-
1
-
-
0142040354
-
Thrombophilias as risk factors for disorders of pregnancy and fetal damage
-
DOI 10.1159/000073589
-
Abbate R, Sofi F, Gensini F, Fatini C, Sticchi E, Fedi S. (2002). Thrombophilias as risk factors for disorders of pregnancy and fetal damage. Pathophysiol Haemost Thromb. 32: 318-321. (Pubitemid 37490561)
-
(2002)
Pathophysiology of Haemostasis and Thrombosis
, vol.32
, Issue.5-6
, pp. 318-321
-
-
Abbate, R.1
Sofi, F.2
Gensini, F.3
Fatini, C.4
Sticchi, E.5
Fedi, S.6
-
2
-
-
18144401263
-
Polymorphisms of genes involved in homocysteine metabolism in preeclampsia and in uncomplicated pregnancies
-
DOI 10.1016/j.ejogrb.2004.08.008
-
Also-Rallo E, Lopez-Quesada E, Urreizti R, Vilaseca MA, Lailla JM, Balcells S et al (2005). Polymorphisms of genes involved in homocysteine metabolism in preeclampsia and in uncomplicated pregnancies. Eur J Obstet Gynecol Reprod Biol. 120: 45-52. (Pubitemid 40615071)
-
(2005)
European Journal of Obstetrics Gynecology and Reproductive Biology
, vol.120
, Issue.1
, pp. 45-52
-
-
Also-Rallo, E.1
Lopez-Quesada, E.2
Urreizti, R.3
Vilaseca, M.A.4
Lailla, J.M.5
Balcells, S.6
Grinberg, D.7
-
3
-
-
75749090996
-
Variations in folate pathway genes are associated with unexplained female infertility
-
Epub ahead of print
-
Altmae S, Stavereus-Evers A, Ruiz JR, Laapere M, Syvanen T, Yngve A et al (2009). Variations in folate pathway genes are associated with unexplained female infertility. Fertil Steril. Epub ahead of print.
-
(2009)
Fertil Steril
-
-
Altmae, S.1
Stavereus-Evers, A.2
Ruiz, J.R.3
Laapere, M.4
Syvanen, T.5
Yngve, A.6
-
4
-
-
0031767657
-
Thrombophilia: A mechanism of disease in women with adverse pregnancy outcome and thrombotic lesions in the placenta
-
Arias F, Romero R, Joist H, Kraus FT (1998). Thrombophilia: a mechanism of disease in women with adverse pregnancy outcome and thrombotic lesions in the placenta. J Matern Fetal Med. 7: 277-286.
-
(1998)
J Matern Fetal Med
, vol.7
, pp. 277-286
-
-
Arias, F.1
Romero, R.2
Joist, H.3
Kraus, F.T.4
-
5
-
-
32544441249
-
Novel mutations in the 5′-UTR of the FOLR1 gene
-
DOI 10.1515/CCLM.2006.029
-
Börjel AK, Ynqve A, Sjöström M, Nilsson TK (2006). Novel mutations in the 5′-UTR of the FOLR1 gene. Clin Chem Lab Med. 44: 161-167. (Pubitemid 43237958)
-
(2006)
Clinical Chemistry and Laboratory Medicine
, vol.44
, Issue.2
, pp. 161-167
-
-
Borjel, A.K.1
Yngve, A.2
Sjostrom, M.3
Nilsson, T.K.4
-
6
-
-
0035989412
-
Prevalence of genetic markers for thrombophilia in recurrent pregnancy loss
-
Carp H, Salomon O, Seidman D, Dardik R, Rosenberg N, Inbal A (2002). Prevalence of genetic markers for thrombophilia in recurrent pregnancy loss. Hum Reprod. 17: 1633-1637. (Pubitemid 34661820)
-
(2002)
Human Reproduction
, vol.17
, Issue.6
, pp. 1633-1637
-
-
Carp, H.1
Salomon, O.2
Seidman, D.3
Dardik, R.4
Rosenberg, N.5
Inbal, A.6
-
7
-
-
0033623867
-
The effect of 677C > T and 1298A > C mutations on plasma homocysteine and 5,10-methylenetetrahydrofolate reductase activity in healthy subjects
-
Chango A, Boisson F, Barbé F, Quilliot D, Droesch S, Pfister M et al (2000). The effect of 677C - >T and 1298A - >C mutations on plasma homocysteine and 5, 10-methylenetetrahydrofolate reductase activity in healthy subjects. Br J Nutr. 83: 593-596. (Pubitemid 30392098)
-
(2000)
British Journal of Nutrition
, vol.83
, Issue.6
, pp. 593-596
-
-
Chango, A.1
Boisson, F.2
Barbe, F.3
Quilliot, D.4
Droesch, S.5
Pfister, M.6
Fillon-Emery, N.7
Lambert, D.8
Fremont, S.9
Rosenblatt, D.S.10
Nicolas, J.P.11
-
8
-
-
0033955432
-
Factor V Leiden and prothrombin G20210A mutations, but not methylenetetrahydrofolate reductase C677T, are associated with recurrent miscarriages
-
Foka ZJ, Lambropoulos AF, Saravelos H, Karas GB, Karavida A, Agorastos T et al (2000). Factor V Leiden and prothrombin G20210A mutations, but not methylenetetrahydrofolate reductase C677T, are associated with recurrent miscarriages. Hum Reprod. 15: 458-462. (Pubitemid 30076732)
-
(2000)
Human Reproduction
, vol.15
, Issue.2
, pp. 458-462
-
-
Foka, Z.J.1
Lambropoulos, A.F.2
Saravelos, H.3
Karas, G.B.4
Karavida, T.5
Agorastos6
Zournatzi, P.E.7
Makris8
Bontis, J.9
Kotsis, A.10
-
9
-
-
0032865186
-
A common mutation A1298C in human methylenetetrahydrofolate reductase gene: Association with plasma total homocysteine and folate concentrations
-
Friedman G, Goldschmidt N, Friedlander Y, Ben-Yehuda A, Selhub J, Babaey S et al (1999). A common mutation A1298C in human methylenetetrahydrofolate reductase gene: association with plasma total homocysteine and folate concentrations. J Nutr. 129: 1656-1661. (Pubitemid 29406617)
-
(1999)
Journal of Nutrition
, vol.129
, Issue.9
, pp. 1656-1661
-
-
Friedman, G.1
Goldschmidt, N.2
Friedlander, Y.3
Ben-Yehuda, A.4
Selhub, J.5
Babaey, S.6
Mendel, M.7
Kidron, M.8
Bar-On, H.9
-
10
-
-
0036019532
-
A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: Relationships with C677T polymorphism and homocysteine/folate metabolism
-
Friso S, Girelli D, Trabetti E, Stranieri C, Olivieri O, Tinazzi E et al (2002). A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: relationships with C677T polymorphism and homocysteine/folate metabolism. Clin Exp Med. 2: 7-12. (Pubitemid 34743942)
-
(2002)
Clinical and Experimental Medicine
, vol.2
, Issue.1
, pp. 7-12
-
-
Friso, S.1
Girelli, D.2
Trabetti, E.3
Stranieri, C.4
Olivieri, O.5
Tinazzi, E.6
Martinelli, N.7
Faccini, G.8
Pignatti, P.F.9
Corrocher, R.10
-
11
-
-
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 et al (1995). A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat. Genet. 10: 111-113.
-
(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
-
12
-
-
0028304102
-
Human methylenetetrahydrofolate reductase: Isolation of cDNA, mapping and mutation identification
-
DOI 10.1038/ng0694-195
-
Goyette P, Sumner JS, Milos R, Duncan AMV, Rosenblatt DS, Matthews RG et al (1994). Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification. Nature Genet. 7: 195-200. (Pubitemid 24174661)
-
(1994)
Nature Genetics
, vol.7
, Issue.2
, pp. 195-200
-
-
Goyette, P.1
Sumner, J.S.2
Milos, R.3
Duncan, A.M.V.4
Rosenblatt, D.S.5
Matthews, R.G.6
Rozen, R.7
-
13
-
-
0031978235
-
Methylene tetrahydrofolate reductase (MTHFR) 677T→C mutation and unexplained early pregnancy loss [1]
-
Grandone E, Margaglione M, Colaizzo D, d'Addedda M, D'Andrea G, Pavone G et al (1998). Methylene tetrahydrofolate reductase (MTHFR) 677T→C mutation and unexplained early pregnancy loss. Thromb Haemost. 79: 1056-1057. (Pubitemid 28224749)
-
(1998)
Thrombosis and Haemostasis
, vol.79
, Issue.5
, pp. 1056-1057
-
-
Grandone, E.1
Margaglione, M.2
Colaizzo, D.3
D'Addedda, M.4
D'Andrea, G.5
Pavone, G.6
Di, M.G.7
-
14
-
-
0033813493
-
Genomic structure and transcript variants of the human methylenetetrahydrofolate reductase gene
-
Homberger A, Linnebank M, Winter C, Willenbring H, Marquardt T, Harms E et al (2000). Genomic structure and transcript variants of the human methylenetetrahydrofolate reductase gene. Eur J Hum Genet. 8: 725-729.
-
(2000)
Eur J Hum Genet
, vol.8
, pp. 725-729
-
-
Homberger, A.1
Linnebank, M.2
Winter, C.3
Willenbring, H.4
Marquardt, T.5
Harms, E.6
-
15
-
-
33751243615
-
Total homocysteine, folate, and cobalamin, and their relation to genetic polymorphisms, lifestyle and body mass index in healthy children and adolescents
-
DOI 10.1203/01.pdr.0000246099.39469.18, PII 0000645020061200000020
-
Huemer M, Vonbion K, Födinger M, Krumpholz R, Hubmann M, Ulmer H et al (2006). Total homocysteine, folate, and cobalamin, and their relation to genetic polymorphisms, lifestyle and body mass index in healthy children and adolescents. Pediatr Res. 60: 764-769. (Pubitemid 44789523)
-
(2006)
Pediatric Research
, vol.60
, Issue.6
, pp. 764-769
-
-
Huemer, M.1
Vonblon, K.2
Fodinger, M.3
Krumpholz, R.4
Hubmann, M.5
Ulmer, H.6
Simma, B.7
-
16
-
-
17844375459
-
Thrombophilic polymorphisms and intrauterine growth restriction
-
DOI 10.1097/01.ede.0000158199.64871.b9
-
Infante-Rivard C, Rivard GE, Guiquet M, Gauthier R (2005). Thrombophilic polymorphisms and intrauterine growth restriction. Epidemiology. 16: 281-287. (Pubitemid 40586701)
-
(2005)
Epidemiology
, vol.16
, Issue.3
, pp. 281-287
-
-
Infante-Rivard, C.1
Rivard, G.-E.2
Guiguet, M.3
Gauthier, R.4
-
17
-
-
33746806663
-
MTHFR C677T polymorphism is not associated with placental abruption or preeclampsia in Finnish women
-
DOI 10.1080/10641950600745137, PII PQ37161V41375434
-
Jaaskelainen E, Keski-Nisula L, Toivonen S, Romppanen EL, Helisalmi S, Punnonen K et al (2006). MTHFR C677T polymorphism is not associated with placental abruption or preeclampsia in Finnish women. Hypertens Pregnancy. 25: 73-80. (Pubitemid 44180348)
-
(2006)
Hypertension in Pregnancy
, vol.25
, Issue.2
, pp. 73-80
-
-
Jaaskelainen, E.1
Keski-Nisula, L.2
Toivonen, S.3
Romppanen, E.-L.4
Helisalmi, S.5
Punnonen, K.6
Heinonen, S.7
-
18
-
-
33645826542
-
Genetic thrombophilic mutations among couples with recurrent miscarriage
-
Jivraj S, Rai R, Underwood J, Regan L (2006). Genetic thrombophilic mutations among couples with recurrent miscarriage. Hum Reprod. 21: 1161-1165.
-
(2006)
Hum Reprod
, vol.21
, pp. 1161-1165
-
-
Jivraj, S.1
Rai, R.2
Underwood, J.3
Regan, L.4
-
19
-
-
0023696435
-
Intermediate Homocysteinemia: A Thermolabile Variant of Methylenetetrahydrofolate Reductase
-
Kang SS, Zhou J, Wong PWK, Kowalisyn J, Strokosch G (1988). Intermediate Homocysteinemia: A Thermolabile Variant of Methylenetetrahydrofolate Reductase. Am J Hum Genet. 43: 414-421.
-
(1988)
Am J Hum Genet
, vol.43
, pp. 414-421
-
-
Kang, S.S.1
Zhou, J.2
Wong, P.W.K.3
Kowalisyn, J.4
Strokosch, G.5
-
20
-
-
0033021552
-
The placenta in maternal hyperhomocysteinaemia
-
Khong TY, Hague WM (1999). The placenta in maternal hyperhomocysteinaemia. Br J Obstet Gynaecol. 106: 273-278.
-
(1999)
Br J Obstet Gynaecol
, vol.106
, pp. 273-278
-
-
Khong, T.Y.1
Hague, W.M.2
-
21
-
-
28044447631
-
5, 10-Methylenetetrahydrofolate reductase polymorphisms and pharmacogenetcs: A new role of single nucleotide polymorphisms in the folate metabolic pathway in human health and disease
-
Kim YI (2005). 5, 10-Methylenetetrahydrofolate reductase polymorphisms and pharmacogenetcs: a new role of single nucleotide polymorphisms in the folate metabolic pathway in human health and disease. Nutr Rev. 63: 398-407.
-
(2005)
Nutr Rev
, vol.63
, pp. 398-407
-
-
Kim, Y.I.1
-
22
-
-
77952579305
-
Methylenetetrahydrofolate reductase (MTHFR) C677T, A1298C and G1793A genotypes, and the relationship between maternal folate intake, tibia lead and infant size birth
-
Kordas K, Ettinger AS, Lamadrid-Figueroa H, Tellez-Rojo MM, Hernandez-Avilla M, Hu H et al (2009). Methylenetetrahydrofolate reductase (MTHFR) C677T, A1298C and G1793A genotypes, and the relationship between maternal folate intake, tibia lead and infant size birth. Br J Nutrition. 2: 1-8.
-
(2009)
Br J Nutrition
, vol.2
, pp. 1-8
-
-
Kordas, K.1
Ettinger, A.S.2
Lamadrid-Figueroa, H.3
Tellez-Rojo, M.M.4
Hernandez-Avilla, M.5
Hu, H.6
-
23
-
-
12544249743
-
Management of thrombophilia in women with PVC
-
Kupfermine MJ (2005). Management of thrombophilia in women with PVC. Thromb Res. 115: 46-50.
-
(2005)
Thromb Res
, vol.115
, pp. 46-50
-
-
Kupfermine, M.J.1
-
24
-
-
0033153189
-
Hypercoagulable state mutation analysis in white patients with early first-trimester recurrent pregnancy loss
-
DOI 10.1016/S0015-0282(99)00133-8, PII S0015028299001338
-
Kutteh WH, Park VM, Deitcher SR (1999). Hypercoagulable state mutation analysis in white patients with early first-trimester recurrent pregnancy loss. Fertil Steril. 71: 1048-1053. (Pubitemid 29252494)
-
(1999)
Fertility and Sterility
, vol.71
, Issue.6
, pp. 1048-1053
-
-
Park, V.M.1
-
25
-
-
0032870680
-
Polymorphism for mutation of cytosine to thymine at location 677 in the methylenetetrahydrofolate reductase gene is associated with recurrent early fetal loss
-
Lissak A, Sharon A, Fruchter O, Kassel A, Sanderovitz J, Abramovici H (1999). Polymorphism for mutation of cytosine to thymine at location 677 in the methylenetetrahydrofolate reductase gene is associated with recurrent early fetal loss. Am J Obstet Gynecol. 181: 126-130.
-
(1999)
Am J Obstet Gynecol
, vol.181
, pp. 126-130
-
-
Lissak, A.1
Sharon, A.2
Fruchter, O.3
Kassel, A.4
Sanderovitz, J.5
Abramovici, H.6
-
26
-
-
0034610031
-
Mutations in coagulation factors in women with unexplained late fetal loss
-
Martinelli I, Taioli E, Cetin I, Marinoni A, Gerosa S, Villa MV et al (2000). Mutations in coagulation factors in women with unexplained late fetal loss. N Engl J Med. 343: 1015-1018.
-
(2000)
N Engl J Med
, vol.343
, pp. 1015-1018
-
-
Martinelli, I.1
Taioli, E.2
Cetin, I.3
Marinoni, A.4
Gerosa, S.5
Villa, M.V.6
-
27
-
-
33748421075
-
G1793A polymorphisms in the methylene-tetrahydrofolate gene: Effect of folic acid on homocysteine levels
-
DOI 10.1002/mnfr.200600020
-
Melo SS, Persuhn DC, Meirelles MS, Jordao AA, Vannucchi H (2006). G1793A polymorphisms in the methylene-tetrahydrofolate gene: effect of folic acid on homocysteine levels. Mol Nutr Food Res. 50: 769-774. (Pubitemid 44342474)
-
(2006)
Molecular Nutrition and Food Research
, vol.50
, Issue.8
, pp. 769-774
-
-
Melo, S.S.1
Persuhn, D.C.2
Meirelles, M.S.3
Jordao, A.A.4
Vannucchi, H.5
-
28
-
-
33244479387
-
Methylenetetrahydrofolate reductase C677T and A1298C polymorphism and changes in homocysteine concentrations in women with idiopathic recurrent pregnancy losses
-
DOI 10.1530/rep.1.00815
-
Mtiraoui N, Zammiti W, Ghazouani L, Braham NJ, Saidi S, Finan RR et al (2006). Methylenetetrahydrofolate reductase C677T and A1298C polymorphism and changes in homocysteine concentrations in women with idiopathic recurrent pregnancy losses. Reproduction. 131: 395-401. (Pubitemid 43273699)
-
(2006)
Reproduction
, vol.131
, Issue.2
, pp. 395-401
-
-
Mtiraoui, N.1
Zammiti, W.2
Ghazouani, L.3
Braham, N.J.4
Saidi, S.5
Finan, R.R.6
Almawi, W.Y.7
Mahjoub, T.8
-
29
-
-
0033638057
-
Hyperhomocysteinemia and recurrent early pregnancy loss: A meta-analysis
-
Nelen WL, Bloom HJ, Steegers EA, den Heijer M, Eskes TK (2000). Hyperhomocysteinemia and recurrent early pregnancy loss: a meta-analysis. Fertil Steril. 74: 1196-1199.
-
(2000)
Fertil Steril
, vol.74
, pp. 1196-1199
-
-
Nelen, W.L.1
Bloom, H.J.2
Steegers, E.A.3
Den Heijer, M.4
Eskes, T.K.5
-
30
-
-
0037079957
-
Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A
-
Rady PL, Szucs S, Grady J, Hudnall SD, Kellner LH, Nitowsky H et al (2002). Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A. Am J Med Genet. 107: 162-168.
-
(2002)
Am J Med Genet
, vol.107
, pp. 162-168
-
-
Rady, P.L.1
Szucs, S.2
Grady, J.3
Hudnall, S.D.4
Kellner, L.H.5
Nitowsky, H.6
-
31
-
-
0038281545
-
Is miscarriage a coagulopathy?
-
Rai R (2003). Is miscarriage a coagulopathy? Curr Opin Obstet Gynecol. 15: 265-268.
-
(2003)
Curr Opin Obstet Gynecol
, vol.15
, pp. 265-268
-
-
Rai, R.1
-
32
-
-
33747050669
-
Recurrent miscarriage
-
DOI 10.1016/S0140-6736(06)69204-0, PII S0140673606692040
-
Rai R, Regan L (2006). Recurrent miscarriage. Lancet. 368: 601-611. (Pubitemid 44209184)
-
(2006)
Lancet
, vol.368
, Issue.9535
, pp. 601-611
-
-
Rai, R.1
Regan, L.2
-
33
-
-
0035139803
-
Hypercoagulable thrombophilic defects and hyperhomocysteinemia in patients with recurrent pregnancy loss
-
Raziel A, Kornberg Y, Friedler S, Schachter M, Sela BA, Ron-El R (2001). Hypercoagulable thrombophilic defects and hyperhomocysteinemia in patients with recurrent pregnancy loss. Am J Reprod Immunol. 45: 65-71. (Pubitemid 32111900)
-
(2001)
American Journal of Reproductive Immunology
, vol.45
, Issue.2
, pp. 65-71
-
-
Raziel, A.1
Kornberg, Y.2
Friedler, S.3
Schachter, M.4
Sela, B.A.5
Ron-El, R.6
-
34
-
-
33751186905
-
Methylenetetrahydrofolate reductase C677T polymorphism and the risk of unexplained recurrent pregnancy loss: A meta-analysis
-
Ren A, Wang H (2006). Methylenetetrahydrofolate reductase C677T polymorphism and the risk of unexplained recurrent pregnancy loss: a meta-analysis. Fertil Steril. 86: 1716-1722.
-
(2006)
Fertil Steril
, vol.86
, pp. 1716-1722
-
-
Ren, A.1
Wang, H.2
-
35
-
-
0037443934
-
Thrombophilic disorders and fetal loss: A meta-analysis
-
DOI 10.1016/S0140-6736(03)12771-7
-
Rey E, Kahn SR, David M, Shrier I (2003).Thrombophilic disorders and fetal loss: a meta-analysis. Lancet. 361: 901-908. (Pubitemid 36335814)
-
(2003)
Lancet
, vol.361
, Issue.9361
, pp. 901-908
-
-
Rey, E.1
Kahn, S.R.2
David, M.3
Shrier, I.4
-
36
-
-
61549141386
-
Maternal MTHFR polymorphisms and risk of spontaneous abortion
-
Rodriguez-Guillen Mdel R, Torres-Sanchez L, Chen J, Galvan-Portillo M, Blanco-Munoz J, Anaya MA et al (2009). Maternal MTHFR polymorphisms and risk of spontaneous abortion. Salud Publica Mex. 51: 19-25.
-
(2009)
Salud Publica Mex
, vol.51
, pp. 19-25
-
-
Rodriguez-Guillen Mdel, R.1
Torres-Sanchez, L.2
Chen, J.3
Galvan-Portillo, M.4
Blanco-Munoz, J.5
Anaya, M.A.6
-
37
-
-
0031687887
-
A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity
-
DOI 10.1006/mgme.1998.2714
-
Weisberg I, Tran P, Christensen B, Sibani S, Rozen R (1998). A second genetic polymorphism in methylenetetrahydrofolate reductese (MTHFR) associated with decreased enzyme activity. Mol Genet Metabol. 64: 169-172. (Pubitemid 28453294)
-
(1998)
Molecular Genetics and Metabolism
, vol.64
, Issue.3
, pp. 169-172
-
-
Weisberg, I.1
Tran, P.2
Christensen, B.3
Sibani, S.4
Rozen, R.5
-
38
-
-
22544443919
-
Roles of methylenetetrahydrofolate reductase C677T polymorphism in repeated pregnancy loss
-
Wiwanitkit V (2005). Roles of methylenetetrahydrofolate reductase C677T polymorphism in repeated pregnancy loss. Clin Appl Thromb Hemost. 11: 343-345.
-
(2005)
Clin Appl Thromb Hemost
, vol.11
, pp. 343-345
-
-
Wiwanitkit, V.1
-
39
-
-
0031971515
-
A second common mutation in the methylenetetrahydrofolate reductase gene: An additional risk factor for neural-tube defects?
-
Van der Put NM, Gabreëls F, Stevens EM, Smeitink JA, Trijbels FJ, Eskes TK et al (1998). A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects? Am J Hum Genet. 62: 1044-1051.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1044-1051
-
-
Van Der Put, N.M.1
Gabreëls, F.2
Stevens, E.M.3
Smeitink, J.A.4
Trijbels, F.J.5
Eskes, T.K.6
-
40
-
-
0035909980
-
Effects of common polymorphisms on the properties of recombinant human methylenetetrahydrofolate reductase
-
DOI 10.1073/pnas.261469998
-
Yamada K, Chen Z, Rozen R, Matthews RG (2001). Effects of common polymorphisms on the properties of recombinant human methylenetetrahydrofolate reductase. Proc Nat Acad Sci. 98: 14853-14858. (Pubitemid 34013934)
-
(2001)
Proceedings of the National Academy of Sciences of the United States of America
, vol.98
, Issue.26
, pp. 14853-14858
-
-
Yamada, K.1
Chen, Z.2
Rozen, R.3
Matthews, R.G.4
-
41
-
-
8444245917
-
Association of pre-eclampsia with hyperhomocysteinaemia and methylenetetrahydrofolate reductase gene C677T polymorphism in a Turkish population
-
DOI 10.1111/j.1479-828X.2004.00283.x
-
Yilmaz H, Unlucerci Y, Gurdol F, Isbilen E, Isbir T (2004). Association of pre-eclampsia with hyperhomocysteinemia and methylenetetrahydrofolate reductase gene C677T polymorphism in a Turkish population. Aust NZJ Obstet Gynaecol. 44: 423-427. (Pubitemid 39485268)
-
(2004)
Australian and New Zealand Journal of Obstetrics and Gynaecology
, vol.44
, Issue.5
, pp. 423-427
-
-
Yilmaz, H.1
Unlucerci, Y.2
Gurdol, F.3
Isbilen, E.4
Isbir, T.5
-
42
-
-
85047696639
-
Increased frequency of combined methylenetetrahydrofolate reductase C677T and A1298C mutated alleles in spontaneously aborted embryos
-
DOI 10.1038/sj/ejhg/5200767
-
Zetterberg H, Regland B, Palmér M, Ricksten A, Palmqvist L, Rymo L et al (2002). Increased frequency of combined methylenetetrahydrofolate reductase C677T and A1298C mutated alleles in spontaneously aborted embryos. Eur J Hum Genet. 10: 113-118. (Pubitemid 34414045)
-
(2002)
European Journal of Human Genetics
, vol.10
, Issue.2
, pp. 113-118
-
-
Zetterberg, H.1
Regland, B.2
Palmer, M.3
Ricksten, A.4
Palmqvist, L.5
Rymo, L.6
Arvanitis, D.A.7
Spandidos, D.A.8
Blennow, K.9
|