Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 125

1.

MTHFR rs1801133 C>T polymorphism is associated with an increased risk of tetralogy of Fallot.

Huang J, Mei J, Jiang L, Jiang Z, Liu H, Ding F.

Biomed Rep. 2014 Mar;2(2):172-176. Epub 2014 Jan 15.

2.

Methylenetetrahydrofolate reductase C677T and reduced folate carrier 80 G>A polymorphisms are associated with an increased risk of conotruncal heart defects.

Gong D, Gu H, Zhang Y, Gong J, Nie Y, Wang J, Zhang H, Liu R, Hu S, Zhang H.

Clin Chem Lab Med. 2012 Feb 4;50(8):1455-61. doi: 10.1515/cclm-2011-0759.

PMID:
22868813
3.

Evidence of gene-gene interactions between MTHFD1 and MTHFR in relation to anterior encephalocele susceptibility in Northeast India.

Dutta HK, Borbora D, Baruah M, Narain K.

Birth Defects Res. 2017 Apr 3;109(6):432-444. doi: 10.1002/bdra.23607. Epub 2017 Feb 20.

PMID:
28398708
4.

Association study of MTHFD1 coding polymorphisms R134K and R653Q with migraine susceptibility.

Sutherland HG, Hermile H, Sanche R, Menon S, Lea RA, Haupt LM, Griffiths LR.

Headache. 2014 Oct;54(9):1506-14. doi: 10.1111/head.12428. Epub 2014 Jul 18.

PMID:
25039261
5.

MiR-196a2 rs11614913 T>C Polymorphism is Associated with an Increased Risk of Tetralogy of Fallot in a Chinese Population.

Huang JB, Mei J, Jiang LY, Jiang ZL, Liu H, Zhang JW, Ding FB.

Acta Cardiol Sin. 2015 Jan;31(1):18-23.

6.

Genetic polymorphisms in the methylenetetrahydrofolate reductase gene (MTHFR) and risk of vitiligo in Han Chinese populations: a genotype-phenotype correlation study.

Chen JX, Shi Q, Wang XW, Guo S, Dai W, Li K, Song P, Wei C, Wang G, Li CY, Gao TW.

Br J Dermatol. 2014 May;170(5):1092-9. doi: 10.1111/bjd.12845.

PMID:
24472005
7.

Tagging SNPs in the MTHFR gene and risk of ischemic stroke in a Chinese population.

Zhou BS, Bu GY, Li M, Chang BG, Zhou YP.

Int J Mol Sci. 2014 May 20;15(5):8931-40. doi: 10.3390/ijms15058931.

8.

Polymorphisms in the MTHFR gene are associated with breast cancer risk and prognosis in a Chinese population.

Lu Q, Jiang K, Li Q, Ji YJ, Chen WL, Xue XH.

Tumour Biol. 2015 May;36(5):3757-62. doi: 10.1007/s13277-014-3016-4. Epub 2015 Jan 8.

PMID:
25566964
9.

MTHFR 677C-->T polymorphism and risk of coronary heart disease: a meta-analysis.

Klerk M, Verhoef P, Clarke R, Blom HJ, Kok FJ, Schouten EG; MTHFR Studies Collaboration Group.

JAMA. 2002 Oct 23-30;288(16):2023-31.

PMID:
12387655
10.

Study on Environmental Causes and SNPs of MTHFR, MS and CBS Genes Related to Congenital Heart Disease.

Shi H, Yang S, Liu Y, Huang P, Lin N, Sun X, Yu R, Zhang Y, Qin Y, Wang L.

PLoS One. 2015 Jun 2;10(6):e0128646. doi: 10.1371/journal.pone.0128646. eCollection 2015.

11.

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. doi: 10.3109/14767058.2013.799648. Epub 2013 Jun 10.

PMID:
23701284
12.

Common Polymorphisms That Affect Folate Transport or Metabolism Modify the Effect of the MTHFR 677C > T Polymorphism on Folate Status.

Bueno O, Molloy AM, Fernandez-Ballart JD, García-Minguillán CJ, Ceruelo S, Ríos L, Ueland PM, Meyer K, Murphy MM.

J Nutr. 2016 Jan;146(1):1-8. doi: 10.3945/jn.115.223685. Epub 2015 Nov 11.

13.

Association analysis between MTHFR genetic polymorphisms and the risk of congenital heart diseases in Chinese Han population.

Zhang Q, Zha D, Dong P, Zhang Y, Zhang W, Liu Y.

J Pharm Pharmacol. 2014 Sep;66(9):1259-64. doi: 10.1111/jphp.12260. Epub 2014 Apr 10.

PMID:
24720776
14.

Associations between polymorphisms in folate-metabolizing genes and pancreatic cancer risk in Japanese subjects.

Nakao H, Wakai K, Ishii N, Kobayashi Y, Ito K, Yoneda M, Mori M, Nojima M, Kimura Y, Endo T, Matsuyama M, Ishii H, Ueno M, Kuruma S, Egawa N, Matsuo K, Hosono S, Ohkawa S, Nakamura K, Tamakoshi A, Takahashi M, Shimada K, Nishiyama T, Kikuchi S, Lin Y.

BMC Gastroenterol. 2016 Jul 29;16(1):83. doi: 10.1186/s12876-016-0503-7.

15.

Association of methylenetetrahydrofolate reductase gene-gene interaction and haplotype with susceptibility to acute lymphoblastic leukemia in Chinese children.

Xia X, Duan Y, Cui J, Jiang J, Lin L, Peng X, Wang Y, Guo B, Liu S, Lei X.

Leuk Lymphoma. 2017 Aug;58(8):1887-1892. doi: 10.1080/10428194.2016.1265117. Epub 2016 Dec 20.

PMID:
27996344
16.

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 3rd, Theriaque DW, Kauwell GP.

J Nutr. 2004 Nov;134(11):2985-90.

17.

Methylenetetrahydrofolate reductase C677T polymorphism and congenital heart disease: a meta-analysis.

Nie Y, Gu H, Gong J, Wang J, Gong D, Cong X, Chen X, Hu S.

Clin Chem Lab Med. 2011 Dec;49(12):2101-8. doi: 10.1515/CCLM.2011.673. Epub 2011 Jul 28.

PMID:
21793799
18.

Methylenetetrahydrofolate reductase C667T polymorphism is associated with increased risk of coronary artery disease in a Chinese population.

Chen W, Hua K, Gu H, Zhang J, Wang L.

Scand J Immunol. 2014 Nov;80(5):346-53. doi: 10.1111/sji.12215.

19.

Association between methylenetetrahydrofolate reductase C677T polymorphism and epilepsy susceptibility: a meta-analysis.

Wu YL, Yang HY, Ding XX, Zhao X, Chen J, Bi P, Sun YH.

Seizure. 2014 Jun;23(6):411-6. doi: 10.1016/j.seizure.2014.01.018. Epub 2014 Feb 2.

20.

Associations of Polymorphisms in MTHFR Gene with the Risk of Age-Related Cataract in Chinese Han Population: A Genotype-Phenotype Analysis.

Wang XB, Qiao C, Wei L, Han YD, Cui NH, Huang ZL, Li ZH, Zheng F, Yan M.

PLoS One. 2015 Dec 21;10(12):e0145581. doi: 10.1371/journal.pone.0145581. eCollection 2015.

Supplemental Content

Support Center