Role of the Angiotensin Type 2 Receptor Gene in Congenital Anomalies of the Kidney and Urinary Tract, CAKUT, of Mice and Men
Open Access
- 1 January 1999
- journal article
- Published by Elsevier in Molecular Cell
- Vol. 3 (1) , 1-10
- https://doi.org/10.1016/s1097-2765(00)80169-0
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Chimeric mice carrying 'regional' targeted deletion of the angiotensin type 1A receptor gene. Evidence against the role for local angiotensin in the in vivo feedback regulation of renin synthesis in juxtaglomerular cells.Journal of Clinical Investigation, 1996
- A comprehensive genetic map of the mouse genomeNature, 1996
- Phocomelia, ectrodactyly, skull defect and urinary system anomaly: Schinzel‐phocomelia syndrome?Clinical Genetics, 1996
- Linkage Mapping of the Angiotensin AT2Receptor Gene (Agtr2) to the Mouse X ChromosomeGenomics, 1995
- Effects on blood pressure and exploratory behaviour of mice lacking angiotensin II type-2 receptorNature, 1995
- The impact of fetal screening on indications for cystourethrography in infantsPediatric Radiology, 1994
- Contralateral renal abnormalities in multicystic-dysplastic kidney diseaseThe Journal of Pediatrics, 1992
- Reflux nephropathy secondary to intrauterine vesicoureteric refluxJournal of Pediatric Surgery, 1990
- Prenatal diagnosis of Weyers syndrome (deficient ulnar and fibular rays with bilateral hydronephrosis)American Journal of Medical Genetics, 1985
- Ueber einige Bildungsfehler der UreterenVirchows Archiv, 1877