Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study - Test2 - elhamkhani - TriplyDB

Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study

Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study

http://www.wikidata.org/entity/Q28269827

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Interferon lambda: a new sword in cancer immunotherapy A variant upstream of IFNL3 (IL28B) creating a new interferon gene IFNL4 is associated with impaired clearance of hepatitis C virus Hepatitis C virus protease inhibitor-resistance mutations: our experience and review Genetic background in nonalcoholic fatty liver disease: A comprehensive review The 2015 Clinical Guidelines for the Diagnosis and Treatment of HIV/AIDS in HIV-Infected Koreans Impact of IL28B, ITPA and PNPLA3 genetic variants on therapeutic outcome and progression of hepatitis C virus infection Natural history and clinical response: "it's the virus, stupid, or is it the host?"Regulation of hepatic innate immunity by hepatitis C virus Natural killer cell responses during viral infections: flexibility and conditioning of innate immunity by experience Hepatitis C virus adaptation to T-cell immune pressure Systematic review with meta-analysis: do interferon lambda 3 polymorphisms predict the outcome of interferon-therapy in hepatitis B infection?Influence of HIV and HCV on T cell antigen presentation and challenges in the development of vaccines MiR-122 in hepatitis B virus and hepatitis C virus dual infection Post-transcriptional regulation of interferons and their signaling pathways Genetic variants at the IFNL3 locus and their association with hepatitis C virus infections reveal novel insights into host-virus interactions Hepatitis C virus genotype 6: virology, epidemiology, genetic variation and clinical implication Targeted induction of interferon-λ in humanized chimeric mouse liver abrogates hepatotropic virus infection Modeling host genetic regulation of influenza pathogenesis in the collaborative cross Copy number variation of genes involved in the hepatitis C virus-human interactome Influence of host resistance on viral adaptation: hepatitis C virus as a case study Female sex and IL28B, a synergism for spontaneous viral clearance in hepatitis C virus (HCV) seroconverters from a community-based cohort Identification of improved IL28B SNPs and haplotypes for prediction of drug response in treatment of hepatitis C using massively parallel sequencing in a cross-sectional European cohort A multicentre molecular analysis of hepatitis B and blood-borne virus coinfections in Viet Nam Relation of IL28B gene polymorphism with biochemical and histological features in hepatitis C virus-induced liver disease Association of IFNL3 rs12979860 and rs8099917 with biochemical predictors of interferon responsiveness in chronic hepatitis C virus infection Hepatitis C virus infection among injection drug users with and without human immunodeficiency virus co-infection Influence of hepatitis C virus and IL28B genotypes on liver stiffness Within-host stochastic emergence dynamics of immune-escape mutants Ribavirin Concentrations Do Not Predict Sustained Virological Response in HIV/HCV-Coinfected Patients Treated with Ribavirin and Pegylated Interferon in the Swiss HIV Cohort Study Systems immunogenetics of vaccines HCV genotype-3a T cell immunity: specificity, function and impact of therapy Impact of IL28B-related single nucleotide polymorphisms on liver histopathology in chronic hepatitis C genotype 2 and 3 An IL28B genotype-based clinical prediction model for treatment of chronic hepatitis C Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy.Pharmacogenetics of hepatitis C: transition from interferon-based therapies to direct-acting antiviral agents Genome-wide association study of spontaneous resolution of hepatitis C virus infection: data from multiple cohorts.Lack of evidence to support the association of a single IL28B genotype SNP rs12979860 with the HTLV-1 clinical outcomes and proviral load.Prioritizing genes responsible for host resistance to influenza using network approaches IL28B polymorphisms and clinical implications for hepatitis C virus infection in Uzbekistan Interleukin28B and inosine triphosphatase help to personalize hepatitis C treatment.

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P2860

Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study

http://www.wikidata.org/entity/Q28269827

description

2010 nî lūn-bûn

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2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2010 թվականի ապրիլին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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Genetic variation in IL28B is ...... genome-wide association study

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Genetic variation in IL28B is ...... genome-wide association study

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Genetic variation in IL28B is ...... genome-wide association study

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Genetic variation in IL28B is ...... genome-wide association study

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4

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Murielle Bochud

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Enos Bernasconi

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Pierre-Yves Bochud

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therapeutic failure