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 *

142 related articles for article (PubMed ID: 11470464)

  • 1. Infant methylenetetrahydrofolate reductase 677TT genotype is a risk factor for congenital heart disease.
    Junker R; Kotthoff S; Vielhaber H; Halimeh S; Kosch A; Koch HG; Kassenböhmer R; Heineking B; Nowak-Göttl U
    Cardiovasc Res; 2001 Aug; 51(2):251-4. PubMed ID: 11470464
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Evaluation of infant methylenetetrahydrofolate reductase genotype, maternal vitamin use, and risk of high versus low level spina bifida defects.
    Volcik KA; Shaw GM; Lammer EJ; Zhu H; Finnell RH
    Birth Defects Res A Clin Mol Teratol; 2003 Mar; 67(3):154-7. PubMed ID: 12797455
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Study of correlationship between congenital heart disease and 5, 10-methylenetetra hydrofolate reductase gene's polymorphism or folacin intakes].
    Li D; Jing XA; Wang HY; Ye WJ; Fan H
    Zhonghua Yu Fang Yi Xue Za Zhi; 2009 Aug; 43(8):700-4. PubMed ID: 20021850
    [TBL] [Abstract][Full Text] [Related]  

  • 4. MTHFR C677T and A1298C gene polymorphisms and their relation to homocysteine level in Egyptian children with congenital heart diseases.
    Zidan HE; Rezk NA; Mohammed D
    Gene; 2013 Oct; 529(1):119-24. PubMed ID: 23933414
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prevalence of methylenetetrahydrofolate reductase C677T and its association with arterial and venous thrombosis in the Chinese population.
    Zheng YZ; Tong J; Do XP; Pu XQ; Zhou BT
    Br J Haematol; 2000 Jun; 109(4):870-4. PubMed ID: 10929044
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The role of vitamin B12 in fasting hyperhomocysteinemia and its interaction with the homozygous C677T mutation of the methylenetetrahydrofolate reductase (MTHFR) gene. A case-control study of patients with early-onset thrombotic events.
    D'Angelo A; Coppola A; Madonna P; Fermo I; Pagano A; Mazzola G; Galli L; Cerbone AM
    Thromb Haemost; 2000 Apr; 83(4):563-70. PubMed ID: 10780318
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Case-control study on the association between four single nucleotide polymorphisms in folate metabolism way and the risk of congenital heart disease].
    Duan S; Li G; Qiu F; Zhao L; Zhao M; Wang L; Feng Z; Ma X
    Wei Sheng Yan Jiu; 2018 Jul; 47(4):536-542. PubMed ID: 30081977
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Methylenetetrahydrofolate reductase C677T polymorphism and congenital heart disease: a meta-analysis.
    Nie Y; Gu H; Gong J; Wang J; Gong D; Cong X; Chen X; Hu S
    Clin Chem Lab Med; 2011 Dec; 49(12):2101-8. PubMed ID: 21793799
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Risk of congenital heart defects is influenced by genetic variation in folate metabolism.
    Christensen KE; Zada YF; Rohlicek CV; Andelfinger GU; Michaud JL; Bigras JL; Richter A; Dubé MP; Rozen R
    Cardiol Young; 2013 Feb; 23(1):89-98. PubMed ID: 22475273
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Methylenetetrahydrofolate Reductase C677T: Hypoplastic Left Heart and Thrombosis.
    Spronk KJ; Olivero AD; Haw MP; Vettukattil JJ
    World J Pediatr Congenit Heart Surg; 2015 Oct; 6(4):643-5. PubMed ID: 26467879
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Evaluation of High Resolution Melting for MTHFR C677T Genotyping in Congenital Heart Disease.
    Wang Y; Zhang H; Yue S; Zhang K; Wang H; Dong R; Yang X; Liu Y; Ma Y
    PLoS One; 2016; 11(3):e0151140. PubMed ID: 26990189
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Association of congenital cardiac defects and the C677T methylenetetrahydrofolate reductase polymorphism.
    Wintner S; Hafner E; Stonek F; Stuempflen I; Metzenbauer M; Philipp K
    Prenat Diagn; 2007 Aug; 27(8):704-8. PubMed ID: 17510921
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Common C677T polymorphism of the methylenetetrahydrofolate reductase gene and the risk of venous thromboembolism: meta-analysis of 31 studies.
    Ray JG; Shmorgun D; Chan WS
    Pathophysiol Haemost Thromb; 2002; 32(2):51-8. PubMed ID: 12214149
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases.
    Lee CN; Su YN; Cheng WF; Lin MT; Wang JK; Wu MH; Hsieh FJ
    Acta Obstet Gynecol Scand; 2005 Dec; 84(12):1134-40. PubMed ID: 16305696
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hyperhomocysteinemia and the MTHFR C677T mutation in Budd-Chiari syndrome.
    Li XM; Wei YF; Hao HL; Hao YB; He LS; Li JD; Mei B; Wang SY; Wang C; Wang JX; Zhu JZ; Liang JQ
    Am J Hematol; 2002 Sep; 71(1):11-4. PubMed ID: 12221667
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Association of congenital cardiovascular malformations with 33 single nucleotide polymorphisms of selected cardiovascular disease-related genes.
    Kuehl K; Loffredo C; Lammer EJ; Iovannisci DM; Shaw GM
    Birth Defects Res A Clin Mol Teratol; 2010 Feb; 88(2):101-10. PubMed ID: 19764075
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Does the interaction between maternal folate intake and the methylenetetrahydrofolate reductase polymorphisms affect the risk of cleft lip with or without cleft palate?
    van Rooij IA; Vermeij-Keers C; Kluijtmans LA; Ocké MC; Zielhuis GA; Goorhuis-Brouwer SM; van der Biezen JJ; Kuijpers-Jagtman AM; Steegers-Theunissen RP
    Am J Epidemiol; 2003 Apr; 157(7):583-91. PubMed ID: 12672677
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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. PubMed ID: 20160465
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association of SNPs in genes involved in folate metabolism with the risk of congenital heart disease.
    Wang B; Liu M; Yan W; Mao J; Jiang D; Li H; Chen Y
    J Matern Fetal Neonatal Med; 2013 Dec; 26(18):1768-77. PubMed ID: 23701284
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Correlationship between congenital heart disease and polymorphism of MTHFR gene].
    Li D; Yu K; Ma Y; Liu Y; Ji L
    Wei Sheng Yan Jiu; 2015 Nov; 44(6):933-8. PubMed ID: 26738386
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.