| Year |
Citation |
Score |
| 2024 |
Li X, Tae HS, Chen S, Yousuf A, Huang L, Zhang J, Jiang T, Adams DJ, Yu R. Dual Antagonism of α9α10 nAChR and GABA Receptor-Coupled Ca2.2 Channels by an Analgesic αO-Conotoxin Analogue. Journal of Medicinal Chemistry. PMID 38217860 DOI: 10.1021/acs.jmedchem.3c00979 |
0.777 |
|
| 2023 |
Arias HR, Tae HS, Micheli L, Yousuf A, Manetti D, Romanelli MN, Ghelardini C, Adams DJ, Di Cesare Mannelli L. 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. PMID 37058425 DOI: 10.1213/ANE.0000000000006461 |
0.655 |
|
| 2022 |
Wang S, Bartels P, Zhao C, Yousuf A, Liu Z, Yu S, Bony AR, Ma X, Dai Q, Sun T, Liu N, Yang M, Yu R, Du W, Adams DJ, et al. A 4/8 Subtype α-Conotoxin Vt1.27 Inhibits N-Type Calcium Channels With Potent Anti-Allodynic Effect. Frontiers in Pharmacology. 13: 881732. PMID 35754473 DOI: 10.3389/fphar.2022.881732 |
0.615 |
|
| 2021 |
Yousuf A, Sadeghi M, Adams DJ. Venom-Derived Peptides Inhibiting Voltage-Gated Sodium and Calcium Channels in Mammalian Sensory Neurons. Advances in Experimental Medicine and Biology. 1349: 3-19. PMID 35138607 DOI: 10.1007/978-981-16-4254-8_1 |
0.735 |
|
| 2021 |
Yousuf A, Wu X, Bony AR, Sadeghi M, Huang YH, Craik DJ, Adams DJ. 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. PMID 34738241 DOI: 10.1111/jnc.15535 |
0.599 |
|
| 2020 |
Arias HR, Ghelardini C, Lucarini E, Tae HS, Yousuf A, Marcovich I, Manetti D, Romanelli MN, Elgoyhen AB, Adams DJ, Di Cesare Mannelli L. ()-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. PMID 33073974 DOI: 10.1021/acschemneuro.0c00476 |
0.748 |
|
| 2020 |
Arias HR, Tae HS, Micheli L, Yousuf A, Ghelardini C, Adams DJ, Di Cesare Mannelli L. Coronaridine congeners decrease neuropathic pain in mice and inhibit α9α10 nicotinic acetylcholine receptors and Ca2.2 channels. Neuropharmacology. 108194. PMID 32540451 DOI: 10.1016/J.Neuropharm.2020.108194 |
0.765 |
|
| 2016 |
Salzer I, Gantumur E, Yousuf A, Boehm S. Control of sensory neuron excitability by serotonin involves 5HT2C receptors and Ca(2+)-activated chloride channels. Neuropharmacology. 110: 277-286. PMID 27511837 DOI: 10.1016/j.neuropharm.2016.08.006 |
0.416 |
|
| 2016 |
Salzer I, Gantumur E, Yousuf A, Boehm S. Control of sensory neuron excitability by serotonin involves 5HT2C receptors and Ca2+-activated chloride channels Neuropharmacology. 110: 277-286. DOI: 10.1016/j.neuropharm.2016.08.006 |
0.312 |
|
| 2012 |
Klinger F, Geier P, Dorostkar MM, Chandaka GK, Yousuf A, Salzer I, Kubista H, Boehm S. Concomitant facilitation of GABAA receptors and KV7 channels by the non-opioid analgesic flupirtine. British Journal of Pharmacology. 166: 1631-42. PMID 22188423 DOI: 10.1111/j.1476-5381.2011.01821.x |
0.32 |
|
| 2011 |
Yousuf A, Klinger F, Schicker K, Boehm S. Nucleotides control the excitability of sensory neurons via two P2Y receptors and a bifurcated signaling cascade. Pain. 152: 1899-908. PMID 21600693 DOI: 10.1016/j.pain.2011.04.016 |
0.476 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2019 |
Mostyn SN, Rawling T, Mohammadi S, Shimmon S, Frangos ZJ, Sarker S, Yousuf A, Vetter I, Ryan RM, Christie MJ, Vandenberg RJ. Development of an N-acyl amino acid that selectively inhibits the glycine transporter 2 to produce analgesia in a rat model of chronic pain. Journal of Medicinal Chemistry. PMID 30714733 DOI: 10.1021/Acs.Jmedchem.8B01775 |
0.27 |
|
| 2019 |
Dekan Z, Sianati S, Yousuf A, Sutcliffe KJ, Gillis A, Mallet C, Singh P, Jin AH, Wang AM, Mohammadi SA, Stewart M, Ratnayake R, Fontaine F, Lacey E, Piggott AM, et al. A tetrapeptide class of biased analgesics from an Australian fungus targets the µ-opioid receptor. Proceedings of the National Academy of Sciences of the United States of America. PMID 31611414 DOI: 10.1073/Pnas.1908662116 |
0.192 |
|
| 2009 |
Yousuf A, Boehm S. Nucleotides excite sensory neurons via two P2Y receptors and a dual signaling cascade Bmc Pharmacology. 9. DOI: 10.1186/1471-2210-9-S2-A17 |
0.167 |
|
| 2018 |
Miess E, Gondin AB, Yousuf A, Steinborn R, Mösslein N, Yang Y, Göldner M, Ruland JG, Bünemann M, Krasel C, Christie MJ, Halls ML, Schulz S, Canals M. Multisite phosphorylation is required for sustained interaction with GRKs and arrestins during rapid μ-opioid receptor desensitization. Science Signaling. 11. PMID 30018083 DOI: 10.1126/Scisignal.Aas9609 |
0.16 |
|
| 2015 |
Yousuf A, Miess E, Sianati S, Du YP, Schulz S, Christie M. The Role of Phosphorylation Sites in Desensitization of μ-Opioid Receptor. Molecular Pharmacology. PMID 25969388 DOI: 10.1124/Mol.115.098244 |
0.15 |
|
| 2024 |
Tae HS, Ortells MO, Yousuf A, Xu SQ, Akk G, Adams DJ, Arias HR. Tabernanthalog and ibogainalog inhibit the α7 and α9α10 nicotinic acetylcholine receptors via different mechanisms and with higher potency than the GABA receptor and Ca2.2 channel. Biochemical Pharmacology. 116183. PMID 38580167 DOI: 10.1016/j.bcp.2024.116183 |
0.12 |
|
| Hide low-probability matches. |