Glutathione peroxidase and catalase enzyme gene polymorphisms in profound congenital hearing loss

Objective: The aim of this study was to search the codon 200 polymorphism on the glutathione peroxidase 1 gene (GPX1) and A/T changes on the promoter region of the catalase gene (CAT) in cochlear implant patients with congenital profound hearing loss

Glutathione peroxidase and catalase enzyme gene polymorphisms in profound congenital hearing loss

Objective: The aim of this study was to search the codon 200 polymorphism on the glutathione peroxidase 1 gene (GPX1) and A/T changes on the promoter region of the catalase gene (CAT) in cochlear implant patients with congenital profound hearing loss

The polymorphisms of the MBL2 and MIF genes associated with Pediatric Cochlear Implant Patients

Objectives: Mannose-binding lectin and macrophage migration inhibitory factor gene polymorphisms are associated with several acute/chronic autoimmune or inflammatory diseases. The aim of this study was to investigate if there was any association between mannose-binding lectin 2 (MBL2) and macrophage migration inhibitory factor (MIF) gene polymorphisms and profound congenital sensorineural hearing loss in children who underwent cochlear implantation

Cytokine gene polymorphisms and expression in Turkish pediatric cochlear implant patients

Objective: We assessed the association between the polymorphisms and expressions of three cytokine genes and clinical parameters in children who underwent cochlear implantation due to profound congenital sensorineural hearing loss

Cytokine gene polymorphisms and expression in Turkish pediatric cochlear implant patients

Objective: We assessed the association between the polymorphisms and expressions of three cytokine genes and clinical parameters in children who underwent cochlear implantation due to profound congenital sensorineural hearing loss