Associated Papers
Structural effect of the H992D/H418D mutation of angiotensin-converting enzyme in the Indian population: implications for health and disease.
Kulshreshtha A et al.
Journal of Biomolecular Structure & Dynamics, 2025
A loss-of-function AGTR1 variant in a critically-ill infant with renal tubular dysgenesis: case presentation and literature review.
Al-Maraghi A et al.
Bmc Nephrology, 2024
Angiotensin II type 1 receptor variants alter endosomal receptor-β-arrestin complex stability and MAPK activation.
Cao Y et al.
The Journal of Biological Chemistry, 2020
Genetic code expansion and photocross-linking identify different β-arrestin binding modes to the angiotensin II type 1 receptor.
Gagnon L et al.
The Journal of Biological Chemistry, 2019
Functional selectivity profiling of the angiotensin II type 1 receptor using pathway-wide BRET signaling sensors.
Namkung Y et al.
Science Signaling, 2018
Genetics of congenital anomalies of the kidney and urinary tract.
Song R et al.
Pediatric Nephrology (berlin, Germany), 2011
Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesis.
Gribouval O et al.
Nature Genetics, 2005
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