These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

113 related articles for article (PubMed ID: 20075510)

  • 1. Investigating the impact of the Down syndrome related common MTHFR 677C>T polymorphism in the Danish population.
    Kokotas H; Grigoriadou M; Mikkelsen M; Giannoulia-Karantana A; Petersen MB
    Dis Markers; 2009; 27(6):279-85. PubMed ID: 20075510
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. The impact of folate pathway polymorphisms combined to nutritional deficiency as a maternal predisposition factor for Down syndrome.
    Santos-Rebouças CB; Corrêa JC; Bonomo A; Fintelman-Rodrigues N; Moura KC; Rodrigues CS; Santos JM; Pimentel MM
    Dis Markers; 2008; 25(3):149-57. PubMed ID: 19096127
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Methylenetetrahydrofolate reductase enzyme polymorphisms as maternal risk for Down syndrome among Turkish women.
    Boduroğlu K; Alanay Y; Koldan B; Tunçbilek E
    Am J Med Genet A; 2004 May; 127A(1):5-10. PubMed ID: 15103709
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Association between MTHFR 1298A>C polymorphism and spontaneous abortion with fetal chromosomal aneuploidy.
    Kim SY; Park SY; Choi JW; Kim DJ; Lee SY; Lim JH; Han JY; Ryu HM; Kim MH
    Am J Reprod Immunol; 2011 Oct; 66(4):252-8. PubMed ID: 21410812
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome.
    Hobbs CA; Sherman SL; Yi P; Hopkins SE; Torfs CP; Hine RJ; Pogribna M; Rozen R; James SJ
    Am J Hum Genet; 2000 Sep; 67(3):623-30. PubMed ID: 10930360
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Abnormal folate metabolism and mutation in the methylenetetrahydrofolate reductase gene may be maternal risk factors for Down syndrome.
    James SJ; Pogribna M; Pogribny IP; Melnyk S; Hine RJ; Gibson JB; Yi P; Tafoya DL; Swenson DH; Wilson VL; Gaylor DW
    Am J Clin Nutr; 1999 Oct; 70(4):495-501. PubMed ID: 10500018
    [TBL] [Abstract][Full Text] [Related]  

  • 8. MTHFR genetic polymorphism as a risk factor in Egyptian mothers with Down syndrome children.
    Meguid NA; Dardir AA; Khass M; Hossieny LE; Ezzat A; El Awady MK
    Dis Markers; 2008; 24(1):19-26. PubMed ID: 18057532
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. [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]  

  • 12. Methylenetetrahydrofolate reductase gene polymorphisms (677C > T and 1298A > C) in Egyptian patients with non-Hodgkin lymphoma.
    Nasr AS; Sami RM; Ibrahim NY
    J Cancer Res Ther; 2012; 8(3):355-60. PubMed ID: 23174714
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Methylenetetrahydrofolate reductase gene polymorphisms in Egyptian Turner Syndrome patients.
    Ismail MF; Zarouk WA; Ruby MO; Mahmoud WM; Gad RS
    Acta Biochim Pol; 2015; 62(3):529-32. PubMed ID: 26217949
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Polymorphisms in folate pathway genes are not associated with somatic nondisjunction in turner syndrome.
    Bispo AV; dos Santos LO; de Barros JV; Duarte AR; Araújo J; Muniz MT; Santos N
    Am J Med Genet A; 2015 Jul; 167(7):1510-7. PubMed ID: 25858821
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Gene polymorphism and folate metabolism: a maternal risk factor for Down syndrome.
    Sheth JJ; Sheth FJ
    Indian Pediatr; 2003 Feb; 40(2):115-23. PubMed ID: 12626825
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic polymorphism of methylenetetrahydrofolate reductase is associated with insulin resistance in Egyptian women with polycystic ovary syndrome.
    Nsrallah AA; Abd-El Fatah AH; Ahmed HS
    J Gene Med; 2019 Apr; 21(4):e3076. PubMed ID: 30743312
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Folate gene polymorphisms and the risk of Down syndrome pregnancies in young Italian women.
    Coppedè F; Marini G; Bargagna S; Stuppia L; Minichilli F; Fontana I; Colognato R; Astrea G; Palka G; Migliore L
    Am J Med Genet A; 2006 May; 140(10):1083-91. PubMed ID: 16596679
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Associations between 2 polymorphisms in the methylenetetrahydrofolate reductase gene and placental abruption.
    Ananth CV; Peltier MR; De Marco C; Elsasser DA; Getahun D; Rozen R; Smulian JC;
    Am J Obstet Gynecol; 2007 Oct; 197(4):385.e1-7. PubMed ID: 17904970
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Maternal folate polymorphisms and the etiology of human nondisjunction.
    Hassold TJ; Burrage LC; Chan ER; Judis LM; Schwartz S; James SJ; Jacobs PA; Thomas NS
    Am J Hum Genet; 2001 Aug; 69(2):434-9. PubMed ID: 11443546
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.