Taylor RW - Search Results

1

Mitochondrial Protein Interaction Mapping Identifies Regulators of Respiratory Chain Function.

Floyd BJ, Wilkerson EM, Veling MT, Minogue CE, Xia C, Beebe ET, Wrobel RL, Cho H, Kremer LS, Alston CL, Gromek KA, Dolan BK, Ulbrich A, Stefely JA, Bohl SL, Werner KM, Jochem A, Westphall MS, Rensvold JW, Taylor RW, Prokisch H, Kim JP, Coon JJ, Pagliarini DJ. Floyd BJ, et al. Among authors: taylor rw. Mol Cell. 2016 Aug 18;63(4):621-632. doi: 10.1016/j.molcel.2016.06.033. Epub 2016 Aug 4. Mol Cell. 2016. PMID: 27499296 Free PMC article.

2

Biochemical assays of respiratory chain complex activity.

Kirby DM, Thorburn DR, Turnbull DM, Taylor RW. Kirby DM, et al. Among authors: taylor rw. Methods Cell Biol. 2007;80:93-119. doi: 10.1016/S0091-679X(06)80004-X. Methods Cell Biol. 2007. PMID: 17445690 Review. No abstract available.

3

Mitochondrial DNA transcription: regulating the power supply.

Taylor RW, Turnbull DM. Taylor RW, et al. Cell. 2007 Jul 27;130(2):211-3. doi: 10.1016/j.cell.2007.07.002. Cell. 2007. PMID: 17662933 Free article.

4

Urine heteroplasmy is the best predictor of clinical outcome in the m.3243A>G mtDNA mutation.

Whittaker RG, Blackwood JK, Alston CL, Blakely EL, Elson JL, McFarland R, Chinnery PF, Turnbull DM, Taylor RW. Whittaker RG, et al. Among authors: taylor rw. Neurology. 2009 Feb 10;72(6):568-9. doi: 10.1212/01.wnl.0000342121.91336.4d. Neurology. 2009. PMID: 19204268 Free PMC article. No abstract available.

5

Age-associated mitochondrial DNA mutations lead to small but significant changes in cell proliferation and apoptosis in human colonic crypts.

Nooteboom M, Johnson R, Taylor RW, Wright NA, Lightowlers RN, Kirkwood TB, Mathers JC, Turnbull DM, Greaves LC. Nooteboom M, et al. Among authors: taylor rw. Aging Cell. 2010 Feb;9(1):96-9. doi: 10.1111/j.1474-9726.2009.00531.x. Epub 2009 Oct 30. Aging Cell. 2010. PMID: 19878146 Free PMC article.

6

A novel mitochondrial MTND5 frameshift mutation causing isolated complex I deficiency, renal failure and myopathy.

Alston CL, Morak M, Reid C, Hargreaves IP, Pope SA, Land JM, Heales SJ, Horvath R, Mundy H, Taylor RW. Alston CL, et al. Among authors: taylor rw. Neuromuscul Disord. 2010 Feb;20(2):131-5. doi: 10.1016/j.nmd.2009.10.010. Epub 2009 Dec 16. Neuromuscul Disord. 2010. PMID: 20018511

7

The investigation and diagnosis of pathogenic mitochondrial DNA mutations in human urothelial cells.

Blackwood JK, Whittaker RG, Blakely EL, Alston CL, Turnbull DM, Taylor RW. Blackwood JK, et al. Among authors: taylor rw. Biochem Biophys Res Commun. 2010 Mar 19;393(4):740-5. doi: 10.1016/j.bbrc.2010.02.072. Epub 2010 Feb 18. Biochem Biophys Res Commun. 2010. PMID: 20171163

8

Detection of mitochondrial DNA variation in human cells.

Krishnan KJ, Blackwood JK, Reeve AK, Turnbull DM, Taylor RW. Krishnan KJ, et al. Among authors: taylor rw. Methods Mol Biol. 2010;628:227-57. doi: 10.1007/978-1-60327-367-1_13. Methods Mol Biol. 2010. PMID: 20238085

9

The pathogenic m.3243A>T mitochondrial DNA mutation is associated with a variable neurological phenotype.

Alston CL, Bender A, Hargreaves IP, Mundy H, Deshpande C, Klopstock T, McFarland R, Horvath R, Taylor RW. Alston CL, et al. Among authors: taylor rw. Neuromuscul Disord. 2010 Jun;20(6):403-6. doi: 10.1016/j.nmd.2010.04.003. Epub 2010 May 14. Neuromuscul Disord. 2010. PMID: 20471262

10

A novel mitochondrial tRNAGlu (MTTE) gene mutation causing chronic progressive external ophthalmoplegia at low levels of heteroplasmy in muscle.

Alston CL, Lowe J, Turnbull DM, Maddison P, Taylor RW. Alston CL, et al. Among authors: taylor rw. J Neurol Sci. 2010 Nov 15;298(1-2):140-4. doi: 10.1016/j.jns.2010.08.014. J Neurol Sci. 2010. PMID: 20810132

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