Jackson S - Search Results

1

The measurement of carnitine and acyl-carnitines: application to the investigation of patients with suspected inherited disorders of mitochondrial fatty acid oxidation.

Bhuiyan AK, Jackson S, Turnbull DM, Aynsley-Green A, Leonard JV, Bartlett K. Bhuiyan AK, et al. Among authors: jackson s. Clin Chim Acta. 1992 May 15;207(3):185-204. doi: 10.1016/0009-8981(92)90118-a. Clin Chim Acta. 1992. PMID: 1327583

2

Combined enzyme defect of mitochondrial fatty acid oxidation.

Jackson S, Kler RS, Bartlett K, Briggs H, Bindoff LA, Pourfarzam M, Gardner-Medwin D, Turnbull DM. Jackson S, et al. J Clin Invest. 1992 Oct;90(4):1219-25. doi: 10.1172/JCI115983. J Clin Invest. 1992. PMID: 1401059 Free PMC article.

3

Quantitation of acyl-CoA and acylcarnitine esters accumulated during abnormal mitochondrial fatty acid oxidation.

Kler RS, Jackson S, Bartlett K, Bindoff LA, Eaton S, Pourfarzam M, Frerman FE, Goodman SI, Watmough NJ, Turnbull DM. Kler RS, et al. Among authors: jackson s. J Biol Chem. 1991 Dec 5;266(34):22932-8. J Biol Chem. 1991. PMID: 1744086 Free article.

4

Deficiency of the pyruvate dehydrogenase complex and of mitochondrial fatty acid oxidation.

Bindoff LA, Birch-Machin MA, Jackson S, Singh Kler R, Bartlett K, Turnbull DM. Bindoff LA, et al. Among authors: jackson s. Rev Neurol (Paris). 1991;147(6-7):526-31. Rev Neurol (Paris). 1991. PMID: 1962058 Review.

5

Characterisation of a novel enzyme of human fatty acid beta-oxidation: a matrix-associated, mitochondrial 2-enoyl-CoA hydratase.

Jackson S, Schaefer J, Middleton B, Turnbull DM. Jackson S, et al. Biochem Biophys Res Commun. 1995 Sep 5;214(1):247-53. doi: 10.1006/bbrc.1995.2281. Biochem Biophys Res Commun. 1995. PMID: 7669045

6

Fatty acid oxidation in peripheral blood cells: characterization and use for the diagnosis of defects of fatty acid oxidation.

Schaefer J, Pourfarzam M, Bartlett K, Jackson S, Turnbull DM. Schaefer J, et al. Among authors: jackson s. Pediatr Res. 1995 Mar;37(3):354-60. doi: 10.1203/00006450-199503000-00017. Pediatr Res. 1995. PMID: 7784145

7

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: jackson s. J Inherit Metab Dis. 1992;15(5):727-32. doi: 10.1007/BF01800014. J Inherit Metab Dis. 1992. PMID: 1434512

8

Combined defect of long-chain 3-hydroxyacyl-CoA dehydrogenase, 2-enoyl-CoA hydratase and 3-oxoacyl-CoA thiolase.

Jackson S, Kler RS, Bartlett K, Pourfarzam M, Aynsley-Green A, Bindoff LA, Turnbull DM. Jackson S, et al. Prog Clin Biol Res. 1992;375:327-37. Prog Clin Biol Res. 1992. PMID: 1438378 No abstract available.

9

Immunoreactive enzyme protein in medium-chain acyl-CoA dehydrogenase deficiency.

Ogilvie I, Jackson S, Bartlett K, Turnbull DM. Ogilvie I, et al. Among authors: jackson s. Biochem Med Metab Biol. 1991 Dec;46(3):373-9. doi: 10.1016/0885-4505(91)90085-y. Biochem Med Metab Biol. 1991. PMID: 1793614

10

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Jackson S, Bartlett K, Land J, Moxon ER, Pollitt RJ, Leonard JV, Turnbull DM. Jackson S, et al. Pediatr Res. 1991 Apr;29(4 Pt 1):406-11. doi: 10.1203/00006450-199104000-00016. Pediatr Res. 1991. PMID: 1830138 Free article.

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