HBV mutation literature information.


  Molecular characterization of hepatitis B virus (HBV) isolated from a pediatric case of acute lymphoid leukemia, with a delayed response to antiviral treatment: a case report.
 PMID: 35361141       2022       BMC pediatrics
Table: E64D
Discussion: cE64D was previously reported to reduce T-cell proliferation in vitro and correlated to HBV-associated liver disease progression.


  Precore/core mutations of hepatitis B virus genotype D arising in different states of infection.
 PMID: 35415256       2022       Clinical and experimental hepatology
Discussion: The present study also demonstrated that the rates of F24Y, E64D, E77Q, L116I, and E180A mutations were higher in the C/HCC patients than the other groups; however, these differences were not statistically significant.
Discussion: They also found that F24Y, E64D, and V91S/T mutations were located in the T-cell epitope regions, and E77Q, A80I/T/V, and L116I were located within the B-cell epitope regions.
Discussion: reported 6 core mutations (F24Y,


  The Correlation Between Hepatitis B Virus Precore/Core Mutations and the Progression of Severe Liver Disease.
 PMID: 30406036       2018       Frontiers in cellular and infection microbiology
Abstract: Six of the seven significant core mutations that were identified in this study were located within immuno-active epitopes; E77Q, A80I/T/V, and L116I were located within B-cell epitopes, and F24Y, E64D, and V91S/T were located within T-cell epitopes.
Abstract: Two precore mutations, W28* and G29D, and six core mutations, F24Y, E64D, E77Q, A80I/T/V, L116I, and E180A were


  HBV core region variability: effect of antiviral treatments on main epitopic regions.
 PMID: 21311107       2011       Antiviral therapy
Abstract: Codons 74 and 77 were the most polymorphic, and the double change E64D-N67T was significantly observed.


  CTL escape mutations of core protein are more frequent in strains of HBeAg negative patients with low levels of HBV DNA.
 PMID: 19748824       2009       Journal of clinical virology
Result: Double amino acid mutations Ile66 and Ser69 were always accompanied with Glu64Asp and never accompanied with Asn67 (p<0.001).



Browser Board

 Co-occurred Entities




   Filtrator