Taylor RW - Search Results

1

High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease.

Bender A, Krishnan KJ, Morris CM, Taylor GA, Reeve AK, Perry RH, Jaros E, Hersheson JS, Betts J, Klopstock T, Taylor RW, Turnbull DM. Bender A, et al. Among authors: taylor rw, taylor ga. Nat Genet. 2006 May;38(5):515-7. doi: 10.1038/ng1769. Epub 2006 Apr 9. Nat Genet. 2006. PMID: 16604074

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

Insulin sensitivity and mitochondrial gene mutation.

Walker M, Taylor RW, Stewart MW, Bindoff LA, Jackson MJ, Alberti GK, Turnbull DM. Walker M, et al. Among authors: taylor rw. Diabetes Care. 1995 Feb;18(2):273-5. doi: 10.2337/diacare.18.2.273. Diabetes Care. 1995. PMID: 7729311 No abstract available.

6

Complex aetiology of type 2 diabetes.

Walker M, Taylor R, Armstrong M, Turnbull DM. Walker M, et al. Br J Hosp Med. 1994 Aug 17-Sep 6;52(4):179. Br J Hosp Med. 1994. PMID: 8000686 No abstract available.

7

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.

8

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.

9

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

10

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

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