Vincent O'Connor, Ph.D

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Mulcahy B, Ibbett P, Holden-Dye L, et al. (2019) The cysteine-string protein homologue, DNJ-14, is dispensable for neuromuscular junction maintenance across ageing. The Journal of Experimental Biology
Pitera AP, Asuni AA, O'Connor V, et al. (2019) Pathogenic tau does not drive activation of the unfolded protein response. The Journal of Biological Chemistry
Dillon J, Franks CJ, Murray C, et al. (2015) Metabotropic Glutamate Receptors: MODULATORS OF CONTEXT-DEPENDENT FEEDING BEHAVIOUR IN C. ELEGANS. The Journal of Biological Chemistry. 290: 15052-65
Calahorro F, Holden-Dye L, O'Connor V. (2015) Analysis of splice variants for the C. elegans orthologue of human neuroligin reveals a developmentally regulated transcript. Gene Expression Patterns : Gep. 17: 69-78
Davies MJ, Cooper M, Perry VH, et al. (2015) Reduced expression of the presynaptic co-chaperone cysteine string protein alpha (CSPα) does not exacerbate experimentally-induced ME7 prion disease. Neuroscience Letters. 589: 138-43
Alessi AM, O'Connor V, Aonuma H, et al. (2014) Dopaminergic modulation of phase reversal in desert locusts. Frontiers in Behavioral Neuroscience. 8: 371
Asuni AA, Gray B, Bailey J, et al. (2014) Analysis of the hippocampal proteome in ME7 prion disease reveals a predominant astrocytic signature and highlights the brain-restricted production of clusterin in chronic neurodegeneration. The Journal of Biological Chemistry. 289: 4532-45
Å iÅ¡kovÃ¡ Z, Reynolds RA, O'Connor V, et al. (2013) Brain region specific pre-synaptic and post-synaptic degeneration are early components of neuropathology in prion disease. Plos One. 8: e55004
Mulcahy B, Holden-Dye L, O'Connor V. (2013) Pharmacological assays reveal age-related changes in synaptic transmission at the Caenorhabditis elegans neuromuscular junction that are modified by reduced insulin signalling. The Journal of Experimental Biology. 216: 492-501
Caleo M, Restani L, Vannini E, et al. (2012) The role of activity in synaptic degeneration in a protein misfolding disease, prion disease. Plos One. 7: e41182