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Items: 1 to 20 of 151

1.

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
2.

Linkage disequilibrium of MTHFR genotypes 677C/T-1298A/C in the German population and association studies in probands with neural tube defects(NTD).

Stegmann K, Ziegler A, Ngo ET, Kohlschmidt N, Schröter B, Ermert A, Koch MC.

Am J Med Genet. 1999 Nov 5;87(1):23-9.

PMID:
10528242
4.

Amniotic fluid homocysteine levels, 5,10-methylenetetrahydrafolate reductase genotypes, and neural tube closure sites.

Wenstrom KD, Johanning GL, Owen J, Johnston KE, Acton S, Cliver S, Tamura T.

Am J Med Genet. 2000 Jan 3;90(1):6-11.

PMID:
10602110
5.

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.

Am J Med Genet. 1999 May 21;84(2):151-7.

PMID:
10323741
7.
8.

Low blood folates in NTD pregnancies are only partly explained by thermolabile 5,10-methylenetetrahydrofolate reductase: low folate status alone may be the critical factor.

Molloy AM, Mills JL, Kirke PN, Ramsbottom D, McPartlin JM, Burke H, Conley M, Whitehead AS, Weir DG, Scott JM.

Am J Med Genet. 1998 Jun 30;78(2):155-9.

PMID:
9674907
9.

Interaction of folate and homocysteine pathway genotypes evaluated in susceptibility to neural tube defects (NTD) in a German population.

Richter B, Stegmann K, Röper B, Böddeker I, Ngo ET, Koch MC.

J Hum Genet. 2001;46(3):105-9.

PMID:
11310576
10.

A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?

van der Put NM, Gabreëls F, Stevens EM, Smeitink JA, Trijbels FJ, Eskes TK, van den Heuvel LP, Blom HJ.

Am J Hum Genet. 1998 May;62(5):1044-51.

11.

Decreased methylene tetrahydrofolate reductase activity due to the 677C-->T mutation in families with spina bifida offspring.

van der Put NM, van den Heuvel LP, Steegers-Theunissen RP, Trijbels FJ, Eskes TK, Mariman EC, den Heyer M, Blom HJ.

J Mol Med (Berl). 1996 Nov;74(11):691-4. Erratum in: J Mol Med 1997 Jan;75(1):69.

PMID:
8956155
12.

Folate levels and N(5),N(10)-methylenetetrahydrofolate reductase genotype (MTHFR) in mothers of offspring with neural tube defects: a case-control study.

Martínez de Villarreal LE, Delgado-Enciso I, Valdéz-Leal R, Ortíz-López R, Rojas-Martínez A, Limón-Benavides C, Sánchez-Peña MA, Ancer-Rodríguez J, Barrera-Saldaña HA, Villarreal-Pérez JZ.

Arch Med Res. 2001 Jul-Aug;32(4):277-82.

PMID:
11440783
13.

Analysis of select folate pathway genes, PAX3, and human T in a Midwestern neural tube defect population.

Trembath D, Sherbondy AL, Vandyke DC, Shaw GM, Todoroff K, Lammer EJ, Finnell RH, Marker S, Lerner G, Murray JC.

Teratology. 1999 May;59(5):331-41.

PMID:
10332959
14.

Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) as a risk factor for coronary artery disease.

Morita H, Taguchi J, Kurihara H, Kitaoka M, Kaneda H, Kurihara Y, Maemura K, Shindo T, Minamino T, Ohno M, Yamaoki K, Ogasawara K, Aizawa T, Suzuki S, Yazaki Y.

Circulation. 1997 Apr 15;95(8):2032-6.

15.

Folate status and neural tube defects.

Molloy AM, Mills JL, Kirke PN, Weir DG, Scott JM.

Biofactors. 1999;10(2-3):291-4.

PMID:
10609896
17.

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.

Mol Genet Metab. 1999 Aug;67(4):317-23.

PMID:
10444342
18.

A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity.

Weisberg I, Tran P, Christensen B, Sibani S, Rozen R.

Mol Genet Metab. 1998 Jul;64(3):169-72.

PMID:
9719624
19.

Evaluation of genetic variants in the reduced folate carrier and in glutamate carboxypeptidase II for spina bifida risk.

Morin I, Devlin AM, Leclerc D, Sabbaghian N, Halsted CH, Finnell R, Rozen R.

Mol Genet Metab. 2003 Jul;79(3):197-200.

PMID:
12855225
20.

The common 'thermolabile' variant of methylene tetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia.

Harmon DL, Woodside JV, Yarnell JW, McMaster D, Young IS, McCrum EE, Gey KF, Whitehead AS, Evans AE.

QJM. 1996 Aug;89(8):571-7.

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