Results 201 to 210 of about 41,836 (256)
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Construction of arginine vasopressin receptor 2-deficient rats by the rGONAD method
Clinical and Experimental NephrologyCongenital nephrogenic diabetes insipidus (NDI) is a hereditary disease characterized by a reduced response to arginine vasopressin in the renal collecting duct. NDI is primarily caused by mutations in the arginine vasopressin receptor 2 (AVPR2). Several animal models have been developed for congenital NDI; however, the appropriate models are limited ...
Ayaka Kamada +12 more
semanticscholar +3 more sources
Expression of Arginine Vasopressin Type 2 Receptor in Canine Mammary Tumours: Preliminary Results
Journal of Comparative Pathology, 2020The aims of this study were to investigate the potential association of arginine vasopressin type 2 receptor (AVPR2) in canine mammary tumours with expression of oestrogen receptors α (ORα) and β (ORβ) and clinicopathological features of the neoplasms. Twenty-six canine mammary tumour samples (11 benign, 15 malignant) were immunolabelled for AVPR2, ORα
Benavente, Micaela Andrea +2 more
openaire +3 more sources
An Enhanced Effect of Arginine Vasopressin in Bradykinin B 2 Receptor Null Mutant Mice [PDF]
Abstract —Under water restriction, arginine vasopressin (AVP) is released and promotes water reabsorption in the distal nephron, mainly through AVP V 2 -receptors. It has been proposed that renal kinins counteract the hydro-osmotic effect of AVP. We hypothesized that kinins acting through B 2
Marcos E. Alfie +4 more
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Fetal lung liquid production is essential for in utero pulmonary development, and the resorption of lung liquid at birth facilitates neonatal transition. Lung liquid also contributes importantly to amniotic fluid volume. Factors that influence lung liquid production/resorption may, therefore, impact fetal pulmonary growth and development as well as ...
Cheryl A. Albuquerque +2 more
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Archives of Physiology and Biochemistry, 2020
Oxidative stress, has been shown to play an important role in the pathophysiology of cardiac remodelling and heart failure. The aim of study is effect of arginine vasopressin (AVP) on apoptosis of cardiomyocyte via its receptors.The cell viability effect of AVP in H9C2 cardiomyocytes was assayed using the MTT method.
Vajihe, Ghorbanzadeh +6 more
openaire +2 more sources
Oxidative stress, has been shown to play an important role in the pathophysiology of cardiac remodelling and heart failure. The aim of study is effect of arginine vasopressin (AVP) on apoptosis of cardiomyocyte via its receptors.The cell viability effect of AVP in H9C2 cardiomyocytes was assayed using the MTT method.
Vajihe, Ghorbanzadeh +6 more
openaire +2 more sources
Journal of Neurotrauma, 2019
Complications in upper and lower urinary function arise after spinal cord injury (SCI), which creates a significant impact on quality of life for those affected.
Jason H. Gumbel +3 more
semanticscholar +1 more source
Complications in upper and lower urinary function arise after spinal cord injury (SCI), which creates a significant impact on quality of life for those affected.
Jason H. Gumbel +3 more
semanticscholar +1 more source
Acta Neuropsychiatrica, 2020
Objective: Gene–environment (GxE) interactions may comprise an important part of the aetiology of depression, and childhood maltreatment (CM), a significant stressor, has consistently been linked to depression.
C. Normann, H. Buttenschøn
semanticscholar +1 more source
Objective: Gene–environment (GxE) interactions may comprise an important part of the aetiology of depression, and childhood maltreatment (CM), a significant stressor, has consistently been linked to depression.
C. Normann, H. Buttenschøn
semanticscholar +1 more source
Acta Neuropsychiatrica, 2019
Objective: Depression is a disorder caused by genetics and environmental factors. The aim of this study was to perform a review investigating the interaction between genetic variations located in genes involved in hypothalamus–pituitary–adrenal axis (HPA-
C. Normann, H. Buttenschøn
semanticscholar +1 more source
Objective: Depression is a disorder caused by genetics and environmental factors. The aim of this study was to perform a review investigating the interaction between genetic variations located in genes involved in hypothalamus–pituitary–adrenal axis (HPA-
C. Normann, H. Buttenschøn
semanticscholar +1 more source

