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G Maga

Showing results (41-50 of 49) with videos related to

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The EMBO Journal|August 15, 1996
A conserved domain of the large subunit of replication factor C binds PCNA and acts like a dominant negative inhibitor of DNA replication in mammalian cellsR Fotedar, R Mossi, P Fitzgerald, et al.
Journal of Medicinal Chemistry|October 30, 1992
L-thymidine is phosphorylated by herpes simplex virus type 1 thymidine kinase and inhibits viral growthS Spadari, G Maga, F Focher, et al.
Nucleic Acids Research|May 10, 2002
Reconstitution of the base excision repair pathway for 7,8-dihydro-8-oxoguanine with purified human proteinsB Pascucci, G Maga, U Hübscher, et al.
The Journal of Biological Chemistry|April 24, 2001
Specific structural determinants are responsible for the antioxidant activity and the cell cycle effects of resveratrolL A Stivala, M Savio, F Carafoli, et al.
The International Journal of Biochemistry & Cell Biology|August 15, 2009
The resveratrol analogue 4,4'-dihydroxy-trans-stilbene inhibits cell proliferation with higher efficiency but different mechanism from resveratrolM Savio, T Coppa, L Bianchi, et al.
Antiviral Chemistry & Chemotherapy|May 20, 2000
Non-nucleoside HIV-1 reverse transcriptase inhibitors: synthesis and biological evaluation of novel quinoxalinylethylpyridylthioureas as potent antiviral agentsG Campiani, M Fabbrini, E Morelli, 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 inhibitorsG Maga, A Ramunno, V Nacci, et al.
Journal of Medicinal Chemistry|November 2, 1999
Pyrrolobenzoxazepinone derivatives as non-nucleoside HIV-1 RT inhibitors: further structure-activity relationship studies and identification of more potent broad-spectrum HIV-1 RT inhibitors with antiviral activityG Campiani, E Morelli, M Fabbrini, et al.
Journal of Medicinal Chemistry|July 21, 2001
Quinoxalinylethylpyridylthioureas (QXPTs) as potent non-nucleoside HIV-1 reverse transcriptase (RT) inhibitors. Further SAR studies and identification of a novel orally bioavailable hydrazine-based antiviral agentG Campiani, F Aiello, M Fabbrini, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
The EMBO Journal|August 15, 1996
A conserved domain of the large subunit of replication factor C binds PCNA and acts like a dominant negative inhibitor of DNA replication in mammalian cellsR Fotedar, R Mossi, P Fitzgerald, et al.
Journal of Medicinal Chemistry|October 30, 1992
L-thymidine is phosphorylated by herpes simplex virus type 1 thymidine kinase and inhibits viral growthS Spadari, G Maga, F Focher, et al.
Nucleic Acids Research|May 10, 2002
Reconstitution of the base excision repair pathway for 7,8-dihydro-8-oxoguanine with purified human proteinsB Pascucci, G Maga, U Hübscher, et al.
The Journal of Biological Chemistry|April 24, 2001
Specific structural determinants are responsible for the antioxidant activity and the cell cycle effects of resveratrolL A Stivala, M Savio, F Carafoli, et al.
The International Journal of Biochemistry & Cell Biology|August 15, 2009
The resveratrol analogue 4,4'-dihydroxy-trans-stilbene inhibits cell proliferation with higher efficiency but different mechanism from resveratrolM Savio, T Coppa, L Bianchi, et al.
Antiviral Chemistry & Chemotherapy|May 20, 2000
Non-nucleoside HIV-1 reverse transcriptase inhibitors: synthesis and biological evaluation of novel quinoxalinylethylpyridylthioureas as potent antiviral agentsG Campiani, M Fabbrini, E Morelli, 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 inhibitorsG Maga, A Ramunno, V Nacci, et al.
Journal of Medicinal Chemistry|November 2, 1999
Pyrrolobenzoxazepinone derivatives as non-nucleoside HIV-1 RT inhibitors: further structure-activity relationship studies and identification of more potent broad-spectrum HIV-1 RT inhibitors with antiviral activityG Campiani, E Morelli, M Fabbrini, et al.
Journal of Medicinal Chemistry|July 21, 2001
Quinoxalinylethylpyridylthioureas (QXPTs) as potent non-nucleoside HIV-1 reverse transcriptase (RT) inhibitors. Further SAR studies and identification of a novel orally bioavailable hydrazine-based antiviral agentG Campiani, F Aiello, M Fabbrini, et al.
Pageof 5