Leclerc D - Search Results

1

Mild Methylenetetrahydrofolate Reductase Deficiency Alters Inflammatory and Lipid Pathways in Liver.

Leclerc D, Christensen KE, Cauvi O, Yang E, Fournelle F, Bahous RH, Malysheva OV, Deng L, Wu Q, Zhou Z, Gao ZH, Chaurand P, Caudill MA, Rozen R. Leclerc D, et al. Mol Nutr Food Res. 2019 Feb;63(3):e1801001. doi: 10.1002/mnfr.201801001. Epub 2018 Nov 23. Mol Nutr Food Res. 2019. PMID: 30408316

2

Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders.

Leclerc D, Campeau E, Goyette P, Adjalla CE, Christensen B, Ross M, Eydoux P, Rosenblatt DS, Rozen R, Gravel RA. Leclerc D, et al. Hum Mol Genet. 1996 Dec;5(12):1867-74. doi: 10.1093/hmg/5.12.1867. Hum Mol Genet. 1996. PMID: 8968737

3

The methionine synthase (Mtr) gene maps to proximal mouse chromosome 13.

Zhang ZX, Leclerc D, Gravel R, Rozen R. Zhang ZX, et al. Among authors: leclerc d. Mamm Genome. 1997 Oct;8(10):787-8. doi: 10.1007/s003359900570. Mamm Genome. 1997. PMID: 9321480 No abstract available.

4

Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects.

Christensen B, Arbour L, Tran P, Leclerc D, Sabbaghian N, Platt R, Gilfix BM, Rosenblatt DS, Gravel RA, Forbes P, Rozen R. Christensen B, et al. Among authors: leclerc d. Am J Med Genet. 1999 May 21;84(2):151-7. doi: 10.1002/(sici)1096-8628(19990521)84:2<151::aid-ajmg12>3.0.co;2-t. Am J Med Genet. 1999. PMID: 10323741

5

A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida.

Wilson A, Platt R, Wu Q, Leclerc D, Christensen B, Yang H, Gravel RA, Rozen R. Wilson A, et al. Among authors: leclerc d. Mol Genet Metab. 1999 Aug;67(4):317-23. doi: 10.1006/mgme.1999.2879. Mol Genet Metab. 1999. PMID: 10444342

6

Molecular cloning, expression and physical mapping of the human methionine synthase reductase gene.

Leclerc D, Odièvre M, Wu Q, Wilson A, Huizenga JJ, Rozen R, Scherer SW, Gravel RA. Leclerc D, et al. Gene. 1999 Nov 15;240(1):75-88. doi: 10.1016/s0378-1119(99)00431-x. Gene. 1999. PMID: 10564814

7

The silent T1317C mutation of methylenetetrahydrofolate reductase should not interfere with MboII restriction isotyping of the reported A1298C mutation.

Sibani S, Leclerc D, Weisberg I I, Rozen R. Sibani S, et al. Among authors: leclerc d. Mol Genet Metab. 1999 Dec;68(4):512. doi: 10.1006/mgme.1999.2945. Mol Genet Metab. 1999. PMID: 10607483 No abstract available.

8

Is the SLC7A10 gene on chromosome 19 a candidate locus for cystinuria?

Leclerc D, Wu Q, Ellis JR, Goodyer P, Rozen R. Leclerc D, et al. Mol Genet Metab. 2001 Aug;73(4):333-9. doi: 10.1006/mgme.2001.3209. Mol Genet Metab. 2001. PMID: 11509015

9

Multiple transcription start sites and alternative splicing in the methylenetetrahydrofolate reductase gene result in two enzyme isoforms.

Tran P, Leclerc D, Chan M, Pai A, Hiou-Tim F, Wu Q, Goyette P, Artigas C, Milos R, Rozen R. Tran P, et al. Among authors: leclerc d. Mamm Genome. 2002 Sep;13(9):483-92. doi: 10.1007/s00335-002-2167-6. Mamm Genome. 2002. PMID: 12370778

10

SLC7A9 mutations in all three cystinuria subtypes.

Leclerc D, Boutros M, Suh D, Wu Q, Palacin M, Ellis JR, Goodyer P, Rozen R. Leclerc D, et al. Kidney Int. 2002 Nov;62(5):1550-9. doi: 10.1046/j.1523-1755.2002.00602.x. Kidney Int. 2002. PMID: 12371955 Free article.

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