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

doi:10.1111/j.1523-1755.2004.00703.x

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Article

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

Kidney international - 1 Jul 2004

Jiang Songshan, Gitlin Jordan, Deng Fang-Ming, Liang Feng-Xia, Lee Andy, Atala Anthony, Bauer Stuart B, Ehrlich Garth D, Feather Sally A, Goldberg Judith D, Goodship Judith A, Goodship Timothy H J, Hermanns Monika, Hu Fen Ze, Jones Katrin E, Malcolm Sue, Mendelsohn Cathy, Preston Robert A, Retik Alan B, Schneck Francis X, Wright Victoria, Ye Xiang Y, Woolf Adrian S, Wu Xue-Ru, Ostrer Harry, Shapiro Ellen, Yu Jun, Sun Tung-Tien

Abstract excerpt

BACKGROUND: Primary vesicoureteral reflux (VUR) is a hereditary disorder characterized by the retrograde flow of urine into the ureters and kidneys. It affects about 1% of the young children and is thus one of the most common hereditary diseases. Its associated nephropathy is an important cause of end-stage renal failure in children and adults. Recent studies indicate that genetic ablation of mouse uroplakin (UP)...

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PMID: 15200408
DOI: 10.1111/j.1523-1755.2004.00703.x

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Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneity.PMID 15200408Read ↗

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

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

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

Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux.Semantic proximity Read ↗

De Novo Uroplakin IIIa Heterozygous Mutations Cause Human Renal Adysplasia Leading to Severe Kidney FailureSemantic 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 ↗

Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral RefluxSemantic proximity Read ↗

A single-center cohort of Canadian children with VUR reveals renal phenotypes important for genetic studies.Semantic proximity Read ↗

Mutations in Uroplakin IIIA Are a Rare Cause of Renal Hypodysplasia in HumansSemantic proximity Read ↗

Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1.Semantic proximity Read ↗

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

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