HBV mutation literature information.


  Hepatitis B virus rtA181T/sW172non-stop mutation may increase resistance fold to adefovir- and entecavir-resistant mutants compared to rtA181T/sW172* mutation.
 PMID: 21933446       2011       BMC cancer
Abstract: BACKGROUND: Development of the hepatitis B virus (HBV) rtA181T/sW172* mutant could occur during prolonged lamivudine (LAM) therapy, conferring cross resistance to adefovir.
Abstract: CONCLUSIONS: Emergence of the rtA181T/sW172* mutant in LAM-resistant patients increased the risk of HCC development in the subsequent courses of antiviral therapy.
Introduction: Because of the overlap between the S and polymerase genes, a great proportion of patients carrying the rtA181T mutation also possessed the


  Antiviral drug-associated potential vaccine-escape hepatitis B virus mutants in Turkish patients with chronic hepatitis B.
 PMID: 21784687       2011       International journal of infectious diseases
Abstract: RESULTS: Seven types of ADAPVEM were detected in the total CHB patients: rtM204V/sI195M, rtM204I/sW196S, rtM204I/sW196L, rtV173L/sE164D, rtA181T/sW172*, rtA181T/


  National survey of hepatitis B virus (HBV) polymorphism in asymptomatic HBV blood donors from 1999 to 2007 in France.
 PMID: 20553432       2010       Transfusion
Abstract: rtA181T/sW172 stop mutation associated with resistance to nucleos(t)ide analogs was detected in two donors suggesting a transmission of these isolates.


  Development of HBV S gene mutants in chronic hepatitis B patients receiving nucleotide/nucleoside analogue therapy.
 PMID: 20516567       2010       Antiviral therapy
Abstract: Among them, the rtA181T/sW172* mutant has a dominant negative secretion effect as well as an increased oncogenic potential.


  Hepatitis B virus rtA181T/sW172non-stop mutation may increase resistance fold to adefovir- and entecavir-resistant mutants compared to rtA181T/sW172* mutation.
 PMID: 20119580       2010       Journal of Korean medical science
Discussion: A large percentage of the cases with rtA181T mutations developed sW172stop mutations.
Discussion: We detected sW172stop and sL173F mutations in 10 of the 13 patients with ADV-resistant rtA181T/V polymerase mutations.
Discussion: Whereas a domain D rtN236T mutation does not overlap with the envelope gene, a mutation at rtA181T can result in a stop mutation in the envelope


  Hepatitis B viral surface mutations in patients with adefovir resistant chronic hepatitis B with A181T/V polymerase mutations.
 PMID: 20119580       2010       Journal of Korean medical science
Abstract: Although sW172stop and sL173F mutations were detected, reduced HBsAg titer was not observed.
Result: AST (P=0.035) and ALT (P=0.009) levels were significantly lower in patients with W172stop/L173F mutation.
Result: Among the patients in Group P, sW172stop (n=5) and sL173F (n=5) mutations were detected.


  Identification of nonsense mutations in hepatitis B virus S gene in patients with hepatocellular carcinoma developed after lamivudine therapy.
 PMID: 19430100       2009       Antiviral therapy
Abstract: NIH3T3 cells stably expressing sL21*, sW156* and sW172* pre-S/S mutants had increased tumourigenicity in nude mice.


  Hepatitis B virus rtA181T/sW172non-stop mutation may increase resistance fold to adefovir- and entecavir-resistant mutants compared to rtA181T/sW172* mutation.
 PMID: 18537180       2008       Hepatology (Baltimore, Md.)
Abstract: CONCLUSION: The rtA181T/sW172* variant has a secretory defect and exerts a dominant negative effect on wild-type HBV virion secretion.
Abstract: In vitro analysis revealed that the rtA181T/sW172* variant is not only defective in secretion of viral particles causing intracellular retention of surface proteins, it also has a dominant negative effect on virion but not subviral particle secretion when coexpressed with the wild type.
Abstract: The selection of rtA181T/sW172* reduced the typical extent of virological breakthrou


  "Molecular analysis of hepatitis B virus ""a"" determinant in asymptomatic and symptomatic Mexican carriers."
 PMID: 17217533       2007       Virology journal
Discussion: In addition, mutation rtA181T is associated with the stop mutation sW172stop in the S gene.



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