-
1
-
-
4344690205
-
Hyperhomocysteinemia, pregnancy complications, and the timing of investigation
-
DOI 10.1097/01.AOG.0000129955.47943.2a
-
Steegers-Theunissen RP, Van Iersel CA, Peer PG, Nelen WL, Steegers EA. Hyperhomocysteinemia, pregnancy complications, and the timing of investigation. Obstet Gynecol 2004;104:336-43. (Pubitemid 40458881)
-
(2004)
Obstetrics and Gynecology
, vol.104
, Issue.2
, pp. 336-343
-
-
Steegers-Theunissen, R.P.1
Van Iersel, C.A.2
Peer, P.G.3
Nelen, W.L.4
Steegers, E.A.5
-
2
-
-
0037120820
-
Plasma folate levels and risk of spontaneous abortion
-
George L, Mills JL, Johansson AL, Nordmark A, Olander B, Granath F, Cnattingius S. Plasma folate levels and risk of spontaneous abortion. JAMA 2002;288:1867-73. (Pubitemid 35168142)
-
(2002)
Journal of the American Medical Association
, vol.288
, Issue.15
, pp. 1867-1873
-
-
George, L.1
Mills, J.L.2
Johansson, A.L.V.3
Nordmark, A.4
Olander, B.5
Granath, F.6
Cnattingius, S.7
-
4
-
-
37349000559
-
Folic acid supplementation in early second trimester and the risk of preeclampsia
-
Wen SW, Chen XK, Rodger M, White RR, Yang Q, Smith GN, Sigal RJ, Perkins SL, Walker MC. Folic acid supplementation in early second trimester and the risk of preeclampsia. Am J Obstet Gynecol 2008: 198:45.e1-7.
-
(2008)
Am J Obstet Gynecol
, vol.198
-
-
Wen, S.W.1
Chen, X.K.2
Rodger, M.3
White, R.R.4
Yang, Q.5
Smith, G.N.6
Sigal, R.J.7
Perkins, S.L.8
Walker, M.C.9
-
5
-
-
0034073977
-
Plasma total homocysteine, pregnancy complications, and adverse pregnancy outcomes: The Hordaland Homocysteine Study
-
Vollset SE, Refsum H, Irgens LM, Emblem BM, Tverdal A, Gjessing HK, Monsen AL, Ueland PM. Plasma total homocysteine, pregnancy complications, and adverse pregnancy outcomes: the Hordaland Homocysteine study. Am J Clin Nutr 2000;71:962-8. (Pubitemid 30176580)
-
(2000)
American Journal of Clinical Nutrition
, vol.71
, Issue.4
, pp. 962-968
-
-
Vollset, S.E.1
Refsum, H.2
Irgens, L.M.3
Emblem, B.M.4
Tverdal, A.5
Gjessing, H.K.6
Monsen, A.L.B.7
Ueland, P.M.8
-
6
-
-
0026571546
-
Intrauterine growth retardation, perinatal death, and maternal homocysteine levels
-
Burke G, Robinson K, Refsum H, Stuart B, Drumm J, Graham I. Intrauterine growth retardation, perinatal death, and maternal homocysteine levels. N Engl J Med 1992;326:69-70.
-
(1992)
N Engl J Med
, vol.326
, pp. 69-70
-
-
Burke, G.1
Robinson, K.2
Refsum, H.3
Stuart, B.4
Drumm, J.5
Graham, I.6
-
7
-
-
32244434573
-
Plasma homocysteine in late pregnancies complicated with preeclampsia and in newborns
-
DOI 10.1055/s-2005-918889
-
Baksu A, Taskin M, Goker N, Baksu B, Uluocak A. Plasma homocysteine inlate pregnancies complicated with preeclampsia and in newborns. Am J Perinatol 2006;23:31-5. (Pubitemid 43214401)
-
(2006)
American Journal of Perinatology
, vol.23
, Issue.1
, pp. 31-35
-
-
Baksu, A.1
Taskin, M.2
Goker, N.3
Baksu, B.4
Uluocak, A.5
-
8
-
-
10044220574
-
Second trimester folate status and preterm birth
-
DOI 10.1016/j.ajog.2004.07.076, PII S0002937804008609
-
Siega-Riz AM, Savitz DA, Zeisel SH, Thorp JM, Herring A. Second trimester folate status and preterm birth. Am J Obstet Gynecol 2004; 191:1851-7. (Pubitemid 39601487)
-
(2004)
American Journal of Obstetrics and Gynecology
, vol.191
, Issue.6
, pp. 1851-1857
-
-
Siega-Riz, A.M.1
Savitz, D.A.2
Zeisel, S.H.3
Thorp, J.M.4
Herring, A.5
-
9
-
-
0027080461
-
Prevention of the first occurrence of neural-tube defects by periconceptional vitamin supplementation
-
Czeizel AE, Dudas I. Prevention ofthe first occurrence of neural-tube defects by periconceptional vitamin supplementation. N Engl J Med 1992;327:1832-5. (Pubitemid 23003073)
-
(1992)
New England Journal of Medicine
, vol.327
, Issue.26
, pp. 1832-1835
-
-
Czeizel, A.E.1
Dudas, I.2
-
10
-
-
0025863475
-
Prevention ofneural tube defects: Results of the Medical Research Council Vitamin Study
-
MRC. MRC Vitamin Study Research Group
-
MRC. Prevention ofneural tube defects: results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group. Lancet 1991;338:131-7.
-
(1991)
Lancet
, vol.338
, pp. 131-137
-
-
-
11
-
-
33846788502
-
Prenatal multivitamin supplementation and rates of congenital anomalies: A meta-analysis
-
Goh YI, Bollano E, Einarson TR, Koren G. Prenatal multivitamin supplementation and rates of congenital anomalies: a meta-analysis. J Obstet Gynaecol Can 2006;28:680-9.
-
(2006)
J Obstet Gynaecol Can
, vol.28
, pp. 680-689
-
-
Goh, Y.I.1
Bollano, E.2
Einarson, T.R.3
Koren, G.4
-
12
-
-
50949104067
-
Changes infrequencies of select congenital anomalies since the onset of folic acid fortification in a Canadian birth defect registry
-
Godwin KA, Sibbald B, Bedard T, Kuzeljevic B, Lowry RB, Arbour L. Changes infrequencies of select congenital anomalies since the onset of folic acid fortification in a Canadian birth defect registry. Can J Public Health 2008;99:271-5.
-
(2008)
Can J Public Health
, vol.99
, pp. 271-275
-
-
Godwin, K.A.1
Sibbald, B.2
Bedard, T.3
Kuzeljevic, B.4
Lowry, R.B.5
Arbour, L.6
-
13
-
-
27644569002
-
Changes in the birth prevalence of selected birth defects after grain fortification with folic acid in the United States: Findings from a multi-state population-based study
-
DOI 10.1002/bdra.20210
-
Canfield MA, Collins JS, Botto LD, Williams LJ, Mai CT, Kirby RS, Pearson K, Devine O, Mulinare J. Changes inthe birth prevalence of selected birth defects after grain fortification with folic acid in the United States: findings from a multi-state population-based study. Birth Defects Res A Clin Mol Teratol 2005;73:679-89. (Pubitemid 41572010)
-
(2005)
Birth Defects Research Part A - Clinical and Molecular Teratology
, vol.73
, Issue.10
, pp. 679-689
-
-
Canfield, M.A.1
Collins, J.S.2
Botto, L.D.3
Williams, L.J.4
Mai, C.T.5
Kirby, R.S.6
Peareon, K.7
Devine, O.8
Mulinare, J.9
-
14
-
-
33846807689
-
Fetal and maternal MTHFR C677T genotype, maternal folate intake and the risk of nonsyndromic oral clefts
-
DOI 10.1002/ajmg.a.31462
-
Chevrier C, Perret C, BahuauM, Zhu H, Nelva A, Herman C, Francannet C, Robert-Gnansia E, Finnell RH, Cordier S. Fetal and maternal MTHFR C677T genotype, maternal folate intake and the risk of nonsyndromic oral clefts. Am J Med Genet A 2007;143:248-57. (Pubitemid 46212215)
-
(2007)
American Journal of Medical Genetics, Part A
, vol.143
, Issue.3
, pp. 248-257
-
-
Chevrier, C.1
Perret, C.2
Bahuau, M.3
Zhu, H.4
Nelva, A.5
Herman, C.6
Francannet, C.7
Robert-Gnansia, E.8
Finnell, R.H.9
Cordier, S.10
-
16
-
-
0242600545
-
Does the interaction between maternal folate intake and the methylenetetrahydrofolate reductase polymorphisms affect the risk of cleft lip with or without cleft palate?
-
DOI 10.1093/aje/kwg005
-
van Rooij IA, Vermeij-Keers C, Kluijtmans LA, Ocke MC, Zielhuis GA, Goorhuis-Brouwer SM, van der Biezen JJ, Kuijpers-Jagtman AM, Steegers-Theunissen RP. Does the interaction between maternal folate intake and the methylenetetrahydrofolate reductase polymorphisms affect the risk of cleft lip with or without cleft palate? Am J Epidemiol 2003;157:583-91. (Pubitemid 36368528)
-
(2003)
American Journal of Epidemiology
, vol.157
, Issue.7
, pp. 583-591
-
-
Van Rooij, I.A.L.M.1
Vermeij-Keers, C.2
Kluijtmans, L.A.J.3
Ocke, M.C.4
Zielhuis, G.A.5
Goorhuis-Brouwer, S.M.6
Van Der, B.J.-J.7
Kuijpers-Jagtman, A.-M.8
Steegers-Theunissen, R.P.M.9
-
17
-
-
1842418757
-
Low erythrocyte folate status and polymorphic variation in folate-related genes are associated with risk of neural tube defect pregnancy
-
DOI 10.1016/j.ymgme.2003.12.010, PII S1096719203002932
-
Relton CL, Wilding CS, Laffling AJ, Jonas PA, Burgess T, Binks K, Tawn EJ, Burn J. Low erythrocyte folate status and polymorphic variation in folate-related genes are associated with risk of neural tube defect pregnancy. Mol Genet Metab 2004;81:273-81. (Pubitemid 38429990)
-
(2004)
Molecular Genetics and Metabolism
, vol.81
, Issue.4
, pp. 273-281
-
-
Relton, C.L.1
Wilding, C.S.2
Laffling, A.J.3
Jonas, P.A.4
Burgess, T.5
Binks, K.6
Tawn, E.J.7
Burn, J.8
-
18
-
-
0030027668
-
Relation between folate status, a common mutation in methylenetetrahydrofolate 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 methylenetetrahydrofolate reductase, and plasma homocysteine concentrations. Circulation 1996;93:7-9. (Pubitemid 26006560)
-
(1996)
Circulation
, vol.93
, Issue.1
, 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
-
19
-
-
0037117501
-
A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status
-
DOI 10.1073/pnas.062066299
-
Friso S, Choi SW, Girelli D, Mason JB, Dolnikowski GG, Bagley PJ, Olivieri O, Jacques PF, Rosenberg IH, Corrocher R, et al. A common mutation inthe 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status. Proc Natl Acad Sci USA 2002;99:5606-11. (Pubitemid 34411596)
-
(2002)
Proceedings of the National Academy of Sciences of the United States of America
, vol.99
, Issue.8
, pp. 5606-5611
-
-
Friso, S.1
Choi, S.-W.2
Girelli, D.3
Mason, J.B.4
Dolnikowski, G.G.5
Bagley, P.J.6
Olivieri, O.7
Jacques, P.F.8
Rosenberg, I.H.9
Corrocher, R.10
Selhub, J.11
-
20
-
-
0032937206
-
Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects
-
DOI 10.1002/(SICI)1096-8628(19990521)84:2<151::AID-AJMG12>3.0.CO;2- T
-
Christensen B, Arbour L, Tran P, Leclerc D, Sabbaghian N, Platt R, Gilfix BM, Rosenblatt DS, Gravel RA, Forbes P, et al. Genetic polymorphisms inmethylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects. Am J Med Genet 1999;84:151-7. (Pubitemid 29201082)
-
(1999)
American Journal of Medical Genetics
, vol.84
, Issue.2
, pp. 151-157
-
-
Christensen, B.1
Arbour, L.2
Tran, P.3
Leclerc, D.4
Sabbaghian, N.5
Platt, R.6
Gilfix, B.M.7
Rosenblatt, D.S.8
Gravel, R.A.9
Forbes, P.10
Rozen, R.11
-
21
-
-
33646500328
-
Genetic variation ofinfant 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 ofinfant reduced folate carrier (A80G) and risk of orofacial defects and congenital heart defects in China. Ann Epidemiol 2006;16:352-6.
-
(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
-
22
-
-
33645473405
-
Maternal MTHFR 677C>T is a risk factor for congenital heart defects: Effect modification by periconceptional folate supplementation
-
van Beynum IM, Kapusta L, den Heijer M, Vermeulen SH, Kouwenberg M, Daniels O, Blom HJ. Maternal MTHFR 677C>T is a risk factor for congenital heart defects: effect modification by periconceptional folate supplementation. Eur Heart J 2006;27:981-7.
-
(2006)
Eur Heart J
, vol.27
, pp. 981-987
-
-
Van Beynum, I.M.1
Kapusta, L.2
Den Heijer, M.3
Vermeulen, S.H.4
Kouwenberg, M.5
Daniels, O.6
Blom, H.J.7
-
23
-
-
33745095012
-
Mitochondrial one-carbon metabolism is adapted to the specific needs of yeast, plants and mammals
-
DOI 10.1002/bies.20420
-
Christensen KE, MacKenzie RE. Mitochondrial one-carbon metabolism isadapted to the specific needs of yeast, plants and mammals. Bioessays 2006;28:595-605. (Pubitemid 43886185)
-
(2006)
BioEssays
, vol.28
, Issue.6
, pp. 595-605
-
-
Christensen, K.E.1
MacKenzie, R.E.2
-
24
-
-
51849127760
-
Folate-mediated one-carbon metabolism
-
Fox JT, Stover PJ. Folate-mediated one-carbon metabolism. Vitam Horm 2008;79:1-44.
-
(2008)
Vitam Horm
, vol.79
, pp. 1-44
-
-
Fox, J.T.1
Stover, P.J.2
-
25
-
-
18644379774
-
A polymorphism, R653Q, in the trifunctional enzyme methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase/formyltetrahydrofolate synthetase is a maternal genetic risk factor for neural tube defects: Report of the birth defects research group
-
DOI 10.1086/344213
-
Brody LC, Conley M, Cox C, Kirke PN, McKeever MP, Mills JL, Molloy AM, O'Leary VB, Parle-McDermott A, Scott JM, et al. A polymorphism, R653Q, inthe trifunctional enzyme methylenetetrahydrofolate dehydrogenase/ methenyltetrahydrofolate cyclohydrolase/formyltetrahydrofolate synthetase is amaternal genetic risk factor for neural tube defects: report of the Birth Defects Research Group. Am J Hum Genet 2002;71:1207-15. (Pubitemid 35305240)
-
(2002)
American Journal of Human Genetics
, vol.71
, Issue.5
, pp. 1207-1215
-
-
Brody, L.C.1
Conley, M.2
Cox, C.3
Kirke, P.N.4
McKeever, M.P.5
Mills, J.L.6
Molloy, A.M.7
O'Leary, V.B.8
Parle-McDermott, A.9
Scott, J.M.10
Swanson, D.A.11
-
26
-
-
33744460203
-
Confirmation of the R653Q polymorphism of the trifunctional C1-synthase enzyme as a maternal risk for neural tube defects in the Irish population
-
DOI 10.1038/sj.ejhg.5201603, PII 5201603
-
Parle-McDermott A, Kirke PN, Mills JL, Molloy AM, Cox C, O'Leary VB, Pangilinan F, Conley M, Cleary L, Brody LC, et al. Confirmation of the R653Q polymorphism of the trifunctional C1-synthase enzyme as a maternal risk for neural tube defects in the Irish population. Eur J Hum Genet 2006;14:768-72. (Pubitemid 43797275)
-
(2006)
European Journal of Human Genetics
, vol.14
, Issue.6
, pp. 768-772
-
-
Parle-McDermott, A.1
Kirke, P.N.2
Mills, J.L.3
Molloy, A.M.4
Cox, C.5
O'Leary, V.B.6
Pangilinan, F.7
Conley, M.8
Cleary, L.9
Brody, L.C.10
Scott, J.M.11
-
27
-
-
31544464705
-
Evaluation of a methylenetetrahydrofolate-dehydrogenase 1958G>A polymorphism for neural tube defect risk
-
DOI 10.1007/s10038-005-0329-6
-
De Marco P, Merello E, Calevo MG, Mascelli S, Raso A, Cama A, Capra V. Evaluation of amethylenetetrahydrofolate-dehydrogenase 1958G>A polymorphism for neural tube defect risk. J Hum Genet 2006; 51:98-103. (Pubitemid 43155452)
-
(2006)
Journal of Human Genetics
, vol.51
, Issue.2
, pp. 98-103
-
-
De Marco, P.1
Merello, E.2
Calevo, M.G.3
Mascelli, S.4
Raso, A.5
Cama, A.6
Capra, V.7
-
28
-
-
52249105530
-
Folate-related gene polymorphisms asrisk factors for cleft lip and cleft palate
-
Mills JL, Molloy AM, Parle-McDermott A, Troendle JF, Brody LC, Conley MR, Cox C, Pangilinan F, Orr DJ, Earley M, et al. Folate-related gene polymorphisms asrisk factors for cleft lip and cleft palate. Birth Defects Res A Clin Mol Teratol 2008;82:636-43.
-
(2008)
Birth Defects Res A Clin Mol Teratol
, vol.82
, pp. 636-643
-
-
Mills, J.L.1
Molloy, A.M.2
Parle-McDermott, A.3
Troendle, J.F.4
Brody, L.C.5
Conley, M.R.6
Cox, C.7
Pangilinan, F.8
Orr, D.J.9
Earley, M.10
-
29
-
-
59749093930
-
The MTHFD1 p.Arg653Gln variant alters enzyme function and increases risk for congenital heart defects
-
Christensen KE, Rohlicek CV, Andelfinger GU, Michaud J, Bigras JL, Richter A, Mackenzie RE, Rozen R. The MTHFD1 p.Arg653Gln variant alters enzyme function and increases risk for congenital heart defects. Hum Mutat 2009;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.L.5
Richter, A.6
Mackenzie, R.E.7
Rozen, R.8
-
30
-
-
19944432029
-
MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae
-
DOI 10.1002/ajmg.a.30354
-
Parle-McDermott A, Mills JL, Kirke PN, Cox C, Signore CC, Kirke S, Molloy AM, O'Leary VB, Pangilinan FJ, O'Herlihy C, et al. MTHFD1 R653Q polymorphism isa maternal genetic risk factor for severe abruptio placentae. Am J Med Genet A 2005;132:365-8. (Pubitemid 40175585)
-
(2005)
American Journal of Medical Genetics
, vol.132 A
, Issue.4
, pp. 365-368
-
-
Parle-McDermott, A.1
Mills, J.L.2
Kirke, P.N.3
Cox, C.4
Signore, C.C.5
Kirke, S.6
Molloy, A.M.7
O'Leary, V.B.8
Pangilinan, F.J.9
O'Herlihy, C.10
Brody, L.C.11
Scott, J.M.12
-
31
-
-
24344491209
-
A polymorphism in the MTHFD1 gene increases a mother's risk of having an unexplained second trimester pregnancy loss
-
DOI 10.1093/molehr/gah204
-
Parle-McDermott A, Pangilinan F, Mills JL, Signore CC, Molloy AM, Cotter A, Conley M, Cox C, Kirke PN, Scott JM, et al. A polymorphism inthe MTHFD1 gene increases a mother's risk of having an unexplained second trimester pregnancy loss. Mol Hum Reprod 2005;11: 477-80. (Pubitemid 41258233)
-
(2005)
Molecular Human Reproduction
, vol.11
, Issue.7
, pp. 477-480
-
-
Parle-McDermott, A.1
Pangilinan, F.2
Mills, J.L.3
Signore, C.C.4
Molloy, A.M.5
Cotter, A.6
Conley, M.7
Cox, C.8
Kirke, P.N.9
Scott, J.M.10
Brody, L.C.11
-
32
-
-
50349095834
-
Onecarbon metabolism enzyme polymorphisms and uteroplacental insufficiency
-
Furness DL, Fenech MF, Khong YT, Romero R, Dekker GA. Onecarbon metabolism enzyme polymorphisms and uteroplacental insufficiency. Am J Obstet Gynecol 2008:199:276.e1-8.
-
(2008)
Am J Obstet Gynecol
, vol.199
-
-
Furness, D.L.1
Fenech, M.F.2
Khong, Y.T.3
Romero, R.4
Dekker, G.A.5
-
33
-
-
59449092734
-
Mthfd1 isan essential gene in mice and alters biomarkers of impaired one-carbon metabolism
-
MacFarlane AJ, Perry CA, Girnary HH, Gao D, Allen RH, Stabler SP, Shane B, Stover PJ. Mthfd1 isan essential gene in mice and alters biomarkers of impaired one-carbon metabolism. J Biol Chem 2009; 284:1533-9.
-
(2009)
J Biol Chem
, vol.284
, pp. 1533-1539
-
-
MacFarlane, A.J.1
Perry, C.A.2
Girnary, H.H.3
Gao, D.4
Allen, R.H.5
Stabler, S.P.6
Shane, B.7
Stover, P.J.8
-
34
-
-
3242795763
-
Methylation demand: A key determinant of homocysteine metabolism
-
Brosnan JT, Jacobs RL, Stead LM, Brosnan ME. Methylation demand: akey determinant of homocysteine metabolism. Acta Biochim Pol 2004;51:405-13. (Pubitemid 38969303)
-
(2004)
Acta Biochimica Polonica
, vol.51
, Issue.2
, pp. 405-413
-
-
Brosnan, J.T.1
Jacobs, R.L.2
Stead, L.M.3
Brosnan, M.E.4
-
36
-
-
0034634630
-
Purification and properties of a folate-catabolizing enzyme
-
Suh JR, Oppenheim EW, Girgis S, Stover PJ. Purification and properties of a folate-catabolizing enzyme. J Biol Chem 2000;275:35646-55.
-
(2000)
J Biol Chem
, vol.275
, pp. 35646-35655
-
-
Suh, J.R.1
Oppenheim, E.W.2
Girgis, S.3
Stover, P.J.4
-
37
-
-
0027160548
-
Elevation of serum cystathionine levels in patients with cobalamin and folate deficiency
-
Stabler SP, Lindenbaum J, Savage DG, Allen RH. Elevation of serum cystathionine levels in patients with cobalamin and folate deficiency. Blood 1993;81:3404-13. (Pubitemid 23172927)
-
(1993)
Blood
, vol.81
, Issue.12
, pp. 3404-3413
-
-
Stabler, S.P.1
Lindenbaum, J.2
Savage, D.G.3
Allen, R.H.4
-
38
-
-
0027182884
-
Elevation of 2-methylcitric acid I and II levels in serum, urine, and cerebrospinal fluid of patients with cobalamin deficiency
-
DOI 10.1016/0026-0495(93)90010-L
-
Allen RH, Stabler SP, Savage DG, Lindenbaum J. Elevation of 2-methylcitric acid I and II levels in serum, urine, and cerebrospinal fluid of patients with cobalamin deficiency. Metabolism 1993;42:978-88. (Pubitemid 23230428)
-
(1993)
Metabolism: Clinical and Experimental
, vol.42
, Issue.8
, pp. 978-988
-
-
Allen, R.H.1
Stabler, S.P.2
Savage, D.G.3
Lindenbaum, J.4
-
39
-
-
0038819954
-
+-dependent methylenetetrahydrofolate dehydrogenase-cyclohydrolase are glycine auxotrophs
-
DOI 10.1074/jbc.M301718200
-
Patel H, Pietro ED, MacKenzie RE. Mammalian fibroblasts lacking mitochondrial NAD+-dependent methylenetetrahydrofolate dehydrogenasecyclohydrolase are glycine auxotrophs. J Biol Chem 2003;278:19436-41. (Pubitemid 36799339)
-
(2003)
Journal of Biological Chemistry
, vol.278
, Issue.21
, pp. 19436-19441
-
-
Patel, H.1
Di, P.E.2
MacKenzie, R.E.3
-
40
-
-
14844297720
-
Disruption of the Mthfd1 gene reveals a monofunctional 10- formyltetrahydrofolate synthetase in mammalian mitochondria
-
DOI 10.1074/jbc.M409380200
-
Christensen KE, Patel H, Kuzmanov U, Mejia NR, MacKenzie RE. Disruption of the mthfd1 gene reveals a monofunctional 10-formyltetrahydrofolate synthetase in mammalian mitochondria. J Biol Chem 2005;280:7597-602. (Pubitemid 40349652)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.9
, pp. 7597-7602
-
-
Christensen, K.E.1
Patel, H.2
Kuzmanov, U.3
Mejia, N.R.4
MacKenzie, R.E.5
-
42
-
-
0025810648
-
Hypoxanthine-maintained two-cell block inmouse embryos: Dependence on glucose and effect of hypoxanthine phosphoribosyltransferase inhibitors
-
Downs SM, Dow MP. Hypoxanthine-maintained two-cell block inmouse embryos: dependence on glucose and effect of hypoxanthine phosphoribosyltransferase inhibitors. Biol Reprod 1991;44:1025-39.
-
(1991)
Biol Reprod
, vol.44
, pp. 1025-1039
-
-
Downs, S.M.1
Dow, M.P.2
-
43
-
-
0026554901
-
Folate deficiency alone does not produce neural tube defects in mice
-
Heid MK, Bills ND, Hinrichs SH, Clifford AJ. Folate deficiency alone does not produce neural tube defects in mice. J Nutr 1992;122:888-94.
-
(1992)
J Nutr
, vol.122
, pp. 888-894
-
-
Heid, M.K.1
Bills, N.D.2
Hinrichs, S.H.3
Clifford, A.J.4
|