Andrew A. George

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Roberts CF, Cao Y, Im W, et al. (2024) Neuroprotective amyloid β N-terminal peptides differentially alter human α7- and α7β2-nicotinic acetylcholine (nACh) receptor single-channel properties. British Journal of Pharmacology
George AA, John SJ, Lucero LM, et al. (2024) Analogs of α-conotoxin PnIC selectively inhibit α7β2- over α7-only subtype nicotinic acetylcholine receptors via a novel allosteric mechanism. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 38: e23374
York JM, Borghese CM, George AA, et al. (2023) A potential cost of evolving epibatidine resistance in poison frogs. Bmc Biology. 21: 144
Whiteaker P, George AA. (2023) Discoveries and future significance of research into amyloid-beta/α7-containing nicotinic acetylcholine receptor (nAChR) interactions. Pharmacological Research. 106743
York JM, Borghese CM, George AA, et al. (2023) A potential cost of evolving epibatidine resistance in poison frogs. Biorxiv : the Preprint Server For Biology
Weltzin MM, George AA, Lukas RJ, et al. (2021) Sleep-related hypermotor epilepsy associated mutations uncover important kinetic roles of α4β2- nicotinic acetylcholine receptor intracellular structures. Plos One. 16: e0247825
George AA, Vieira JM, Xavier-Jackson C, et al. (2020) Implications of oligomeric amyloid-beta (oAβ42) signaling through α7β2-nicotinic acetylcholine receptors (nAChR) on basal forebrain cholinergic neuronal intrinsic excitability and cognitive decline. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience
Weltzin MM, George AA, Lukas RJ, et al. (2019) Distinctive single-channel properties of α4β2-nicotinic acetylcholine receptor isoforms. Plos One. 14: e0213143
George AA, Bloy A, Miwa JM, et al. (2017) Isoform-specific mechanisms of α3β4*-nicotinic acetylcholine receptor modulation by the prototoxin lynx1. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology
Ochoa V, George AA, Nishi R, et al. (2015) The prototoxin LYPD6B modulates heteromeric α3β4-containing nicotinic acetylcholine receptors, but not α7 homomers. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology
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