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

Biology of inherited coagulopathies: factor IX.

Hematology/oncology clinics of North America - 1 Oct 1992

Larson P J, High K A

Abstract excerpt

Characterization of the functional domains of FIX and related vitamin K-dependent proteins has been enhanced by the isolation and characterization of the genes encoding these proteins. A better understanding of the interactions between FIX's activators, cofactors, and substrate, FX, has been gained through the study of naturally occurring variants isolated from patients with hemophilia B and genetically...

Read the complete abstract on PubMed

Topics

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

Share to Amino Acid Sequence
Share to Fetal Diseases
Share to Genes

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Genetic Carrier Screening

Share to Molecular Sequence Data

Share to Mutation

Share to Polymorphism, Restriction Fragment Length

Share to Prenatal Diagnosis

Source

Identifiers

PMID: 1356960

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Biology of inherited coagulopathies: factor IX.PMID 1356960Read ↗

Progress in the molecular biology of inherited bleeding disordersSemantic proximity Read ↗

The Clinical Genetics of Hemophilia B (Factor IX Deficiency)Semantic proximity Read ↗

Inherited factor VII deficiency: molecular genetics and pathophysiology.Semantic proximity Read ↗

Molecular basis of inherited factor XIII deficiency: identification of multiple mutations provides insights into protein function.Semantic proximity Read ↗

Biology of inherited coagulopathies: von Willebrand factor.Semantic proximity Read ↗

Deficiencies in factors IX and VIII: what is now known.Semantic proximity Read ↗

Factor XI deficiency--from molecular genetics to clinical management.Semantic proximity Read ↗

Inherited factor X deficiency: molecular genetics and pathophysiology.Semantic proximity Read ↗

Molecular and functional basis of hereditary factor IX defects.Semantic proximity Read ↗

The Molecular Basis of FIX Deficiency in Hemophilia B.Semantic proximity Read ↗

Why factor XI deficiency is a clinical concern.Semantic proximity Read ↗

Phenotypic characterization of haemophilia B – Understanding the underlying biology of coagulation factor IXSemantic proximity Read ↗

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