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Leonardo Pardo

Showing results (11-20 of 122) with videos related to

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Plos One|September 15, 2011
Molecular basis of ligand dissociation in β-adrenergic receptorsAngel González, Tomas Perez-Acle, Leonardo Pardo, et al.
Methods in Enzymology|January 22, 2013
The role of hydrophobic amino acids in the structure and function of the rhodopsin family of G protein-coupled receptorsGianluigi Caltabiano, Angel Gonzalez, Arnau Cordomí, et al.
Biochemistry|September 10, 2008
Activation of the mu opioid receptor involves conformational rearrangements of multiple transmembrane domainsWei Xu, Arantxa Sanz, Leonardo Pardo, et al.
Advances in Experimental Medicine and Biology|October 26, 2013
Modeling of G protein-coupled receptors using crystal structures: from monomers to signaling complexesAngel Gonzalez, Arnau Cordomí, Minos Matsoukas, et al.
Journal of Chemical Information and Modeling|October 5, 2013
Ligand binding determinants for angiotensin II type 1 receptor from computer simulationsMinos-Timotheos Matsoukas, Arnau Cordomí, Santiago Ríos, et al.
Advances in Pharmacology (San Diego, Calif.)|May 18, 2020
The computational modeling of allosteric modulation of metabotropic glutamate receptorsLaura Pérez-Benito, Claudia Llinas Del Torrent, Leonardo Pardo, et al.
Chembiochem : a European Journal of Chemical Biology|December 19, 2006
The role of internal water molecules in the structure and function of the rhodopsin family of G protein-coupled receptorsLeonardo Pardo, Xavier Deupi, Nicole Dölker, et al.
Journal of Structural Biology|September 22, 2009
Influence of the g- conformation of Ser and Thr on the structure of transmembrane helicesXavier Deupi, Mireia Olivella, Arantxa Sanz, et al.
Current Pharmaceutical Design|January 11, 2012
The G-protein coupled receptor family: actors with many facesGeorge Liapakis, Liapakis George, Arnau Cordomí, et al.
Molecular Endocrinology (Baltimore, Md.)|March 30, 2002
Lysine 183 and glutamic acid 157 of the TSH receptor: two interacting residues with a key role in determining specificity toward TSH and human CGGuillaume Smits, Cédric Govaerts, Isabelle Nubourgh, et al.
Pageof 13

Showing results (11-20 of 122) with videos related to

Sort By:
Pageof 13
Plos One|September 15, 2011
Molecular basis of ligand dissociation in β-adrenergic receptorsAngel González, Tomas Perez-Acle, Leonardo Pardo, et al.
Methods in Enzymology|January 22, 2013
The role of hydrophobic amino acids in the structure and function of the rhodopsin family of G protein-coupled receptorsGianluigi Caltabiano, Angel Gonzalez, Arnau Cordomí, et al.
Biochemistry|September 10, 2008
Activation of the mu opioid receptor involves conformational rearrangements of multiple transmembrane domainsWei Xu, Arantxa Sanz, Leonardo Pardo, et al.
Advances in Experimental Medicine and Biology|October 26, 2013
Modeling of G protein-coupled receptors using crystal structures: from monomers to signaling complexesAngel Gonzalez, Arnau Cordomí, Minos Matsoukas, et al.
Journal of Chemical Information and Modeling|October 5, 2013
Ligand binding determinants for angiotensin II type 1 receptor from computer simulationsMinos-Timotheos Matsoukas, Arnau Cordomí, Santiago Ríos, et al.
Advances in Pharmacology (San Diego, Calif.)|May 18, 2020
The computational modeling of allosteric modulation of metabotropic glutamate receptorsLaura Pérez-Benito, Claudia Llinas Del Torrent, Leonardo Pardo, et al.
Chembiochem : a European Journal of Chemical Biology|December 19, 2006
The role of internal water molecules in the structure and function of the rhodopsin family of G protein-coupled receptorsLeonardo Pardo, Xavier Deupi, Nicole Dölker, et al.
Journal of Structural Biology|September 22, 2009
Influence of the g- conformation of Ser and Thr on the structure of transmembrane helicesXavier Deupi, Mireia Olivella, Arantxa Sanz, et al.
Current Pharmaceutical Design|January 11, 2012
The G-protein coupled receptor family: actors with many facesGeorge Liapakis, Liapakis George, Arnau Cordomí, et al.
Molecular Endocrinology (Baltimore, Md.)|March 30, 2002
Lysine 183 and glutamic acid 157 of the TSH receptor: two interacting residues with a key role in determining specificity toward TSH and human CGGuillaume Smits, Cédric Govaerts, Isabelle Nubourgh, et al.
Pageof 13