Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population
    
Yazarlar (7)
Goknur Kalkan Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Serbulent Yigit Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Doç. Dr. Nevin KARAKUŞ Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Omer Ates Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Dr. Öğr. Üyesi Nihan BOZKURT Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Atiye Ozdemir Tokat State Hospital, Türkiye
Gunseli Sefika Pancar Tokat State Hospital, Türkiye
Makale Türü Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı Gene (Q4)
Dergi ISSN 0378-1119 Wos Dergi Scopus Dergi
Dergi Tarandığı Indeksler SCI
Makale Dili İngilizce Basım Tarihi 11-2013
Cilt / Sayı / Sayfa 530 / 1 / 109–112 DOI 10.1016/j.gene.2013.08.016
Özet
ObjectiveMethylene-tetrahydrofolate reductase (MTHFR) is a key enzyme regulating folate metabolism and it is thought to influence DNA methylation and nucleic acid synthesis. Mutations in the MTHFR gene have been associated with several autoimmune disorders in previous studies. Alopecia areata (AA) is considered to be a tissue-specific autoimmune disease as the hair follicle has been targeted and antibodies to their own hair follicle structures have been developed. Since there is a common shared pathway between AA and other autoimmune disorders, we aimed to investigate a possible association between the MTHFR gene C677T mutation and AA susceptibility in the Turkish population.MethodsThe study included 136 patients affected by AA and 130 healthy controls. Genomic DNA was isolated and genotyped using a polymerase chain reaction (PCR)-based restriction fragment length polymorphism …
Anahtar Kelimeler
Alopecia areata | C677T mutation | MTHFR gene
Science Direct
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
Google Scholar 23
Scopus 1
Web of Science 13
Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population

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