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Items: 1 to 20 of 34

1.

Associations Between MTHFR Polymorphisms and the Risk of Potentially Malignant Oral Disorders.

Senghore T, Li YF, Sung FC, Tsai MH, Hua CH, Liu CS, Hung MF, Yeh CC.

Anticancer Res. 2018 Jul;38(7):4021-4026. doi: 10.21873/anticanres.12690.

PMID:
29970526
2.

MTHFR 677C → T genotype modulates the effect of a 5-year supplementation with B-vitamins on homocysteine concentration: The SU.FOL.OM3 randomized controlled trial.

Fezeu LK, Ducros V, Guéant JL, Guilland JC, Andreeva VA, Hercberg S, Galan P.

PLoS One. 2018 May 29;13(5):e0193352. doi: 10.1371/journal.pone.0193352. eCollection 2018.

3.

The relationship between of ACE I/D and the MTHFR C677T polymorphisms in the pathophysiology of type 2 diabetes mellitus in a population of Brazilian obese patients.

Pirozzi FF, Belini Junior E, Okumura JV, Salvarani M, Bonini-Domingos CR, Ruiz MA.

Arch Endocrinol Metab. 2018 Feb;62(1):21-26. doi: 10.20945/2359-3997000000005.

4.

Association of parental methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism in couples with unexplained recurrent pregnancy loss.

Sah AK, Shrestha N, Joshi P, Lakha R, Shrestha S, Sharma L, Chandra A, Singh N, Kc Y, Rijal B.

BMC Res Notes. 2018 Apr 5;11(1):233. doi: 10.1186/s13104-018-3321-x.

5.

The Role of MTHFR Genotype in Colorectal Cancer Susceptibility in Taiwan.

Lin KM, Yang MD, Tsai CW, Chang WS, Hsiao CL, Jeng LB, Yueh TC, Lee MC, Bau DT.

Anticancer Res. 2018 Apr;38(4):2001-2006.

PMID:
29599316
6.

Two Common MTHFR Gene Polymorphisms (C677T and A1298C) and Fetal Congenital Heart Disease Risk: An Updated Meta-Analysis with Trial Sequential Analysis.

Zhang R, Huo C, Wang X, Dang B, Mu Y, Wang Y.

Cell Physiol Biochem. 2018;45(6):2483-2496. doi: 10.1159/000488267. Epub 2018 Mar 15.

7.

3'-UTR Polymorphisms of MTHFR and TS Associated with Osteoporotic Vertebral Compression Fracture Susceptibility in Postmenopausal Women.

Ahn TK, Kim JO, Kim HW, Park HS, Shim JH, Ropper AE, Han IB, Kim NK.

Int J Mol Sci. 2018 Mar 12;19(3). pii: E824. doi: 10.3390/ijms19030824.

8.

Computational analysis for the determination of deleterious nsSNPs in human MTHFR gene.

Desai M, Chauhan JB.

Comput Biol Chem. 2018 Jun;74:20-30. doi: 10.1016/j.compbiolchem.2018.02.022. Epub 2018 Feb 27.

PMID:
29524840
9.

The SNP Rs915014 in MTHFR Regulated by MiRNA Associates with Atherosclerosis.

Liu X, Wang L, Chi H, Wang J, Zheng Q, Li J, Li Y, Yang D.

Cell Physiol Biochem. 2018;45(3):1149-1155. doi: 10.1159/000487355. Epub 2018 Feb 8.

10.

Correlation between global methylation level of peripheral blood leukocytes and serum C reactive protein level modified by MTHFR polymorphism: a cross-sectional study.

Nojima M, Iwasaki M, Kasuga Y, Yokoyama S, Onuma H, Nishimura H, Kusama R, Yoshida T, Tsugane S.

BMC Cancer. 2018 Feb 13;18(1):184. doi: 10.1186/s12885-018-4089-z.

11.

Association of MTHFR gene polymorphisms with migraine in North Indian population.

Kaur S, Ali A, Pandey AK, Singh B.

Neurol Sci. 2018 Apr;39(4):691-698. doi: 10.1007/s10072-018-3276-7. Epub 2018 Feb 9.

PMID:
29427165
12.

Association of elevated homocysteine levels and Methylenetetrahydrofolate reductase (MTHFR) 1298 A > C polymorphism with Vitiligo susceptibility in Gujarat.

Jadeja SD, Mansuri MS, Singh M, Patel H, Marfatia YS, Begum R.

J Dermatol Sci. 2018 May;90(2):112-122. doi: 10.1016/j.jdermsci.2018.01.003. Epub 2018 Jan 31.

PMID:
29395581
13.

A possible synergistic effect of MTHFR C677T polymorphism on homocysteine level variations increased risk for ischemic stroke.

Li A, Shi Y, Xu L, Zhang Y, Zhao H, Li Q, Zhao X, Cao X, Zheng H, He Y.

Medicine (Baltimore). 2017 Dec;96(51):e9300. doi: 10.1097/MD.0000000000009300.

14.

Manifestations of neurological symptoms and thromboembolism in adults with MTHFR-deficiency.

Rommer PS, Zschocke J, Fowler B, Födinger M, Konstantopoulou V, Möslinger D, Stögmann E, Suess E, Baumgartner M, Auff E, Sunder-Plassmann G.

J Neurol Sci. 2017 Dec 15;383:123-127. doi: 10.1016/j.jns.2017.10.035. Epub 2017 Nov 6.

PMID:
29246599
15.

MTHFR C677T gene polymorphism and the severity of coronary lesions in acute coronary syndrome.

Li MN, Wang HJ, Zhang NR, Xuan L, Shi XJ, Zhou T, Chen B, Zhang J, Li H.

Medicine (Baltimore). 2017 Dec;96(49):e9044. doi: 10.1097/MD.0000000000009044.

16.

Association between MTHFR variant and diabetic neuropathy.

Kakavand Hamidi A, Radfar M, Amoli MM.

Pharmacol Rep. 2018 Feb;70(1):1-5. doi: 10.1016/j.pharep.2017.04.017. Epub 2017 Apr 26.

PMID:
29222982
17.

MTHFR A1298C and C677T Polymorphisms Are Associated with Increased Risk of Venous Thromboembolism: A Retrospective Chart Review Study.

Liu F, Silva D, Malone MV, Seetharaman K.

Acta Haematol. 2017;138(4):208-215. doi: 10.1159/000480447. Epub 2017 Dec 7. Review.

PMID:
29212064
18.

MTHFR A1298C polymorphisms reduce the risk of congenital heart defects: a meta-analysis from 16 case-control studies.

Yu D, Zhuang Z, Wen Z, Zang X, Mo X.

Ital J Pediatr. 2017 Dec 4;43(1):108. doi: 10.1186/s13052-017-0425-1. Review.

20.

The MTHFR polymorphism affect the susceptibility of HCC and the prognosis of HCC liver transplantation.

Wang C, Xie H, Lu D, Ling Q, Jin P, Li H, Zhuang R, Xu X, Zheng S.

Clin Transl Oncol. 2018 Apr;20(4):448-456. doi: 10.1007/s12094-017-1729-8. Epub 2017 Nov 28.

PMID:
29185200

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