-
2
-
-
0030862457
-
Contribution of birth defects and genetic diseases to pediatric hospitalizations. A population-based study
-
Yoon PW, Olney RS, Khoury MJ, Sappenfield WM, Chavez GF, Taylor D. Contribution of birth defects and genetic diseases to pediatric hospitalizations. A population-based study. Arch Pediatr Adolesc Med 1997; 151:1096-103.
-
(1997)
Arch Pediatr Adolesc Med
, vol.151
, pp. 1096-1103
-
-
Yoon, P.W.1
Olney, R.S.2
Khoury, M.J.3
Sappenfield, W.M.4
Chavez, G.F.5
Taylor, D.6
-
3
-
-
0028277755
-
Estimates of the economic costs of birth defects
-
Waitzman NJ, Romano PS, Scheffler RM. Estimates of the economic costs of birth defects. Inquiry 1994; 31:188-205.
-
(1994)
Inquiry
, vol.31
, pp. 188-205
-
-
Waitzman, N.J.1
Romano, P.S.2
Scheffler, R.M.3
-
4
-
-
20344362942
-
Annual summary of vital statistics—2003
-
Martin JA, Kochanek KD, Strobino DM, Guyer B, MacGillivray I. Annual summary of vital statistics—2003. Pediatrics 2005; 115:619-34.
-
(2005)
Pediatrics
, vol.115
, pp. 619-634
-
-
Martin, J.A.1
Kochanek, K.D.2
Strobino, D.M.3
Guyer, B.4
Macgillivray, I.5
-
6
-
-
0016428740
-
An analysis of migratory behavior of avian cephalic neural crest cells
-
Noden DM. An analysis of migratory behavior of avian cephalic neural crest cells. Dev Biol 1975; 42:106-30.
-
(1975)
Dev Biol
, vol.42
, pp. 106-130
-
-
Noden, D.M.1
-
7
-
-
0018155576
-
The control of avian cephalic neural crest cytodifferentiation. I. Skeletal and connective tissues
-
Noden DM. The control of avian cephalic neural crest cytodifferentiation. I. Skeletal and connective tissues. Dev Biol 1978; 67:296-312.
-
(1978)
Dev Biol
, vol.67
, pp. 296-312
-
-
Noden, D.M.1
-
8
-
-
0018115551
-
The control of avian cephalic neural crest cytodifferentiation. II. Neural tissues
-
Noden DM. The control of avian cephalic neural crest cytodifferentiation. II. Neural tissues. Dev Biol 1978; 67:313-29.
-
(1978)
Dev Biol
, vol.67
, pp. 313-329
-
-
Noden, D.M.1
-
9
-
-
0021088311
-
The embryonic origins of avian cephalic and cervical muscles and associated connective tissues
-
Noden DM. The embryonic origins of avian cephalic and cervical muscles and associated connective tissues. Am J Anat 1983; 168:257-76.
-
(1983)
Am J Anat
, vol.168
, pp. 257-276
-
-
Noden, D.M.1
-
10
-
-
0034444312
-
Molecular determinants of neural crest migration
-
Maschhoff KL, Baldwin HS. Molecular determinants of neural crest migration. Am J Med Genet 2000; 97:280-88.
-
(2000)
Am J Med Genet
, vol.97
, pp. 280-288
-
-
Maschhoff, K.L.1
Baldwin, H.S.2
-
11
-
-
0032884078
-
Mice lacking the folic acid-binding protein Folbp1 are defective in early embryonic development
-
Piedrahita JA, Oetama B, Bennett GD, van Waes J, Kamen BA, Richardson J, Lacey SW, Anderson RG, Finnell RH. Mice lacking the folic acid-binding protein Folbp1 are defective in early embryonic development. Nat Genet 1999; 23:228-32.
-
(1999)
Nat Genet
, vol.23
, pp. 228-232
-
-
Piedrahita, J.A.1
Oetama, B.2
Bennett, G.D.3
Van Waes, J.4
Kamen, B.A.5
Richardson, J.6
Lacey, S.W.7
Erson, R.G.8
Finnell, R.H.9
-
12
-
-
0032813393
-
Expression patterns of folate binding proteins one and two in the developing mouse embryo
-
Barber RC, Bennett GD, Greer KA, Finnell RH. Expression patterns of folate binding proteins one and two in the developing mouse embryo. Mol Genet Metab 1999; 66:31-39.
-
(1999)
Mol Genet Metab
, vol.66
, pp. 31-39
-
-
Barber, R.C.1
Bennett, G.D.2
Greer, K.A.3
Finnell, R.H.4
-
13
-
-
0037217759
-
Spatial and temporal expression of folatebinding protein 1 (Fbp1) is closely associated with anterior neural tube closure in mice
-
Saitsu H, Ishibashi M, Nakano H, Shiota K. Spatial and temporal expression of folatebinding protein 1 (Fbp1) is closely associated with anterior neural tube closure in mice. Dev Dyn 2003; 226:112-17.
-
(2003)
Dev Dyn
, vol.226
, pp. 112-117
-
-
Saitsu, H.1
Ishibashi, M.2
Nakano, H.3
Shiota, K.4
-
14
-
-
0028799948
-
Maternal peri-conceptional use of multivitamins and reduced risk for conotruncal heart defects and limb deficiencies among offspring
-
Shaw GM, O’Malley CD, Wasserman CR, Tolarova MM, Lammer EJ. Maternal peri-conceptional use of multivitamins and reduced risk for conotruncal heart defects and limb deficiencies among offspring. Am J Med Genet 1995; 59:536-45.
-
(1995)
Am J Med Genet
, vol.59
, pp. 536-545
-
-
Shaw, G.M.1
O’Malley, C.D.2
Wasserman, C.R.3
Tolarova, M.M.4
Lammer, E.J.5
-
15
-
-
0141995096
-
Neural and orofacial defects in Folp1 knockout mice [corrected]
-
Tang LS, Finnell RH. Neural and orofacial defects in Folp1 knockout mice [corrected]. Birth Defects Res A Clin Mol Teratol 2003; 67:209-18.
-
(2003)
Birth Defects Res a Clin Mol Teratol
, vol.67
, pp. 209-218
-
-
Tang, L.S.1
Finnell, R.H.2
-
16
-
-
0035552975
-
Polymorphisms in the methylenetetrahydrofolate reductase gene: Clinical consequences
-
Schwahn B, Rozen R. Polymorphisms in the methylenetetrahydrofolate reductase gene: Clinical consequences. Am J Pharmacogenomics 2001; 1:189-201.
-
(2001)
Am J Pharmacogenomics
, vol.1
, pp. 189-201
-
-
Schwahn, B.1
Rozen, R.2
-
17
-
-
0032771346
-
Homocysteine metabolism
-
Selhub J. Homocysteine metabolism. Annu Rev Nutr 1999; 19:217-46.
-
(1999)
Annu Rev Nutr
, vol.19
, pp. 217-246
-
-
Selhub, J.1
-
18
-
-
1542373560
-
Molecular basis of homocysteine toxicity in humans
-
Jakubowski H. Molecular basis of homocysteine toxicity in humans. Cell Mol Life Sci2004; 61:470-87.
-
(2004)
Cell Mol Life Sci
, vol.61
, pp. 470-487
-
-
Jakubowski, H.1
-
19
-
-
0033981289
-
Homocysteine thiolactone: Metabolic origin and protein homocysteiny-lation in humans
-
Jakubowski H. Homocysteine thiolactone: Metabolic origin and protein homocysteiny-lation in humans. J Nutr 2000; 130:377S-81S.
-
(2000)
J Nutr
, vol.130
, pp. 377-8155
-
-
Jakubowski, H.1
-
20
-
-
33644504239
-
Increased plasma protein homocysteinylation in hemodialysis patients
-
Perna AF, Satta E, Acanfora F, Lombardi C, Ingrosso D, De Santo NG. Increased plasma protein homocysteinylation in hemodialysis patients. Kidney Int 2006; 69:869-76.
-
(2006)
Kidney Int
, vol.69
, pp. 869-876
-
-
Perna, A.F.1
Satta, E.2
Acanfora, F.3
Lombardi, C.4
Ingrosso, D.5
De Santo, N.G.6
-
21
-
-
0030188563
-
The oxidant stress of hyperhomocyst(E)inemia
-
Loscalzo J. The oxidant stress of hyperhomocyst(e)inemia. J Clin Invest 1996; 98:5-7.
-
(1996)
J Clin Invest
, vol.98
, pp. 5-7
-
-
Loscalzo, J.1
-
22
-
-
0002205882
-
Teratogenic effects of pteroylglutamic acid deficiency in the rat
-
Nelson MM. Teratogenic effects of pteroylglutamic acid deficiency in the rat. Ciba Foundation Symp Cong Malfs 1960:134-57.
-
(1960)
Ciba Foundation Symp Cong Malfs
, pp. 134-157
-
-
Nelson, M.M.1
-
23
-
-
0038643838
-
Multiple congenital abnormalities in the rat resulting from riboflavin deficiency induced by the antimetabolite galactoflavin
-
Nelson MM, Baird CD, Wright HV, Evans HM. Multiple congenital abnormalities in the rat resulting from riboflavin deficiency induced by the antimetabolite galactoflavin. J Nutr 1956; 58:125-34.
-
(1956)
J Nutr
, vol.58
, pp. 125-134
-
-
Nelson, M.M.1
Baird, C.D.2
Wright, H.V.3
Evans, H.M.4
-
24
-
-
0000900060
-
Appearance of skeletal abnormalities in the offspring of rats reared on a deficient diet
-
Warkany J, Nelson RC. Appearance of skeletal abnormalities in the offspring of rats reared on a deficient diet. Science 1940; 92:383-84.
-
(1940)
Science
, vol.92
, pp. 383-384
-
-
Warkany, J.1
Nelson, R.C.2
-
25
-
-
0032410553
-
Direct effect of vitamins at the time of palatal fusion
-
Natsume N, Nagatsu Y, Kawai T. Direct effect of vitamins at the time of palatal fusion. Plast Reconstr Surg 1998; 102:2512-13.
-
(1998)
Plast Reconstr Surg
, vol.102
, pp. 2512-2513
-
-
Natsume, N.1
Nagatsu, Y.2
Kawai, T.3
-
26
-
-
4143082484
-
Embryonic development of folate binding protein-1 (Folbpl) knockout mice: Effects of the chemical form, dose, and timing of maternal folate supplementation
-
Spiegelstein O, Mitchell LE, Merriweather MY, Wicker NJ, Zhang Q, Lammer EJ, Finnell RH. Embryonic development of folate binding protein-1 (Folbpl) knockout mice: Effects of the chemical form, dose, and timing of maternal folate supplementation. Dev Dyn 2004; 231:221-31.
-
(2004)
Dev Dyn
, vol.231
, pp. 221-231
-
-
Spiegelstein, O.1
Mitchell, L.E.2
Merriweather, M.Y.3
Wicker, N.J.4
Zhang, Q.5
Lammer, E.J.6
Finnell, R.H.7
-
27
-
-
3242889813
-
Developmental consequences of abnormal folate transport during murine heart morphogenesis
-
Tang LS, Wlodarczyk BJ, Santillano DR, Miranda RC, Finnell RH. Developmental consequences of abnormal folate transport during murine heart morphogenesis. Birth Defects Res A Clin Mol Teratol 2004; 70:449-58.
-
(2004)
Birth Defects Res a Clin Mol Teratol
, vol.70
, pp. 449-458
-
-
Tang, L.S.1
Wlodarczyk, B.J.2
Santillano, D.R.3
Miranda, R.C.4
Finnell, R.H.5
-
28
-
-
0036324926
-
DNA methylation in Folbp1 knockout mice supplemented with folic acid during gestation
-
Finnell RH, Spiegelstein O, Wlodarczyk B, Triplett A, Pogribny IP, Melnyk S, James JS. DNA methylation in Folbp1 knockout mice supplemented with folic acid during gestation. JNutr 2002; 132:2457S-61S.
-
(2002)
Jnutr
, vol.132
, pp. 2457-6155
-
-
Finnell, R.H.1
Spiegelstein, O.2
Wlodarczyk, B.3
Triplett, A.4
Pogribny, I.P.5
Melnyk, S.6
James, J.S.7
-
29
-
-
47749100055
-
Embryonic development in the reduced folate carrier knockout mouse is modulated by maternal folate supplementation
-
Gelineau-van Waes J, Heller S, Bauer LK, Wilberding J, Maddox JR, Aleman F, Rosenquist TH, Finnell RH. Embryonic development in the reduced folate carrier knockout mouse is modulated by maternal folate supplementation. Birth Defects Res A Clin Mol Teratol2008; 82:494-507.
-
(2008)
Birth Defects Res a Clin Mol Teratol
, vol.82
, pp. 494-507
-
-
Gelineau-Van Waes, J.1
Heller, S.2
Bauer, L.K.3
Wilberding, J.4
Maddox, J.R.5
Aleman, F.6
Rosenquist, T.H.7
Finnell, R.H.8
-
30
-
-
0036328028
-
Folate status: Effects on pathways of colorectal carcinogenesis
-
Choi SW, Mason JB. Folate status: Effects on pathways of colorectal carcinogenesis. J Nutr2002; 132:2413S-18S.
-
(2002)
J Nutr
, vol.132
, pp. 1855-2413
-
-
Choi, S.W.1
Mason, J.B.2
-
31
-
-
10644297327
-
Folate and DNA methylation during in utero development and aging
-
McKay JA, Williams EA, Mathers JC. Folate and DNA methylation during in utero development and aging. Biochem Soc Trans 2004; 32:1006-07.
-
(2004)
Biochem Soc Trans
, vol.32
, pp. 1006-1007
-
-
McKay, J.A.1
Williams, E.A.2
Mathers, J.C.3
-
32
-
-
0025863475
-
Prevention of neural tube defects: Results of the Medical Research Council Vitamin Study
-
MRC Vitamin Study Research Group. Prevention of neural tube defects: Results of the Medical Research Council Vitamin Study. Lancet 1991; 338:131-37.
-
(1991)
Lancet
, vol.338
, pp. 131-137
-
-
-
33
-
-
0027080461
-
Prevention of the first occurrence of neural-tube defects by peri-conceptional vitamin supplementation
-
Czeizel AE, Dudas I. Prevention of the first occurrence of neural-tube defects by peri-conceptional vitamin supplementation. N Engl J Med 1992; 327:1832-35.
-
(1992)
N Engl J Med
, vol.327
, pp. 1832-1835
-
-
Czeizel, A.E.1
Dudas, I.2
-
34
-
-
0028803474
-
A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects
-
Whitehead AS, Gallagher P, Mills JL, Kirke PN, Burke H, Molloy AM, Weir DG, Shields DC, Scott JM. A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects. QJM 1995; 88:763-66.
-
(1995)
QJM
, vol.88
, pp. 763-766
-
-
Whitehead, A.S.1
Gallagher, P.2
Mills, J.L.3
Kirke, P.N.4
Burke, H.5
Molloy, A.M.6
Weir, D.G.7
Shields, D.C.8
Scott, J.M.9
-
35
-
-
0028833677
-
Homocysteine metabolism in pregnancies complicated by neural-tube defects
-
Mills JL, McPartlin JM, Kirke PN, Lee YJ, Conley MR, Weir DG, Scott JM. Homocysteine metabolism in pregnancies complicated by neural-tube defects. Lancet 1995; 345:149-51.
-
(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
-
36
-
-
33750930659
-
Maternal hyperhomocysteinaemia is a risk factor for congenital heart disease
-
Verkleij-Hagoort AC, Verlinde M, Ursem NT, Lindemans J, Helbing WA, Ottenkamp J, Siebel FM, et al. Maternal hyperhomocysteinaemia is a risk factor for congenital heart disease. BJOG 2006; 113:1412-18.
-
(2006)
BJOG
, vol.113
, pp. 1412-1418
-
-
Verkleij-Hagoort, A.C.1
Verlinde, M.2
Ursem, N.T.3
Lindemans, J.4
Helbing, W.A.5
Ottenkamp, J.6
Siebel, F.M.7
-
37
-
-
34247844422
-
Hyperhomocysteinemia and MTHFR polymorphisms in association with orofacial clefts and congenital heart defects: A meta-analysis
-
Verkleij-Hagoort A, Bliek J, Sayed-Tabatabaei F, Ursem N, Steegers E, Steegers-Theunissen R. Hyperhomocysteinemia and MTHFR polymorphisms in association with orofacial clefts and congenital heart defects: A meta-analysis. Am J Med Genet A 2007; 143:952-60.
-
(2007)
Am J Med Genet A
, vol.143
, pp. 952-960
-
-
Verkleij-Hagoort, A.1
Bliek, J.2
Sayed-Tabatabaei, F.3
Ursem, N.4
Steegers, E.5
Steegers-Theunissen, R.6
-
38
-
-
0036328453
-
Gene-nutrient interactions and DNA methylation
-
Friso S, Choi SW. Gene-nutrient interactions and DNA methylation. J Nutr 2002; 132:2382S-87S.
-
(2002)
J Nutr
, vol.132
, pp. 2382-8785
-
-
Friso, S.1
Choi, S.W.2
-
39
-
-
0017360453
-
Embryotoxicity of the folate antagonist methotrexate in rats and rabbits
-
Jordan RL, Wilson JG, Schumacher HJ. Embryotoxicity of the folate antagonist methotrexate in rats and rabbits. Teratology 1977; 15:73-79.
-
(1977)
Teratology
, vol.15
, pp. 73-79
-
-
Jordan, R.L.1
Wilson, J.G.2
Schumacher, H.J.3
-
40
-
-
0007605941
-
Stress as an etiologic factor in the development of cleft palate
-
Peer LA, Strean LP. Stress as an etiologic factor in the development of cleft palate. Plast Reconstr Surg 1956; 18:1-8.
-
(1956)
Plast Reconstr Surg
, vol.18
, pp. 1-8
-
-
Peer, L.A.1
Strean, L.P.2
-
42
-
-
0017127533
-
Cardiac defects in children of mothers receiving anticonvulsant therapy during pregnancy
-
Anderson RC. Cardiac defects in children of mothers receiving anticonvulsant therapy during pregnancy. J Pediatr 1976; 89:318-19.
-
(1976)
J Pediatr
, vol.89
, pp. 318-319
-
-
Anderson, R.C.1
-
43
-
-
0023156494
-
Anticonvulsants, folate levels, and pregnancy outcome: A prospective study
-
Dansky LV, Andermann E, Rosenblatt D, Sherwin AL, Andermann F. Anticonvulsants, folate levels, and pregnancy outcome: A prospective study. Ann Neurol 1987; 21:176-82.
-
(1987)
Ann Neurol
, vol.21
, pp. 176-182
-
-
Dansky, L.V.1
Ermann, E.2
Rosenblatt, D.3
Sherwin, A.L.4
Ermann, F.5
-
44
-
-
0026281619
-
Parental epilepsy, anticonvulsant drugs, and reproductive outcome: Epidemiologic and experimental findings spanning three decades; 2: Human studies
-
Dansky LV, Finnell RH. Parental epilepsy, anticonvulsant drugs, and reproductive outcome: Epidemiologic and experimental findings spanning three decades; 2: Human studies. Reprod Toxicol 1991; 5:301-35.
-
(1991)
Reprod Toxicol
, vol.5
, pp. 301-335
-
-
Dansky, L.V.1
Finnell, R.H.2
-
45
-
-
0026302402
-
Diurnal variation of folate concentrations in mouse embryo and plasma: The protective effect of folinic acid on valproic-acid-induced teratogenicity is time dependent
-
Wegner C, Nau H. Diurnal variation of folate concentrations in mouse embryo and plasma: The protective effect of folinic acid on valproic-acid-induced teratogenicity is time dependent. Reprod Toxicol 1991; 5:465-71.
-
(1991)
Reprod Toxicol
, vol.5
, pp. 465-471
-
-
Wegner, C.1
Nau, H.2
-
46
-
-
0026848306
-
Alteration of embryonic folate metabolism by valproic acid during organogenesis: Implications for mechanism of teratogenesis
-
Wegner C, Nau H. Alteration of embryonic folate metabolism by valproic acid during organogenesis: Implications for mechanism of teratogenesis. Neurology 1992; 42:17-24.
-
(1992)
Neurology
, vol.42
, pp. 17-24
-
-
Wegner, C.1
Nau, H.2
-
47
-
-
0023942345
-
Maternal drug histories and congenital malformations: Limb reduction defects and oral clefts
-
Hill L, Murphy M, McDowall M, Paul AH. Maternal drug histories and congenital malformations: Limb reduction defects and oral clefts. J Epidemiol Community Health1988; 42:1-7.
-
(1988)
J Epidemiol Community Health
, vol.42
, pp. 1-7
-
-
Hill, L.1
Murphy, M.2
McDowall, M.3
Paul, A.H.4
-
48
-
-
0029171533
-
Orofacial clefts and maternal anticonvulsant use
-
Shaw GM, Wasserman CR, O’Malley CD, Lammer EJ, Finnell RH. Orofacial clefts and maternal anticonvulsant use. Reprod Toxicol 1995; 9:97-98.
-
(1995)
Reprod Toxicol
, vol.9
, pp. 97-98
-
-
Shaw, G.M.1
Wasserman, C.R.2
O’Malley, C.D.3
Lammer, E.J.4
Finnell, R.H.5
-
49
-
-
0015518918
-
Maternal epilepsy and abnormalities of the fetus and newborn
-
Speidel BD, Meadow SR. Maternal epilepsy and abnormalities of the fetus and newborn. Lancet 1972; 2:839-43.
-
(1972)
Lancet
, vol.2
, pp. 839-843
-
-
Speidel, B.D.1
Meadow, S.R.2
-
50
-
-
0034959518
-
Repeated neural tube defects and valproate monotherapy suggest a pharmacogenetic abnormality
-
Duncan S, Mercho S, Lopes-Cendes I, Seni MH, Benjamin A, Dubeau F, Andermann F, Andermann E. Repeated neural tube defects and valproate monotherapy suggest a pharmacogenetic abnormality. Epilepsia 2001; 42:750-53.
-
(2001)
Epilepsia
, vol.42
, pp. 750-753
-
-
Duncan, S.1
Mercho, S.2
Lopes-Cendes, I.3
Seni, M.H.4
Benjamin, A.5
Dubeau, F.6
Ermann, F.7
Ermann, E.8
-
51
-
-
0033066533
-
Congenital malformations due to antiepileptic drugs
-
Kaneko S, Battino D, Andermann E, Wada K, Kan R, Takeda A, Nakane Y, et al.Congenital malformations due to antiepileptic drugs. Epilepsy Res 1999; 33:145-58.
-
(1999)
Epilepsy Res
, vol.33
, pp. 145-158
-
-
Kaneko, S.1
Battino, D.2
Ermann, E.3
Wada, K.4
Kan, R.5
Takeda, A.6
Nakane, Y.7
-
52
-
-
33846010780
-
Plasma vitamin values and antiepileptic therapy: Case reports of pregnancy outcomes affected by a neural tube defect
-
Candito M, Naimi M, Boisson C, Rudigoz JC, Gaucherand P, Gueant JL, Luton D, VanObberghen E. Plasma vitamin values and antiepileptic therapy: Case reports of pregnancy outcomes affected by a neural tube defect. Birth Defects Res A Clin Mol Teratol2007; 79:62-64.
-
(2007)
Birth Defects Res a Clin Mol Teratol
, vol.79
, pp. 62-64
-
-
Candito, M.1
Naimi, M.2
Boisson, C.3
Rudigoz, J.C.4
Gaucherand, P.5
Gueant, J.L.6
Luton, D.7
Vanobberghen, E.8
-
53
-
-
0030025013
-
Purification and characterization of folate binding proteins from rat placenta
-
da Costa M, Rothenberg SP. Purification and characterization of folate binding proteins from rat placenta. Biochim Biophys Acta 1996; 1292:23-30.
-
(1996)
Biochim Biophys Acta
, vol.1292
, pp. 23-30
-
-
Da Costa, M.1
Rothenberg, S.P.2
-
55
-
-
0347988053
-
Autoantibodies against folate receptors in women with a pregnancy complicated by a neural-tube defect
-
Rothenberg SP, da Costa MP, Sequeira JM, Cracco J, Roberts JL, Weedon J, Quadros EV. Autoantibodies against folate receptors in women with a pregnancy complicated by a neural-tube defect. N Engl J Med 2004; 350:134-42.
-
(2004)
N Engl J Med
, vol.350
, pp. 134-142
-
-
Rothenberg, S.P.1
Da Costa, M.P.2
Sequeira, J.M.3
Cracco, J.4
Roberts, J.L.5
Weedon, J.6
Quadros, E.V.7
-
56
-
-
0023225457
-
Purification, properties, and immunological characterization of folate-binding proteins from human leukemia cells
-
Sadasivan E, da Costa M, Rothenberg SP, Brink L. Purification, properties, and immunological characterization of folate-binding proteins from human leukemia cells. Biochim Biophys Acta 1987; 925:36-47.
-
(1987)
Biochim Biophys Acta
, vol.925
, pp. 36-47
-
-
Sadasivan, E.1
Da Costa, M.2
Rothenberg, S.P.3
Brink, L.4
-
57
-
-
17844383222
-
Role of Folbp1 in the regional regulation of apoptosis and cell proliferation in the developing neural tube and craniofacies
-
Tang LS, Santillano DR, Wlodarczyk BJ, Miranda RC, Finnell RH. Role of Folbp1 in the regional regulation of apoptosis and cell proliferation in the developing neural tube and craniofacies. Am J Med Genet C Semin Med Genet 2005; 135:48-58.
-
(2005)
Am J Med Genet C Semin Med Genet
, vol.135
, pp. 48-58
-
-
Tang, L.S.1
Santillano, D.R.2
Wlodarczyk, B.J.3
Miranda, R.C.4
Finnell, R.H.5
-
58
-
-
33646788784
-
Pathophysiological consequences of homocysteine excess
-
Jakubowski H. Pathophysiological consequences of homocysteine excess. JNutr 2006; 136:1741S-49S.
-
(2006)
Jnutr
, vol.136
, pp. 1741S-1749S
-
-
Jakubowski, H.1
-
59
-
-
2542618547
-
Autoantibodies against N-homocysteinylated proteins in humans: Implications for atherosclerosis
-
Undas A, Perla J, Lacinski M, Trzeciak W, Kazmierski R, Jakubowski H. Autoantibodies against N-homocysteinylated proteins in humans: Implications for atherosclerosis. Stroke 2004; 35:1299-304.
-
(2004)
Stroke
, vol.35
, pp. 1299-1304
-
-
Undas, A.1
Perla, J.2
Lacinski, M.3
Trzeciak, W.4
Kazmierski, R.5
Jakubowski, H.6
-
60
-
-
0037083014
-
Maternal periconcep-tional vitamin use, genetic variation of infant reduced folate carrier (A80G), and risk of spina bifida
-
Shaw GM, Lammer EJ, Zhu H, Baker MW, Neri E, Finnell RH. Maternal periconcep-tional vitamin use, genetic variation of infant reduced folate carrier (A80G), and risk of spina bifida. Am J Med Genet 2002; 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
-
61
-
-
0031785528
-
Infant C677T mutation in MTHFR, maternal periconceptional vitamin use, and cleft lip
-
Shaw GM, Rozen R, Finnell RH, Todoroff K, Lammer EJ. Infant C677T mutation in MTHFR, maternal periconceptional vitamin use, and cleft lip. Am J Med Genet 1998; 80:196-98.
-
(1998)
Am J Med Genet
, vol.80
, pp. 196-198
-
-
Shaw, G.M.1
Rozen, R.2
Finnell, R.H.3
Todoroff, K.4
Lammer, E.J.5
-
62
-
-
0032125774
-
Maternal vitamin use, genetic variation of infant methylenetetrahydrofolate reductase, and risk for spina bifida
-
Shaw GM, Rozen R, Finnell RH, Wasserman CR, Lammer EJ. Maternal vitamin use, genetic variation of infant methylenetetrahydrofolate reductase, and risk for spina bifida. Am J Epidemiol 1998; 148:30-37.
-
(1998)
Am J Epidemiol
, vol.148
, pp. 30-37
-
-
Shaw, G.M.1
Rozen, R.2
Finnell, R.H.3
Wasserman, C.R.4
Lammer, E.J.5
-
63
-
-
0141894138
-
Genetic variation of infant reduced folate carrier (A80G) and risk of orofacial and conotruncal heart defects
-
Shaw GM, Zhu H, Lammer EJ, Yang W, Finnell RH. Genetic variation of infant reduced folate carrier (A80G) and risk of orofacial and conotruncal heart defects. Am J Epidemiol2003; 158:747-52.
-
(2003)
Am J Epidemiol
, vol.158
, pp. 747-752
-
-
Shaw, G.M.1
Zhu, H.2
Lammer, E.J.3
Yang, W.4
Finnell, R.H.5
-
64
-
-
0036644017
-
Testing for genetic associations with the PAX gene family in a spina bifida population
-
Volcik KA, Blanton SH, Kruzel MC, Townsend IT, Tyerman GH, Mier RJ, Northrup H. Testing for genetic associations with the PAX gene family in a spina bifida population. Am J Med Genet 2002; 110:195-202.
-
(2002)
Am J Med Genet
, vol.110
, pp. 195-202
-
-
Volcik, K.A.1
Blanton, S.H.2
Kruzel, M.C.3
Townsend, I.T.4
Tyerman, G.H.5
Mier, R.J.6
Northrup, H.7
-
65
-
-
0141925974
-
Evaluation of infant methyl-enetetrahydrofolate reductase genotype, maternal vitamin use, and risk of high versus low level spina bifida defects
-
Volcik KA, Shaw GM, Lammer EJ, Zhu H, Finnell RH. Evaluation of infant methyl-enetetrahydrofolate reductase genotype, maternal vitamin use, and risk of high versus low level spina bifida defects. Birth Defects Res Part A Clin Mol Teratol 2003; 67:154-57.
-
(2003)
Birth Defects Res Part a Clin Mol Teratol
, vol.67
, pp. 154-157
-
-
Volcik, K.A.1
Shaw, G.M.2
Lammer, E.J.3
Zhu, H.4
Finnell, R.H.5
-
66
-
-
0037341890
-
Homocysteine remethylation enzyme polymorphisms and increased risks for neural tube defects
-
Zhu H, Wicker NJ, Shaw GM, Lammer EJ, Hendricks K, Suarez L, Canfield M, Finnell RH. Homocysteine remethylation enzyme polymorphisms and increased risks for neural tube defects. Mol Genet Metab 2003; 78:216-21.
-
(2003)
Mol Genet Metab
, vol.78
, pp. 216-221
-
-
Zhu, H.1
Wicker, N.J.2
Shaw, G.M.3
Lammer, E.J.4
Hendricks, K.5
Suarez, L.6
Canfield, M.7
Finnell, R.H.8
-
67
-
-
0032954923
-
Infant methionine synthase variants and risk for spina bifida
-
Shaw GM, Todoroff K, Finnell RH, Lammer EJ, Leclerc D, Gravel RA, Rozen R. Infant methionine synthase variants and risk for spina bifida. JMed Genet 1999; 36:86-87.
-
(1999)
Jmed Genet
, vol.36
, pp. 86-87
-
-
Shaw, G.M.1
Todoroff, K.2
Finnell, R.H.3
Lammer, E.J.4
Leclerc, D.5
Gravel, R.A.6
Rozen, R.7
-
68
-
-
0033516526
-
Maternal vitamin use, infant C677T mutation in MTHFR, and isolated cleft palate risk
-
Shaw GM, Todoroff K, Finnell RH, Rozen R, Lammer EJ. Maternal vitamin use, infant C677T mutation in MTHFR, and isolated cleft palate risk. Am J Med Genet 1999; 85:84-85.
-
(1999)
Am J Med Genet
, vol.85
, pp. 84-85
-
-
Shaw, G.M.1
Todoroff, K.2
Finnell, R.H.3
Rozen, R.4
Lammer, E.J.5
-
69
-
-
0034190659
-
5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: A HuGE review
-
Botto LD, Yang Q. 5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: A HuGE review. Am J Epidemiol 2000; 151:862-77.
-
(2000)
Am J Epidemiol
, vol.151
, pp. 862-877
-
-
Botto, L.D.1
Yang, Q.2
-
70
-
-
0032751289
-
Role of the C677T polymorphism at the MTHFR gene on risk to nonsyndromic cleft lip with/without cleft palate: Results from a case-control study in Brazil
-
Gaspar DA, Pavanello RC, Zatz M, Passos-Bueno MR, Andre M, Steman S, Wyszynski DF, Matiolli SR. Role of the C677T polymorphism at the MTHFR gene on risk to nonsyndromic cleft lip with/without cleft palate: Results from a case-control study in Brazil. Am J Med Genet 1999; 87:197-99.
-
(1999)
Am J Med Genet
, vol.87
, pp. 197-199
-
-
Gaspar, D.A.1
Pavanello, R.C.2
Zatz, M.3
Passos-Bueno, M.R.4
Re, M.5
Steman, S.6
Wyszynski, D.F.7
Matiolli, S.R.8
-
71
-
-
0032802054
-
Methylenetetrahydrofolate reductase thermolabile variant and oral clefts
-
Mills JL, Kirke PN, Molloy AM, Burke H, Conley MR, Lee YJ, Mayne PD, Weir DG, Scott JM. Methylenetetrahydrofolate reductase thermolabile variant and oral clefts. Am J Med Genet 1999; 86:71-74.
-
(1999)
Am J Med Genet
, vol.86
, pp. 71-74
-
-
Mills, J.L.1
Kirke, P.N.2
Molloy, A.M.3
Burke, H.4
Conley, M.R.5
Lee, Y.J.6
Mayne, P.D.7
Weir, D.G.8
Scott, J.M.9
-
72
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
-
Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Matthews RG, Boers GJ, et al. A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase. Nat Genet 1995; 10:111-13.
-
(1995)
Nat Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
Goyette, P.4
Sheppard, C.A.5
Matthews, R.G.6
Boers, G.J.7
-
73
-
-
0031971515
-
Second common mutation in the methylenetetrahydrofo-late reductase gene: An additional risk factor for neural-tube defects
-
van der Put NM, Gabreels F, Stevens EM, Smeitink JA, Trijbels FJ, Eskes TK, van den Heuvel LP, Blom HJ. A second common mutation in the methylenetetrahydrofo-late reductase gene: An additional risk factor for neural-tube defects? Am J Hum Genet1998; 62:1044-51.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1044-1051
-
-
Van Der Put, N.M.1
Gabreels, F.2
Stevens, E.M.3
Smeitink, J.A.4
Trijbels, F.J.5
Eskes, T.K.6
Van Den Heuvel, L.P.7
Blom, H.8
-
74
-
-
0030027668
-
Relation between folate status, a common mutation in methylenetetrahydro-folate reductase, and plasma homocysteine concentrations
-
Jacques PF, Bostom AG, Williams RR, Ellison RC, Eckfeldt JH, Rosenberg IH, Selhub J, Rozen R. Relation between folate status, a common mutation in methylenetetrahydro-folate reductase, and plasma homocysteine concentrations. Circulation 1996; 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
-
75
-
-
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; 64:169-72.
-
(1998)
Mol Genet Metab
, vol.64
, pp. 169-172
-
-
Weisberg, I.1
Tran, P.2
Christensen, B.3
Sibani, S.4
Rozen, R.5
-
76
-
-
0034743914
-
The 1298A-->C polymorphism in methylenetetrahydrofolate reductase (MTHFR): In vitro expression and association with homocysteine
-
Weisberg IS, Jacques PF, Selhub J, Bostom AG, Chen Z, Curtis Ellison R, Eckfeldt JH, Rozen R. The 1298A-->C polymorphism in methylenetetrahydrofolate reductase (MTHFR): In vitro expression and association with homocysteine. Atherosclerosis2001; 156:409-15.
-
(2001)
Atherosclerosis
, vol.156
, pp. 409-415
-
-
Weisberg, I.S.1
Jacques, P.F.2
Selhub, J.3
Bostom, A.G.4
Chen, Z.5
Curtis Ellison, R.6
Eckfeldt, J.H.7
Rozen, R.8
-
77
-
-
38849187271
-
Folate and one-carbon metabolism gene polymorphisms and their associations with oral facial clefts
-
Boyles AL, Wilcox AJ, Taylor JA, Meyer K, Fredriksen A, Ueland PM, Drevon CA, Vollset SE, Lie RT. Folate and one-carbon metabolism gene polymorphisms and their associations with oral facial clefts. Am J Med Genet A 2008; 146A:440-49.
-
(2008)
Am J Med Genet A
, vol.146A
, pp. 440-449
-
-
Boyles, A.L.1
Wilcox, A.J.2
Taylor, J.A.3
Meyer, K.4
Fredriksen, A.5
Ueland, P.M.6
Drevon, C.A.7
Vollset, S.E.8
Lie, R.T.9
-
78
-
-
0027145847
-
Maternal plasma folate and vitamin B12 are independent risk factors for neural tube defects
-
Kirke PN, Molloy AM, Daly LE, Burke H, Weir DG, Scott JM. Maternal plasma folate and vitamin B12 are independent risk factors for neural tube defects. Q J Med 1993; 86:703-08.
-
(1993)
Q J Med
, vol.86
, pp. 703-708
-
-
Kirke, P.N.1
Molloy, A.M.2
Daly, L.E.3
Burke, H.4
Weir, D.G.5
Scott, J.M.6
-
79
-
-
0028844492
-
Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida
-
van der Put NM, Steegers-Theunissen RP, Frosst P, Trijbels FJ, Eskes TK, van den Heuvel LP, Mariman EC, den Heyer M, Rozen R, Blom HJ. Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida. Lancet 1995; 346:1070-71.
-
(1995)
Lancet
, vol.346
, pp. 1070-1071
-
-
Van Der Put, N.M.1
Steegers-Theunissen, R.P.2
Frosst, P.3
Trijbels, F.J.4
Eskes, T.K.5
Van Den Heuvel, L.P.6
Mariman, E.C.7
Den Heyer, M.8
Rozen, R.9
Blom, H.J.10
-
80
-
-
0029849703
-
Decreased methylene tetrahydrofolate reductase activity due to the 677C-->T mutation in families with spina bifida offspring
-
van der Put NM, van den Heuvel LP, Steegers-Theunissen RP, Trijbels FJ, Eskes TK, Mariman EC, den Heyer M, Blom HJ. Decreased methylene tetrahydrofolate reductase activity due to the 677C-->T mutation in families with spina bifida offspring. J Mol Med1996; 74:691-94.
-
(1996)
J Mol Med
, vol.74
, pp. 691-694
-
-
Van Der Put, N.M.1
Van Den Heuvel, L.P.2
Steegers-Theunissen, R.P.3
Trijbels, F.J.4
Eskes, T.K.5
Mariman, E.C.6
Den Heyer, M.7
Blom, H.J.8
-
81
-
-
0030018760
-
5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects
-
Ou CY, Stevenson RE, Brown VK, Schwartz CE, Allen WP, Khoury MJ, Rozen R, Oakley GP Jr, Adams MJ Jr. 5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects. Am J Med Genet 1996; 63:610-14.
-
(1996)
Am J Med Genet
, vol.63
, pp. 610-614
-
-
Ou, C.Y.1
Stevenson, R.E.2
Brown, V.K.3
Schwartz, C.E.4
Allen, W.P.5
Khoury, M.J.6
Rozen, R.7
Oakley, G.P.8
Adams, M.J.9
-
82
-
-
31944431893
-
Homocysteine metabolism in families from southern Italy with neural tube defects: Role of genetic and nutritional determinants
-
Grandone E, Corrao AM, Colaizzo D, Vecchione G, Di Girgenti C, Paladini D, Sardella L, et al. Homocysteine metabolism in families from southern Italy with neural tube defects: Role of genetic and nutritional determinants. Prenat Diagn 2006; 26:1-5.
-
(2006)
Prenat Diagn
, vol.26
, pp. 1-5
-
-
Grandone, E.1
Corrao, A.M.2
Colaizzo, D.3
Vecchione, G.4
Di Girgenti, C.5
Paladini, D.6
Sardella, L.7
-
83
-
-
3242881463
-
Metabolic effects and the methylenetetrahydrofo-late reductase (MTHFR) polymorphism associated with neural tube defects in southern Brazil
-
Felix TM, Leistner S, Giugliani R. Metabolic effects and the methylenetetrahydrofo-late reductase (MTHFR) polymorphism associated with neural tube defects in southern Brazil. Birth Defects Res A Clin Mol Teratol 2004; 70:459-63.
-
(2004)
Birth Defects Res a Clin Mol Teratol
, vol.70
, pp. 459-463
-
-
Felix, T.M.1
Leistner, S.2
Giugliani, R.3
-
84
-
-
0035987006
-
Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population
-
De Marco P, Calevo MG, Moroni A, Arata L, Merello E, Finnell RH, Zhu H, Andreussi L, Cama A, Capra V. Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population. J Hum Genet 2002; 47:319-24.
-
(2002)
J Hum Genet
, vol.47
, pp. 319-324
-
-
De Marco, P.1
Calevo, M.G.2
Moroni, A.3
Arata, L.4
Merello, E.5
Finnell, R.H.6
Zhu, H.7
Reussi, L.8
Cama, A.9
Capra, V.10
-
85
-
-
0242669376
-
Reduced folate carrier polymorphism (80A-->G) and neural tube defects
-
De Marco P, Calevo MG, Moroni A, Merello E, Raso A, Finnell RH, Zhu H, Andreussi L, Cama A, Capra V. Reduced folate carrier polymorphism (80A-->G) and neural tube defects. Eur J Hum Genet 2003; 11:245-52.
-
(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
Reussi, L.8
Cama, A.9
Capra, V.10
-
86
-
-
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 RH. Reduced folate carrier gene is a risk factor for neural tube defects in a Chinese population. Birth Defects Res A Clin Mol Teratol2005; 73:430-33.
-
(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
-
87
-
-
33646500328
-
Genetic variation of infant reduced folate carrier (A80G) and risk of orofacial defects and congenital heart defects in China
-
Pei L, Zhu H, Zhu J, Ren A, Finnell RH, Li Z. Genetic variation of infant reduced folate carrier (A80G) and risk of orofacial defects and congenital heart defects in China. Ann Epidemiol 2006; 16:352-56.
-
(2006)
Ann Epidemiol
, vol.16
, pp. 352-356
-
-
Pei, L.1
Zhu, H.2
Zhu, J.3
Ren, A.4
Finnell, R.H.5
Li, Z.6
-
88
-
-
0031815048
-
Infant TGF-alpha genotype, orofacial clefts, and maternal periconceptional multivitamin use
-
Shaw GM, Wasserman CR, Murray JC, Lammer EJ. Infant TGF-alpha genotype, orofacial clefts, and maternal periconceptional multivitamin use. Cleft Palate Craniofac J 1998; 35:366-70.
-
(1998)
Cleft Palate Craniofac J
, vol.35
, pp. 366-370
-
-
Shaw, G.M.1
Wasserman, C.R.2
Murray, J.C.3
Lammer, E.J.4
-
89
-
-
0036844005
-
Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida
-
Doolin MT, Barbaux S, McDonnell M, Hoess K, Whitehead AS, Mitchell LE. Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida. Am J Hum Genet 2002; 71:1222-26.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1222-1226
-
-
Doolin, M.T.1
Barbaux, S.2
McDonnell, M.3
Hoess, K.4
Whitehead, A.S.5
Mitchell, L.E.6
-
91
-
-
0029968027
-
Is mutated MTHFR a risk factor for neural tube defects?
-
Posey DL, Khoury MJ, Mulinare J, Adams MJ Jr, Ou CY. Is mutated MTHFR a risk factor for neural tube defects? Lancet 1996; 347:686-87.
-
(1996)
Lancet
, vol.347
, pp. 686-687
-
-
Posey, D.L.1
Khoury, M.J.2
Mulinare, J.3
Adams, M.J.4
Ou, C.Y.5
-
92
-
-
0023214676
-
Is disordered folate metabolism the basis for the genetic predisposition to neural tube defects?
-
Yates JR, Ferguson-Smith MA, Shenkin A, Guzman-Rodriguez R, White M, Clark BJ. Is disordered folate metabolism the basis for the genetic predisposition to neural tube defects? Clin Genet 1987; 31:279-87.
-
(1987)
Clin Genet
, vol.31
, pp. 279-287
-
-
Yates, J.R.1
Ferguson-Smith, M.A.2
Shenkin, A.3
Guzman-Rodriguez, R.4
White, M.5
Clark, B.J.6
-
93
-
-
0026610678
-
Folate and vitamin B12 concentrations in maternal and fetal blood, and amniotic fluid in second trimester pregnancies complicated by neural tube defects
-
Economides DL, Ferguson J, Mackenzie IZ, Darley J, Ware II, Holmes-Siedle M. Folate and vitamin B12 concentrations in maternal and fetal blood, and amniotic fluid in second trimester pregnancies complicated by neural tube defects. Br J Obstet Gynaecol1992; 99:23-25.
-
(1992)
Br J Obstet Gynaecol
, vol.99
, pp. 23-25
-
-
Economides, D.L.1
Ferguson, J.2
Mackenzie, I.Z.3
Darley, J.4
Ware, I.I.5
Holmes-Siedle, M.6
-
94
-
-
0026509087
-
Maternal vitamin levels during pregnancies producing infants with neural tube defects
-
Mills JL, Tuomilehto J, Yu KF, Colman N, Blaner WS, Koskela P, Rundle WE, Forman M, Toivanen L, Rhoads GG. Maternal vitamin levels during pregnancies producing infants with neural tube defects. J Pediatr 1992; 120:863-71.
-
(1992)
J Pediatr
, vol.120
, pp. 863-871
-
-
Mills, J.L.1
Tuomilehto, J.2
Yu, K.F.3
Colman, N.4
Blaner, W.S.5
Koskela, P.6
Rundle, W.E.7
Forman, M.8
Toivanen, L.9
Rhoads, G.G.10
-
95
-
-
0021889431
-
Maternal serum folate and vitamin B12 concentrations in pregnancies associated with neural tube defects
-
Molloy AM, Kirke P, Hillary I, Weir DG, Scott JM. Maternal serum folate and vitamin B12 concentrations in pregnancies associated with neural tube defects. Arch Dis Child1985; 60:660-65.
-
(1985)
Arch Dis Child
, vol.60
, pp. 660-665
-
-
Molloy, A.M.1
Kirke, P.2
Hillary, I.3
Weir, D.G.4
Scott, J.M.5
-
96
-
-
0034994046
-
Folate, homocysteine and neural tube defects: An overview
-
van der Put NM, van Straaten HW, Trijbels FJ, Blom HJ. Folate, homocysteine and neural tube defects: An overview. Exp Biol Med (Maywood) 2001; 226:243-70.
-
(2001)
Exp Biol Med (Maywood)
, vol.226
, pp. 243-270
-
-
Van Der Put, N.M.1
Van Straaten, H.W.2
Trijbels, F.J.3
Blom, H.J.4
-
98
-
-
0041305877
-
Membrane transport of folates
-
Matherly LH, Goldman DI. Membrane transport of folates. Vitam Horm 2003; 66:403-56.
-
(2003)
Vitam Horm
, vol.66
, pp. 403-456
-
-
Matherly, L.H.1
Goldman, D.I.2
-
99
-
-
0032807982
-
Carrier-mediated membrane transport of folates in mammalian cells
-
Sirotnak FM, Tolner B. Carrier-mediated membrane transport of folates in mammalian cells. Annu Rev Nutr 1999; 19:91-122.
-
(1999)
Annu Rev Nutr
, vol.19
, pp. 91-122
-
-
Sirotnak, F.M.1
Tolner, B.2
-
100
-
-
2942752383
-
Reduced-folate carrier (RFC) is expressed in placenta and yolk sac, as well as in cells of the developing forebrain, hindbrain, neural tube, craniofacial region, eye, limb buds and heart
-
Maddox DM, Manlapat A, Roon P, Prasad P, Ganapathy V, Smith SB. Reduced-folate carrier (RFC) is expressed in placenta and yolk sac, as well as in cells of the developing forebrain, hindbrain, neural tube, craniofacial region, eye, limb buds and heart. BMC Dev Biol 2003; 3:6.
-
(2003)
BMC Dev Biol
, vol.3
, pp. 6
-
-
Maddox, D.M.1
Manlapat, A.2
Roon, P.3
Prasad, P.4
Ganapathy, V.5
Smith, S.B.6
-
101
-
-
0035797082
-
Localization of the murine reduced folate carrier as assessed by immunohistochemical analysis
-
Wang Y, Zhao R, Russell RG, Goldman ID. Localization of the murine reduced folate carrier as assessed by immunohistochemical analysis. Biochim Biophys Acta 2001; 1513:49-54.
-
(2001)
Biochim Biophys Acta
, vol.1513
, pp. 49-54
-
-
Wang, Y.1
Zhao, R.2
Russell, R.G.3
Goldman, I.D.4
-
102
-
-
0024415796
-
Molecular cloning and characterization of the human folate-binding protein cDNA from placenta and malignant tissue culture (KB) cells
-
Elwood PC. Molecular cloning and characterization of the human folate-binding protein cDNA from placenta and malignant tissue culture (KB) cells. J Biol Chem 1989; 264:14893-901.
-
(1989)
J Biol Chem
, vol.264
, pp. 14893-14901
-
-
Elwood, P.C.1
-
103
-
-
0024440701
-
Homologous membrane folate binding proteins in human placenta: Cloning and sequence of a cDNA
-
Ratnam M, Marquardt H, Duhring JL, Freisheim JH. Homologous membrane folate binding proteins in human placenta: Cloning and sequence of a cDNA. Biochemistry1989; 28:8249-54.
-
(1989)
Biochemistry
, vol.28
, pp. 8249-8254
-
-
Ratnam, M.1
Marquardt, H.2
Duhring, J.L.3
Freisheim, J.H.4
-
104
-
-
0027417620
-
Expression of the human placental folate receptor transcript is regulated in human tissues. Organization and full nucleotide sequence of the gene
-
Page ST, Owen WC, Price K, Elwood PC. Expression of the human placental folate receptor transcript is regulated in human tissues. Organization and full nucleotide sequence of the gene. JMol Biol 1993; 229:1175-83.
-
(1993)
Jmol Biol
, vol.229
, pp. 1175-1183
-
-
Page, S.T.1
Owen, W.C.2
Price, K.3
Elwood, P.C.4
-
105
-
-
0028301752
-
Differential regulation of folate receptor isoforms in normal and malignant tissues in vivo and in established cell lines. Physiologic and clinical implications
-
Ross JF, Chaudhuri PK, Ratnam M. Differential regulation of folate receptor isoforms in normal and malignant tissues in vivo and in established cell lines. Physiologic and clinical implications. Cancer 1994; 73:2432-43.
-
(1994)
Cancer
, vol.73
, pp. 2432-2443
-
-
Ross, J.F.1
Chaudhuri, P.K.2
Ratnam, M.3
-
106
-
-
33751244559
-
Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption
-
Qiu A, Jansen M, Sakaris A, Min SH, Chattopadhyay S, Tsai E, Sandoval C, Zhao R, Akabas MH, Goldman ID. Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption. Cell 2006; 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
-
107
-
-
24144468186
-
The intestinal heme transporter revealed
-
Rouault TA. The intestinal heme transporter revealed. Cell 2005; 122:649-51.
-
(2005)
Cell
, vol.122
, pp. 649-651
-
-
Rouault, T.A.1
-
108
-
-
78649836356
-
Folic acid prevents conotruncal malformations in Folbp1 knockout mice: Role of folate in cardiac neural crest cell survival and migration
-
Jansen G, Peters G, eds., Heilbronn, Germany: Kluwer Academic Publishers
-
Gelineau-van Waes J, Aleman F, Maddox J, Bauer L, Wilberding J, Rosenquist T, Finnell R. Folic acid prevents conotruncal malformations in Folbp1 knockout mice: Role of folate in cardiac neural crest cell survival and migration. In: Jansen G, Peters G, eds., Chemistry and Biology of Pteridines and Folates. Heilbronn, Germany: Kluwer Academic Publishers, 2007:483-502.
-
(2007)
Chemistry and Biology of Pteridines and Folates
, pp. 483-502
-
-
Gelineau-Van Waes, J.1
Aleman, F.2
Maddox, J.3
Bauer, L.4
Wilberding, J.5
Rosenquist, T.6
Finnell, R.7
-
109
-
-
13444282095
-
Developmental consequences of in utero sodium arsenate exposure in mice with folate transport deficiencies
-
Spiegelstein O, Gould A, Wlodarczyk B, Tsie M, Lu X, Le C, Troen A, et al.Developmental consequences of in utero sodium arsenate exposure in mice with folate transport deficiencies. Toxicol Appl Pharmacol 2005; 203:18-26.
-
(2005)
Toxicol Appl Pharmacol
, vol.203
, pp. 18-26
-
-
Spiegelstein, O.1
Gould, A.2
Wlodarczyk, B.3
Tsie, M.4
Lu, X.5
Le, C.6
Troen, A.7
-
110
-
-
34250827739
-
Cardiovascular abnormalities in Folr1 knockout mice and folate rescue
-
Zhu H, Wlodarczyk BJ, Scott M, Yu W, Merriweather M, Gelineau-van Waes J, Schwartz RJ, Finnell RH. Cardiovascular abnormalities in Folr1 knockout mice and folate rescue. Birth Defects Res A Clin Mol Teratol 2007; 79:257-68.
-
(2007)
Birth Defects Res a Clin Mol Teratol
, vol.79
, pp. 257-268
-
-
Zhu, H.1
Wlodarczyk, B.J.2
Scott, M.3
Yu, W.4
Merriweather, M.5
Gelineau-Van Waes, J.6
Schwartz, R.J.7
Finnell, R.H.8
-
111
-
-
13444291027
-
Folate transport gene inactivation in mice increases sensitivity to colon carcinogenesis
-
Ma DW, Finnell RH, Davidson LA, Callaway ES, Spiegelstein O, Piedrahita JA, Salbaum JM, et al. Folate transport gene inactivation in mice increases sensitivity to colon carcinogenesis. Cancer Res 2005; 65:887-97.
-
(2005)
Cancer Res
, vol.65
, pp. 887-897
-
-
Ma, D.W.1
Finnell, R.H.2
Davidson, L.A.3
Callaway, E.S.4
Spiegelstein, O.5
Piedrahita, J.A.6
Salbaum, J.M.7
-
112
-
-
0035894337
-
Arsenic-induced congenital malformations in genetically susceptible folate binding protein-2 knockout mice
-
Wlodarczyk B, Spiegelstein O, Gelineau-van Waes J, Vorce RL, Lu X, Le CX, Finnell RH. Arsenic-induced congenital malformations in genetically susceptible folate binding protein-2 knockout mice. Toxicol Appl Pharmacol 2001; 177:238-46.
-
(2001)
Toxicol Appl Pharmacol
, vol.177
, pp. 238-246
-
-
Wlodarczyk, B.1
Spiegelstein, O.2
Gelineau-Van Waes, J.3
Vorce, R.L.4
Lu, X.5
Le, C.X.6
Finnell, R.H.7
-
114
-
-
0035971190
-
Rescue of embryonic lethality in reduced folate carrier-deficient mice by maternal folic acid supplementation reveals early neonatal failure of hematopoietic organs
-
Zhao R, Russell RG, Wang Y, Liu L, Gao F, Kneitz B, Edelmann W, Goldman ID. Rescue of embryonic lethality in reduced folate carrier-deficient mice by maternal folic acid supplementation reveals early neonatal failure of hematopoietic organs. J Biol Chem2001; 276:10224-28.
-
(2001)
J Biol Chem
, vol.276
, pp. 10224-10228
-
-
Zhao, R.1
Russell, R.G.2
Wang, Y.3
Liu, L.4
Gao, F.5
Kneitz, B.6
Edelmann, W.7
Goldman, I.D.8
-
115
-
-
0035282903
-
Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomo-cysteinemia and decreased methylation capacity, with neuropathology and aortic lipid deposition
-
Chen Z, Karaplis AC, Ackerman SL, Pogribny IP, Melnyk S, Lussier-Cacan S, Chen MF, et al. Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomo-cysteinemia and decreased methylation capacity, with neuropathology and aortic lipid deposition. Hum Mol Genet 2001; 10:433-43.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 433-443
-
-
Chen, Z.1
Karaplis, A.C.2
Ackerman, S.L.3
Pogribny, I.P.4
Melnyk, S.5
Lussier-Cacan, S.6
Chen, M.F.7
-
116
-
-
0030986598
-
Strain-dependent alterations in the expression of folate pathway genes following teratogenic exposure to valproic acid in a mouse model
-
Finnell RH, Wlodarczyk BC, Craig JC, Piedrahita JA, Bennett GD. Strain-dependent alterations in the expression of folate pathway genes following teratogenic exposure to valproic acid in a mouse model. Am J Med Genet 1997; 70:303-11.
-
(1997)
Am J Med Genet
, vol.70
, pp. 303-311
-
-
Finnell, R.H.1
Wlodarczyk, B.C.2
Craig, J.C.3
Piedrahita, J.A.4
Bennett, G.D.5
-
117
-
-
0027198703
-
Absorption of pteroylpo-lyglutamates in mothers of infants with neural tube defects
-
Bower C, Stanley FJ, Croft M, de Klerk N, Davis RE, Nicol DJ. Absorption of pteroylpo-lyglutamates in mothers of infants with neural tube defects. Br J Nutr 1993; 69:827-34.
-
(1993)
Br J Nutr
, vol.69
, pp. 827-834
-
-
Bower, C.1
Stanley, F.J.2
Croft, M.3
De Klerk, N.4
Davis, R.E.5
Nicol, D.J.6
-
118
-
-
0027280589
-
Maternal folate status and the risk for neural tube defects. The role of dietary folate
-
Bower C, Stanley FJ, Nicol DJ. Maternal folate status and the risk for neural tube defects. The role of dietary folate. Ann N YAcad Sci 1993; 678:146-55.
-
(1993)
Ann N Yacad Sci
, vol.678
, pp. 146-155
-
-
Bower, C.1
Stanley, F.J.2
Nicol, D.J.3
-
119
-
-
0023747114
-
Amniotic fluid folate, vitamin B12 and transcobalamins in neural tube defects
-
Gardiki-Kouidou P, Seller MJ. Amniotic fluid folate, vitamin B12 and transcobalamins in neural tube defects. Clin Genet 1988; 33:441-48.
-
(1988)
Clin Genet
, vol.33
, pp. 441-448
-
-
Gardiki-Kouidou, P.1
Seller, M.J.2
-
120
-
-
0027983904
-
The methylfolate axis in neural tube defects: In vitro characterisation and clinical investigation
-
Lucock MD, Wild J, Schorah CJ, Levene MI, Hartley R. The methylfolate axis in neural tube defects: In vitro characterisation and clinical investigation. Biochem Med Metab Biol 1994; 52:101-14.
-
(1994)
Biochem Med Metab Biol
, vol.52
, pp. 101-114
-
-
Lucock, M.D.1
Wild, J.2
Schorah, C.J.3
Levene, M.I.4
Hartley, R.5
-
121
-
-
0026507989
-
Nutrient levels in amniotic fluid from women with normal and neural tube defect pregnancies
-
Weekes EW, Tamura T, Davis RO, Birch R, Vaughn WH, Franklin JC, Barganier C, Cosper P, Finley SC, Finley WH. Nutrient levels in amniotic fluid from women with normal and neural tube defect pregnancies. Biol Neonate 1992; 61:226-31.
-
(1992)
Biol Neonate
, vol.61
, pp. 226-231
-
-
Weekes, E.W.1
Tamura, T.2
Davis, R.O.3
Birch, R.4
Vaughn, W.H.5
Franklin, J.C.6
Barganier, C.7
Cosper, P.8
Finley, S.C.9
Finley, W.H.10
-
122
-
-
0027222697
-
Investigation of factors influencing folate status in women who have had a neural tube defect-affected infant
-
Wild J, Schorah CJ, Sheldon TA, Smithells RW. Investigation of factors influencing folate status in women who have had a neural tube defect-affected infant. Br J Obstet Gynaecol 1993; 100:546-49.
-
(1993)
Br J Obstet Gynaecol
, vol.100
, pp. 546-549
-
-
Wild, J.1
Schorah, C.J.2
Sheldon, T.A.3
Smithells, R.W.4
-
123
-
-
0027231447
-
Possible abnormalities of folate and vitamin B12 metabolism associated with neural tube defects
-
Schorah CJ, Habibzadeh N, Wild J, Smithells RW, Seller MJ. Possible abnormalities of folate and vitamin B12 metabolism associated with neural tube defects. Ann N Y Acad Sci 1993; 678:81-91.
-
(1993)
Ann N Y Acad Sci
, vol.678
, pp. 81-91
-
-
Schorah, C.J.1
Habibzadeh, N.2
Wild, J.3
Smithells, R.W.4
Seller, M.J.5
-
124
-
-
43749104028
-
Microarray analysis of E9.5 reduced folate carrier (RFC1; Slc19a1) knockout embryos reveals altered expression of genes in the cubilin-megalin multiligand endocytic receptor complex
-
Gelineau-van Waes J, Maddox JR, Smith LM, van Waes M, Wilberding J, Eudy JD, Bauer LK, Finnell RH. Microarray analysis of E9.5 reduced folate carrier (RFC1; Slc19a1) knockout embryos reveals altered expression of genes in the cubilin-megalin multiligand endocytic receptor complex. BMC Genomics 2008; 9:156.
-
(2008)
BMC Genomics
, vol.9
, pp. 156
-
-
Gelineau-Van Waes, J.1
Maddox, J.R.2
Smith, L.M.3
Van Waes, M.4
Wilberding, J.5
Eudy, J.D.6
Bauer, L.K.7
Finnell, R.H.8
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