-
1
-
-
0026034240
-
Thermolabile methylenetetrahydrofolate reductase: An inherited risk factor for coronary artery disease
-
Kang SS, Wong PWK, Susmano A, Sora J, Norusis M, Ruggie N. Thermolabile methylenetetrahydrofolate reductase: an inherited risk factor for coronary artery disease. Am J Hum Genet 1991; 48: 536-45.
-
(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
-
2
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
-
Frosst P, Blom HJ, Milos R, et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 1995; 10: 111-13.
-
(1995)
Nat Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
-
3
-
-
4143088796
-
Spina bifida, 677T→C mutation and role of folate
-
de Franchis R, Sebastio G, Mandato C, Andria G, Mastroiacovo P. Spina bifida, 677T→C mutation and role of folate. Lancet 1995; 346: 1703.
-
(1995)
Lancet
, vol.346
, pp. 1703
-
-
De Franchis, R.1
Sebastio, G.2
Mandato, C.3
Andria, G.4
Mastroiacovo, P.5
-
4
-
-
0029800387
-
Methylenetetrahydrofolate reductase mutation and neural tube defects
-
Kirke PN, Mills JL, Whitehead AS, Molloy A, Scott JM. Methylenetetrahydrofolate reductase mutation and neural tube defects. Lancet 1996; 348: 1037-38.
-
(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
-
5
-
-
0027421353
-
Thermolabile defect of methylenetetrahydrofolate reductase in coronary artery disease
-
Kang SS, Passen EL, Ruggie N, Wong PWK, Sora H. Thermolabile defect of methylenetetrahydrofolate reductase in coronary artery disease. Circulation 1993; 88: 1463-69.
-
(1993)
Circulation
, vol.88
, pp. 1463-1469
-
-
Kang, S.S.1
Passen, E.L.2
Ruggie, N.3
Wong, P.W.K.4
Sora, H.5
-
6
-
-
0028890671
-
Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia
-
Engbersen AMT, Franken DG, Boers GHJ, Stevens EMB, Trijbels FJM, Blom HJ. Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia. Am J Hum Genet 1995; 56: 142-50.
-
(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
-
7
-
-
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, et al. 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 1996; 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
-
8
-
-
0028803474
-
A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects
-
Whitehead AS, Gallagher P, Mills JL, et al. A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects. Q J Med 1995; 88: 763-66.
-
(1995)
Q J Med
, vol.88
, pp. 763-766
-
-
Whitehead, A.S.1
Gallagher, P.2
Mills, J.L.3
-
9
-
-
0028844492
-
Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida
-
van der Put NMJ, Steegers-Theunissen RPM, Frosst P, et al. Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida. Lancet 1995; 346: 1070-71.
-
(1995)
Lancet
, vol.346
, pp. 1070-1071
-
-
Van Der Put, N.M.J.1
Steegers-Theunissen, R.P.M.2
Frosst, P.3
-
10
-
-
0023696435
-
Intermediate homocysteinemia: A thermolabile variant of methylenetetrahydrofolate reductase
-
Kang SS, Zhou J, Wong PWK, Kowalisyn J, Strokosch G. Intermediate homocysteinemia: a thermolabile variant of methylenetetrahydrofolate reductase. Am J Hum Genet 1988; 43: 414-21.
-
(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
-
11
-
-
0026544977
-
Microbiological assay on microtitre plates of folate in serum red cells
-
O'Broin S, Kelleher B. Microbiological assay on microtitre plates of folate in serum red cells. J Clin Pathol 1992; 45: 344-47.
-
(1992)
J Clin Pathol
, vol.45
, pp. 344-347
-
-
O'Broin, S.1
Kelleher, B.2
-
13
-
-
0026747176
-
Dibrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease
-
Smith CAD, Gough AD, Leigh PN, et al. Dibrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease. Lancet 1992; 339: 1375-77.
-
(1992)
Lancet
, vol.339
, pp. 1375-1377
-
-
Smith, C.A.D.1
Gough, A.D.2
Leigh, P.N.3
-
14
-
-
0025873535
-
Homocysteinuria due to 5,10 methylenetetrahydrofolate reductase deficiency revealed by stroke in adult siblings
-
Visy JM, LeCoz P, Chadefaux B, et al. Homocysteinuria due to 5,10 methylenetetrahydrofolate reductase deficiency revealed by stroke in adult siblings. Neurology 1991; 41: 1313-15.
-
(1991)
Neurology
, vol.41
, pp. 1313-1315
-
-
Visy, J.M.1
LeCoz, P.2
Chadefaux, B.3
-
16
-
-
0022387408
-
Comparison of folic acid coenzyme distribution patterns in patients with methylenetetrahydrofolate reductase and methionine synthetase deficiencies
-
Baumgartner ER, Stokstad ELR, Wick H, Watson JE, Kusano G. Comparison of folic acid coenzyme distribution patterns in patients with methylenetetrahydrofolate reductase and methionine synthetase deficiencies. PediatrRes 1985; 19: 1288-92.
-
(1985)
PediatrRes
, vol.19
, pp. 1288-1292
-
-
Baumgartner, E.R.1
Stokstad, E.L.R.2
Wick, H.3
Watson, J.E.4
Kusano, G.5
-
18
-
-
0029066299
-
A quantitative assessment of plasma homocysteine as a risk factor for vascular disease
-
Boushey CJ, Beresford SAA, Omenn GS, Motulsky AG. A quantitative assessment of plasma homocysteine as a risk factor for vascular disease. JAMA 1995; 274: 1049-57.
-
(1995)
JAMA
, vol.274
, pp. 1049-1057
-
-
Boushey, C.J.1
Beresford, S.2
Omenn, G.S.3
Motulsky, A.G.4
-
19
-
-
0030027668
-
Relation between folate status, a common mutation in methylenetetrahydrofolate reductase and plasma homocysteine concentrations
-
Jacques PF, Bostom AG, Williams RR, et al. Relation between folate status, a common mutation in methylenetetrahydrofolate reductase and plasma homocysteine concentrations. Circulation 1996; 93: 7-9.
-
(1996)
Circulation
, vol.93
, pp. 7-9
-
-
Jacques, P.F.1
Bostom, A.G.2
Williams, R.R.3
-
20
-
-
0028863219
-
Folate levels and neural tube defects: Implications for prevention
-
Daly LE, Kirke PN, Molloy AM, Weir DG, Scott JM. Folate levels and neural tube defects: implications for prevention. JAMA 1995; 274: 1698-702.
-
(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
|