| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/S00467-006-0390-1 |
| P2888 | exact match | https://scigraph.springernature.com/pub.10.1007/s00467-006-0390-1 |
| P932 | PMC publication ID | 6904386 |
| P698 | PubMed publication ID | 17216254 |
| P5875 | ResearchGate publication ID | 6585763 |
| P50 | author | Luisa Murer | Q44237018 |
| P2093 | author name string | Elisa Benetti | |
| Lina Artifoni | |||
| P2860 | cites work | Genetic determination of nephrogenesis: the Pax/Eya/Six gene network. | Q52096291 |
| Deregulation of Pax-2 expression in transgenic mice generates severe kidney abnormalities. | Q52226238 | ||
| Expression of Nuclear Transcription Factor PAX2 in Renal Biopsies of Juvenile Nephronophthisis | Q57980393 | ||
| De Novo Uroplakin IIIa Heterozygous Mutations Cause Human Renal Adysplasia Leading to Severe Kidney Failure | Q59382431 | ||
| Interleukin-8 and CXCR1 Receptor Functional Polymorphisms and Susceptibility to Acute Pyelonephritis | Q61409830 | ||
| Vesicoureteric reflux: segregation analysis | Q70101713 | ||
| The molecular control of renal branching morphogenesis: current knowledge and emerging insights | Q34792534 | ||
| Primary ureteral reflux: emerging insights from molecular and genetic studies | Q35086254 | ||
| The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney | Q35934032 | ||
| Role of the renin-angiotensin system in the development of the ureteric bud and renal collecting system | Q36155390 | ||
| Vesicoureteric reflux and renal malformations: a developmental problem | Q36376471 | ||
| Hereditary vesicoureteric reflux: phenotypic variation and family screening | Q40886029 | ||
| Unravelling the genetics of vesicoureteric reflux: a common familial disorder | Q40957103 | ||
| HDR syndrome (hypoparathyroidism, sensorineural deafness, renal dysplasia) associated with del(10)(p13). | Q41671947 | ||
| Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindreds | Q42653487 | ||
| Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneity | Q44939092 | ||
| A locus for renal malformations including vesico-ureteric reflux on chromosome 13q33-34. | Q52022384 | ||
| A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family | Q24318377 | ||
| A gene locus for branchio-otic syndrome maps to chromosome 14q21.3-q24.3 | Q24676647 | ||
| SALL1 mutation analysis in Townes-Brocks syndrome: twelve novel mutations and expansion of the phenotype | Q28266426 | ||
| Familial nephrosis, nerve deafness, and hypoparathyroidism | Q28286402 | ||
| How they begin and how they end: classic and new theories for the development and deterioration of congenital anomalies of the kidney and urinary tract, CAKUT. | Q33728700 | ||
| Ablation of uroplakin III gene results in small urothelial plaques, urothelial leakage, and vesicoureteral reflux | Q33925813 | ||
| SALL1 mutations in Townes-Brocks syndrome and related disorders | Q34096518 | ||
| Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1. | Q34145616 | ||
| Mutation of PAX2 in two siblings with renal-coloboma syndrome | Q34373971 | ||
| Paradigm shift from classic anatomic theories to contemporary cell biological views of CAKUT. | Q34534588 | ||
| Molecular mechanisms of human embryogenesis: developmental pathogenesis of renal tract malformations | Q34575106 | ||
| Coordinating early kidney development: lessons from gene targeting | Q34718165 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 6 | |
| P304 | page(s) | 788-797 | |
| P577 | publication date | 2007-01-10 | |
| P1433 | published in | Pediatric Nephrology | Q15749796 |
| P1476 | title | Embryology and genetics of primary vesico-ureteric reflux and associated renal dysplasia | |
| P478 | volume | 22 |
| Q36484807 | A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity |
| Q37535775 | A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract development. |
| Q28264027 | Association between congenital defects in papillary outgrowth and functional obstruction in Crim1 mutant mice |
| Q90730001 | Association of vesicoureteral reflux and gastroesophageal reflux disease in children: A population-based study |
| Q51862664 | Concomitant vesicoureteral reflux and gastroesophageal reflux: an analytic cross-sectional study. |
| Q99630787 | Congenital Anomalies of the Kidney and Urinary Tract: A Clinical Review |
| Q80089130 | Continuing medical education: introducing four papers on vesicoureteral reflux |
| Q35547763 | Demographic features and antibiotic resistance among children hospitalized for urinary tract infection in northwest Iran |
| Q26749409 | Dermatoglyphics in kidney diseases: a review |
| Q81359140 | Diagnosing papillorenal syndrome: see the optic papilla |
| Q37034904 | Diagnostic accuracy of magnetic resonance voiding cystourethrography for detecting vesico-ureteral reflux in children and adolescents |
| Q95471779 | Editorial comment |
| Q37078188 | Gene discovery and vesicoureteric reflux |
| Q37351552 | Genetic and developmental basis for urinary tract obstruction |
| Q36658504 | Genetics of Vesicoureteral Reflux |
| Q39485603 | Genetics of vesicoureteral reflux. |
| Q50482421 | Heterozygous non-synonymous ROBO2 variants are unlikely to be sufficient to cause familial vesicoureteric reflux. |
| Q38570411 | Kruppel-like factor 5 is required for formation and differentiation of the bladder urothelium |
| Q38054159 | Lower urinary tract function in childhood; normal development and common functional disturbances |
| Q37164109 | Management and etiology of the unilateral multicystic dysplastic kidney: a review. |
| Q42111744 | Morphological, molecular and FTIR spectroscopic analysis during the differentiation of kidney cells from pluripotent stem cells. |
| Q56774780 | PAX2 polymorphisms and congenital abnormalities of the kidney and urinary tract in a Brazilian pediatric population: evidence for a role in vesicoureteral reflux |
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