Arsalan Yousuf
Affiliations: | 2019- | University of Wollongong, Australia |
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| Li X, Tae HS, Chen S, et al. (2024) Dual Antagonism of α9α10 nAChR and GABA Receptor-Coupled Ca2.2 Channels by an Analgesic αO-Conotoxin Analogue. Journal of Medicinal Chemistry |
| Arias HR, Tae HS, Micheli L, et al. (2023) The Antinociceptive Activity of (E)-3-(thiophen-2-yl)-N-(p-tolyl)acrylamide in Mice Is Reduced by (E)-3-(furan-2-yl)-N-methyl-N-(p-tolyl)acrylamide Through Opposing Modulatory Mechanisms at the α7 Nicotinic Acetylcholine Receptor. Anesthesia and Analgesia |
| Wang S, Bartels P, Zhao C, et al. (2022) A 4/8 Subtype α-Conotoxin Vt1.27 Inhibits N-Type Calcium Channels With Potent Anti-Allodynic Effect. Frontiers in Pharmacology. 13: 881732 |
| Yousuf A, Sadeghi M, Adams DJ. (2021) Venom-Derived Peptides Inhibiting Voltage-Gated Sodium and Calcium Channels in Mammalian Sensory Neurons. Advances in Experimental Medicine and Biology. 1349: 3-19 |
| Yousuf A, Wu X, Bony AR, et al. (2021) ɑO-Conotoxin GeXIVA isomers modulate N-type calcium (Ca 2.2) channels and inwardly-rectifying potassium (GIRK) channels via GABA receptor activation. Journal of Neurochemistry |
| Arias HR, Ghelardini C, Lucarini E, et al. (2020) ()-3-Furan-2-yl---tolyl-acrylamide and its Derivative DM489 Decrease Neuropathic Pain in Mice Predominantly by α7 Nicotinic Acetylcholine Receptor Potentiation. Acs Chemical Neuroscience |
| Arias HR, Tae HS, Micheli L, et al. (2020) Coronaridine congeners decrease neuropathic pain in mice and inhibit α9α10 nicotinic acetylcholine receptors and Ca2.2 channels. Neuropharmacology. 108194 |
| Salzer I, Gantumur E, Yousuf A, et al. (2016) Control of sensory neuron excitability by serotonin involves 5HT2C receptors and Ca(2+)-activated chloride channels. Neuropharmacology. 110: 277-286 |
| Salzer I, Gantumur E, Yousuf A, et al. (2016) Control of sensory neuron excitability by serotonin involves 5HT2C receptors and Ca2+-activated chloride channels Neuropharmacology. 110: 277-286 |
| Klinger F, Geier P, Dorostkar MM, et al. (2012) Concomitant facilitation of GABAA receptors and KV7 channels by the non-opioid analgesic flupirtine. British Journal of Pharmacology. 166: 1631-42 |