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

T280M and V249I polymorphisms of fractalkine receptor CX3CR1 and ischemic cerebrovascular disease.

Neuroscience letters - 10 Feb 2005

Hattori Hidenori, Ito Daisuke, Tanahashi Norio, Murata Mitsuru, Saito Ikuo, Watanabe Kiyoaki, Suzuki Norihiro

Abstract excerpt

The contribution to atherosclerosis of two CX3CR1 single nucleotide polymorphisms, V249I and T280M has been recently reported. The atherosclerosis of intracranial vessels is thought to be the major pathological mechanism of ischemic stroke. In this study, we investigated the risk of ischemic stroke associated with fractalkine receptor CX3CR1 polymorphisms. We investigated the T280M and V249I mutations in the...

Read the complete abstract on PubMed

Topics

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

Share to Cerebrovascular Disorders
Share to Confidence Intervals

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to CX3C Chemokine Receptor 1

Share to Isoleucine

Share to Methionine

Share to Receptors, Chemokine

Share to Threonine

Share to Valine

Source

Identifiers

PMID: 15644279
DOI: 10.1016/j.neulet.2004.10.042

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

T280M and V249I polymorphisms of fractalkine receptor CX3CR1 and ischemic cerebrovascular disease.PMID 15644279Read ↗

Two polymorphisms in the Fractalkine receptor CX3CR1 gene influence the development of atherosclerosis: a meta-analysis.Semantic proximity Read ↗

Polymorphisms of fractalkine receptor CX3CR1 gene in patients with symptomatic and asymptomatic carotid artery stenosis.Semantic proximity Read ↗

Internal carotid artery occlusive disease and polymorphisms of fractalkine receptor CX3CR1: a genetic risk factor.Semantic proximity Read ↗

Effects of fractalkine receptor variants on common carotid artery intima-media thickness.Semantic proximity Read ↗

Role of the fractalkine receptor CX3CR1 polymorphisms V249I and T280M as risk factors for early-onset coronary artery disease in patients with no classic risk factors.Semantic proximity Read ↗

Relationship between CX3CR1 genetic polymorphism and carotid atherosclerosis.Semantic proximity Read ↗

Polymorphism in the fractalkine receptor CX3CR1 as a genetic risk factor for coronary artery disease.Semantic proximity Read ↗

Opposite effects of CX3CR1 receptor polymorphisms V249I and T280M on the development of acute coronary syndrome. A possible implication of fractalkine in inflammatory activation.Semantic proximity Read ↗

An association study between polymorphisms of the fractalkine receptor gene, CX3CR1, and cerebral infarction in the Han Chinese population.Semantic proximity Read ↗

Association of V249I and T280M variants of fractalkine receptor CX3CR1 with carotid intima-media thickness in a mexican population with type 2 diabetes.Semantic proximity Read ↗

Association of polymorphisms in the chemokine receptor CX3CR1 gene with coronary artery disease.Semantic proximity Read ↗

CX3CR1 receptor polymorphisms, Th1 cell recruitment, and acute myocardial infarction outcome: looking for a link.Semantic proximity Read ↗

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