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Items: 1 to 20 of 24

1.

Screening of the C677T mutation on the methylenetetrahydrofolate reductase gene in French patients with neural tube defects.

Mornet E, Muller F, Lenvoisé-Furet A, Delezoide AL, Col JY, Simon-Bouy B, Serre JL.

Hum Genet. 1997 Oct;100(5-6):512-4.

PMID:
9341863
2.

Analysis of folates using combined affinity and ion-pair chromatography.

Bagley PJ, Selhub J.

Methods Enzymol. 1997;281:16-25. No abstract available.

PMID:
9250962
3.

The 677C-->T mutation in the methylenetetrahydrofolate reductase gene: associations with plasma total homocysteine levels and risk of coronary atherosclerotic disease.

Verhoef P, Kok FJ, Kluijtmans LA, Blom HJ, Refsum H, Ueland PM, Kruyssen DA.

Atherosclerosis. 1997 Jul 11;132(1):105-13.

PMID:
9247365
4.

Genetic predisposition to hyperhomocysteinemia: deficiency of methylenetetrahydrofolate reductase (MTHFR).

Rozen R.

Thromb Haemost. 1997 Jul;78(1):523-6. Review. No abstract available.

PMID:
9198208
5.

Methylenetetrahydrofolate reductase polymorphism, dietary interactions, and risk of colorectal cancer.

Ma J, Stampfer MJ, Giovannucci E, Artigas C, Hunter DJ, Fuchs C, Willett WC, Selhub J, Hennekens CH, Rozen R.

Cancer Res. 1997 Mar 15;57(6):1098-102.

8.

Homocysteine and risk of premature coronary heart disease. Evidence for a common gene mutation.

Gallagher PM, Meleady R, Shields DC, Tan KS, McMaster D, Rozen R, Evans A, Graham IM, Whitehead AS.

Circulation. 1996 Nov 1;94(9):2154-8.

9.

A methylenetetrahydrofolate reductase polymorphism and the risk of colorectal cancer.

Chen J, Giovannucci E, Kelsey K, Rimm EB, Stampfer MJ, Colditz GA, Spiegelman D, Willett WC, Hunter DJ.

Cancer Res. 1996 Nov 1;56(21):4862-4.

10.

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.

Am J Med Genet. 1996 Jun 28;63(4):610-4.

PMID:
8826441
11.

Distribution in healthy and coronary populations of the methylenetetrahydrofolate reductase (MTHFR) C677T mutation.

Wilcken DE, Wang XL, Sim AS, McCredie RM.

Arterioscler Thromb Vasc Biol. 1996 Jul;16(7):878-82.

12.

Elevated total plasma homocysteine and 677C-->T mutation of the 5,10-methylenetetrahydrofolate reductase gene in thrombotic vascular disease.

de Franchis R, Mancini FP, D'Angelo A, Sebastio G, Fermo I, de Stefano V, Margaglione M, Mazzola G, di Minno G, Andria G.

Am J Hum Genet. 1996 Jul;59(1):262-4. No abstract available.

13.

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.

Circulation. 1996 Jan 1;93(1):7-9.

14.

Is mutated MTHFR a risk factor for neural tube defects?

Posey DL, Khoury MJ, Mulinare J, Adams MJ Jr, Ou CY.

Lancet. 1996 Mar 9;347(9002):686-7. No abstract available.

PMID:
8596396
15.

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.

Am J Hum Genet. 1996 Jan;58(1):35-41.

16.

Spina bifida, 677T-->C mutation, and role of folate.

de Franchis R, Sebastio G, Mandato C, Andria G, Mastroiacovo P.

Lancet. 1995 Dec 23-30;346(8991-8992):1703. No abstract available.

PMID:
8551837
17.

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

Goyette P, Sumner JS, Milos R, Duncan AM, Rosenblatt DS, Matthews RG, Rozen R.

Nat Genet. 1994 Jun;7(2):195-200. Erratum in: Nat Genet. 1994 Aug;7(4):551.

PMID:
7920641
18.

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase.

Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Matthews RG, Boers GJ, den Heijer M, Kluijtmans LA, van den Heuvel LP, et al.

Nat Genet. 1995 May;10(1):111-3.

PMID:
7647779
19.

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.

Lancet. 1995 Oct 21;346(8982):1070-1.

PMID:
7564788
20.

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