276 related articles for article (PubMed ID: 22918506)
1. Polymorphisms in antithrombin and in tissue factor pathway inhibitor genes are associated with recurrent pregnancy loss.
Guerra-Shinohara EM; Bertinato JF; Tosin Bueno C; Cordeiro da Silva K; Burlacchini de Carvalho MH; Pulcineli Vieira Francisco R; Zugaib M; Cerda A; Morelli VM
Thromb Haemost; 2012 Oct; 108(4):693-700. PubMed ID: 22918506
[TBL] [Abstract][Full Text] [Related]
2. The association of idiopathic recurrent pregnancy loss with polymorphisms in hemostasis-related genes.
Cao Y; Zhang Z; Xu J; Yuan W; Wang J; Huang X; Shen Y; Du J
Gene; 2013 Nov; 530(2):248-52. PubMed ID: 23954867
[TBL] [Abstract][Full Text] [Related]
3. Tissue factor pathway inhibitor polymorphisms in women with and without a history of venous thrombosis and the effects of postmenopausal hormone therapy.
Opstad TB; Eilertsen AL; Høibraaten E; Skretting G; Sandset PM
Blood Coagul Fibrinolysis; 2010 Sep; 21(6):516-21. PubMed ID: 20453636
[TBL] [Abstract][Full Text] [Related]
4. Pregnancy-associated plasma protein-A polymorphism and the risk of recurrent pregnancy loss.
Suzuki K; Sata F; Yamada H; Saijo Y; Tsuruga N; Minakami H; Kishi R
J Reprod Immunol; 2006 Jun; 70(1-2):99-108. PubMed ID: 16540175
[TBL] [Abstract][Full Text] [Related]
5. IL-10 gene promoter and intron polymorphisms and changes in IL-10 secretion in women with idiopathic recurrent miscarriage.
Qaddourah RH; Magdoud K; Saldanha FL; Mahmood N; Mustafa FE; Mahjoub T; Almawi WY
Hum Reprod; 2014 May; 29(5):1025-34. PubMed ID: 24626804
[TBL] [Abstract][Full Text] [Related]
6. Vascular endothelial growth factor-A gene polymorphisms in women with recurrent pregnancy loss.
Eller AG; Branch DW; Nelson L; Porter TF; Silver RM
J Reprod Immunol; 2011 Jan; 88(1):48-52. PubMed ID: 20977975
[TBL] [Abstract][Full Text] [Related]
7. Polymorphisms of the tissue factor pathway inhibitor gene are associated with venous thromboembolism in the antiphospholipid syndrome and carriers of factor V Leiden.
Lincz LF; Adams MJ; Scorgie FE; Thom J; Baker RI; Seldon M
Blood Coagul Fibrinolysis; 2007 Sep; 18(6):559-64. PubMed ID: 17762532
[TBL] [Abstract][Full Text] [Related]
8. C-reactive protein gene variants associated with recurrent pregnancy loss independent of CRP serum levels: a case-control study.
Ahmed SK; Mahmood N; Malalla ZH; Alsobyani FM; Al-Kiyumi IS; Almawi WY
Gene; 2015 Sep; 569(1):136-40. PubMed ID: 26013044
[TBL] [Abstract][Full Text] [Related]
9. Thrombin-activatable fibrinolysis inhibitor polymorphisms and recurrent pregnancy loss.
Masini S; Ticconi C; Gravina P; Tomassini M; Pietropolli A; Forte V; Federici G; Piccione E; Bernardini S
Fertil Steril; 2009 Aug; 92(2):694-702. PubMed ID: 18774564
[TBL] [Abstract][Full Text] [Related]
10. Association of endothelial nitric oxide synthase gene variants (-786 T>C, intron 4 b/a VNTR and 894 G>T) with idiopathic recurrent pregnancy loss: A case-control study with haplotype and in silico analysis.
Azani A; Hosseinzadeh A; Azadkhah R; Zonouzi AAP; Zonouzi AP; Aftabi Y; Khani H; Heidary L; Danaii S; Bargahi N; Pouladi N; Hosseini SM
Eur J Obstet Gynecol Reprod Biol; 2017 Aug; 215():93-100. PubMed ID: 28605668
[TBL] [Abstract][Full Text] [Related]
11. Functional characterization of polymorphisms in the human TFPI gene.
Skretting G; Stavik B; Landvik NE; Myklebust CF; Iversen N; Zienolddiny S; Sandset PM
Biochem Biophys Res Commun; 2010 Jun; 397(1):106-11. PubMed ID: 20519147
[TBL] [Abstract][Full Text] [Related]
12. Association of polymorphisms/haplotypes of the genes encoding vascular endothelial growth factor and its KDR receptor with recurrent pregnancy loss.
Su MT; Lin SH; Lee IW; Chen YC; Kuo PL
Hum Reprod; 2011 Apr; 26(4):758-64. PubMed ID: 21257617
[TBL] [Abstract][Full Text] [Related]
13. Interleukin-18 promoter polymorphisms and risk of idiopathic recurrent pregnancy loss in a Tunisian population.
Messaoudi S; Dandana M; Magdoud K; Meddeb S; Ben Slama N; Hizem S; Mahjoub T
J Reprod Immunol; 2012 Mar; 93(2):109-13. PubMed ID: 22386125
[TBL] [Abstract][Full Text] [Related]
14. Matrix metalloproteinases 1, 2, 3 and 9 functional single-nucleotide polymorphisms in idiopathic recurrent spontaneous abortion.
Pereza N; Ostojić S; Volk M; Kapović M; Peterlin B
Reprod Biomed Online; 2012 May; 24(5):567-75. PubMed ID: 22406112
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Association study of vascular endothelial growth factor polymorphisms with the risk of recurrent spontaneous abortion.
Lee HH; Hong SH; Shin SJ; Ko JJ; Oh D; Kim NK
Fertil Steril; 2010 Mar; 93(4):1244-7. PubMed ID: 19131057
[TBL] [Abstract][Full Text] [Related]
17. Association of TFPI polymorphisms rs8176592, rs10931292, and rs10153820 with venous thrombosis: A meta-analysis.
Zhang Y; Pang A; Zhao L; Guo Q; Zhang Z; Zhu X; Wei R; Yin X; Wang B; Li X
Medicine (Baltimore); 2019 Mar; 98(12):e14978. PubMed ID: 30896671
[TBL] [Abstract][Full Text] [Related]
18. Analysis of a T-287C polymorphism in the tissue factor pathway inhibitor gene and identification of a repressor element in the promoter.
Amini Nekoo A; Iles D
Thromb Res; 2008; 121(6):813-9. PubMed ID: 17931693
[TBL] [Abstract][Full Text] [Related]
19. Polymorphisms in factor V and antithrombin III gene in recurrent pregnancy loss: a case-control study in Indian population.
Sharma A; Bhakuni T; Ranjan R; Kumar R; Kishor K; Kamal VK; Mahapatra M; Jairajpuri MA; Saxena R
J Thromb Thrombolysis; 2015 May; 39(4):481-8. PubMed ID: 25771983
[TBL] [Abstract][Full Text] [Related]
20. +1040 C/T polymorphism in coding region of thrombin-activatable fibrinolysis inhibitor gene and the risk of idiopathic recurrent fetal loss.
Pruner I; Djordjevic V; Miljic P; Kovac M; Antonijevic N; Rakicevic L; Radojkovic D
Blood Coagul Fibrinolysis; 2010 Oct; 21(7):679-82. PubMed ID: 20729722
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
