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Article

Fructosamine 3-kinase and glyoxalase I polymorphisms and their association with soluble RAGE and adhesion molecules in diabetes.

Physiological research - 1 Jan 2014

Škrha J, Muravská A, Flekač M, Horová E, Novák J, Novotný A, Prázný M, Škrha J, Kvasnička J, Landová L, Jáchymová M, Zima T, Kalousová M

Abstract excerpt

Advanced glycation end-products (AGEs) are key players in pathogenesis of long-term vascular diabetes complications. Several enzymes such as fructosamine 3-kinase (FN3K) and glyoxalase I (GLO I) are crucial in preventing glycation processes. The aim of our study was to evaluate an association of FN3K (rs1056534, rs3848403) and GLO1 rs4746 polymorphisms with parameters of endothelial dysfunction and soluble...

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Share to Biomarkers
Share to Cell Adhesion Molecules
Share to Diabetes Mellitus, Type 1
Share to Diabetes Mellitus, Type 2
Share to Lactoylglutathione Lyase
Share to Phosphotransferases (Alcohol Group Acceptor)
Share to Receptor for Advanced Glycation End Products
Share to Receptors, Immunologic

Source

Identifiers

PMID: 24908234
DOI: 10.33549/physiolres.932790

Genes

GLO1

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