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pro vyhledávání: '"Beril Erdem Tuncdemir"'
Publikováno v:
ACS Omega, Vol 7, Iss 23, Pp 20195-20203 (2022)
Externí odkaz:
https://doaj.org/article/1eaff31224e84cd78b1f76e88920ef78
Autor:
Beril, Erdem Tuncdemir
Publikováno v:
Journal of Receptors and Signal Transduction. 42:573-579
Loss-of-function mutations of the arginine vasopressin receptor 2 gene (AVPR2) cause Nephrogenic diabetes insipidus (NDI). AVPR2 is a kind of G protein coupled receptor (GPCR) and mainly couples with Gαs protein leading to cAMP accumulation in the c
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
Publikováno v:
European journal of pharmacology. 865
Nephrogenic Diabetes Insipidus is a rare disorder which is characterized by severe water imbalance in the body. The disease can be acquired or inherited. AVPR2 (arginine vasopressin type 2 receptor) mutations are responsible for genetical type of the