Search research articles
Contact Us
Filters
Showing results (1-10 of 4) with videos related to
Page
of 1
Sort By:
Current Drug Metabolism
|
August 24, 2004
HIV-1 reverse transcriptase inhibitors: current issues and future perspectives
G A Locatelli, R Cancio, S Spadari, et al.
Journal of Molecular Biology
|
November 8, 2001
Hepatitis C virus NS3 NTPase/helicase: different stereoselectivity in nucleoside triphosphate utilisation suggests that NTPase and helicase activities are coupled by a nucleotide-dependent rate limiting step
G A Locatelli, G Gosselin, S Spadari, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 29, 2001
Okazaki fragment processing: modulation of the strand displacement activity of DNA polymerase delta by the concerted action of replication protein A, proliferating cell nuclear antigen, and flap endonuclease-1
G Maga, G Villani, V Tillement, et al.
The Journal of Biological Chemistry
|
September 27, 2001
The stereoselective targeting of a specific enzyme-substrate complex is the molecular mechanism for the synergic inhibition of HIV-1 reverse transcriptase by (R)-(-)-PPO464: a novel generation of nonnucleoside inhibitors
G Maga, A Ramunno, V Nacci, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 4) with videos related to
Sort By:
Page
of 1
Current Drug Metabolism
|
August 24, 2004
HIV-1 reverse transcriptase inhibitors: current issues and future perspectives
G A Locatelli, R Cancio, S Spadari, et al.
Journal of Molecular Biology
|
November 8, 2001
Hepatitis C virus NS3 NTPase/helicase: different stereoselectivity in nucleoside triphosphate utilisation suggests that NTPase and helicase activities are coupled by a nucleotide-dependent rate limiting step
G A Locatelli, G Gosselin, S Spadari, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 29, 2001
Okazaki fragment processing: modulation of the strand displacement activity of DNA polymerase delta by the concerted action of replication protein A, proliferating cell nuclear antigen, and flap endonuclease-1
G Maga, G Villani, V Tillement, et al.
The Journal of Biological Chemistry
|
September 27, 2001
The stereoselective targeting of a specific enzyme-substrate complex is the molecular mechanism for the synergic inhibition of HIV-1 reverse transcriptase by (R)-(-)-PPO464: a novel generation of nonnucleoside inhibitors
G Maga, A Ramunno, V Nacci, et al.
Page
of 1