Turnbull DM - Search Results

1

Cell-permeable succinate prodrugs bypass mitochondrial complex I deficiency.

Ehinger JK, Piel S, Ford R, Karlsson M, Sjövall F, Frostner EÅ, Morota S, Taylor RW, Turnbull DM, Cornell C, Moss SJ, Metzsch C, Hansson MJ, Fliri H, Elmér E. Ehinger JK, et al. Among authors: turnbull dm. Nat Commun. 2016 Aug 9;7:12317. doi: 10.1038/ncomms12317. Nat Commun. 2016. PMID: 27502960 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. Among authors: turnbull dm. J Inherit Metab Dis. 1992;15(5):727-32. doi: 10.1007/BF01800014. J Inherit Metab Dis. 1992. PMID: 1434512

3

Tissue specific defect of complex I of the mitochondrial respiratory chain.

Watmough NJ, Birch-Machin MA, Bindoff LA, Aynsley-Green A, Simpson K, Ragan CI, Sherratt HS, Turnbull DM. Watmough NJ, et al. Among authors: turnbull dm. Biochem Biophys Res Commun. 1989 Apr 28;160(2):623-7. doi: 10.1016/0006-291x(89)92478-9. Biochem Biophys Res Commun. 1989. PMID: 2719685

4

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: turnbull dm. Pediatr Nephrol. 1995 Aug;9(4):407-11. doi: 10.1007/BF00866711. Pediatr Nephrol. 1995. PMID: 7577396

5

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: turnbull dm. 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.

6

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. Among authors: turnbull dm. J Biol Chem. 1994 Feb 4;269(5):3523-8. J Biol Chem. 1994. PMID: 8106394 Free article.

7

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. Among authors: turnbull dm. 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.

8

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. Among authors: turnbull dm. Biochim Biophys Acta. 1993 Jun 19;1181(3):261-5. doi: 10.1016/0925-4439(93)90030-5. Biochim Biophys Acta. 1993. PMID: 8391327

9

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: turnbull dm. 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

10

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. Among authors: turnbull dm. Diabetologia. 1996 Mar;39(3):322-8. doi: 10.1007/BF00418348. Diabetologia. 1996. PMID: 8721778

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