Angiotensin II type 2 receptor gene is not responsible for familial vesicoureteral reflux

Journal of Urology

Volumn 168, Issue 3, 2002, Pages 1138-1141

  Yoneda, Akihiro ^a   Cascio, Salvatore ^a   Green, Andrew ^a   Barton, David ^a   Puri, Prem ^a  

^a UNIVERSITY COLLEGE DUBLIN   (Ireland)

Author keywords

Angiotensins; Genes; Vesico ureteral reflux

Indexed keywords

ALANINE; ANGIOTENSIN 2 RECEPTOR; GENOMIC DNA; GLYCINE;

AMINO ACID SUBSTITUTION; ARTICLE; CONTROLLED STUDY; FAMILIAL DISEASE; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENE MUTATION; GENETIC POLYMORPHISM; HUMAN; INCIDENCE; KIDNEY ANOMALY; MAJOR CLINICAL STUDY; MALE; MEGAURETER; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PRIORITY JOURNAL; RENIN ANGIOTENSIN ALDOSTERONE SYSTEM; URETER MALFORMATION; URETEROPELVIC JUNCTION OBSTRUCTION; VESICOURETERAL REFLUX;

EID: 0036718403     PISSN: 00225347     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-5347(05)64611-3     Document Type: Article

References (23)

1. Urinary tract infection and renal damage in sibling vesicoureteral reflux
2. Vesico-ureteral reflux: A genetic condition?
3. Vesicoureteric reflux and renal injury
4. Renal transplantation and chronic dialysis in children and adolescents: The 1993 annual report of the North American Pediatric Renal Transplant Cooperative Study
5. Vesicoureteric reflux and reflux nephropathy
6. The transmission of vesicoureteral reflux from parent to child
7. Vesicoureteric reflux: Segregation analysis
8. Unravelling the genetics of vesicoureteric reflux: A common familial disorder
9. A theory on the nature of transmission of congenital vesicoureteral reflux
10. A family study of vesicoureteric reflux
11. Familial vesicoureteral reflux: A prospective study
12. Sibling vesicoureteral reflux in multiple gestation births
13. Mutation of PAX2 in two siblings with renalcoloboma syndrome
14. Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux
15. Absence of PAX2 gene mutations in patients with primary familial vesicoureteric reflux
16. Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1
17. Renin-angiotensin genes in renal development and the occurrence and progression of renal diseases
18. Role of the angiotensin type 2 receptor gene in congenital anomalies of the kidney and urinary tract, CAKUT, of mice and men
19. Angiotensin type 2 receptor is important in the normal development of the ureter
20. Angiotensin II, type 2 receptor in the development of vesico-ureteric reflux
21. A molecular and genetic view of human renal and urinary tract malformations
22. Role of the angiotensin receptor in the development of the mammalian kidney and urinary tract
23. Congenital anomalies of the kidney and urinary tract-role of the loss of function mutation in the pluripotent angiotensin type 2 receptor gene