… identify drugresistancemutations in the protease, reversetranscriptase and integrase regions … necessarily associate together mutations found in one area of the pol gene product with …
… Secondly, we did not generate in vitro drugsusceptibility or replication capacity data on the strains in this study, so it was not possible to discern whether changes in mutational profiles …
… Our discovery of minor mutations against integraseinhibitors in a country that does not routinely use them for other than last-step rescue therapy highlights the possibility that …
T Imamichi - Current pharmaceutical design, 2004 - ingentaconnect.com
… In this review, mechanisms of action of licensed RTIs and PIs, and drugresistance will be described. The mechanisms of IN inhibitors and entry inhibitors are described in detail in other …
SY Rhee, K Sankaran, V Varghese, MA Winters… - Journal of …, 2016 - Am Soc Microbiol
… Therefore, we restricted our analysis of ARV-naive sequences to those lacking any of the 93 surveillance drugresistancemutations (SDRMs) that have become established markers of …
D Tekin, D Gokengin, H Onay… - Journal of Medical …, 2021 - Wiley Online Library
… to investigate the mutations in protease (PR), reversetranscriptase (RT), and integrase (IN) … , which were referred for HIV-1 drugresistance testing during 2017. A nested polymerase …
C Charpentier, M Karmochkine, D Laureillard… - HIV …, 2008 - Wiley Online Library
… used second-generation integraseinhibitors. Moreover, RAL-… reversetranscriptaseinhibitors (NRTIs and NNRTIs, respectively), proteaseinhibitors (PIs) and fusion inhibitors. The safety …
AC Chrysostomou, C Topcu, DC Stylianou… - Infection, Genetics and …, 2020 - Elsevier
… drugresistance analysis of all HIV-1 antiretroviral agents (reversetranscriptase, protease and integraseinhibitors) are increasingly in demand due to introduction of integraseinhibitors …