Morphogenesis of hepatitis B virus and its subviral envelope particles.

Notably, HepaRG cells support both viral entry and production of cccDNA [36] and are thus suitable for the study of a large number of steps in the HBV life cycle.. In 2007, Schulze

We have developed a model based on Semliki forest virus (SFV) replicon vectors, in which the production of the HCV core protein in mammalian cells leads to the

NS2 Interferes with the Mitochondrial Cytochrome c Release Induced by CIDE-B—Although it was reported that mitochon- drial localization and dimerization are required for CIDE-B

Phosphorylation of the Arginine-Rich C-Terminal Domains of the Hepatitis B Virus (HBV) Core Protein as a Fine Regulator of the Interaction between HBc and Nucleic

However, early studies of cells infected with the JFH-1 virus showed that the core protein was detected at the surface of lipid droplets or in association with the ER membranes

HBV M protein production did not lead to formation of intracellular filamentous or spherical subviral envelope particles, although the pSFV1-MHBs adw construct also

Cross-neutralizing properties of antibodies induced by immunization with chimeric S+E1-S, S+E2-S or S+E1-S+E2-S particles in the presence of AddaVax ® adjuvant against

Antibodies produced in small-animal models in response to immunization with chimeric HBV-HCV subviral particles bearing the full-length HCV genotype 1a envelope E2