نتایج جستجو برای: ymdd mutation

تعداد نتایج: 291493  

Journal: :jundishapur journal of microbiology 0
sepide ezzatpanah fard blood transfusion research center, high institute for research and education in transfusion medicine, tehran, ir iran; department of microbiology, shahid beheshti university of medical sciences, tehran, ir iran zohreh sharifi blood transfusion research center, high institute for research and education in transfusion medicine, tehran, ir iran; blood transfusion research center, high institute for research and education in transfusion medicine, tehran, ir iran. email: seyed masoud hosseini department of microbiology, shahid beheshti university of medical sciences, tehran, ir iran mahmood mahmoodian shooshtari blood transfusion research center, high institute for research and education in transfusion medicine, tehran, ir iran

conclusions this study showed that the presence of mutation at codons rtl80v, rtl180m and rtm204v in a, b and c domains is associated with higher viral load and resistance to lamivudine (3tc) respectively. results about 6% (3 of 50) of samples were hbeag positive and 94% (47 of 50) of patients were hbeag negative by elisa method. the patients' alt level was between 16 and 95 iu/l with the mean ...

Journal: :Antimicrobial agents and chemotherapy 2005
S Balakrishna Pai A Mithat Bozdayi Rekha B Pai Tolunay Beker Mustafa Sarioglu Ahmet R Turkyilmaz Jason Grier Cihan Yurdaydin Raymond F Schinazi

The emergence of resistance to lamivudine has been one of the major stumbling blocks to successful treatment and control of hepatitis B virus (HBV) infections. The major mechanism of resistance has been attributed to the alteration in the YMDD motif of the HBV polymerase due to an amino acid change of rtM204 to V/I and an accompanying rtL180M conversion. A novel mutation pattern in a patient ha...

2015
Rahim Rahimi Seyed Younes Hosseini Mohammad Reza Fattahi Masood Sepehrimanesh Alireza Safarpour Seyed Ali Malekhosseini Maryam Nejabat Mahboobeh Khodadad Maryam Ardebili

BACKGROUND Recurrence of Hepatitis B Virus infection in patients undergoing liver transplanted (LT) is a serious and often fatal problem. Lamivudine (LAM) and Hepatitis B Immunoglobulin (HBIG) are widely used to manage hepatitis B recurrence after liver transplantation. However, the outcomes in patients are less elucidated. OBJECTIVES The current study aimed to evaluate the YMDD motif mutatio...

Journal: :Enfermedades infecciosas y microbiologia clinica 2004
Pilar León Francisco Pozo José M Echevarría

BACKGROUND Treatment for chronic hepatitis B with lamivudine is often hampered by the emergence of point mutations in the YMDD motif of the HBV DNA polymerase gene that confer drug resistance. This usually occurs after several months of therapy, but early detection of lamivudine-resistant mutants has been reported among patients in South Korea. Data from Japan and France suggest that naturally ...

Journal: :Nucleic acids research 1998
L F Rezende W C Drosopoulos V R Prasad

A common target for therapies against human immuno-deficiency virus type 1 (HIV-1) is the viral reverse transcriptase (RT). Treatment with the widely used nucleoside analog (-)-2', 3'-deoxy-3'-thiacytidine (3TC) leads to the development of resistance-conferring mutations at residue M184 within the YMDD motif of RT. First, variants of HIV with the M184I substitution appear transiently, followed ...

Journal: :Molecular medicine reports 2016
Shaolong Chen Jing Wu Erli Gu Yaojie Shen Feifei Wang Wenhong Zhang

Virological breakthrough is a clinical manifestation in patients infected with chronic hepatitis B (CHB), who undergo treatment with nucleoside/nucleotide analogs (NUCs). The current understanding of the underlying mechanism of virological breakthrough is limited. Ultra‑deep pyrosequencing (UDPS) is a novel and powerful tool used to investigate minor viral variants and viral evolution. The pres...

Journal: :Therapeutics and Clinical Risk Management 2008
Hans Ludger Tillmann

SEVERAL OPTIONS FOR THE TREATMENT OF HEPATITIS B HAVE BEEN LICENSED IN THE LAST YEARS: interferon, pegylated interferon, lamivudine, adefovir, entecavir, and telbivudine. In addition tenofovir has been licensed in the EU and is expected to be licensed in the USA in 2008. The antivirals can be divided into "lamivudine-like" and "adefovir-like", which clinically differ in their capacity to induce...

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