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

Abnormal melt curve profile during prothrombin 20210G --> A analysis due to the 20209C --> T variant.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Oct 2006

Dunn S Terence, Allen Richard A, Bates Francesca, McNamara Victoria, Comp Philip

Abstract excerpt

The common factor II 20210G --> A mutation, located in the 3'-untranslated region, is an important risk factor for the development of thromboembolic disorders, especially in Caucasians. A number of methods are employed for clinical laboratory diagnosis of this mutation, some of which are capable of detecting adjacent 3'-end sequence variations. We present results from an African deep vein thrombosis patient...

Read the complete abstract on PubMed

Topics

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

Share to DNA Probes
Share to Nucleic Acid Denaturation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Nucleic Acid Hybridization

Share to Point Mutation

Share to Prothrombin

Share to Reverse Transcriptase Polymerase Chain Reaction

Share to Temperature

Share to Venous Thrombosis

Source

Identifiers

PMID: 16988559
DOI: 10.1097/01.mbc.0000245303.95138.01

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

Abnormal melt curve profile during prothrombin 20210G --> A analysis due to the 20209C --> T variant.PMID 16988559Read ↗

Detection of a novel point mutation of the prothrombin gene at position 20209.Semantic proximity Read ↗

The prothrombin nt20210 A allele as a risk factor for venous thromboembolism: detection of heterozygous and homozygous carriers by alternative methods.Semantic proximity Read ↗

Factor V Leiden and FII 20210 testing in thromboembolic disorders.Semantic proximity Read ↗

A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis.Semantic proximity Read ↗

The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis.Semantic proximity Read ↗

A Rare Prothrombin Gene Mutation C20209T in a South African Patient with Pulmonary Embolism in Pregnancy: a Case Study and Systematic Review.Semantic proximity Read ↗

Rapid multiplex analysis for the factor V Leiden and prothrombin G20210A mutations associated with hereditary thrombophilia.Semantic proximity Read ↗

The 20210 G → A mutation in the 3′‐untranslated region of the prothrombin gene and the risk for arterial thrombotic diseaseSemantic proximity Read ↗

The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease.Semantic proximity Read ↗

The prothrombin 20210 G to A variation and thrombosis.Semantic proximity Read ↗

Reliable genotyping of the G-20210-A mutation of coagulation factor II (prothrombin).Semantic proximity Read ↗

G20210A is a functional mutation in the prothrombin gene; effect on protein levels and 3'-end formation.Semantic proximity Read ↗

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