    Prispievatelia: M Azim Ansari Vincent Pedergnana Camilla L C Ip a ďalší

    Zdroj: Nat Genet
    Nature genetics, vol. 49, no. 5, pp. 666-673

    Popis súboru: application/pdf; 666 - +

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    Zdroj: Front Cell Infect Microbiol
    Frontiers in Cellular and Infection Microbiology, Vol 9 (2019)
    CONICET Digital (CONICET)
    Consejo Nacional de Investigaciones Científicas y Técnicas
    Frontiers in Cellular and Infection Microbiology, 9:284

    Predmety: 0301 basic medicine, PML-NBs disruption, Gene Expression, Promyelocytic Leukemia Protein, Viral Nonstructural Proteins, FOS: Health sciences, Cell Nucleus/metabolism [MeSH], Viral Nonstructural Proteins/genetics [MeSH], Cell Line [MeSH], Cell Nucleus/metabolism, Dengue Virus/physiology [MeSH], Gene Expression [MeSH], Host-Pathogen Interactions [MeSH], Virus Replication [MeSH], Protein Binding, Dengue/metabolism, Promyelocytic Leukemia Protein/metabolism, Protein Transport [MeSH], Viral Nonstructural Proteins/metabolism [MeSH], Host-Pathogen Interactions, Viral Nonstructural Proteins/genetics, Promyelocytic Leukemia Protein/metabolism [MeSH], Humans, Dengue/metabolism [MeSH], Protein Isoforms [MeSH], Protein Isoforms, Humans [MeSH], Dengue/virology [MeSH], Protein Transport, Dengue Virus/classification, Dengue/virology, Serogroup, Viral Nonstructural Proteins/metabolism, Protein Binding [MeSH], Dengue Virus/classification [MeSH], Dengue Virus/physiology, Cell Line, Serogroup [MeSH], Virus Replication, Gene, Dengue virus, Promyelocytic leukemia protein, Dengue, Cellular and Infection Microbiology, Acute promyelocytic leukemia, 0303 health sciences, Ebola Virus Research and Outbreaks, NON-STRUCTURAL PROTEIN 5 POLYMERASE, QR1-502, 3. Good health, Infectious Diseases, Medicine, Viral Hemorrhagic Fevers and Zoonotic Infections, promyelocytic leukemia protein, Microbiology, 03 medical and health sciences, Virology, Health Sciences, Genetics, Retinoic acid, Global Impact of Arboviral Diseases, PML isoform, DENGUE VIRUS, Biology, PROMYELOCYTIC LEUKEMIA PROTEIN, non-structural protein 5 polymerase, Cell Nucleus, dengue virus, Public Health, Environmental and Occupational Health, PML-NBS DISRUPTION, Dengue Virus, Dengue fever, PML ISOFORM, FOS: Biological sciences

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    Zdroj: World Journal of Gastroenterology. 22:3418-3431

    Predmety: Male, 0301 basic medicine, chronic - drug therapy, Antiviral agents - adverse effects, Recombinant proteins - adverse effects, Hepacivirus, Polyethylene Glycols, 0302 clinical medicine, viral - blood, Interferon-alpha - adverse effects, Viral load, Treatment outcome, Middle aged, Imidazoles - adverse effects, chronic - diagnosis, chronic - virology, Interleukins - genetics, Oligopeptides - adverse effects, Polyethylene glycols - adverse effects, Polyethylene glycols - therapeutic use, Oligopeptides - therapeutic use, Imidazoles, Middle Aged, Hepatitis C, 3. Good health, Drug Therapy, Combination, Female, Drug therapy, Oligopeptides, Adult, Imidazoles - therapeutic use, Adolescent, Genotype, Antiviral agents - therapeutic use, Recombinant proteins - therapeutic use, Antiviral Agents, viral - genetics, Viral nonstructural proteins - antagonists & inhibitors, Interferon-alpha - therapeutic use, 03 medical and health sciences, Chronic hepatitis C, Daclatasvir, Direct-acting antiviral, Genotype 1b, Liver disease, NS5A inhibitor, Aged, Drug Resistance, Viral, Hepatitis C, Chronic, Humans, Interferon-alpha, Interleukins, Polymorphism, Genetic, RNA, Viral, Recombinant Proteins, Ribavirin, Time Factors, Treatment Outcome, Viral Load, Viral Nonstructural Proteins, Young Adult, Gastroenterology, Polymorphism, combination, chronic - genetics, Time factors, Hepacivirus - genetics, Ribavirin - therapeutic use, Young adult, Drug resistance, RNA, Viral nonstructural proteins - genetics, Hepacivirus - drug effects, Carbamates, Interferons, genetic, Ribavirin - adverse effects

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    Zdroj: Journal of Virology
    J Virol
    Cong, Y, Ulasli, M, Schepers, H, Mauthe, M, V'kovski, P, Kriegenburg, F, Thiel, V, de Haan, C A M & Reggiori, F 2020, ' Nucleocapsid Protein Recruitment to Replication-Transcription Complexes Plays a Crucial Role in Coronaviral Life Cycle ', Journal of Virology, vol. 94, no. 4, e01925-19 . https://doi.org/10.1128/JVI.01925-19

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