-
1
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase
-
Frosst P., Blom H.J., Milos R., Goyette P., Sheppard C.A., Matthews R.G., et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 10 (1995) 111-113
-
(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
-
2
-
-
0026034240
-
Thermolabile methylenetetrahydrofolate reductase: an inherited risk factor for coronary artery disease
-
Kang S.S., Wong P.W.K., Susmano A., Sora J., Norusis M., and Ruggie N. Thermolabile methylenetetrahydrofolate reductase: an inherited risk factor for coronary artery disease. Am J Hum Genet 48 (1991) 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
-
3
-
-
0029800387
-
Methylenetetrahydrofolate reductase mutation and neural tube defects
-
Kirke P.N., Mills J.L., Whitehead A.S., Molloy A., and Scott J.M. Methylenetetrahydrofolate reductase mutation and neural tube defects. Lancet 348 (1996) 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
-
4
-
-
4143088796
-
Spina bifida, 677TC mutation and role of folate
-
de Franchis R., Sebastio G., Mandato C., Andria G., and Mastroiacovo P. Spina bifida, 677TC mutation and role of folate. Lancet 346 (1995) 1703
-
(1995)
Lancet
, vol.346
, pp. 1703
-
-
de Franchis, R.1
Sebastio, G.2
Mandato, C.3
Andria, G.4
Mastroiacovo, P.5
-
5
-
-
0028890671
-
Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia
-
Engbersen A.M.T., Franken D.G., Boers G.H.J., Stevens E.M.B., Trijbels F.J.M., and Blom H.J. Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia. Am J Hum Genet 56 (1995) 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
-
6
-
-
12744269673
-
Distribution of 5, 10 methylenetetrahydrofolate reductase and its association with red blood cell 5-methyltetrahyrofolate in the healthy Iranians
-
Golbahar J., Fathi Z., and Tamadon M.A. Distribution of 5, 10 methylenetetrahydrofolate reductase and its association with red blood cell 5-methyltetrahyrofolate in the healthy Iranians. Clin Nutr 24 (2005) 83-87
-
(2005)
Clin Nutr
, vol.24
, pp. 83-87
-
-
Golbahar, J.1
Fathi, Z.2
Tamadon, M.A.3
-
7
-
-
0023696435
-
Intermediate homocysteinemia: a thermolabile variant of methylenetetrahydrofolate reductase
-
Kang S.S., Zhou J., Wong P.W.K., Kowalisyn J., and Strokosch G. Intermediate homocysteinemia: a thermolabile variant of methylenetetrahydrofolate reductase. Am J Hum Genet 43 (1988) 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
-
-
0037163849
-
MTHFR Studies Collaboration Group. MTHFR 677C → T polymorphism and risk of coronary heart disease: a meta-analysis
-
Klerk M., Verhoef P., Clarke R., Blom H.J., Kok F.J., and Schouten E.G. MTHFR Studies Collaboration Group. MTHFR 677C → T polymorphism and risk of coronary heart disease: a meta-analysis. JAMA 288 (2002) 2023-2031
-
(2002)
JAMA
, vol.288
, pp. 2023-2031
-
-
Klerk, M.1
Verhoef, P.2
Clarke, R.3
Blom, H.J.4
Kok, F.J.5
Schouten, E.G.6
-
9
-
-
0012739367
-
Spina bifida and folate-related genes: a study of gene-gene interactions
-
de Franchis R., Botto L.D., Sebastio G., Ricci R., Iolascon A., Capra V., et al. Spina bifida and folate-related genes: a study of gene-gene interactions. Genet Med 4 (2002) 126-130
-
(2002)
Genet Med
, vol.4
, pp. 126-130
-
-
de Franchis, R.1
Botto, L.D.2
Sebastio, G.3
Ricci, R.4
Iolascon, A.5
Capra, V.6
-
10
-
-
0030018760
-
5,10-Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects
-
Ou C.Y., Stevenson R.E., Brown V.K., Schwartz C.E., Allen W.P., Khoury M.J., et al. 5,10-Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects. Am J Med Genet 63 (1996) 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
-
11
-
-
0025278455
-
Elevated plasma homocyst(e)ine concentration as a possible independent risk factor for stroke
-
Coull B.M., Malinow M.R., Beamer N., Sexton G., Nordt F., and de Garmo P. Elevated plasma homocyst(e)ine concentration as a possible independent risk factor for stroke. Stroke 21 (1990) 572-576
-
(1990)
Stroke
, vol.21
, pp. 572-576
-
-
Coull, B.M.1
Malinow, M.R.2
Beamer, N.3
Sexton, G.4
Nordt, F.5
de Garmo, P.6
-
12
-
-
0030776695
-
Features, symptoms, and neurophysiological findings in stroke associated with hyperhomocysteinemia
-
Evers S., Koch H.G., Grotemeyer K.H., Lange B., Deufel T., and Ringelstein E.B. Features, symptoms, and neurophysiological findings in stroke associated with hyperhomocysteinemia. Arch Neurol 54 (1997) 1276-1282
-
(1997)
Arch Neurol
, vol.54
, pp. 1276-1282
-
-
Evers, S.1
Koch, H.G.2
Grotemeyer, K.H.3
Lange, B.4
Deufel, T.5
Ringelstein, E.B.6
-
13
-
-
0028936881
-
Role of blood pressure, uric acid, and hemorheological parameters on plasma homocyst(e)ine concentration
-
Malinow M.R., Levenson J., Giral P., Nieto F.J., Razavian M., Segond P., et al. Role of blood pressure, uric acid, and hemorheological parameters on plasma homocyst(e)ine concentration. Atherosclerosis 114 (1995) 175-183
-
(1995)
Atherosclerosis
, vol.114
, pp. 175-183
-
-
Malinow, M.R.1
Levenson, J.2
Giral, P.3
Nieto, F.J.4
Razavian, M.5
Segond, P.6
-
14
-
-
0031831064
-
Common mutation in methylenetetrahydrofolate reductase. Correlation with homocysteine and other risk factors for vascular disease
-
Motti C., Gnasso A., Bernardini S., Massoud R., Pastore A., Rampa P., et al. Common mutation in methylenetetrahydrofolate reductase. Correlation with homocysteine and other risk factors for vascular disease. Atherosclerosis 139 (1998) 377-383
-
(1998)
Atherosclerosis
, vol.139
, pp. 377-383
-
-
Motti, C.1
Gnasso, A.2
Bernardini, S.3
Massoud, R.4
Pastore, A.5
Rampa, P.6
-
15
-
-
0033529386
-
Serum uric acid and risk for cardiovascular disease and death: the Framingham Heart Study
-
Culleton B.F., Larson M.G., Kannel W.B., and Levy D. Serum uric acid and risk for cardiovascular disease and death: the Framingham Heart Study. Ann Intern Med 131 (1999) 7-13
-
(1999)
Ann Intern Med
, vol.131
, pp. 7-13
-
-
Culleton, B.F.1
Larson, M.G.2
Kannel, W.B.3
Levy, D.4
-
16
-
-
0031942817
-
Serum uric acid is a strong predictor of stroke in patients with non-insulin-dependent diabetes mellitus
-
Lehto S., Niskanen L., Ronnemaa T., and Laakso M. Serum uric acid is a strong predictor of stroke in patients with non-insulin-dependent diabetes mellitus. Stroke 29 (1998) 635-639
-
(1998)
Stroke
, vol.29
, pp. 635-639
-
-
Lehto, S.1
Niskanen, L.2
Ronnemaa, T.3
Laakso, M.4
-
17
-
-
0021077501
-
Inheritance and alcohol as factors influencing plasma uric acid levels
-
Whitfield J.B., and Martin N.G. Inheritance and alcohol as factors influencing plasma uric acid levels. Acta Genet Med Gemellol Roma 32 (1983) 117-126
-
(1983)
Acta Genet Med Gemellol Roma
, vol.32
, pp. 117-126
-
-
Whitfield, J.B.1
Martin, N.G.2
-
18
-
-
0026548215
-
Genetic control of the renal clearance of urate: a study of twins
-
Emmerson B.T., Nagel S.L., Duffy D.L., and Martin N.G. Genetic control of the renal clearance of urate: a study of twins. Ann Rheum Dis 51 (1992) 375-377
-
(1992)
Ann Rheum Dis
, vol.51
, pp. 375-377
-
-
Emmerson, B.T.1
Nagel, S.L.2
Duffy, D.L.3
Martin, N.G.4
-
19
-
-
0014222377
-
Enzyme defect associated with a sex-linked human neurological disorder and excessive purine synthesis
-
Seegmiller J.E., Rosenbloom F.M., and Kelly W.N. Enzyme defect associated with a sex-linked human neurological disorder and excessive purine synthesis. Science 155 (1967) 1682-1684
-
(1967)
Science
, vol.155
, pp. 1682-1684
-
-
Seegmiller, J.E.1
Rosenbloom, F.M.2
Kelly, W.N.3
-
20
-
-
0015634609
-
Human erythrocyte phosphoribosylpyrophosphate synthetase mutationaly altered in regulatory properties
-
Sperling O., Persky-Brosh S., Boer P., and De Vries A. Human erythrocyte phosphoribosylpyrophosphate synthetase mutationaly altered in regulatory properties. Biochem Med 7 (1973) 389-395
-
(1973)
Biochem Med
, vol.7
, pp. 389-395
-
-
Sperling, O.1
Persky-Brosh, S.2
Boer, P.3
De Vries, A.4
-
21
-
-
0033928273
-
The C677T mutation in the methylene tetrahydrofolate reductase gene increases serum uric acid in elderly men
-
Zuo M., Nishio H., Lee M.J., Maejima K., Mimura S., and Sumino K. The C677T mutation in the methylene tetrahydrofolate reductase gene increases serum uric acid in elderly men. J Hum Genet 45 (2000) 257-262
-
(2000)
J Hum Genet
, vol.45
, pp. 257-262
-
-
Zuo, M.1
Nishio, H.2
Lee, M.J.3
Maejima, K.4
Mimura, S.5
Sumino, K.6
-
22
-
-
17644428015
-
The relationships between plasma total homocysteine and selected atherosclerotic risk factors according to the C677T methylenetetrahydrofolate reductase gene in Japanese
-
Lwin H., Yoshiike N., Yokoyama T., Saito K., Date C., and Tanaka H. The relationships between plasma total homocysteine and selected atherosclerotic risk factors according to the C677T methylenetetrahydrofolate reductase gene in Japanese. Eur J Cardiovasc Prev Rehabil 12 (2005) 182-184
-
(2005)
Eur J Cardiovasc Prev Rehabil
, vol.12
, pp. 182-184
-
-
Lwin, H.1
Yoshiike, N.2
Yokoyama, T.3
Saito, K.4
Date, C.5
Tanaka, H.6
-
23
-
-
0013950540
-
Hyperuricemia in primary and renal hypertension
-
Cannon P.J., Stason W.B., Demartini F.E., Sommers S.C., and Laragh J.H. Hyperuricemia in primary and renal hypertension. N Engl J Med 275 (1966) 457-464
-
(1966)
N Engl J Med
, vol.275
, pp. 457-464
-
-
Cannon, P.J.1
Stason, W.B.2
Demartini, F.E.3
Sommers, S.C.4
Laragh, J.H.5
-
24
-
-
0034630917
-
Serum uric acid and cardiovascular mortality the NHANES I epidemiologic follow-up study, 1971-1992. National Health and Nutrition Examination Survey
-
Fang J., and Alderman M.H. Serum uric acid and cardiovascular mortality the NHANES I epidemiologic follow-up study, 1971-1992. National Health and Nutrition Examination Survey. JAMA 283 (2000) 2404-2410
-
(2000)
JAMA
, vol.283
, pp. 2404-2410
-
-
Fang, J.1
Alderman, M.H.2
-
25
-
-
0030248466
-
Relationships between serum uric acid and lipids in healthy subjects
-
Russo C., Olivieri O., Girelli D., Guarini P., and Corrocher R. Relationships between serum uric acid and lipids in healthy subjects. Prev Med 25 (1996) 611-616
-
(1996)
Prev Med
, vol.25
, pp. 611-616
-
-
Russo, C.1
Olivieri, O.2
Girelli, D.3
Guarini, P.4
Corrocher, R.5
-
26
-
-
0023852684
-
A DNA polymorphism of an apoprotein gene associates with the hypertriglyceridaemia of primary gout
-
Ferns G.A., Lanham J., Dieppe P., and Galton D.J. A DNA polymorphism of an apoprotein gene associates with the hypertriglyceridaemia of primary gout. Hum Genet 78 (1988) 55-59
-
(1988)
Hum Genet
, vol.78
, pp. 55-59
-
-
Ferns, G.A.1
Lanham, J.2
Dieppe, P.3
Galton, D.J.4
-
27
-
-
0028962657
-
Apolipoprotein E phenotypes in patients with gout: relation with hypertriglyceridaemia
-
Moriwaki Y., Yamamoto T., Takahashi S., Tsutsumi Z., and Higashino K. Apolipoprotein E phenotypes in patients with gout: relation with hypertriglyceridaemia. Ann Rheum Dis 54 (1995) 351-354
-
(1995)
Ann Rheum Dis
, vol.54
, pp. 351-354
-
-
Moriwaki, Y.1
Yamamoto, T.2
Takahashi, S.3
Tsutsumi, Z.4
Higashino, K.5
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