Yousuf A - Search Results

1

Control of sensory neuron excitability by serotonin involves 5HT2C receptors and Ca(2+)-activated chloride channels.

Salzer I, Gantumur E, Yousuf A, Boehm S. Salzer I, et al. Among authors: yousuf a. Neuropharmacology. 2016 Nov;110(Pt A):277-286. doi: 10.1016/j.neuropharm.2016.08.006. Epub 2016 Aug 7. Neuropharmacology. 2016. PMID: 27511837 Free PMC article.

2

Nucleotides control the excitability of sensory neurons via two P2Y receptors and a bifurcated signaling cascade.

Yousuf A, Klinger F, Schicker K, Boehm S. Yousuf A, et al. Pain. 2011 Aug;152(8):1899-1908. doi: 10.1016/j.pain.2011.04.016. Epub 2011 May 19. Pain. 2011. PMID: 21600693 Free PMC article.

3

Concomitant facilitation of GABAA receptors and KV7 channels by the non-opioid analgesic flupirtine.

Klinger F, Geier P, Dorostkar MM, Chandaka GK, Yousuf A, Salzer I, Kubista H, Boehm S. Klinger F, et al. Among authors: yousuf a. Br J Pharmacol. 2012 Jul;166(5):1631-42. doi: 10.1111/j.1476-5381.2011.01821.x. Br J Pharmacol. 2012. PMID: 22188423 Free PMC article.

4

Coronaridine congeners decrease neuropathic pain in mice and inhibit α9α10 nicotinic acetylcholine receptors and Ca_V2.2 channels.

Arias HR, Tae HS, Micheli L, Yousuf A, Ghelardini C, Adams DJ, Di Cesare Mannelli L. Arias HR, et al. Among authors: yousuf a. Neuropharmacology. 2020 Sep 15;175:108194. doi: 10.1016/j.neuropharm.2020.108194. Epub 2020 Jun 12. Neuropharmacology. 2020. PMID: 32540451

5

(E)-3-Furan-2-yl-N-p-tolyl-acrylamide and its Derivative DM489 Decrease Neuropathic Pain in Mice Predominantly by α7 Nicotinic Acetylcholine Receptor Potentiation.

Arias HR, Ghelardini C, Lucarini E, Tae HS, Yousuf A, Marcovich I, Manetti D, Romanelli MN, Elgoyhen AB, Adams DJ, Di Cesare Mannelli L. Arias HR, et al. Among authors: yousuf a. ACS Chem Neurosci. 2020 Nov 4;11(21):3603-3614. doi: 10.1021/acschemneuro.0c00476. Epub 2020 Oct 19. ACS Chem Neurosci. 2020. PMID: 33073974

6

Venom-Derived Peptides Inhibiting Voltage-Gated Sodium and Calcium Channels in Mammalian Sensory Neurons.

Yousuf A, Sadeghi M, Adams DJ. Yousuf A, et al. Adv Exp Med Biol. 2021;1349:3-19. doi: 10.1007/978-981-16-4254-8_1. Adv Exp Med Biol. 2021. PMID: 35138607

7

A 4/8 Subtype α-Conotoxin Vt1.27 Inhibits N-Type Calcium Channels With Potent Anti-Allodynic Effect.

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, Dai Q. Wang S, et al. Among authors: yousuf a. Front Pharmacol. 2022 Apr 29;13:881732. doi: 10.3389/fphar.2022.881732. eCollection 2022. Front Pharmacol. 2022. PMID: 35754473 Free PMC article.

8

Role of Phosphorylation Sites in Desensitization of µ-Opioid Receptor.

Yousuf A, Miess E, Sianati S, Du YP, Schulz S, Christie MJ. Yousuf A, et al. Mol Pharmacol. 2015 Oct;88(4):825-35. doi: 10.1124/mol.115.098244. Epub 2015 May 12. Mol Pharmacol. 2015. PMID: 25969388

9

ɑO-Conotoxin GeXIVA isomers modulate N-type calcium (Ca_V 2.2) channels and inwardly-rectifying potassium (GIRK) channels via GABA_B receptor activation.

Yousuf A, Wu X, Bony AR, Sadeghi M, Huang YH, Craik DJ, Adams DJ. Yousuf A, et al. J Neurochem. 2022 Jan;160(2):154-171. doi: 10.1111/jnc.15535. Epub 2021 Nov 15. J Neurochem. 2022. PMID: 34738241 Free article.

10

Multisite phosphorylation is required for sustained interaction with GRKs and arrestins during rapid μ-opioid receptor desensitization.

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. Miess E, et al. Among authors: yousuf a. Sci Signal. 2018 Jul 17;11(539):eaas9609. doi: 10.1126/scisignal.aas9609. Sci Signal. 2018. PMID: 30018083

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