Samuel Evans
ARC Grant-Funded Researcher A
School of Biomedicine
Faculty of Health and Medical Sciences
ECR with an interest in Toll-Like Receptor signalling and protein interactions. In particular their relevance to pathological pain and altered neural function.
My current work involves developing novel techniques for detection of immune signalling at the receptor level. This work aims improve our ability to study activation of innate immune receptors and the early stages of their signalling pathways. Innate immune receptors are important for numerous processes, from threat detection, reproduction, and nervous system function. Therefore, developing tools to better understand their mechanism of action has the potential to impact multiple fields, including, immunology and vaccine development, pain, addiction, and reproductive biology.
Previously, I worked with Toll-Like Receptors to investigate the relationship with neuronal ion channel TRPV1, attempting to understand the effect that immune signalling has on neural function. Known as neuroimmune signalling, these interactions are believed to play an important role in establishing and maintaining chronic pain. Unfortunately, effective treatment of chronic pain is currently lacking, and greater understanding of these mechanisms is a potential pathway to novel treatment strategies.
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Appointments
Date Position Institution name 2019 - ongoing Grant Funded Researcher University of Adelaide -
Education
Date Institution name Country Title University of Adelaide, Adelaide Australia Bachelor of Health Science (Honours) University of Adelaide, Adelaide Australia Bachelor of Science University of Adelaide Australia PhD (Medicine) -
Research Interests
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Journals
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Book Chapters
Year Citation 2022 Mustafa, S., Evans, S., Barry, B., Barratt, D., Wang, Y., Lin, C., . . . Hutchinson, M. R. (2022). Toll-Like Receptor 4 in Pain: Bridging Molecules-to-Cells-to-Systems.. In V. Kumar (Ed.), Toll-like Receptors in Health and Disease. Handbook of Experimental Pharmacology (Vol. 276, pp. 239-273). Springer Berlin Heidelberg.
DOI Scopus2 Europe PMC2
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