BACKGROUND AND AIMS:A recent meta-analysis revealed that the genotype PNPLA3 rs738409 GG is associated with a higher risk of hepatic steatosis (HS) in Caucasian patients with chronic hepatitis C (CHC). However, controversial results were found regarding Asian populations. Furthermore, previous studies have shown a negative association between interferon lambda 3 (IFNL3) rs12979860 CC and HS in Caucasian CHC patients, but there have been no reports indicating any such association in Asian populations. In this study, then, we investigated the association of PNPLA3 and IFNL3 polymorphisms with HS in Asian CHC patients. METHODS:We enrolled consecutive CHC patients who underwent liver biopsy prior to antiviral therapy. We excluded those patients...
This study analysed the impact of PNPLA3 variants on liver histology of 168 HIV/hepatitis C virus (H...
Background and Objectives: Hepatic diseases are an important public health problem. All patients wit...
Background: An isoleucine.methionine mutation at position 148 in the PNPLA3 gene (p.I148M, rs738409)...
Background/Purpose: Prdevious meta-analyses assess whether or not patatin-like phospholipase domain ...
Background The PNPLA3/Adiponutrin rs738409 C/G single nucleotide polymorphism is associated with the...
Abstract Background Prospective studies have shown that 80% of acute hepatitis C virus (HCV) cases p...
Hepatitis C virus (HCV) has been associated with high prevalence of steatosis and fibrosis. The impa...
BACKGROUND & AIMS: Steatosis is a prominent feature of hepatitis C, especially in patients infec...
AbstractHepatitis C virus (HCV) has been associated with high prevalence of steatosis and fibrosis. ...
BACKGROUND: Hepatitis C virus (HCV) infection is associated with the development of cirrhosis and he...
Hepatitis C virus (HCV) infection is associated with the development of cirrhosis and hepatocellular...
Only 20% of patients with chronic hepatitis C (CHC) will develop cirrhosis, and fibrosis progression...
Background Homozygosity for the PNPLA3 p.I148M polymorphism influences steatosis and fibrogenesis in...
The impact of hepatic steatosis on interferon therapy for patients with chronic hepatitis C (CHC) ha...
BACKGROUND: An isoleucine>methionine mutation at position 148 in the PNPLA3 gene (p.I148M, rs738409)...
This study analysed the impact of PNPLA3 variants on liver histology of 168 HIV/hepatitis C virus (H...
Background and Objectives: Hepatic diseases are an important public health problem. All patients wit...
Background: An isoleucine.methionine mutation at position 148 in the PNPLA3 gene (p.I148M, rs738409)...
Background/Purpose: Prdevious meta-analyses assess whether or not patatin-like phospholipase domain ...
Background The PNPLA3/Adiponutrin rs738409 C/G single nucleotide polymorphism is associated with the...
Abstract Background Prospective studies have shown that 80% of acute hepatitis C virus (HCV) cases p...
Hepatitis C virus (HCV) has been associated with high prevalence of steatosis and fibrosis. The impa...
BACKGROUND & AIMS: Steatosis is a prominent feature of hepatitis C, especially in patients infec...
AbstractHepatitis C virus (HCV) has been associated with high prevalence of steatosis and fibrosis. ...
BACKGROUND: Hepatitis C virus (HCV) infection is associated with the development of cirrhosis and he...
Hepatitis C virus (HCV) infection is associated with the development of cirrhosis and hepatocellular...
Only 20% of patients with chronic hepatitis C (CHC) will develop cirrhosis, and fibrosis progression...
Background Homozygosity for the PNPLA3 p.I148M polymorphism influences steatosis and fibrogenesis in...
The impact of hepatic steatosis on interferon therapy for patients with chronic hepatitis C (CHC) ha...
BACKGROUND: An isoleucine>methionine mutation at position 148 in the PNPLA3 gene (p.I148M, rs738409)...
This study analysed the impact of PNPLA3 variants on liver histology of 168 HIV/hepatitis C virus (H...
Background and Objectives: Hepatic diseases are an important public health problem. All patients wit...
Background: An isoleucine.methionine mutation at position 148 in the PNPLA3 gene (p.I148M, rs738409)...