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Items: 1 to 20 of 202

1.

One-carbon genetic variants and the role of MTHFD1 1958G>A in liver and colon cancer risk according to global DNA methylation.

Moruzzi S, Guarini P, Udali S, Ruzzenente A, Guglielmi A, Conci S, Pattini P, Martinelli N, Olivieri O, Tammen SA, Choi SW, Friso S.

PLoS One. 2017 Oct 2;12(10):e0185792. doi: 10.1371/journal.pone.0185792. eCollection 2017.

2.

Methylenetetrahydrofolate Dehydrogenase 1 Polymorphisms Modify the Associations of Plasma Glycine and Serine With Risk of Acute Myocardial Infarction in Patients With Stable Angina Pectoris in WENBIT (Western Norway B Vitamin Intervention Trial).

Ding Y, Pedersen ER, Svingen GF, Helgeland Ø, Gregory JF, Løland KH, Meyer K, Tell GS, Ueland PM, Nygård OK.

Circ Cardiovasc Genet. 2016 Dec;9(6):541-547. doi: 10.1161/CIRCGENETICS.116.001483. Epub 2016 Nov 21.

PMID:
27872106
3.

MTHFD1 regulates nuclear de novo thymidylate biosynthesis and genome stability.

Field MS, Kamynina E, Stover PJ.

Biochimie. 2016 Jul;126:27-30. doi: 10.1016/j.biochi.2016.02.001. Epub 2016 Feb 4.

4.

B vitamin treatments modify the risk of myocardial infarction associated with a MTHFD1 polymorphism in patients with stable angina pectoris.

Ding YP, Pedersen EK, Johansson S, Gregory JF 3rd, Ueland PM, Svingen GF, Helgeland Ø, Meyer K, Fredriksen Å, Nygård OK.

Nutr Metab Cardiovasc Dis. 2016 Jun;26(6):495-501. doi: 10.1016/j.numecd.2015.12.009. Epub 2015 Dec 23.

5.

Paternal transmission of MTHFD1 G1958A variant predisposes to neural tube defects in the offspring.

Prasoona KR, Sunitha T, Srinadh B, Deepika ML, Kumari TM, Jyothy A.

Dev Med Child Neurol. 2016 Jun;58(6):625-31. doi: 10.1111/dmcn.12929. Epub 2015 Sep 22.

6.

Polymorphisms in MTHFD1 Gene and Susceptibility to Neural Tube Defects: A Case-Control Study in a Chinese Han Population with Relatively Low Folate Levels.

Wu J, Bao Y, Lu X, Wu L, Zhang T, Guo J, Yang J.

Med Sci Monit. 2015 Sep 4;21:2630-7. doi: 10.12659/MSM.895155.

7.

Human mutations in methylenetetrahydrofolate dehydrogenase 1 impair nuclear de novo thymidylate biosynthesis.

Field MS, Kamynina E, Watkins D, Rosenblatt DS, Stover PJ.

Proc Natl Acad Sci U S A. 2015 Jan 13;112(2):400-5. doi: 10.1073/pnas.1414555112. Epub 2014 Dec 29.

8.

MTHFD1 polymorphism as maternal risk for neural tube defects: a meta-analysis.

Zheng J, Lu X, Liu H, Zhao P, Li K, Li L.

Neurol Sci. 2015 Apr;36(4):607-16. doi: 10.1007/s10072-014-2035-7. Epub 2014 Dec 13.

PMID:
25502174
9.

A pilot study on the contribution of folate gene variants in the cognitive function of ADHD probands.

Saha T, Dutta S, Rajamma U, Sinha S, Mukhopadhyay K.

Neurochem Res. 2014 Nov;39(11):2058-67. doi: 10.1007/s11064-014-1393-0. Epub 2014 Jul 31.

PMID:
25079255
10.

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
11.

Association between MTHFD1 G1958A polymorphism and neural tube defects susceptibility: a meta-analysis.

Jiang J, Zhang Y, Wei L, Sun Z, Liu Z.

PLoS One. 2014 Jun 30;9(6):e101169. doi: 10.1371/journal.pone.0101169. eCollection 2014.

12.

Lack of association between MTHFD1 G401A polymorphism and ovarian cancer susceptibility.

Cui Y, Jing Y, Sun Z.

Tumour Biol. 2014 Apr;35(4):3385-9. doi: 10.1007/s13277-013-1446-z. Epub 2013 Nov 28.

PMID:
24287951
13.

Lack of association between methylenetetrahydrofolate dehydrogenase 1 G1958A polymorphism and prostate cancer risk: a meta-analysis.

Liu G, Qi C, Xu Q, Wu B, Wang Y, Xue C.

Tumour Biol. 2014 Mar;35(3):2029-33. doi: 10.1007/s13277-013-1269-y. Epub 2013 Oct 3.

PMID:
24197977
14.

Association of methylenetetrahydrofolate dehydrogenase 1 polymorphisms with cancer: a meta-analysis.

Zhang H, Ma H, Li L, Zhang Z, Xu Y.

PLoS One. 2013 Jul 19;8(7):e69366. doi: 10.1371/journal.pone.0069366. Print 2013.

15.

Head and neck carconogenesis: impact of MTHFD1 G1958A polymorphism.

Silva LM, Silva JN, Galbiatti AL, Succi M, Ruiz MT, Raposo LS, Maniglia JV, Pavarino-Bertelli EC, Goloni-Bertollo EM.

Rev Assoc Med Bras (1992). 2011 Mar-Apr;57(2):194-9. English, Portuguese.

16.

A neonate with antiphospholipid syndrome and inherited thrombophilia.

Canpolat FE, Cekmez F.

Pediatr Hematol Oncol. 2011 Apr;28(3):251-2. doi: 10.3109/08880018.2010.536300. Epub 2011 Jan 27. No abstract available.

PMID:
21271780
17.

Methylenetetrahydrofolate dehydrogenase (MTHFD) enzyme polymorphism as a maternal risk factor for trisomy 21: a clinical study.

Neagos D, Cretu R, Tutulan-Cunita A, Stoian V, Bohiltea LC.

J Med Life. 2010 Oct-Dec;3(4):454-7.

18.

The MTHFD1 c.1958 G>A polymorphism and recurrent spontaneous abortions.

Crişan TO, Trifa A, Farcaş M, Militaru M, Netea M, Pop I, Popp R.

J Matern Fetal Neonatal Med. 2011 Jan;24(1):189-92. doi: 10.3109/14767051003702794. Epub 2010 Mar 24.

PMID:
20334533
20.

Analysis of the MTHFD1 promoter and risk of neural tube defects.

Carroll N, Pangilinan F, Molloy AM, Troendle J, Mills JL, Kirke PN, Brody LC, Scott JM, Parle-McDermott A.

Hum Genet. 2009 Apr;125(3):247-56. doi: 10.1007/s00439-008-0616-3. Epub 2009 Jan 8.

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