Ara
Toplam kayıt 14, listelenen: 1-10
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 ...
Role of Leptin (rs7799039) and Leptin Receptor (rs1137101) Gene Polymorphisms in the Development of Uterine Leiomyoma
(Kuwait Medical Assoc, 2017)
Objective: To evaluate whether there is an association between leptin (rs7799039) and leptin receptor (rs1137101) gene polymorphisms and risk of Uterine Leiomyoma (ULM) development Design: Controlled prospective study ...
Evaluation of serum trail level and DR4 gene variants as biomarkers for vitiligo patients
(Wiley-Blackwell, 2016)
[No abstract available]
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 ...
The effect of FOXO gene family variants and global DNA methylation on RRMS disease
(Wiley, 2019)
5th Congress of the European-Academy-of-Neurology
Assessment of COL1A1 and MMP9 expression in patients with dermatochalasis
(Springer, 2020)
Purpose Dermatochalasis is a clinical condition characterized by loss of elasticity of eyelid skin and soft tissue, which typically affects the elderly population. The aim of this study is to investigate the mRNA expression ...
Association of Synapsin III Gene with Adult Attention Deficit Hyperactivity Disorder
(Mary Ann Liebert, Inc, 2013)
It was aimed to investigate the association of the synapsin III gene -196 G> A and -631 C>G polymorphisms that takes place in an encoding presynaptic protein, with adult attention deficit hyperactivity disorder (ADHD). One ...
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 ...
Association of SNAP-25 Gene Ddel and Mnll Polymorphisms with Adult Attention Deficit Hyperactivity Disorder
(Korean Neuropsychiatric Assoc, 2014)
Objective The synaptosomal-associated protein of 25 kDa (SNAP-25) gene is a presynaptic plasma membrane protein and an integral component of the vesicle docking and fusion machinery mediating secretion of neurotransmitters. ...
Novel Fructose-1,6-bisphosphatase Gene Mutation in Two Siblings
(Mary Ann Liebert, Inc, 2013)
Fructose-1,6-bisphosphatase (FBPase) deficiency is an autosomal, recessively inherited disease that progresses with severe hypoglycemia, and metabolic attacks result in a defect in gluconeogenesis. If not appropriately ...