-
1
-
-
1842331509
-
Plasma homocysteine as a risk factor for vascular disease, The European Concerted Action Project
-
Graham, I. M., Daly, L. E., Refsum, H. M., Plasma homocysteine as a risk factor for vascular disease, The European Concerted Action Project, JAMA 1997, 277, 1775-1781.
-
(1997)
JAMA
, vol.277
, pp. 1775-1781
-
-
Graham, I.M.1
Daly, L.E.2
Refsum, H.M.3
-
2
-
-
0035098961
-
Methylenetetrahydrofolate reductase
-
Rosenblatt, D. S., Methylenetetrahydrofolate reductase, Clin. Invest. Med. 2001, 24, 56-59.
-
(2001)
Clin. Invest. Med
, vol.24
, pp. 56-59
-
-
Rosenblatt, D.S.1
-
3
-
-
0036137128
-
Methylenetetrahydrofolate reductase gene polymorphism, hyperhomocysteinemia, and cardiovascular diseases in chronic hemodialysis patients
-
Morimoto, K., Haneda, T., Okamoto, K., Ishida, H. et al., Methylenetetrahydrofolate reductase gene polymorphism, hyperhomocysteinemia, and cardiovascular diseases in chronic hemodialysis patients, Nephron 2002, 90, 43-50.
-
(2002)
Nephron
, vol.90
, pp. 43-50
-
-
Morimoto, K.1
Haneda, T.2
Okamoto, K.3
Ishida, H.4
-
4
-
-
0036237438
-
Methylenetetrahydrofolate reductase genotype, vitamin B12, and folate influence plasma homocysteine in hemodialysis patients
-
Nakamura, T., Saionji, K., Hiejima, Y., Hirayama, H. et al., Methylenetetrahydrofolate reductase genotype, vitamin B12, and folate influence plasma homocysteine in hemodialysis patients, Am. J Kidney Dis. 2002, 39, 1032-1039.
-
(2002)
Am. J Kidney Dis
, vol.39
, pp. 1032-1039
-
-
Nakamura, T.1
Saionji, K.2
Hiejima, Y.3
Hirayama, H.4
-
5
-
-
0028487161
-
Human methylenetetrahydrofolate reductase: Isolation of cDNA, mapping and mutation identification
-
Goyette, P., Sumner, J. S., Milos, R., Duncan, A. M. V. et al., Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification, Nat. Genet. 1994, 7, 195-200.
-
(1994)
Nat. Genet
, vol.7
, pp. 195-200
-
-
Goyette, P.1
Sumner, J.S.2
Milos, R.3
Duncan, A.M.V.4
-
6
-
-
0031904465
-
Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR)
-
Goyette, P., Pai, A., Milos, R., Frosst, P. et al., Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR), Mamm. Genome 1998, 9, 652-656.
-
(1998)
Mamm. Genome
, vol.9
, pp. 652-656
-
-
Goyette, P.1
Pai, A.2
Milos, R.3
Frosst, P.4
-
7
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
-
Frosst, P., Blom, H. J., Milos, R., Goyette, P. et al., A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase, Nat. Genet. 1995, 10, 111-113.
-
(1995)
Nat. Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
Goyette, P.4
-
8
-
-
0030610090
-
The mutation Ala 677-Val in the methylenetetrahydrofolate 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. et al., The mutation Ala 677-Val in the methylenetetrahydrofolate reductase gene: a risk factor for arterial disease and venous thrombosis, Thromb. Haemost. 1997, 77, 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
-
9
-
-
0032984676
-
Hyperhomocysteinemia in chronic renal disease
-
Bostom, A. G., Culleton, B. F., Hyperhomocysteinemia in chronic renal disease, J. Am. Soc. Nephrol. 1999, 10, 891-900.
-
(1999)
J. Am. Soc. Nephrol
, vol.10
, pp. 891-900
-
-
Bostom, A.G.1
Culleton, B.F.2
-
10
-
-
0033736584
-
A C677T mutation in the methylenetetrahydrofolate reductase gene modifies serum cysteine in dialysis patients
-
Kimura, H., Gejyo, F., Suzuki, S., Takeda, T. et al., A C677T mutation in the methylenetetrahydrofolate reductase gene modifies serum cysteine in dialysis patients, Am. J. Kidney Dis. 2000, 36, 925-933.
-
(2000)
Am. J. Kidney Dis
, vol.36
, pp. 925-933
-
-
Kimura, H.1
Gejyo, F.2
Suzuki, S.3
Takeda, T.4
-
11
-
-
0034964403
-
Association of two MTHFR polymorphisms with total homocysteine plasma levels in dialysis patients
-
Fodinger, M., Buchmayer, G., Heinz, A., Association of two MTHFR polymorphisms with total homocysteine plasma levels in dialysis patients, Am. J Kidney Dis. 2001, 35, 77-84.
-
(2001)
Am. J Kidney Dis
, vol.35
, pp. 77-84
-
-
Fodinger, M.1
Buchmayer, G.2
Heinz, A.3
-
12
-
-
0031971515
-
A second common mutation in the methylenetetrahydrofolate reductase gene: An additional risk factor for neural-tube defects?
-
Van Der Put, N. M., Gabreels, F., Stevens, E. M., Smeitink, J. A. et al., A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects? Am. J Hum. Genet. 1998, 62, 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
-
13
-
-
0031687887
-
A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity
-
Weisberg, I., Tran, P., Christensen, B., Sibani, S., Rozen, R., A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity, Mol. Genet. Metab. 1998, 64, 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
-
14
-
-
0032865186
-
A common mutation A1298C in human methylenetetrahydrofolate reductase gene: Association with plasma total homocysteine and folate concentrations
-
Friedman, G., Goldschimidt, N., Friedlander, Y., Yehuda, A. B. et al., A common mutation A1298C in human methylenetetrahydrofolate reductase gene: association with plasma total homocysteine and folate concentrations, J. Nutr. 1999, 129, 1656-1661.
-
(1999)
J. Nutr
, vol.129
, pp. 1656-1661
-
-
Friedman, G.1
Goldschimidt, N.2
Friedlander, Y.3
Yehuda, A.B.4
-
15
-
-
0037079957
-
Genetic polymorphisms of methylenetetrahydrofolate reductase and methionine synthase reductase in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A
-
Rady, P. L., Szucs, S., Grady, J., Hundnall, S. D. et al., Genetic polymorphisms of methylenetetrahydrofolate reductase and methionine synthase reductase in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A, Am. J. Med. Genet. 2002, 107, 162-168.
-
(2002)
Am. J. Med. Genet
, vol.107
, pp. 162-168
-
-
Rady, P.L.1
Szucs, S.2
Grady, J.3
Hundnall, S.D.4
-
16
-
-
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. 1988, 1, 1215.
-
(1988)
Nucleic Acids Res
, vol.1
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
17
-
-
0030610090
-
The mutation Ala677Val in the methylene tetrahydrofolate reductase gene: A risk factor for arterial disease and venous thrombosis
-
Arruda, V. R., Zuben, P. M., Chiaparini, L. C., AnnichinoBizzacchi, J. M., Costa, F. F., The mutation Ala677Val in the methylene tetrahydrofolate reductase gene: a risk factor for arterial disease and venous thrombosis, Thromb. Haemost. 1997, 77, 818-821.
-
(1997)
Thromb. Haemost
, vol.77
, pp. 818-821
-
-
Arruda, V.R.1
Zuben, P.M.2
Chiaparini, L.C.3
AnnichinoBizzacchi, J.M.4
Costa, F.F.5
-
18
-
-
0035057410
-
C677T and A1298C polymorphisms of the MTHFR gene: Incidence and effects of combined genotypes on plasma fasting and post-methionine load homocysteine in vascular disease
-
Hanson, N. Q., Aras, O., Yang, F., Tsai, M. Y., C677T and A1298C polymorphisms of the MTHFR gene: incidence and effects of combined genotypes on plasma fasting and post-methionine load homocysteine in vascular disease, Clin. Chem. 2001, 47, 661 -666.
-
(2001)
Clin. Chem
, vol.47
, pp. 661-666
-
-
Hanson, N.Q.1
Aras, O.2
Yang, F.3
Tsai, M.Y.4
-
20
-
-
36649017650
-
Hyperhomocysteinemia in chronic renal failure
-
Sarta, E., Perna, A. F., Lombard C., Acanfora, F. et al., Hyperhomocysteinemia in chronic renal failure, G. Ital. Nefrol. 2006, 23, 480-489.
-
(2006)
G. Ital. Nefrol
, vol.23
, pp. 480-489
-
-
Sarta, E.1
Perna, A.F.2
Lombard, C.3
Acanfora, F.4
-
21
-
-
0032986906
-
Effect of folic acid and betaine on fasting and postmethionine-loading plasma homocysteine and methionine levels in chronic haemodialysis patients
-
Van Guldener, C., Janssen, M. J. F. M., Meer, K., Donker, A. J., Stehouwer, C. D., Effect of folic acid and betaine on fasting and postmethionine-loading plasma homocysteine and methionine levels in chronic haemodialysis patients, J. Inter. Med. 1999, 245, 175-183.
-
(1999)
J. Inter. Med
, vol.245
, pp. 175-183
-
-
Van Guldener, C.1
Janssen, M.J.F.M.2
Meer, K.3
Donker, A.J.4
Stehouwer, C.D.5
-
22
-
-
0032731968
-
Evidence of altered homocysteine metabolism in chronic renal failure
-
Henning, B. F., Rielzler, R., Tepel, M., Evidence of altered homocysteine metabolism in chronic renal failure, Nephron 1999, 53, 314-322.
-
(1999)
Nephron
, vol.53
, pp. 314-322
-
-
Henning, B.F.1
Rielzler, R.2
Tepel, M.3
-
23
-
-
2442527727
-
Homocysteine metabolism in renal failure
-
Perna, A. F., Ingrosso, D., Satta, E., Lombardi, C. et al., Homocysteine metabolism in renal failure, Curr Opin Clin Nutr Metab Care, 2004, 7, 53-57.
-
(2004)
Curr Opin Clin Nutr Metab Care
, vol.7
, pp. 53-57
-
-
Perna, A.F.1
Ingrosso, D.2
Satta, E.3
Lombardi, C.4
-
24
-
-
0030946890
-
Clinical Chemistry and molecular biology of homocysteine metabolism: Un update
-
Miner, S. E. S., Evrovski, J., Cole, D. E. C., Clinical Chemistry and molecular biology of homocysteine metabolism: un update, Clin. Biochem. 1997, 30, 189-201.
-
(1997)
Clin. Biochem
, vol.30
, pp. 189-201
-
-
Miner, S.E.S.1
Evrovski, J.2
Cole, D.E.C.3
-
25
-
-
0030851289
-
Mutation (677 C to T) in the methylenetetrahydrofolate reductase gene aggravates hyperhomocysteinemia in hemodialysis patients
-
Fodinger, M., Mannhalter, C., Wolfi, G., Pabinger, I., Muller, E. et al., Mutation (677 C to T) in the methylenetetrahydrofolate reductase gene aggravates hyperhomocysteinemia in hemodialysis patients, Kidney Int. 1997, 52, 517-523.
-
(1997)
Kidney Int
, vol.52
, pp. 517-523
-
-
Fodinger, M.1
Mannhalter, C.2
Wolfi, G.3
Pabinger, I.4
Muller, E.5
-
26
-
-
0034058544
-
The C677T methylenetetrahydrofolate reductase gene mutation in hemodialysis patients
-
Kimura, H., Gejyo, F., Suzuki, S., Miyazaki, R., The C677T methylenetetrahydrofolate reductase gene mutation in hemodialysis patients, J Am. Soc. Nephrol. 2000, 11, 885-893.
-
(2000)
J Am. Soc. Nephrol
, vol.11
, pp. 885-893
-
-
Kimura, H.1
Gejyo, F.2
Suzuki, S.3
Miyazaki, R.4
-
27
-
-
0038159610
-
Homocysteine, folate, vitamin B12 levels, and C677T MTHFR mutation in children with renal failure
-
Canepa, A., Carrea, A., Caridi, L. D., Minniti, R. C., Cerone, R., et al., Homocysteine, folate, vitamin B12 levels, and C677T MTHFR mutation in children with renal failure, Pediatr. Nephrol. 2003, 18, 225-229.
-
(2003)
Pediatr. Nephrol
, vol.18
, pp. 225-229
-
-
Canepa, A.1
Carrea, A.2
Caridi, L.D.3
Minniti, R.C.4
Cerone, R.5
-
28
-
-
0036377016
-
The common mutation C677T and A1298C in the human methylenetetrahydrofolate reductase gene are associated with hyperhomocysteinemia and cardiovascular disease in hemodialysis patients
-
Haviv, Y. S., Shpichinetsky, V., Goldschimit, N., Abou Atta, I., Benyehuda, A., et al., The common mutation C677T and A1298C in the human methylenetetrahydrofolate reductase gene are associated with hyperhomocysteinemia and cardiovascular disease in hemodialysis patients, Nephron 2002, 92, 120-126.
-
(2002)
Nephron
, vol.92
, pp. 120-126
-
-
Haviv, Y.S.1
Shpichinetsky, V.2
Goldschimit, N.3
Abou Atta, I.4
Benyehuda, A.5
-
29
-
-
33748421075
-
polymorphisms in the methylenetetrahydrofolate gene: Effect of folic acid on homocysteine levels
-
Melo, S. S., Persuhn, D. C., Meirelles, M. S., Jordão, A. A., Vannucchi, H., G1793A polymorphisms in the methylenetetrahydrofolate gene: Effect of folic acid on homocysteine levels, Mol. Nutr. Food Res. 2006, 50, 769-774.
-
(1793)
Mol. Nutr. Food Res
, vol.2006
, Issue.50
, pp. 769-774
-
-
Melo, S.S.1
Persuhn, D.C.2
Meirelles, M.S.3
Jordão, A.A.4
Vannucchi, H.G.5
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