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Chemical Biology & Drug Design
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April 12, 2011
Comparative QSAR analyses of competitive CYP2C9 inhibitors using three-dimensional molecular descriptors
Viney Lather, Miguel X Fernandes
Chemical Biology & Drug Design
|
February 27, 2009
Quantitative structure-activity relationship models with receptor-dependent descriptors for predicting peroxisome proliferator-activated receptor activities of thiazolidinedione and oxazolidinedione derivatives
Viney Lather, Visvaldas Kairys, Miguel X Fernandes
European Biophysics Journal : EBJ
|
October 12, 2005
Lipid membrane-induced optimization for ligand-receptor docking: recent tools and insights for the "membrane catalysis" model
Miguel A R B Castanho, Miguel X Fernandes
Biophysical Journal
|
December 24, 2002
Brownian dynamics simulation of rigid particles of arbitrary shape in external fields
Miguel X Fernandes, José García de la Torre
Journal of Chemical Information and Computer Sciences
|
November 24, 2004
Comparing ligand interactions with multiple receptors via serial docking
Miguel X Fernandes, Visvaldas Kairys, Michael K Gilson
Journal of Chemical Information and Modeling
|
January 24, 2006
Screening drug-like compounds by docking to homology models: a systematic study
Visvaldas Kairys, Miguel X Fernandes, Michael K Gilson
Analytical Chemistry
|
January 21, 2025
Introducing the Adsorption Energy Distribution Calculation for Two-Component Competitive Adsorption Isotherm Data
Abdul Haseeb, Yosief Wondmagegne, Miguel X Fernandes, et al.
Foods (Basel, Switzerland)
|
December 7, 2019
Prediction of Terpenoid Toxicity Based on a Quantitative Structure-Activity Relationship Model
Rosa Perestrelo, Catarina Silva, Miguel X Fernandes, et al.
The Journal of Biological Chemistry
|
July 17, 2016
Phosphorylation of Mineralocorticoid Receptor Ligand Binding Domain Impairs Receptor Activation and Has a Dominant Negative Effect over Non-phosphorylated Receptors
Rubén Jiménez-Canino, Miguel X Fernandes, Diego Alvarez de la Rosa
Current Pharmaceutical Design
|
July 26, 2012
Structure and ligand-based design of P-glycoprotein inhibitors: a historical perspective
Andreia Palmeira, Emilia Sousa, M Helena Vasconcelos, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 48) with videos related to
Sort By:
Page
of 5
Chemical Biology & Drug Design
|
April 12, 2011
Comparative QSAR analyses of competitive CYP2C9 inhibitors using three-dimensional molecular descriptors
Viney Lather, Miguel X Fernandes
Chemical Biology & Drug Design
|
February 27, 2009
Quantitative structure-activity relationship models with receptor-dependent descriptors for predicting peroxisome proliferator-activated receptor activities of thiazolidinedione and oxazolidinedione derivatives
Viney Lather, Visvaldas Kairys, Miguel X Fernandes
European Biophysics Journal : EBJ
|
October 12, 2005
Lipid membrane-induced optimization for ligand-receptor docking: recent tools and insights for the "membrane catalysis" model
Miguel A R B Castanho, Miguel X Fernandes
Biophysical Journal
|
December 24, 2002
Brownian dynamics simulation of rigid particles of arbitrary shape in external fields
Miguel X Fernandes, José García de la Torre
Journal of Chemical Information and Computer Sciences
|
November 24, 2004
Comparing ligand interactions with multiple receptors via serial docking
Miguel X Fernandes, Visvaldas Kairys, Michael K Gilson
Journal of Chemical Information and Modeling
|
January 24, 2006
Screening drug-like compounds by docking to homology models: a systematic study
Visvaldas Kairys, Miguel X Fernandes, Michael K Gilson
Analytical Chemistry
|
January 21, 2025
Introducing the Adsorption Energy Distribution Calculation for Two-Component Competitive Adsorption Isotherm Data
Abdul Haseeb, Yosief Wondmagegne, Miguel X Fernandes, et al.
Foods (Basel, Switzerland)
|
December 7, 2019
Prediction of Terpenoid Toxicity Based on a Quantitative Structure-Activity Relationship Model
Rosa Perestrelo, Catarina Silva, Miguel X Fernandes, et al.
The Journal of Biological Chemistry
|
July 17, 2016
Phosphorylation of Mineralocorticoid Receptor Ligand Binding Domain Impairs Receptor Activation and Has a Dominant Negative Effect over Non-phosphorylated Receptors
Rubén Jiménez-Canino, Miguel X Fernandes, Diego Alvarez de la Rosa
Current Pharmaceutical Design
|
July 26, 2012
Structure and ligand-based design of P-glycoprotein inhibitors: a historical perspective
Andreia Palmeira, Emilia Sousa, M Helena Vasconcelos, et al.
Page
of 5