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

No association of the -105 promoter polymorphism of the selenoprotein S encoding gene SEPS1 with cerebrovascular disease.

European journal of neurology - 1 Oct 2007

Hyrenbach S, Pezzini A, del Zotto E, Giossi A, Lichy C, Kloss M, Werner I, Padovani A, Brandt T, Grond-Ginsbach C

Abstract excerpt

A common pro-inflammatory promoter variant of the selenoprotein S encoding gene (SEPS1) was studied in young stroke patients from Italy and Germany and in healthy control subjects. The -105A-allele was found in 56 of 205 (27.3%) patients with ischemic stroke IS because of a spontaneous cervical a...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Cerebrovascular Disorders
Share to CAD gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Membrane Proteins

Share to Polymorphism, Genetic

Share to Promoter Regions, Genetic

Share to Risk Factors

Share to Selenoproteins

Source

Identifiers

PMID: 17880573
DOI: 10.1111/j.1468-1331.2007.01898.x

Genes

CAD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17880573-2026-09-02.2. 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

No association of the -105 promoter polymorphism of the selenoprotein S encoding gene SEPS1 with cerebrovascular disease.PMID 17880573Read ↗

Association of selenoprotein S gene polymorphism with ischemic stroke in a Chinese case-control study.Semantic proximity Read ↗

Variation in the selenoprotein S gene locus is associated with coronary heart disease and ischemic stroke in two independent Finnish cohorts.Semantic proximity Read ↗

The I/D polymorphism of the ACE1 gene is not associated with ischaemic stroke in Spanish individuals.Semantic proximity Read ↗

The SEPS1 G-105A polymorphism is associated with risk of spontaneous preterm birth in a Chinese population.Semantic proximity Read ↗

Polymorphisms in the selenoprotein S gene: lack of association with autoimmune inflammatory diseases.Semantic proximity Read ↗

The ICAM-1 E469K gene polymorphism is a risk factor for spontaneous cervical artery dissection.Semantic proximity Read ↗

The combined effect of paraoxonase promoter and coding region polymorphisms on the risk of arterial ischemic stroke among young adults.Semantic proximity Read ↗

MTHFR C677T, FII G20210A, FV Leiden G1691A, NOS3 intron 4 VNTR, and APOE epsilon4 gene polymorphisms are not associated with spontaneous cervical artery dissection.Semantic proximity Read ↗

Variation in the estrogen receptor alpha gene and risk of stroke: the Rotterdam Study.Semantic proximity Read ↗

Association of functional VKORC1 promoter polymorphism with occurrence and clinical aspects of ischemic stroke in a Greek population.Semantic proximity Read ↗

Association of promoter polymorphism of apolipoprotein E gene with cerebral vasospasm after spontaneous SAH.Semantic proximity Read ↗

Lack of association between genetic variations in the KALRN region and ischemic stroke.Semantic proximity Read ↗

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