-
1
-
-
0025756673
-
Hyperhomocysteinemia: an independent risk factor for vascular disease
-
Clarke R., Daly L., Robinson K., Naughten E., Cahalane S., Fowler B., et al. Hyperhomocysteinemia: an independent risk factor for vascular disease. N Engl J Med 324 (1991) 1149-1155
-
(1991)
N Engl J Med
, vol.324
, pp. 1149-1155
-
-
Clarke, R.1
Daly, L.2
Robinson, K.3
Naughten, E.4
Cahalane, S.5
Fowler, B.6
-
2
-
-
0026684554
-
A prospective study of plasma homocyst(e)ine and risk of myocardial infarction in US physicians
-
Stampfer M.J., Malinow M.R., Willett W.C., Newcomer L.M., Upson B., Ullmann D., et al. A prospective study of plasma homocyst(e)ine and risk of myocardial infarction in US physicians. JAMA 268 (1992) 877-881
-
(1992)
JAMA
, vol.268
, pp. 877-881
-
-
Stampfer, M.J.1
Malinow, M.R.2
Willett, W.C.3
Newcomer, L.M.4
Upson, B.5
Ullmann, D.6
-
3
-
-
0029066299
-
A quantitative assessment of plasma homocysteine as a risk factor for vascular disease. Probable benefits of increasing folic acid intakes
-
Boushey C.J., Beresford S.A., Omenn G.S., and Motulsky A.G. A quantitative assessment of plasma homocysteine as a risk factor for vascular disease. Probable benefits of increasing folic acid intakes. JAMA 274 (1995) 1049-1057
-
(1995)
JAMA
, vol.274
, pp. 1049-1057
-
-
Boushey, C.J.1
Beresford, S.A.2
Omenn, G.S.3
Motulsky, A.G.4
-
4
-
-
0029655527
-
Nutritional ecogenetics: homocysteine-related arteriosclerotic vascular disease, neural tube defects, and folic acid
-
Motulsky A.G. Nutritional ecogenetics: homocysteine-related arteriosclerotic vascular disease, neural tube defects, and folic acid. Am J Hum Genet 58 (1996) 17-20
-
(1996)
Am J Hum Genet
, vol.58
, pp. 17-20
-
-
Motulsky, A.G.1
-
5
-
-
0023243925
-
Homocysteinemia due to folate deficiency
-
Kang S.S., Wong P.W., and Norusis M. Homocysteinemia due to folate deficiency. Metabolism 36 (1987) 458-462
-
(1987)
Metabolism
, vol.36
, pp. 458-462
-
-
Kang, S.S.1
Wong, P.W.2
Norusis, M.3
-
6
-
-
0027392610
-
Vitamin B-12, vitamin B-6, and folate nutritional status in men with hyperhomocysteinemia
-
Ubbink J.B., Vermaak W.J., van der Merwe A., and Becker P.J. Vitamin B-12, vitamin B-6, and folate nutritional status in men with hyperhomocysteinemia. Am J Clin Nutr 57 (1993) 47-53
-
(1993)
Am J Clin Nutr
, vol.57
, pp. 47-53
-
-
Ubbink, J.B.1
Vermaak, W.J.2
van der Merwe, A.3
Becker, P.J.4
-
7
-
-
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., and 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
-
8
-
-
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., Metthews 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
Metthews, R.G.6
-
9
-
-
0030826587
-
Thermolabile methylenetetrahydrofolate reductase in coronary artery disease
-
Kluijtmans L.A., Kastelein J.J., Lindemans J., Boers G.H., Heil S.G., Bruschke A.V., et al. Thermolabile methylenetetrahydrofolate reductase in coronary artery disease. Circulation 96 (1997) 2573-2578
-
(1997)
Circulation
, vol.96
, pp. 2573-2578
-
-
Kluijtmans, L.A.1
Kastelein, J.J.2
Lindemans, J.3
Boers, G.H.4
Heil, S.G.5
Bruschke, A.V.6
-
10
-
-
0030610090
-
The mutation Ala677àVal in the methylene tetrahydrofolate reductase gene: a risk factor for arterial disease and venous thrombosis
-
Arruda V.R., von Zuben P.M., Chiaparini L.C., Annichino-Bizzacchi J.M., and Costa F.F. The mutation Ala677àVal in the methylene tetrahydrofolate reductase gene: a risk factor for arterial disease and venous thrombosis. Thromb Haemost 77 (1997) 818-821
-
(1997)
Thromb Haemost
, vol.77
, pp. 818-821
-
-
Arruda, V.R.1
von Zuben, P.M.2
Chiaparini, L.C.3
Annichino-Bizzacchi, J.M.4
Costa, F.F.5
-
11
-
-
0031049530
-
A common mutation in methylenetetrahydrofolate reductase gene is not a major risk of coronary artery disease or myocardial infarction
-
Brugada R., and Marian A.J. A common mutation in methylenetetrahydrofolate reductase gene is not a major risk of coronary artery disease or myocardial infarction. Atherosclerosis 128 (1997) 107-112
-
(1997)
Atherosclerosis
, vol.128
, pp. 107-112
-
-
Brugada, R.1
Marian, A.J.2
-
12
-
-
0035864638
-
Identification of six methylenetetrahydrofolate reductase (MTHFR) genotypes resulting from common polymorphisms: impact on plasma homocysteine levels and development of coronary artery disease
-
Meisel C., Cascorbi I., Gerloff T., Stangl V., Laule M., Muller J.M., et al. Identification of six methylenetetrahydrofolate reductase (MTHFR) genotypes resulting from common polymorphisms: impact on plasma homocysteine levels and development of coronary artery disease. Atherosclerosis 154 (2001) 651-668
-
(2001)
Atherosclerosis
, vol.154
, pp. 651-668
-
-
Meisel, C.1
Cascorbi, I.2
Gerloff, T.3
Stangl, V.4
Laule, M.5
Muller, J.M.6
-
13
-
-
0030859681
-
A mutation in the methylenetetrahydrofolate reductase gene is not associated with increased risk for coronary artery disease or myocardial infarction
-
Anderson J.L., King G.J., Thomson M.J., Todd M., Bair T.L., Muhlestein J.B., et al. A mutation in the methylenetetrahydrofolate reductase gene is not associated with increased risk for coronary artery disease or myocardial infarction. J Am Coll Cardiol 30 (1997) 1206-1211
-
(1997)
J Am Coll Cardiol
, vol.30
, pp. 1206-1211
-
-
Anderson, J.L.1
King, G.J.2
Thomson, M.J.3
Todd, M.4
Bair, T.L.5
Muhlestein, J.B.6
-
14
-
-
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
-
15
-
-
0031971515
-
A second mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neutral tube defects?
-
van der Put N.M., Gabreels F., Stevens E.M., Smeitink J.A., Trijbels F.J., Eskes T.K., et al. A second mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neutral tube defects?. Am J Hum Genet 62 (1998) 1044-1051
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1044-1051
-
-
van der Put, N.M.1
Gabreels, F.2
Stevens, E.M.3
Smeitink, J.A.4
Trijbels, F.J.5
Eskes, T.K.6
-
16
-
-
0030993597
-
Loss of heterozygosity at the 5,10-methylenetetrahydrofolate reductase locus in human ovarian carcinomas
-
Viel A., Dall'Agnese L., Simone F., Canzonieri V., Capozzi E., Visentin M.C., et al. Loss of heterozygosity at the 5,10-methylenetetrahydrofolate reductase locus in human ovarian carcinomas. Br J Cancer 75 (1997) 1105-1110
-
(1997)
Br J Cancer
, vol.75
, pp. 1105-1110
-
-
Viel, A.1
Dall'Agnese, L.2
Simone, F.3
Canzonieri, V.4
Capozzi, E.5
Visentin, M.C.6
-
17
-
-
0034743914
-
The 1298A3C polymorphism in methylenetetrahydrofolate reductase (MTHFR): in vitro expression and association with homocysteine
-
Weisberg I.S., Jacques P.F., Selhub J., Bostom A.G., Chen Z., Curtis Ellison R., et al. The 1298A3C polymorphism in methylenetetrahydrofolate reductase (MTHFR): in vitro expression and association with homocysteine. Atherosclerosis 156 (2001) 409-415
-
(2001)
Atherosclerosis
, vol.156
, pp. 409-415
-
-
Weisberg, I.S.1
Jacques, P.F.2
Selhub, J.3
Bostom, A.G.4
Chen, Z.5
Curtis Ellison, R.6
-
18
-
-
0034606262
-
The homozygous C677T mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for migraine
-
Kowa H., Yasui K., Takeshima T., Urakami K., Sakai F., and Nakashima K. The homozygous C677T mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for migraine. Am J Med Genet 96 (2000) 762-764
-
(2000)
Am J Med Genet
, vol.96
, pp. 762-764
-
-
Kowa, H.1
Yasui, K.2
Takeshima, T.3
Urakami, K.4
Sakai, F.5
Nakashima, K.6
-
19
-
-
0033607241
-
Polymorphisms in the methylenetetrahydrofolate reductase gene are associated with susceptibility to acute leukemia in adults
-
Skibola C.F., Smith M.T., Kane E., Roman E., Rollinson S., Cartwright R.A., et al. Polymorphisms in the methylenetetrahydrofolate reductase gene are associated with susceptibility to acute leukemia in adults. Proc Natl Acad Sci USA 96 (1999) 12810-12815
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 12810-12815
-
-
Skibola, C.F.1
Smith, M.T.2
Kane, E.3
Roman, E.4
Rollinson, S.5
Cartwright, R.A.6
-
20
-
-
0000262278
-
GENEPOP (V.1.2) A population genetics software for exact tests and ecumenicism
-
Raymont M., and Rousset F. GENEPOP (V.1.2) A population genetics software for exact tests and ecumenicism. J Hered 95 (1995) 248-249
-
(1995)
J Hered
, vol.95
, pp. 248-249
-
-
Raymont, M.1
Rousset, F.2
-
21
-
-
0003300707
-
Arlequin: a software for population genetic data analysis
-
University of Geneva, Switzerland
-
Schneider S., Kueffer J.M., and Roessli D. Arlequin: a software for population genetic data analysis. Genetics and Biometry Laboratory (2000), University of Geneva, Switzerland
-
(2000)
Genetics and Biometry Laboratory
-
-
Schneider, S.1
Kueffer, J.M.2
Roessli, D.3
-
22
-
-
0035071957
-
A new statistical method for haplotype reconstruction from population data
-
Stephens M., Smith N.J., and Donnelly P. A new statistical method for haplotype reconstruction from population data. Am J Hum Genet 68 (2001) 978-989
-
(2001)
Am J Hum Genet
, vol.68
, pp. 978-989
-
-
Stephens, M.1
Smith, N.J.2
Donnelly, P.3
-
23
-
-
0021566877
-
Estimating F-statistics for the analysis of population structure
-
Weir B., and Cockerham C. Estimating F-statistics for the analysis of population structure. Evolution 38 (1984) 1358-1370
-
(1984)
Evolution
, vol.38
, pp. 1358-1370
-
-
Weir, B.1
Cockerham, C.2
-
24
-
-
49549119880
-
-
Goudet J. FSTAT, a program to estimate and test gene diversities and fixation indices (version 2.9.3). 2001. Available from www.unil.ch/izea/softwares/fstat.html. Updated from Goudet (1995).
-
Goudet J. FSTAT, a program to estimate and test gene diversities and fixation indices (version 2.9.3). 2001. Available from www.unil.ch/izea/softwares/fstat.html. Updated from Goudet (1995).
-
-
-
-
25
-
-
0000625869
-
Analyzing tables of statistical tests
-
Rice W.R. Analyzing tables of statistical tests. Evolution 43 (1989) 223-225
-
(1989)
Evolution
, vol.43
, pp. 223-225
-
-
Rice, W.R.1
-
26
-
-
13444309753
-
Polymorphism of the ACE gene is associated with extent and severity of coronary disease
-
Mendonça I., Freitas A.I., Sousa A.C., Gomes S., Faria P., Drumond A., et al. Polymorphism of the ACE gene is associated with extent and severity of coronary disease. Rev Port Cardiol 23 (2004) 1605-1611
-
(2004)
Rev Port Cardiol
, vol.23
, pp. 1605-1611
-
-
Mendonça, I.1
Freitas, A.I.2
Sousa, A.C.3
Gomes, S.4
Faria, P.5
Drumond, A.6
-
28
-
-
0028788020
-
Total plasma homocysteine and cardiovascular risk profile. The Hordaland Homocysteine Study
-
Nygard O., Vollset S.E., Refsum H., Stensvold I., Tverdal A., Nordrehaug J.E., et al. Total plasma homocysteine and cardiovascular risk profile. The Hordaland Homocysteine Study. JAMA 274 (1995) 1526-1533
-
(1995)
JAMA
, vol.274
, pp. 1526-1533
-
-
Nygard, O.1
Vollset, S.E.2
Refsum, H.3
Stensvold, I.4
Tverdal, A.5
Nordrehaug, J.E.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
-
-
0031457858
-
Homocyst(e)ine and risk of cardiovascular disease in the Multiple Risk Factor Intervention Trial
-
Evans R.W., Shaten B.J., Hempel J.D., Cutler J.A., and Kuller L.H. Homocyst(e)ine and risk of cardiovascular disease in the Multiple Risk Factor Intervention Trial. Arterioscler Thromb Vasc Biol 17 (1997) 1947-1953
-
(1997)
Arterioscler Thromb Vasc Biol
, vol.17
, pp. 1947-1953
-
-
Evans, R.W.1
Shaten, B.J.2
Hempel, J.D.3
Cutler, J.A.4
Kuller, L.H.5
-
31
-
-
0033304841
-
Hyperhomocysteinemia and the endocrine system: implications for atherosclerosis and thrombosis
-
Fonseca V., Guba S.C., and Fink L.M. Hyperhomocysteinemia and the endocrine system: implications for atherosclerosis and thrombosis. Endocr Rev 20 (1999) 738-759
-
(1999)
Endocr Rev
, vol.20
, pp. 738-759
-
-
Fonseca, V.1
Guba, S.C.2
Fink, L.M.3
-
32
-
-
39949084495
-
Association of polymorphism in the thermolabile 5,10-methylene tetrahydrofolate reductase gene and hyperhomocysteinemia with coronary artery disease
-
Alam M.A., Husain S.A., Narang R., Chauhan S.S., Kabra M., and Vasisht S. Association of polymorphism in the thermolabile 5,10-methylene tetrahydrofolate reductase gene and hyperhomocysteinemia with coronary artery disease. Mol Cell Biochem 310 (2007) 111-117
-
(2007)
Mol Cell Biochem
, vol.310
, pp. 111-117
-
-
Alam, M.A.1
Husain, S.A.2
Narang, R.3
Chauhan, S.S.4
Kabra, M.5
Vasisht, S.6
-
33
-
-
33947170999
-
Thermolabile methylenetetrahydrofolate reductase C677T polymorphism and homocysteine are risk factors for coronary artery disease in Moroccan population
-
[Electronic Publication]
-
Bennouar N., Allami A., Azeddoug H., Bendris A., Laraqui A., El Jaffali A., et al. Thermolabile methylenetetrahydrofolate reductase C677T polymorphism and homocysteine are risk factors for coronary artery disease in Moroccan population. J Biomed Biotechnol (2007) [Electronic Publication]
-
(2007)
J Biomed Biotechnol
-
-
Bennouar, N.1
Allami, A.2
Azeddoug, H.3
Bendris, A.4
Laraqui, A.5
El Jaffali, A.6
-
34
-
-
34548492494
-
Relation between plasma homocysteine, gene polymorphisms of homocysteine metabolism-related enzymes, and angiographically proven coronary artery disease
-
Laraqui A., Allami A., Carrié A., Raisonnier A., Coiffard A.S., Benkouka F., et al. Relation between plasma homocysteine, gene polymorphisms of homocysteine metabolism-related enzymes, and angiographically proven coronary artery disease. Eur J Intern Med 18 (2007) 474-483
-
(2007)
Eur J Intern Med
, vol.18
, pp. 474-483
-
-
Laraqui, A.1
Allami, A.2
Carrié, A.3
Raisonnier, A.4
Coiffard, A.S.5
Benkouka, F.6
-
35
-
-
2342485635
-
Methylenetetrahydrofolate reductase gene C677T and A1298C polymorphisms, plasma homocysteine, folate, and vitamin B12 levels and the extent of coronary artery disease
-
Kölling K., Ndrepepa G., Koch W., Braun S., Mehilli J., Schömig A., et al. Methylenetetrahydrofolate reductase gene C677T and A1298C polymorphisms, plasma homocysteine, folate, and vitamin B12 levels and the extent of coronary artery disease. Am J Cardiol. 93 (2004) 1201-1206
-
(2004)
Am J Cardiol.
, vol.93
, pp. 1201-1206
-
-
Kölling, K.1
Ndrepepa, G.2
Koch, W.3
Braun, S.4
Mehilli, J.5
Schömig, A.6
-
36
-
-
0033533527
-
Homocyst(e)ine and cardiovascular disease: a critical review of the epidemiologic evidence
-
Eikelboom J.W., Lonn E., Genest Jr. J., Hankey G., and Yusuf S. Homocyst(e)ine and cardiovascular disease: a critical review of the epidemiologic evidence. Ann Intern Med 131 (1999) 363-375
-
(1999)
Ann Intern Med
, vol.131
, pp. 363-375
-
-
Eikelboom, J.W.1
Lonn, E.2
Genest Jr., J.3
Hankey, G.4
Yusuf, S.5
-
37
-
-
0034023742
-
Homocysteine and atherothrombosis-mechanisms for injury
-
Thambyrajah J., and Townend J.N. Homocysteine and atherothrombosis-mechanisms for injury. Eur Heart J 21 (2000) 967-974
-
(2000)
Eur Heart J
, vol.21
, pp. 967-974
-
-
Thambyrajah, J.1
Townend, J.N.2
-
38
-
-
0030188563
-
The oxidant stress of hyperhomocyst(e)inemia
-
Loscalzo J. The oxidant stress of hyperhomocyst(e)inemia. J Clin Invest 98 (1996) 5-7
-
(1996)
J Clin Invest
, vol.98
, pp. 5-7
-
-
Loscalzo, J.1
-
39
-
-
0035906327
-
The role of folic acid and vitamin B12 in genomic stability of human cells
-
Fenech M. The role of folic acid and vitamin B12 in genomic stability of human cells. Mutat Res 475 (2001) 57-67
-
(2001)
Mutat Res
, vol.475
, pp. 57-67
-
-
Fenech, M.1
-
40
-
-
0034703084
-
Increase in plasma homocysteine associated with parallel increases in plasma S-adenosylhomocysteine and lymphocyte DNA hypomethylation
-
Yi P., Melnyk S., Pogribna M., Pogribny I.P., Hine R.J., and James S.J. Increase in plasma homocysteine associated with parallel increases in plasma S-adenosylhomocysteine and lymphocyte DNA hypomethylation. J Biol Chem 275 (2000) 29318-29323
-
(2000)
J Biol Chem
, vol.275
, pp. 29318-29323
-
-
Yi, P.1
Melnyk, S.2
Pogribna, M.3
Pogribny, I.P.4
Hine, R.J.5
James, S.J.6
-
41
-
-
0034966495
-
Plasma homocysteine, methylenetetrahydrofolate reductase mutation and carotid damage in elderly healthy women
-
Passaro A., Vanini A., Calzoni F., Alberti L., Zamboni P.F., Fellin R., et al. Plasma homocysteine, methylenetetrahydrofolate reductase mutation and carotid damage in elderly healthy women. Atherosclerosis 157 (2001) 175-180
-
(2001)
Atherosclerosis
, vol.157
, pp. 175-180
-
-
Passaro, A.1
Vanini, A.2
Calzoni, F.3
Alberti, L.4
Zamboni, P.F.5
Fellin, R.6
-
42
-
-
0032005443
-
C677T (thermolabile alanine/valine) polymorphism in methylenetetrahydrofolate reductase (MTHFR): its frequency and impact on plasma homocysteine concentration in different European populations. EARS group
-
Gudnason V., Stansbie D., Scott J., Bowron A., Nicaud V., and Humphries S. C677T (thermolabile alanine/valine) polymorphism in methylenetetrahydrofolate reductase (MTHFR): its frequency and impact on plasma homocysteine concentration in different European populations. EARS group. Atherosclerosis 136 (1998) 347-354
-
(1998)
Atherosclerosis
, vol.136
, pp. 347-354
-
-
Gudnason, V.1
Stansbie, D.2
Scott, J.3
Bowron, A.4
Nicaud, V.5
Humphries, S.6
-
43
-
-
0141590217
-
Genetic polymorphisms in folate and homocysteine metabolism as risk factors for DNA damage
-
Botto N., Andreassi M.G., Manfredi S., Masetti S., Cocci F., Colombo M.G., et al. Genetic polymorphisms in folate and homocysteine metabolism as risk factors for DNA damage. Eur J Hum Genet 11 (2003) 671-678
-
(2003)
Eur J Hum Genet
, vol.11
, pp. 671-678
-
-
Botto, N.1
Andreassi, M.G.2
Manfredi, S.3
Masetti, S.4
Cocci, F.5
Colombo, M.G.6
-
44
-
-
0035057410
-
C677T and A1298C polymorphisms of the methylenetetrahydrofolate reductase gene: incidence and effect of combined genotypes on plasma fasting and post-methionine load homocysteine in vascular disease
-
Hanson N.Q., Omer A., Yang F., and Tsai M.Y. C677T and A1298C polymorphisms of the methylenetetrahydrofolate reductase gene: incidence and effect of combined genotypes on plasma fasting and post-methionine load homocysteine in vascular disease. Clin Chem 47 (2001) 661-666
-
(2001)
Clin Chem
, vol.47
, pp. 661-666
-
-
Hanson, N.Q.1
Omer, A.2
Yang, F.3
Tsai, M.Y.4
-
45
-
-
0029806746
-
Methylenetetrahydrofolate reductase polymorphism, plasma folate, homocysteine, and risk of myocardial infarction in US physicians
-
Malinow M.R., Willett W.C., and Rozen R. Methylenetetrahydrofolate reductase polymorphism, plasma folate, homocysteine, and risk of myocardial infarction in US physicians. Circulation 94 (1996) 2410-2416
-
(1996)
Circulation
, vol.94
, pp. 2410-2416
-
-
Malinow, M.R.1
Willett, W.C.2
Rozen, R.3
-
46
-
-
0029806746
-
Methylenetetrahydrofolate reductase polymorphism, plasma folate, homocysteine, and risk of myocardial infarction in US physicians
-
Ma J., Stampfer M.J., Hennekens C.H., Frosst P., Selhub J., Horsford J., et al. Methylenetetrahydrofolate reductase polymorphism, plasma folate, homocysteine, and risk of myocardial infarction in US physicians. Circulation 94 (1996) 2410-2416
-
(1996)
Circulation
, vol.94
, pp. 2410-2416
-
-
Ma, J.1
Stampfer, M.J.2
Hennekens, C.H.3
Frosst, P.4
Selhub, J.5
Horsford, J.6
-
48
-
-
27644488218
-
Prevalence of genetic risk factors for coronary artery disease in Corsica island (France)
-
Falchi A., Giovannoni L., Piras I.S., Calo C.M., Moral P., Vona G., et al. Prevalence of genetic risk factors for coronary artery disease in Corsica island (France). Exp Mol Path 79 (2005) 210-213
-
(2005)
Exp Mol Path
, vol.79
, pp. 210-213
-
-
Falchi, A.1
Giovannoni, L.2
Piras, I.S.3
Calo, C.M.4
Moral, P.5
Vona, G.6
-
49
-
-
0031687887
-
A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity
-
Weisberg I., Tran P., Christensen B., Sibani S., and Rozen R. A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity. Mol Genet Metab 64 (1998) 169-172
-
(1998)
Mol Genet Metab
, vol.64
, pp. 169-172
-
-
Weisberg, I.1
Tran, P.2
Christensen, B.3
Sibani, S.4
Rozen, R.5
-
50
-
-
0032923453
-
A second mutation in the methylenetetrahydrofolate reductase gene and the risk of venous thrombotic disease
-
Franco R.F., Morelli V., Lourenco D., Maffei F.H., Tavella M.H., Piccinato C.E., et al. A second mutation in the methylenetetrahydrofolate reductase gene and the risk of venous thrombotic disease. Br J Haematol 105 (1999) 556-559
-
(1999)
Br J Haematol
, vol.105
, pp. 556-559
-
-
Franco, R.F.1
Morelli, V.2
Lourenco, D.3
Maffei, F.H.4
Tavella, M.H.5
Piccinato, C.E.6
-
51
-
-
0032822750
-
Methylenetetrahydrofolate reductase (MTHFR): the incidence of mutations C677T and A1298C in the Ashkenazi Jewish population
-
Rady P.L., Tyring S.K., Hudnall S.D., Vargas T., Kellner L.H., Nitowsky H., et al. Methylenetetrahydrofolate reductase (MTHFR): the incidence of mutations C677T and A1298C in the Ashkenazi Jewish population. Am J Med Genet 86 (1999) 380-384
-
(1999)
Am J Med Genet
, vol.86
, pp. 380-384
-
-
Rady, P.L.1
Tyring, S.K.2
Hudnall, S.D.3
Vargas, T.4
Kellner, L.H.5
Nitowsky, H.6
-
52
-
-
0033794925
-
Neonatal and fetal methylenetetrahydrofolate reductase genetic polymorphisms: an examination of C677T and A1298C mutations
-
Isotalo P.A., Wells G.A., and Donnelly J.G. Neonatal and fetal methylenetetrahydrofolate reductase genetic polymorphisms: an examination of C677T and A1298C mutations. Am J Hum Genet 67 (2000) 986-990
-
(2000)
Am J Hum Genet
, vol.67
, pp. 986-990
-
-
Isotalo, P.A.1
Wells, G.A.2
Donnelly, J.G.3
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