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 *

158 related articles for article (PubMed ID: 22179537)

  • 1. Functional variant in methionine synthase reductase intron-1 significantly increases the risk of congenital heart disease in the Han Chinese population.
    Zhao JY; Yang XY; Gong XH; Gu ZY; Duan WY; Wang J; Ye ZZ; Shen HB; Shi KH; Hou J; Huang GY; Jin L; Qiao B; Wang HY
    Circulation; 2012 Jan; 125(3):482-90. PubMed ID: 22179537
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Functional variant in methionine synthase reductase intron-1 is associated with pleiotropic congenital malformations.
    Cheng H; Li H; Bu Z; Zhang Q; Bai B; Zhao H; Li RK; Zhang T; Xie J
    Mol Cell Biochem; 2015 Sep; 407(1-2):51-6. PubMed ID: 26045171
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Lower Circulating Folate Induced by a Fidgetin Intronic Variant Is Associated With Reduced Congenital Heart Disease Susceptibility.
    Wang D; Wang F; Shi KH; Tao H; Li Y; Zhao R; Lu H; Duan W; Qiao B; Zhao SM; Wang H; Zhao JY
    Circulation; 2017 May; 135(18):1733-1748. PubMed ID: 28302752
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. MTRR 66A>G polymorphism in relation to congenital heart defects.
    van Beynum IM; Kouwenberg M; Kapusta L; den Heijer M; van der Linden IJ; Daniels O; Blom HJ
    Clin Chem Lab Med; 2006; 44(11):1317-23. PubMed ID: 17087642
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic variation in folate metabolism is associated with the risk of conotruncal heart defects in a Chinese population.
    Wang X; Wei H; Tian Y; Wu Y; Luo L
    BMC Pediatr; 2018 Aug; 18(1):287. PubMed ID: 30165839
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic variants reducing MTR gene expression increase the risk of congenital heart disease in Han Chinese populations.
    Zhao JY; Qiao B; Duan WY; Gong XH; Peng QQ; Jiang SS; Lu CQ; Chen YJ; Shen HB; Huang GY; Jin L; Wang HY
    Eur Heart J; 2014 Mar; 35(11):733-42. PubMed ID: 23798577
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Analysis of MTR and MTRR Polymorphisms for Neural Tube Defects Risk Association.
    Wang Y; Liu Y; Ji W; Qin H; Wu H; Xu D; Tukebai T; Wang Z
    Medicine (Baltimore); 2015 Sep; 94(35):e1367. PubMed ID: 26334892
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Relationship between methionine synthase, methionine synthase reductase genetic polymorphisms and deep vein thrombosis among South Indians.
    Naushad SM; Jain Jamal MN; Prasad CK; Rama Devi AR
    Clin Chem Lab Med; 2008; 46(1):73-9. PubMed ID: 18034637
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association of three missense mutations in the homocysteine-related MTHFR and MTRR gene with risk of polycystic ovary syndrome in Southern Chinese women.
    Feng W; Zhang Y; Pan Y; Zhang Y; Liu M; Huang Y; Xiao Y; Mo W; Jiao J; Wang X; Tian D; Yang L; Ma Y
    Reprod Biol Endocrinol; 2021 Jan; 19(1):5. PubMed ID: 33407572
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Methylenetetrahydrofolate reductase and methionine synthase reductase gene polymorphisms in ethnic Han women from Linyi].
    Zhang YL; Lu YQ; Li HF; Rui XY; Zhang LJ; Wu CY; Fang AM; Wang GX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Dec; 29(6):705-8. PubMed ID: 23225055
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 5,10-Methylenetetrahydrofolate reductase (MTHFR), methionine synthase (MTRR), and methionine synthase reductase (MTR) gene polymorphisms and adult meningioma risk.
    Zhang J; Zhou YW; Shi HP; Wang YZ; Li GL; Yu HT; Xie XY
    J Neurooncol; 2013 Nov; 115(2):233-9. PubMed ID: 23959833
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A66G and C524T polymorphisms of the methionine synthase reductase gene are associated with congenital heart defects in the Chinese Han population.
    Zeng W; Liu L; Tong Y; Liu HM; Dai L; Mao M
    Genet Mol Res; 2011 Oct; 10(4):2597-605. PubMed ID: 22057956
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Three genetic polymorphisms of homocysteine-metabolizing enzymes and risk of coronary heart disease: a meta-analysis based on 23 case-control studies.
    Chen L; Liu L; Hong K; Hu J; Cheng X
    DNA Cell Biol; 2012 Feb; 31(2):238-49. PubMed ID: 21780915
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association of Single Nucleotide Polymorphisms (SNPs) in Genes Encoding for Folate Metabolising Enzymes with Glioma and Meningioma in Indian Population.
    Kumawat R; Gowda SH; Debnath E; Rashid S; Niwas R; Gupta Y; Upadaya AD; Suri A; Chandra PS; Gupta DK; Lakshmy R; Sarkar C; Sinha S; Chosdol K
    Asian Pac J Cancer Prev; 2018 Dec; 19(12):3415-3425. PubMed ID: 30583664
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Association of maternal methionine synthase reductase gene polymorphisms with the risk of congenital heart disease in offspring: a hospital-based case-control study.
    Wei J; Wang T; Song X; Liu Y; Shu J; Sun M; Diao J; Li J; Li Y; Chen L; Zhang S; Huang P; Qin J
    J Matern Fetal Neonatal Med; 2023 Dec; 36(1):2211201. PubMed ID: 37183022
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Folate, vitamin B12, homocysteine and polymorphisms in folate metabolizing genes in children with congenital heart disease and their mothers.
    Elizabeth KE; Praveen SL; Preethi NR; Jissa VT; Pillai MR
    Eur J Clin Nutr; 2017 Dec; 71(12):1437-1441. PubMed ID: 28876333
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations.
    Gaughan DJ; Kluijtmans LA; Barbaux S; McMaster D; Young IS; Yarnell JW; Evans A; Whitehead AS
    Atherosclerosis; 2001 Aug; 157(2):451-6. PubMed ID: 11472746
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Effects of polymorphisms of methionine synthase and methionine synthase reductase on total plasma homocysteine in the NHLBI Family Heart Study.
    Jacques PF; Bostom AG; Selhub J; Rich S; Ellison RC; Eckfeldt JH; Gravel RA; Rozen R;
    Atherosclerosis; 2003 Jan; 166(1):49-55. PubMed ID: 12482550
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Homocysteine Metabolism Gene Polymorphisms (MTHFR C677T, MTHFR A1298C, MTR A2756G and MTRR A66G) Jointly Elevate the Risk of Folate Deficiency.
    Li WX; Dai SX; Zheng JJ; Liu JQ; Huang JF
    Nutrients; 2015 Aug; 7(8):6670-87. PubMed ID: 26266420
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.