Rozen R - Search Results

1

Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease.

Kluijtmans LA, van den Heuvel LP, Boers GH, Frosst P, Stevens EM, van Oost BA, den Heijer M, Trijbels FJ, Rozen R, Blom HJ. Kluijtmans LA, et al. Among authors: rozen r. Am J Hum Genet. 1996 Jan;58(1):35-41. Am J Hum Genet. 1996. PMID: 8554066 Free PMC article.

2

Purification and characterization of methylenetetrahydrofolate reductase from human cadaver liver.

Zhou J, Kang SS, Wong PW, Fournier B, Rozen R. Zhou J, et al. Among authors: rozen r. Biochem Med Metab Biol. 1990 Jun;43(3):234-42. doi: 10.1016/0885-4505(90)90029-z. Biochem Med Metab Biol. 1990. PMID: 2383427

3

Chromosomal localization of the gene for the human trifunctional enzyme, methylenetetrahydrofolate dehydrogenase-methenyltetrahydrofolate cyclohydrolase-formyltetrahydrofolate synthetase.

Rozen R, Barton D, Du J, Hum DW, MacKenzie RE, Francke U. Rozen R, et al. Am J Hum Genet. 1989 Jun;44(6):781-6. Am J Hum Genet. 1989. PMID: 2786332 Free PMC article.

4

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida.

van der Put NM, Steegers-Theunissen RP, Frosst P, Trijbels FJ, Eskes TK, van den Heuvel LP, Mariman EC, den Heyer M, Rozen R, Blom HJ. van der Put NM, et al. Among authors: rozen r. Lancet. 1995 Oct 21;346(8982):1070-1. doi: 10.1016/s0140-6736(95)91743-8. Lancet. 1995. PMID: 7564788 Free article.

5

Seven novel mutations in the methylenetetrahydrofolate reductase gene and genotype/phenotype correlations in severe methylenetetrahydrofolate reductase deficiency.

Goyette P, Frosst P, Rosenblatt DS, Rozen R. Goyette P, et al. Among authors: rozen r. Am J Hum Genet. 1995 May;56(5):1052-9. Am J Hum Genet. 1995. PMID: 7726158 Free PMC article.

6

Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification.

Goyette P, Sumner JS, Milos R, Duncan AM, Rosenblatt DS, Matthews RG, Rozen R. Goyette P, et al. Among authors: rozen r. Nat Genet. 1994 Jun;7(2):195-200. doi: 10.1038/ng0694-195. Nat Genet. 1994. PMID: 7920641

7

Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations.

Jacques PF, Bostom AG, Williams RR, Ellison RC, Eckfeldt JH, Rosenberg IH, Selhub J, Rozen R. Jacques PF, et al. Among authors: rozen r. Circulation. 1996 Jan 1;93(1):7-9. doi: 10.1161/01.cir.93.1.7. Circulation. 1996. PMID: 8616944

8

Haplotype identity between individuals who share a CFTR mutation allele "identical by descent": demonstration of the usefulness of the haplotype-sharing concept for gene mapping in real populations.

de Vries HG, van der Meulen MA, Rozen R, Halley DJ, Scheffer H, ten Kate LP, Buys CH, te Meerman GJ. de Vries HG, et al. Among authors: rozen r. Hum Genet. 1996 Sep;98(3):304-9. doi: 10.1007/s004390050211. Hum Genet. 1996. PMID: 8707298

9

5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects.

Ou CY, Stevenson RE, Brown VK, Schwartz CE, Allen WP, Khoury MJ, Rozen R, Oakley GP Jr, Adams MJ Jr. Ou CY, et al. Among authors: rozen r. Am J Med Genet. 1996 Jun 28;63(4):610-4. doi: 10.1002/(SICI)1096-8628(19960628)63:4<610::AID-AJMG15>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8826441

10

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.

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