Mahsa Sadeghi

Affiliations: 
2015-2018 Illawarra Health & Medical Research Institute (IHMRI) University of Wollongong, Australia 
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"Mahsa Sadeghi"
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Publications

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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
Belgi A, Burnley JV, MacRaild CA, et al. (2021) Alkyne-Bridged α-Conotoxin Vc1.1 Potently Reverses Mechanical Allodynia in Neuropathic Pain Models. Journal of Medicinal Chemistry
Dai Q, Liu Z, Ning H, et al. (2019) Structures, functions of two novel α-conotoxins from conus snails in South China Sea Toxicon. 158: S26-S27
Sadeghi M, Carstens BB, Callaghan BP, et al. (2018) Structure-activity studies reveal the molecular basis for GABAB-receptor mediated inhibition of high voltage-activated calcium channels by α-conotoxin Vc1.1. Acs Chemical Biology
Sadeghi M, Erickson A, Castro J, et al. (2018) Contribution of membrane receptor signalling to chronic visceral pain. The International Journal of Biochemistry & Cell Biology
Liu Z, Bartels P, Sadeghi M, et al. (2018) A novel α-conopeptide Eu1.6 inhibits N-type (CaV2.2) calcium channels and exhibits potent analgesic activity. Scientific Reports. 8: 1004
Sadeghi M, McArthur JR, Finol-Urdaneta RK, et al. (2017) Analgesic conopeptides targeting G protein-coupled receptors reduce excitability of sensory neurons. Neuropharmacology
Carstens BB, Berecki G, Daniel JT, et al. (2016) Structure-Activity Studies of Cysteine-Rich α-Conotoxins that Inhibit High Voltage-Activated Calcium Channels via GABAB Receptor Activation Reveal a Minimal Functional Motif. Angewandte Chemie (International Ed. in English)
Sadeghi M, Tzschentke TM, Christie MJ. (2015) μ-Opioid receptor activation and noradrenaline transport inhibition by tapentadol in rat single locus coeruleus neurons. British Journal of Pharmacology. 172: 460-8
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