-
1
-
-
4444305073
-
Prevalence of MTHFR gene polymorphisms (C677T and A1298C) among Tamilians
-
Angeline T, Jeyaraj N, Granito S, Tsongalis GJ: Prevalence of MTHFR gene polymorphisms (C677T and A1298C) among Tamilians. Exp Mol Pathol 77:85-88, 2004
-
(2004)
Exp Mol Pathol
, vol.77
, pp. 85-88
-
-
Angeline, T.1
Jeyaraj, N.2
Granito, S.3
Tsongalis, G.J.4
-
3
-
-
0032937206
-
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, et al: Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects. Am J Med Genet 84:151-157, 1999
-
(1999)
Am J Med Genet
, vol.84
, pp. 151-157
-
-
Christensen, B.1
Arbour, L.2
Tran, P.3
Leclerc, D.4
Sabbaghian, N.5
Platt, R.6
-
4
-
-
0027080461
-
Prevention of the first occurrence of neural-tube defects by periconceptional vitamin supplementation
-
Czeizel AE, Dudás I: Prevention of the first occurrence of neural-tube defects by periconceptional vitamin supplementation. N Engl J Med 327:1832-1835, 1992
-
(1992)
N Engl J Med
, vol.327
, pp. 1832-1835
-
-
Czeizel, A.E.1
Dudás, I.2
-
5
-
-
34047188626
-
MTHFR 677C→T and 1298A→C polymorphisms: Evaluation of maternal genotypic risk and association with level of neural tube defect
-
Dalal A, Pradhan M, Tiwari D, Behari S, Singh U, Mallik GK, et al: MTHFR 677C→T and 1298A→C polymorphisms: evaluation of maternal genotypic risk and association with level of neural tube defect. Gynecol Obstet Invest 63:146-150, 2007
-
(2007)
Gynecol Obstet Invest
, vol.63
, pp. 146-150
-
-
Dalal, A.1
Pradhan, M.2
Tiwari, D.3
Behari, S.4
Singh, U.5
Mallik, G.K.6
-
6
-
-
0027455468
-
Methionine but not folinic acid or vitamin B-12 alters the frequency of neural tube defects in Axd mutant mice
-
Essien FB, Wannberg SL: Methionine but not folinic acid or vitamin B-12 alters the frequency of neural tube defects in Axd mutant mice. J Nutr 123:27-34, 1993
-
(1993)
J Nutr
, vol.123
, pp. 27-34
-
-
Essien, F.B.1
Wannberg, S.L.2
-
7
-
-
0029049553
-
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, et al: A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 10:111-113, 1995
-
(1995)
Nat Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
Goyette, P.4
Sheppard, C.A.5
Matthews, R.G.6
-
8
-
-
0344211885
-
Frequency of the thermolabile variant C677T in the MTHFR gene and lack of association with neural tube defects in the State of Yucatan, Mexico
-
González-Herrera L, García-Escalante G, Castillo-Zapata I, Canto-Herrera J, Ceballos-Quintal J, Pinto-Escalante D, et al: Frequency of the thermolabile variant C677T in the MTHFR gene and lack of association with neural tube defects in the State of Yucatan, Mexico. Clin Genet 62:394-398, 2002
-
(2002)
Clin Genet
, vol.62
, pp. 394-398
-
-
González-Herrera, L.1
García-Escalante, G.2
Castillo-Zapata, I.3
Canto-Herrera, J.4
Ceballos-Quintal, J.5
Pinto-Escalante, D.6
-
9
-
-
0028304102
-
Human methylenetetrahydrofolate reductase: Isolation of cDNA mapping and mutation identification
-
Erratum in Nat Genet 7:551, 1994
-
Goyette P, Sumner JS, Milos R, Duncan AM, Rosenblatt DS, Matthews RG, et al: Human methylenetetrahydrofolate reductase: isolation of cDNA mapping and mutation identification. Nat Genet 7:195-200, 1994 (Erratum in Nat Genet 7:551, 1994)
-
(1994)
Nat Genet
, vol.7
, pp. 195-200
-
-
Goyette, P.1
Sumner, J.S.2
Milos, R.3
Duncan, A.M.4
Rosenblatt, D.S.5
Matthews, R.G.6
-
10
-
-
0031033593
-
Inositol prevents folate-resistant neural tube defects in the mouse
-
Greene ND, Copp AJ: Inositol prevents folate-resistant neural tube defects in the mouse. Nat Med 3:60-66, 1997
-
(1997)
Nat Med
, vol.3
, pp. 60-66
-
-
Greene, N.D.1
Copp, A.J.2
-
11
-
-
0026034240
-
Thermolabile methylenetetrahydrofolate reductase: An inherited risk factor for coronary artery disease
-
Kang SS, Wong PW, Susmano A, Sora J, Norusis M, Ruggie N: Thermolabile methylenetetrahydrofolate reductase: an inherited risk factor for coronary artery disease. Am J Hum Genet 48:536-545, 1991
-
(1991)
Am J Hum Genet
, vol.48
, pp. 536-545
-
-
Kang, S.S.1
Wong, P.W.2
Susmano, A.3
Sora, J.4
Norusis, M.5
Ruggie, N.6
-
12
-
-
0023696435
-
Intermediate homocysteinemia: A thermolabile variant of methylenetetrahydrofolate reductase
-
Kang SS, Zhou J, Wong PW, Kowalisyn J, Strokosch G: Intermediate homocysteinemia: a thermolabile variant of methylenetetrahydrofolate reductase. Am J Hum Genet 43:414-421, 1988
-
(1988)
Am J Hum Genet
, vol.43
, pp. 414-421
-
-
Kang, S.S.1
Zhou, J.2
Wong, P.W.3
Kowalisyn, J.4
Strokosch, G.5
-
13
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller SA, Dykes DD, Polesky HF: A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16:1215, 1988
-
(1988)
Nucleic Acids Res
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
14
-
-
0025863475
-
Prevention of neural tube defects: Results of the Medical Research Council Vitamin Study
-
MRC Vitamin Study Research Group
-
MRC Vitamin Study Research Group: Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. Lancet 338:131-137, 1991
-
(1991)
Lancet
, vol.338
, pp. 131-137
-
-
-
15
-
-
0036488108
-
A low prevalence of the C677T mutation in the methylenetetrahydrofolate reductase gene in Asian Indians
-
Mukherjee M, Joshi S, Bagadi S, Dalvi M, Rao A, Shetty KR: A low prevalence of the C677T mutation in the methylenetetrahydrofolate reductase gene in Asian Indians. Clin Genet 61:155-159, 2002
-
(2002)
Clin Genet
, vol.61
, pp. 155-159
-
-
Mukherjee, M.1
Joshi, S.2
Bagadi, S.3
Dalvi, M.4
Rao, A.5
Shetty, K.R.6
-
16
-
-
0031828880
-
Methylenetetrahydrofolate reductase polymorphism affects the change in homocysteine and folate concentrations resulting from low dose folic acid supplementation in women with unexplained recurrent miscarriages
-
Nelen WL, Blom HJ, Thomas CM, Steegers EA, Boers GH, Eskes TK: Methylenetetrahydrofolate reductase polymorphism affects the change in homocysteine and folate concentrations resulting from low dose folic acid supplementation in women with unexplained recurrent miscarriages. J Nutr 128:1336-1341, 1998
-
(1998)
J Nutr
, vol.128
, pp. 1336-1341
-
-
Nelen, W.L.1
Blom, H.J.2
Thomas, C.M.3
Steegers, E.A.4
Boers, G.H.5
Eskes, T.K.6
-
17
-
-
0030018760
-
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, et al: 5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects. Am J Med Genet 63:610-614, 1996
-
(1996)
Am J Med Genet
, vol.63
, pp. 610-614
-
-
Ou, C.Y.1
Stevenson, R.E.2
Brown, V.K.3
Schwartz, C.E.4
Allen, W.P.5
Khoury, M.J.6
-
18
-
-
0041630889
-
Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defects
-
Rampersaud E, Melvin EC, Siegel D, Mehltretter L, Dickerson ME, George TM, et al: Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defects. Clin Genet 63:210-214, 2003
-
(2003)
Clin Genet
, vol.63
, pp. 210-214
-
-
Rampersaud, E.1
Melvin, E.C.2
Siegel, D.3
Mehltretter, L.4
Dickerson, M.E.5
George, T.M.6
-
19
-
-
0033365197
-
The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother
-
Shields DC, Kirke PN, Mills JL, Ramsbottom D, Molloy AM, Burke H, et al: The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother. Am J Hum Genet 64:1045-1055, 1999
-
(1999)
Am J Hum Genet
, vol.64
, pp. 1045-1055
-
-
Shields, D.C.1
Kirke, P.N.2
Mills, J.L.3
Ramsbottom, D.4
Molloy, A.M.5
Burke, H.6
-
20
-
-
0033527788
-
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, et al: Linkage disequilibrium of MTHFR genotypes 677C/T-1298A/C in the German population and association studies in probands with neural tube defects(NTD). Am J Med Genet 87:23-29, 1999
-
(1999)
Am J Med Genet
, vol.87
, pp. 23-29
-
-
Stegmann, K.1
Ziegler, A.2
Ngo, E.T.3
Kohlschmidt, N.4
Schröter, B.5
Ermert, A.6
-
21
-
-
0031066138
-
Is the common 677C.T mutation in the methylenetetrahydrofolate reductase gene a risk factor for neural tube defects? A meta-analysis
-
van der Put NM, Eskes TK, Blom HJ: Is the common 677C.T mutation in the methylenetetrahydrofolate reductase gene a risk factor for neural tube defects? A meta-analysis. QJM 90:111-115, 1997
-
(1997)
QJM
, vol.90
, pp. 111-115
-
-
Van Der Put, N.M.1
Eskes, T.K.2
Blom, H.J.3
-
22
-
-
0028844492
-
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, et al: Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida. Lancet 346:1070-1071, 1995
-
(1995)
Lancet
, vol.346
, pp. 1070-1071
-
-
Van Der Put, N.M.1
Steegers-Theunissen, R.P.2
Frosst, P.3
Trijbels, F.J.4
Eskes, T.K.5
Van Den Heuvel, L.P.6
-
23
-
-
0029849703
-
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, et al: Decreased methylene tetrahydrofolate reductase activity due to the 677C->T mutation in families with spina bifida offspring. J Mol Med 74:691-694, 1996
-
(1996)
J Mol Med
, vol.74
, pp. 691-694
-
-
Van Der Put, N.M.1
Van Den Heuvel, L.P.2
Steegers-Theunissen, R.P.3
Trijbels, F.J.4
Eskes, T.K.5
Mariman, E.C.6
-
24
-
-
0034994046
-
Folate, homocysteine and neural tube defects: An overview
-
van der Put NM, van Straaten HW, Trijbels FJ, Blom HJ: Folate, homocysteine and neural tube defects: an overview. Exp Biol Med (Maywood) 226:243-270, 2001
-
(2001)
Exp Biol Med (Maywood)
, vol.226
, pp. 243-270
-
-
Van Der Put, N.M.1
Van Straaten, H.W.2
Trijbels, F.J.3
Blom, H.J.4
-
25
-
-
0028803474
-
A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects
-
Whitehead AS, Gallagher P, Mills JL, Kirke PN, Burke H, Molloy AM, et al: A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects. QJM 88:763-766, 1995
-
(1995)
QJM
, vol.88
, pp. 763-766
-
-
Whitehead, A.S.1
Gallagher, P.2
Mills, J.L.3
Kirke, P.N.4
Burke, H.5
Molloy, A.M.6
|