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Antiviral Res ; 204: 105369, 2022 08.
Article in English | MEDLINE | ID: mdl-35738347

ABSTRACT

In our ongoing efforts to identify baloxavir resistance markers, we demonstrated that the influenza A polymerase acidic (PA) protein E23R substitution is genetically stable, increases baloxavir EC50 values (13- to 19-fold vs. wild-type), synergizes with PA I38T, and only modestly decreases viral fitness. E23R is, therefore, a potential threat to baloxavir treatment efficacy.


Subject(s)
Influenza A virus , Influenza, Human , Thiepins , Amino Acid Substitution , Antiviral Agents/pharmacology , Antiviral Agents/therapeutic use , Dibenzothiepins , Drug Resistance, Viral/genetics , Humans , Influenza A virus/genetics , Influenza, Human/drug therapy , Morpholines , Oxazines/pharmacology , Oxazines/therapeutic use , Pyridines/pharmacology , Pyridones/pharmacology , Pyridones/therapeutic use , Thiepins/pharmacology , Thiepins/therapeutic use , Triazines/pharmacology , Triazines/therapeutic use
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