Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

+1040 C/T polymorphism in coding region of thrombin-activatable fibrinolysis inhibitor gene and the risk of idiopathic recurrent fetal loss.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Oct 2010

Pruner Iva, Djordjevic Valentina, Miljic Predrag, Kovac Mirjana, Antonijevic Nebojsa, Rakicevic Ljiljana, Radojkovic Dragica

Abstract excerpt

Recurrent fetal loss (RFL) is common health problem affecting up to 5% of women of reproductive age. It has been shown that plasma thrombin-activatable fibrinolysis inhibitor (TAFI) concentrations increase during pregnancy and return to baseline levels soon after delivery. The +1040C/T single nucleotide polymorphism in coding region of TAFI gene is associated with TAFI blood levels. The aim of our study was to...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Abortion, Habitual
Share to Carboxypeptidase B2

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Case-Control Studies

Share to Genetic Association Studies

Share to Open Reading Frames

Share to Pregnancy

Share to Young Adult

Source

Identifiers

PMID: 20729722
DOI: 10.1097/MBC.0b013e32833e426d

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

+1040 C/T polymorphism in coding region of thrombin-activatable fibrinolysis inhibitor gene and the risk of idiopathic recurrent fetal loss.PMID 20729722Read ↗

Thrombin-activatable fibrinolysis inhibitor polymorphisms and recurrent pregnancy loss.Semantic proximity Read ↗

Thrombin-Activatable Fibrinolysis Inhibitor Gene Polymorphism (TAFI1040C/T) in Women With Recurrent Spontaneous Abortion.Semantic proximity Read ↗

Association between thrombophilia gene polymorphisms and recurrent pregnancy loss risk in the Iranian populationSemantic proximity Read ↗

Thrombophilia and Recurrent Pregnancy Loss: The Enigma Continues.Semantic proximity Read ↗

Polymorphisms in antithrombin and in tissue factor pathway inhibitor genes are associated with recurrent pregnancy loss.Semantic proximity Read ↗

The association of idiopathic recurrent pregnancy loss with polymorphisms in hemostasis-related genes.Semantic proximity Read ↗

Thrombophilic gene polymorphisms and recurrent pregnancy loss: a systematic review and meta-analysis.Semantic proximity Read ↗

[Patients with inherited trombophilia and recurrent pregnancy loss: incidence].Semantic proximity Read ↗

Etiology of hypercoagulable state in women with recurrent fetal loss without other causes of miscarriage from Southern Italy: new clinical target for antithrombotic therapySemantic proximity Read ↗

Genetic regulation of recurrent spontaneous abortion in humansSemantic proximity Read ↗

Inherited thrombophilia and recurrent pregnancy loss: a single-center case-control study in North-Western AlgeriaSemantic proximity Read ↗

Genetic association of five plasminogen activator inhibitor-1 (PAI-1) polymorphisms and idiopathic recurrent pregnancy loss in Korean women.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.