Rocio Finol-Urdaneta
Affiliations: | 2016- | University of Wollongong, Australia |
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| Finol-Urdaneta RK, Belovanovic A, Micic-Vicovac M, et al. (2020) Marine Toxins Targeting Kv1 Channels: Pharmacological Tools and Therapeutic Scaffolds. Marine Drugs. 18 |
| Luna-Ramirez K, Csoti A, McArthur JR, et al. (2019) Structural basis of the potency and selectivity of Urotoxin, a potent Kv1 blocker from scorpion venom. Biochemical Pharmacology. 113782 |
| Wang Y, Finol-Urdaneta RK, Ngo VA, et al. (2019) Author Correction: Bases of Bacterial Sodium Channel Selectivity Among Organic Cations. Scientific Reports. 9: 18992 |
| Wang Y, Finol-Urdaneta RK, Ngo VA, et al. (2019) Bases of Bacterial Sodium Channel Selectivity Among Organic Cations. Scientific Reports. 9: 15260 |
| Finol-Urdaneta RK, McArthur JR, Korkosh VS, et al. (2019) Extremely Potent Block of Bacterial Voltage-Gated Sodium Channels by µ-Conotoxin PIIIA. Marine Drugs. 17 |
| McArthur JR, Finol-Urdaneta RK, Adams DJ. (2019) Analgesic TRPV1-active compounds inhibit native and recombinant T-type (Ca 3) calcium channels. British Journal of Pharmacology |
| Cordeiro S, Finol-Urdaneta RK, Köpfer D, et al. (2018) Conotoxin κM-RIIIJ, a tool targeting asymmetric heteromeric K1 channels. Proceedings of the National Academy of Sciences of the United States of America |
| Finol-Urdaneta RK, McArthur JR, Goldschen-Ohm MP, et al. (2018) Batrachotoxin acts as a stent to hold open homotetrameric prokaryotic voltage-gated sodium channels. The Journal of General Physiology |
| Harvey PJ, Kurniawan ND, Finol-Urdaneta RK, et al. (2018) NMR Structure of μ-Conotoxin GIIIC: Leucine 18 Induces Local Repacking of the N-Terminus Resulting in Reduced Na Channel Potency. Molecules (Basel, Switzerland). 23 |
| Sadeghi M, McArthur JR, Finol-Urdaneta RK, et al. (2017) Analgesic conopeptides targeting G protein-coupled receptors reduce excitability of sensory neurons. Neuropharmacology |