HBV mutation literature information.


  Polymorphism rtQ215H in primary resistance to adefovir dipivoxil in hepatitis B virus infection: a case report.
 PMID: 21686872       2009       BMJ case reports
Abstract: Virological evaluations showed two well-known LAM-related mutations (rtL180M and rtM204I) in addition to reverse-transcriptase rtQ215H.


  New approaches in the management of chronic hepatitis B: role of tenofovir.
 PMID: 21694884       2009       Infection and drug resistance
Method: In one patient a HBV subpopulation with mutations rtM204V, rtL180M, and rtA194T could be detected.
Method: In vitro studies show that the rtA194T mutation alone resulted in a 7.6-fold decrease in susceptibility, but in conjunction with rtM204V and rtL180M led to a more than 10-fold decrease in susceptibility to TDF.
Method: The other patient presented with mutations in the HBV polymerase of rtM204V, rt PMID: 18171343       2008       Journal of gastroenterology and hepatology
Abstract: After 32 months, the rtM204V mutation was predominant, accompanied by the lamivudine-resistant rtL180M mutation.
Abstract: BACKGROUND AND AIM: Resistance to lamivudine therapy of chronic hepatitis B virus (HBV) infection occurs by mutation in the YMDD motif of the reverse transcriptase (rt) domain (rtM204V/I) of the virus polymerase, and is usually accompanied by rtL180M mutation.


  Hepatitis B virus genotypes and resistance mutations in patients under long term lamivudine therapy: characterization of genotype G in Brazil.
 PMID: 18211717       2008       BMC microbiology
Abstract: All three showed the double mutation L180M/M204V and displayed a large genetic divergence when compared with other full-length genotype G isolates.
Abstract: Fifteen patients showed the L180M/M204V lamivudine resistant double mutation.
Result: Fifteen patients showed the well-known double rtL180M/rtM204V mutation.


  Comprehensive evaluation of hepatitis B virus reverse transcriptase substitutions associated with entecavir resistance.
 PMID: 18435459       2008       Hepatology (Baltimore, Md.)
Abstract: Two of these substitutions are associated with lamivudine resistance (LVDr) in the tyrosine-methionine-aspartate-aspartate (YMDD) motif (rtM204V and rtL180M), whereas the other occurs at one or more positions specifically associated with ETV resistance (ETVr): rtT184, rtS202, or rtM250.


  [Mutations of HBV polymerase gene sequence in lamivudine-resistant chronic hepatitis B patients].
 PMID: 18504191       2008       Nan fang yi ke da xue xue bao
Abstract: RESULTS: Lamivudine resistant mutation was detected in 103 patients, and the major mutations included rtL180M+rtM204V and rtM204I, accounting for 58.3% and 22.3%, respectively.


  Rolling circle amplification, a powerful tool for genetic and functional studies of complete hepatitis B virus genomes from low-level infections and for directly probing covalently closed circular DNA.
 PMID: 18606836       2008       Antimicrobial agents and chemotherapy
1Abstract: Only the genomes from the last biopsy specimen obtained after the emergence of lamivudine resistance contained the lamivudine resistance-associated mutations rtL180M and rtM204V (""rt"" indicates reverse transcriptase domain)."


  Selection of an entecavir-resistant mutant despite prolonged hepatitis B virus DNA suppression, in a chronic hepatitis B patient with preexistent lamivudine resistance: successful rescue therapy with tenofovir.
 PMID: 18617782       2008       European journal of gastroenterology & hepatology
Abstract: Sequence analysis revealed the presence of rtL180M and rtM204V lamivudine-resistant-associated mutations at the start of entecavir treatment.


  [A five-year analysis of HBV mutations in a multidrug-resistant patient with chronic hepatitis B].
 PMID: 18647526       2008       Zhonghua gan zang bing za zhi
Abstract: RESULTS: Several mutations were identified in succession, including LAM-resistant mutations M204I/V and L180M+M204V, ETV-resistant mutation S202G, and HBeAg nonsense mutation G1896A.


  Supportive role played by precore and preS2 genomic changes in the establishment of lamivudine-resistant hepatitis B virus.
 PMID: 18713056       2008       The Journal of infectious diseases
Abstract: BACKGROUND: Hepatitis B virus (HBV) establishes lamivudine resistance via the resistance-causative rtM204V/I mutation and the replication-compensatory rtL180M mutation.
Abstract: CONCLUSIONS: Both the precore-defective mutation and the preS2 deletion may play a supportive role in the replication of lamivudine-resistant HBV, which may be a reason for there being no need for the compensatory rtL180M mutation in lamivudine-resistant HBV possessing the precore and preS2 genomic changes.
Abstract: However, both lamivudine-resistant viruses with and those without rt



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