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

The Val34Leu genetic variation in the A subunit of coagulation factor XIII in recurrent spontaneous abortion.

Systems biology in reproductive medicine - 1 Oct 2011

Bagheri Morteza, Rad Isa Abdi, Omrani Mir Davood, Nanbaksh Fariba

Abstract excerpt

The present study was carried out to assess the frequencies of factor XIII (FXIII) Val34Leu genetic variation in the patients with recurrent spontaneous abortion and healthy fertile women of Azeri Turkish origin. A total of 54 patients with recurrent spontaneous abortion and 46 healthy fertile women as controls were studied for the FXIII Val34Leu genetic variation by a RFLP-PCR method. Statistical analysis showed...

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 Factor XIII

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Leucine

Share to Point Mutation

Share to Polymerase Chain Reaction

Share to Polymorphism, Restriction Fragment Length

Share to Pregnancy

Share to Valine

Source

Identifiers

PMID: 21548851
DOI: 10.3109/19396368.2011.576308

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

The Val34Leu genetic variation in the A subunit of coagulation factor XIII in recurrent spontaneous abortion.PMID 21548851Read ↗

Polymorphisms of plasminogen activator inhibitor-1, angiotensin converting enzyme and coagulation factor XIII genes in patients with recurrent spontaneous abortion.Semantic proximity Read ↗

Prevalence of coagulation factor XIII and plasminogen activator inhibitor-1 gene polymorphisms among Egyptian women suffering from unexplained primary recurrent miscarriage.Semantic proximity Read ↗

Association of the F13A1 Val34Leu polymorphism and recurrent pregnancy loss: A meta-analysis.Semantic proximity Read ↗

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

Polymorphisms of the angiotensin converting enzyme gene in Iranian Azeri Turkish women with unexplained recurrent pregnancy loss.Semantic proximity Read ↗

The association between thrombophilic gene mutations and recurrent pregnancy loss.Semantic proximity Read ↗

Investigating Association of Three Polymorphisms of Coagulation Factor XIII and Recurrent Pregnancy Loss.Semantic proximity Read ↗

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

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

Detection of human platelets antigen polymorphism (HPA-1 and HPA-3) and human factor XIII mutation in Sudanese women with recurrent pregnancy loss.Semantic proximity Read ↗

Role of the HLA-G regulatory region polymorphisms in idiopathic recurrent spontaneous abortions (RSA).Semantic proximity Read ↗

Thrombophilic mutations and polymorphisms, alone or in combination, and recurrent spontaneous abortion.Semantic proximity Read ↗

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