Argel Estrada-Mondragón

University of Queensland, Saint Lucia, Queensland, Australia 
Molecular Neurobiology
"Argel Estrada-Mondragón"
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Téllez-Arreola JL, Martínez-Torres A, Flores-Moran AE, et al. (2022) Analysis of the MCTP Amino Acid Sequence Reveals the Conservation of Putative Calcium- and Lipid-Binding Pockets Within the C2 Domains In Silico. Journal of Molecular Evolution
Estrada-Mondragon A, Ottosson NE, Wu X, et al. (2020) Electrostatic Interactions of Negatively Charged DHAA Derivatives with the Voltage-Gated Potassium Channel Kv7.2/7.3 Biophysical Journal. 118
Hénault CM, Govaerts C, Spurny R, et al. (2019) A lipid site shapes the agonist response of a pentameric ligand-gated ion channel. Nature Chemical Biology
Atif M, Smith JJ, Estrada-Mondragon A, et al. (2019) GluClR-mediated inhibitory postsynaptic currents reveal targets for ivermectin and potential mechanisms of ivermectin resistance. Plos Pathogens. 15: e1007570
Rosas-Arellano A, Estrada-Mondragón A, Mantellero CA, et al. (2018) The adjustment of γ-aminobutyric acid tonic subunits in Huntington's disease: from transcription to translation to synaptic levels into the neostriatum. Neural Regeneration Research. 13: 584-590
Atif M, Estrada-Mondragon A, Nguyen B, et al. (2017) Effects of glutamate and ivermectin on single glutamate-gated chloride channels of the parasitic nematode H. contortus. Plos Pathogens. 13: e1006663
Lynch JW, Zhang Y, Talwar S, et al. (2017) Glycine Receptor Drug Discovery. Advances in Pharmacology (San Diego, Calif.). 79: 225-253
Moreau CJ, Revilloud J, Caro LN, et al. (2017) Tuning the allosteric regulation of artificial muscarinic and dopaminergic ligand-gated potassium channels by protein engineering of G protein-coupled receptors. Scientific Reports. 7: 41154
Soh MS, Estrada-Mondragon A, Durisic N, et al. (2017) Probing the structural mechanism of partial agonism in glycine receptors using the fluorescent artificial amino acid, ANAP. Acs Chemical Biology
Limon A, Estrada-Mondragon A, Reyes-Ruiz JM, et al. (2016) Dipicrylamine Modulates GABAρ1 Receptors through Interactions with Residues in the TM4 and Cys-loop Domains. Molecular Pharmacology
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