-
1
-
-
0028863219
-
Folate levels and neural tube defects: Implications for prevention
-
Daly LE, Kirke PN, Molloy AM, Weir DG, Scott JM (1995): Folate levels and neural tube defects: Implications for prevention. JAMA 274:1698-1702.
-
(1995)
JAMA
, vol.274
, pp. 1698-1702
-
-
Daly, L.E.1
Kirke, P.N.2
Molloy, A.M.3
Weir, D.G.4
Scott, J.M.5
-
2
-
-
4143088796
-
Spina bifida, 677T → C mutation and role of folate
-
de Franchis R, Sebastio G, Mandato C, Andria G, Mastroiacovo P (1995): Spina bifida, 677T → C mutation and role of folate. Lancet 346:1703.
-
(1995)
Lancet
, vol.346
, pp. 1703
-
-
De Franchis, R.1
Sebastio, G.2
Mandato, C.3
Andria, G.4
Mastroiacovo, P.5
-
3
-
-
0028890671
-
Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia
-
Engbersen AMT, Franken DG, Boers GHJ, Stevens EMB, Trijbels FJM, Blom HJ (1995): Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia. Am J Hum Genet 56: 142-150.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 142-150
-
-
Engbersen, A.M.T.1
Franken, D.G.2
Boers, G.H.J.3
Stevens, E.M.B.4
Trijbels, F.J.M.5
Blom, H.J.6
-
4
-
-
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, Boers GJH, den Heijer M, Kluijtmans LAJ, van den Heuvel LP, Rozen R (1995): A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase. Nature Genet 10: 111-113.
-
(1995)
Nature 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
Boers, G.J.H.7
Den Heijer, M.8
Kluijtmans, L.A.J.9
Van Den Heuvel, L.P.10
Rozen, R.11
-
5
-
-
0029738540
-
The common "thermolabile" variant of methylenetetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia
-
Harmon D, Woodside JV, Yarnell JWG, McMaster D, Young IS, McCrum EE, Gey KF, Whitehead AS, Evans AE (1996): The common "thermolabile" variant of methylenetetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia. Q J Med 89:571-577.
-
(1996)
Q J Med
, vol.89
, pp. 571-577
-
-
Harmon, D.1
Woodside, J.V.2
Yarnell, J.W.G.3
McMaster, D.4
Young, I.S.5
McCrum, E.E.6
Gey, K.F.7
Whitehead, A.S.8
Evans, A.E.9
-
6
-
-
0026034240
-
Thermolabile methylenetetrahydrofolate reductase: An inherited risk factor for coronary artery disease
-
Kang SS, Wong PWK, Susmano A, Sora J, Norusis M, Ruggie N (1991): Thermolabile methylenetetrahydrofolate reductase: An inherited risk factor for coronary artery disease. Am J Hum Genet 48:536-545.
-
(1991)
Am J Hum Genet
, vol.48
, pp. 536-545
-
-
Kang, S.S.1
Wong, P.W.K.2
Susmano, A.3
Sora, J.4
Norusis, M.5
Ruggie, N.6
-
7
-
-
0023696435
-
Intermediate homocysteinemia: A thermolabile variant of methylenetetrahydrofolate reductase
-
Kang SS, Zhou J, Wong PWK, Kowalisyn J, Strokosch G (1988): Intermediate homocysteinemia: A thermolabile variant of methylenetetrahydrofolate reductase. Am J Hum Genet 43:414-421.
-
(1988)
Am J Hum Genet
, vol.43
, pp. 414-421
-
-
Kang, S.S.1
Zhou, J.2
Wong, P.W.K.3
Kowalisyn, J.4
Strokosch, G.5
-
8
-
-
0025860071
-
Microbiological assay for vitamin B12 performed in 96-well microtitre plates
-
Kelleher BP, O'Broin SD (1991): Microbiological assay for vitamin B12 performed in 96-well microtitre plates. J Clin Pathol 44:592-595.
-
(1991)
J Clin Pathol
, vol.44
, pp. 592-595
-
-
Kelleher, B.P.1
O'Broin, S.D.2
-
9
-
-
0029800387
-
Methylenetetrahydrofolate reductase mutation and neural tube defects
-
Kirke PN, Mills JL, Whitehead AS, Molloy A, Scott JM (1996): Methylenetetrahydrofolate reductase mutation and neural tube defects. Lancet 348:1037-1038.
-
(1996)
Lancet
, vol.348
, pp. 1037-1038
-
-
Kirke, P.N.1
Mills, J.L.2
Whitehead, A.S.3
Molloy, A.4
Scott, J.M.5
-
11
-
-
0029655724
-
Molecular genetic analysis in mild hyperhomocysteinemia: A common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease
-
Kluijtmans LAJ, van den Heuvel LPW, Boers GHJ, Frosst P, Stevens EMB, van Oost BA, den Heijer M, Trijbels FJM, Rozen R, Blom HJ (1996): Molecular genetic analysis in mild hyperhomocysteinemia: A common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease. Am J Hum Genet 58: 35-41.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 35-41
-
-
Kluijtmans, L.A.J.1
Van Den Heuvel, L.P.W.2
Boers, G.H.J.3
Frosst, P.4
Stevens, E.M.B.5
Van Oost, B.A.6
Den Heijer, M.7
Trijbels, F.J.M.8
Rozen, R.9
Blom, H.J.10
-
12
-
-
0028833677
-
Homocysteine metabolism in pregnancies complicated by neural tube defects
-
Mills JL, McPartlin JM, Kirke PN, Lee YJ, Conley MR, Weir DG, Scott JM (1995): Homocysteine metabolism in pregnancies complicated by neural tube defects. Lancet 345:149-151.
-
(1995)
Lancet
, vol.345
, pp. 149-151
-
-
Mills, J.L.1
McPartlin, J.M.2
Kirke, P.N.3
Lee, Y.J.4
Conley, M.R.5
Weir, D.G.6
Scott, J.M.7
-
13
-
-
0030955502
-
Association of thermolabile variant of 5,10-methylenetetrahydrofolate reductase with low red-cell folates: Implications for folate intake recommendations
-
Molloy AM, Daly S, Mills JL, Kirke PN, Whitehead AS, Ramsbottom D, Conley MR, Weir DG, Scott JM (1997): Association of thermolabile variant of 5,10-methylenetetrahydrofolate reductase with low red-cell folates: Implications for folate intake recommendations. Lancet 349: 1591-1593.
-
(1997)
Lancet
, vol.349
, pp. 1591-1593
-
-
Molloy, A.M.1
Daly, S.2
Mills, J.L.3
Kirke, P.N.4
Whitehead, A.S.5
Ramsbottom, D.6
Conley, M.R.7
Weir, D.G.8
Scott, J.M.9
-
14
-
-
0026544977
-
Microbiological assay on microtitre plates of folate in serum and red cells
-
O'Broin S, Kelleher B (1992): Microbiological assay on microtitre plates of folate in serum and red cells. J Clin Pathol 45:344-347.
-
(1992)
J Clin Pathol
, vol.45
, pp. 344-347
-
-
O'Broin, S.1
Kelleher, B.2
-
15
-
-
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, Rozen R, Oakley GP Jr, Adams MJ Jr (1996): 5,10-Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects. Am J Med Genet 63:610-614.
-
(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
Rozen, R.7
Oakley Jr., G.P.8
Adams Jr., M.J.9
-
16
-
-
0029886679
-
Methylenetetrahydrofolate reductase and neural tube defects
-
Papapetrou C, Lynch SA, Bum J, Edwards YH (1996): Methylenetetrahydrofolate reductase and neural tube defects. Lancet 348:58.
-
(1996)
Lancet
, vol.348
, pp. 58
-
-
Papapetrou, C.1
Lynch, S.A.2
Bum, J.3
Edwards, Y.H.4
-
17
-
-
0029968027
-
Is mutated MTHFR a risk factor for neural tube defects?
-
Posey DL, Khoury MJ, Mulinare J, Adams MJ Jr. Ou C-Y (1996): Is mutated MTHFR a risk factor for neural tube defects? Lancet 347:686.
-
(1996)
Lancet
, vol.347
, pp. 686
-
-
Posey, D.L.1
Khoury, M.J.2
Mulinare, J.3
Adams Jr., M.J.4
Ou, C.-Y.5
-
18
-
-
0026747176
-
Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease
-
Smith CA, Gough AC, Leigh PN, Summers BA, Harding AE, Maraganore DM, Sturman SG, Schapira AH, Williams AC, Spurr NK, Wolf CR (1992): Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease. Lancet 339:1375-1377.
-
(1992)
Lancet
, vol.339
, pp. 1375-1377
-
-
Smith, C.A.1
Gough, A.C.2
Leigh, P.N.3
Summers, B.A.4
Harding, A.E.5
Maraganore, D.M.6
Sturman, S.G.7
Schapira, A.H.8
Williams, A.C.9
Spurr, N.K.10
Wolf, C.R.11
-
19
-
-
0029028236
-
Neural tube defects and elevated homocysteine levels in amniotic fluid
-
Steegers-Theunissen RPM, Boers GH, Blom HJ, Nijhuis JG, Thomas CMG, Borm GF, Eskes TK (1995): Neural tube defects and elevated homocysteine levels in amniotic fluid. Am J Obstet Gynecol 172:1436-1441.
-
(1995)
Am J Obstet Gynecol
, vol.172
, pp. 1436-1441
-
-
Steegers-Theunissen, R.P.M.1
Boers, G.H.2
Blom, H.J.3
Nijhuis, J.G.4
Thomas, C.M.G.5
Borm, G.F.6
Eskes, T.K.7
-
20
-
-
0028149224
-
Maternal hyperhomocysteinemia: A risk factor for neural-tube defects?
-
Steegers-Theunissen RPM, Boers GHJ, Trijbels FJM, Finkelstein JD, Blom HJ, Thomas CMG, Borm GF, Wouters MGAJ, Eskes TKAB (1994): Maternal hyperhomocysteinemia: A risk factor for neural-tube defects? Metabolism 43:1475-1480.
-
(1994)
Metabolism
, vol.43
, pp. 1475-1480
-
-
Steegers-Theunissen, R.P.M.1
Boers, G.H.J.2
Trijbels, F.J.M.3
Finkelstein, J.D.4
Blom, H.J.5
Thomas, C.M.G.6
Borm, G.F.7
Wouters, M.G.A.J.8
Eskes, T.K.A.B.9
-
21
-
-
0025848779
-
Rapid high-performance liquid chromatographic assay for total homocysteine levels in human serum
-
Ubbink JB, Vermaak WJH, Bissbort S (1991): Rapid high-performance liquid chromatographic assay for total homocysteine levels in human serum. J Chromatogr 565:441-446.
-
(1991)
J Chromatogr
, vol.565
, pp. 441-446
-
-
Ubbink, J.B.1
Vermaak, W.J.H.2
Bissbort, S.3
-
22
-
-
0028556581
-
Prevention of neural tube defects by and toxicity of L-homocysteine in cultured postimplantation rat embryos
-
van Aerts LAG, Blom HJ, Deabreu RA, Trijbels FJM, Eskes TK, Copius Peereboom-Stegeman JHG, Noordhoek J (1994): Prevention of neural tube defects by and toxicity of L-homocysteine in cultured postimplantation rat embryos. Teratology 50:348-360.
-
(1994)
Teratology
, vol.50
, pp. 348-360
-
-
Van Aerts, L.A.G.1
Blom, H.J.2
Deabreu, R.A.3
Trijbels, F.J.M.4
Eskes, T.K.5
Copius Peereboom-Stegeman, J.H.G.6
Noordhoek, J.7
-
23
-
-
0028844492
-
Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida
-
van der Put NMJ, Steegers-Theunissen RPM, Frosst P, Trijbels FJM, Eskes TKAB, van den Heuvel LP, Mariman ECM, den Heyer M, Rozen R, Blom HJ (1995): Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida. Lancet 346:1070-1071.
-
(1995)
Lancet
, vol.346
, pp. 1070-1071
-
-
Van Der Put, N.M.J.1
Steegers-Theunissen, R.P.M.2
Frosst, P.3
Trijbels, F.J.M.4
Eskes, T.K.A.B.5
Van Den Heuvel, L.P.6
Mariman, E.C.M.7
Den Heyer, M.8
Rozen, R.9
Blom, H.J.10
-
24
-
-
0029849703
-
Decreased methylene tetrahydrofolate reductase activity due to the 677C → T mutation in families with spina bifida offspring
-
van der Put NMJ, van den Heuvel LP, Steegers Theunissen RPM, Trijbels FJM, Eskes TKAB, Mariman ECM, den Heyer M, Blom HJ (1996): Decreased methylene tetrahydrofolate reductase activity due to the 677C → T mutation in families with spina bifida offspring. J Mol Med 74:691-694.
-
(1996)
J Mol Med
, vol.74
, pp. 691-694
-
-
Van Der Put, N.M.J.1
Van Den Heuvel, L.P.2
Steegers Theunissen, R.P.M.3
Trijbels, F.J.M.4
Eskes, T.K.A.B.5
Mariman, E.C.M.6
Den Heyer, M.7
Blom, H.J.8
-
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, Weir DG, Shields DC, Scott JM (1995): A genetic defect in 5,10-methylenetetrahydrofolate reductase in neural tube defects. Q J Med 88:763-766.
-
(1995)
Q J Med
, 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
Weir, D.G.7
Shields, D.C.8
Scott, J.M.9
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