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Items: 1 to 20 of 145

1.

Methionine synthase A2756G and methylenetetrahydrofolate reductase A1298C polymorphisms are not risk factors for idiopathic venous thromboembolism.

Salomon O, Rosenberg N, Zivelin A, Steinberg DM, Kornbrot N, Dardik R, Inbal A, Seligsohn U.

Hematol J. 2001;2(1):38-41.

PMID:
11920232
3.
6.

Methylenetetrahydrofolate reductase C677T genotype and venous thromboembolic disease.

Couturaud F, Oger E, Abalain JH, Chenu E, Guias B, Floch HH, Mercier B, Mottier D, Leroyer C.

Respiration. 2000;67(6):657-61.

PMID:
11124649
7.

Polymorphisms in MTHFR, MS and CBS genes and homocysteine levels in a Pakistani population.

Yakub M, Moti N, Parveen S, Chaudhry B, Azam I, Iqbal MP.

PLoS One. 2012;7(3):e33222. doi: 10.1371/journal.pone.0033222. Epub 2012 Mar 21.

8.

Genetic polymorphisms associated with acute pulmonary embolism and deep venous thrombosis.

Nizankowska-Mogilnicka E, Adamek L, Grzanka P, Domagala TB, Sanak M, Krzanowski M, Szczeklik A.

Eur Respir J. 2003 Jan;21(1):25-30.

9.

Single and combined prothrombotic factors in patients with idiopathic venous thromboembolism: prevalence and risk assessment.

Salomon O, Steinberg DM, Zivelin A, Gitel S, Dardik R, Rosenberg N, Berliner S, Inbal A, Many A, Lubetsky A, Varon D, Martinowitz U, Seligsohn U.

Arterioscler Thromb Vasc Biol. 1999 Mar;19(3):511-8.

10.
11.
12.

Interaction of MTHFR C677T and A1298C, and MTR A2756G gene polymorphisms in breast cancer risk in a population in Northeast Brazil.

de Cássia Carvalho Barbosa R, da Costa DM, Cordeiro DE, Vieira AP, Rabenhorst SH.

Anticancer Res. 2012 Nov;32(11):4805-11.

PMID:
23155246
14.

No evidence for an increased risk of venous thrombosis in patients with factor V Leiden by the homozygous 677 C to T mutation in the methylenetetrahydrofolate-reductase gene.

Rintelen C, Mannhalter C, Lechner K, Eichinger S, Kyrle PA, Papagiannopoulos M, Schneider B, Pabinger I.

Blood Coagul Fibrinolysis. 1999 Mar;10(2):101-5.

PMID:
10192659
15.

Lack of association between the C677T mutation in the 5,10-methylenetetrahydrofolate reductase gene and venous thromboembolism in Northwestern Greece.

Zalavras ChG, Giotopoulou S, Dokou E, Mitsis M, Ioannou HV, Tzolou A, Kolaitis N, Vartholomatos G.

Int Angiol. 2002 Sep;21(3):268-71.

PMID:
12384649
16.

Association between MTHFR C677T, MTHFR A1298C and MS A2756G polymorphisms and risk of cervical intraepithelial neoplasia II/III and cervical cancer: a meta-analysis.

Zhu J, Wu L, Kohlmeier M, Ye F, Cai W.

Mol Med Rep. 2013 Sep;8(3):919-27. doi: 10.3892/mmr.2013.1589. Epub 2013 Jul 16.

PMID:
23864153
17.

Interaction between hyperhomocysteinemia, mutated methylenetetrahydrofolatereductase (MTHFR) and inherited thrombophilic factors in recurrent venous thrombosis.

Keijzer MB, den Heijer M, Blom HJ, Bos GM, Willems HP, Gerrits WB, Rosendaal FR.

Thromb Haemost. 2002 Nov;88(5):723-8.

PMID:
12428084
18.

Genetic variations observed in arterial and venous thromboembolism--relevance for therapy, risk prevention and prognosis.

Harrington DJ, Malefora A, Schmeleva V, Kapustin S, Papayan L, Blinov M, Harrington P, Mitchell M, Savidge GF.

Clin Chem Lab Med. 2003 Apr;41(4):496-500.

PMID:
12747593
19.

Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations.

Grandone E, Margaglione M, Colaizzo D, D'Andrea G, Cappucci G, Brancaccio V, Di Minno G.

Am J Obstet Gynecol. 1998 Nov;179(5):1324-8.

PMID:
9822524
20.

Serum homocysteine, thermolabile variant of methylene tetrahydrofolate reductase (MTHFR), and venous thromboembolism: Longitudinal Investigation of Thromboembolism Etiology (LITE).

Tsai AW, Cushman M, Tsai MY, Heckbert SR, Rosamond WD, Aleksic N, Yanez ND, Psaty BM, Folsom AR.

Am J Hematol. 2003 Mar;72(3):192-200. Erratum in: Am J Hematol. 2007 Nov;82(11):1031-2.

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