In Vitro Selection of Mutations in the Human Immunodeficiency Virus Type 1 Reverse Transcriptase That Decrease Susceptibility to (−)-β-d-Dioxolane-Guanosine and Suppress Resistance to 3′-Azido-3′-Deoxythymidine

Míreanna Comhchosúla

• Relationship between 3′-Azido-3′-Deoxythymidine Resistance and Primer Unblocking Activity in Foscarnet-Resistant Mutants of Human Immunodeficiency Virus Type 1 Reverse Transcriptase
  le: Meyer, Peter R., et al.
  Foilsithe: (2003)
• 3′-Azido-3′-Deoxythymidine (AZT) and AZT-Resistant Reverse Transcriptase Can Increase the In Vivo Mutation Rate of Human Immunodeficiency Virus Type 1
  le: Mansky, Louis M., et al.
  Foilsithe: (2000)
• 3'-Azido-3'-deoxythymidine triphosphate as an inhibitor and substrate of purified human immunodeficiency virus reverse transcriptase.
  le: St Clair, M H, et al.
  Foilsithe: (1987)
• Sanctuary growth of human immunodeficiency virus in the presence of 3'-azido-3'-deoxythymidine.
  le: Medina, D J, et al.
  Foilsithe: (1995)
• Phosphorylation of 3'-azido-3'-deoxythymidine and selective interaction of the 5'-triphosphate with human immunodeficiency virus reverse transcriptase.
  le: Furman, P A, et al.
  Foilsithe: (1986)