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Mitochondrial DNA mutations in human colonic crypt stem cells.
Taylor RW, Barron MJ, Borthwick GM, Gospel A, Chinnery PF, Samuels DC, Taylor GA, Plusa SM, Needham SJ, Greaves LC, Kirkwood TB, Turnbull DM. Taylor RW, et al. Among authors: samuels dc. J Clin Invest. 2003 Nov;112(9):1351-60. doi: 10.1172/JCI19435. J Clin Invest. 2003. PMID: 14597761 Free PMC article.
What causes mitochondrial DNA deletions in human cells?
Krishnan KJ, Reeve AK, Samuels DC, Chinnery PF, Blackwood JK, Taylor RW, Wanrooij S, Spelbrink JN, Lightowlers RN, Turnbull DM. Krishnan KJ, et al. Among authors: samuels dc. Nat Genet. 2008 Mar;40(3):275-9. doi: 10.1038/ng.f.94. Nat Genet. 2008. PMID: 18305478 Review.
Epigenetics, epidemiology and mitochondrial DNA diseases.
Chinnery PF, Elliott HR, Hudson G, Samuels DC, Relton CL. Chinnery PF, et al. Among authors: samuels dc. Int J Epidemiol. 2012 Feb;41(1):177-87. doi: 10.1093/ije/dyr232. Epub 2012 Jan 28. Int J Epidemiol. 2012. PMID: 22287136 Free PMC article. Review.
Universal heteroplasmy of human mitochondrial DNA.
Payne BA, Wilson IJ, Yu-Wai-Man P, Coxhead J, Deehan D, Horvath R, Taylor RW, Samuels DC, Santibanez-Koref M, Chinnery PF. Payne BA, et al. Among authors: samuels dc. Hum Mol Genet. 2013 Jan 15;22(2):384-90. doi: 10.1093/hmg/dds435. Epub 2012 Oct 16. Hum Mol Genet. 2013. PMID: 23077218 Free PMC article.
181 results