-
1
-
-
18144400600
-
Tracking of physical activity, fitness, body composition and diet from adolescence to young adulthood: The Young Hearts Project, Northern Ireland
-
Boreham, C., Robson, P. J., Gallagher, A. M., Cran, G. W., Savage, J. M. & Murray, L. J. (2004) Tracking of physical activity, fitness, body composition and diet from adolescence to young adulthood: The Young Hearts Project, Northern Ireland. Int J Behav Nutr Phys Act 1, 14.
-
(2004)
Int J Behav Nutr Phys Act
, vol.1
, pp. 14
-
-
Boreham, C.1
Robson, P.J.2
Gallagher, A.M.3
Cran, G.W.4
Savage, J.M.5
Murray, L.J.6
-
2
-
-
0027467970
-
Coronary risk factors in schoolchildren
-
Boreham, C., Savage, J. M., Primrose, D., Cran, G. & Strain, J. (1993) Coronary risk factors in schoolchildren. Arch Dis Child 68, 182-186.
-
(1993)
Arch Dis Child
, vol.68
, pp. 182-186
-
-
Boreham, C.1
Savage, J.M.2
Primrose, D.3
Cran, G.4
Strain, J.5
-
3
-
-
0033805360
-
A polymorphism (80G->A) in the reduced folate carrier gene and its associations with folate status and homocysteinemia
-
Chango, A., Emery-Fillon, N., De Courcy, G. P., Lambert, D., Pfister, M., Rosenblatt, D. S. & Nicolas, J. P. (2000) A polymorphism (80G->A) in the reduced folate carrier gene and its associations with folate status and homocysteinemia. Mol Genet Metab 70, 310-315.
-
(2000)
Mol Genet Metab
, vol.70
, pp. 310-315
-
-
Chango, A.1
Emery-Fillon, N.2
De Courcy, G.P.3
Lambert, D.4
Pfister, M.5
Rosenblatt, D.S.6
Nicolas, J.P.7
-
4
-
-
0027080461
-
Prevention of the first occurrence of neural-tube defects by periconceptional vitamin supplementation
-
Czeizel, A. E. & Dudas, I. (1992) Prevention of the first occurrence of neural-tube defects by periconceptional vitamin supplementation. N Engl J Med 327, 1832-1835.
-
(1992)
N Engl J Med
, vol.327
, pp. 1832-1835
-
-
Czeizel, A.E.1
Dudas, I.2
-
5
-
-
0242669376
-
Reduced folate carrier polymorphism (80A->G) and neural tube defects
-
De Marco, P., Calevo, M. G., Moroni, A., Merello, E., Raso, A., Finnell, R. H., Zhu, H., Andreussi, L., Cama, A. & Capra, V. (2003) Reduced folate carrier polymorphism (80A->G) and neural tube defects. Eur J Hum Genet 11, 245-252.
-
(2003)
Eur J Hum Genet
, vol.11
, pp. 245-252
-
-
De Marco, P.1
Calevo, M.G.2
Moroni, A.3
Merello, E.4
Raso, A.5
Finnell, R.H.6
Zhu, H.7
Andreussi, L.8
Cama, A.9
Capra, V.10
-
6
-
-
9244264949
-
Contribution of common polymorphisms in reduced folate carrier and gamma-glutamylhydrolase to methotrexate polyglutamate levels in patients with rheumatoid arthritis
-
Dervieux, T., Kremer, J., Lein, D. O., Capps, R., Barham, R., Meyer, G., Smith, K., Caldwell, J. & Furst, D. E. (2004) Contribution of common polymorphisms in reduced folate carrier and gamma-glutamylhydrolase to methotrexate polyglutamate levels in patients with rheumatoid arthritis. Pharmacogenetics 14, 733-739.
-
(2004)
Pharmacogenetics
, vol.14
, pp. 733-739
-
-
Dervieux, T.1
Kremer, J.2
Lein, D.O.3
Capps, R.4
Barham, R.5
Meyer, G.6
Smith, K.7
Caldwell, J.8
Furst, D.E.9
-
7
-
-
33645635701
-
Interactions among polymorphisms in folate-metabolizing genes and serum total homocysteine concentrations in a healthy elderly population
-
Devlin, A. M., Clarke, R., Birks, J., Evans, J. G. & Halsted, C. H. (2006) Interactions among polymorphisms in folate-metabolizing genes and serum total homocysteine concentrations in a healthy elderly population. Am J Clin Nutr 83, 708-713.
-
(2006)
Am J Clin Nutr
, vol.83
, pp. 708-713
-
-
Devlin, A.M.1
Clarke, R.2
Birks, J.3
Evans, J.G.4
Halsted, C.H.5
-
8
-
-
34848881628
-
Large-scale population-based metabolic phenotyping of thirteen genetic polymorphisms related to one-carbon metabolism
-
Fredriksen, A., Meyer, K., Ueland, P. M., Vollset, S. E., Grotmol, T. & Schneede, J. (2007) Large-scale population-based metabolic phenotyping of thirteen genetic polymorphisms related to one-carbon metabolism. Hum Mutat 28, 856-865.
-
(2007)
Hum Mutat
, vol.28
, pp. 856-865
-
-
Fredriksen, A.1
Meyer, K.2
Ueland, P.M.3
Vollset, S.E.4
Grotmol, T.5
Schneede, J.6
-
9
-
-
0036856206
-
A longitudinal study through adolescence to adulthood: The Young Hearts Project, Northern Ireland
-
Gallagher, A. M., Savage, J. M., Murray, L. J., Davey Smith, G., Young, I. S., Robson, P. J., Neville, C. E., Cran, G., Strain, J. J. & Boreham, C. A. (2002) A longitudinal study through adolescence to adulthood: The Young Hearts Project, Northern Ireland. Public Health 116, 332-340.
-
(2002)
Public Health
, vol.116
, pp. 332-340
-
-
Gallagher, A.M.1
Savage, J.M.2
Murray, L.J.3
Davey Smith, G.4
Young, I.S.5
Robson, P.J.6
Neville, C.E.7
Cran, G.8
Strain, J.J.9
Boreham, C.A.10
-
10
-
-
0029738540
-
The common 'thermolabile' variant of methylene tetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia
-
Harmon, D. L., Woodside, J. V., Yarnell, J. W., McMaster, D., Young, I. S., McCrum, E. E., Gey, K. F., Whitehead, A. S. & Evans, A. E. (1996) The common 'thermolabile' variant of methylene tetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia. QJM 89, 571-577. http://snp500cancer.nci.nih.gov.
-
(1996)
QJM
, vol.89
, pp. 571-577
-
-
Harmon, D.L.1
Woodside, J.V.2
Yarnell, J.W.3
McMaster, D.4
Young, I.S.5
McCrum, E.E.6
Gey, K.F.7
Whitehead, A.S.8
Evans, A.E.9
-
11
-
-
0030027668
-
Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations
-
Jacques, P. F., Bostom, A. G., Williams, R. R., Ellison, R. C., Eckfeldt, J. H., Rosenberg, I. H., Selhub, J. & Rozen, R. (1996) Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations. Circulation 93, 7-9.
-
(1996)
Circulation
, vol.93
, pp. 7-9
-
-
Jacques, P.F.1
Bostom, A.G.2
Williams, R.R.3
Ellison, R.C.4
Eckfeldt, J.H.5
Rosenberg, I.H.6
Selhub, J.7
Rozen, R.8
-
12
-
-
3042784787
-
Impact of the MTHFR C677T polymorphism on risk of neural tube defects: Case-control study
-
Kirke, P. N., Mills, J. L., Molloy, A. M., Brody, L. C., O'Leary, V. B., Daly, L., Murray, S., Conley, M., Mayne, P. D., Smith, O. & Scott, J. M. (2004) Impact of the MTHFR C677T polymorphism on risk of neural tube defects: Case-control study. BMJ 328, 1535-1536.
-
(2004)
BMJ
, vol.328
, pp. 1535-1536
-
-
Kirke, P.N.1
Mills, J.L.2
Molloy, A.M.3
Brody, L.C.4
O'Leary, V.B.5
Daly, L.6
Murray, S.7
Conley, M.8
Mayne, P.D.9
Smith, O.10
Scott, J.M.11
-
13
-
-
0038446637
-
Genetic and nutritional factors contributing to hyperhomocysteinemia in young adults
-
Kluijtmans, L. A., Young, I. S., Boreham, C. A., Murray, L., McMaster, D., McNulty, H., Strain, J. J., McPartlin, J., Scott, J. M. & Whitehead, A. S. (2003) Genetic and nutritional factors contributing to hyperhomocysteinemia in young adults. Blood 101, 2483-2488.
-
(2003)
Blood
, vol.101
, pp. 2483-2488
-
-
Kluijtmans, L.A.1
Young, I.S.2
Boreham, C.A.3
Murray, L.4
McMaster, D.5
McNulty, H.6
Strain, J.J.7
McPartlin, J.8
Scott, J.M.9
Whitehead, A.S.10
-
14
-
-
0037110469
-
Polymorphism G80A in the reduced folate carrier gene and its relationship to methotrexate plasma levels and outcome of childhood acute lymphoblastic leukemia
-
Laverdiere, C., Chiasson, S., Costea, I., Moghrabi, A. & Krajinovic, M. (2002) Polymorphism G80A in the reduced folate carrier gene and its relationship to methotrexate plasma levels and outcome of childhood acute lymphoblastic leukemia. Blood 100, 3832-3834.
-
(2002)
Blood
, vol.100
, pp. 3832-3834
-
-
Laverdiere, C.1
Chiasson, S.2
Costea, I.3
Moghrabi, A.4
Krajinovic, M.5
-
15
-
-
0033808685
-
Folic acid: Nutritional biochemistry, molecular biology, and role in disease processes
-
Lucock, M. (2000) Folic acid: Nutritional biochemistry, molecular biology, and role in disease processes. Mol Genet Metab 71, 121-138.
-
(2000)
Mol Genet Metab
, vol.71
, pp. 121-138
-
-
Lucock, M.1
-
16
-
-
0041305877
-
Membrane transport of folates
-
Matherly, L. H. & Goldman, D. I. (2003) Membrane transport of folates. Vitam Horm 66, 403-456.
-
(2003)
Vitam Horm
, vol.66
, pp. 403-456
-
-
Matherly, L.H.1
Goldman, D.I.2
-
17
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller, S. A., Dykes, D. D. & Polesky, H. F. (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16, 1215.
-
(1988)
Nucleic Acids Res
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
18
-
-
0028833677
-
Homocysteine metabolism in pregnancies complicated by neural-tube defects
-
Mills, J. L., McPartlin, J. M., Kirke, P. N., Lee, Y. J., Conley, M. R., Weir, D. G. & Scott, J. M. (1995) Homocysteine metabolism in pregnancies complicated by neural-tube defects. Lancet 345, 149-151.
-
(1995)
Lancet
, vol.345
, pp. 149-151
-
-
Mills, J.L.1
McPartlin, J.M.2
Kirke, P.N.3
Lee, Y.J.4
Conley, M.R.5
Weir, D.G.6
Scott, J.M.7
-
19
-
-
0030744634
-
Microbiological assay for serum, plasma, and red cell folate using cryopreserved, microtiter plate method
-
Molloy, A. M. & Scott, J. M. (1997) Microbiological assay for serum, plasma, and red cell folate using cryopreserved, microtiter plate method. Methods Enzymol 281, 43-53.
-
(1997)
Methods Enzymol
, vol.281
, pp. 43-53
-
-
Molloy, A.M.1
Scott, J.M.2
-
20
-
-
0037677623
-
Evaluation of genetic variants in the reduced folate carrier and in glutamate carboxypeptidase II for spina bifida risk
-
Morin, I., Devlin, A. M., Leclerc, D., Sabbaghian, N., Halsted, C. H., Finnell, R. & Rozen, R. (2003) Evaluation of genetic variants in the reduced folate carrier and in glutamate carboxypeptidase II for spina bifida risk. Mol Genet Metab 79, 197-200.
-
(2003)
Mol Genet Metab
, vol.79
, pp. 197-200
-
-
Morin, I.1
Devlin, A.M.2
Leclerc, D.3
Sabbaghian, N.4
Halsted, C.H.5
Finnell, R.6
Rozen, R.7
-
21
-
-
0025863475
-
Prevention of neural tube defects: Results of the Medical Research Council Vitamin Study
-
MRC Vitamin Study Research Group
-
MRC Vitamin Study Research Group (1991) Prevention of neural tube defects: Results of the Medical Research Council Vitamin Study. Lancet 338, 131-137.
-
(1991)
Lancet
, vol.338
, pp. 131-137
-
-
-
22
-
-
33645118135
-
Reduced folate carrier polymorphisms and neural tube defect risk
-
O'leary, V. B., Pangilinan, F., Cox, C., Parle-Mcdermott, A., Conley, M., Molloy, A. M., Kirke, P. N., Mills, J. L., Brody, L. C. & Scott, J. M. (2006) Reduced folate carrier polymorphisms and neural tube defect risk. Mol Genet Metab 87, 364-369.
-
(2006)
Mol Genet Metab
, vol.87
, pp. 364-369
-
-
O'leary, V.B.1
Pangilinan, F.2
Cox, C.3
Parle-Mcdermott, A.4
Conley, M.5
Molloy, A.M.6
Kirke, P.N.7
Mills, J.L.8
Brody, L.C.9
Scott, J.M.10
-
23
-
-
20544439668
-
Reduced folate carrier gene is a risk factor for neural tube defects in a Chinese population
-
Pei, L., Zhu, H., Ren, A., Li, Z., Hao, L. & Finnell, R. H. (2005) Reduced folate carrier gene is a risk factor for neural tube defects in a Chinese population. Birth Defects Res A Clin Mol Teratol 73, 430-433.
-
(2005)
Birth Defects Res A Clin Mol Teratol
, vol.73
, pp. 430-433
-
-
Pei, L.1
Zhu, H.2
Ren, A.3
Li, Z.4
Hao, L.5
Finnell, R.H.6
-
24
-
-
0242525248
-
Genetic susceptibility to neural tube defect pregnancy varies with offspring phenotype
-
Relton, C. L., Wilding, C. S., Jonas, P. A., Lynch, S. A., Tawn, E. J. & Burn, J. (2003) Genetic susceptibility to neural tube defect pregnancy varies with offspring phenotype. Clin Genet 64, 424-428.
-
(2003)
Clin Genet
, vol.64
, pp. 424-428
-
-
Relton, C.L.1
Wilding, C.S.2
Jonas, P.A.3
Lynch, S.A.4
Tawn, E.J.5
Burn, J.6
-
25
-
-
1842418757
-
Low erythrocyte folate status and polymorphic variation in folate-related genes are associated with risk of neural tube defect pregnancy
-
Relton, C. L., Wilding, C. S., Laffling, A. J., Jonas, P. A., Burgess, T., Binks, K., Tawn, E. J. & Burn, J. (2004) Low erythrocyte folate status and polymorphic variation in folate-related genes are associated with risk of neural tube defect pregnancy. Mol Genet Metab 81, 273-281.
-
(2004)
Mol Genet Metab
, vol.81
, pp. 273-281
-
-
Relton, C.L.1
Wilding, C.S.2
Laffling, A.J.3
Jonas, P.A.4
Burgess, T.5
Binks, K.6
Tawn, E.J.7
Burn, J.8
-
26
-
-
0037083014
-
Maternal periconceptional vitamin use, genetic variation of infant reduced folate carrier (A80G), and risk of spina bifida
-
Shaw, G. M., Lammer, E. J., Zhu, H., Baker, M. W., Neri, E. & Finnell, R. H. (2002) Maternal periconceptional vitamin use, genetic variation of infant reduced folate carrier (A80G), and risk of spina bifida. Am J Med Genet 108, 1-6.
-
(2002)
Am J Med Genet
, vol.108
, pp. 1-6
-
-
Shaw, G.M.1
Lammer, E.J.2
Zhu, H.3
Baker, M.W.4
Neri, E.5
Finnell, R.H.6
-
27
-
-
4644243438
-
Polymorphisms and haplotypes in folate-metabolizing genes and risk of non-Hodgkin lymphoma
-
Skibola, C. F., Forrest, M. S., Coppede, F., Agana, L., Hubbard, A., Smith, M. T., Bracci, P. M. & Holly, E. A. (2004) Polymorphisms and haplotypes in folate-metabolizing genes and risk of non-Hodgkin lymphoma. Blood 104, 2155-2162.
-
(2004)
Blood
, vol.104
, pp. 2155-2162
-
-
Skibola, C.F.1
Forrest, M.S.2
Coppede, F.3
Agana, L.4
Hubbard, A.5
Smith, M.T.6
Bracci, P.M.7
Holly, E.A.8
-
28
-
-
0025848779
-
Rapid high-performance liquid chromatographic assay for total homocysteine levels in human serum
-
Ubbink, J. B., Hayward Vermaak, W. J. & Bissbort, S. (1991) Rapid high-performance liquid chromatographic assay for total homocysteine levels in human serum. J Chromatogr 565, 441-446.
-
(1991)
J Chromatogr
, vol.565
, pp. 441-446
-
-
Ubbink, J.B.1
Hayward Vermaak, W.J.2
Bissbort, S.3
-
29
-
-
21844441674
-
Genetic determinants of folate status in Central Bohemia
-
Vesela, K., Pavlikova, M., Janosikova, B., Andel, M., Zvarova, J., Hyanek, J. & Kozich, V. (2005) Genetic determinants of folate status in Central Bohemia. Physiol Res 54, 295-303.
-
(2005)
Physiol Res
, vol.54
, pp. 295-303
-
-
Vesela, K.1
Pavlikova, M.2
Janosikova, B.3
Andel, M.4
Zvarova, J.5
Hyanek, J.6
Kozich, V.7
-
30
-
-
20044382841
-
Studies of reduced folate carrier 1 (RFC1) A80G and 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms with neural tube and orofacial cleft defects
-
Vieira, A. R., Murray, J. C., Trembath, D., Orioli, I. M., Castilla, E. E., Cooper, M. E., Marazita, M. L., Lennon-Graham, F. & Speer, M. (2005) Studies of reduced folate carrier 1 (RFC1) A80G and 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms with neural tube and orofacial cleft defects. Am J Med Genet A 135, 220-223.
-
(2005)
Am J Med Genet A
, vol.135
, pp. 220-223
-
-
Vieira, A.R.1
Murray, J.C.2
Trembath, D.3
Orioli, I.M.4
Castilla, E.E.5
Cooper, M.E.6
Marazita, M.L.7
Lennon-Graham, F.8
Speer, M.9
-
31
-
-
0346037346
-
The human reduced folate carrier gene is regulated by the AP2 and sp1 transcription factor families and a functional 61-base pair polymorphism
-
Whetstine, J. R., Witt, T. L. & Matherly, L. H. (2002) The human reduced folate carrier gene is regulated by the AP2 and sp1 transcription factor families and a functional 61-base pair polymorphism. J Biol Chem 277, 43873-43880.
-
(2002)
J Biol Chem
, vol.277
, pp. 43873-43880
-
-
Whetstine, J.R.1
Witt, T.L.2
Matherly, L.H.3
-
32
-
-
0037513238
-
Effects of the glutamate carboxypeptidase II (GCP2 1561C>T) and reduced folate carrier (RFC1 80G>A) allelic variants on folate and total homocysteine levels in kidney transplant patients
-
Winkelmayer, W. C., Eberle, C., Sunder-Plassmann, G. & Fodinger, M. (2003) Effects of the glutamate carboxypeptidase II (GCP2 1561C>T) and reduced folate carrier (RFC1 80G>A) allelic variants on folate and total homocysteine levels in kidney transplant patients. Kidney Int 63, 2280-2285.
-
(2003)
Kidney Int
, vol.63
, pp. 2280-2285
-
-
Winkelmayer, W.C.1
Eberle, C.2
Sunder-Plassmann, G.3
Fodinger, M.4
-
33
-
-
24744443273
-
G80A reduced folate carrier SNP modulates cellular uptake of folate and affords protection against thrombosis via a non homocysteine related mechanism
-
Yates, Z. & Lucock, M. (2005) G80A reduced folate carrier SNP modulates cellular uptake of folate and affords protection against thrombosis via a non homocysteine related mechanism. Life Sci 77, 2735-2742.
-
(2005)
Life Sci
, vol.77
, pp. 2735-2742
-
-
Yates, Z.1
Lucock, M.2
|