162 related articles for article (PubMed ID: 27110516)
1. Methylenetetrahydrofolate Reductase C677T and A1298C Polymorphisms in Male Partners of Recurrent Miscarriage Couples.
Tara SS; Ghaemimanesh F; Zarei S; Reihani-Sabet F; Pahlevanzadeh Z; Modarresi MH; Jeddi-Tehrani M
J Reprod Infertil; 2015; 16(4):193-8. PubMed ID: 27110516
[TBL] [Abstract][Full Text] [Related]
2. Methylenetetrahydrofolate reductase C677T and A1298C polymorphism and changes in homocysteine concentrations in women with idiopathic recurrent pregnancy losses.
Mtiraoui N; Zammiti W; Ghazouani L; Braham NJ; Saidi S; Finan RR; Almawi WY; Mahjoub T
Reproduction; 2006 Feb; 131(2):395-401. PubMed ID: 16452733
[TBL] [Abstract][Full Text] [Related]
3. Evidence of Paternal N5, N10 - Methylenetetrahydrofolate Reductase (MTHFR) C677T Gene Polymorphism in Couples with Recurrent Spontaneous Abortions (RSAs) in Kolar District- A South West of India.
Vanilla S; Dayanand CD; Kotur PF; Kutty MA; Vegi PK
J Clin Diagn Res; 2015 Feb; 9(2):BC15-8. PubMed ID: 25859445
[TBL] [Abstract][Full Text] [Related]
4. Methylenetetrahydrofolate Reductase C677T and A1298C Polymorphism in Iranian Women With Idiopathic Recurrent Pregnancy Losses.
Yousefian E; Kardi MT; Allahveisi A
Iran Red Crescent Med J; 2014 Jul; 16(7):e16763. PubMed ID: 25237572
[TBL] [Abstract][Full Text] [Related]
5. The importance of homozygous polymorphisms of methylenetetrahydrofolate reductase gene in romanian patients with idiopathic venous thromboembolism.
Hotoleanu C; Trifa A; Popp R; Fodor D
Balkan Med J; 2013 Jun; 30(2):197-203. PubMed ID: 25207100
[TBL] [Abstract][Full Text] [Related]
6. Association between maternal, fetal and paternal MTHFR gene C677T and A1298C polymorphisms and risk of recurrent pregnancy loss: a comprehensive evaluation.
Yang Y; Luo Y; Yuan J; Tang Y; Xiong L; Xu M; Rao X; Liu H
Arch Gynecol Obstet; 2016 Jun; 293(6):1197-211. PubMed ID: 26530235
[TBL] [Abstract][Full Text] [Related]
7. Interactions between genetic variants involved in the folate metabolic pathway and serum lipid, homocysteine levels on the risk of recurrent spontaneous abortion.
Lin Z; Li Q; Sun Y; Huang J; Wang W; Fu J; Xu J; Zeng D
Lipids Health Dis; 2019 Jun; 18(1):143. PubMed ID: 31200713
[TBL] [Abstract][Full Text] [Related]
8. The early-onset preeclampsia is associated with MTHFR and FVL polymorphisms.
Salimi S; Saravani M; Yaghmaei M; Fazlali Z; Mokhtari M; Naghavi A; Farajian-Mashhadi F
Arch Gynecol Obstet; 2015 Jun; 291(6):1303-12. PubMed ID: 25480409
[TBL] [Abstract][Full Text] [Related]
9. Association of Methylenetetrahydrofolate Reductase C677T and A1298C Gene Polymorphisms With Recurrent Pregnancy Loss in Syrian Women.
Al-Achkar W; Wafa A; Ammar S; Moassass F; Jarjour RA
Reprod Sci; 2017 Sep; 24(9):1275-1279. PubMed ID: 28814189
[TBL] [Abstract][Full Text] [Related]
10. Association of inherited thrombophilia mutations and their combinations among palestinian women with unexplained recurrent miscarriage.
Najjar AA; Hassouna I; Srour MA; Ibrahim HM; Assi RY; Abd El Latif HM
Thromb J; 2024 Feb; 22(1):20. PubMed ID: 38351006
[TBL] [Abstract][Full Text] [Related]
11. The Impact of Methylenetetrahydrofolate Reductase (MTHFR) Sperm Methylation and Variants on Semen Parameters and the Chance of Recurrent Pregnancy Loss in the Couple.
Poorang S; Abdollahi S; Anvar Z; Tabei SMB; Jahromi BN; Moein-Vaziri N; Gharesi-Fard B; Banaei M; Dastgheib SA
Clin Lab; 2018 Jul; 64(7):1121-1128. PubMed ID: 30146842
[TBL] [Abstract][Full Text] [Related]
12. [Polymorphism of methylenetetrahydrofolate reductase and sensitivity of stomach cancer to fluoropyrimidine-based chemotherapy].
Gao CM; Lu JW; Toshiro T; Wu JZ; Cao HX; Chen HQ; Feng JF; Kazuo T
Zhonghua Liu Xing Bing Xue Za Zhi; 2004 Dec; 25(12):1054-8. PubMed ID: 15769364
[TBL] [Abstract][Full Text] [Related]
13. Methylenetetrahydrofolate Reductase gene polymorphism in children with allergic rhinitis.
Dogru M; Aydin H; Aktas A; Cırık AA
Allergol Immunopathol (Madr); 2015; 43(6):579-83. PubMed ID: 25796308
[TBL] [Abstract][Full Text] [Related]
14. Plasminogen activator inhibitor-1, factor V, factor II and methylenetetrahydrofolate reductase polymorphisms in women with recurrent miscarriage.
Pietropolli A; Giuliani E; Bruno V; Patrizi L; Piccione E; Ticconi C
J Obstet Gynaecol; 2014 Apr; 34(3):229-34. PubMed ID: 24484533
[TBL] [Abstract][Full Text] [Related]
15. [Case-control study on the association between four single nucleotide polymorphisms in folate metabolism way and the risk of congenital heart disease].
Duan S; Li G; Qiu F; Zhao L; Zhao M; Wang L; Feng Z; Ma X
Wei Sheng Yan Jiu; 2018 Jul; 47(4):536-542. PubMed ID: 30081977
[TBL] [Abstract][Full Text] [Related]
16. Methylenetetrahydrofolate reductase gene polymorphisms in Egyptian Turner Syndrome patients.
Ismail MF; Zarouk WA; Ruby MO; Mahmoud WM; Gad RS
Acta Biochim Pol; 2015; 62(3):529-32. PubMed ID: 26217949
[TBL] [Abstract][Full Text] [Related]
17. Genetic polymorphisms of methylenetetrahydrofolate reductase and susceptibility to colorectal cancer.
Cao HX; Gao CM; Takezaki T; Wu JZ; Ding JH; Liu YT; Li SP; Su P; Cao J; Hamajima N; Tajima K
Asian Pac J Cancer Prev; 2008; 9(2):203-8. PubMed ID: 18712959
[TBL] [Abstract][Full Text] [Related]
18. Methylenetetrahydrofolate reductase gene polymorphisms: association with risk for pediatric acute lymphoblastic leukemia in north Indians.
Sood S; Das R; Trehan A; Ahluwalia J; Sachdeva MU; Varma N; Bansal D; Marwaha RK
Leuk Lymphoma; 2010 May; 51(5):928-32. PubMed ID: 20367562
[TBL] [Abstract][Full Text] [Related]
19. Mutations C677T and A1298C of the 5,10-methylenetetrahydrofolate reductase gene and fasting plasma homocysteine levels are not associated with the increased risk of venous thromboembolic disease.
Domagala TB; Adamek L; Nizankowska E; Sanak M; Szczeklik A
Blood Coagul Fibrinolysis; 2002 Jul; 13(5):423-31. PubMed ID: 12138370
[TBL] [Abstract][Full Text] [Related]
20. Methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms in breast cancer: a Sardinian preliminary case-control study.
Castiglia P; Sanna V; Azara A; De Miglio MR; Murgia L; Pira G; Sanges F; Fancellu A; Carru C; Bisail M; Muroni MR
Int J Med Sci; 2019; 16(8):1089-1095. PubMed ID: 31523170
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
