161 related articles for article (PubMed ID: 28702146)
1. Are polymorphisms in MTRR A66G and MTHFR C677T genes associated with congenital heart diseases in Iranian population?
Noori N; Miri-Moghaddam E; Dejkam A; Garmie Y; Bazi A
Caspian J Intern Med; 2017; 8(2):83-90. PubMed ID: 28702146
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Interactions between genetic variants involved in the folate metabolic pathway and serum lipid, homocysteine levels on the risk of recurrent spontaneous abortion.
Lin Z; Li Q; Sun Y; Huang J; Wang W; Fu J; Xu J; Zeng D
Lipids Health Dis; 2019 Jun; 18(1):143. PubMed ID: 31200713
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Association of MTHFR (C677T, A1298C) and MTRR A66G polymorphisms with fatty acids profile and risk of neural tube defects.
Nasri K; Ben Jamaa N; Gaigi SS; Feki M; Marrakchi R
Birth Defects Res; 2024 May; 116(5):e2333. PubMed ID: 38716581
[TBL] [Abstract][Full Text] [Related]
6. Gender-specific interactions of MTHFR C677T and MTRR A66G polymorphisms with overweight/obesity on serum lipid levels in a Chinese Han population.
Zhi X; Yang B; Fan S; Wang Y; Wei J; Zheng Q; Sun G
Lipids Health Dis; 2016 Oct; 15(1):185. PubMed ID: 27793164
[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. 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]
9. 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]
10. A Association of
Raigani M; Lakpour N; Soleimani M; Johari B; Sadeghi MR
Int J Fertil Steril; 2021 Jan; 15(1):20-25. PubMed ID: 33497043
[TBL] [Abstract][Full Text] [Related]
11. MTRR and MTHFR polymorphism: link to Down syndrome?
O'Leary VB; Parle-McDermott A; Molloy AM; Kirke PN; Johnson Z; Conley M; Scott JM; Mills JL
Am J Med Genet; 2002 Jan; 107(2):151-5. PubMed ID: 11807890
[TBL] [Abstract][Full Text] [Related]
12. Association between MTHFR C677T and A1298C, and MTRR A66G polymorphisms and susceptibility to schizophrenia in a Syrian study cohort.
Lajin B; Alhaj Sakur A; Michati R; Alachkar A
Asian J Psychiatr; 2012 Jun; 5(2):144-9. PubMed ID: 22813657
[TBL] [Abstract][Full Text] [Related]
13. Joint associations of folate, homocysteine and MTHFR, MTR and MTRR gene polymorphisms with dyslipidemia in a Chinese hypertensive population: a cross-sectional study.
Li WX; Lv WW; Dai SX; Pan ML; Huang JF
Lipids Health Dis; 2015 Sep; 14():101. PubMed ID: 26337056
[TBL] [Abstract][Full Text] [Related]
14. Additive Interaction of MTHFR C677T and MTRR A66G Polymorphisms with Being Overweight/Obesity on the Risk of Type 2 Diabetes.
Zhi X; Yang B; Fan S; Li Y; He M; Wang D; Wang Y; Wei J; Zheng Q; Sun G
Int J Environ Res Public Health; 2016 Dec; 13(12):. PubMed ID: 27983710
[TBL] [Abstract][Full Text] [Related]
15. Methionine Synthase Reductase Gene A66G Polymorphism is Associated with Risk of Colorectal Cancer.
Matsuo K; Hamajima N; Hirai T; Kato T; Inoue M; Takezaki T; Tajima K
Asian Pac J Cancer Prev; 2002; 3(4):353-359. PubMed ID: 12716294
[TBL] [Abstract][Full Text] [Related]
16. Genetic polymorphisms in MTHFR (C677T, A1298C), MTR (A2756G) and MTRR (A66G) genes associated with pathological characteristics of prostate cancer in the Ecuadorian population.
López-Cortés A; Jaramillo-Koupermann G; Muñoz MJ; Cabrera A; Echeverría C; Rosales F; Vivar N; Paz-y-Miño C
Am J Med Sci; 2013 Dec; 346(6):447-54. PubMed ID: 23459165
[TBL] [Abstract][Full Text] [Related]
17. Association between decreased vitamin levels and MTHFR, MTR and MTRR gene polymorphisms as determinants for elevated total homocysteine concentrations in pregnant women.
Barbosa PR; Stabler SP; Machado AL; Braga RC; Hirata RD; Hirata MH; Sampaio-Neto LF; Allen RH; Guerra-Shinohara EM
Eur J Clin Nutr; 2008 Aug; 62(8):1010-21. PubMed ID: 17522601
[TBL] [Abstract][Full Text] [Related]
18. MTR, MTRR, and MTHFR Gene Polymorphisms and Susceptibility to Nonsyndromic Cleft Lip With or Without Cleft Palate.
Wang W; Jiao XH; Wang XP; Sun XY; Dong C
Genet Test Mol Biomarkers; 2016 Jun; 20(6):297-303. PubMed ID: 27167580
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]