Johnson A - Search Results

1

A case of the carbohydrate-deficient glycoprotein syndrome type 1 (CDGS type 1) with normal phosphomannomutase activity.

Charlwood J, Clayton P, Johnson A, Keir G, Mian N, Winchester B. Charlwood J, et al. Among authors: johnson a. J Inherit Metab Dis. 1997 Nov;20(6):817-26. doi: 10.1023/a:1005380003902. J Inherit Metab Dis. 1997. PMID: 9427152

2

The underglycosylation of plasma alpha 1-antitrypsin in congenital disorders of glycosylation type I is not random.

Mills K, Mills PB, Clayton PT, Mian N, Johnson AW, Winchester BG. Mills K, et al. Glycobiology. 2003 Feb;13(2):73-85. doi: 10.1093/glycob/cwg026. Epub 2002 Dec 17. Glycobiology. 2003. PMID: 12626422

3

Congenital disorders of glycosylation type I leads to altered processing of N-linked glycans, as well as underglycosylation.

Mills P, Mills K, Clayton P, Johnson A, Whitehouse D, Winchester B. Mills P, et al. Among authors: johnson a. Biochem J. 2001 Oct 15;359(Pt 2):249-54. doi: 10.1042/0264-6021:3590249. Biochem J. 2001. PMID: 11583570 Free PMC article.

4

Ataxia associated with increased plasma concentrations of pristanic acid, phytanic acid and C27 bile acids but normal fibroblast branched-chain fatty acid oxidation.

Clayton PT, Johnson AW, Mills KA, Lynes GW, Wilson J, Casteels M, Mannaerts G. Clayton PT, et al. Among authors: johnson aw. J Inherit Metab Dis. 1996;19(6):761-8. doi: 10.1007/BF01799170. J Inherit Metab Dis. 1996. PMID: 8982949

5

Identification of alpha(1)-antitrypsin variants in plasma with the use of proteomic technology.

Mills K, Mills PB, Clayton PT, Johnson AW, Whitehouse DB, Winchester BG. Mills K, et al. Among authors: johnson aw. Clin Chem. 2001 Nov;47(11):2012-22. Clin Chem. 2001. PMID: 11673370

6

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.

Mills PB, Mills K, Johnson AW, Clayton PT, Winchester BG. Mills PB, et al. Among authors: johnson aw. Proteomics. 2001 Jun;1(6):778-86. doi: 10.1002/1615-9861(200106)1:6<778::AID-PROT778>3.0.CO;2-H. Proteomics. 2001. PMID: 11677785

7

The use of automated electrospray ionization tandem MS for the diagnosis of inborn errors of metabolism from dried blood spots.

Johnson AW, Mills K, Clayton PT. Johnson AW, et al. Biochem Soc Trans. 1996 Aug;24(3):932-8. doi: 10.1042/bst0240932. Biochem Soc Trans. 1996. PMID: 8878877 No abstract available.

8

Application of magnetic chromatography to the isolation of lysosomes from fibroblasts of patients with lysosomal storage disorders.

Diettrich O, Mills K, Johnson AW, Hasilik A, Winchester BG. Diettrich O, et al. Among authors: johnson aw. FEBS Lett. 1998 Dec 28;441(3):369-72. doi: 10.1016/s0014-5793(98)01578-6. FEBS Lett. 1998. PMID: 9891973 Free article.

9

The identification of unusual bile acid metabolites by tandem mass spectrometry: use of low-energy collision-induced dissociation to produce informative spectra.

Lemonde HA, Johnson AW, Clayton PT. Lemonde HA, et al. Among authors: johnson aw. Rapid Commun Mass Spectrom. 1999;13(12):1159-64. doi: 10.1002/(SICI)1097-0231(19990630)13:12<1159::AID-RCM636>3.0.CO;2-#. Rapid Commun Mass Spectrom. 1999. PMID: 10390861

10

A method for the quantitation of conjugated bile acids in dried blood spots using electrospray ionization-mass spectrometry.

Mills KA, Mushtaq I, Johnson AW, Whitfield PD, Clayton PT. Mills KA, et al. Among authors: johnson aw. Pediatr Res. 1998 Mar;43(3):361-8. doi: 10.1203/00006450-199803000-00009. Pediatr Res. 1998. PMID: 9505275

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