Karen J. Smillie - Publications

University of Edinburgh, Edinburgh, Scotland, United Kingdom 

24 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Harper CB, Smillie KJ. Current molecular approaches to investigate presynaptic dysfunction. Journal of Neurochemistry. PMID 33544872 DOI: 10.1111/jnc.15316  0.48
2021 Cousin MA, Smillie KJ. Monitoring Activity-Dependent Bulk Endocytosis in Primary Neuronal Culture Using Large Fluorescent Dextrans. Methods in Molecular Biology (Clifton, N.J.). 2233: 101-111. PMID 33222130 DOI: 10.1007/978-1-0716-1044-2_7  1
2020 Harper CB, Small C, Davenport EC, Low DW, Smillie KJ, Martínez-Mármol R, Meunier FA, Cousin MA. An epilepsy-associated SV2A mutation disrupts synaptotagmin-1 expression and activity-dependent trafficking. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 32341095 DOI: 10.1523/JNEUROSCI.0210-20.2020  1
2019 McAdam RL, Morton A, Gordon SL, Alterman JF, Khvorova A, Cousin MA, Smillie KJ. Loss of huntingtin function slows synaptic vesicle endocytosis in striatal neurons from the htt mouse model of Huntington's disease. Neurobiology of Disease. 134: 104637. PMID 31614197 DOI: 10.1016/j.nbd.2019.104637  1
2019 Kokotos AC, Harper CB, Marland JRK, Smillie KJ, Cousin MA, Gordon SL. Synaptophysin sustains presynaptic performance by preserving vesicular synaptobrevin-II levels. Journal of Neurochemistry. PMID 31216055 DOI: 10.1111/jnc.14797  1
2018 Cousin MA, Gordon SL, Smillie KJ. Using FM Dyes to Monitor Clathrin-Mediated Endocytosis in Primary Neuronal Culture. Methods in Molecular Biology (Clifton, N.J.). 1847: 239-249. PMID 30129022 DOI: 10.1007/978-1-4939-8719-1_18  1
2016 Nicholson-Fish JC, Smillie KJ, Cousin MA. Monitoring activity-dependent bulk endocytosis with the genetically-encoded reporter VAMP4-pHluorin. Journal of Neuroscience Methods. PMID 27015791 DOI: 10.1016/j.jneumeth.2016.03.011  1
2016 Gordon SL, Harper CB, Smillie KJ, Cousin MA. A Fine Balance of Synaptophysin Levels Underlies Efficient Retrieval of Synaptobrevin II to Synaptic Vesicles. Plos One. 11: e0149457. PMID 26871701 DOI: 10.1371/journal.pone.0149457  1
2016 Marland JR, Smillie KJ, Cousin MA. Synaptic Vesicle Recycling Is Unaffected in the Ts65Dn Mouse Model of Down Syndrome. Plos One. 11: e0147974. PMID 26808141 DOI: 10.1371/journal.pone.0147974  1
2015 Nicholson-Fish JC, Kokotos AC, Gillingwater TH, Smillie KJ, Cousin MA. VAMP4 Is an Essential Cargo Molecule for Activity-Dependent Bulk Endocytosis. Neuron. PMID 26607000 DOI: 10.1016/j.neuron.2015.10.043  1
2015 Nicholson-Fish JC, Cousin MA, Smillie KJ. Phosphatidylinositol 3-Kinase Couples Localised Calcium Influx to Activation of Akt in Central Nerve Terminals. Neurochemical Research. PMID 26198194 DOI: 10.1007/s11064-015-1663-5  1
2014 Kavanagh DM, Smyth AM, Martin KJ, Dun A, Brown ER, Gordon S, Smillie KJ, Chamberlain LH, Wilson RS, Yang L, Lu W, Cousin MA, Rickman C, Duncan RR. A molecular toggle after exocytosis sequesters the presynaptic syntaxin1a molecules involved in prior vesicle fusion. Nature Communications. 5: 5774. PMID 25517944 DOI: 10.1038/ncomms6774  1
2013 Smillie KJ, Pawson J, Perkins EM, Jackson M, Cousin MA. Control of synaptic vesicle endocytosis by an extracellular signalling molecule. Nature Communications. 4: 2394. PMID 23999152 DOI: 10.1038/ncomms3394  1
2012 Smillie KJ, Cousin MA. Akt/PKB controls the activity-dependent bulk endocytosis of synaptic vesicles. Traffic (Copenhagen, Denmark). 13: 1004-11. PMID 22487004 DOI: 10.1111/j.1600-0854.2012.01365.x  1
2012 Quan A, Xue J, Wielens J, Smillie KJ, Anggono V, Parker MW, Cousin MA, Graham ME, Robinson PJ. Phosphorylation of syndapin I F-BAR domain at two helix-capping motifs regulates membrane tubulation. Proceedings of the National Academy of Sciences of the United States of America. 109: 3760-5. PMID 22355135 DOI: 10.1073/pnas.1108294109  1
2011 Xue J, Graham ME, Novelle AE, Sue N, Gray N, McNiven MA, Smillie KJ, Cousin MA, Robinson PJ. Calcineurin selectively docks with the dynamin Ixb splice variant to regulate activity-dependent bulk endocytosis. The Journal of Biological Chemistry. 286: 30295-303. PMID 21730063 DOI: 10.1074/jbc.M111.273110  1
2011 Smillie KJ, Cousin MA. The Role of GSK3 in Presynaptic Function. International Journal of Alzheimer's Disease. 2011: 263673. PMID 21547219 DOI: 10.4061/2011/263673  1
2010 Clayton EL, Sue N, Smillie KJ, O'Leary T, Bache N, Cheung G, Cole AR, Wyllie DJ, Sutherland C, Robinson PJ, Cousin MA. Dynamin I phosphorylation by GSK3 controls activity-dependent bulk endocytosis of synaptic vesicles. Nature Neuroscience. 13: 845-51. PMID 20526333 DOI: 10.1038/nn.2571  1
2009 Clayton EL, Anggono V, Smillie KJ, Chau N, Robinson PJ, Cousin MA. The phospho-dependent dynamin-syndapin interaction triggers activity-dependent bulk endocytosis of synaptic vesicles. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 7706-17. PMID 19535582 DOI: 10.1523/JNEUROSCI.1976-09.2009  1
2006 Anggono V, Smillie KJ, Graham ME, Valova VA, Cousin MA, Robinson PJ. Syndapin I is the phosphorylation-regulated dynamin I partner in synaptic vesicle endocytosis. Nature Neuroscience. 9: 752-60. PMID 16648848 DOI: 10.1038/nn1695  1
2005 Smillie KJ, Evans GJ, Cousin MA. Developmental change in the calcium sensor for synaptic vesicle endocytosis in central nerve terminals. Journal of Neurochemistry. 94: 452-8. PMID 15998295 DOI: 10.1111/j.1471-4159.2005.03213.x  1
2005 Smillie KJ, Cousin MA. Dynamin I phosphorylation and the control of synaptic vesicle endocytosis. Biochemical Society Symposium. 87-97. PMID 15649133  1
2003 Cousin MA, Malladi CS, Tan TC, Raymond CR, Smillie KJ, Robinson PJ. Synapsin I-associated phosphatidylinositol 3-kinase mediates synaptic vesicle delivery to the readily releasable pool. The Journal of Biological Chemistry. 278: 29065-71. PMID 12754199 DOI: 10.1074/jbc.M302386200  1
2002 Pang S, Wang W, Rich B, David R, Chang YT, Carbunaru G, Myers SE, Howie AF, Smillie KJ, Mason JI. A novel nonstop mutation in the stop codon and a novel missense mutation in the type II 3beta-hydroxysteroid dehydrogenase (3beta-HSD) gene causing, respectively, nonclassic and classic 3beta-HSD deficiency congenital adrenal hyperplasia. The Journal of Clinical Endocrinology and Metabolism. 87: 2556-63. PMID 12050213 DOI: 10.1210/jcem.87.6.8559  1
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