Chris Dunning - Publications

Biology University of York, York, England, United Kingdom 

7 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
2015 Keenan S, Lewis PA, Wetherill SJ, Dunning CJ, Evans GJ. The N2-Src neuronal splice variant of C-Src has altered SH3 domain ligand specificity and a higher constitutive activity than N1-Src. Febs Letters. 589: 1995-2000. PMID 26026271 DOI: 10.1016/j.febslet.2015.05.033  0.76
2015 Cohen SI, Arosio P, Presto J, Kurudenkandy FR, Biverstål H, Dolfe L, Dunning C, Yang X, Frohm B, Vendruscolo M, Johansson J, Dobson CM, Fisahn A, Knowles TP, Linse S. A molecular chaperone breaks the catalytic cycle that generates toxic Aβ oligomers. Nature Structural & Molecular Biology. 22: 207-13. PMID 25686087 DOI: 10.1038/nsmb.2971  0.76
2015 Grey M, Dunning CJ, Gaspar R, Grey C, Brundin P, Sparr E, Linse S. Acceleration of α-synuclein aggregation by exosomes. The Journal of Biological Chemistry. 290: 2969-82. PMID 25425650 DOI: 10.1074/jbc.M114.585703  0.76
2013 Dunning CJ, George S, Brundin P. What's to like about the prion-like hypothesis for the spreading of aggregated α-synuclein in Parkinson disease? Prion. 7: 92-7. PMID 23360753 DOI: 10.4161/pri.23806  0.76
2012 Dunning CJ, Reyes JF, Steiner JA, Brundin P. Can Parkinson's disease pathology be propagated from one neuron to another? Progress in Neurobiology. 97: 205-19. PMID 22115849 DOI: 10.1016/j.pneurobio.2011.11.003  0.76
2007 Dunning CJ, McKenzie M, Sugiana C, Lazarou M, Silke J, Connelly A, Fletcher JM, Kirby DM, Thorburn DR, Ryan MT. Human CIA30 is involved in the early assembly of mitochondrial complex I and mutations in its gene cause disease. The Embo Journal. 26: 3227-37. PMID 17557076 DOI: 10.1038/sj.emboj.7601748  0.76
2004 Kirby DM, McFarland R, Ohtake A, Dunning C, Ryan MT, Wilson C, Ketteridge D, Turnbull DM, Thorburn DR, Taylor RW. Mutations of the mitochondrial ND1 gene as a cause of MELAS. Journal of Medical Genetics. 41: 784-9. PMID 15466014 DOI: 10.1136/jmg.2004.020537  0.76
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