| review article | Q7318358 |
| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1037169999 |
| P356 | DOI | 10.1046/J.1523-1755.2002.00188.X |
| P2888 | exact match | https://scigraph.springernature.com/pub.10.1046/j.1523-1755.2002.00188.x |
| P698 | PubMed publication ID | 11849443 |
| P5875 | ResearchGate publication ID | 11512784 |
| P2093 | author name string | Yoichi Miyazaki | |
| John C Pope | |||
| Iekuni Ichikawa | |||
| F Douglas Stephens | |||
| Fumiyo Kuwayama | |||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | paradigm shift | Q689971 |
| P304 | page(s) | 889-898 | |
| P577 | publication date | 2002-03-01 | |
| P1433 | published in | Kidney International | Q6404823 |
| P1476 | title | Paradigm shift from classic anatomic theories to contemporary cell biological views of CAKUT. | |
| P478 | volume | 61 |
| Q37363254 | A genome-wide scan for genes involved in primary vesicoureteric reflux. |
| Q47800870 | A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral reflux |
| 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. |
| Q40286826 | Activin A is an endogenous inhibitor of ureteric bud outgrowth from the Wolffian duct |
| Q53133244 | An unusual case of S-shaped malformation of the ipsilateral kidney with normal contralateral kidney. |
| Q88458468 | Association between cord blood cystatin C levels and early mortality of neonates with congenital abnormalities of the kidney and urinary tract: a single-center, retrospective cohort study |
| Q56774769 | Association of angiotensin type 2 receptor gene polymorphisms with ureteropelvic junction obstruction in Brazilian patients |
| Q40223314 | Branching morphogenesis of the ureteric epithelium during kidney development is coordinated by the opposing functions of GDNF and Sprouty1. |
| Q91991382 | Clinico-Biochemical Profile of Children with Congenital Anomalies of the Kidney and Urinary Tract: A Cross-Sectional Study |
| Q47775900 | Coexistent duplication of urethra and a refluxing ectopic ureter presenting as recurrent epididymo-orchitis in a child |
| Q84121434 | Complications and long-term outcome of primary obstructive megaureter in childhood |
| Q43116254 | Congenital anomalies of kidney and urinary tract in siblings: An uncommon condition |
| Q38270948 | Congenital anomalies of the kidney and urinary tract: an embryogenetic review |
| Q24310775 | Deficiency of intrarenal angiotensin II type 2 receptor impairs paired homeo box-2 and N-myc expression during nephrogenesis |
| Q38822350 | Developmental Genetics and Congenital Anomalies of the Kidney and Urinary Tract |
| Q64984008 | Developmental pathology of congenital kidney and urinary tract anomalies. |
| Q28587600 | Distal ureter morphogenesis depends on epithelial cell remodeling mediated by vitamin A and Ret |
| Q36740991 | Double homozygous missense mutations in DACH1 and BMP4 in a patient with bilateral cystic renal dysplasia |
| Q92135557 | Embryology and Morphological (Mal)Development of UPJ |
| Q51997234 | Embryology and genetics of primary vesico-ureteric reflux and associated renal dysplasia. |
| Q37028863 | Evaluation of reflux nephropathy, pyelonephritis and renal dysplasia |
| Q52578627 | Expression profiles of congenital renal dysplasia reveal new insights into renal development and disease. |
| Q58333230 | Familial multicystic dysplastic kidney |
| Q28579892 | Gata3 acts downstream of beta-catenin signaling to prevent ectopic metanephric kidney induction |
| Q34256093 | Genes in the ureteric budding pathway: association study on vesico-ureteral reflux patients. |
| Q47224735 | Genetic basis of human congenital anomalies of the kidney and urinary tract |
| Q79105221 | Genetic disorders of human congenital anomalies of the kidney and urinary tract (CAKUT) |
| Q35097858 | Genetic etiology of renal agenesis: fine mapping of Renag1 and identification of Kit as the candidate functional gene |
| Q33968487 | Genetic kidney diseases |
| Q38731983 | Genetics of Congenital Anomalies of the Kidney and Urinary Tract: The Current State of Play. |
| Q36658504 | Genetics of Vesicoureteral Reflux |
| Q41238162 | Genetics of kidney development: pathogenesis of renal anomalies |
| Q39371197 | Genetics of vesicoureteral reflux and congenital anomalies of the kidney and urinary tract. |
| Q39485603 | Genetics of vesicoureteral reflux. |
| Q28509829 | Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental disease |
| Q36411148 | Going in circles: conserved mechanisms control radial patterning in the urinary and digestive tracts |
| Q50482421 | Heterozygous non-synonymous ROBO2 variants are unlikely to be sufficient to cause familial vesicoureteric reflux. |
| Q37330869 | Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis |
| Q37241467 | Impact of Kidney Disease on Survival in Neonatal Extracorporeal Life Support. |
| Q52566089 | Implication of genetic variations in congenital obstructive nephropathy. |
| Q79081704 | In the case of urinary tract malformation, when is it necessary to check for a genetic cause? |
| Q47155566 | Involvement of the bone morphogenic protein/SMAD signaling pathway in the etiology of congenital anomalies of the kidney and urinary tract accompanied by cryptorchidism. |
| Q33525015 | Kidney development in the absence of Gdnf and Spry1 requires Fgf10. |
| Q37778484 | Kidney development: two tales of tubulogenesis |
| Q51907012 | L1CAM mutation in a boy with hydrocephalus and duplex kidneys. |
| Q35884248 | Linkage study of 14 candidate genes and loci in four large Dutch families with vesico-ureteral reflux |
| Q44788075 | Long-term risk of chronic kidney disease in unilateral multicystic dysplastic kidney |
| Q79768855 | MR urography in children |
| Q34103492 | Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract |
| Q33692509 | Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract |
| Q24338673 | Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development |
| Q35836481 | Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract |
| Q54040009 | Narrowing critical regions and determining penetrance for selected 18q- phenotypes. |
| Q27320477 | Noninvasive assessment of antenatal hydronephrosis in mice reveals a critical role for Robo2 in maintaining anti-reflux mechanism |
| Q50100394 | Novel Insights into the Pathogenesis of Monogenic Congenital Anomalies of the Kidney and Urinary Tract. |
| Q30441412 | Obstructive nephropathy: towards biomarker discovery and gene therapy |
| Q27011303 | Pediatric febrile urinary tract infections: the current state of play |
| Q37786621 | Postnatal management of congenital bilateral renal hypodysplasia. |
| Q24302641 | Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: results of the ESCAPE study |
| Q53473853 | Prioritization and burden analysis of rare variants in 208 candidate genes suggest they do not play a major role in CAKUT. |
| Q36561449 | Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux |
| Q42794542 | Renal cell carcinoma arising in ipsilateral duplex system |
| Q38724083 | Renal dysplasia in the neonate |
| Q36369898 | Renal scar formation after urinary tract infection in children |
| Q24318341 | SIX2 and BMP4 mutations associate with anomalous kidney development |
| Q51275833 | Side-to-side and interpolar renal duplications: the nonpolar variety. |
| Q26862475 | Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans |
| Q37078422 | TNXB mutations can cause vesicoureteral reflux |
| Q42019386 | Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tract |
| Q37666573 | The adverse renal effects of prostaglandin-synthesis inhibition in the fetus and the newborn |
| Q90712113 | The copy number variation landscape of congenital anomalies of the kidney and urinary tract |
| Q51958032 | The fate of prenatally diagnosed primary nonrefluxing megaureter: do we have reliable predictors for spontaneous resolution? |
| Q28588665 | The leucine zipper putative tumor suppressor 2 protein LZTS2 regulates kidney development |
| Q58095875 | Transcription Factor 21 Is Required for Branching Morphogenesis and Regulates the Gdnf-Axis in Kidney Development |
| Q36023297 | UG4 enhancer-driven GATA-2 and bone morphogenetic protein 4 complementation remedies the CAKUT phenotype in Gata2 hypomorphic mutant mice |
| Q55313563 | Urinary Anomalies in 22q11.2 Deletion (DiGeorge syndrome): From Copy Number Variations to Single-Gene Determinants of Phenotype. |
| Q36207459 | Urine excretion strategy for stem cell-generated embryonic kidneys |
| Q36689787 | Uroplakins: new molecular players in the biology of urinary tract malformations. |
| Q37719873 | Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association |
| Q35842436 | Whole-exome sequencing identifies mutations of TBC1D1 encoding a Rab-GTPase-activating protein in patients with congenital anomalies of the kidneys and urinary tract (CAKUT). |
| Q85936967 | [Primary megaureter] |
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