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Year Number of Results
2005 1
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Page 1
Mitochondrial DNA and genetic disease.
Krishnan KJ, Turnbull DM. Krishnan KJ, et al. Essays Biochem. 2010;47:139-51. doi: 10.1042/bse0470139. Essays Biochem. 2010. PMID: 20533905 Review.
A neurological perspective on mitochondrial disease.
McFarland R, Taylor RW, Turnbull DM. McFarland R, et al. Lancet Neurol. 2010 Aug;9(8):829-40. doi: 10.1016/S1474-4422(10)70116-2. Lancet Neurol. 2010. PMID: 20650404 Review.
A diagnostic tattoo.
Whittaker RG, Turnbull DM. Whittaker RG, et al. Clin Genet. 2009 Jan;75(1):37-8. doi: 10.1111/j.1399-0004.2008.01103.x. Clin Genet. 2009. PMID: 19128396
Mitochondrial DNA mutations and human disease.
Tuppen HA, Blakely EL, Turnbull DM, Taylor RW. Tuppen HA, et al. Biochim Biophys Acta. 2010 Feb;1797(2):113-28. doi: 10.1016/j.bbabio.2009.09.005. Epub 2009 Sep 15. Biochim Biophys Acta. 2010. PMID: 19761752 Free article. Review.
Translation termination in human mitochondrial ribosomes.
Richter R, Pajak A, Dennerlein S, Rozanska A, Lightowlers RN, Chrzanowska-Lightowlers ZM. Richter R, et al. Biochem Soc Trans. 2010 Dec;38(6):1523-6. doi: 10.1042/BST0381523. Biochem Soc Trans. 2010. PMID: 21118119 Review.
Mitochondrial DNA mutations and ageing.
Greaves LC, Turnbull DM. Greaves LC, et al. Biochim Biophys Acta. 2009 Oct;1790(10):1015-20. doi: 10.1016/j.bbagen.2009.04.018. Epub 2009 May 4. Biochim Biophys Acta. 2009. PMID: 19409965 Review.
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. Nat Genet. 2008 Mar;40(3):275-9. doi: 10.1038/ng.f.94. Nat Genet. 2008. PMID: 18305478 Review.
97 results