2024

• Li, X., Tae, H., Chen, S., Yousuf, A., Huang, L., Zhang, J., Jiang, T., Adams, D., Yu, R. (2024). Dual Antagonism of α9α10 nAChR and GABAB Receptor-Coupled CaV2.2 Channels by an Analgesic αO-Conotoxin Analogue. Journal of Medicinal Chemistry, 67(2), 971-987. [More Information]
• Tae, H., Ortells, M., Yousuf, A., Xu, S., Akk, G., Adams, D., Arias, H. (2024). Tabernanthalog and ibogainalog inhibit the α7 and α9α10 nicotinic acetylcholine receptors via different mechanisms and with higher potency than the GABAA receptor and CaV2.2 channel. Biochemical Pharmacology, 223, 116183. [More Information]

2023

• Arias, H., Tae, H., Micheli, L., Yousuf, A., Manetti, D., Romanelli, M., Ghelardini, C., Adams, D., Di Cesare Mannelli, L. (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, 137(3), 691-701. [More Information]

2022

• Yousuf, A., Wu, X., Bony, A., Sadeghi, M., Huang, Y., Craik, D., Adams, D. (2022). ɑO-Conotoxin GeXIVA isomers modulate N-type calcium (CaV2.2) channels and inwardly-rectifying potassium (GIRK) channels via GABAB receptor activation. Journal of Neurochemistry, 160(2), 154-171. [More Information]
• Wang, S., Bartels, P., Zhao, C., Yousuf, A., Liu, Z., Yu, S., Bony, A., Ma, X., Dai, Q., Sun, T., 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. [More Information]

2020

• Arias, H., Ghelardini, C., Lucarini, E., Tae, H., Yousuf, A., Marcovich, I., Manetti, D., Romanelli, M., Elgoyhen, A., Adams, D., et al (2020). (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. ACS Chemical Neuroscience, 11(21), 3603-3614. [More Information]
• Arias, H., Tae, H., Micheli, L., Yousuf, A., Ghelardini, C., Adams, D., Di Cesare Mannelli, L. (2020). Coronaridine congeners decrease neuropathic pain in mice and inhibit α9α10 nicotinic acetylcholine receptors and CaV2.2 channels. Neuropharmacology, 175. [More Information]

2019

• Dekan, Z., Sianati, S., Yousuf, A., Sutcliffe, K., Gillis, A., Mallet, C., Wang, A., Singh, P., Jin, A., Mohammadi, S., Du, Y., Christie, M., et al (2019). 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, 116(44), 22353-22358. [More Information]
• Mostyn, S., Rawling, T., Mohammadi, S., Shimmon, S., Frangos, Z., Sarker, S., Yousuf, A., Vetter, I., Ryan, R., Christie, M., Vandenberg, R. (2019). 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, 62(5), 2466-2484. [More Information]

2018

• Miess, E., Gondin, A., Yousuf, A., Steinborn, R., Mosslein, N., Yang, Y., Goldner, M., Ruland, J., Bunemann, M., Krasel, C., Christie, M., et al (2018). Multisite phosphorylation is required for sustained interaction with GRKs and arrestins during rapid mu-opioid receptor desensitization. Science Signaling, 11(539), 1-15. [More Information]

2016

• Salzer, I., Gantumur, E., Yousuf, A., Boehm, S. (2016). Control of sensory neuron excitability by serotonin involves 5HT2C receptors and Ca(2+)-activated chloride channels. Neuropharmacology, 110, 277-286. [More Information]

2015

• Yousuf, A., Miess, E., Sianati, S., Du, Y., Schulz, S., Christie, M. (2015). The Role of Phosphorylation Sites in Desensitization of u-Opioid Receptor. Molecular Pharmacology, 88(4), 825-835. [More Information]

2012

• Klinger, F., Geier, P., Dorostkar, M., Chandaka, G., Yousuf, A., Salzer, I., Kubista, H., Boehm, S. (2012). Concomitant facilitation of GABAA receptors and Kv7 channels by the non-opioid analgesic flupirtine. British Journal of Pharmacology, 166(5), 1631-1642. [More Information]

2011

• Yousuf, A., Klinger, F., Schicker, K., Boehm, S. (2011). Nucleotides control the excitability of sensory neurons via two P2Y receptors and a bifurcated signalling cascade. Pain, 152(8), 1899-1908. [More Information]
• Yousuf, A., Boehm, S. (2011). Nucleotides excite sensory neurons via two P2Y receptors and a dual signaling cascade. 12th Austrian Neuroscience Association Meeting, Not-Known.

2010

• Yousuf, A., Boehm, S. (2010). Nucleotides excite sensory neurons via two P2Y receptors and a dual signaling cascade. European Pain School 2010, Not-Known.
• Yousuf, A., Boehm, S. (2010). Nucleotides excite sensory neurons via two P2Y receptors and a dual signaling cascade. 6th Young Scientist Association of the Medical University of Vienna PhD Symposium, Not-Known.

2009

• Ibrahim, M., Khan, S., Zafar, Y., Mansoor, S., Yousuf, A., Mukhtar, Z. (2009). Expression of a full length Arabidopsis vacuolar H+-pyrophosphatase (AVP1) gene in tobacco (Nicotiana tabbacum) to increase tolerance to drought and salt stresses. Journal of Phytology, 1(6).
• Yousuf, A., Boehm, S. (2009). Nucleotides excite sensory neurons via two P2Y receptors and a dual signaling cascade. 15th Scientific Symposium of the Austrian Pharmacological Society (APHAR), Not-Known: BioMed Central.
• Yousuf, A., Boehm, S. (2009). Nucleotides excite sensory neurons via two P2Y receptors and a dual signaling cascade. 5th Young Scientist Association of the Medical University of Vienna PhD Symposium, Not-Known.