Turnbull DM - Search Results

1

The length of cytochrome c oxidase-negative segments in muscle fibres in patients with mtDNA myopathy.

Elson JL, Samuels DC, Johnson MA, Turnbull DM, Chinnery PF. Elson JL, et al. Among authors: turnbull dm. Neuromuscul Disord. 2002 Nov;12(9):858-64. doi: 10.1016/s0960-8966(02)00047-0. Neuromuscul Disord. 2002. PMID: 12398838 Clinical Trial.

2

Accumulation of mitochondrial DNA mutations in ageing, cancer, and mitochondrial disease: is there a common mechanism?

Chinnery PF, Samuels DC, Elson J, Turnbull DM. Chinnery PF, et al. Among authors: turnbull dm. Lancet. 2002 Oct 26;360(9342):1323-5. doi: 10.1016/S0140-6736(02)11310-9. Lancet. 2002. PMID: 12414225

3

A novel sporadic mutation in cytochrome c oxidase subunit II as a cause of rhabdomyolysis.

McFarland R, Taylor RW, Chinnery PF, Howell N, Turnbull DM. McFarland R, et al. Among authors: turnbull dm. Neuromuscul Disord. 2004 Feb;14(2):162-6. doi: 10.1016/j.nmd.2003.10.011. Neuromuscul Disord. 2004. PMID: 14733964

4

Sporadic mitochondrial myopathy due to a new mutation in the mitochondrial tRNASer(UCN) gene.

Bidooki S, Jackson MJ, Johnson MA, Chrzanowska-Lightowlers ZM, Taylor RW, Venables G, Lightowlers RN, Turnbull DM, Bindoff LA. Bidooki S, et al. Among authors: turnbull dm. Neuromuscul Disord. 2004 Jul;14(7):417-20. doi: 10.1016/j.nmd.2004.03.004. Neuromuscul Disord. 2004. PMID: 15210164

5

Progressive depletion of mtDNA in mitochondrial myopathy.

Durham SE, Brown DT, Turnbull DM, Chinnery PF. Durham SE, et al. Among authors: turnbull dm. Neurology. 2006 Aug 8;67(3):502-4. doi: 10.1212/01.wnl.0000227961.55640.2f. Neurology. 2006. PMID: 16894115

6

Cardiomyopathy is common in patients with the mitochondrial DNA m.3243A>G mutation and correlates with mutation load.

Hollingsworth KG, Gorman GS, Trenell MI, McFarland R, Taylor RW, Turnbull DM, MacGowan GA, Blamire AM, Chinnery PF. Hollingsworth KG, et al. Among authors: turnbull dm. Neuromuscul Disord. 2012 Jul;22(7):592-6. doi: 10.1016/j.nmd.2012.03.001. Epub 2012 Apr 17. Neuromuscul Disord. 2012. PMID: 22513320 Free PMC article.

7

Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCR.

He L, Chinnery PF, Durham SE, Blakely EL, Wardell TM, Borthwick GM, Taylor RW, Turnbull DM. He L, et al. Among authors: turnbull dm. Nucleic Acids Res. 2002 Jul 15;30(14):e68. doi: 10.1093/nar/gnf067. Nucleic Acids Res. 2002. PMID: 12136116 Free PMC article.

8

Can mitochondrial DNA mutations cause sperm dysfunction?

Spiropoulos J, Turnbull DM, Chinnery PF. Spiropoulos J, et al. Among authors: turnbull dm. Mol Hum Reprod. 2002 Aug;8(8):719-21. doi: 10.1093/molehr/8.8.719. Mol Hum Reprod. 2002. PMID: 12149402

9

Changes in the human mitochondrial genome after treatment of malignant disease.

Wardell TM, Ferguson E, Chinnery PF, Borthwick GM, Taylor RW, Jackson G, Craft A, Lightowlers RN, Howell N, Turnbull DM. Wardell TM, et al. Among authors: turnbull dm. Mutat Res. 2003 Apr 9;525(1-2):19-27. doi: 10.1016/s0027-5107(02)00313-5. Mutat Res. 2003. PMID: 12650902

10

Genotypes from patients indicate no paternal mitochondrial DNA contribution.

Taylor RW, McDonnell MT, Blakely EL, Chinnery PF, Taylor GA, Howell N, Zeviani M, Briem E, Carrara F, Turnbull DM. Taylor RW, et al. Among authors: turnbull dm. Ann Neurol. 2003 Oct;54(4):521-4. doi: 10.1002/ana.10673. Ann Neurol. 2003. PMID: 14520666

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