Mitchell LE - Search Results

1

Folate and homocysteine phenotypes: Comparative findings using research and clinical laboratory data.

Mitchell LE, Morales M, Khartulyari S, Huang Y, Murphy K, Mei M, Von Feldt JM, Blair IA, Whitehead AS. Mitchell LE, et al. Clin Biochem. 2009 Aug;42(12):1275-81. doi: 10.1016/j.clinbiochem.2009.04.014. Epub 2009 May 8. Clin Biochem. 2009. PMID: 19427846 Free PMC article.

2

Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida.

Doolin MT, Barbaux S, McDonnell M, Hoess K, Whitehead AS, Mitchell LE. Doolin MT, et al. Among authors: mitchell le. Am J Hum Genet. 2002 Nov;71(5):1222-6. doi: 10.1086/344209. Epub 2002 Oct 9. Am J Hum Genet. 2002. PMID: 12375236 Free PMC article.

3

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. Among authors: mitchell le. 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

4

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. Among authors: mitchell le. Hum Genet. 2004 Jan;114(2):182-5. doi: 10.1007/s00439-003-1039-9. Epub 2003 Oct 25. Hum Genet. 2004. PMID: 14586640

5

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. Among authors: mitchell le. 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

6

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. Among authors: mitchell le. Atherosclerosis. 2004 Jun;174(2):315-22. doi: 10.1016/j.atherosclerosis.2004.01.023. Atherosclerosis. 2004. PMID: 15136061 Clinical Trial.

7

A common ABCC2 promoter polymorphism is not a determinant of the risk of spina bifida.

Jensen LE, Wall AM, Cook M, Hoess K, Thorn CF, Whitehead AS, Mitchell LE. Jensen LE, et al. Among authors: mitchell le. Birth Defects Res A Clin Mol Teratol. 2004 Jun;70(6):396-9. doi: 10.1002/bdra.20023. Birth Defects Res A Clin Mol Teratol. 2004. PMID: 15211708

8

Spina bifida.

Mitchell LE, Adzick NS, Melchionne J, Pasquariello PS, Sutton LN, Whitehead AS. Mitchell LE, et al. Lancet. 2004 Nov 20-26;364(9448):1885-95. doi: 10.1016/S0140-6736(04)17445-X. Lancet. 2004. PMID: 15555669 Review.

9

The NAT1 C1095A polymorphism, maternal multivitamin use and smoking, and the risk of spina bifida.

Jensen LE, Hoess K, Whitehead AS, Mitchell LE. Jensen LE, et al. Among authors: mitchell le. Birth Defects Res A Clin Mol Teratol. 2005 Jul;73(7):512-6. doi: 10.1002/bdra.20143. Birth Defects Res A Clin Mol Teratol. 2005. PMID: 15959877

10

Maternal genotype for the monocyte chemoattractant protein 1 A(-2518)G promoter polymorphism is associated with the risk of spina bifida in offspring.

Jensen LE, Etheredge AJ, Brown KS, Mitchell LE, Whitehead AS. Jensen LE, et al. Among authors: mitchell le. Am J Med Genet A. 2006 May 15;140(10):1114-8. doi: 10.1002/ajmg.a.31212. Am J Med Genet A. 2006. PMID: 16596675 No abstract available.

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