Taylor RW - Search Results

1

A novel point mutation in the mitochondrial tRNA(Trp) gene produces a neurogastrointestinal syndrome.

Maniura-Weber K, Taylor RW, Johnson MA, Chrzanowska-Lightowlers Z, Morris AA, Charlton CP, Turnbull DM, Bindoff LA. Maniura-Weber K, et al. Among authors: taylor rw. Eur J Hum Genet. 2004 Jun;12(6):509-12. doi: 10.1038/sj.ejhg.5201185. Eur J Hum Genet. 2004. PMID: 15054399

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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