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

[α-2β-adrenoreceptor gene polymorphism in patients with disorders of cardiac conduction].

Kardiologiia - 1 Jan 2013

Chernova A A, Nikulina S Iu, Tret'iakova S S, Maksimov V N, Voevoda M I, Chernov V N

Abstract excerpt

The article is devoted to the role of insertion-deletion polymorphism of -2-adrenoreceptor gene in development of hereditary disorders of cardiac conduction. We examined 71 patients with atrioventricular blocks and 92 patients with sick sinus node syndrome. Statistically significant preponderance of homozygous genotype DD of ADRA2B gene was found in both groups. Associations of alleles with male or female gender...

Read the complete abstract on PubMed

Topics

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

Share to Atrioventricular Block
Share to Heart Conduction System

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Homozygote

Share to Receptors, Adrenergic, alpha-2

Share to Severity of Illness Index

Share to Sex Factors

Share to Siberia

Share to Sick Sinus Syndrome

Source

Identifiers

PMID: 24087960

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

[α-2β-adrenoreceptor gene polymorphism in patients with disorders of cardiac conduction].PMID 24087960Read ↗

[The role of alfa-2-beta-adrenoreceptor in development of ventricular conduction disturbance].Semantic proximity Read ↗

[Association of 2B-adrenergic receptor gene polymorphism with disturbances of cardiac conduction].Semantic proximity Read ↗

[Polymorphisms of 2B-adrenergic receptor and endothelial NO-Synthase genes in genesis of the hereditary sick sinus node syndrome].Semantic proximity Read ↗

[Manifestations of polymorphism of β1-adrenoreceptors in patients with newly diagnosed cardiac rhythm disorders].Semantic proximity Read ↗

[Sudden cardiac death and polymorphism of genes-candidates of cardiovascular diseases].Semantic proximity Read ↗

[Genetic predisposition to development of atrial fibrillation in patients with hypertensive disease].Semantic proximity Read ↗

[Genetic predictors of sick sinus node syndrome].Semantic proximity Read ↗

[Relationship between polymorphism of non-coding regions of human mitochondrial genome and primary cardiac conduction disorders].Semantic proximity Read ↗

[Polymorphisms of beta2-adrenergic receptor].Semantic proximity Read ↗

[Polymorphisms of α-2-β-adrenergic receptor and endothelial NO-synthase genes in patients with atrial fibrillation].Semantic proximity Read ↗

[Ser49gly polymorphism as predictor of development of hereditary sick sinus node syndrome].Semantic proximity Read ↗

Association of ADRB1 gene polymorphism with atrial fibrillation.Semantic proximity Read ↗

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