Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Merve Özcan Türkmen"'
Publikováno v:
Journal of Cytology, Vol 40, Iss 4, Pp 177-183 (2023)
Background: Autophagy is a catabolic process whereby organelles and long-lived proteins are recycled through lysosomes to maintain cellular homeostasis. This process is being widely studied using culture techniques and animal models; however, cervico
Externí odkaz:
https://doaj.org/article/f741d66f3cc04c0bbae095cdd74b1358
Publikováno v:
Online Türk Sağlık Bilimleri Dergisi.
Objective: It is important to investigate the interactions of drugs used in the treatment process of COVID-19 with cellular mechanisms. In this study, the aim was to investigate the interactions of Dexamethasone, Favipiravir, and Hydroxychloroquine d
Publikováno v:
Endocrine. 74:658-665
Purpose Familial neurohypophyseal diabetes insipidus (FNDI), a rare disorder, which is clinically characterized by polyuria and polydipsia, results from mutations in the arginine vasopressin-neurophysin II (AVP-NPII) gene. The aim of this study was t
The radioimmunoassay (RIA) method is widely used to determine the levels of arginine vasopressin (AVP) in studies, especially in cell culture studies. However, there are many difficulties and disadvantages in performing this method. Therefore, this s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd916dc45978abbd7fa8f1526c410edf
https://hdl.handle.net/20.500.12451/9900
https://hdl.handle.net/20.500.12451/9900
Autor:
Merve Özcan Türkmen, Aslı Çelebi Tayfur, Aysun Çaltik Yilmaz, Tugce Karaduman, Hatice Mergen, Ayşe Derya Buluş, Bahar Büyükkaragöz, Dilara Sahin
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology.
Objective Congenital nephrogenic diabetes insipidus (CNDI) is a rare inherited disorder characterized by a renal insensitivity to arginine vasopressin (AVP). In the majority of the cases, CNDI is caused by mutations in the arginine vasopressin recept