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Items: 1 to 20 of 298

1.

Genetic variation in genes of folate metabolism and neural-tube defect risk.

van der Linden IJ, Afman LA, Heil SG, Blom HJ.

Proc Nutr Soc. 2006 May;65(2):204-15. Review.

PMID:
16672082
2.

Neural tube defects and a disturbed folate dependent homocysteine metabolism.

van der Put NM, Blom HJ.

Eur J Obstet Gynecol Reprod Biol. 2000 Sep;92(1):57-61. Review.

PMID:
10986435
3.

Folate, homocysteine and neural tube defects: an overview.

van der Put NM, van Straaten HW, Trijbels FJ, Blom HJ.

Exp Biol Med (Maywood). 2001 Apr;226(4):243-70. Review.

PMID:
11368417
4.

C677T polymorphism of the methylenetetrahydrofolate reductase gene does not affect folic acid, vitamin B12, and homocysteine serum levels in Turkish children with neural tube defects.

Erdogan MO, Yildiz SH, Solak M, Eser O, Cosar E, Eser B, Koken R, Buyukbas S.

Genet Mol Res. 2010 Jun 22;9(2):1197-203. doi: 10.4238/vol9-2gmr816.

5.

Polymorphisms in genes involved in folate metabolism as risk factors for NTDs.

De Marco P, Calevo MG, Moroni A, Arata L, Merello E, Cama A, Finnell RH, Andreussi L, Capra V.

Eur J Pediatr Surg. 2001 Dec;11 Suppl 1:S14-7.

PMID:
11813127
6.

Folic acid, methylation and neural tube closure in humans.

Blom HJ.

Birth Defects Res A Clin Mol Teratol. 2009 Apr;85(4):295-302. doi: 10.1002/bdra.20581. Review.

PMID:
19301298
7.

Interaction of folate and homocysteine pathway genotypes evaluated in susceptibility to neural tube defects (NTD) in a German population.

Richter B, Stegmann K, Röper B, Böddeker I, Ngo ET, Koch MC.

J Hum Genet. 2001;46(3):105-9.

PMID:
11310576
8.

Nutritional and genetic determinants of vitamin B and homocysteine metabolisms in neural tube defects: a multicenter case-control study.

Candito M, Rivet R, Herbeth B, Boisson C, Rudigoz RC, Luton D, Journel H, Oury JF, Roux F, Saura R, Vernhet I, Gaucherand P, Muller F, Guidicelli B, Heckenroth H, Poulain P, Blayau M, Francannet C, Roszyk L, Brustié C, Staccini P, Gérard P, Fillion-Emery N, Guéant-Rodriguez RM, Van Obberghen E, Guéant JL.

Am J Med Genet A. 2008 May 1;146A(9):1128-33. doi: 10.1002/ajmg.a.32199.

PMID:
18386810
9.

Genetic basis of neural tube defects. II. Genes correlated with folate and methionine metabolism.

Gos M Jr, Szpecht-Potocka A.

J Appl Genet. 2002;43(4):511-24. Review.

PMID:
12441636
10.

Folate status and neural tube defects.

Molloy AM, Mills JL, Kirke PN, Weir DG, Scott JM.

Biofactors. 1999;10(2-3):291-4.

PMID:
10609896
11.

Is mutated serine hydroxymethyltransferase (SHMT) involved in the etiology of neural tube defects?

Heil SG, Van der Put NM, Waas ET, den Heijer M, Trijbels FJ, Blom HJ.

Mol Genet Metab. 2001 Jun;73(2):164-72.

PMID:
11386852
12.

Investigation of folate pathway gene polymorphisms and the incidence of neural tube defects in a Texas hispanic population.

Barber R, Shalat S, Hendricks K, Joggerst B, Larsen R, Suarez L, Finnell R.

Mol Genet Metab. 2000 May;70(1):45-52.

PMID:
10833330
13.

The curly-tail (ct) mouse, an animal model of neural tube defects, displays altered homocysteine metabolism without folate responsiveness or a defect in Mthfr.

Tran P, Hiou-Tim F, Frosst P, Lussier-Cacan S, Bagley P, Selhub J, Bottiglieri T, Rozen R.

Mol Genet Metab. 2002 Aug;76(4):297-304.

PMID:
12208134
14.

Folate status, homocysteine metabolism, and methylene tetrahydrofolate reductase genotype in rural South African blacks with a history of pregnancy complicated by neural tube defects.

Ubbink JB, Christianson A, Bester MJ, Van Allen MI, Venter PA, Delport R, Blom HJ, van der Merwe A, Potgieter H, Vermaak WJ.

Metabolism. 1999 Feb;48(2):269-74.

PMID:
10024094
15.

The search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects.

Molloy AM, Brody LC, Mills JL, Scott JM, Kirke PN.

Birth Defects Res A Clin Mol Teratol. 2009 Apr;85(4):285-94. doi: 10.1002/bdra.20566. Review.

PMID:
19235830
16.

Low erythrocyte folate status and polymorphic variation in folate-related genes are associated with risk of neural tube defect pregnancy.

Relton CL, Wilding CS, Laffling AJ, Jonas PA, Burgess T, Binks K, Tawn EJ, Burn J.

Mol Genet Metab. 2004 Apr;81(4):273-81.

PMID:
15059614
17.

Etiology, pathogenesis and prevention of neural tube defects.

Padmanabhan R.

Congenit Anom (Kyoto). 2006 Jun;46(2):55-67. Review.

PMID:
16732763
18.

Abnormal folate metabolism and genetic polymorphism of the folate pathway in a child with Down syndrome and neural tube defect.

Al-Gazali LI, Padmanabhan R, Melnyk S, Yi P, Pogribny IP, Pogribna M, Bakir M, Hamid ZA, Abdulrazzaq Y, Dawodu A, James SJ.

Am J Med Genet. 2001 Oct 1;103(2):128-32.

PMID:
11568918
19.

Low blood folates in NTD pregnancies are only partly explained by thermolabile 5,10-methylenetetrahydrofolate reductase: low folate status alone may be the critical factor.

Molloy AM, Mills JL, Kirke PN, Ramsbottom D, McPartlin JM, Burke H, Conley M, Whitehead AS, Weir DG, Scott JM.

Am J Med Genet. 1998 Jun 30;78(2):155-9.

PMID:
9674907
20.

Maternal one-carbon metabolism, MTHFR and TCN2 genotypes and neural tube defects in India.

Godbole K, Gayathri P, Ghule S, Sasirekha BV, Kanitkar-Damle A, Memane N, Suresh S, Sheth J, Chandak GR, Yajnik CS.

Birth Defects Res A Clin Mol Teratol. 2011 Sep;91(9):848-56. doi: 10.1002/bdra.20841. Epub 2011 Jul 18.

PMID:
21770021

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