Rozen R - Search Results

1

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: rozen r. Mamm Genome. 1997 Oct;8(10):787-8. doi: 10.1007/s003359900570. Mamm Genome. 1997. PMID: 9321480 No abstract available.

2

The methylenetetrahydrofolate reductase (Mthfr) gene maps to distal mouse chromosome 4.

Frosst P, Zhang Z, Pai A, Rozen R. Frosst P, et al. Among authors: rozen r. Mamm Genome. 1996 Nov;7(11):864-5. doi: 10.1007/s003359900255. Mamm Genome. 1996. PMID: 8875901 No abstract available.

3

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: rozen r. Hum Mol Genet. 1996 Dec;5(12):1867-74. doi: 10.1093/hmg/5.12.1867. Hum Mol Genet. 1996. PMID: 8968737

4

Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR).

Goyette P, Pai A, Milos R, Frosst P, Tran P, Chen Z, Chan M, Rozen R. Goyette P, et al. Among authors: rozen r. Mamm Genome. 1998 Aug;9(8):652-6. doi: 10.1007/s003359900838. Mamm Genome. 1998. PMID: 9680386

5

Infant methionine synthase variants and risk for spina bifida.

Shaw GM, Todoroff K, Finnell RH, Lammer EJ, Leclerc D, Gravel RA, Rozen R. Shaw GM, et al. Among authors: rozen r. J Med Genet. 1999 Jan;36(1):86-7. J Med Genet. 1999. PMID: 9950377 Free PMC article. No abstract available.

6

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: rozen r. 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

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

8

A polymorphism of the methionine synthase gene: association with plasma folate, vitamin B12, homocyst(e)ine, and colorectal cancer risk.

Ma J, Stampfer MJ, Christensen B, Giovannucci E, Hunter DJ, Chen J, Willett WC, Selhub J, Hennekens CH, Gravel R, Rozen R. Ma J, et al. Among authors: rozen r. Cancer Epidemiol Biomarkers Prev. 1999 Sep;8(9):825-9. Cancer Epidemiol Biomarkers Prev. 1999. PMID: 10498402

9

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

10

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: rozen r. Mol Genet Metab. 1999 Dec;68(4):512. doi: 10.1006/mgme.1999.2945. Mol Genet Metab. 1999. PMID: 10607483 No abstract available.

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