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Quantitative Structure-Activity Relationship
 
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 Breast cancer resistance protein (BCRP/ABCG2): new inhibitors and QSAR studies by a 3D linear solvation energy approach Nicolle, Edwige; Boccard, Julien; Guilet, David; Dijoux-Franca, Marie-Geneviève; ... Boumendjel, Ahcène 2009
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 A 3D linear solvation energy model to quantify the affinity of flavonoid derivatives toward P-glycoprotein Boccard, Julien; Bajot, Fania; Di Pietro, Attilio; Rudaz, Serge; ... Carrupt, Pierre-Alain 2009
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 QSAR analysis and molecular modeling of ABCG2-specific inhibitors Nicolle, Edwige; Boumendjel, A.; Macalou, S.; Genoux, E.; ... Di Pietro, A. 2009
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 Structure-antioxidant activity relationships in a series of NO-donor phenols Tosco, Paolo; Marini, Elisabetta; Rolando, Barbara; Lazzarato, Loretta; ... Gasco, Alberto 2008
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 Quantitative structure-permeation relationship for iontophoretic transport across the skin Mudry, B.; Carrupt, Pierre-Alain; Guy, Richard H.; Delgado-Charro, M. B. 2007
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 D-LogP: an alignment-free 3D description of local lipophilicity for QSAR studies Gomar, J.; Giraud, E.; Turner, D.; Lahana, R.; Carrupt, Pierre-Alain 2004
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 Quantitative structure-permeation relationships (QSPeRs) to predict skin permeation: a critical evaluation Geinoz, S.; Guy, Richard H.; Testa, Bernard; Carrupt, Pierre-Alain 2004
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 Synthesis and three-dimensional quantitative structure-activity relationship analysis of H3 receptor antagonists containing a neutral heterocyclic polar group Rivara, S.; Mor, M.; Bordi, F.; Silva, C.; ... Testa, Bernard 2003
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 Quantitative structure-permeation relationships for solute transport across silicone membranes Geinoz, S.; Rey, S.; Boss, G.; Bunge, A. L.; ... Testa, Bernard 2002
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 Inhibition of monoamine oxidases by functionalized coumarin derivatives: biological activities, QSARs, and 3D-QSARs Gnerre, Carmela; Catto, M.; Leonetti, F.; Weber, P.; ... Testa, Bernard 2000