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Modelling biochemical features of mitochondrial neuropathology.
Bird MJ, Thorburn DR, Frazier AE. Bird MJ, et al. Among authors: frazier ae. Biochim Biophys Acta. 2014 Apr;1840(4):1380-92. doi: 10.1016/j.bbagen.2013.10.017. Epub 2013 Oct 23. Biochim Biophys Acta. 2014. PMID: 24161927 Review.
Mutations in the UQCC1-interacting protein, UQCC2, cause human complex III deficiency associated with perturbed cytochrome b protein expression.
Tucker EJ, Wanschers BF, Szklarczyk R, Mountford HS, Wijeyeratne XW, van den Brand MA, Leenders AM, Rodenburg RJ, Reljić B, Compton AG, Frazier AE, Bruno DL, Christodoulou J, Endo H, Ryan MT, Nijtmans LG, Huynen MA, Thorburn DR. Tucker EJ, et al. Among authors: frazier ae. PLoS Genet. 2013;9(12):e1004034. doi: 10.1371/journal.pgen.1004034. Epub 2013 Dec 26. PLoS Genet. 2013. PMID: 24385928 Free PMC article.
Functional characterization of Friedreich ataxia iPS-derived neuronal progenitors and their integration in the adult brain.
Bird MJ, Needham K, Frazier AE, van Rooijen J, Leung J, Hough S, Denham M, Thornton ME, Parish CL, Nayagam BA, Pera M, Thorburn DR, Thompson LH, Dottori M. Bird MJ, et al. Among authors: frazier ae. PLoS One. 2014 Jul 7;9(7):e101718. doi: 10.1371/journal.pone.0101718. eCollection 2014. PLoS One. 2014. PMID: 25000412 Free PMC article.
46 results