Ara
Toplam kayıt 3, listelenen: 1-3
Investigation of genetic variations of IL17 for vitiligo disease
(Kuwait Medical Assoc, 2019)
Objective: Vitiligo is a disorder of pigmentation characterized by the presence of depigmented skin macules due to a chronic and progressive loss of melanocytes from the cutaneous epidermis. Among many different etiologic ...
GPR30 Gene Polymorphisms Are Associated with Gynecomastia Risk in Adolescents
(Karger, 2015)
Aim: The G protein-coupled receptor, GPR30, which is a third estrogen receptor, has been shown to mediate estrogenic effects on the essential features of human breast cancer cells. The aim of this study was to evaluate the ...
Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency
(Galenos Yayincilik, 2016)
Objective: Deficiency of steroid 5-alpha reductase type 2 (5 alpha RD2) is a rare autosomal recessive disorder caused by mutations in the SRD5A2 gene. A defect in the 5-alpha reductase enzyme, which ensures conversion of ...