BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

250 related articles for article (PubMed ID: 11568918)

  • 1. 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; 103(2):128-32. PubMed ID: 11568918
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects.
    Christensen B; Arbour L; Tran P; Leclerc D; Sabbaghian N; Platt R; Gilfix BM; Rosenblatt DS; Gravel RA; Forbes P; Rozen R
    Am J Med Genet; 1999 May; 84(2):151-7. PubMed ID: 10323741
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Altered folate metabolism and disposition in mothers affected by a spina bifida pregnancy: influence of 677c --> t methylenetetrahydrofolate reductase and 2756a --> g methionine synthase genotypes.
    Lucock M; Daskalakis I; Briggs D; Yates Z; Levene M
    Mol Genet Metab; 2000 May; 70(1):27-44. PubMed ID: 10833329
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Folate levels and N(5),N(10)-methylenetetrahydrofolate reductase genotype (MTHFR) in mothers of offspring with neural tube defects: a case-control study.
    Martínez de Villarreal LE; Delgado-Enciso I; Valdéz-Leal R; Ortíz-López R; Rojas-Martínez A; Limón-Benavides C; Sánchez-Peña MA; Ancer-Rodríguez J; Barrera-Saldaña HA; Villarreal-Pérez JZ
    Arch Med Res; 2001; 32(4):277-82. PubMed ID: 11440783
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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. PubMed ID: 11813127
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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. PubMed ID: 11310576
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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. PubMed ID: 12208134
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic basis of neural tube defects. II. Genes correlated with folate and methionine metabolism.
    Gos M; Szpecht-Potocka A
    J Appl Genet; 2002; 43(4):511-24. PubMed ID: 12441636
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Methylene tetrahydrofolate reductase mutations as genetic risk factors for neural tube defects (NTF)].
    Mierzejewska E
    Med Wieku Rozwoj; 1999; 3(4):521-7. PubMed ID: 10910677
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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. PubMed ID: 10986435
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida.
    Wilson A; Platt R; Wu Q; Leclerc D; Christensen B; Yang H; Gravel RA; Rozen R
    Mol Genet Metab; 1999 Aug; 67(4):317-23. PubMed ID: 10444342
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Folate and homocysteine metabolism and gene polymorphisms in the etiology of Down syndrome.
    Rosenblatt DS
    Am J Clin Nutr; 1999 Oct; 70(4):429-30. PubMed ID: 10500007
    [No Abstract]   [Full Text] [Related]  

  • 16. Does prenatal screening for 5,10-methylenetetrahydrofolate reductase (MTHFR) mutations in high-risk neural tube defect pregnancies make sense?
    Finnell RH; Shaw GM; Lammer EJ; Volcik KA
    Genet Test; 2002; 6(1):47-52. PubMed ID: 12180076
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Abnormal folate metabolism in mothers with Down syndrome offspring: review of the literature.
    Eskes TK
    Eur J Obstet Gynecol Reprod Biol; 2006 Feb; 124(2):130-3. PubMed ID: 16169148
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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. PubMed ID: 10833330
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 9(2):1197-203. PubMed ID: 20589617
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association of neural tube defects with maternal alterations and genetic polymorphisms in one-carbon metabolic pathway.
    Cai CQ; Fang YL; Shu JB; Zhao LS; Zhang RP; Cao LR; Wang YZ; Zhi XF; Cui HL; Shi OY; Liu W
    Ital J Pediatr; 2019 Mar; 45(1):37. PubMed ID: 30867013
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.