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Article

3'-UTR OLR1/LOX-1 gene polymorphism and endothelial dysfunction: molecular and vascular data in never-treated hypertensive patients.

Internal and emergency medicine - 1 Apr 2014

Sciacqua Angela, Presta Ivan, Perticone Maria, Tassone Eliezer J, Andreozzi Francesco, Quitadamo Maria Chiara, Sangiuolo Federica Carla, Sesti Giorgio, Perticone Francesco

Abstract excerpt

Endothelial dysfunction represents an independent predictor for clinical events. Genetic background may promote deleterious alterations of endothelial physiology. The aim of the study was to investigate the relationship between the rs1050283 polymorphism in the 3'-UTR of OLR1/LOX-1 gene and endothelial dysfunction in 178 never-treated hypertensive patients and 36 healthy subjects. The rs1050283 C/T single...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to 3' Untranslated Regions
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Share to Polymorphism, Single Nucleotide
Share to Scavenger Receptors, Class E
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Source

Identifiers

PMID: 23054405
DOI: 10.1007/s11739-012-0857-y

Genes

LOX
OLR1

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.

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