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 *

144 related articles for article (PubMed ID: 22057956)

  • 1. 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]  

  • 2. Analysis of MTR and MTRR Gene Polymorphisms in Chinese Patients With Ventricular Septal Defect.
    Su J; Li Z
    Appl Immunohistochem Mol Morphol; 2018; 26(10):769-774. PubMed ID: 29293099
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A66G and C524T polymorphisms of methionine synthase reductase gene are linked to the development of acyanotic congenital heart diseases in Egyptian children.
    Hassan FM; Khattab AA; Abo El Fotoh WMM; Zidan RS
    Gene; 2017 Sep; 629():59-63. PubMed ID: 28778621
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Methionine Synthase Reductase-A66G and -C524T Single Nucleotide Polymorphisms and Prostate Cancer: A Case-Control Trial.
    Basir A
    Asian Pac J Cancer Prev; 2019 May; 20(5):1445-1451. PubMed ID: 31127906
    [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. Analysis of MTHFR and MTRR Gene Polymorphisms in Iranian Ventricular Septal Defect Subjects.
    Pishva SR; Vasudevan R; Etemad A; Heidari F; Komara M; Ismail P; Othman F; Karimi A; Sabri MR
    Int J Mol Sci; 2013 Jan; 14(2):2739-52. PubMed ID: 23358257
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Geographical distribution of MTHFR C677T, A1298C and MTRR A66G gene polymorphisms in China: findings from 15357 adults of Han nationality.
    Yang B; Liu Y; Li Y; Fan S; Zhi X; Lu X; Wang D; Zheng Q; Wang Y; Wang Y; Sun G
    PLoS One; 2013; 8(3):e57917. PubMed ID: 23472119
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. Associations of MTHFR C677T and MTRR A66G gene polymorphisms with metabolic syndrome: a case-control study in Northern China.
    Yang B; Fan S; Zhi X; Wang D; Li Y; Wang Y; Wang Y; Wei J; Zheng Q; Sun G
    Int J Mol Sci; 2014 Nov; 15(12):21687-702. PubMed ID: 25429430
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Association between methionine synthase reductase A66G polymorphism and the risk of congenital heart defects: evidence from eight case-control studies.
    Yu D; Yang L; Shen S; Fan C; Zhang W; Mo X
    Pediatr Cardiol; 2014 Oct; 35(7):1091-8. PubMed ID: 24913415
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Genetic variant in MTRR, but not MTR, is associated with risk of congenital heart disease: an integrated meta-analysis.
    Cai B; Zhang T; Zhong R; Zou L; Zhu B; Chen W; Shen N; Ke J; Lou J; Wang Z; Sun Y; Liu L; Song R
    PLoS One; 2014; 9(3):e89609. PubMed ID: 24595101
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Influence of methionine synthase (A2756G) and methionine synthase reductase (A66G) polymorphisms on plasma homocysteine levels and relation to risk of coronary artery disease.
    Laraqui A; Allami A; Carrié A; Coiffard AS; Benkouka F; Benjouad A; Bendriss A; Kadiri N; Bennouar N; Benomar A; Guedira A; Raisonnier A; Fellati S; Srairi JE; Benomar M
    Acta Cardiol; 2006 Feb; 61(1):51-61. PubMed ID: 16485733
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Association of MTHFR C677T, MTHFR A1298C, and MTRR A66G Polymorphisms with Neural Tube Defects in Tunisian Parents.
    Nasri K; Midani F; Kallel A; Ben Jemaa N; Aloui M; Boulares M; Lassoued M; Ben Halima M; Ben Wafi S; Soussi M; Mahjoubi I; Baara A; Ben Fradj MK; Omar S; Feki M; Jemaa R; Gaigi SS; Marrakchi R
    Pathobiology; 2019; 86(4):190-200. PubMed ID: 31238314
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association between methionine synthase reductase A66G polymorphism and primary infertility in Chinese males.
    Li XY; Ye JZ; Ding XP; Zhang XH; Ma TJ; Zhong R; Ren HY
    Genet Mol Res; 2015 Apr; 14(2):3491-500. PubMed ID: 25966116
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Gene polymorphisms involved in folate and methionine metabolism and increased risk of sporadic colorectal adenocarcinoma.
    Guimarães JL; Ayrizono Mde L; Coy CS; Lima CS
    Tumour Biol; 2011 Oct; 32(5):853-61. PubMed ID: 21603981
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.