There is currently no universally accepted numbering convention for the antiviral drug-related resistance mutations in the reverse transcriptase (rt) domain of the human hepatitis B virus (HBV) polymerase. The published inconsistencies have resulted from different HBV genotypes. A standardized numbering system for HBV polymerase is proposed. The new system is based on functional observations of HBV surface gene proteins (preS1, preS2, and HBsAg) and on the current convention used for human immunodeficiency virus type 1 (HIV-1) polymerase proteins (protease, rt, and integrase), in which the amino acid numbering restarts at the first codon position of each domain. The HBV polymerase protein can be divided into 4 domains (terminal protein, spa...
The replication of human herpesvirus-6 (HHV-6) DNA is catalyzed by the viral DNA polymerase pU38 and...
Objective: To complete mutation existence in reverse transcriptase domain of the viral Polymerase.Me...
Selection of amino acid substitutions associated with resistance to nucleos(t)ide-analog (NA) therap...
There is currently no universally accepted numbering convention for the antiviral drug-related resis...
<p>The values are presented as the percent nucleotide mutations (upper panel) or amino acid substitu...
Prolonged administration of nucleoside analogues for chronic hepatitis B may result in the emergence...
Drug resistance resulting from reverse transcriptase (RI) mutations is one of the main obstacles to ...
Aim: To explore nucleoside/nucleotide analogues resistance mutations in hepatitis B virus (HBV) reve...
To explore functional domains in the hepatitis B virus (HBV) polymerase, two naturally occurring HBV...
textabstractA new hepatitis B virus variant selected during lamivudine treatment was detected, in wh...
Nous avons développé la base HBVdb (http://hbvdb.ibcp.fr) pour permettre aux chercheurs d'étudier le...
We have analyzed 11 independent mutations located at various domains of the polymerase gene (pol) of...
Resistance to anti-viral drugs is a global problem in the treatment of HBV. Around 350 million peopl...
High rate of viral replication and lacking of proofreading activity in hepatitis B virus (HBV) polym...
We developed HBVdb (http://hbvdb.ibcp.fr) to allow researchers to investigate the geneticcharacteris...
The replication of human herpesvirus-6 (HHV-6) DNA is catalyzed by the viral DNA polymerase pU38 and...
Objective: To complete mutation existence in reverse transcriptase domain of the viral Polymerase.Me...
Selection of amino acid substitutions associated with resistance to nucleos(t)ide-analog (NA) therap...
There is currently no universally accepted numbering convention for the antiviral drug-related resis...
<p>The values are presented as the percent nucleotide mutations (upper panel) or amino acid substitu...
Prolonged administration of nucleoside analogues for chronic hepatitis B may result in the emergence...
Drug resistance resulting from reverse transcriptase (RI) mutations is one of the main obstacles to ...
Aim: To explore nucleoside/nucleotide analogues resistance mutations in hepatitis B virus (HBV) reve...
To explore functional domains in the hepatitis B virus (HBV) polymerase, two naturally occurring HBV...
textabstractA new hepatitis B virus variant selected during lamivudine treatment was detected, in wh...
Nous avons développé la base HBVdb (http://hbvdb.ibcp.fr) pour permettre aux chercheurs d'étudier le...
We have analyzed 11 independent mutations located at various domains of the polymerase gene (pol) of...
Resistance to anti-viral drugs is a global problem in the treatment of HBV. Around 350 million peopl...
High rate of viral replication and lacking of proofreading activity in hepatitis B virus (HBV) polym...
We developed HBVdb (http://hbvdb.ibcp.fr) to allow researchers to investigate the geneticcharacteris...
The replication of human herpesvirus-6 (HHV-6) DNA is catalyzed by the viral DNA polymerase pU38 and...
Objective: To complete mutation existence in reverse transcriptase domain of the viral Polymerase.Me...
Selection of amino acid substitutions associated with resistance to nucleos(t)ide-analog (NA) therap...