Ara
Toplam kayıt 34, listelenen: 11-20
Endothelin-1 Lys198Asn and rs10478694 polymorphism in ischemic stroke.
(Scientific Publishers India, 2017)
Objective: In this study, we aimed to investigate the relationship between ischemic cerebrovascular diseases and Lys198Asn and rs10478694 polymorphism of Endothelin-1 gene, a strong vasoconstrictor. Materials and Methods: ...
IGF2BP2 gene polymorphism in patients with psoriasis.
(Allied Acad, 2017)
Psoriasis is a chronic inflammatory disease with genetic transmission, the etiology of which has not been completely clarified yet. Insulin-like Growth Factor Binding Protein 2 (IGF2BP2) plays a role in growth, development, ...
Chromosomal Translocation t (10; 19) (q11.2; q13.4) in an Infertile Male
(Aves, 2014)
Chromosomal rearrangements are usually associated with male factor infertility. We report here a 34-year-old man suffering from primary infertility for 15 years. The cytogenetic analysis and investigation of Y-chromosome ...
Differential Expression of MicroRNAs in Chronic Obstructive Pulmonary Disease
(Wroclaw Medical Univ, 2016)
Background. This study aimed to investigate the associations of miRNA with COPD patients. Objectives. Chronic obstructive pulmonary disease (COPD) is characterized by progressive and largely irreversible airflow limitation. ...
Evaluation of RELN gene polymorphism in children with autism spectrum disorder
(Cumhuriyet Univ Tip Fak Psikiyatri Anabilim Dali, 2018)
Objective: With increasing frequency of autism spectrum disorder (ASD) in recent years, etiology has not yet been fully elucidated. Multiple hypotheses have been proposed to explain autism etiology including genetic, ...
Influence of omega-3 fatty acid on orthodontic tooth movement in rats: A biochemical, histological, immunohistochemical and gene expression study
(Wiley, 2019)
Structured Abstract Objective The aim of this study was to investigate the effects of omega-3 fatty acids on orthodontic tooth movement. Setting and Sample Population For this study, 56 12-week-old adult male Wistar albino ...
Methylation of cation-chloride cotransporters NKCC1 and KCC2 in patients with juvenile myoclonic epilepsy
(Springer-Verlag Italia Srl, 2019)
The etiology of juvenile myoclonic epilepsy (JME) is still unknown and the process of elaboration of multiple genetic mechanisms is ongoing. The aim of this study was to investigate the potential role of NKCC1 (SCL12A2) ...
Sirtuin gene polymorphisms are associated with chronic obstructive pulmonary disease in patients in Mugla province
(Termedia Publishing House Ltd, 2014)
Introduction: Chronic obstructive pulmonary disease (COPD) is an irreversible progressive chronic inflammatory disease that causes shortness of breath in consequence of a decrease in pulmonary functions. The pulmonary ...
The rs3768777-G allele of ITGAV gene is associated with rheumatoid arthritis
(Springer Heidelberg, 2014)
Integrin alpha v beta 3 (vitronectin receptor) plays a prominent role in angiogenesis, a key pathogenic feature of rheumatoid arthritis (RA). Moreover, integrin alpha(V) (ITGAV) subunit gene has been associated with a ...
Expression changes of antioxidant, apoptotic, anti-apoptotic genes and miR-15b-34a-21-98 in over tissue by using erythromycin, quinacrine and tetracycline in non-surgical sterilization
(Springer, 2014)
In the present study, effects on expression of antioxidant, apoptotic and anti-apoptotic genes (GSR, GRX3, SOD1, RAI-NOS, HSP7, BAX, Bc1-2, CASP3 and MDH1) of substances being used in non-surgical sterilization such as ...