-
1
-
-
0031801285
-
Methylenetetrahydrofolate reductase and methionine synthase: Biochemistry and molecular biology
-
Matthews R.G., Sheppard C., Goulding C. Methylenetetrahydrofolate reductase and methionine synthase: biochemistry and molecular biology. Eur. J. Pediatr. 157(Suppl. 2):1998;S54-S59.
-
(1998)
Eur. J. Pediatr.
, vol.157
, Issue.SUPPL. 2
-
-
Matthews, R.G.1
Sheppard, C.2
Goulding, C.3
-
2
-
-
0031733260
-
Hyperhomocysteinemia and venous thrombosis: A meta-analysis
-
den-Heijer M., Rosendaal F.R., Blom H.J., Gerrits W.B., Bos G.M. Hyperhomocysteinemia and venous thrombosis: a meta-analysis. Thromb. Haemost. 80:1998;874-877.
-
(1998)
Thromb. Haemost.
, vol.80
, pp. 874-877
-
-
Den-Heijer, M.1
Rosendaal, F.R.2
Blom, H.J.3
Gerrits, W.B.4
Bos, G.M.5
-
4
-
-
0032497941
-
Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease: The result of a meta-analysis
-
Brattstrom L., Wilcken D.E., Ohrvik J., Brudin L. Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease: the result of a meta-analysis. Circulation. 98:1998;2520-2526.
-
(1998)
Circulation
, vol.98
, pp. 2520-2526
-
-
Brattstrom, L.1
Wilcken, D.E.2
Ohrvik, J.3
Brudin, L.4
-
5
-
-
0037163849
-
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., Schouten E.G. 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
-
6
-
-
10544249877
-
Human methionine synthase: CDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders
-
Leclerc D., Campeau E., Goyette P., Adjalla C.E., Christensen B., Ross M.et al. Human methionine synthase: CDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders. Hum. Mol. Genet. 5:1996;1867-1874.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1867-1874
-
-
Leclerc, D.1
Campeau, E.2
Goyette, P.3
Adjalla, C.E.4
Christensen, B.5
Ross, M.6
-
7
-
-
0030804226
-
Sequence analysis of the coding region of human methionine synthase: Relevance to hyperhomocysteinaemia in neural-tube defects and vascular disease
-
Van-Der-Put N.M., Van-Der-Molen E.F., Kluijtmans L.A.J., Heil S.G., Trijbels J.M.F., Eskes T.K.A.B.et al. Sequence analysis of the coding region of human methionine synthase: Relevance to hyperhomocysteinaemia in neural-tube defects and vascular disease. QJM. 90:1997;517.
-
(1997)
QJM
, vol.90
, pp. 517
-
-
Van-Der-Put, N.M.1
Van-Der-Molen, E.F.2
Kluijtmans, L.A.J.3
Heil, S.G.4
Trijbels, J.M.F.5
Eskes, T.K.A.B.6
-
8
-
-
0031030585
-
Human methionine synthase. cDNA cloning, gene localization, and expression
-
Chen L.H., Liu M.L., Hwang H.Y., Chen L.S., Korenberg J., Shane B. Human methionine synthase. cDNA cloning, gene localization, and expression. J. Biol. Chem. 272:1997;3628-3634.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 3628-3634
-
-
Chen, L.H.1
Liu, M.L.2
Hwang, H.Y.3
Chen, L.S.4
Korenberg, J.5
Shane, B.6
-
9
-
-
0030612756
-
The 677C→T mutation in the methylenetetrahydrofolate reductase gene: Associations with plasma total homocysteine levels and risk of coronary atherosclerotic disease
-
Verhoef P., Kok F.J., Kluijtmans L.A., Blom H.J., Refsum H., Ueland P.M.et al. The 677C→T mutation in the methylenetetrahydrofolate reductase gene: associations with plasma total homocysteine levels and risk of coronary atherosclerotic disease. Atherosclerosis. 132:1997;105-113.
-
(1997)
Atherosclerosis
, vol.132
, pp. 105-113
-
-
Verhoef, P.1
Kok, F.J.2
Kluijtmans, L.A.3
Blom, H.J.4
Refsum, H.5
Ueland, P.M.6
-
10
-
-
0028949953
-
Is hyperhomocysteinaemia a risk factor for recurrent venous thrombosis?
-
den-Heijer M., Blom H.J., Gerrits W.B., Rosendaal F.R., Haak H.L., Wijermans P.W.et al. Is hyperhomocysteinaemia a risk factor for recurrent venous thrombosis? Lancet. 345:1995;882-885.
-
(1995)
Lancet
, vol.345
, pp. 882-885
-
-
Den-Heijer, M.1
Blom, H.J.2
Gerrits, W.B.3
Rosendaal, F.R.4
Haak, H.L.5
Wijermans, P.W.6
-
11
-
-
0028913608
-
Three different methods for the determination of total homocysteine in plasma
-
te Poele-Pothoff M., van-den-Berg M., Franken D.G., Boers G.H., Jakobs C., de-Kroon I.F.et al. Three different methods for the determination of total homocysteine in plasma. Ann. Clin. Biochem. 32:1995;20.
-
(1995)
Ann. Clin. Biochem.
, vol.32
, pp. 20
-
-
Te Poele-Pothoff, M.1
Van-Den-Berg, M.2
Franken, D.G.3
Boers, G.H.4
Jakobs, C.5
De-Kroon, I.F.6
-
12
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller S.A., Dykes D.D., Polesky H.F. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 16:1988;1215.
-
(1988)
Nucleic Acids Res.
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
13
-
-
0002051637
-
Polymorphisms of folate and cobalamin metabolism
-
R. Carmel, & D.W. Jacobsen. Cambridge: Cambridge Univ. Press
-
Rozen R. Polymorphisms of folate and cobalamin metabolism. Carmel R., Jacobsen D.W. Homocysteine in health and disease. 2001;259-270 Cambridge Univ. Press, Cambridge.
-
(2001)
Homocysteine in Health and Disease
, pp. 259-270
-
-
Rozen, R.1
-
14
-
-
0032713815
-
Methionine synthase D919G polymorphism is a significant but modest determinant of circulating homocysteine concentrations
-
Harmon D.L., Shields D.C., Woodside J.V., McMaster D., Yarnell J.W.G., Young I.S.et al. Methionine synthase D919G polymorphism is a significant but modest determinant of circulating homocysteine concentrations. Gen. Epidemiol. 17:1999;298-309.
-
(1999)
Gen. Epidemiol.
, vol.17
, pp. 298-309
-
-
Harmon, D.L.1
Shields, D.C.2
Woodside, J.V.3
McMaster, D.4
Yarnell, J.W.G.5
Young, I.S.6
-
15
-
-
0034670081
-
Effect of heterozygosity for the methionine synthase 2756 A→G mutation on the risk for recurrent cardiovascular events
-
Hyndman ME, Bridge PJ, Warnica JW, Fick G, Parsons, HG. Effect of heterozygosity for the methionine synthase 2756 A→G mutation on the risk for recurrent cardiovascular events. Am. J. Cardiol. 2000;86: 1144-6,A9.
-
(2000)
Am. J. Cardiol.
, vol.86
, pp. 1144-1146
-
-
Hyndman, M.E.1
Bridge, P.J.2
Warnica, J.W.3
Fick, G.4
Parsons, H.G.5
-
16
-
-
0032966833
-
Polymorphism of the methionine synthase gene-association with homocysteine metabolism and late-onset vascular diseases in the Japanese population
-
Morita H., Kurihara H., Sugiyama T., Hamada C., Kurihara Y., Shindo T.et al. Polymorphism of the methionine synthase gene-association with homocysteine metabolism and late-onset vascular diseases in the Japanese population. Arteriol. Thromb. Vasc. Biol. 19:1999;298-302.
-
(1999)
Arteriol. Thromb. Vasc. Biol.
, vol.19
, pp. 298-302
-
-
Morita, H.1
Kurihara, H.2
Sugiyama, T.3
Hamada, C.4
Kurihara, Y.5
Shindo, T.6
-
17
-
-
0034168107
-
The role of vitamin B12 in fasting hyperhomocysteinemia and its interaction with the homozygous C677T mutation of the methylenetetrahydrofolate reductase (MTHFR) gene - A case-control study of patients with early-onset thrombotic events
-
D'-Angelo A., Coppola A., Madonna P., Fermo I., Pagano A., Mazzola G.et al. The role of vitamin B12 in fasting hyperhomocysteinemia and its interaction with the homozygous C677T mutation of the methylenetetrahydrofolate reductase (MTHFR) gene - a case-control study of patients with early-onset thrombotic events. Thromb. Haemost. 83:2000;563-570.
-
(2000)
Thromb. Haemost.
, vol.83
, pp. 563-570
-
-
D'-Angelo, A.1
Coppola, A.2
Madonna, P.3
Fermo, I.4
Pagano, A.5
Mazzola, G.6
-
18
-
-
0032878590
-
A polymorphism of the methionine synthase gene: Association with plasma folate, vitamin B-12, homocyst(e)ine, and colorectal cancer risk
-
Ma J., Stampfer M.J., Christensen B., Giovannucci E., Hunter D.J., Chen J.et al. A polymorphism of the methionine synthase gene: association with plasma folate, vitamin B-12, homocyst(e)ine, and colorectal cancer risk. Cancer Epidemiol. Biomark. Prev. 8:1999;825-829.
-
(1999)
Cancer Epidemiol. Biomark. Prev.
, vol.8
, pp. 825-829
-
-
Ma, J.1
Stampfer, M.J.2
Christensen, B.3
Giovannucci, E.4
Hunter, D.J.5
Chen, J.6
-
19
-
-
0034827634
-
Genetic defects as important factors for moderate hyperhomocysteinemia
-
Geisel J., Zimbelmann I., Schorr H., Knapp J.P., Bodis M., Hubner U.et al. Genetic defects as important factors for moderate hyperhomocysteinemia. Clin. Chem. Lab. Med. 39:2001;698-704.
-
(2001)
Clin. Chem. Lab. Med.
, vol.39
, pp. 698-704
-
-
Geisel, J.1
Zimbelmann, I.2
Schorr, H.3
Knapp, J.P.4
Bodis, M.5
Hubner, U.6
-
20
-
-
0032773207
-
Relationship between total plasma homocysteine, polymorphisms of homocysteine metabolism related enzymes, risk factors and coronary artery disease in the Australian hospital-based population
-
Wang X.L., Duarte N., Cai H., Adachi T., Sim A.S., Cranney G.et al. Relationship between total plasma homocysteine, polymorphisms of homocysteine metabolism related enzymes, risk factors and coronary artery disease in the Australian hospital-based population. Atherosclerosis. 146:1999;133-140.
-
(1999)
Atherosclerosis
, vol.146
, pp. 133-140
-
-
Wang, X.L.1
Duarte, N.2
Cai, H.3
Adachi, T.4
Sim, A.S.5
Cranney, G.6
-
21
-
-
20244366362
-
Genetic causes of mild hyperhomocysteinemia in patients with premature occlusive coronary artery diseases
-
Tsai M.Y., Welge B.G., Hanson N.Q., Bignell M.K., Vessey J., Schwichtenberg K.et al. Genetic causes of mild hyperhomocysteinemia in patients with premature occlusive coronary artery diseases. Atherosclerosis. 143:1999;163-170.
-
(1999)
Atherosclerosis
, vol.143
, pp. 163-170
-
-
Tsai, M.Y.1
Welge, B.G.2
Hanson, N.Q.3
Bignell, M.K.4
Vessey, J.5
Schwichtenberg, K.6
-
22
-
-
0033999287
-
Polygenic influence on plasma homocysteine: Association of two prevalent mutations, the 844ins68 of cystathionine beta-synthase and A(2756)G of methionine synthase, with lowered plasma homocysteine levels
-
Tsai M.Y., Bignell M., Yang F., Welge B.G., Graham K.J., Hanson N.Q. Polygenic influence on plasma homocysteine: association of two prevalent mutations, the 844ins68 of cystathionine beta-synthase and A(2756)G of methionine synthase, with lowered plasma homocysteine levels. Atherosclerosis. 149:2000;131-137.
-
(2000)
Atherosclerosis
, vol.149
, pp. 131-137
-
-
Tsai, M.Y.1
Bignell, M.2
Yang, F.3
Welge, B.G.4
Graham, K.J.5
Hanson, N.Q.6
-
23
-
-
0035864635
-
Influence of a methionine synthase (D919G) polymorphism on plasma homocysteine and folate levels and relation to risk of myocardial infarction
-
Chen J., Stampfer M.J., Ma J., Selhub J., Malinow M.R., Hennekens C.H.et al. Influence of a methionine synthase (D919G) polymorphism on plasma homocysteine and folate levels and relation to risk of myocardial infarction. Atherosclerosis. 154:2001;667-672.
-
(2001)
Atherosclerosis
, vol.154
, pp. 667-672
-
-
Chen, J.1
Stampfer, M.J.2
Ma, J.3
Selhub, J.4
Malinow, M.R.5
Hennekens, C.H.6
-
24
-
-
0032415394
-
The frequency of a common mutation of the methionine synthase gene in the Australian population and its relation to smoking and coronary artery disease
-
Wang X.L., Cai H., Cranney G., Wilcken D.E. The frequency of a common mutation of the methionine synthase gene in the Australian population and its relation to smoking and coronary artery disease. J. Cardiovasc. Risk. 5:1998;289-295.
-
(1998)
J. Cardiovasc. Risk
, vol.5
, pp. 289-295
-
-
Wang, X.L.1
Cai, H.2
Cranney, G.3
Wilcken, D.E.4
-
25
-
-
0034044549
-
Altered folate metabolism and disposition in mothers affected by a spina bifida pregnancy: Influence of 677c→t methylenetetrahydrofolate reductase and 2756a→g methionine synthase genotypes
-
Lucock M., Daskalakis I., Briggs D., Yates Z., Levene M. Altered folate metabolism and disposition in mothers affected by a spina bifida pregnancy: influence of 677c→t methylenetetrahydrofolate reductase and 2756a→g methionine synthase genotypes. Mol. Genet. Metab. 70:2000;27-44.
-
(2000)
Mol. Genet. Metab.
, vol.70
, pp. 27-44
-
-
Lucock, M.1
Daskalakis, I.2
Briggs, D.3
Yates, Z.4
Levene, M.5
-
26
-
-
0031595492
-
Vitamins B6, B12, and folate: Association with plasma total homocysteine and risk of coronary atherosclerosis
-
Siri P.W., Verhoef P., Kok F.J. Vitamins B6, B12, and folate: association with plasma total homocysteine and risk of coronary atherosclerosis. J. Am. Coll. Nutr. 17:1998;435-441.
-
(1998)
J. Am. Coll. Nutr.
, vol.17
, pp. 435-441
-
-
Siri, P.W.1
Verhoef, P.2
Kok, F.J.3
-
27
-
-
0029924647
-
Homocysteine metabolism and risk of myocardial infarction: Relation with vitamins B6, B12, and folate
-
Verhoef P., Stampfer M.J., Buring J.E., Gaziano J.M., Allen R.H., Stabler S.P.et al. Homocysteine metabolism and risk of myocardial infarction: relation with vitamins B6, B12, and folate. Am. J. Epidemiol. 143:1996;845-859.
-
(1996)
Am. J. Epidemiol.
, vol.143
, pp. 845-859
-
-
Verhoef, P.1
Stampfer, M.J.2
Buring, J.E.3
Gaziano, J.M.4
Allen, R.H.5
Stabler, S.P.6
-
28
-
-
0032501963
-
Low circulating folate and vitamin B6 concentrations: Risk factors for stroke, peripheral vascular disease, and coronary artery disease. European COMAC Group
-
Robinson K., Arheart K., Refsum H., Brattstrom L., Boers G., Ueland P.et al. Low circulating folate and vitamin B6 concentrations: risk factors for stroke, peripheral vascular disease, and coronary artery disease. European COMAC Group. Circulation. 97:1998;437-443.
-
(1998)
Circulation
, vol.97
, pp. 437-443
-
-
Robinson, K.1
Arheart, K.2
Refsum, H.3
Brattstrom, L.4
Boers, G.5
Ueland, P.6
-
29
-
-
0032555167
-
Prospective study of coronary heart disease incidence in relation to fasting total homocysteine, related genetic polymorphisms, and B vitamins: The atherosclerosis risk in communities (ARIC) study
-
Folsom A.R., Nieto F.J., McGovern P.G., Tsai M.Y., Malinow M.R., Eckfeldt J.H.et al. Prospective study of coronary heart disease incidence in relation to fasting total homocysteine, related genetic polymorphisms, and B vitamins: the atherosclerosis risk in communities (ARIC) study. Circulation. 98:1998;204-210.
-
(1998)
Circulation
, vol.98
, pp. 204-210
-
-
Folsom, A.R.1
Nieto, F.J.2
McGovern, P.G.3
Tsai, M.Y.4
Malinow, M.R.5
Eckfeldt, J.H.6
-
30
-
-
0028267831
-
Plasma homocyst(e)ine, folate, and vitamin B-12 concentrations and risk for early-onset coronary artery disease
-
Pancharuniti N., Lewis C.A., Sauberlich H.E., Perkins L.L., Go R.C., Alvarez J.O.et al. Plasma homocyst(e)ine, folate, and vitamin B-12 concentrations and risk for early-onset coronary artery disease. Am. J. Clin. Nutr. 59:1994;940-948.
-
(1994)
Am. J. Clin. Nutr.
, vol.59
, pp. 940-948
-
-
Pancharuniti, N.1
Lewis, C.A.2
Sauberlich, H.E.3
Perkins, L.L.4
Go, R.C.5
Alvarez, J.O.6
-
31
-
-
0030812224
-
The association of vitamin b 12 and folate blood levels with mortality and cardiovascular morbidity incidence in the old old: The Bronx aging study
-
Zeitlin A., Frishman W.H., Chang C.J. The association of vitamin b 12 and folate blood levels with mortality and cardiovascular morbidity incidence in the old old: the Bronx aging study. Am. J. Ther. 4:1997;275-281.
-
(1997)
Am. J. Ther.
, vol.4
, pp. 275-281
-
-
Zeitlin, A.1
Frishman, W.H.2
Chang, C.J.3
|