-
1
-
-
77951950464
-
Folate bioavailability: Implications for establishing recommendations and optimizing status
-
Caudill, M.A. (2010) Folate bioavailability: implications for establishing recommendations and optimizing status. Am. J. Clin. Nutr. 91, 1455S - 60S.
-
(2010)
Am. J. Clin. Nutr.
, vol.91
-
-
Caudill, M.A.1
-
2
-
-
20444431586
-
Integrating the issues of folate bioavailability, intake and metabolism in the era of fortification
-
Gregory, J., Quinlivan, E.P. and Davis, S.R. (2005) Integrating the issues of folate bioavailability, intake and metabolism in the era of fortification. Trends Food Sci. Technol. 16, 229 - 40.
-
(2005)
Trends Food Sci. Technol.
, vol.16
, pp. 229-240
-
-
Gregory, J.1
Quinlivan, E.P.2
Davis, S.R.3
-
3
-
-
33750107341
-
Choline: Critical role during fetal development and dietary requirements in adults
-
Zeisel, S.H. (2006) Choline: critical role during fetal development and dietary requirements in adults. Annu. Rev. Nutr. 26, 229 - 50.
-
(2006)
Annu. Rev. Nutr.
, vol.26
, pp. 229-250
-
-
Zeisel, S.H.1
-
4
-
-
23444435961
-
Polymorphism of the PEMT gene and susceptibility to nonalcoholic fatty liver disease (NAFLD)
-
Song, J., daCosta, K.A., Fischer, L.M., Kohlmeier, M., Kwock, L., Wang, S. and Zeisel, S.H. (2005) Polymorphism of the PEMT gene and susceptibility to nonalcoholic fatty liver disease (NAFLD). FASEB. J. 19, 1266 - 71.
-
(2005)
FASEB. J.
, vol.19
, pp. 1266-1271
-
-
Song, J.1
daCosta, K.A.2
Fischer, L.M.3
Kohlmeier, M.4
Kwock, L.5
Wang, S.6
Zeisel, S.H.7
-
5
-
-
73149092115
-
Betaine for nonalcoholic fatty liver disease: Results of a randomized placebo-controlled trial
-
Abdelmalek, M.F., Sanderson, S.O., Angulo, P., Soldevila-Pico, C., Liu, C., Peter, J., Keach, J., Cave, M., Chen, T., McClain, C.J. and Lindor, K.D. (2009) Betaine for nonalcoholic fatty liver disease: results of a randomized placebo-controlled trial. Hepatology 50, 1818 - 26.
-
(2009)
Hepatology
, vol.50
, pp. 1818-1826
-
-
Abdelmalek, M.F.1
Sanderson, S.O.2
Angulo, P.3
Soldevila-Pico, C.4
Liu, C.5
Peter, J.6
Keach, J.7
Cave, M.8
Chen, T.9
McClain, C.J.10
Lindor, K.D.11
-
6
-
-
78149479415
-
Betaine improves nonalcoholic fatty liver and associated hepatic insulin resistance: A potential mechanism for hepatoprotection by betaine
-
Kathirvel, E., Morgan, K., Nandgiri, G., Sandoval, B.C., Caudill, M.A., Bottiglieri, T., French, S.W. and Morgan, T.R. (2010) Betaine improves nonalcoholic fatty liver and associated hepatic insulin resistance: a potential mechanism for hepatoprotection by betaine. Am. J. Physiol. Gastrointest. Liver Physiol. 299, G1068 - G1077.
-
(2010)
Am. J. Physiol. Gastrointest. Liver Physiol.
, vol.299
-
-
Kathirvel, E.1
Morgan, K.2
Nandgiri, G.3
Sandoval, B.C.4
Caudill, M.A.5
Bottiglieri, T.6
French, S.W.7
Morgan, T.R.8
-
7
-
-
77955042574
-
Folate and choline interrelationships: Metabolic and potential health implications
-
(Bailey, L.B., ed.) second ed., CRC Press, Boca Raton
-
Caudill, M.A. (2009) Folate and choline interrelationships: metabolic and potential health implications. In: Folate Health and Disease. (Bailey, L.B., ed.) second ed., pp. 449, CRC Press, Boca Raton.
-
(2009)
Folate Health and Disease
, pp. 449
-
-
Caudill, M.A.1
-
8
-
-
0003844776
-
-
Institute of Medicine. National Academy of Sciences USA. National Academics Press, Washington, D.C.
-
Institute of Medicine. National Academy of Sciences USA. (1998) Dietary reference intakes for thiamin, riboflavin, niacin, vitamin B6, folate, vitamin B12, pantothenic acid, biotin and choline. National Academics Press, Washington, D.C.
-
(1998)
Dietary reference intakes for thiamin, riboflavin, niacin, vitamin B6, folate, vitamin B12, pantothenic acid, biotin and choline
-
-
-
9
-
-
0035670159
-
Bioavailability and bioefficacy of folate and folic acid in man
-
Brouwer, I.A., van Dusseldorp, M., West, C.E. and Steegers-Theunissen, R.P.M. (2001) Bioavailability and bioefficacy of folate and folic acid in man. Nutr. Res. Revs. 14, 267 - 93.
-
(2001)
Nutr. Res. Revs.
, vol.14
, pp. 267-293
-
-
Brouwer, I.A.1
van Dusseldorp, M.2
West, C.E.3
Steegers-Theunissen, R.P.M.4
-
10
-
-
85057908352
-
Genetic variation: Effect on folate metabolism and health
-
(Bailey, L.B., ed.) second ed., CRC Press, Boca Raton
-
Christensen, K.E. and Rozen R. (2009) Genetic variation: effect on folate metabolism and health. In: Folate Health and Disease. (Bailey, L.B., ed.) second ed., p. 75, CRC Press, Boca Raton.
-
(2009)
Folate Health and Disease
, pp. 75
-
-
Christensen, K.E.1
Rozen, R.2
-
11
-
-
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., Boers, G.J.H., den Heijer, M., Kluijtmans, L.A.J., van den Heuvel, L.P. and Rozen, R. (1995) A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nature Genet. 10, 111 - 3.
-
(1995)
Nature 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
Boers, G.J.H.7
den Heijer, M.8
Kluijtmans, L.A.J.9
van den Heuvel, L.P.10
Rozen, R.11
-
12
-
-
0038446637
-
Genetic and nutritional factors contributing to hyperhomocysteinemia in young adults
-
Kluijtmans, L.A.J., Young, I.S., Boreham, C.A., Murray, L, McMaster, D., McNulty, H., Strain, J.J., McPartlin, J., Scott, J.M. and Whitehead, A.S. (2003) Genetic and nutritional factors contributing to hyperhomocysteinemia in young adults. Blood 101, 2483 - 8.
-
(2003)
Blood
, vol.101
, pp. 2483-2488
-
-
Kluijtmans, L.A.J.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
-
13
-
-
0032895522
-
The structure and properties of methylenetetrahydrofolate reductase from Escherichia coli suggest how folate ameliorates human hyperhomocysteinemia
-
Guenther, B.D., Sheppard, C.A., Tran, P., Rozen, R., Matthews, R.G. and Ludwig, M.L. (1999) The structure and properties of methylenetetrahydrofolate reductase from Escherichia coli suggest how folate ameliorates human hyperhomocysteinemia. Nat. Struct. Biol. 6, 359 - 65.
-
(1999)
Nat. Struct. Biol.
, vol.6
, pp. 359-365
-
-
Guenther, B.D.1
Sheppard, C.A.2
Tran, P.3
Rozen, R.4
Matthews, R.G.5
Ludwig, M.L.6
-
14
-
-
0035909980
-
Effects of common polymorphisms on the properties of recombinant human methylenetetrahydrofolate reductase
-
Yamada, K., Chen, Z., Rozen, R., and Matthews, R.G. (2001) Effects of common polymorphisms on the properties of recombinant human methylenetetrahydrofolate reductase. PNAS 98, 14853 - 8.
-
(2001)
PNAS
, vol.98
, pp. 14853-8
-
-
Yamada, K.1
Chen, Z.2
Rozen, R.3
Matthews, R.G.4
-
15
-
-
0041326346
-
Geographical and ethnic variation of the 677C > T allele of the 5,10 methylenetetrahydrofolate reductase (MTHFR): Findings from over 7000 newborns from 16 areas world wide
-
Wilcken, B., Bamforth, F., Li, Z., Zhu, H., Ritvanen, A., Redlund, M., Stoll, C., Alembik, Y., Dott, Db. Czeizel, A.E., Gelman-Kohan, Z., Scarano, G., Bianca, S., Ettore, G., Tenconi, R., Bellato, S., Scala, I., Mutchinick, O.M., Lopez, M.A., de Walle, H., Hofstra, R., Joutchenko, L., Kavteladze, L., Bermejo, E., Martinez-Frias, M.L., Gallagher, M., Erickson, J.D., Vollset, S.E., Mastroiacovo, P., Andria, G. and Botto, L.D. (2003) Geographical and ethnic variation of the 677C > T allele of the 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas world wide. J. Med. Genet. 40, 619 - 25.
-
(2003)
J. Med. Genet.
, vol.40
-
-
Wilcken, B.1
Bamforth, F.2
Li, Z.3
Zhu, H.4
Ritvanen, A.5
Redlund, M.6
Stoll, C.7
Alembik, Y.8
Dott, D.9
Czeizel, A.E.10
Gelman-Kohan, Z.11
Scarano, G.12
Bianca, S.13
Ettore, G.14
Tenconi, R.15
Bellato, S.16
Scala, I.17
Mutchinick, O.M.18
Lopez, M.A.19
de Walle, H.20
Hofstra, R.21
Joutchenko, L.22
Kavteladze, L.23
Bermejo, E.24
Martinez-Frias, M.L.25
Gallagher, M.26
Erickson, J.D.27
Vollset, S.E.28
Mastroiacovo, P.29
Andria, G.30
Botto, L.D.31
more..
-
16
-
-
33645652119
-
Prevalence of methylenetetrahydrofolate reductase 677T and 1298C alleles and folate status: A comparative study in Mexican, West African, and European populations
-
Gueant-Rodriguez, R., Gueant, J., Debard, R., Thirion, S., Hong, L.X., Bronowicki, J., Namour, F., Chabi, N.W., Sanni, A., Anello, G., Bosco, P., Romano, C., Amouzou, E., Arrieta, H.R., Sanchez, B.E., Romano, A., Herbeth, B., Guilland, J. and Mutchinick, O.M. (2006) Prevalence of methylenetetrahydrofolate reductase 677T and 1298C alleles and folate status: a comparative study in Mexican, West African, and European populations. Am. J. Clin. Nutr. 83, 701 - 7.
-
(2006)
Am. J. Clin. Nutr.
, vol.83
-
-
Gueant-Rodriguez, R.1
Gueant, J.2
Debard, R.3
Thirion, S.4
Hong, L.X.5
Bronowicki, J.6
Namour, F.7
Chabi, N.W.8
Sanni, A.9
Anello, G.10
Bosco, P.11
Romano, C.12
Amouzou, E.13
Arrieta, H.R.14
Sanchez, B.E.15
Romano, A.16
Herbeth, B.17
Guilland, J.18
Mutchinick, O.M.19
-
17
-
-
47249164811
-
Prevalence and effects of gene-gene and gene-nutrient interactions on serum folate and serum total homocysteine concentrations in the United States: Findings from the third National Health and Nutrition Examination Survey DNA Bank
-
Yang, Q., Botto, L.D., Gallagher, M., Friedman, J.M., Sanders, C.L., Koontz, D., Nikolova, S., Erickson, J.D. and Steinberg, K. (2008) Prevalence and effects of gene-gene and gene-nutrient interactions on serum folate and serum total homocysteine concentrations in the United States: findings from the third National Health and Nutrition Examination Survey DNA Bank. Am. J. Clin. Nutr. 88, 232 - 46.
-
(2008)
Am. J. Clin. Nutr.
, vol.88
, pp. 232-246
-
-
Yang, Q.1
Botto, L.D.2
Gallagher, M.3
Friedman, J.M.4
Sanders, C.L.5
Koontz, D.6
Nikolova, S.7
Erickson, J.D.8
Steinberg, K.9
-
18
-
-
77951628918
-
Lifestyle and genetic determinants of folate and vitamin B12 levels in a general adult population
-
Thuesen, B.H., Husemoen, L.L.N., Oveson, L., Jorgensen, T., Fenger, M. and Linneberg, A. (2010) Lifestyle and genetic determinants of folate and vitamin B12 levels in a general adult population. Br. J. Nutr. 103, 1195 - 204.
-
(2010)
Br. J. Nutr.
, vol.103
, pp. 1195-1204
-
-
Thuesen, B.H.1
Husemoen, L.L.N.2
Oveson, L.3
Jorgensen, T.4
Fenger, M.5
Linneberg, A.6
-
19
-
-
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. and Schneede, J. (2007) Large-scale population-based metabolic phenotyping of thirteen genetic polymorphisms related to one-carbon metabolism. Hum. Mutat. 28, 856 - 65.
-
(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
-
20
-
-
0038671834
-
Methylenetetrahydrofolate reductase 677C > T variant modulates folate status response to controlled folate intakes in young women
-
Guinotte, C.L., Burns, M.G., Axume, J.A., Hata, H., Urrutia, T.F., Alamilla, A., McCabe, D., Singgih, A., Cogger, E.A. and Caudill, M.A. (2003) Methylenetetrahydrofolate reductase 677C > T variant modulates folate status response to controlled folate intakes in young women. J. Nutr. 133, 1272 - 80.
-
(2003)
J. Nutr.
, vol.133
, pp. 1272-1280
-
-
Guinotte, C.L.1
Burns, M.G.2
Axume, J.A.3
Hata, H.4
Urrutia, T.F.5
Alamilla, A.6
McCabe, D.7
Singgih, A.8
Cogger, E.A.9
Caudill, M.A.10
-
21
-
-
0345601004
-
Folate status response to controlled folate intake is affected by the methylenetetrahydrofolate reductase 677C > T polymorphism in young women
-
Shelnutt, K.P., Kauwell, G.P.A., Chapman, C.M., Gregory, J.F., Maneval, D.R., Browdy, A.A., Theriaque, D.W. and Bailey, L.B. (2003) Folate status response to controlled folate intake is affected by the methylenetetrahydrofolate reductase 677C > T polymorphism in young women. J. Nutr. 133, 4107 - 11.
-
(2003)
J. Nutr.
, vol.133
, pp. 4107-4111
-
-
Shelnutt, K.P.1
Kauwell, G.P.A.2
Chapman, C.M.3
Gregory, J.F.4
Maneval, D.R.5
Browdy, A.A.6
Theriaque, D.W.7
Bailey, L.B.8
-
22
-
-
38149118639
-
Folate intake at RDA levels is inadequate for Mexican American men with the methylenetetrahydrofolate reductase 677TT genotype
-
Solis, C., Veenema, K., Ivanov, A.A., Tran, S., Li, R., Wang, W., Moriarty, M., Maletz, C.V. and Caudill, M.A. (2008) Folate intake at RDA levels is inadequate for Mexican American men with the methylenetetrahydrofolate reductase 677TT genotype. J. Nutr. 138, 67 - 72.
-
(2008)
J. Nutr.
, vol.138
, pp. 67-72
-
-
Solis, C.1
Veenema, K.2
Ivanov, A.A.3
Tran, S.4
Li, R.5
Wang, W.6
Moriarty, M.7
Maletz, C.V.8
Caudill, M.A.9
-
23
-
-
33644863502
-
Riboflavin lowers homocysteine in individuals homozygous for the MTHFR 677C > T polymorphism
-
McNulty, H., Dowey, L.C., Strain, J.J., Dunne, A., Ward, M., Molloy, A.M., McAnena, L.B., Hughes, J.P., Hannon-Fletcher, M. and Scott, J.M. (2006) Riboflavin lowers homocysteine in individuals homozygous for the MTHFR 677C > T polymorphism. Circulation 113, 74 - 80.
-
(2006)
Circulation
, vol.113
, pp. 74-80
-
-
McNulty, H.1
Dowey, L.C.2
Strain, J.J.3
Dunne, A.4
Ward, M.5
Molloy, A.M.6
McAnena, L.B.7
Hughes, J.P.8
Hannon-Fletcher, M.9
Scott, J.M.10
-
24
-
-
64049097931
-
Choline intake, plasma riboflavin, and the phosphatidylethanolamine N-methyltransferase G5465 A genotype predict plasma homocysteine in folate-deplete Mexican-American men with the methylenetetrahydrofolate reductase 677TT genotype
-
Caudill, M.A., Dellschaft, N., Solis, C., Hinkis, S., Ivanov, A.A., Nash-Barboza, S., Randall, K.E., Jackson, B., Solomita, G.N. and Vermeylen, F.(2009) Choline intake, plasma riboflavin, and the phosphatidylethanolamine N-methyltransferase G5465 A genotype predict plasma homocysteine in folate-deplete Mexican-American men with the methylenetetrahydrofolate reductase 677TT genotype. J. Nutr. 139, 727 - 33.
-
(2009)
J. Nutr.
, vol.139
-
-
Caudill, M.A.1
Dellschaft, N.2
Solis, C.3
Hinkis, S.4
Ivanov, A.A.5
Nash-Barboza, S.6
Randall, K.E.7
Jackson, B.8
Solomita, G.N.9
Vermeylen, F.10
-
25
-
-
45849118692
-
The prevalence of folate-remedial MTHFR enzyme variants in humans
-
Marini, N.J., Gin, J., Ziegle, J., Keho, K.H., Ginzinger, D., Gilbert, D.A. and Rine, J. (2008). The prevalence of folate-remedial MTHFR enzyme variants in humans. PNAS 105, 8055 - 60.
-
(2008)
PNAS
, vol.105
, pp. 8055-8060
-
-
Marini, N.J.1
Gin, J.2
Ziegle, J.3
Keho, K.H.4
Ginzinger, D.5
Gilbert, D.A.6
Rine, J.7
-
26
-
-
33750118717
-
Additional food folate derived exclusively from natural sources improves folate status in women with the MTHFR 677 CC or TT genotype
-
Hung, J., Yang, T.L., Urrutia, T.F., Li, R., Perry, C.A., Hata, H., Cogger, E.A., Moriarty, D.J. and Caudill, M.A. (2006) Additional food folate derived exclusively from natural sources improves folate status in women with the MTHFR 677 CC or TT genotype. J. Nutr. Biochem. 17, 728 - 34.
-
(2006)
J. Nutr. Biochem.
, vol.17
, pp. 728-734
-
-
Hung, J.1
Yang, T.L.2
Urrutia, T.F.3
Li, R.4
Perry, C.A.5
Hata, H.6
Cogger, E.A.7
Moriarty, D.J.8
Caudill, M.A.9
-
27
-
-
18444363017
-
Methylenetetrahydrofolate reductase 677C->T genotype modulates homocysteine responses to a folate-rich diet or a low-dose folic acid supplement: A randomized control trial
-
Ashfield-Watt, P.A.L., Pullin, C.H., Whiting, J.M, Clark, Z.E., Moat, S.J., Newcombe, R.G., Burr, M.L., Lewis, M.J., Powers, H.J. and McDowell, I.F.W. (2002) Methylenetetrahydrofolate reductase 677C->T genotype modulates homocysteine responses to a folate-rich diet or a low-dose folic acid supplement: a randomized control trial. Am. J. Clin. Nutr. 76, 180 - 6.
-
(2002)
Am. J. Clin. Nutr.
, vol.76
, pp. 180-186
-
-
Ashfield-Watt, P.A.L.1
Pullin, C.H.2
Whiting, J.M.3
Clark, Z.E.4
Moat, S.J.5
Newcombe, R.G.6
Burr, M.L.7
Lewis, M.J.8
Powers, H.J.9
McDowell, I.F.W.10
-
28
-
-
0031687887
-
A Second Genetic Polymorphism in Methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity
-
Weisberg, I., Tran, P., Christensen, B., Sahar, S. and Rozen, R. (1998) A Second Genetic Polymorphism in Methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity. Mol. Genet. Metab. 64, 169 - 172.
-
(1998)
Mol. Genet. Metab.
, vol.64
, pp. 169-172
-
-
Weisberg, I.1
Tran, P.2
Christensen, B.3
Sahar, S.4
Rozen, R.5
-
29
-
-
0031971515
-
A second common mutation in the methylenetetrahydrofolate reductase gene: An additional risk factor for neural-tube defects?
-
van der Put, N.M.J., Gabreels, F., Stevens, E.M.B., Smeitink, J.A.M., Trijbels, F.J.M., Eskes, T.K.A.B., van den Heuvel, L.P. and Blom, H.J. (1998) A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects? Am. J. Hum. Genet. 62, 1044 - 51.
-
(1998)
Am. J. Hum. Genet.
, vol.62
-
-
van der Put, N.M.J.1
Gabreels, F.2
Stevens, E.M.B.3
Smeitink, J.A.M.4
Trijbels, F.J.M.5
Eskes, T.K.A.B.6
van den Heuvel, L.P.7
Blom, H.J.8
-
30
-
-
33645081745
-
Human methylenetetrahydrofolate reductase pharmacogenomics: Gene resequencing and functional genomics
-
Martin, Y.N., Salavaggione, O.E., Eckloff, B.W., Wieben, E.D., Schaid, D.J. and Weinshilboum, R.M. (2006) Human methylenetetrahydrofolate reductase pharmacogenomics: gene resequencing and functional genomics. Pharma. & Geno. 16, 265 - 77.
-
(2006)
Pharma. & Geno.
, vol.16
, pp. 265-277
-
-
Martin, Y.N.1
Salavaggione, O.E.2
Eckloff, B.W.3
Wieben, E.D.4
Schaid, D.J.5
Weinshilboum, R.M.6
-
31
-
-
0037276240
-
Genotype and haplotype distributions of MTHFR 677C > T and 1298A > C single nucleotide polymorphisms: A meta-analysis
-
Ogino, S. and Wilson, R.B. (2003) Genotype and haplotype distributions of MTHFR 677C > T and 1298A > C single nucleotide polymorphisms: a meta-analysis. J. Hum. Genet. 48, 1 - 7.
-
(2003)
J. Hum. Genet.
, vol.48
, pp. 1-7
-
-
Ogino, S.1
Wilson, R.B.2
-
32
-
-
33947239251
-
Functional inference of the methylenetetrahydrofolate reductase 677 C > T and 1298A>C polymorphisms from a large-scale epidemiological study
-
Ulvik, A., Ueland, P.M., Fredriksen, A., Meyer, K., Vollset, S.E., Hoff, G. and Schneede, J. (2007) Functional inference of the methylenetetrahydrofolate reductase 677 C > T and 1298A>C polymorphisms from a large-scale epidemiological study. Hum. Genet. 121, 57 - 64.
-
(2007)
Hum. Genet.
, vol.121
, pp. 57-64
-
-
Ulvik, A.1
Ueland, P.M.2
Fredriksen, A.3
Meyer, K.4
Vollset, S.E.5
Hoff, G.6
Schneede, J.7
-
33
-
-
33751244559
-
Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption
-
Qiu, A., Jansen, M., Sakaris, A., Min, S.H., Chattopadhyay, S., Tsai, E., Sandoval, C., Zhao, R., Akabas, M.H. and Goldman, I.D. (2006) Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption. Cell 127, 917 - 28.
-
(2006)
Cell
, vol.127
, pp. 917-928
-
-
Qiu, A.1
Jansen, M.2
Sakaris, A.3
Min, S.H.4
Chattopadhyay, S.5
Tsai, E.6
Sandoval, C.7
Zhao, R.8
Akabas, M.H.9
Goldman, I.D.10
-
34
-
-
34548026299
-
The Spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption
-
Zhao, R., Min, S.H., Qui, A., Sakaris, A., Goldberg, G.L., Sandoval, C., Malatack, J.J., Rosenblatt, D.S. and Goldman, I.D. (2007) The Spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption. Blood 110, 1147 - 52.
-
(2007)
Blood
, vol.110
, pp. 1147-1152
-
-
Zhao, R.1
Min, S.H.2
Qui, A.3
Sakaris, A.4
Goldberg, G.L.5
Sandoval, C.6
Malatack, J.J.7
Rosenblatt, D.S.8
Goldman, I.D.9
-
35
-
-
0033805360
-
A polymorphism (80G>A) in the reduced folate carrier gene and its associations with folate status and homocysteinemia
-
Chango, A., Emery-Fillon, N., Potier de Courcy, G., Lambert, D., Pfister, M., Rosenblatt, D.S. and 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 - 15.
-
(2000)
Mol. Genet. Metab.
, vol.70
, pp. 310-315
-
-
Chango, A.1
Emery-Fillon, N.2
Potier de Courcy, G.3
Lambert, D.4
Pfister, M.5
Rosenblatt, D.S.6
Nicolas, J.P.7
-
36
-
-
0035187308
-
Single nucleotide polymorphisms in the human reduced folate carrier: Characterization of a high-frequency G/A variant at position 80 and transport properties of the His(27) and Arg (27) carriers
-
Whetstine, J.R., Gifford, A.J., Witt, T., Liu, X.Y., Flatley, R.M., Norris, M., Haber, M., Taub, J.W., Ravindranath, Y. and Matherly, L.H. (2001) Single nucleotide polymorphisms in the human reduced folate carrier: characterization of a high-frequency G/A variant at position 80 and transport properties of the His(27) and Arg (27) carriers. Clin. Cancer Res. 7, 3416 - 22.
-
(2001)
Clin. Cancer Res.
, vol.7
, pp. 3416-3422
-
-
Whetstine, J.R.1
Gifford, A.J.2
Witt, T.3
Liu, X.Y.4
Flatley, R.M.5
Norris, M.6
Haber, M.7
Taub, J.W.8
Ravindranath, Y.9
Matherly, L.H.10
-
37
-
-
68549104398
-
The reduced folate carrier (SLC19 A1) c. 80G>A polymorphism is associated with red cell folate concentrations among women
-
Stanislawska-Sachadyn, A., Mitchell, L.E., Woodside, J.V., Buckley, P.T., Kealey, C., Young, I.S., Scott, J.M., Murray, L., Boreham, C.A., McNulty, H., Strain, J.J. and Whitehead, A.S. (2009) The reduced folate carrier (SLC19 A1) c. 80G>A polymorphism is associated with red cell folate concentrations among women. Ann. Hum. Genet. 73, 484 - 491.
-
(2009)
Ann. Hum. Genet.
, vol.73
, pp. 484-491
-
-
Stanislawska-Sachadyn, A.1
Mitchell, L.E.2
Woodside, J.V.3
Buckley, P.T.4
Kealey, C.5
Young, I.S.6
Scott, J.M.7
Murray, L.8
Boreham, C.A.9
McNulty, H.10
Strain, J.J.11
Whitehead, A.S.12
-
38
-
-
54049150738
-
Relationships between gene polymorphisms of folate-related proteins and vitamins and metabolites in pregnant women and neonates
-
Lopreato, F.R., Stabler, S.P., Carvalho, F.R., Hirata, R.D.C., Hirata, M.H., Robi, D.L., Sampaio-Neto, L.F., Allen, R.H. and Guerra-Shinohara, E.M. (2008) Relationships between gene polymorphisms of folate-related proteins and vitamins and metabolites in pregnant women and neonates. Clin. Chim. Acta 398, 135 - 9.
-
(2008)
Clin. Chim. Acta
, vol.398
, pp. 135-139
-
-
Lopreato, F.R.1
Stabler, S.P.2
Carvalho, F.R.3
Hirata, R.D.C.4
Hirata, M.H.5
Robi, D.L.6
Sampaio-Neto, L.F.7
Allen, R.H.8
Guerra-Shinohara, E.M.9
-
39
-
-
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. and 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 - 13.
-
(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
-
40
-
-
38049060817
-
Folic acid, Vitamin B-12, Vitamin B-6
-
(Stipanuk, M., ed.), second ed., Saunders Elsevier, St. Louis, MO
-
Shane, B. (2006) Folic acid, Vitamin B-12, Vitamin B-6. In: Biochemical, Physiological, Molecular Aspects of Human Nutrition.(Stipanuk, M., ed.) second ed., pp.693, Saunders Elsevier, St. Louis, MO.
-
(2006)
Biochemical, Physiological, Molecular Aspects of Human Nutrition
, pp. 693
-
-
Shane, B.1
-
41
-
-
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., Peng, K., Shane, B., Evans, A.E. and Whitehead, A.S. (1999) Methionine synthase D919G polymorphism is a significant but modest determinant of circulating homocysteine concentrations. Genet. Epidemiol. 17, 298 - 309.
-
(1999)
Genet. 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
Peng, K.7
Shane, B.8
Evans, A.E.9
Whitehead, A.S.10
-
42
-
-
49349102119
-
Association between decreased vitamin levels and MTHFR, MTR and MTRR gene polymorphisms as determinants for elevated total homocysteine concentrations in pregnant women
-
Barbosa, P.R., Stabler, S.P., Machado, A.L.K., Braga, R.C., Hirata, R.D.C., Hirata, M.H., Sampaio-Neto, L.F., Allen, R.H. and Guerra-Shinohara, E.M. (2008) Association between decreased vitamin levels and MTHFR, MTR and MTRR gene polymorphisms as determinants for elevated total homocysteine concentrations in pregnant women. Eur. J. Clin. Nutr. 62, 1010 - 21.
-
(2008)
Eur. J. Clin. Nutr.
, vol.62
, pp. 1010-1021
-
-
Barbosa, P.R.1
Stabler, S.P.2
Machado, A.L.K.3
Braga, R.C.4
Hirata, R.D.C.5
Hirata, M.H.6
Sampaio-Neto, L.F.7
Allen, R.H.8
Guerra-Shinohara, E.M.9
-
43
-
-
7944239638
-
Methionine synthase reductase 66 A>G polymorphism is associated with increased plasma homocysteine concentration when combined with the homozygous methylenetetrahydrofolate reductase 677C > T variant
-
Vaughn, J.D., Bailey, L.B., Shelnutt, K.P., von-Castel Dunwoody, K.M., Maneval, D.R., Davis, S.R., Quinlivan, E.P., Gregory, J.F., Theriaque, D.W. and Kauwell, G.P.A. (2004) Methionine synthase reductase 66 A>G polymorphism is associated with increased plasma homocysteine concentration when combined with the homozygous methylenetetrahydrofolate reductase 677C > T variant. J. Nutr. 134, 2985 - 90.
-
(2004)
J. Nutr.
, vol.134
, pp. 2985-2990
-
-
Vaughn, J.D.1
Bailey, L.B.2
Shelnutt, K.P.3
von-Castel Dunwoody, K.M.4
Maneval, D.R.5
Davis, S.R.6
Quinlivan, E.P.7
Gregory, J.F.8
Theriaque, D.W.9
Kauwell, G.P.A.10
-
44
-
-
0942290719
-
New 19bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR): A risk factor for spina bifida acting in mothers during pregnancy?
-
Johnson, W.G., Stenroos, E.S., Spychala, J.R., Chatkput, S., Ming, S.X. and Buyske, S. (2004) New 19bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR): a risk factor for spina bifida acting in mothers during pregnancy? Am. J. Med. Genet. 124 A, 339 - 45.
-
(2004)
Am. J. Med. Genet.
, vol.124 A
, pp. 339-345
-
-
Johnson, W.G.1
Stenroos, E.S.2
Spychala, J.R.3
Chatkput, S.4
Ming, S.X.5
Buyske, S.6
-
45
-
-
33845531853
-
Molecular genetic analysis of the human dihydrofolate reductase gene: Relation with plasma total homocysteine, serum and red blood cell folate levels
-
Gellekink, H., Blom, H.J., van der Linden, I.J.M. and den Heijer, M. (2007) Molecular genetic analysis of the human dihydrofolate reductase gene: relation with plasma total homocysteine, serum and red blood cell folate levels. Euro. J. Hum. Genet.15, 103 - 7.
-
(2007)
Euro. J. Hum. Genet.
, vol.15
-
-
Gellekink, H.1
Blom, H.J.2
van der Linden, I.J.M.3
den Heijer, M.4
-
46
-
-
34147122502
-
A functional 19-base pair deletion polymorphism of dihydrofolate reductase (DHFR) and risk of breast cancer in multivitamin users
-
Xu, X., Gammon, M.D., Wetmur, J.G., Rao, M., Gaudet, M.M, Teitelbaum, S.L., Britton, J.A., Neugut, A.I., Santella, R.M. and Chen, J. (2007) A functional 19-base pair deletion polymorphism of dihydrofolate reductase (DHFR) and risk of breast cancer in multivitamin users. Am. J. Clin. Nutr. 85, 1098 - 102.
-
(2007)
Am. J. Clin. Nutr.
, vol.85
, pp. 1098-1102
-
-
Xu, X.1
Gammon, M.D.2
Wetmur, J.G.3
Rao, M.4
Gaudet, M.M.5
Teitelbaum, S.L.6
Britton, J.A.7
Neugut, A.I.8
Santella, R.M.9
Chen, J.10
-
47
-
-
57349115474
-
A 19-base pair deletion polymorphism in dihydrofolate reductase is associated with increased unmetabolized folic acid in plasma and decreased red blood cell folate
-
Kalmbach, R.D., Choumenkovitch, S.F., Troen, A.P., Jacques, P.F., D'Agostino, R. and Selhub, J. (2008) A 19-base pair deletion polymorphism in dihydrofolate reductase is associated with increased unmetabolized folic acid in plasma and decreased red blood cell folate. J. Nutr. 138, 2323 - 7.
-
(2008)
J. Nutr.
, vol.138
, pp. 2323-2327
-
-
Kalmbach, R.D.1
Choumenkovitch, S.F.2
Troen, A.P.3
Jacques, P.F.4
D'Agostino, R.5
Selhub, J.6
-
48
-
-
34249903333
-
The 19-bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR) may decrease rather than increase risk for spina bifi da in the Irish population
-
Parle-McDermott, A., Pangilinan, F., Mills, J.L., Kirke, P.N., Gibney, E.R., Troendle, J., O'Leary, V.B., Molloy, A.M., Conley, M., Scott, J.M. and Brody, L.C. (2007) The 19-bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR) may decrease rather than increase risk for spina bifi da in the Irish population. Am. J. Med. Genet. part A. 143 A, 1174 - 80.
-
(2007)
Am. J. Med. Genet. part A.
, vol.143 A
, pp. 1174-1180
-
-
Parle-Mcdermott, A.1
Pangilinan, F.2
Mills, J.L.3
Kirke, P.N.4
Gibney, E.R.5
Troendle, J.6
O'Leary, V.B.7
Molloy, A.M.8
Conley, M.9
Scott, J.M.10
Brody, L.C.11
-
49
-
-
34047248403
-
Variation and expression of dihydrofolate reductase (DHFR) in relation to spina bifida
-
van der Linden, I.J.M., Nguyen, U., Heil, S.G., Franke, B., Vloet, S., Gellekink, H., den Heijer, M. and Blom, H.J. (2007) Variation and expression of dihydrofolate reductase (DHFR) in relation to spina bifida. Mol. Gen. & Metab. 9, 98 - 103.
-
(2007)
Mol. Gen. & Metab.
, vol.9
, pp. 98-103
-
-
van der Linden, I.J.M.1
Nguyen, U.2
Heil, S.G.3
Franke, B.4
Vloet, S.5
Gellekink, H.6
den Heijer, M.7
Blom, H.J.8
-
50
-
-
41149145923
-
An insertion/deletion polymorphism of the dihydrofolate reductase (DHFR) gene is associated with serum and red blood cell folate concentrations in women
-
Stanislawska-Sachadyn, A., Brown, K.S., Mitchell, L.E., Woodside, J.V., Young, I.S., Scott, J.M., Murray, L., Boreham, C.A., McNulty, H., Strain, J.J. and Whitehead, A.S. (2008) An insertion/deletion polymorphism of the dihydrofolate reductase (DHFR) gene is associated with serum and red blood cell folate concentrations in women. Hum. Genet. 123, 289 - 95.
-
(2008)
Hum. Genet.
, vol.123
, pp. 289-295
-
-
Stanislawska-Sachadyn, A.1
Brown, K.S.2
Mitchell, L.E.3
Woodside, J.V.4
Young, I.S.5
Scott, J.M.6
Murray, L.7
Boreham, C.A.8
McNulty, H.9
Strain, J.J.10
Whitehead, A.S.11
-
51
-
-
70349324816
-
The extremely slow and variable activity of dihydrofolate reductase in human liver and its implications for high folic acid intake
-
Bailey, S.W. and Ayling, J.E. (2009) The extremely slow and variable activity of dihydrofolate reductase in human liver and its implications for high folic acid intake. PNAS 106, 15424 - 9.
-
(2009)
PNAS
, vol.106
, pp. 15424-9
-
-
Bailey, S.W.1
Ayling, J.E.2
-
52
-
-
85057943345
-
Folate biochemical pathways and their regulation
-
(Bailey, L.B., ed.) second ed., CRC Press, Boca Raton, FL
-
Stover, P.J. (2009) Folate biochemical pathways and their regulation. In: Folate Health and Disease. (Bailey, L.B., ed.) second ed., p. 49, CRC Press, Boca Raton, FL.
-
(2009)
Folate Health and Disease
, pp. 49
-
-
Stover, P.J.1
-
53
-
-
0031969348
-
Molecular genetic ana lysis of the gene encoding the trifunctional enzyme MTHFD (me-thylenetetrahydrofolate-dehydrogenase, methenylte-tra hydrofolate-cyclohydrolase, formyltetrahydrofola-te synthetase) in patients with neural tube defects
-
Hol, F.A., van der Put, N.M.J., Geurds, M.P.A., Heil, S.G., Trijbels, F.J.M., Hamel, B.C.J., Mariman, E.C.M. and Blom, H.J. (1998) Molecular genetic ana lysis of the gene encoding the trifunctional enzyme MTHFD (me-thylenetetrahydrofolate-dehydrogenase, methenylte-tra hydrofolate-cyclohydrolase, formyltetrahydrofola-te synthetase) in patients with neural tube defects. Clin. Genet. 53, 119 - 25.
-
(1998)
Clin. Genet.
, vol.53
, pp. 119-125
-
-
Hol, F.A.1
van der Put, N.M.J.2
Geurds, M.P.A.3
Heil, S.G.4
Trijbels, F.J.M.5
Hamel, B.C.J.6
Mariman, E.C.M.7
Blom, H.J.8
-
54
-
-
27644581598
-
Genetic variation of folate-mediated one-carbon transfer pathways predicts susceptibility to choline deficiency in humans
-
Kohlmeier, M. da Costa, K., Fischer, L.M. and Zeisel, S.H. (2005) Genetic variation of folate-mediated one-carbon transfer pathways predicts susceptibility to choline deficiency in humans. PNAS 102, 16025 - 30.
-
(2005)
PNAS
, vol.102
-
-
Kohlmeier, M.1
da Costa, K.2
Fischer, L.M.3
Zeisel, S.H.4
-
55
-
-
62149129730
-
Genetic variants in phosphatidyletha-nolami ne N-methyltransferase (PEMT) and me-thylenetetrahydrofolate dehydrogenase (MTHFD1) influence biomarkers of choline metabolism when folate intake is restricted
-
Ivanov, A., Nash-Barboza, S., Hinkis, S. and Caudill, M.A. (2009) Genetic variants in phosphatidyletha-nolami ne N-methyltransferase (PEMT) and me-thylenetetrahydrofolate dehydrogenase (MTHFD1) influence biomarkers of choline metabolism when folate intake is restricted. JADA 109, 313 - 8.
-
(2009)
JADA
, vol.109
, pp. 313-318
-
-
Ivanov, A.1
Nash-Barboza, S.2
Hinkis, S.3
Caudill, M.A.4
-
56
-
-
34547782307
-
Phosphatidylethanolamine N-methyltransferase (PEMT) gene expression is induced by estrogen in human and mouse primary hepatocytes
-
Resseguie, M., Song, J.N., Niculescu, M.D., da Costa, K.A., Randall, T.A. and Zeisel, S.H. (2007) Phosphatidylethanolamine N-methyltransferase (PEMT) gene expression is induced by estrogen in human and mouse primary hepatocytes. FASEB J. 21, 2622 - 32.
-
(2007)
FASEB J.
, vol.21
, pp. 2622-2632
-
-
Resseguie, M.1
Song, J.N.2
Niculescu, M.D.3
da Costa, K.A.4
Randall, T.A.5
Zeisel, S.H.6
-
57
-
-
59749093930
-
The MTHFD1 p.Arg653Gln variant alters enzyme function and increases risk for congenital heart defects
-
Christensen, K.E., Rohlicek, C.V., Andelfinger, G.U., Michaud, J., Bigras, J., Richter, A., MacKenzie, R.E. and Rozen, R. (2009) The MTHFD1 p.Arg653Gln variant alters enzyme function and increases risk for congenital heart defects. Hum. Mutat. 30, 212 - 20.
-
(2009)
Hum. Mutat.
, vol.30
, pp. 212-220
-
-
Christensen, K.E.1
Rohlicek, C.V.2
Andelfinger, G.U.3
Michaud, J.4
Bigras, J.5
Richter, A.6
Mackenzie, R.E.7
Rozen, R.8
-
58
-
-
38749098623
-
Folate intake and the MTHFR C677T genotype influence choline status in young Mexican American women
-
Abratte, C.M., Wang, W., Li, R., Moriarty, D.J. and Caudill, M.A. (2008) Folate intake and the MTHFR C677T genotype influence choline status in young Mexican American women. J. Nutr. Biochem. 19, 158 - 65.
-
(2008)
J. Nutr. Biochem.
, vol.19
, pp. 158-165
-
-
Abratte, C.M.1
Wang, W.2
Li, R.3
Moriarty, D.J.4
Caudill, M.A.5
-
59
-
-
51749099188
-
Adequate intake levels of choline are sufficient for preventing elevations in serum markers of liver dysfunction in Mexican American men but are not optimal for minimizing plasma total homocysteine after a methionine load
-
Veenema, K., Solis, C., Li, R., Wange, W., Maletz, C.V., Abratte, C. and Caudill, M.A. (2008) Adequate intake levels of choline are sufficient for preventing elevations in serum markers of liver dysfunction in Mexican American men but are not optimal for minimizing plasma total homocysteine after a methionine load. Am. J. Clin. Nutr. 88, 685 - 92.
-
(2008)
Am. J. Clin. Nutr.
, vol.88
-
-
Veenema, K.1
Solis, C.2
Li, R.3
Wange, W.4
Maletz, C.V.5
Abratte, C.6
Caudill, M.A.7
-
60
-
-
57049125142
-
Choline status is not a reliable indicator of moderate changes in dietary choline consumption in premenopausal women
-
Abratte, C.M., Wang, W., Li, R., Axume, J., Moriarty, D.J. and Caudill, M.A. (2009) Choline status is not a reliable indicator of moderate changes in dietary choline consumption in premenopausal women. J. Nutr. Biochem. 20, 62 - 9.
-
(2009)
J. Nutr. Biochem.
, vol.20
, pp. 62-69
-
-
Abratte, C.M.1
Wang, W.2
Li, R.3
Axume, J.4
Moriarty, D.J.5
Caudill, M.A.6
-
61
-
-
77951458462
-
Choline intake exceeding current dietary recommendations preserves markers of cellular methylation in a genetic subgroup of folate-compromised men
-
Shin, W., Yan, J., Abratte, C.M., Vermeylen, F. and Caudill, M.A. (2010) Choline intake exceeding current dietary recommendations preserves markers of cellular methylation in a genetic subgroup of folate-compromised men. J. Nutr. 140, 975 - 80.
-
(2010)
J. Nutr.
, vol.140
, pp. 975-980
-
-
Shin, W.1
Yan, J.2
Abratte, C.M.3
Vermeylen, F.4
Caudill, M.A.5
-
62
-
-
79251524576
-
MTHFR C677T genotype influences the isotopic enrichment of one-carbon metabolites in folate-compromised men consuming d9-choline
-
Yan, J., Wang, W., Gregory, J.F., Malysheva, O., Brenna, J.T., Stabler, S.P., Allen, R.H. and Caudill, M.A. MTHFR C677T genotype influences the isotopic enrichment of one-carbon metabolites in folate-compromised men consuming d9-choline. Am. J. Clin. Nutr. 2011; 93: 348 - 55.
-
(2011)
Am. J. Clin. Nutr.
, vol.93
-
-
Yan, J.1
Wang, W.2
Gregory, J.F.3
Malysheva, O.4
Brenna, J.T.5
Stabler, S.P.6
Allen, R.H.7
Caudill, M.A.8
-
63
-
-
72249114913
-
One-carbon metabolism-genome interactions in folate-associated pathologies
-
Stover, P.J. (2009) One-carbon metabolism-genome interactions in folate-associated pathologies. J. Nutr. 139, 2402 - 2405.
-
(2009)
J. Nutr.
, vol.139
, pp. 2402-2405
-
-
Stover, P.J.1
-
64
-
-
35548959261
-
B-vitamins, genotype and disease causality
-
Haggarty, P. (2007) B-vitamins, genotype and disease causality. Proc. Nutr. Soc. 66, 539 - 47.
-
(2007)
Proc. Nutr. Soc.
, vol.66
, pp. 539-547
-
-
Haggarty, P.1
-
65
-
-
77951702343
-
Genetic heterogeneity in human disease
-
McClellan, J. and King, M.C. (2010) Genetic heterogeneity in human disease. Cell. 141, 210 - 17.
-
(2010)
Cell.
, vol.141
, pp. 210-217
-
-
McClellan, J.1
King, M.C.2
-
66
-
-
74049120835
-
Total folate and folic acid intake from foods and dietary supplements in the United States: 2003 - 2006.
-
Bailey, R.L., Dodd, K.W., Gahche, J.J., Dwyer, J.T., McDowell, M.A., Yetley, E.A., Sempos, C.A., Burt, V.L., Radimer, K.L. and Picciano, M.F. (2010) Total folate and folic acid intake from foods and dietary supplements in the United States: 2003 - 2006. Am. J. Clin. Nutr. 9, 231 - 7.
-
(2010)
Am. J. Clin. Nutr.
, vol.9
, pp. 231-237
-
-
Bailey, R.L.1
Dodd, K.W.2
Gahche, J.J.3
Dwyer, J.T.4
McDowell, M.A.5
Yetley, E.A.6
Sempos, C.A.7
Burt, V.L.8
Radimer, K.L.9
Picciano, M.F.10
-
67
-
-
58649098775
-
Clinical utility of genotyping the 677C > T variant of methylenetetrahydrofolate reductase in humans is decreased in the post-folic acid fortifi cation era
-
Tsai, M.Y., Loria, C.M., Cao, J., Kim, Y., Siscovick, D., Schreiner, P.J. and Hanson, N.Q. (2009) Clinical utility of genotyping the 677C > T variant of methylenetetrahydrofolate reductase in humans is decreased in the post-folic acid fortifi cation era. J. Nutr. 139, 33 - 7.
-
(2009)
J. Nutr.
, vol.139
, pp. 33-37
-
-
Tsai, M.Y.1
Loria, C.M.2
Cao, J.3
Kim, Y.4
Siscovick, D.5
Schreiner, P.J.6
Hanson, N.Q.7
-
68
-
-
79953786557
-
DRI research synthesis workshop summary
-
Institute of Medicine. National Academy of Sciences USA, National Academies Press, Washington, D.C.
-
Institute of Medicine. National Academy of Sciences USA. (2006) DRI research synthesis workshop summary. Dietary reference intakes for thiamin, riboflavin, niacin, vitamin B6, folate, vitamin B12, pantothenic acid, biotin and choline. pp. 35 - 48, National Academies Press, Washington, D.C.
-
(2006)
Dietary reference intakes for thiamin, riboflavin, niacin, vitamin B6, folate, vitamin B12, pantothenic acid, biotin and choline
-
-
-
69
-
-
34047182610
-
Human nutrition and genetic variation
-
Stover, P.J. (2007) Human nutrition and genetic variation. Food Nutr. Bull. 28, S101 - 15.
-
(2007)
Food Nutr. Bull.
, vol.28
-
-
Stover, P.J.1
-
70
-
-
63649102730
-
Does the MTHFR 677C > T variant affect the Recommended Dietary Allowance for folate in the US population?
-
Robitaille, J., Hamner, H.C., Cogswell, M.E. and Yang, Q. (2009) Does the MTHFR 677C > T variant affect the Recommended Dietary Allowance for folate in the US population? Am. J. Clin. Nutr. 89, 1269 - 73.
-
(2009)
Am. J. Clin. Nutr.
, vol.89
-
-
Robitaille, J.1
Hamner, H.C.2
Cogswell, M.E.3
Yang, Q.4
|