-
1
-
-
70449245071
-
Study of somatic chromosomes from 9 mongoloid children
-
Lejeune J, Gautier M, Turpin R (1959) Study of somatic chromosomes from 9 mongoloid children. C R Hebd Seances Acad Sci 248(11):1721-1722
-
(1959)
C R Hebd Seances Acad Sci
, vol.248
, Issue.11
, pp. 1721-1722
-
-
Lejeune, J.1
Gautier, M.2
Turpin, R.3
-
2
-
-
0034969415
-
Homocysteine metabolism in children with Down syndrome: In vitro modulation
-
Pogribna M, Melnyk S, Pogribny I, Chango A, Yi P, James J (2001) Homocysteine metabolism in children with Down syndrome: in vitro modulation. Am J Hum Genet 69(1):88-95
-
(2001)
Am J Hum Genet
, vol.69
, Issue.1
, pp. 88-95
-
-
Pogribna, M.1
Melnyk, S.2
Pogribny, I.3
Chango, A.4
Yi, P.5
James, J.6
-
3
-
-
34547120441
-
Plasma amino acids and neopterin in healthy persons with Down's syndrome
-
Coppus AW, Fekkes D, Verhoeven WM, Tuinier S, Egger JI, Van Duijn CM (2007) Plasma amino acids and neopterin in healthy persons with Down's syndrome. J Neural Transm 114(8):1041-1045
-
(2007)
J Neural Transm
, vol.114
, Issue.8
, pp. 1041-1045
-
-
Coppus, A.W.1
Fekkes, D.2
Verhoeven, W.M.3
Tuinier, S.4
Egger, J.I.5
Van Duijn, C.M.6
-
4
-
-
41149124341
-
The MTR A2756G polymorphism is associated with an increase of plasma homocysteine concentration in Brazilian individuals with Down syndrome
-
Biselli JM, Goloni-Bertollo EM, Haddad R, Eberlin MN, Pavarino-Bertelli EC (2008) The MTR A2756G polymorphism is associated with an increase of plasma homocysteine concentration in Brazilian individuals with Down syndrome. Braz J Med Biol Res 41(1):34-40
-
(2008)
Braz J Med Biol Res
, vol.41
, Issue.1
, pp. 34-40
-
-
Biselli, J.M.1
Goloni-Bertollo, E.M.2
Haddad, R.3
Eberlin, M.N.4
Pavarino-Bertelli, E.C.5
-
5
-
-
33750338304
-
Does Down's syndrome support the homocysteine theory of atherogenesis? Experience in elderly subjects with trisomy 21
-
Licastro F, Marocchi A, Penco S, Porcellini E, Lio D, Dogliotti G et al (2006) Does Down's syndrome support the homocysteine theory of atherogenesis? Experience in elderly subjects with trisomy 21. Arch Gerontol Geriatr 43(3):317-318
-
(2006)
Arch Gerontol Geriatr
, vol.43
, Issue.3
, pp. 317-318
-
-
Licastro, F.1
Marocchi, A.2
Penco, S.3
Porcellini, E.4
Lio, D.5
Dogliotti, G.6
-
6
-
-
0034880973
-
Amino acid quantitation in aqueous matrices via trap and release membrane introduction mass spectrometry: Homocysteine in human plasma
-
Haddad R, Mendes MA, Hoehr NF, Eberlin MN (2001) Amino acid quantitation in aqueous matrices via trap and release membrane introduction mass spectrometry: homocysteine in human plasma. Analyst 126:1212-1215
-
(2001)
Analyst
, vol.126
, pp. 1212-1215
-
-
Haddad, R.1
Mendes, M.A.2
Hoehr, N.F.3
Eberlin, M.N.4
-
7
-
-
33746190611
-
Alpha1D-adrenoceptor-induced relaxation on rat carotid artery is impaired during the endothelial dysfunction evoked in the early stages of hyperhomocysteinemia
-
De Andrade CR, Fukada SY, Olivon VC, De Godoy MA, Haddad R, Eberlin MN et al (2006) Alpha1D-adrenoceptor-induced relaxation on rat carotid artery is impaired during the endothelial dysfunction evoked in the early stages of hyperhomocysteinemia. Eur J Pharmacol 543(1-3):83-91
-
(2006)
Eur J Pharmacol
, vol.543
, Issue.1-3
, pp. 83-91
-
-
De Andrade, C.R.1
Fukada, S.Y.2
Olivon, V.C.3
De Godoy, M.A.4
Haddad, R.5
Eberlin, M.N.6
-
8
-
-
49049101852
-
Determination of serum methylmalonic acid by alkylative extraction and liquid chromatography coupled to tandem mass spectrometry
-
Carvalho VM, Kok F (2008) Determination of serum methylmalonic acid by alkylative extraction and liquid chromatography coupled to tandem mass spectrometry. Anal Biochem 381(1-3):67-73
-
(2008)
Anal Biochem
, vol.381
, Issue.1-3
, pp. 67-73
-
-
Carvalho, V.M.1
Kok, F.2
-
9
-
-
0032231635
-
Measurement and use of total plasma homocysteine
-
American Society of Human Genetics/American College of Medical Genetics Test and Technology Transfer Committee Working Group. ASHG/ACMG Statement
-
American Society of Human Genetics/American College of Medical Genetics Test and Technology Transfer Committee Working Group. ASHG/ACMG Statement (1998) Measurement and use of total plasma homocysteine. Am J Hum Genet 63:1541-1543
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1541-1543
-
-
-
10
-
-
0033882025
-
Cobalamin and folate evaluation: Measurement of methylmalonic acid and homocysteinevs vitamin B (12) and folate
-
Klee GG (2000) Cobalamin and folate evaluation: measurement of methylmalonic acid and homocysteinevs vitamin B (12) and folate. Clin Chem 46(8 Pt 2):1277-1283
-
(2000)
Clin Chem
, vol.46
, Issue.8 PART 2
, pp. 1277-1283
-
-
Klee, G.G.1
-
11
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller SA, Dykes DD Polesky HF (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16(3):1215
-
(1988)
Nucleic Acids Res
, vol.16
, Issue.3
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
12
-
-
33845202083
-
Cystathionineβ-synthase T833C/844INS68 polymorphism: A family-based study on mentally retarded children
-
Dutta S, Sinha S, Chattopadhyay A, Gangopadhyay PK, Mukhopadhyay J, Singh M et al (2005) Cystathionineβ-synthase T833C/844INS68 polymorphism: a family-based study on mentally retarded children. Behav Brain Funct 1:25
-
(2005)
Behav Brain Funct
, vol.1
, pp. 25
-
-
Dutta, S.1
Sinha, S.2
Chattopadhyay, A.3
Gangopadhyay, P.K.4
Mukhopadhyay, J.5
Singh, M.6
-
13
-
-
0345373993
-
Effect of glutamate carboxypeptidase II and reduced folate carrier polymorphisms on folate and total homocysteine concentrations in dialysis patients
-
Födinger M, Dierkes J, Skoupy S, Röhrer C, Hagen W, Puttinger H et al (2003) Effect of glutamate carboxypeptidase II and reduced folate carrier polymorphisms on folate and total homocysteine concentrations in dialysis patients. J Am Soc Nephrol 14(5):1314-1319
-
(2003)
J Am Soc Nephrol
, vol.14
, Issue.5
, pp. 1314-1319
-
-
Födinger, M.1
Dierkes, J.2
Skoupy, S.3
Röhrer, C.4
Hagen, W.5
Puttinger, H.6
-
14
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A common mutation in Methylenetetrahydrofolatereductase
-
Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Matthews RG et al (1995) A candidate genetic risk factor for vascular disease: a common mutation in Methylenetetrahydrofolatereductase. Nat Genet 10(1):111-113
-
(1995)
Nat Genet
, vol.10
, Issue.1
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
Goyette, P.4
Sheppard, C.A.5
Matthews, R.G.6
-
15
-
-
0031969348
-
Molecular genetic analysis of the gene encoding the trifunctional enzyme MTHFD (methylenetetrahydrofolate-dehydrogenase, methenyltetrahydrofolate- cyclohydrolase, formyltetrahydrofolate synthetase) in patients with neural tube defects
-
Hol FA, Van Der Put N M J, Geurds M P A, Blom HJ (1998) Molecular genetic analysis of the gene encoding the trifunctional enzyme MTHFD (methylenetetrahydrofolate-dehydrogenase, methenyltetrahydrofolate- cyclohydrolase, formyltetrahydrofolate synthetase) in patients with neural tube defects. Clin Genet 53(2):119-125
-
(1998)
Clin Genet
, vol.53
, Issue.2
, pp. 119-125
-
-
Hol, F.A.1
Van Der Put, N.M.J.2
Geurds, M.P.A.3
Blom, H.J.4
-
16
-
-
0142154026
-
776C>G polymorphism of the transcobalamin II gene as a risk factor for spina bifida
-
Pietrzyk JJ, Bik-Multanowski M (2003) 776C>G polymorphism of the transcobalamin II gene as a risk factor for spina bifida. Mol Genet Metab 80(3):364
-
(2003)
Mol Genet Metab
, vol.80
, Issue.3
, pp. 364
-
-
Pietrzyk, J.J.1
Bik-Multanowski, M.2
-
17
-
-
77956235500
-
Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome
-
Locke AE, Dooley KJ, Tinker SW, Cheong SY, Feingold E, Allen EG et al (2010) Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome. Genet Epidemiol 34(6):613-623
-
(2010)
Genet Epidemiol
, vol.34
, Issue.6
, pp. 613-623
-
-
Locke, A.E.1
Dooley, K.J.2
Tinker, S.W.3
Cheong, S.Y.4
Feingold, E.5
Allen, E.G.6
-
18
-
-
84868542794
-
Down syndrome as a model of DNA polymerase beta haploinsufficiency and accelerated aging
-
Epub Ahead of Print
-
Patterson D, Cabelof DC (2011) Down syndrome as a model of DNA polymerase beta haploinsufficiency and accelerated aging. Mech Ageing Dev [Epub Ahead of Print]
-
(2011)
Mech Ageing Dev
-
-
Patterson, D.1
Cabelof, D.C.2
-
19
-
-
16544380413
-
Homocysteine concentrations in adults with trisomy 21: Effect of B vitamins and genetic polymorphisms
-
Fillon-Emery N, Chango A, Mircher C, Barbé F, Bléhaut H, Herbeth B et al (2004) Homocysteine concentrations in adults with trisomy 21: effect of B vitamins and genetic polymorphisms. Am J Clin Nutr 80(6):1551-1557
-
(2004)
Am J Clin Nutr
, vol.80
, Issue.6
, pp. 1551-1557
-
-
Fillon-Emery, N.1
Chango, A.2
Mircher, C.3
Barbé, F.4
Bléhaut, H.5
Herbeth, B.6
-
20
-
-
33947239251
-
Functional inference of the methylenetetrahydrofolatereductase 677C>T and 1298A>C polymorphisms from a large-scale epidemiological study
-
Ulvik A, Ueland PM, Fredriksen A, Meyer K, Vollset SE, Hoff G et al (2007) Functional inference of the methylenetetrahydrofolatereductase 677C>T and 1298A>C polymorphisms from a large-scale epidemiological study. Hum Genet 121(1):57-64
-
(2007)
Hum Genet
, vol.121
, Issue.1
, pp. 57-64
-
-
Ulvik, A.1
Ueland, P.M.2
Fredriksen, A.3
Meyer, K.4
Vollset, S.E.5
Hoff, G.6
-
21
-
-
32044453846
-
Influence of methionine synthase (A2756G) and methionine synthase reductase (A66G) polymorphisms on plasma homocysteine levels and relation to risk of coronary artery disease
-
Laraqui A, Allami A, Carrie A, Coiffard AS, Benkouka F, Benjouad A (2006) Influence of methionine synthase (A2756G) and methionine synthase reductase (A66G) polymorphisms on plasma homocysteine levels and relation to risk of coronary artery disease. Acta Cardiol 61(1):51-61
-
(2006)
Acta Cardiol
, vol.61
, Issue.1
, pp. 51-61
-
-
Laraqui, A.1
Allami, A.2
Carrie, A.3
Coiffard, A.S.4
Benkouka, F.5
Benjouad, A.6
-
22
-
-
0034747726
-
Increased prevalence of combined MTR and MTHFR genotypes among individuals with severely elevated total homocysteine plasma levels
-
Feix A, Fritsche-Polanz R, Kletzmayr J, Vychytil A, Hörl WH, Sunder-Plassmann G et al (2001) Increased prevalence of combined MTR and MTHFR genotypes among individuals with severely elevated total homocysteine plasma levels. Am J Kidney Dis 38(5):956-964
-
(2001)
Am J Kidney Dis
, vol.38
, Issue.5
, pp. 956-964
-
-
Feix, A.1
Fritsche-Polanz, R.2
Kletzmayr, J.3
Vychytil, A.4
Hörl, W.H.5
Sunder-Plassmann, G.6
-
23
-
-
0038446637
-
Genetic and nutritional factors contributing to hyperhomocysteinemia in young adults
-
Kluijtmans LA, Young IS, Boreham CA, Murray L, McMaster D, McNulty H et al (2003) Genetic and nutritional factors contributing to hyperhomocysteinemia in young adults. Blood 101(7):2483-2488
-
(2003)
Blood
, vol.101
, Issue.7
, pp. 2483-2488
-
-
Kluijtmans, L.A.1
Young, I.S.2
Boreham, C.A.3
Murray, L.4
McMaster, D.5
McNulty, H.6
-
24
-
-
79957461263
-
TT genotype of the methylenetetrahydrofolate reductase C677T polymorphism is an important determinant for homocysteine levels in multi-ethnic Malaysian ischaemic stroke patients
-
Mejia Mohamed EH, Tan KS, Ali JM, Mohamed Z (2011) TT genotype of the methylenetetrahydrofolate reductase C677T polymorphism is an important determinant for homocysteine levels in multi-ethnic Malaysian ischaemic stroke patients. Ann Acad Med Singapore 40(4):186-191
-
(2011)
Ann Acad Med Singapore
, vol.40
, Issue.4
, pp. 186-191
-
-
Mejia Mohamed, E.H.1
Tan, K.S.2
Ali, J.M.3
Mohamed, Z.4
-
25
-
-
79959797206
-
Genetic and environmental determinants of plasma total homocysteine levels: Impact of population-wide folate fortification
-
Nagele P, Meissner K, Francis A, Födinger M, Saccone NL (2011) Genetic and environmental determinants of plasma total homocysteine levels: impact of population-wide folate fortification. Pharmacogenet Genomics 21(7):426-441
-
(2011)
Pharmacogenet Genomics
, vol.21
, Issue.7
, pp. 426-441
-
-
Nagele, P.1
Meissner, K.2
Francis, A.3
Födinger, M.4
Saccone, N.L.5
-
26
-
-
0034743914
-
The 1298A→C polymorphism in methylenetetrahydrofolatereductase (MTHFR): In vitro expression and association with Homocysteine
-
Weisberg IS, Jacques PF, Selhub J, Bostom AG, Chen Z, Curtis Ellison R et al (2001) The 1298A→C polymorphism in methylenetetrahydrofolatereductase (MTHFR): in vitro expression and association with Homocysteine. Atherosclerosis 156(2):409-415
-
(2001)
Atherosclerosis
, vol.156
, Issue.2
, 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
-
27
-
-
0042194787
-
Methionine synthase (MTR) 2756 (A ->G) polymorphism, double heterozygosity methionine synthase 2756 AG/methionine synthase reductase (MTRR) 66 AG, and elevated homocysteinemia are three risk factors for having a child with Down syndrome
-
Bosco P, Guéant-Rodriguez RM, Anello G, Barone C, Namour F, Caraci F et al (2003) Methionine synthase (MTR) 2756(A ->G) polymorphism, double heterozygosity methionine synthase 2756 AG/methionine synthase reductase (MTRR) 66 AG, and elevated homocysteinemia are three risk factors for having a child with Down syndrome. Am J Med Genet A 121 A (3):219-224
-
(2003)
Am J Med Genet A
, vol.121 A
, Issue.3
, pp. 219-224
-
-
Bosco, P.1
Guéant-Rodriguez, R.M.2
Anello, G.3
Barone, C.4
Namour, F.5
Caraci, F.6
-
28
-
-
76749137605
-
Transcobalamin-II variants, decreased vitamin B12 availability and increased risk of frailty
-
Matteini AM, Walston JD, Bandeen-Roche K, Arking DE, Allen RH, Fried L P C et al (2010) Transcobalamin-II variants, decreased vitamin B12 availability and increased risk of frailty. J Nutr Health Aging 14(1):73-77
-
(2010)
J Nutr Health Aging
, vol.14
, Issue.1
, pp. 73-77
-
-
Matteini, A.M.1
Walston, J.D.2
Bandeen-Roche, K.3
Arking, D.E.4
Allen, R.H.5
Fried, L.P.C.6
-
29
-
-
33845508214
-
Betainehomocysteine S-methyltransferase: Just a regulator of homocysteine metabolism?
-
Pajares MA, Pérez-Sala D (2006) Betainehomocysteine S-methyltransferase: just a regulator of homocysteine metabolism? Cell Mol Life Sci 63(23):2792-2803
-
(2006)
Cell Mol Life Sci
, vol.63
, Issue.23
, pp. 2792-2803
-
-
Pajares, M.A.1
Pérez-Sala, D.2
-
30
-
-
49949114320
-
MTHFD1 gene: Role in disease susceptibility and pharmacogenetics
-
Krajinovic M (2008) MTHFD1 gene: role in disease susceptibility and pharmacogenetics. Pharmacogenomics 9(7):829-832
-
(2008)
Pharmacogenomics
, vol.9
, Issue.7
, pp. 829-832
-
-
Krajinovic, M.1
-
31
-
-
44649202769
-
Human betaine-homocysteine methyltransferase (BHMT) and BHMT2: Common gene sequence variation and functional characterization
-
Li F, Feng Q, Lee C, Wang S, Pelleymounter LL, Moon I (2008) Human betaine-homocysteine methyltransferase (BHMT) and BHMT2: common gene sequence variation and functional characterization. Mol Genet Metab 94:326-335
-
(2008)
Mol Genet Metab
, vol.94
, pp. 326-335
-
-
Li, F.1
Feng, Q.2
Lee, C.3
Wang, S.4
Pelleymounter, L.L.5
Moon, I.6
-
32
-
-
79955864329
-
Choline and betaine in health and disease
-
Ueland PM (2011) Choline and betaine in health and disease. J Inherit Metab Dis 34(1):3-15
-
(2011)
J Inherit Metab Dis
, vol.34
, Issue.1
, pp. 3-15
-
-
Ueland, P.M.1
-
33
-
-
0042322356
-
Common variant in betaine-homocysteinemethyltransferase (BHMT) and risk for spina bifida
-
Morin I, Platt R, Weisberg I, Sabbaghian N, Wu Q, Garrow TA et al (2003) Common variant in betaine-homocysteinemethyltransferase (BHMT) and risk for spina bifida. Am J Med Genet 119 A (2): 172-176
-
(2003)
Am J Med Genet
, vol.119 A
, Issue.2
, pp. 172-176
-
-
Morin, I.1
Platt, R.2
Weisberg, I.3
Sabbaghian, N.4
Wu, Q.5
Garrow, T.A.6
-
34
-
-
0038124366
-
Investigations of a common genetic variant in betaine-homocysteine methyltransferase (BHMT) in coronary artery disease
-
Weisberg IS, Park E, Ballman KV, Berger P, Nunn M, Suh DS et al (2003) Investigations of a common genetic variant in betaine-homocysteine methyltransferase (BHMT) in coronary artery disease. Atherosclerosis 167(2):205-214
-
(2003)
Atherosclerosis
, vol.167
, Issue.2
, pp. 205-214
-
-
Weisberg, I.S.1
Park, E.2
Ballman, K.V.3
Berger, P.4
Nunn, M.5
Suh, D.S.6
-
35
-
-
46749120334
-
Polymorphisms in genes related to folate and cobalamin metabolism and the associations with complex birth defects
-
Brouns R, Ursem N, Lindemans J, Hop W, Pluijm S, Steegers E et al (2008) Polymorphisms in genes related to folate and cobalamin metabolism and the associations with complex birth defects. Prenat Diagn 28(6):485-493
-
(2008)
Prenat Diagn
, vol.28
, Issue.6
, pp. 485-493
-
-
Brouns, R.1
Ursem, N.2
Lindemans, J.3
Hop, W.4
Pluijm, S.5
Steegers, E.6
-
36
-
-
0035865701
-
Transcobalamin codon 259 polymorphism in HT-29 and Caco-2 cells and in Caucasians: Relation to transcobalamin and homocysteine concentration in blood
-
Namour F, Olivier J, Abdelmouttaleb I, Adjalla C, Debard R, Salvat C et al (2001) Transcobalamin codon 259 polymorphism in HT-29 and Caco-2 cells and in Caucasians: relation to transcobalamin and homocysteine concentration in blood. Blood 97(4):1092-1098
-
(2001)
Blood
, vol.97
, Issue.4
, pp. 1092-1098
-
-
Namour, F.1
Olivier, J.2
Abdelmouttaleb, I.3
Adjalla, C.4
Debard, R.5
Salvat, C.6
-
37
-
-
0037100425
-
Transcobalamin II 775G>C polymorphism and indices of vitamin B12 status in healthy older adults
-
Miller JW, Ramos MI, Garrod MG, Flynn MA, Green R (2002) Transcobalamin II 775G>C polymorphism and indices of vitamin B12 status in healthy older adults. Blood 100(2):718-720
-
(2002)
Blood
, vol.100
, Issue.2
, pp. 718-720
-
-
Miller, J.W.1
Ramos, M.I.2
Garrod, M.G.3
Flynn, M.A.4
Green, R.5
-
38
-
-
77951207405
-
The TCN2 776CNG polymorphism correlates with vitamin B (12) cellular delivery in healthy adult populations
-
Castro R, Barroso M, Rocha M, Esse R, Ramos R, Ravasco P et al (2010) The TCN2 776CNG polymorphism correlates with vitamin B (12) cellular delivery in healthy adult populations. Clin Biochem 43(7-8):645-649
-
(2010)
Clin Biochem
, vol.43
, Issue.7-8
, pp. 645-649
-
-
Castro, R.1
Barroso, M.2
Rocha, M.3
Esse, R.4
Ramos, R.5
Ravasco, P.6
-
39
-
-
34848881628
-
Large-scale population-based metabolic phenotyping of thirteen genetic polymorphisms related to one-carbon metabolism
-
Fredriksen A, Meyer K, Ueland PM, Vollset SE, Grotmol T, Schneede J (2007) Large-scale population-based metabolic phenotyping of thirteen genetic polymorphisms related to one-carbon metabolism. Hum Mutat 28(9):856-865
-
(2007)
Hum Mutat
, vol.28
, Issue.9
, pp. 856-865
-
-
Fredriksen, A.1
Meyer, K.2
Ueland, P.M.3
Vollset, S.E.4
Grotmol, T.5
Schneede, J.6
-
40
-
-
33847176545
-
Polymorphism C776G in the transcobalamin II gene and homocysteine, folate and vitamin B12 concentrations. Association with MTHFR C677T and A1298C and MTRR A66G polymorphisms in healthy children
-
Aléssio AC, Höehr NF, Siqueira LH, Bydlowski SP, Annichino-Bizzacchi JM (2007) Polymorphism C776G in the transcobalamin II gene and homocysteine, folate and vitamin B12 concentrations. Association with MTHFR C677T and A1298C and MTRR A66G polymorphisms in healthy children. Thromb Res 119(5):571-577
-
(2007)
Thromb Res
, vol.119
, Issue.5
, pp. 571-577
-
-
Aléssio, A.C.1
Höehr, N.F.2
Siqueira, L.H.3
Bydlowski, S.P.4
Annichino-Bizzacchi, J.M.5
-
41
-
-
81055134843
-
Transcobalamin polymorphism 67A->G, but not 776C->G, affects serum holotranscobalamin in a cohort of healthy middle-aged men and women
-
Riedel BM, Molloy AM, Meyer K, Fredriksen A, Ulvik A, Schneede J et al (2011) Transcobalamin polymorphism 67A->G, but not 776C->G, affects serum holotranscobalamin in a cohort of healthy middle-aged men and women. J Nutr 141(10):1784-1790
-
(2011)
J Nutr
, vol.141
, Issue.10
, pp. 1784-1790
-
-
Riedel, B.M.1
Molloy, A.M.2
Meyer, K.3
Fredriksen, A.4
Ulvik, A.5
Schneede, J.6
-
42
-
-
80052580390
-
Maternal one-carbon metabolism, MTHFR and TCN2 genotypes and neural tube defects in India
-
Godbole K, Gayathri P, Ghule S, Sasirekha BV, Kanitkar-Damle A, Memane N et al (2011) Maternal one-carbon metabolism, MTHFR and TCN2 genotypes and neural tube defects in India. Birth Defects Res A Clin Mol Teratol 91(9):848-856
-
(2011)
Birth Defects Res A Clin Mol Teratol
, vol.91
, Issue.9
, pp. 848-856
-
-
Godbole, K.1
Gayathri, P.2
Ghule, S.3
Sasirekha, B.V.4
Kanitkar-Damle, A.5
Memane, N.6
-
43
-
-
0036721305
-
Polymorphisms in the Transcobalamin gene: Association with plasma homocysteine in healthy individuals and vascular disease patients
-
Lievers K J A, Afman LA, Kluijtmans L A J, Boers G H D, Verhoef P, Den Heijer M et al (2002) Polymorphisms in the Transcobalamin gene: association with plasma homocysteine in healthy individuals and vascular disease patients. Clin Chem 48(9):1383-1389
-
(2002)
Clin Chem
, vol.48
, Issue.9
, pp. 1383-1389
-
-
Lievers, K.J.A.1
Afman, L.A.2
Kluijtmans, L.A.J.3
Boers, G.H.D.4
Verhoef, P.5
Den Heijer, M.6
-
44
-
-
33645339255
-
The effect of MTHFR (C677T) genotype on plasma homocysteine concentrations in healthy children is influenced by gender
-
Papoutsakis C, Yiannakouris N, Manios Y, Papaconstantinou E, Magkos F et al (2006) The effect of MTHFR (C677T) genotype on plasma homocysteine concentrations in healthy children is influenced by gender. Eur J Clin Nutr 60(2):155-162
-
(2006)
Eur J Clin Nutr
, vol.60
, Issue.2
, pp. 155-162
-
-
Papoutsakis, C.1
Yiannakouris, N.2
Manios, Y.3
Papaconstantinou, E.4
Magkos, F.5
-
45
-
-
0032587458
-
Plasma homocysteine concentrations in a Belgian School-age population
-
De Laet C, Wautrecht JC, Brasseur D, Dramaix M, Boeynaems J-M, Decuyper J et al (1999) Plasma homocysteine concentrations in a Belgian School-age population. Am J Clin Nutr 69:968-972
-
(1999)
Am J Clin Nutr
, vol.69
, pp. 968-972
-
-
De Laet, C.1
Wautrecht, J.C.2
Brasseur, D.3
Dramaix, M.4
Boeynaems, J.-M.5
Decuyper, J.6
-
46
-
-
14944346294
-
Plasma homocysteine concentrations in Greek children are influenced by an interaction between the methylenetetrahydrofolate Redustase C677T genotype and folate status
-
Papoutsakis C, Yiannakouris N, Manios Y, Papakonstantinou E, Magkos F, Schulpis KH et al (2005) Plasma homocysteine concentrations in Greek children are influenced by an interaction between the methylenetetrahydrofolate Redustase C677T genotype and folate status. J Nutr 135:383-388
-
(2005)
J Nutr
, vol.135
, pp. 383-388
-
-
Papoutsakis, C.1
Yiannakouris, N.2
Manios, Y.3
Papakonstantinou, E.4
Magkos, F.5
Schulpis, K.H.6
-
47
-
-
33947595649
-
Reference range of total serum homocysteine level and dietary indexes in healthy Greek schoolchildren aged 6-15 years
-
Papandreou D, Mavromichalis I, Makedou A, Rousso I, Arvanitidou M (2006) Reference range of total serum homocysteine level and dietary indexes in healthy Greek schoolchildren aged 6-15 years. Br J Nutr 96(4):719-724
-
(2006)
Br J Nutr
, vol.96
, Issue.4
, pp. 719-724
-
-
Papandreou, D.1
Mavromichalis, I.2
Makedou, A.3
Rousso, I.4
Arvanitidou, M.5
-
48
-
-
0038168733
-
Homocysteine and methylmalonic acid in diagnosis and risk assessment from infancy to adolescence
-
Monsen AL, Ueland PM (2003) Homocysteine and methylmalonic acid in diagnosis and risk assessment from infancy to adolescence. Am J Clin Nutr 78(1):7-21
-
(2003)
Am J Clin Nutr
, vol.78
, Issue.1
, pp. 7-21
-
-
Monsen, A.L.1
Ueland, P.M.2
-
49
-
-
80455132504
-
Vitamin B 12 deficiency & levels of metabolites in an apparently normal urban south Indian elderly population
-
Shobha V, Tarey SD, Singh RG, Shetty P, Unni US, Srinivasan K, et al. (2011) Vitamin B 12 deficiency & levels of metabolites in an apparently normal urban south Indian elderly population. Indian J Med Res 134(4):432-439
-
(2011)
Indian J Med Res
, vol.134
, Issue.4
, pp. 432-439
-
-
Shobha, V.1
Tarey, S.D.2
Singh, R.G.3
Shetty, P.4
Unni, U.S.5
Srinivasan, K.6
-
51
-
-
0033551352
-
The effect of folic acid fortification on plasma folate and total homocysteine concentrations
-
Jacques PF, Selhub J, Bostom AG, Wilson P W F, Rosenberg IH (1999) The effect of folic acid fortification on plasma folate and total homocysteine concentrations. N Engl J Med 340:1449-1454
-
(1999)
N Engl J Med
, vol.340
, pp. 1449-1454
-
-
Jacques, P.F.1
Selhub, J.2
Bostom, A.G.3
Wilson, P.W.F.4
Rosenberg, I.H.5
|