167 related articles for article (PubMed ID: 21687976)
1. Polymorphism C1420T of Serine hydroxymethyltransferase gene on maternal risk for Down syndrome.
Marucci GH; Zampieri BL; Biselli JM; Valentin S; Bertollo EM; Eberlin MN; Haddad R; Riccio MF; Vannucchi H; Carvalho VM; Pavarino EC
Mol Biol Rep; 2012 Mar; 39(3):2561-6. PubMed ID: 21687976
[TBL] [Abstract][Full Text] [Related]
2. DHFR 19-bp deletion and SHMT C1420T polymorphisms and metabolite concentrations of the folate pathway in individuals with Down syndrome.
Mendes CC; Raimundo AM; Oliveira LD; Zampieri BL; Marucci GH; Biselli JM; Goloni-Bertollo EM; Eberlin MN; Haddad R; Riccio MF; Vannucchi H; Carvalho VM; Pavarino ÉC
Genet Test Mol Biomarkers; 2013 Apr; 17(4):274-7. PubMed ID: 23421317
[TBL] [Abstract][Full Text] [Related]
3. 19-base pair deletion polymorphism of the dihydrofolate reductase (DHFR) gene: maternal risk of Down syndrome and folate metabolism.
Mendes CC; Biselli JM; Zampieri BL; Goloni-Bertollo EM; Eberlin MN; Haddad R; Riccio MF; Vannucchi H; Carvalho VM; Pavarino-Bertelli EC
Sao Paulo Med J; 2010 Jul; 128(4):215-8. PubMed ID: 21120433
[TBL] [Abstract][Full Text] [Related]
4. Role of folate-homocysteine pathway gene polymorphisms and nutritional cofactors in Down syndrome: A triad study.
Sukla KK; Jaiswal SK; Rai AK; Mishra OP; Gupta V; Kumar A; Raman R
Hum Reprod; 2015 Aug; 30(8):1982-93. PubMed ID: 26040482
[TBL] [Abstract][Full Text] [Related]
5. Evaluation of C677T and A1298C polymorphisms of the MTHFR gene as maternal risk factors for Down syndrome and congenital heart defects.
Brandalize AP; Bandinelli E; dos Santos PA; Roisenberg I; Schüler-Faccini L
Am J Med Genet A; 2009 Oct; 149A(10):2080-7. PubMed ID: 19725133
[TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 11386852
[TBL] [Abstract][Full Text] [Related]
7. Genetic polymorphisms modulate the folate metabolism of Brazilian individuals with Down syndrome.
Biselli JM; Zampieri BL; Goloni-Bertollo EM; Haddad R; Fonseca MF; Eberlin MN; Vannucchi H; Carvalho VM; Pavarino EC
Mol Biol Rep; 2012 Oct; 39(10):9277-84. PubMed ID: 22903356
[TBL] [Abstract][Full Text] [Related]
8. Maternal polymorphisms 677C-T and 1298A-C of MTHFR, and 66A-G MTRR genes: is there any relationship between polymorphisms of the folate pathway, maternal homocysteine levels, and the risk for having a child with Down syndrome?
Martínez-Frías ML; Pérez B; Desviat LR; Castro M; Leal F; Rodríguez L; Mansilla E; Martínez-Fernández ML; Bermejo E; Rodríguez-Pinilla E; Prieto D; Ugarte M;
Am J Med Genet A; 2006 May; 140(9):987-97. PubMed ID: 16575899
[TBL] [Abstract][Full Text] [Related]
9. Abnormal folic acid-homocysteine metabolism as maternal risk factors for Down syndrome in Japan.
Takamura N; Kondoh T; Ohgi S; Arisawa K; Mine M; Yamashita S; Aoyagi K
Eur J Nutr; 2004 Oct; 43(5):285-7. PubMed ID: 15309447
[TBL] [Abstract][Full Text] [Related]
10. [Folate gene polymorphism and the risk of Down syndrome pregnancies in young Chinese women].
Liao YP; Bao MS; Liu CQ; Liu H; Zhang D
Yi Chuan; 2010 May; 32(5):461-6. PubMed ID: 20466634
[TBL] [Abstract][Full Text] [Related]
11. Betaine-homocysteine methyltransferase 742G>A polymorphism and risk of down syndrome offspring in a Brazilian population.
Amorim MR; Moura CM; Gomes AD; Barboza HN; Lopes RB; Ribeiro MG; Costa Lima MA
Mol Biol Rep; 2013 Aug; 40(8):4685-9. PubMed ID: 23645037
[TBL] [Abstract][Full Text] [Related]
12. Polymorphisms in methionine synthase, methionine synthase reductase and serine hydroxymethyltransferase, folate and alcohol intake, and colon cancer risk.
Steck SE; Keku T; Butler LM; Galanko J; Massa B; Millikan RC; Sandler RS
J Nutrigenet Nutrigenomics; 2008; 1(4):196-204. PubMed ID: 19776626
[TBL] [Abstract][Full Text] [Related]
13. Maternal risk for Down syndrome is modulated by genes involved in folate metabolism.
Zampieri BL; Biselli JM; Goloni-Bertollo EM; Vannucchi H; Carvalho VM; Cordeiro JA; Pavarino EC
Dis Markers; 2012; 32(2):73-81. PubMed ID: 22377700
[TBL] [Abstract][Full Text] [Related]
14. Association of MTHFR C677T and SHMT(1) C1420T with susceptibility to ESCC and GCA in a high incident region of Northern China.
Wang Y; Guo W; He Y; Chen Z; Wen D; Zhang X; Wang N; Li Y; Ge H; Zhang J
Cancer Causes Control; 2007 Mar; 18(2):143-52. PubMed ID: 17206530
[TBL] [Abstract][Full Text] [Related]
15. Genetic polymorphisms involved in folate metabolism and elevated plasma concentrations of homocysteine: maternal risk factors for Down syndrome in Brazil.
Biselli JM; Goloni-Bertollo EM; Zampieri BL; Haddad R; Eberlin MN; Pavarino-Bertelli EC
Genet Mol Res; 2008 Jan; 7(1):33-42. PubMed ID: 18273817
[TBL] [Abstract][Full Text] [Related]
16. [The relationship between polymorphism of gene involved in folate metabolism, homocysteine level and risk of Down syndrome].
Wang W; Xie W; Wang Xy
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Oct; 24(5):533-7. PubMed ID: 17922421
[TBL] [Abstract][Full Text] [Related]
17. DNMT3B C46359T and SHMT1 C1420T polymorphisms in the folate pathway in carcinogenesis of head and neck.
Succi M; de Castro TB; Galbiatti AL; Arantes LM; da Silva JN; Maniglia JV; Raposo LS; Pavarino EC; Goloni-Bertollo EM
Mol Biol Rep; 2014 Feb; 41(2):581-9. PubMed ID: 24362509
[TBL] [Abstract][Full Text] [Related]
18. Double aneuploidy (48,XXY,+21) of maternal origin in a child born to a 13-year-old mother: evaluation of the maternal folate metabolism.
Biselli JM; Machado FB; Zampieri BL; Alves da Silva AF; Goloni-Bertollo EM; Haddad R; Eberlin MN; Vannucchi H; Carvalho VM; Medina-Acosta E; Pavarino-Bertelli EC
Genet Couns; 2009; 20(3):225-34. PubMed ID: 19852428
[TBL] [Abstract][Full Text] [Related]
19. Methionine synthase (MTR) 2756 (A --> G) polymorphism, double heterozygosity methionine synthase 2756 AG/methionine synthase reductase (MTRR) 66 AG, and elevated homocysteinemia are three risk factors for having a child with Down syndrome.
Bosco P; Guéant-Rodriguez RM; Anello G; Barone C; Namour F; Caraci F; Romano A; Romano C; Guéant JL
Am J Med Genet A; 2003 Sep; 121A(3):219-24. PubMed ID: 12923861
[TBL] [Abstract][Full Text] [Related]
20. The biochemical structure and function of methylenetetrahydrofolate reductase provide the rationale to interpret the epidemiological results on the risk for infants with Down syndrome.
Martínez-Frías ML
Am J Med Genet A; 2008 Jun; 146A(11):1477-82. PubMed ID: 18446861
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
