Published in Kidney Int on August 01, 2004
Patterning the renal vascular bed. Semin Cell Dev Biol (2014) 0.83
BIM deficiency differentially impacts the function of kidney endothelial and epithelial cells through modulation of their local microenvironment. Am J Physiol Renal Physiol (2011) 0.81
Podocyte-specific expression of angiopoietin-2 causes proteinuria and apoptosis of glomerular endothelia. J Am Soc Nephrol (2007) 2.06
Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux. Am J Hum Genet (2007) 1.85
Renal tract malformations: perspectives for nephrologists. Nat Clin Pract Nephrol (2008) 1.83
Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein. Nat Genet (2003) 1.71
Angiopoietin-1 therapy enhances fibrosis and inflammation following folic acid-induced acute renal injury. Kidney Int (2008) 1.70
Centriolar satellites are assembly points for proteins implicated in human ciliopathies, including oral-facial-digital syndrome 1. J Cell Sci (2011) 1.64
Peritubular capillary loss after mouse acute nephrotoxicity correlates with down-regulation of vascular endothelial growth factor-A and hypoxia-inducible factor-1 alpha. Am J Pathol (2003) 1.63
Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebs. Nat Genet (2005) 1.51
Convergent extension movements and ciliary function are mediated by ofd1, a zebrafish orthologue of the human oral-facial-digital type 1 syndrome gene. Hum Mol Genet (2008) 1.46
OFD1 is a centrosomal/basal body protein expressed during mesenchymal-epithelial transition in human nephrogenesis. J Am Soc Nephrol (2004) 1.43
Teashirt 3 is necessary for ureteral smooth muscle differentiation downstream of SHH and BMP4. Development (2008) 1.42
Primary vesicoureteric reflux as a predictor of renal damage in children hospitalized with urinary tract infection: a systematic review and meta-analysis. J Am Soc Nephrol (2003) 1.37
Genetic analyses reveal a requirement for Dicer1 in the mouse urogenital tract. Mamm Genome (2009) 1.31
HNF1B mutations associate with hypomagnesemia and renal magnesium wasting. J Am Soc Nephrol (2009) 1.29
Activation of the orphan endothelial receptor Tie1 modifies Tie2-mediated intracellular signaling and cell survival. FASEB J (2007) 1.27
Protein restriction in pregnancy is associated with increased apoptosis of mesenchymal cells at the start of rat metanephrogenesis. Kidney Int (2002) 1.26
Mutations in HPSE2 cause urofacial syndrome. Am J Hum Genet (2010) 1.24
Solitary functioning kidney and diverse genital tract malformations associated with hepatocyte nuclear factor-1beta mutations. Kidney Int (2002) 1.18
De novo Uroplakin IIIa heterozygous mutations cause human renal adysplasia leading to severe kidney failure. J Am Soc Nephrol (2005) 1.15
The planar cell polarity gene Vangl2 is required for mammalian kidney-branching morphogenesis and glomerular maturation. Hum Mol Genet (2010) 1.10
OFD1, the gene mutated in oral-facial-digital syndrome type 1, is expressed in the metanephros and in human embryonic renal mesenchymal cells. J Am Soc Nephrol (2003) 1.08
A paradoxical teratogenic mechanism for retinoic acid. Proc Natl Acad Sci U S A (2012) 1.08
Maternal diet programs embryonic kidney gene expression. Physiol Genomics (2005) 1.03
Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux. J Am Soc Nephrol (2009) 0.99
Fras1, a basement membrane-associated protein mutated in Fraser syndrome, mediates both the initiation of the mammalian kidney and the integrity of renal glomeruli. Hum Mol Genet (2008) 0.99
Targeted glomerular angiopoietin-1 therapy for early diabetic kidney disease. J Am Soc Nephrol (2013) 0.98
LRIG2 mutations cause urofacial syndrome. Am J Hum Genet (2013) 0.97
Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneity. Kidney Int (2004) 0.96
Ureter myogenesis: putting Teashirt into context. J Am Soc Nephrol (2009) 0.95
Immunohistochemical analysis of Sonic hedgehog signalling in normal human urinary tract development. J Anat (2007) 0.94
Albuminuria is associated with too few glomeruli and too much testosterone. Kidney Int (2013) 0.93
Development of embryonic stem cells in recombinant kidneys. Organogenesis (2012) 0.92
Galectin-3 associates with the primary cilium and modulates cyst growth in congenital polycystic kidney disease. Am J Pathol (2006) 0.92
Severe hyperglycemia after renal transplantation in a pediatric patient with a mutation of the hepatocyte nuclear factor-1beta gene. Am J Kidney Dis (2002) 0.90
Implication of Wt1 in the pathogenesis of nephrogenic failure in a mouse model of retinoic acid-induced caudal regression syndrome. Am J Pathol (2005) 0.90
The P2X7 ATP receptor modulates renal cyst development in vitro. Biochem Biophys Res Commun (2004) 0.90
Analysis of TSHZ2 and TSHZ3 genes in congenital pelvi-ureteric junction obstruction. Nephrol Dial Transplant (2009) 0.90
Circulating angiopoietin-2 is a marker for early cardiovascular disease in children on chronic dialysis. PLoS One (2013) 0.89
P2X(7) receptors are expressed during mouse nephrogenesis and in collecting duct cysts of the cpk/cpk mouse. Exp Nephrol (2002) 0.89
Dysmorphogenesis of kidney cortical peritubular capillaries in angiopoietin-2-deficient mice. Am J Pathol (2004) 0.89
Angiopoietin correlates with glomerular capillary loss in anti-glomerular basement membrane glomerulonephritis. Kidney Int (2002) 0.88
Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome. Am J Hum Genet (2011) 0.88
Corticosteroid-induced kidney dysmorphogenesis is associated with deregulated expression of known cystogenic molecules, as well as Indian hedgehog. Am J Physiol Renal Physiol (2009) 0.88
Vascular endothelial growth factor administration does not improve microvascular disease in the salt-dependent phase of post-angiotensin II hypertension. Am J Physiol Renal Physiol (2006) 0.87
Sprouty1 haploinsufficiency prevents renal agenesis in a model of Fraser syndrome. J Am Soc Nephrol (2012) 0.86
Renal malformations associated with mutations of developmental genes: messages from the clinic. Pediatr Nephrol (2010) 0.86
Vascular endothelial growth factor stimulates embryonic urinary bladder development in organ culture. BJU Int (2006) 0.86
Microarray interrogation of human metanephric mesenchymal cells highlights potentially important molecules in vivo. Physiol Genomics (2006) 0.85
Unraveling the genetic landscape of bladder development in mice. J Urol (2009) 0.85
Urinary outflow obstruction increases apoptosis and deregulates Bcl-2 and Bax expression in the fetal ovine bladder. Am J Pathol (2003) 0.85
Vascular endothelial growth factor mediates hypoxic stimulated embryonic bladder growth in organ culture. J Urol (2007) 0.85
Ex vivo modeling of chemical synergy in prenatal kidney cystogenesis. PLoS One (2013) 0.84
Renal hypoplasia and dysplasia: starting to put the puzzle together. J Am Soc Nephrol (2006) 0.84
Using stem and progenitor cells to recapitulate kidney development and restore renal function. Curr Opin Organ Transplant (2014) 0.84
Mutational analyses of UPIIIA, SHH, EFNB2 and HNF1beta in persistent cloaca and associated kidney malformations. J Pediatr Urol (2007) 0.84
Primary, nonsyndromic vesicoureteric reflux and nephropathy in sibling pairs: a United Kingdom cohort for a DNA bank. Clin J Am Soc Nephrol (2011) 0.83
Congential obstructive nephropathy gets complicated. Kidney Int (2003) 0.81
Mutation analyses of Uroplakin II in children with renal tract malformations. Nephrol Dial Transplant (2006) 0.81
Generation of mice with a conditional null Fraser syndrome 1 (Fras1) allele. Genesis (2012) 0.81
Cytokeratin 15 marks basal epithelia in developing ureters and is upregulated in a subset of urothelial cell carcinomas. PLoS One (2013) 0.79
Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney disease. Pediatr Nephrol (2015) 0.78
Effects of in utero bladder outflow obstruction on fetal sheep detrusor contractility, compliance and innervation. J Urol (2002) 0.78
Autosomal dominant inheritance of non-syndromic renal hypoplasia and dysplasia: dramatic variation in clinical severity in a single kindred. Nephrol Dial Transplant (2006) 0.78
Angiogenesis and autosomal dominant polycystic kidney disease. Pediatr Nephrol (2012) 0.77
Immunolocalization of cystinosin, the protein defective in cystinosis. J Am Soc Nephrol (2002) 0.77
Similar renal outcomes in children with ADPKD diagnosed by screening or presenting with symptoms. Pediatr Nephrol (2010) 0.76
Radiotelemetered urodynamics of obstructed ovine fetal bladders: correlations with ex vivo cystometry and renal histopathology. BJU Int (2007) 0.76
Expression of Fraser syndrome genes in normal and polycystic murine kidneys. Pediatr Nephrol (2011) 0.76
Renal FMD may not confer a familial hypertensive risk nor is it caused by ACTA2 mutations. Pediatr Nephrol (2011) 0.75
Perinatal renal disease. Semin Fetal Neonatal Med (2007) 0.75
Organ culture of intact metanephric kidneys. Methods Mol Med (2003) 0.75