Austen Milnerwood

Affiliations: 
2016- McGill University, Montreal, QC, Canada 
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"Austen Milnerwood"
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Parents

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Lynn Raymond grad student 2004-
Kerry PSJ Murphy grad student 2000-2004
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Publications

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Volpicelli-Daley LA, Abdelmotilib H, Liu Z, et al. (2016) G2019S-LRRK2 Expression Augments α-Synuclein Sequestration into Inclusions in Neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 36: 7415-27
Dallérac GM, Cummings DM, Hirst MC, et al. (2016) Changes in Dopamine Signalling Do Not Underlie Aberrant Hippocampal Plasticity in a Mouse Model of Huntington's Disease. Neuromolecular Medicine
Volta M, Milnerwood AJ, Farrer MJ. (2015) Insights from late-onset familial parkinsonism on the pathogenesis of idiopathic Parkinson's disease. The Lancet. Neurology. 14: 1054-64
Volta M, Cataldi S, Beccano-Kelly D, et al. (2015) Chronic and acute LRRK2 silencing has no long-term behavioral effects, whereas wild-type and mutant LRRK2 overexpression induce motor and cognitive deficits and altered regulation of dopamine release. Parkinsonism & Related Disorders. 21: 1156-63
Dallérac GM, Levasseur G, Vatsavayai SC, et al. (2015) Dysfunctional Dopaminergic Neurones in Mouse Models of Huntington's Disease: A Role for SK3 Channels. Neuro-Degenerative Diseases. 15: 93-108
Beccano-Kelly DA, Volta M, Munsie LN, et al. (2015) LRRK2 overexpression alters glutamatergic presynaptic plasticity, striatal dopamine tone, postsynaptic signal transduction, motor activity and memory. Human Molecular Genetics. 24: 1336-49
Beccano-Kelly DA, Kuhlmann N, Tatarnikov I, et al. (2014) Synaptic function is modulated by LRRK2 and glutamate release is increased in cortical neurons of G2019S LRRK2 knock-in mice. Frontiers in Cellular Neuroscience. 8: 301
Walker MD, Volta M, Cataldi S, et al. (2014) Behavioral deficits and striatal DA signaling in LRRK2 p.G2019S transgenic rats: a multimodal investigation including PET neuroimaging. Journal of Parkinson's Disease. 4: 483-98
Araki E, Tsuboi Y, Daechsel J, et al. (2014) A novel DCTN1 mutation with late-onset parkinsonism and frontotemporal atrophy. Movement Disorders : Official Journal of the Movement Disorder Society. 29: 1201-4
Coquinco A, Kojic L, Wen W, et al. (2014) A microfluidic based in vitro model of synaptic competition. Molecular and Cellular Neurosciences. 60: 43-52
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