Coronary Artery Disease Is Related to Methylation Disorders Caused by the c.1286AC IMTHFR/I Polymorphism and to Low Serum 5-MTHF and Folic Acid Concentrations—Preliminary Results

Background: Single nucleotide polymorphisms in gene encoding is the key enzyme in the folates pathway, methyltetrahydrofolate reductase (MTHFR), which causes methylation disorders associated with coronary artery disease (CAD). We evaluated associations between methylation disorders caused by MTHFR g...

Ausführliche Beschreibung

Bibliographische Detailangaben

Veröffentlicht in:	Reports (MDPI) 2024-01, Vol.7 (1)
Hauptverfasser:	Pietruszyńska-Reszetarska, Agnieszka, Pietruszyński, Robert, Majsterek, Ireneusz, Popławski, Tomasz, Skrzypek, Maciej, Kolesińska, Beata, Waśko, Joanna, Kapusta, Joanna, Watała, Cezary, Irzmański, Robert
Format:	Artikel
Sprache:	eng
Schlagworte:	Coronary heart disease Folic acid Genes Genetic aspects Genetic polymorphisms Health aspects Medical research Medicine, Experimental Methylation Physiological aspects
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!