The L80I substitution in the reverse transcriptase domain of the hepatitis B virus polymerase is associated with lamivudine resistance and enhanced viral replication in vitro. [electronic resource]
- Antimicrobial agents and chemotherapy Jul 2007
- 2285-92 p. digital
Publication Type: Journal Article; Research Support, N.I.H., Extramural
0066-4804
10.1128/AAC.01499-06 doi
Amino Acid Motifs Amino Acid Sequence Amino Acid Substitution Binding Sites Carcinoma, Hepatocellular--pathology Cell Line, Tumor Conserved Sequence DNA-Directed DNA Polymerase--chemistry Drug Resistance, Viral Hepatitis B virus--drug effects Humans In Vitro Techniques Lamivudine--pharmacology Liver Neoplasms--pathology Models, Molecular Molecular Sequence Data Mutagenesis, Site-Directed Protein Structure, Secondary Protein Structure, Tertiary Reverse Transcriptase Inhibitors--pharmacology Sequence Homology, Amino Acid Virus Replication