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Copper modulates the large dense core vesicle secretory pathway in PC12 cells.
Duncan C, Bica L, Crouch PJ, Caragounis A, Lidgerwood GE, Parker SJ, Meyerowitz J, Volitakis I, Liddell JR, Raghupathi R, Paterson BM, Duffield MD, Cappai R, Donnelly PS, Grubman A, Camakaris J, Keating DJ, White AR. Duncan C, et al. Among authors: keating dj. Metallomics. 2013 Jun;5(6):700-14. doi: 10.1039/c3mt20231c. Metallomics. 2013. PMID: 23661118
A new 'dual' in the crown for electrochemistry.
Duffield MD, Keating DJ. Duffield MD, et al. Among authors: keating dj. J Neurochem. 2011 Dec;119(5):899-900. doi: 10.1111/j.1471-4159.2011.07508.x. J Neurochem. 2011. PMID: 21955320 Free article. No abstract available.
A Syntenic Cross Species Aneuploidy Genetic Screen Links RCAN1 Expression to β-Cell Mitochondrial Dysfunction in Type 2 Diabetes.
Peiris H, Duffield MD, Fadista J, Jessup CF, Kashmir V, Genders AJ, McGee SL, Martin AM, Saiedi M, Morton N, Carter R, Cousin MA, Kokotos AC, Oskolkov N, Volkov P, Hough TA, Fisher EM, Tybulewicz VL, Busciglio J, Coskun PE, Becker A, Belichenko PV, Mobley WC, Ryan MT, Chan JY, Laybutt DR, Coates PT, Yang S, Ling C, Groop L, Pritchard MA, Keating DJ. Peiris H, et al. Among authors: keating dj. PLoS Genet. 2016 May 19;12(5):e1006033. doi: 10.1371/journal.pgen.1006033. eCollection 2016 May. PLoS Genet. 2016. PMID: 27195491 Free PMC article.
Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder.
Kumar R, Corbett MA, Smith NJ, Jolly LA, Tan C, Keating DJ, Duffield MD, Utsumi T, Moriya K, Smith KR, Hoischen A, Abbott K, Harbord MG, Compton AG, Woenig JA, Arts P, Kwint M, Wieskamp N, Gijsen S, Veltman JA, Bahlo M, Gleeson JG, Haan E, Gecz J. Kumar R, et al. Among authors: keating dj. Hum Mol Genet. 2015 Apr 1;24(7):2000-10. doi: 10.1093/hmg/ddu614. Epub 2014 Dec 11. Hum Mol Genet. 2015. PMID: 25504045
110 results