-
1
-
-
70349646312
-
MTHFR polymorphisms and 5-FU-based adjuvant chemotherapy in colorectal cancer
-
Afzal S, Jensen SA, Vainer B, et al. 2009. MTHFR polymorphisms and 5-FU-based adjuvant chemotherapy in colorectal cancer. Ann Oncol 20:1660-1666.
-
(2009)
Ann Oncol
, vol.20
, pp. 1660-1666
-
-
Afzal, S.1
Jensen, S.A.2
Vainer, B.3
-
2
-
-
44849125653
-
A simple and cost-effective protocol for DNA isolation from buccal epithelial cells
-
Aidar M, Line SR. 2007. A simple and cost-effective protocol for DNA isolation from buccal epithelial cells. Braz Dent J 18:148-152.
-
(2007)
Braz Dent J
, vol.18
, pp. 148-152
-
-
Aidar, M.1
Line, S.R.2
-
3
-
-
84876799487
-
Polymorphisms at regions 1p22 1 (rs560426) and 8q24 (rs1530300) are risk markers for nonsyndromic cleft lip and/or palate in the Brazilian population
-
Bagordakis E, Paranaiba LM, Brito LA, et al. 2013. Polymorphisms at regions 1p22.1 (rs560426) and 8q24 (rs1530300) are risk markers for nonsyndromic cleft lip and/or palate in the Brazilian population. Am J Med Genet A 161:1177-1180.
-
(2013)
Am J Med Genet A
, vol.161
, pp. 1177-1180
-
-
Bagordakis, E.1
Paranaiba, L.M.2
Brito, L.A.3
-
4
-
-
0034101255
-
New standard for dietary folate intake in pregnant woman
-
Bailey LB. 2000. New standard for dietary folate intake in pregnant woman. Am J Clin Nutr 71:1304s-1307s.
-
(2000)
Am J Clin Nutr
, vol.71
, pp. 1304s-1307s
-
-
Bailey, L.B.1
-
5
-
-
33745591590
-
The genetic structure of human populations studied through short insertiondeletion polymorphisms
-
Bastos-Rodrigues L, Pimenta JR, Pena SD. 2006. The genetic structure of human populations studied through short insertiondeletion polymorphisms. Ann Hum Genet 70:658-665.
-
(2006)
Ann Hum Genet
, vol.70
, pp. 658-665
-
-
Bastos-Rodrigues, L.1
Pimenta, J.R.2
Pena, S.D.3
-
8
-
-
38849187271
-
Folate and onecarbonmetabolism gene polymorphisms and their associations with oral facial clefts
-
Boyles AL, Wilcox AJ, Taylor JA, et al. 2008. Folate and onecarbonmetabolism gene polymorphisms and their associations with oral facial clefts. Am J Med Genet A 146A:440-449.
-
(2008)
Am J Med Genet A
, vol.146A
, pp. 440-449
-
-
Boyles, A.L.1
Wilcox, A.J.2
Taylor, J.A.3
-
9
-
-
34347330123
-
Polymorphisms in genes MTHFR MTR and MTRR are not risk factors for cleft lip/palate in South Brazil
-
Brandalize AP, Bandinelli E, Borba JB, et al. 2007. Polymorphisms in genes MTHFR, MTR and MTRR are not risk factors for cleft lip/palate in South Brazil. Braz J Med Biol Res 40:787-791.
-
(2007)
Braz J Med Biol Res
, vol.40
, pp. 787-791
-
-
Brandalize, A.P.1
Bandinelli, E.2
Borba, J.B.3
-
10
-
-
78649585815
-
Maternal polymorphisms in folic acid metabolic genes are associated with nonsyndromic cleft lip and/or palate in the Brazilian population
-
Bufalino A, Ribeiro Paranaíba LM, et al. 2010. Maternal polymorphisms in folic acid metabolic genes are associated with nonsyndromic cleft lip and/or palate in the Brazilian population. Birth Defects Res A ClinMol Teratol 88:980-986.
-
(2010)
Birth Defects Res A ClinMol Teratol
, vol.88
, pp. 980-986
-
-
Bufalino, A.1
Ribeiro Paranaíba, L.M.2
-
11
-
-
84871490239
-
Association study between methylenetetrahydrofolate reductase polymorphisms and unexplained recurrent pregnancy loss: a meta-analysis
-
Cao Y, Xu J, Zhang Z, et al. 2013. Association study between methylenetetrahydrofolate reductase polymorphisms and unexplained recurrent pregnancy loss: a meta-analysis. Gene 514:105-111.
-
(2013)
Gene
, vol.514
, pp. 105-111
-
-
Cao, Y.1
Xu, J.2
Zhang, Z.3
-
12
-
-
33846807689
-
Fetal and maternal MTHFR C677T genotype, maternal folate intake and the risk of nonsyndromic oral clefts
-
Chevrier C, Perret C, Bahuau M, et al. 2007. Fetal and maternal MTHFR C677T genotype, maternal folate intake and the risk of nonsyndromic oral clefts. Am J Med Genet A 143:248-257.
-
(2007)
Am J Med Genet A
, vol.143
, pp. 248-257
-
-
Chevrier, C.1
Perret, C.2
Bahuau, M.3
-
13
-
-
84892874052
-
MTHFR rs2274976 Polymorphism Is a Risk Marker for Nonsyndromic Cleft Lip with or without Cleft Palate in the Brazilian Population
-
de Aquino SN, Hoshi R, Bagordakis E, et al. 2014. MTHFR rs2274976 Polymorphism Is a Risk Marker for Nonsyndromic Cleft Lip with or without Cleft Palate in the Brazilian Population. Birth Defects Res A Clin Mol Teratol 100:30-35.
-
(2014)
Birth Defects Res A Clin Mol Teratol
, vol.100
, pp. 30-35
-
-
de Aquino, S.N.1
Hoshi, R.2
Bagordakis, E.3
-
14
-
-
84878027505
-
Polymorphisms in FGF12, VCL CX43 and VAX1 in Brazilian patients with nonsyndromic cleft lip with or without cleft palate
-
de Aquino SN, Messetti AC, Bagordakis E, et al. 2013. Polymorphisms in FGF12, VCL, CX43 and VAX1 in Brazilian patients with nonsyndromic cleft lip with or without cleft palate. BMC Med Genet 14:53.
-
(2013)
BMC Med Genet
, vol.14
, pp. 53
-
-
de Aquino, S.N.1
Messetti, A.C.2
Bagordakis, E.3
-
15
-
-
79951800135
-
Cleft lip and palate: understanding genetic and environmental influences
-
Dixon MJ, Marazita ML, Beaty TH, Murray JC. 2011. Cleft lip and palate: understanding genetic and environmental influences. Nat Rev Genet 12:167-178.
-
(2011)
Nat Rev Genet
, vol.12
, pp. 167-178
-
-
Dixon, M.J.1
Marazita, M.L.2
Beaty, T.H.3
Murray, J.C.4
-
16
-
-
34447120219
-
Inference of population structure using multilocus genotype data: dominant markers and null alleles
-
Falush D, Stephens M, Pritchard JK. 2007. Inference of population structure using multilocus genotype data: dominant markers and null alleles. Mol Ecol Notes 7:574-578.
-
(2007)
Mol Ecol Notes
, vol.7
, pp. 574-578
-
-
Falush, D.1
Stephens, M.2
Pritchard, J.K.3
-
17
-
-
84874682370
-
Polymorphisms in GABRB3 and oral clefting in the Brazilian population
-
Filezio MR, Bagordakis E, de Aquino SN, et al. 2013. Polymorphisms in GABRB3 and oral clefting in the Brazilian population. DNA Cell Biol 32:125-129.
-
(2013)
DNA Cell Biol
, vol.32
, pp. 125-129
-
-
Filezio, M.R.1
Bagordakis, E.2
de Aquino, S.N.3
-
18
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase
-
Frosst P, Blom HJ, Milos R, 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
-
19
-
-
4043169859
-
Maternal MTHFR interacts with the offspring's BCL3 genotypes, but not with TGFA, in increasing risk to nonsyndromic cleft lip with or without cleft palate
-
Gaspar DA, Matioli SR, de Cassia Pavanello R. 2004. Maternal MTHFR interacts with the offspring's BCL3 genotypes, but not with TGFA, in increasing risk to nonsyndromic cleft lip with or without cleft palate. Eur J Hum Genet 12:521-526.
-
(2004)
Eur J Hum Genet
, vol.12
, pp. 521-526
-
-
Gaspar, D.A.1
Matioli, S.R.2
de Cassia Pavanello, R.3
-
20
-
-
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, et al. 1999. 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 87:197-199.
-
(1999)
Am J Med Genet
, vol.87
, pp. 197-199
-
-
Gaspar, D.A.1
Pavanello, R.C.2
Zatz, M.3
-
21
-
-
0028304102
-
Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation
-
Goyette P, Summer JS, Milos R. 1994. Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation. Nat Genet 7:195-200.
-
(1994)
Nat Genet
, vol.7
, pp. 195-200
-
-
Goyette, P.1
Summer, J.S.2
Milos, R.3
-
22
-
-
0032845227
-
Abnormal folate metabolism and mutation in the methylenetetrahydrofolate reductase gene may be maternal risk factors for Down syndrome
-
James SJ, Pogribna M, Pogribny IP, et al. 1999. Abnormal folate metabolism and mutation in the methylenetetrahydrofolate reductase gene may be maternal risk factors for Down syndrome. Am J Clin Nutr 70:495-501.
-
(1999)
Am J Clin Nutr
, vol.70
, pp. 495-501
-
-
James, S.J.1
Pogribna, M.2
Pogribny, I.P.3
-
23
-
-
0026034240
-
Thermolabile methylenetetrahydrofolate reductase: an inherited risk factor for coronary artery disease
-
Kang SS, Wong PW, Susmano A, et al. 1991. Thermolabile methylenetetrahydrofolate reductase: an inherited risk factor for coronary artery disease. Am J Hum Genet 48:536-545.
-
(1991)
Am J Hum Genet
, vol.48
, pp. 536-545
-
-
Kang, S.S.1
Wong, P.W.2
Susmano, A.3
-
24
-
-
78449235688
-
Folic acid flour fortification: impact on the frequencies of 52 congenital anomaly types in three South American countries
-
López-Camelo JS, Castilla EE, Orioli IM. 2010. Folic acid flour fortification: impact on the frequencies of 52 congenital anomaly types in three South American countries. Am J Med Genet A 152A:2444-2458.
-
(2010)
Am J Med Genet A
, vol.152A
, pp. 2444-2458
-
-
López-Camelo, J.S.1
Castilla, E.E.2
Orioli, I.M.3
-
25
-
-
84859565662
-
Association between MTHFR polymorphisms and orofacial clefts risk: a meta-analysis
-
Luo YL, Cheng YL, Ye P, et al. 2012. Association between MTHFR polymorphisms and orofacial clefts risk: a meta-analysis. Birth Defects Res A Clin Mol Teratol 94:237-244.
-
(2012)
Birth Defects Res A Clin Mol Teratol
, vol.94
, pp. 237-244
-
-
Luo, Y.L.1
Cheng, Y.L.2
Ye, P.3
-
26
-
-
33845303205
-
Methylenetetrahydrofolate reductase haplotype tag single-nucleotide polymorphisms and risk of breast cancer
-
Martin YN, Olson JE, Ingle JN, et al. 2006. Methylenetetrahydrofolate reductase haplotype tag single-nucleotide polymorphisms and risk of breast cancer. Cancer Epidemiol Biomarkers Prev 15: 2322-2324.
-
(2006)
Cancer Epidemiol Biomarkers Prev
, vol.15
, pp. 2322-2324
-
-
Martin, Y.N.1
Olson, J.E.2
Ingle, J.N.3
-
27
-
-
0035254496
-
C677T variant form at the MTHFR gene and CL/P: a risk factor for mothers
-
Martinelli M, Scapoli L, Pezzetti F, et al. 2001. C677T variant form at the MTHFR gene and CL/P: a risk factor for mothers? Am J Med Genet 98:357-360.
-
(2001)
Am J Med Genet
, vol.98
, pp. 357-360
-
-
Martinelli, M.1
Scapoli, L.2
Pezzetti, F.3
-
28
-
-
0032802054
-
Methylenetetrahy drofolate reductase thermolabile variant and oral clefts
-
Mills JL, Kirke PN, Molloy AM, et al. 1999. Methylenetetrahy drofolate reductase thermolabile variant and oral clefts. Am J Med Genet 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
-
30
-
-
2942754073
-
Associations between maternal methylenetetrahydrofolate reductase polymorphisms and adverse outcomes of pregnancy: the Hordaland Homocysteine Study
-
Nurk E, Tell GS, Refsum H, et al. 2004. Associations between maternal methylenetetrahydrofolate reductase polymorphisms and adverse outcomes of pregnancy: the Hordaland Homocysteine Study. Am J Med 117:26-31.
-
(2004)
Am J Med
, vol.117
, pp. 26-31
-
-
Nurk, E.1
Tell, G.S.2
Refsum, H.3
-
32
-
-
33645925310
-
Structural perturbations in the Ala?Val polymorphism of methylenetetrahydrofolate reductase: how binding of folates may protect against inactivation
-
Pejchal R, Campbell E, Guenther BD, et al. 2006. Structural perturbations in the Ala?Val polymorphism of methylenetetrahydrofolate reductase: how binding of folates may protect against inactivation. Biochemistry 45:4808-4818.
-
(2006)
Biochemistry
, vol.45
, pp. 4808-4818
-
-
Pejchal, R.1
Campbell, E.2
Guenther, B.D.3
-
33
-
-
79951895658
-
The genomic ancestry of individuals from different geographical regions of Brazil is more uniform than expected
-
Pena SDJ, Di Pietro G, Fuchshuber-Moraes M, et al. 2011. The genomic ancestry of individuals from different geographical regions of Brazil is more uniform than expected. PLoS One 6: e17063.
-
(2011)
PLoS One
, vol.6
, pp. e17063
-
-
Pena, S.D.J.1
Di Pietro, G.2
Fuchshuber-Moraes, M.3
-
34
-
-
7244219970
-
Maternal MTHFR variant forms increase the risk in offspring of isolated nonsyndromic cleft lip with or without cleft palate
-
Pezzetti F, Martinelli M, Scapoli L, et al. 2004. Maternal MTHFR variant forms increase the risk in offspring of isolated nonsyndromic cleft lip with or without cleft palate. Hum Mutat 24:104-105.
-
(2004)
Hum Mutat
, vol.24
, pp. 104-105
-
-
Pezzetti, F.1
Martinelli, M.2
Scapoli, L.3
-
35
-
-
67649341466
-
Methylenetetrahydrofolate reductase deficiency and low dietary folate increase embryonic delay and placental abnormalities in mice
-
Pickell L, Deqiang L, Brown K, et al. 2009. Methylenetetrahydrofolate reductase deficiency and low dietary folate increase embryonic delay and placental abnormalities in mice. Birth Defects Res 85:531-541.
-
(2009)
Birth Defects Res
, vol.85
, pp. 531-541
-
-
Pickell, L.1
Deqiang, L.2
Brown, K.3
-
36
-
-
0036256811
-
Folate and the face: evaluating the evidence for the influence of folate genes on craniofacial development
-
Prescott NJ, Malcolm S. 2002. Folate and the face: evaluating the evidence for the influence of folate genes on craniofacial development. Cleft Palate Craniofac J 39:327-331.
-
(2002)
Cleft Palate Craniofac J
, vol.39
, pp. 327-331
-
-
Prescott, N.J.1
Malcolm, S.2
-
37
-
-
0034118493
-
Inference of population structure using multilocus genotype data
-
Pritchard JK, Stephens M, Donnelly P. 2000. Inference of population structure using multilocus genotype data. Genetics 155:945- 959.
-
(2000)
Genetics
, vol.155
, pp. 945-959
-
-
Pritchard, J.K.1
Stephens, M.2
Donnelly, P.3
-
38
-
-
0037529367
-
Persistence of vitamin B12 insufficiency among elderly women after folic acid food fortifycation
-
Ray JG, Vermeulen MJ, Langman LJ, et al. 2003. Persistence of vitamin B12 insufficiency among elderly women after folic acid food fortifycation. Clin Biochem 36:387-391.
-
(2003)
Clin Biochem
, vol.36
, pp. 387-391
-
-
Ray, J.G.1
Vermeulen, M.J.2
Langman, L.J.3
-
39
-
-
0000443712
-
Inherited disorders of folate transport and metabolism
-
In: Scriver CR, Beaudet AL, Sly S, Valle D, editors., 7th ed. New-York: McGraw-Hill
-
Rosenblatt DS. 1995. Inherited disorders of folate transport and metabolism. In: Scriver CR, Beaudet AL, Sly S, Valle D, editors. The metabolic and molecular bases of inherited disease. 7th ed. New-York: McGraw-Hill. pp. 3111-3128.
-
(1995)
The metabolic and molecular bases of inherited disease
, pp. 3111-3128
-
-
Rosenblatt, D.S.1
-
40
-
-
43749114271
-
Role of genetic and nongenetic factors for fluorouracil treatment-related severe toxicity: a prospective clinical trial by the German 5-FU Toxicity Study Group
-
Schwab M, Zanger UM, Marx C, et al. 2008. Role of genetic and nongenetic factors for fluorouracil treatment-related severe toxicity: a prospective clinical trial by the German 5-FU Toxicity Study Group. J Clin Oncol 26:2131-2138.
-
(2008)
J Clin Oncol
, vol.26
, pp. 2131-2138
-
-
Schwab, M.1
Zanger, U.M.2
Marx, C.3
-
41
-
-
84876096274
-
Association between C677T and A1298C MTHFR gene polymorphism and nonsyndromic orofacial clefts in the Turkish population: a caseparent study
-
Semic-Jusufagic A, Bircan R, Celebiler O, et al. 2012. Association between C677T and A1298C MTHFR gene polymorphism and nonsyndromic orofacial clefts in the Turkish population: a caseparent study. Turk J Pediatr 54:617-625.
-
(2012)
Turk J Pediatr
, vol.54
, pp. 617-625
-
-
Semic-Jusufagic, A.1
Bircan, R.2
Celebiler, O.3
-
42
-
-
0031785528
-
Infant C677T mutation in MTHFR, maternal periconceptional vitamin use, and cleft lip
-
Shaw GM, Rozen R, Finnell RH, et al. 1998. Infant C677T mutation in MTHFR, maternal periconceptional vitamin use, and cleft lip. Am J Med Genet 80:196-198.
-
(1998)
Am J Med Genet
, vol.80
, pp. 196-198
-
-
Shaw, G.M.1
Rozen, R.2
Finnell, R.H.3
-
43
-
-
0042415793
-
Maternal 677CT/1298AC genotype of the MTHFR gene as a risk factor for cleft lip
-
Shotelersuk V, Ittiwut C, Siriwan P, Angspatt A. 2003. Maternal 677CT/1298AC genotype of the MTHFR gene as a risk factor for cleft lip. J Med Genet 40:64.
-
(2003)
J Med Genet
, vol.40
, pp. 64
-
-
Shotelersuk, V.1
Ittiwut, C.2
Siriwan, P.3
Angspatt, A.4
-
44
-
-
77955293372
-
Parent-of-origin effects for MSX1 in a Chilean population with nonsyndromic cleft lip/ palate
-
Suazo J, Santos JL, Jara L, Blanco R. 2010. Parent-of-origin effects for MSX1 in a Chilean population with nonsyndromic cleft lip/ palate. Am J Med Genet A 152A:2011-2016.
-
(2010)
Am J Med Genet A
, vol.152A
, pp. 2011-2016
-
-
Suazo, J.1
Santos, J.L.2
Jara, L.3
Blanco, R.4
-
45
-
-
0029022223
-
Reduced recurrence of orofacial clefts after periconceptional supplementation with high-dose folic acid and multivitamins
-
Tolarova M, Harris J. 1995. Reduced recurrence of orofacial clefts after periconceptional supplementation with high-dose folic acid and multivitamins. Teratology 51:71-78.
-
(1995)
Teratology
, vol.51
, pp. 71-78
-
-
Tolarova, M.1
Harris, J.2
-
46
-
-
0031971515
-
A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?
-
van der Put NMJ, Gabreels F, Stevens EM, 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.J.1
Gabreels, F.2
Stevens, E.M.3
-
47
-
-
0028844492
-
Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida
-
van der Put NMJ, Steegers-Theunissen RPM, Frosst P, et al. 1995. Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida. Lancet 346:1070-1071.
-
(1995)
Lancet
, vol.346
, pp. 1070-1071
-
-
van der Put, N.M.J.1
Steegers-Theunissen, R.P.M.2
Frosst, P.3
-
48
-
-
0242600545
-
Does the interaction between maternal folate intake and the methylenetetrahydrofolate reductase polymorphisms affect the risk of cleft lip with or without cleft palate?
-
van Rooij IA, Vermeij-Keers C, Kluijtmans LA, et al. 2003. 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 157:583- 591.
-
(2003)
Am J Epidemiol
, vol.157
, pp. 583-591
-
-
van Rooij, I.A.1
Vermeij-Keers, C.2
Kluijtmans, L.A.3
-
49
-
-
84919426885
-
Association of tagging SNPs in the MTHFR gene with risk of type 2 diabetes mellitus and serum homocysteine levels in a Chinese population
-
Wang H, Hu C, Xiao SH, Wan B. 2014. Association of tagging SNPs in the MTHFR gene with risk of type 2 diabetes mellitus and serum homocysteine levels in a Chinese population. Dis Markers 2014:725731.
-
(2014)
Dis Markers
, vol.2014
, pp. 725731
-
-
Wang, H.1
Hu, C.2
Xiao, S.H.3
Wan, B.4
-
50
-
-
84876851366
-
Methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphism and risk of preeclampsia: an updated meta-analysis based on 51 studies
-
Wang XM, Wu HY, Qiu XJ. 2013a. Methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphism and risk of preeclampsia: an updated meta-analysis based on 51 studies. Arch Med Res 44:159-168.
-
(2013)
Arch Med Res
, vol.44
, pp. 159-168
-
-
Wang, X.M.1
Wu, H.Y.2
Qiu, X.J.3
-
51
-
-
84874851939
-
MTHFR C677T polymorphism and risk of congenital heart defects: evidence from 29 case-control and TDT studies
-
Wang W, Wang Y, Gong F, et al. 2013b. MTHFR C677T polymorphism and risk of congenital heart defects: evidence from 29 case-control and TDT studies. PLoS One 8:e58041.
-
(2013)
PLoS One
, vol.8
, pp. e58041
-
-
Wang, W.1
Wang, Y.2
Gong, F.3
-
52
-
-
73649119864
-
Folic acid and orofacial clefts: a review of the evidence
-
Wehby Gl, Murray JC. 2010. Folic acid and orofacial clefts: a review of the evidence. Oral Dis 16:11-19.
-
(2010)
Oral Dis
, vol.16
, pp. 11-19
-
-
Wehby, Gl1
Murray, J.C.2
-
53
-
-
0035957379
-
Methylenetetrahydrofolate reductase (MTHFR) polymorphisms and risk of molecularly defined subtypes of childhood acute leukemia
-
Wiemels JL, Smith RN, Taylor GM, et al. 2001. Methylenetetrahydrofolate reductase (MTHFR) polymorphisms and risk of molecularly defined subtypes of childhood acute leukemia. Proc Natl Acad Sci U S A 98:4004-4009.
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 4004-4009
-
-
Wiemels, J.L.1
Smith, R.N.2
Taylor, G.M.3
-
54
-
-
0035909980
-
Effects of common polymorphisms on the properties of human methylenetetrahydrofolate reductase
-
Yamada K, Chen Z, Rozen R, Matthews RG. 2001. Effects of common polymorphisms on the properties of human methylenetetrahydrofolate reductase. Proc Natl Acad Sci U S A 98:14853- 14858.
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 14853-14858
-
-
Yamada, K.1
Chen, Z.2
Rozen, R.3
Matthews, R.G.4
-
55
-
-
84899099724
-
Association between MTHFR C677T and A1298C polymorphisms and NSCL/P risk in Asians: A meta-analysis
-
Zhao M, Ren Y, Shen L, et al. 2014. Association between MTHFR C677T and A1298C polymorphisms and NSCL/P risk in Asians: A meta-analysis. PLoS One 9:e88242.
-
(2014)
PLoS One
, vol.9
, pp. e88242
-
-
Zhao, M.1
Ren, Y.2
Shen, L.3
-
56
-
-
84901303119
-
Tagging SNPs in the MTHFR gene and risk of ischemic stroke in a Chinese population
-
Zhou BS, Bu GY, Li M, Chang BG, Zhou YP. 2014. Tagging SNPs in the MTHFR gene and risk of ischemic stroke in a Chinese population. Int J Mol Sci 15:8931-8940.
-
(2014)
Int J Mol Sci
, vol.15
, pp. 8931-8940
-
-
Zhou, B.S.1
Bu, G.Y.2
Li, M.3
Chang, B.G.4
Zhou, Y.P.5
-
57
-
-
75449117469
-
MTHFR, TGFB3, and TGFA polymorphisms and their association with the risk of non-syndromic cleft lip and cleft palate in China
-
Zhu J, Hao L, Li S, et al. 2010. MTHFR, TGFB3, and TGFA polymorphisms and their association with the risk of non-syndromic cleft lip and cleft palate in China. Am J Med Genet Part A 152: 291-298.
-
(2010)
Am J Med Genet Part A
, vol.152
, pp. 291-298
-
-
Zhu, J.1
Hao, L.2
Li, S.3
-
58
-
-
33644859355
-
Variable contribution of the MTHFR C677T polymorphism to non-syndromic cleft lip and palate risk in China
-
Zhu J, Ren A, Hao L, et al. 2006. Variable contribution of the MTHFR C677T polymorphism to non-syndromic cleft lip and palate risk in China. Am J Med Genet Part A 140:551-557.
-
(2006)
Am J Med Genet Part A
, vol.140
, pp. 551-557
-
-
Zhu, J.1
Ren, A.2
Hao, L.3
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