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Frauke Christ

Showing results (41-50 of 116) with videos related to

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Bioorganic & Medicinal Chemistry|August 30, 2013
Discovery of a novel 5-carbonyl-1H-imidazole-4-carboxamide class of inhibitors of the HIV-1 integrase-LEDGF/p75 interactionErik Serrao, Zhong-Liang Xu, Bikash Debnath, et al.
Plos One|October 3, 2012
A symmetric region of the HIV-1 integrase dimerization interface is essential for viral replicationErik Serrao, Wannes Thys, Jonas Demeulemeester, et al.
Journal of Medicinal Chemistry|May 6, 2014
Investigation of a novel series of 2-hydroxyisoquinoline-1,3(2H,4H)-diones as human immunodeficiency virus type 1 integrase inhibitorsVirginie Suchaud, Fabrice Bailly, Cedric Lion, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 21, 2013
Single-cell imaging of HIV-1 provirus (SCIP)Cristina Di Primio, Valentina Quercioli, Awatef Allouch, et al.
European Journal of Medicinal Chemistry|April 23, 2016
2-hydroxyisoquinoline-1,3(2H,4H)-diones (HIDs) as human immunodeficiency virus type 1 integrase inhibitors: Influence of the alkylcarboxamide substitution of position 4Muriel Billamboz, Virginie Suchaud, Fabrice Bailly, et al.
Molecular Informatics|August 23, 2016
Rational Design, Synthesis and Evaluation of Coumarin Derivatives as Protein-protein Interaction InhibitorsLaura De Luca, Fatima E Agharbaoui, Rosaria Gitto, et al.
Bioorganic & Medicinal Chemistry|July 16, 2010
New chloro,fluorobenzylindole derivatives as integrase strand-transfer inhibitors (INSTIs) and their mode of actionStefania Ferro, Laura De Luca, Maria Letizia Barreca, et al.
The Journal of Biological Chemistry|July 27, 2014
The HIV-1 integrase mutant R263A/K264A is 2-fold defective for TRN-SR2 binding and viral nuclear importStéphanie De Houwer, Jonas Demeulemeester, Wannes Thys, et al.
Antiviral Research|July 20, 2011
4-[1-(4-Fluorobenzyl)-4-hydroxy-1H-indol-3-yl]-2-hydroxy-4-oxobut-2-enoic acid as a prototype to develop dual inhibitors of HIV-1 integration processLaura De Luca, Rosaria Gitto, Frauke Christ, et al.
Journal of Medicinal Chemistry|November 16, 2012
Design of a novel cyclotide-based CXCR4 antagonist with anti-human immunodeficiency virus (HIV)-1 activityTeshome L Aboye, Helen Ha, Subhabrata Majumder, et al.
Pageof 12

Showing results (41-50 of 116) with videos related to

Sort By:
Pageof 12
Bioorganic & Medicinal Chemistry|August 30, 2013
Discovery of a novel 5-carbonyl-1H-imidazole-4-carboxamide class of inhibitors of the HIV-1 integrase-LEDGF/p75 interactionErik Serrao, Zhong-Liang Xu, Bikash Debnath, et al.
Plos One|October 3, 2012
A symmetric region of the HIV-1 integrase dimerization interface is essential for viral replicationErik Serrao, Wannes Thys, Jonas Demeulemeester, et al.
Journal of Medicinal Chemistry|May 6, 2014
Investigation of a novel series of 2-hydroxyisoquinoline-1,3(2H,4H)-diones as human immunodeficiency virus type 1 integrase inhibitorsVirginie Suchaud, Fabrice Bailly, Cedric Lion, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 21, 2013
Single-cell imaging of HIV-1 provirus (SCIP)Cristina Di Primio, Valentina Quercioli, Awatef Allouch, et al.
European Journal of Medicinal Chemistry|April 23, 2016
2-hydroxyisoquinoline-1,3(2H,4H)-diones (HIDs) as human immunodeficiency virus type 1 integrase inhibitors: Influence of the alkylcarboxamide substitution of position 4Muriel Billamboz, Virginie Suchaud, Fabrice Bailly, et al.
Molecular Informatics|August 23, 2016
Rational Design, Synthesis and Evaluation of Coumarin Derivatives as Protein-protein Interaction InhibitorsLaura De Luca, Fatima E Agharbaoui, Rosaria Gitto, et al.
Bioorganic & Medicinal Chemistry|July 16, 2010
New chloro,fluorobenzylindole derivatives as integrase strand-transfer inhibitors (INSTIs) and their mode of actionStefania Ferro, Laura De Luca, Maria Letizia Barreca, et al.
The Journal of Biological Chemistry|July 27, 2014
The HIV-1 integrase mutant R263A/K264A is 2-fold defective for TRN-SR2 binding and viral nuclear importStéphanie De Houwer, Jonas Demeulemeester, Wannes Thys, et al.
Antiviral Research|July 20, 2011
4-[1-(4-Fluorobenzyl)-4-hydroxy-1H-indol-3-yl]-2-hydroxy-4-oxobut-2-enoic acid as a prototype to develop dual inhibitors of HIV-1 integration processLaura De Luca, Rosaria Gitto, Frauke Christ, et al.
Journal of Medicinal Chemistry|November 16, 2012
Design of a novel cyclotide-based CXCR4 antagonist with anti-human immunodeficiency virus (HIV)-1 activityTeshome L Aboye, Helen Ha, Subhabrata Majumder, et al.
Pageof 12