303 related articles for article (PubMed ID: 28865601)
1. Relationship of the MTHFD1 (rs2236225), eNOS (rs1799983), CBS (rs2850144) and ACE (rs4343) gene polymorphisms in a population of Iranian pediatric patients with congenital heart defects.
Khatami M; Ratki FM; Tajfar S; Akrami F
Kaohsiung J Med Sci; 2017 Sep; 33(9):442-448. PubMed ID: 28865601
[TBL] [Abstract][Full Text] [Related]
2. [G894T (NOS3) and G1958A (MTHFD1) gene polymorphisms and risk of ischemic heart disease in Yucatan, Mexico].
García-González I; Solís-Cárdenas Ade J; Flores-Ocampo JA; Alejos-Mex R; Herrera-Sánchez LF; González-Herrera LJ
Clin Investig Arterioscler; 2015; 27(2):64-73. PubMed ID: 25304051
[TBL] [Abstract][Full Text] [Related]
3. Association of main folate metabolic pathway gene polymorphisms with neural tube defects in Han population of Northern China.
Fang Y; Zhang R; Zhi X; Zhao L; Cao L; Wang Y; Cai C
Childs Nerv Syst; 2018 Apr; 34(4):725-729. PubMed ID: 29392422
[TBL] [Abstract][Full Text] [Related]
4. MTHFD1 formyltetrahydrofolate synthetase deficiency, a model for the MTHFD1 R653Q variant, leads to congenital heart defects in mice.
Christensen KE; Deng L; Bahous RH; Jerome-Majewska LA; Rozen R
Birth Defects Res A Clin Mol Teratol; 2015 Dec; 103(12):1031-8. PubMed ID: 26408344
[TBL] [Abstract][Full Text] [Related]
5. [Association of maternal
Chen Q; Huang P; Song XL; Liu YP; Sun MT; Wang TT; Zhang SM; Qin JB
Zhongguo Dang Dai Er Ke Za Zhi; 2022 Jul; 24(7):797-805. PubMed ID: 35894196
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Moderate folic acid supplementation and MTHFD1-synthetase deficiency in mice, a model for the R653Q variant, result in embryonic defects and abnormal placental development.
Christensen KE; Hou W; Bahous RH; Deng L; Malysheva OV; Arning E; Bottiglieri T; Caudill MA; Jerome-Majewska LA; Rozen R
Am J Clin Nutr; 2016 Nov; 104(5):1459-1469. PubMed ID: 27707701
[TBL] [Abstract][Full Text] [Related]
8. Association between SNPs and hepatotoxicity in patients with primary central nervous system lymphoma on high-dose methotrexate therapy.
Zhao Q; Cui Y; Zeng C; Ren X; Yu K; Lin S; Zhao Z; Mei S
J Pharm Pharmacol; 2021 Oct; 73(11):1480-1490. PubMed ID: 34254644
[TBL] [Abstract][Full Text] [Related]
9. Maternal Mthfd1 disruption impairs fetal growth but does not cause neural tube defects in mice.
Beaudin AE; Perry CA; Stabler SP; Allen RH; Stover PJ
Am J Clin Nutr; 2012 Apr; 95(4):882-91. PubMed ID: 22378735
[TBL] [Abstract][Full Text] [Related]
10. The MTHFD1 p.Arg653Gln variant alters enzyme function and increases risk for congenital heart defects.
Christensen KE; Rohlicek CV; Andelfinger GU; Michaud J; Bigras JL; Richter A; Mackenzie RE; Rozen R
Hum Mutat; 2009 Feb; 30(2):212-20. PubMed ID: 18767138
[TBL] [Abstract][Full Text] [Related]
11. Association between genetic polymorphisms of ACE & eNOS and diabetic nephropathy.
Huo P; Zhang D; Guan X; Mei Y; Zheng H; Feng X
Mol Biol Rep; 2015 Jan; 42(1):27-33. PubMed ID: 25227524
[TBL] [Abstract][Full Text] [Related]
12. Association of MTHFD1 gene polymorphisms and maternal smoking with risk of congenital heart disease: a hospital-based case-control study.
Song X; Li Q; Diao J; Li J; Li Y; Zhang S; Zhao L; Chen L; Wei J; Shu J; Liu Y; Sun M; Huang P; Wang T; Qin J
BMC Pregnancy Childbirth; 2022 Jan; 22(1):88. PubMed ID: 35100977
[TBL] [Abstract][Full Text] [Related]
13. Association analysis of CbetaS 844ins68 and MTHFD1 G1958A polymorphisms with Alzheimer's disease in Chinese.
Bi XH; Zhao HL; Zhang ZX; Liu Q; Zhang JW
J Neural Transm (Vienna); 2010 Apr; 117(4):499-503. PubMed ID: 20217437
[TBL] [Abstract][Full Text] [Related]
14. Association of the genetic polymorphisms of the ACE gene and the eNOS gene with lupus nephropathy in northern Chinese population.
Li X; An J; Guo R; Jin Z; Li Y; Zhao Y; Lu F; Lian H; Liu P; Zhao Y; Jin X
BMC Med Genet; 2010 Jun; 11():94. PubMed ID: 20540812
[TBL] [Abstract][Full Text] [Related]
15. The association between an endothelial nitric oxide synthase gene polymorphism and coronary heart disease in young people and the underlying mechanism.
Chen XJ; Qiu CG; Kong XD; Ren SM; Dong JZ; Gu HP; Chen YW; Tao HL; Sarbesh J
Mol Med Rep; 2018 Mar; 17(3):3928-3934. PubMed ID: 29359785
[TBL] [Abstract][Full Text] [Related]
16. Genetic variants of the endothelial NO synthase gene (eNOS) may confer increased risk of sporadic congenital heart disease.
Zhou K; Wang Y; Peng W; Sun J; Qing YM; Mo XM
Genet Mol Res; 2014 May; 13(2):3805-11. PubMed ID: 24938467
[TBL] [Abstract][Full Text] [Related]
17. Association between MTHFD1 polymorphisms and neural tube defect susceptibility.
Meng J; Han L; Zhuang B
J Neurol Sci; 2015 Jan; 348(1-2):188-94. PubMed ID: 25524527
[TBL] [Abstract][Full Text] [Related]
18. A novel mouse model for genetic variation in 10-formyltetrahydrofolate synthetase exhibits disturbed purine synthesis with impacts on pregnancy and embryonic development.
Christensen KE; Deng L; Leung KY; Arning E; Bottiglieri T; Malysheva OV; Caudill MA; Krupenko NI; Greene ND; Jerome-Majewska L; MacKenzie RE; Rozen R
Hum Mol Genet; 2013 Sep; 22(18):3705-19. PubMed ID: 23704330
[TBL] [Abstract][Full Text] [Related]
19. Relation between endothelial nitric oxide synthase genetic polymorphisms and pulmonary arterial hypertension in newborns with congenital heart disease.
Lin QF; Rao JH; Luo SM; Wang QM; Deng LF; Chen X; Chen CD; Chen YF
Clin Exp Hypertens; 2022 Aug; 44(6):567-572. PubMed ID: 35699093
[TBL] [Abstract][Full Text] [Related]
20. Common 894G>T single nucleotide polymorphism in the gene coding for endothelial nitric oxide synthase (eNOS) and risk of congenital heart defects.
van Beynum IM; Mooij C; Kapusta L; Heil S; den Heijer M; Blom HJ
Clin Chem Lab Med; 2008; 46(10):1369-75. PubMed ID: 18844489
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
