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Article

No pathogenic mutations in the uroplakin III gene of 25 patients with primary vesicoureteral reflux.

The Journal of urology - 1 Feb 2004

Giltay Jacques C, van de Meerakker Judith, van Amstel Hans-Krisian Ploos, de Jong Tom P V M

Abstract excerpt

PURPOSE: The uroplakin III (UPIII) knockout mouse provides a good model for human primary vesicoureteral reflux (VUR). Since to our knowledge no causative genes in human VUR have been identified to date, we wondered whether the UPIII gene might be involved in human primary VUR. Therefore, the UPI...

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Identifiers

PMID: 14713856
DOI: 10.1097/01.ju.0000094802.50650.3d

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-14713856-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

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Research trail→

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No pathogenic mutations in the uroplakin III gene of 25 patients with primary vesicoureteral reflux.PMID 14713856Read ↗

Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneity.Semantic proximity Read ↗

Uroplakin III is not a major candidate gene for primary vesicoureteral reflux.Semantic proximity Read ↗

Mutation analyses of Uroplakin II in children with renal tract malformations.Semantic proximity Read ↗

ROBO2 gene variants in children with primary nonsyndromic vesicoureteral reflux with or without renal hypoplasia/dysplasia.Semantic proximity Read ↗

Genes in the ureteric budding pathway: association study on vesico-ureteral reflux patients.Semantic proximity Read ↗

G-protein beta3 subunit gene C825T polymorphism in patients with vesico-ureteric reflux.Semantic proximity Read ↗

Heterozygous non-synonymous ROBO2 variants are unlikely to be sufficient to cause familial vesicoureteric reflux.Semantic proximity Read ↗

No evidence for AT2R gene derangement in human urinary tract anomalies.Semantic proximity Read ↗

Estimation of the relationship between the polymorphisms of selected genes: ACE, AGTR1, TGFβ1 and GNB3 with the occurrence of primary vesicoureteral reflux.Semantic proximity Read ↗

Absence of PAX2 gene mutations in patients with primary familial vesicoureteric reflux.Semantic proximity Read ↗

Gene deletion in urothelium by specific expression of Cre recombinaseSemantic proximity Read ↗

TGF-beta1 gene polymorphisms and primary vesicoureteral reflux in childhood.Semantic proximity Read ↗

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