Gravel RA - Search Results

1

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. Among authors: gravel ra. Gene. 1999 Nov 15;240(1):75-88. doi: 10.1016/s0378-1119(99)00431-x. Gene. 1999. PMID: 10564814

2

Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria.

Leclerc D, Wilson A, Dumas R, Gafuik C, Song D, Watkins D, Heng HH, Rommens JM, Scherer SW, Rosenblatt DS, Gravel RA. Leclerc D, et al. Among authors: gravel ra. Proc Natl Acad Sci U S A. 1998 Mar 17;95(6):3059-64. doi: 10.1073/pnas.95.6.3059. Proc Natl Acad Sci U S A. 1998. PMID: 9501215 Free PMC article.

3

Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism.

Wilson A, Leclerc D, Rosenblatt DS, Gravel RA. Wilson A, et al. Among authors: gravel ra. Hum Mol Genet. 1999 Oct;8(11):2009-16. doi: 10.1093/hmg/8.11.2009. Hum Mol Genet. 1999. PMID: 10484769

4

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

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

5

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. Among authors: gravel ra. Hum Mol Genet. 1996 Dec;5(12):1867-74. doi: 10.1093/hmg/5.12.1867. Hum Mol Genet. 1996. PMID: 8968737

6

Functionally null mutations in patients with the cblG-variant form of methionine synthase deficiency.

Wilson A, Leclerc D, Saberi F, Campeau E, Hwang HY, Shane B, Phillips JA 3rd, Rosenblatt DS, Gravel RA. Wilson A, et al. Among authors: gravel ra. Am J Hum Genet. 1998 Aug;63(2):409-14. doi: 10.1086/301976. Am J Hum Genet. 1998. PMID: 9683607 Free PMC article.

7

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: gravel ra. Mol Genet Metab. 1999 Aug;67(4):317-23. doi: 10.1006/mgme.1999.2879. Mol Genet Metab. 1999. PMID: 10444342

8

Isolation of a cDNA encoding human holocarboxylase synthetase by functional complementation of a biotin auxotroph of Escherichia coli.

León-Del-Rio A, Leclerc D, Akerman B, Wakamatsu N, Gravel RA. León-Del-Rio A, et al. Among authors: gravel ra. Proc Natl Acad Sci U S A. 1995 May 9;92(10):4626-30. doi: 10.1073/pnas.92.10.4626. Proc Natl Acad Sci U S A. 1995. PMID: 7753853 Free PMC article.

9

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: gravel ra. 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

10

Structure of the PCCA gene and distribution of mutations causing propionic acidemia.

Campeau E, Desviat LR, Leclerc D, Wu X, Pérez B, Ugarte M, Gravel RA. Campeau E, et al. Among authors: gravel ra. Mol Genet Metab. 2001 Sep-Oct;74(1-2):238-47. doi: 10.1006/mgme.2001.3210. Mol Genet Metab. 2001. PMID: 11592820

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