AAAAAA

   
Results: 1-17 |
Results: 17
Analysis by matrix assisted laser desorption/ionisation-time of flight mass spectrometry of the post-translational modifications of alpha(1)-antitrypsin isoforms separated by two-dimensional polyacrylamide gel electrophoresis
Authors: Mills, PB Mills, K Johnson, AW Clayton, PT Winchester, BG
Citation: Pb. Mills et al., Analysis by matrix assisted laser desorption/ionisation-time of flight mass spectrometry of the post-translational modifications of alpha(1)-antitrypsin isoforms separated by two-dimensional polyacrylamide gel electrophoresis, PROTEOMICS, 1(6), 2001, pp. 778-786
New synthesis of (+/-)-alpha-CMBHC and its confirmation as a metabolite ofalpha-tocopherol (Vitamin E)
Authors: Pope, SAS Burtin, GE Clayton, PT Madge, DJ Muller, DPR
Citation: Sas. Pope et al., New synthesis of (+/-)-alpha-CMBHC and its confirmation as a metabolite ofalpha-tocopherol (Vitamin E), BIO MED CH, 9(5), 2001, pp. 1337-1343
Clinical consequences of defects in peroxisomal beta-oxidation
Authors: Clayton, PT
Citation: Pt. Clayton, Clinical consequences of defects in peroxisomal beta-oxidation, BIOCH SOC T, 29, 2001, pp. 298-305
Applications of mass spectrometry in the study of inborn errors of metabolism
Authors: Clayton, PT
Citation: Pt. Clayton, Applications of mass spectrometry in the study of inborn errors of metabolism, J INH MET D, 24(2), 2001, pp. 139-150
Features of carnitine palmitoyltransferase type I deficiency
Authors: Olpin, SE Allen, J Bonham, JR Clark, S Clayton, PT Calvin, J Downing, M Ives, K Jones, S Manning, NJ Pollitt, RJ Standing, SJ Tanner, MS
Citation: Se. Olpin et al., Features of carnitine palmitoyltransferase type I deficiency, J INH MET D, 24(1), 2001, pp. 35-42
Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion
Authors: Clayton, PT Eaton, S Aynsley-Green, A Edginton, M Hussain, K Krywawych, S Datta, V Malingre, HEM Berger, R van den Berg, IET
Citation: Pt. Clayton et al., Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion, J CLIN INV, 108(3), 2001, pp. 457-465
Identification of alpha(1)-antitrypsin variants in plasma with the use of proteomic technology
Authors: Mills, K Mills, PB Clayton, PT Johnson, AW Whitehouse, DB Winchester, BG
Citation: K. Mills et al., Identification of alpha(1)-antitrypsin variants in plasma with the use of proteomic technology, CLIN CHEM, 47(11), 2001, pp. 2012-2022
Mutations in the gene encoding peroxisomal alpha-methylacyl-CoA racemase cause adult-onset sensory motor neuropathy
Authors: Ferdinandusse, S Denis, S Clayton, PT Graham, A Rees, JE Allen, JT McLean, BN Brown, AY Vreken, P Waterham, HR Wanders, RJA
Citation: S. Ferdinandusse et al., Mutations in the gene encoding peroxisomal alpha-methylacyl-CoA racemase cause adult-onset sensory motor neuropathy, NAT GENET, 24(2), 2000, pp. 188-191
A strategy for the identification of site-specific glycosylation in glycoproteins using MALDI TOF MS
Authors: Mills, K Johnson, AW Diettrich, O Clayton, PT Winchester, BG
Citation: K. Mills et al., A strategy for the identification of site-specific glycosylation in glycoproteins using MALDI TOF MS, TETRAHEDR-A, 11(1), 2000, pp. 75-93
Effect of intravenous lipid emulsions on hepatic cholesterol metabolism
Authors: Whitfield, PD Clayton, PT Muller, DPR
Citation: Pd. Whitfield et al., Effect of intravenous lipid emulsions on hepatic cholesterol metabolism, J PED GASTR, 30(5), 2000, pp. 538-546
Phenylalanine supplementation improves the phenylalanine profile in tyrosinaemia
Authors: Wilson, CJ Van Wyk, KG Leonard, JV Clayton, PT
Citation: Cj. Wilson et al., Phenylalanine supplementation improves the phenylalanine profile in tyrosinaemia, J INH MET D, 23(7), 2000, pp. 677-683
A new method for the analysis of urinary vitamin E metabolites and the tentative identification of a novel group of compounds
Authors: Pope, SAS Clayton, PT Muller, DPR
Citation: Sas. Pope et al., A new method for the analysis of urinary vitamin E metabolites and the tentative identification of a novel group of compounds, ARCH BIOCH, 381(1), 2000, pp. 8-15
Screening of newborn infants for cholestatic hepatobiliary disease - Does test fufil screening criteria? Reply
Authors: Clayton, PT Logan, S
Citation: Pt. Clayton et S. Logan, Screening of newborn infants for cholestatic hepatobiliary disease - Does test fufil screening criteria? Reply, BR MED J, 319(7222), 1999, pp. 1436-1436
Screening of newborn infants for cholestatic hepatobiliary disease with tandem mass spectrometry
Authors: Mushtaq, I Logan, S Morris, M Johnson, AW Wade, AM Kelly, D Clayton, PT
Citation: I. Mushtaq et al., Screening of newborn infants for cholestatic hepatobiliary disease with tandem mass spectrometry, BR MED J, 319(7208), 1999, pp. 471-477
The identification of unusual bile acid metabolites by tandem mass spectrometry: Use of low-energy collision-induced dissociation to produce informative spectra
Authors: Lemonde, HA Johnson, AW Clayton, PT
Citation: Ha. Lemonde et al., The identification of unusual bile acid metabolites by tandem mass spectrometry: Use of low-energy collision-induced dissociation to produce informative spectra, RAP C MASS, 13(12), 1999, pp. 1159-1164
Outcome of medium chain acyl-CoA dehydrogenase deficiency after diagnosis
Authors: Wilson, CJ Champion, MP Collins, JE Clayton, PT Leonard, JV
Citation: Cj. Wilson et al., Outcome of medium chain acyl-CoA dehydrogenase deficiency after diagnosis, ARCH DIS CH, 80(5), 1999, pp. 459-462
An inborn error of bile acid synthesis (3 beta-hydroxy-Delta(5)-C-27-steroid dehydrogenase deficiency) presenting as malabsorption leading to rickets
Authors: Akobeng, AK Clayton, PT Miller, V Super, M Thomas, AG
Citation: Ak. Akobeng et al., An inborn error of bile acid synthesis (3 beta-hydroxy-Delta(5)-C-27-steroid dehydrogenase deficiency) presenting as malabsorption leading to rickets, ARCH DIS CH, 80(5), 1999, pp. 463-465
Risultati: 1-17 |