182 related articles for article (PubMed ID: 28758112)
1. Parental Genetic Variants, MTHFR 677C>T and MTRR 66A>G, Associated Differently with Fetal Congenital Heart Defect.
Guo QN; Wang HD; Tie LZ; Li T; Xiao H; Long JG; Liao SX
Biomed Res Int; 2017; 2017():3043476. PubMed ID: 28758112
[TBL] [Abstract][Full Text] [Related]
2. Variants c.677 C>T, c.1298 A>C in
Zhang Y; Zhan W; Du Q; Wu L; Ding H; Liu F; Yin A
Genet Test Mol Biomarkers; 2020 Nov; 24(11):717-722. PubMed ID: 33121283
[No Abstract] [Full Text] [Related]
3. Methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) gene polymorphisms as risk factors for hepatocellular carcinoma in a Korean population.
Kwak SY; Kim UK; Cho HJ; Lee HK; Kim HJ; Kim NK; Hwang SG
Anticancer Res; 2008; 28(5A):2807-11. PubMed ID: 19035314
[TBL] [Abstract][Full Text] [Related]
4. The roles of
Xu A; Wang W; Jiang X
Biosci Rep; 2018 Dec; 38(6):. PubMed ID: 30333252
[No Abstract] [Full Text] [Related]
5. Methionine synthase reductase 66A->G polymorphism is associated with increased plasma homocysteine concentration when combined with the homozygous methylenetetrahydrofolate reductase 677C->T variant.
Vaughn JD; Bailey LB; Shelnutt KP; Dunwoody KM; Maneval DR; Davis SR; Quinlivan EP; Gregory JF; Theriaque DW; Kauwell GP
J Nutr; 2004 Nov; 134(11):2985-90. PubMed ID: 15514263
[TBL] [Abstract][Full Text] [Related]
6. The methionine synthase reductase 66A>G polymorphism is a maternal risk factor for spina bifida.
van der Linden IJ; den Heijer M; Afman LA; Gellekink H; Vermeulen SH; Kluijtmans LA; Blom HJ
J Mol Med (Berl); 2006 Dec; 84(12):1047-54. PubMed ID: 17024475
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Association between genetic polymorphisms in folate-related enzyme genes and infertile men with non-obstructive azoospermia.
Kim SY; Lim JW; Kim JW; Park SY; Seo JT
Syst Biol Reprod Med; 2015; 61(5):286-92. PubMed ID: 26196053
[TBL] [Abstract][Full Text] [Related]
9. Maternal polymorphisms 677C-T and 1298A-C of MTHFR, and 66A-G MTRR genes: is there any relationship between polymorphisms of the folate pathway, maternal homocysteine levels, and the risk for having a child with Down syndrome?
Martínez-Frías ML; Pérez B; Desviat LR; Castro M; Leal F; Rodríguez L; Mansilla E; Martínez-Fernández ML; Bermejo E; Rodríguez-Pinilla E; Prieto D; Ugarte M;
Am J Med Genet A; 2006 May; 140(9):987-97. PubMed ID: 16575899
[TBL] [Abstract][Full Text] [Related]
10. Methylenetetrahydrofolate reductase and methionine synthase reductase gene polymorphisms and protection from microvascular complications in adolescents with type 1 diabetes.
Wiltshire EJ; Mohsin F; Chan A; Donaghue KC
Pediatr Diabetes; 2008 Aug; 9(4 Pt 2):348-53. PubMed ID: 18774994
[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. Germline variation in the MTHFR and MTRR genes determines the nadir of bone density in pediatric acute lymphoblastic leukemia: a prospective study.
te Winkel ML; de Muinck Keizer-Schrama SM; de Jonge R; van Beek RD; van der Sluis IM; Hop WC; Pieters R; van den Heuvel-Eibrink MM
Bone; 2011 Mar; 48(3):571-7. PubMed ID: 20955826
[TBL] [Abstract][Full Text] [Related]
13. Polymorphism in one-carbon metabolism pathway affects survival of gastric cancer patients: Large and comprehensive study.
Zhao T; Gu D; Xu Z; Huo X; Shen L; Wang C; Tang Y; Wu P; He J; Gong W; He ML; Chen J
Oncotarget; 2015 Apr; 6(11):9564-76. PubMed ID: 25840420
[TBL] [Abstract][Full Text] [Related]
14. Different effects of maternal homocysteine concentration, MTHFR and MTRR genetic polymorphisms on the occurrence of fetal aneuploidy.
Guo QN; Wang L; Liu ZY; Wang HD; Wang L; Long JG; Liao SX
Reprod Biomed Online; 2022 Dec; 45(6):1207-1215. PubMed ID: 36210274
[TBL] [Abstract][Full Text] [Related]
15. Role of parental folate pathway single nucleotide polymorphisms in altering the susceptibility to neural tube defects in South India.
Naushad SM; Devi AR
J Perinat Med; 2010; 38(1):63-9. PubMed ID: 20047525
[TBL] [Abstract][Full Text] [Related]
16. Polymorphisms in genes related to folate and cobalamin metabolism and the associations with complex birth defects.
Brouns R; Ursem N; Lindemans J; Hop W; Pluijm S; Steegers E; Steegers-Theunissen R
Prenat Diagn; 2008 Jun; 28(6):485-93. PubMed ID: 18435414
[TBL] [Abstract][Full Text] [Related]
17. Triplex tetra-primer ARMS-PCR method for the simultaneous detection of MTHFR c.677C>T and c.1298A>C, and MTRR c.66A>G polymorphisms of the folate-homocysteine metabolic pathway.
Lajin B; Alachkar A; Sakur AA
Mol Cell Probes; 2012 Feb; 26(1):16-20. PubMed ID: 22074746
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [Association of MTHFR and MTRR genes polymorphisms with non-disjunctions of chromosomes 18 and 21].
Guo Q; Wang H; Yang K; Zhang B; Li T; Liao S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun; 32(3):395-9. PubMed ID: 26037359
[TBL] [Abstract][Full Text] [Related]
20. Effects of methionine synthase and methionine synthase reductase polymorphisms on hypertension susceptibility.
Kim YR; Kang SH; Hong SH
Genes Genomics; 2020 Apr; 42(4):477-483. PubMed ID: 32146711
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
