The Role of Bradykinin Receptors in Hereditary Angioedema Due to C1-Inhibitor Deficiency
Background: Hereditary angioedema (HAE) is a rare, genetic disease caused by the decreased level or function of the C1 inhibitor. The primary mediator of symptoms in HAE is bradykinin acting through its two receptors, namely receptors 1 (BR1) and 2 (BR2). Although BR2 is well characterized, the role...
Main Authors: | Wojciech Dyga, Aleksander Obtulowicz, Tomasz Mikolajczyk, Anna Bogdali, Pawel Dubiela, Krystyna Obtulowicz |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2022-09-01
|
Series: | International Journal of Molecular Sciences |
Subjects: | |
Online Access: | https://www.mdpi.com/1422-0067/23/18/10332 |
Similar Items
-
The Role of Bradykinin Receptors in the Etiopathogenesis of Chronic Spontaneous Urticaria
by: Aleksander Obtulowicz, et al.
Published: (2021-10-01) -
Abdominal and pelvic imaging in the diagnosis of acute abdominal attacks in patients with hereditary angioedema due to C1-inhibitor deficiency
by: Piotr Obtułowicz, et al.
Published: (2021-08-01) -
Mutant plasminogen in hereditary angioedema is bypassing FXII/kallikrein to generate bradykinin
by: Stefan Hintze, et al.
Published: (2023-01-01) -
Bradykinin-induced angioedema in the emergency department
by: Jacques Hébert, et al.
Published: (2022-03-01) -
Bradykinin Metabolism and Drug-Induced Angioedema
by: Sylwia Smolinska, et al.
Published: (2023-07-01)