Taylor RW - Search Results

1

Pathogenic mtDNA mutations causing mitochondrial myopathy: The need for muscle biopsy.

Hardy SA, Blakely EL, Purvis AI, Rocha MC, Ahmed S, Falkous G, Poulton J, Rose MR, O'Mahony O, Bermingham N, Dougan CF, Ng YS, Horvath R, Turnbull DM, Gorman GS, Taylor RW. Hardy SA, et al. Among authors: taylor rw. Neurol Genet. 2016 Jun 23;2(4):e82. doi: 10.1212/NXG.0000000000000082. eCollection 2016 Aug. Neurol Genet. 2016. PMID: 27536729 Free PMC article.

2

Measurement of acyl-CoA dehydrogenase activity in cultured skin fibroblasts and blood platelets.

Taylor RW, Jackson S, Pourfarzam M, Bartlett K, Turnbull DM. Taylor RW, et al. J Inherit Metab Dis. 1992;15(5):727-32. doi: 10.1007/BF01800014. J Inherit Metab Dis. 1992. PMID: 1434512

3

Neonatal Fanconi syndrome due to deficiency of complex III of the respiratory chain.

Morris AA, Taylor RW, Birch-Machin MA, Jackson MJ, Coulthard MG, Bindoff LA, Welch RJ, Howell N, Turnbull DM. Morris AA, et al. Among authors: taylor rw. Pediatr Nephrol. 1995 Aug;9(4):407-11. doi: 10.1007/BF00866711. Pediatr Nephrol. 1995. PMID: 7577396

4

Medium chain acyl-CoA dehydrogenase deficiency caused by a deletion of exons 11 and 12.

Morris AA, Taylor RW, Lightowlers RN, Aynsley-Green A, Bartlett K, Turnbull DM. Morris AA, et al. Among authors: taylor rw. Hum Mol Genet. 1995 Apr;4(4):747-9. doi: 10.1093/hmg/4.4.747. Hum Mol Genet. 1995. PMID: 7633427 No abstract available.

5

The control of mitochondrial oxidations by complex III in rat muscle and liver mitochondria. Implications for our understanding of mitochondrial cytopathies in man.

Taylor RW, Birch-Machin MA, Bartlett K, Lowerson SA, Turnbull DM. Taylor RW, et al. J Biol Chem. 1994 Feb 4;269(5):3523-8. J Biol Chem. 1994. PMID: 8106394 Free article.

6

Defects of oxidative phosphorylation in man.

Taylor RW, Birch-Machin MA, Lowerson S, Sherratt HS, West IC, Bartlett K, Turnbull DM. Taylor RW, et al. Biochem Soc Trans. 1993 Aug;21 ( Pt 3)(3):804-7. doi: 10.1042/bst0210804. Biochem Soc Trans. 1993. PMID: 8224514 Review. No abstract available.

7

Succinate-cytochrome c reductase: assessment of its value in the investigation of defects of the respiratory chain.

Taylor RW, Birch-Machin MA, Bartlett K, Turnbull DM. Taylor RW, et al. Biochim Biophys Acta. 1993 Jun 19;1181(3):261-5. doi: 10.1016/0925-4439(93)90030-5. Biochim Biophys Acta. 1993. PMID: 8391327

8

Human insulin receptor substrate-1: variant sequences in familial non-insulin-dependent diabetes mellitus.

Armstrong M, Haldane F, Taylor RW, Humphriss D, Berrish T, Stewart MW, Turnbull DM, Alberti KG, Walker M. Armstrong M, et al. Among authors: taylor rw. Diabet Med. 1996 Feb;13(2):133-8. doi: 10.1002/(SICI)1096-9136(199602)13:2<133::AID-DIA7>3.0.CO;2-2. Diabet Med. 1996. PMID: 8641117

9

Variant sequences of the Hexokinase II gene in familial NIDDM.

Taylor RW, Printz RL, Armstrong M, Granner DK, Alberti KG, Turnbull DM, Walker M. Taylor RW, et al. Diabetologia. 1996 Mar;39(3):322-8. doi: 10.1007/BF00418348. Diabetologia. 1996. PMID: 8721778

10

MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNA.

Taylor RW, Chinnery PF, Haldane F, Morris AA, Bindoff LA, Wilson J, Turnbull DM. Taylor RW, et al. Ann Neurol. 1996 Sep;40(3):459-62. doi: 10.1002/ana.410400318. Ann Neurol. 1996. PMID: 8797538

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