Winchester BG - Search Results

1

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: winchester bg. 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

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. Among authors: winchester bg. Glycobiology. 2003 Feb;13(2):73-85. doi: 10.1093/glycob/cwg026. Epub 2002 Dec 17. Glycobiology. 2003. PMID: 12626422

3

Diagnosis of congenital disorders of glycosylation type-I using protein chip technology.

Mills K, Mills P, Jackson M, Worthington V, Beesley C, Mann A, Clayton P, Grunewald S, Keir G, Young L, Langridge J, Mian N, Winchester B. Mills K, et al. Proteomics. 2006 Apr;6(7):2295-304. doi: 10.1002/pmic.200500682. Proteomics. 2006. PMID: 16552784

4

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: winchester bg. Clin Chem. 2001 Nov;47(11):2012-22. Clin Chem. 2001. PMID: 11673370

5

Mass spectrometric analysis of glycans in elucidating the pathogenesis of CDG type IIx.

Mills PB, Mills K, Mian N, Winchester BG, Clayton PT. Mills PB, et al. Among authors: winchester bg. J Inherit Metab Dis. 2003;26(2-3):119-34. doi: 10.1023/a:1024476915278. J Inherit Metab Dis. 2003. PMID: 12889655 Review.

6

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. Biochem J. 2001 Oct 15;359(Pt 2):249-54. doi: 10.1042/0264-6021:3590249. Biochem J. 2001. PMID: 11583570 Free PMC article.

7

Discovery of a new biomarker for the mucopolysaccharidoses (MPS), dipeptidyl peptidase IV (DPP-IV; CD26), by SELDI-TOF mass spectrometry.

Beesley CE, Young EP, Finnegan N, Jackson M, Mills K, Vellodi A, Cleary M, Winchester BG. Beesley CE, et al. Among authors: winchester bg. Mol Genet Metab. 2009 Apr;96(4):218-24. doi: 10.1016/j.ymgme.2008.12.002. Epub 2009 Jan 18. Mol Genet Metab. 2009. PMID: 19153055

8

Synthesis of novel internal standards for the quantitative determination of plasma ceramide trihexoside in Fabry disease by tandem mass spectrometry.

Mills K, Johnson A, Winchester B. Mills K, et al. FEBS Lett. 2002 Mar 27;515(1-3):171-6. doi: 10.1016/s0014-5793(02)02491-2. FEBS Lett. 2002. PMID: 11943216 Free article.

9

GM1-gangliosidosis in a cross-bred dog confirmed by detection of GM1-ganglioside using electrospray ionisation-tandem mass spectrometry.

Whitfield P, Johnson AW, Dunn KA, Delauche AJ, Winchester BG, Franklin RJ. Whitfield P, et al. Among authors: winchester bg. Acta Neuropathol. 2000 Oct;100(4):409-14. doi: 10.1007/s004010000187. Acta Neuropathol. 2000. PMID: 10985700

10

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: winchester bg. FEBS Lett. 1998 Dec 28;441(3):369-72. doi: 10.1016/s0014-5793(98)01578-6. FEBS Lett. 1998. PMID: 9891973 Free article.

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