Association analysis of three ABCB1 (MDR1) gene variants (C1236T, G2677A/T and C3435T) and their genotype/haplotype combinations with the familial Mediterranean fever
 
Yazarlar (6)
Prof. Dr. Aydin Rustemoglu Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Guvem Gumus-Akay
Ankara Üniversitesi, Türkiye
Doç. Dr. Nevin KARAKUŞ Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Prof. Dr. Serbulent Yigit Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Server Sahin
Dumlupinar Üniversitesi, Türkiye
Turker Tasliyurt Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Makale Türü Özgün Makale (ESCI dergilerinde yayınlanan tam makale)
Dergi Adı Xenobiotica
Dergi ISSN 0049-8254 Wos Dergi Scopus Dergi
Makale Dili İngilizce Basım Tarihi 10-2014
Cilt / Sayı / Sayfa 44 / 10 / 933–940 DOI 10.3109/00498254.2014.915071
Makale Linki https://www.tandfonline.com/doi/abs/10.3109/00498254.2014.915071
UAK Araştırma Alanları
Tıbbi Biyoloji
Özet
1. Familial Mediterranean fever (FMF) is considered an autosomal recessive disorder, associated with a single gene named Mediterranean fever (MEFV). The aim of this study was to perform genotyping and haplotyping analysis of the multidrug resistance (ATP-binding cassette, subfamily B, member 1 – ABCB1) gene in FMF patients.2. Three ABCB1 gene polymorphisms (C1236T, G2677T/A and C3435T) were analyzed in 309 FMF patients and 250 healthy control subjects. All subjects were genotyped by PCR–restriction fragment length polymorphism analysis, and statistical analysis was performed using the Arlequin 3.1.1 and SPSS 16.0 software packages.3. The CT genotype frequency of the C3435T polymorphism (p = 0.003), the CT–GT–CT (C1236T–G2677T/A–C3435T) triple genotype (p = 0.001) and the C–G (C1236T–G2677T/A) haplotype (p = 0.030) were more common in the FMF patients. The CT …
Anahtar Kelimeler
ABCB1 | FMF | Haplotype | Polymorphism | Turkey