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

Physiopathology and regulation of factor XIII.

Thrombosis and haemostasis - 1 Jul 2001

Ichinose A

Abstract excerpt

Factor XIII is a plasma transglutaminase. Transglutaminases are at least 8 enzymes which cross-link a number of proteins. This type of reaction not only enhances the original functions of substrate proteins, but also adds new functions to them. Factor XIII in plasma is a tetramer (A2B2), and the A subunit contains the active site. Although transglutaminases are homologous, the nucleotide sequences in their...

Read the complete abstract on PubMed

Topics

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

Share to Factor XIII
Share to Factor XIII Deficiency
Share to Gene Expression Regulation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Protein Structure, Tertiary

Share to Transglutaminases

Source

Identifiers

PMID: 11487042

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

Physiopathology and regulation of factor XIII.PMID 11487042Read ↗

Blood coagulation factor XIII and factor XIII deficiency.Semantic proximity Read ↗

Coagulation factor XIII deficiency. Diagnosis, prevalence and management of inherited and acquired forms.Semantic proximity Read ↗

Factor XIII deficiency.Semantic proximity Read ↗

Factor XIII Deficiency.Semantic proximity Read ↗

Factor XIII Deficiency: Laboratory, Molecular, and Clinical AspectsSemantic proximity Read ↗

Phenotypic and genetic analyses of four cases of coagulation factor XII deficiency.Semantic proximity Read ↗

Impaired protein folding, dimer formation, and heterotetramer assembly cause intra- and extracellular instability of a Y283C mutant of the A subunit for coagulation factor XIII.Semantic proximity Read ↗

Factor XIII deficiency.Semantic proximity Read ↗

Factor XIII-A is involved in the regulation of gene expression in alternatively activated human macrophagesSemantic proximity Read ↗

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

Factor XIII-A in Diseases: Role Beyond Blood Coagulation.Semantic proximity Read ↗

Novel Insights into Heterozygous Factor XIII Deficiency.Semantic proximity Read ↗

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