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Cited by 3 publications
(1 citation statement)
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“…HIV-1 infection is highly diverse with the circulation of subtypes A (50–80%), D (10–20%), and C (5–15%) and multiple recombinants (10–20%) [ 13 , 14 ]. Extensive genetic heterogeneity is driven by several factors, such as the lack of proofreading ability of the reverse transcriptase (RT) [ 15 ], the rapid turnover of HIV-1 in vivo [ 16 ], host-selective immune pressures [ 17 ], leading to drug resistance selection pressure, and recombination events during replication [ 18 ]. HIV type 1 is divided into groups M, N, O, and P, more than 90% of HIV infections are derived from HIV-1 group M, and the rest are minor groups [ 19 , 20 ].…”
Section: Introductionmentioning
confidence: 99%
“…HIV-1 infection is highly diverse with the circulation of subtypes A (50–80%), D (10–20%), and C (5–15%) and multiple recombinants (10–20%) [ 13 , 14 ]. Extensive genetic heterogeneity is driven by several factors, such as the lack of proofreading ability of the reverse transcriptase (RT) [ 15 ], the rapid turnover of HIV-1 in vivo [ 16 ], host-selective immune pressures [ 17 ], leading to drug resistance selection pressure, and recombination events during replication [ 18 ]. HIV type 1 is divided into groups M, N, O, and P, more than 90% of HIV infections are derived from HIV-1 group M, and the rest are minor groups [ 19 , 20 ].…”
Section: Introductionmentioning
confidence: 99%