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

Association of Thrombomodulin Gene C1418T Polymorphism with Susceptibility to Kawasaki Disease in Chinese Children.

Disease markers - 1 Jan 2018

Lu Yapeng, Liu Rui, Zha Luting, Yuan Shan, Tian Lang, Chen Jia, Huang Lihua, Yang Zuocheng

Abstract excerpt

Kawasaki disease (KD) is an acute systemic vasculitis that predominantly affects children and can result in coronary artery lesions (CALs). Thrombomodulin (TM) is a critical cofactor in the protein C anticoagulant system. The TM C1418T (rs1042579) polymorphism is associated with a high risk of cardiac-cerebral vascular diseases. But the association of the TM C1418T polymorphism with susceptibility to KD, CAL...

Read the complete abstract on PubMed

Topics

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

Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Child, Preschool

Share to Mucocutaneous Lymph Node Syndrome

Share to Organic Chemicals

Share to Polymorphism, Single Nucleotide

Share to Thrombomodulin

Source

Open in PubMed Open full text

Identifiers

PMID: 30008974
DOI: 10.1155/2018/1064380
PMCID: PMC6020540

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association of Thrombomodulin Gene C1418T Polymorphism with Susceptibility to Kawasaki Disease in Chinese Children.PMID 30008974Read ↗

Association of SNP (rs1042579) in thrombomodulin gene and plasma thrombomodulin level in North Indian children with Kawasaki disease.Semantic proximity Read ↗

Update of genetic susceptibility in patients with Kawasaki diseaseSemantic proximity Read ↗

Association study of polymorphism in Thrombomodulin gene [rs1042579] with cardiovascular disease.Semantic proximity Read ↗

Promoter polymorphism (rs3755724, -55C/T) of tissue inhibitor of metalloproteinase 4 (TIMP4) as a risk factor for Kawasaki disease with coronary artery lesions in a Korean population.Semantic proximity Read ↗

The IL-1B Gene Polymorphisms rs16944 and rs1143627 Contribute to an Increased Risk of Coronary Artery Lesions in Southern Chinese Children with Kawasaki DiseaseSemantic proximity Read ↗

ITPKC polymorphism (rs7251246 T > C), coronary artery aneurysms, and thrombosis in patients with Kawasaki disease in a Southern Han Chinese population.Semantic proximity Read ↗

[Research advances in genetic polymorphisms in Kawasaki disease].Semantic proximity Read ↗

Validation of genome-wide associated variants for Kawasaki disease in a Taiwanese case-control sample.Semantic proximity Read ↗

Single-nucleotide polymorphism rs7251246 in ITPKC is associated with susceptibility and coronary artery lesions in Kawasaki disease.Semantic proximity Read ↗

ITPKC single nucleotide polymorphism associated with the Kawasaki disease in a Taiwanese population.Semantic proximity Read ↗

The Roles of Genetic Factors in Kawasaki Disease: A Systematic Review and Meta-analysis of Genetic Association Studies.Semantic proximity Read ↗

TARC/CCL17 gene polymorphisms and expression associated with susceptibility and coronary artery aneurysm formation in Kawasaki disease.Semantic proximity Read ↗

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