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

The BC genotype of the VNTR polymorphism of platelet glycoprotein Ibalpha is overrepresented in patients with recurrent stroke regardless of aspirin therapy.

Cerebrovascular diseases (Basel, Switzerland) - 1 Jan 2007

Cervera A, Tàssies D, Obach V, Amaro S, Reverter J C, Chamorro A

Abstract excerpt

BACKGROUND: The contribution of genetic factors to aspirin treatment failure (ATF) for secondary prevention is not settled in patients with ischemic stroke. METHODS: We assessed the polymorphisms VNTR (A, B, C, D) of glycoprotein (GP) Ibalpha, 807C/T of GP Ia/IIa, and Pl(A1/A2) of GP IIb/IIIa, an...

Read the complete abstract on PubMed

Topics

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

Share to Aspirin
Share to Patient Compliance
Share to Platelet Aggregation Inhibitors

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Platelet Glycoprotein GPIb-IX Complex

Share to Platelet Glycoprotein GPIIb-IIIa Complex

Share to Secondary Prevention

Share to Stroke

Share to Treatment Failure

Source

Identifiers

PMID: 17630485
DOI: 10.1159/000104485

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17630485-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The BC genotype of the VNTR polymorphism of platelet glycoprotein Ibalpha is overrepresented in patients with recurrent stroke regardless of aspirin therapy.PMID 17630485Read ↗

Variable number of tandem repeats polymorphism of platelet glycoprotein Ib alpha in Chinese people and CC genotype with aspirin sensitivity in patients with cerebral infarction.Semantic proximity Read ↗

Association between platelet glycoprotein Ibalpha genotype and ischemic cerebrovascular disease.Semantic proximity Read ↗

Suboptimal response to clopidogrel: a genetic risk factor for recurrent ischaemic stroke.Semantic proximity Read ↗

Genetic variants of platelet glycoprotein receptors and risk of stroke in young women.Semantic proximity Read ↗

Platelet glycoprotein Ib alpha receptor polymorphisms and recurrent ischaemic events in acute coronary syndrome patients.Semantic proximity Read ↗

Role of platelet glycoprotein polymorphisms in cardiovascular diseases.Semantic proximity Read ↗

Platelet glycoprotein gene Ia C807T, HPA-3, and Ibα VNTR polymorphisms are associated with increased ischemic stroke risk: Evidence from a comprehensive meta-analysis.Semantic proximity Read ↗

Platelet GP IIIa PlA and GP Ib variable number tandem repeat polymorphisms and markers of platelet activation in acute stroke.Semantic proximity Read ↗

Platelet glycoprotein Ibalpha Kozak polymorphism is associated with an increased risk of ischemic stroke.Semantic proximity Read ↗

The GNB3 C825T Polymorphism Is Associated With Decreased Risk of Recurrence of Large-Artery Atherosclerotic Acute Ischemic Stroke.Semantic proximity Read ↗

The contribution of genetic factors to thrombotic and bleeding outcomes in coronary patients randomised to IIb/IIIa antagonists.Semantic proximity Read ↗

Platelet glycoprotein IIb/IIIa polymorphism HPA-3 b/b is associated with increased risk of ischemic stroke in patients under 60 years of age.Semantic proximity Read ↗

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