Brown KS - Search Results

1

Quantification of intracellular homocysteine by stable isotope dilution liquid chromatography/tandem mass spectrometry.

Huang Y, Lu ZY, Brown KS, Whitehead AS, Blair IA. Huang Y, et al. Among authors: brown ks. Biomed Chromatogr. 2007 Jan;21(1):107-12. doi: 10.1002/bmc.735. Biomed Chromatogr. 2007. PMID: 17121413

2

The thymidylate synthase tandem repeat polymorphism is not associated with homocysteine concentrations in healthy young subjects.

Brown KS, Kluijtmans LA, Young IS, McNulty H, Mitchell LE, Yarnell JW, Woodside JV, Boreham CA, McMaster D, Murray L, Strain JJ, Whitehead AS. Brown KS, et al. Hum Genet. 2004 Jan;114(2):182-5. doi: 10.1007/s00439-003-1039-9. Epub 2003 Oct 25. Hum Genet. 2004. PMID: 14586640

3

A common insertion/deletion polymorphism of the thymidylate synthase (TYMS) gene is a determinant of red blood cell folate and homocysteine concentrations.

Kealey C, Brown KS, Woodside JV, Young I, Murray L, Boreham CA, McNulty H, Strain JJ, McPartlin J, Scott JM, Whitehead AS. Kealey C, et al. Among authors: brown ks. Hum Genet. 2005 Apr;116(5):347-53. doi: 10.1007/s00439-004-1243-2. Epub 2005 Jan 29. Hum Genet. 2005. PMID: 15682292

4

Mild folate deficiency induces a proatherosclerotic phenotype in endothelial cells.

Brown KS, Huang Y, Lu ZY, Jian W, Blair IA, Whitehead AS. Brown KS, et al. Atherosclerosis. 2006 Nov;189(1):133-41. doi: 10.1016/j.atherosclerosis.2005.12.018. Epub 2006 Feb 15. Atherosclerosis. 2006. PMID: 16469322

5

Evidence for sex differences in the determinants of homocysteine concentrations.

Stanisławska-Sachadyn A, Woodside JV, Brown KS, Young IS, Murray L, McNulty H, Strain JJ, Boreham CA, Scott JM, Whitehead AS, Mitchell LE. Stanisławska-Sachadyn A, et al. Among authors: brown ks. Mol Genet Metab. 2008 Apr;93(4):355-62. doi: 10.1016/j.ymgme.2007.11.004. Epub 2008 Jan 3. Mol Genet Metab. 2008. PMID: 18180190 Free article.

6

An insertion/deletion polymorphism of the dihydrofolate reductase (DHFR) gene is associated with serum and red blood cell folate concentrations in women.

Stanisławska-Sachadyn A, Brown KS, Mitchell LE, Woodside JV, Young IS, Scott JM, Murray L, Boreham CA, McNulty H, Strain JJ, Whitehead AS. Stanisławska-Sachadyn A, et al. Among authors: brown ks. Hum Genet. 2008 Apr;123(3):289-95. doi: 10.1007/s00439-008-0475-y. Epub 2008 Feb 5. Hum Genet. 2008. PMID: 18247058

7

Genetic evidence that nitric oxide modulates homocysteine: the NOS3 894TT genotype is a risk factor for hyperhomocystenemia.

Brown KS, Kluijtmans LA, Young IS, Woodside J, Yarnell JW, McMaster D, Murray L, Evans AE, Boreham CA, McNulty H, Strain JJ, Mitchell LE, Whitehead AS. Brown KS, et al. Arterioscler Thromb Vasc Biol. 2003 Jun 1;23(6):1014-20. doi: 10.1161/01.ATV.0000071348.70527.F4. Epub 2003 Apr 10. Arterioscler Thromb Vasc Biol. 2003. PMID: 12689917

8

Evidence that the risk of spina bifida is influenced by genetic variation at the NOS3 locus.

Brown KS, Cook M, Hoess K, Whitehead AS, Mitchell LE. Brown KS, et al. Birth Defects Res A Clin Mol Teratol. 2004 Mar;70(3):101-6. doi: 10.1002/bdra.20002. Birth Defects Res A Clin Mol Teratol. 2004. PMID: 15039923

9

The 5,10-methylenetetrahydrofolate reductase C677T polymorphism interacts with smoking to increase homocysteine.

Brown KS, Kluijtmans LA, Young IS, Murray L, McMaster D, Woodside JV, Yarnell JW, Boreham CA, McNulty H, Strain JJ, McPartlin J, Scott JM, Mitchell LE, Whitehead AS. Brown KS, et al. Atherosclerosis. 2004 Jun;174(2):315-22. doi: 10.1016/j.atherosclerosis.2004.01.023. Atherosclerosis. 2004. PMID: 15136061 Clinical Trial.

10

Monocyte chemoattractant protein-1: plasma concentrations and A(-2518)G promoter polymorphism of its gene in systemic lupus erythematosus.

Brown KS, Nackos E, Morthala S, Jensen LE, Whitehead AS, Von Feldt JM. Brown KS, et al. J Rheumatol. 2007 Apr;34(4):740-6. J Rheumatol. 2007. PMID: 17407231

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