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Items: 1 to 20 of 187

2.

[A case-control study on the risk factors of neural tube defects in Shanxi province].

Wang F, Yang YF, Li PZ.

Zhonghua Liu Xing Bing Xue Za Zhi. 2008 Aug;29(8):771-4. Chinese.

PMID:
19103110
3.
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.

[Study on the relations between genetic polymorphisms in methylenetetrahydrofolate reductase, methionine synthase and the risk of pancreatic cancer].

Wang L, Lin DX, Lu XH, Miao XP, Li H.

Zhonghua Liu Xing Bing Xue Za Zhi. 2006 Jan;27(1):50-4. Chinese.

PMID:
16737574
6.

Polymorphisms of 5,10-methylenetetrahydrofolate reductase and cystathionine beta-synthase genes as a risk factor for neural tube defects in Sétif, Algeria.

Houcher B, Bourouba R, Djabi F, Yilmaz E, Eğin Y, Akar N.

Pediatr Neurosurg. 2009;45(6):472-7. doi: 10.1159/000283086. Epub 2010 Feb 16.

PMID:
20160465
7.

Interaction of MTHFR C677T and A1298C, and MTR A2756G gene polymorphisms in breast cancer risk in a population in Northeast Brazil.

de Cássia Carvalho Barbosa R, da Costa DM, Cordeiro DE, Vieira AP, Rabenhorst SH.

Anticancer Res. 2012 Nov;32(11):4805-11.

PMID:
23155246
8.

Methylenetetrahydrofolate reductase C677T and methionine synthase A2756G polymorphisms influence on leukocyte genomic DNA methylation level.

Weiner AS, Boyarskikh UA, Voronina EN, Mishukova OV, Filipenko ML.

Gene. 2014 Jan 1;533(1):168-72. doi: 10.1016/j.gene.2013.09.098. Epub 2013 Oct 5.

PMID:
24103477
9.
10.

Association between MTHFR C677T, MTHFR A1298C and MS A2756G polymorphisms and risk of cervical intraepithelial neoplasia II/III and cervical cancer: a meta-analysis.

Zhu J, Wu L, Kohlmeier M, Ye F, Cai W.

Mol Med Rep. 2013 Sep;8(3):919-27. doi: 10.3892/mmr.2013.1589. Epub 2013 Jul 16.

PMID:
23864153
11.

MTHFR C677T polymorphism as a risk factor of neural tube defects in Malay: a case control study.

Hayati AR, Zainal AI, Tan GC, Ong LC, Khoo TB.

Med J Malaysia. 2008 Dec;63(5):379-83.

12.

Impact of 5,10-methylenetetrahydrofolate reductase gene polymorphism on neural tube defects.

Harisha PN, Devi BI, Christopher R, Kruthika-Vinod TP.

J Neurosurg Pediatr. 2010 Oct;6(4):364-7. doi: 10.3171/2010.8.PEDS1072.

PMID:
20887110
13.

Methionine synthase A2756G polymorphism may predict ulcerative colitis and methylenetetrahydrofolate reductase C677T pancolitis, in Central China.

Chen M, Peyrin-Biroulet L, Xia B, Guéant-Rodriguez RM, Bronowicki JP, Bigard MA, Guéant JL.

BMC Med Genet. 2008 Aug 13;9:78. doi: 10.1186/1471-2350-9-78.

14.

A1298C polymorphism of the MTHFR gene and neural tube defects in the state of Yucatan, Mexico.

Gonzalez-Herrera L, Castillo-Zapata I, Garcia-Escalante G, Pinto-Escalante D.

Birth Defects Res A Clin Mol Teratol. 2007 Aug;79(8):622-6.

PMID:
17621650
15.

Association of MTHFR C677T, MTHFR A1298C, and MTRR A66G Polymorphisms with Neural Tube Defects in Tunisian Parents.

Nasri K, Midani F, Kallel A, Ben Jemaa N, Aloui M, Boulares M, Lassoued M, Ben Halima M, Ben Wafi S, Soussi M, Mahjoubi I, Baara A, Ben Fradj MK, Omar S, Feki M, Jemaa R, Gaigi SS, Marrakchi R.

Pathobiology. 2019;86(4):190-200. doi: 10.1159/000499498. Epub 2019 Jun 25.

PMID:
31238314
16.
17.

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.

J Hum Genet. 2002;47(6):319-24.

PMID:
12111380
18.

Analysis of the MTHFR 1298A-->C and 677C-->T polymorphisms as risk factors for neural tube defects.

Parle-McDermott A, Mills JL, Kirke PN, O'Leary VB, Swanson DA, Pangilinan F, Conley M, Molloy AM, Cox C, Scott JM, Brody LC.

J Hum Genet. 2003;48(4):190-3. Epub 2003 Mar 5.

PMID:
12730722
19.

Methylenetetrahydrofolate reductase and methionine synthase polymorphisms and risk of bladder cancer in a Tunisian population.

Ouerhani S, Oliveira E, Marrakchi R, Ben Slama MR, Sfaxi M, Ayed M, Chebil M, Amorim A, El Gaaied AB, Prata MJ.

Cancer Genet Cytogenet. 2007 Jul 1;176(1):48-53.

PMID:
17574963
20.

Association of MTRRA66G polymorphism (but not of MTHFR C677T and A1298C, MTRA2756G, TCN C776G) with homocysteine and coronary artery disease in the French population.

Guéant-Rodriguez RM, Juilliére Y, Candito M, Adjalla CE, Gibelin P, Herbeth B, Van Obberghen E, Gueánt JL.

Thromb Haemost. 2005 Sep;94(3):510-5.

PMID:
16268464

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