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Defects in human methionine synthase in cblG patients.
Gulati S, Baker P, Li YN, Fowler B, Kruger W, Brody LC, Banerjee R. Gulati S, et al. Among authors: brody lc. Hum Mol Genet. 1996 Dec;5(12):1859-65. doi: 10.1093/hmg/5.12.1859. Hum Mol Genet. 1996. PMID: 8968736
Targeted disruption of the methionine synthase gene in mice.
Swanson DA, Liu ML, Baker PJ, Garrett L, Stitzel M, Wu J, Harris M, Banerjee R, Shane B, Brody LC. Swanson DA, et al. Among authors: brody lc. Mol Cell Biol. 2001 Feb;21(4):1058-65. doi: 10.1128/MCB.21.4.1058-1065.2001. Mol Cell Biol. 2001. PMID: 11158293 Free PMC article.
A polymorphism, R653Q, in the trifunctional enzyme methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase/formyltetrahydrofolate synthetase is a maternal genetic risk factor for neural tube defects: report of the Birth Defects Research Group.
Brody LC, Conley M, Cox C, Kirke PN, McKeever MP, Mills JL, Molloy AM, O'Leary VB, Parle-McDermott A, Scott JM, Swanson DA. Brody LC, et al. Am J Hum Genet. 2002 Nov;71(5):1207-15. doi: 10.1086/344213. Epub 2002 Oct 16. Am J Hum Genet. 2002. PMID: 12384833 Free PMC article.
206 results