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THE AMINO ACID N136 IN HIV-1 REVERSE TRANSCRIPTASE (RT) MAINTAINS EFFICIENT ASSOCIATION OF BOTH RT SUBUNITS AND ENABLES THE RATIONAL DESIGN OF NOVEL RT INHIBITORS
Jan Balzarini, Joeri Auxerx, Fatima Rodriguez-Barrios, Allel Chedad, Viktor Farkas, Francesca Ceccherini-Silberstein, Carlos Garcia-Aparicio, Sonsoles Velazquez, Erik De Clercq, Carlo-Federico Perno, Maria-Jose Camarasa and Federico Gago
Molecular Pharmacology April 15, 2005, DOI: https://doi.org/10.1124/mol.105.012435
Jan Balzarini
Joeri Auxerx
Fatima Rodriguez-Barrios
Allel Chedad
Viktor Farkas
Francesca Ceccherini-Silberstein
Carlos Garcia-Aparicio
Sonsoles Velazquez
Erik De Clercq
Carlo-Federico Perno
Maria-Jose Camarasa
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OtherArticle
THE AMINO ACID N136 IN HIV-1 REVERSE TRANSCRIPTASE (RT) MAINTAINS EFFICIENT ASSOCIATION OF BOTH RT SUBUNITS AND ENABLES THE RATIONAL DESIGN OF NOVEL RT INHIBITORS
Jan Balzarini, Joeri Auxerx, Fatima Rodriguez-Barrios, Allel Chedad, Viktor Farkas, Francesca Ceccherini-Silberstein, Carlos Garcia-Aparicio, Sonsoles Velazquez, Erik De Clercq, Carlo-Federico Perno, Maria-Jose Camarasa and Federico Gago
Molecular Pharmacology April 15, 2005, DOI: https://doi.org/10.1124/mol.105.012435
OtherArticle
THE AMINO ACID N136 IN HIV-1 REVERSE TRANSCRIPTASE (RT) MAINTAINS EFFICIENT ASSOCIATION OF BOTH RT SUBUNITS AND ENABLES THE RATIONAL DESIGN OF NOVEL RT INHIBITORS
Jan Balzarini, Joeri Auxerx, Fatima Rodriguez-Barrios, Allel Chedad, Viktor Farkas, Francesca Ceccherini-Silberstein, Carlos Garcia-Aparicio, Sonsoles Velazquez, Erik De Clercq, Carlo-Federico Perno, Maria-Jose Camarasa and Federico Gago
Molecular Pharmacology April 15, 2005, DOI: https://doi.org/10.1124/mol.105.012435
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