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Iron and HFE or TfR1 mutations as comorbid factors for development and progression of chronic hepatitis C.
No role of the -2518 promoter polymorphism of monocyte chemotactic protein-1 in chronic hepatitis C.
Marked hyperbilirubinemia associated with the heme oxygenase-1 gene promoter microsatellite polymorphism in a boy with autoimmune hemolytic anemia.
Variants in interferon-alpha pathway genes and response to pegylated interferon-Alpha2a plus ribavirin for treatment of chronic hepatitis C virus infection in the hepatitis C antiviral long-term treatment against cirrhosis trial.
A functional serotonin transporter gene polymorphism and depressive effects associated with interferon-alpha treatment.
YKL-40 genetic polymorphisms and the risk of liver disease progression in patients with advanced fibrosis due to chronic hepatitis C.
A variant upstream of IFNL3 (IL28B) creating a new interferon gene IFNL4 is associated with impaired clearance of hepatitis C virus.
Comparison of functional variants in IFNL4 and IFNL3 for association with HCV clearance.
Genetic factors that affect nonalcoholic fatty liver disease: A systematic clinical review.
Genetic Polymorphisms Implicated in Nonalcoholic Liver Disease or Selected Other Disorders Have No Influence on Drug-Induced Liver Injury.