A. Cortés

发表

Moonlighting Adenosine Deaminase: A Target Protein for Drug Development

J. Mallol, C. Lluis, V. Casadó, 2015, Medicinal research reviews.

Interactions between Calmodulin, Adenosine A2A, and Dopamine D2 Receptors*

K. Fuxe, D. Marcellino, L. Agnati, 2009, The Journal of Biological Chemistry.

Cocaine Inhibits Dopamine D2 Receptor Signaling via Sigma-1-D2 Receptor Heteromers

J. Mallol, C. Lluis, R. Franco, 2013, PloS one.

Direct involvement of σ-1 receptors in the dopamine D1 receptor-mediated effects of cocaine

K. Fuxe, D. Marcellino, J. Mallol, 2010, Proceedings of the National Academy of Sciences.

Targeting the dopamine D3 receptor: an overview of drug design strategies

V. Casadó, A. Cortés, E. Moreno, 2016, Expert opinion on drug discovery.

Old and new ways to calculate the affinity of agonists and antagonists interacting with G-protein-coupled monomeric and dimeric receptors: the receptor-dimer cooperativity index.

F. Ciruela, J. Mallol, C. Lluis, 2007, Pharmacology & therapeutics.

The Two-State Dimer Receptor Model: A General Model for Receptor Dimers

K. Fuxe, F. Ciruela, J. Mallol, 2006, Molecular Pharmacology.

Orexin–Corticotropin-Releasing Factor Receptor Heteromers in the Ventral Tegmental Area as Targets for Cocaine

J. Mallol, C. Lluis, S. Ferré, 2015, The Journal of Neuroscience.

Basic Concepts in G-Protein-Coupled Receptor Homo- and Heterodimerization

J. Mallol, C. Lluis, R. Franco, 2007, TheScientificWorldJournal.

Functional Selectivity of Allosteric Interactions within G Protein–Coupled Receptor Oligomers: The Dopamine D1-D3 Receptor Heterotetramer

J. Mallol, C. Lluis, S. Ferré, 2014, Molecular Pharmacology.

α2A- and α2C-Adrenoceptors as Potential Targets for Dopamine and Dopamine Receptor Ligands

J. Meiler, S. Ferré, V. Casadó, 2018, Molecular Neurobiology.

The heterotetrameric structure of the adenosine A1-dopamine D1 receptor complex: Pharmacological implication for restless legs syndrome.

V. Casadó, A. Cortés, E. Moreno, 2019, Advances in pharmacology.

Intracellular calcium levels determine differential modulation of allosteric interactions within G protein-coupled receptor heteromers.

M. Kreutz, J. Mallol, C. Lluis, 2014, Chemistry & biology.

Allosteric interactions between agonists and antagonists within the adenosine A2A receptor-dopamine D2 receptor heterotetramer

N. Volkow, S. Schiffmann, J. Mallol, 2015, Proceedings of the National Academy of Sciences.

Human adenosine deaminase as an allosteric modulator of human A1 adenosine receptor: abolishment of negative cooperativity for [3H](R)‐pia binding to the caudate nucleus

J. Mallol, C. Lluis, R. Franco, 2008, Journal of neurochemistry.

Adenosine A2A receptor-antagonist/dopamine D2 receptor-agonist bivalent ligands as pharmacological tools to detect A2A-D2 receptor heteromers.

C. Lluis, R. Franco, F. Albericio, 2009, Journal of medicinal chemistry.

Dimer-based model for heptaspanning membrane receptors.

K. Fuxe, F. Ciruela, J. Mallol, 2005, Trends in biochemical sciences.