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Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tractSIX2 and BMP4 mutations associate with anomalous kidney developmentThe Good and Bad of β-Catenin in Kidney Development and Renal DysplasiaPediatric febrile urinary tract infections: the current state of playAntennas of organ morphogenesis: the roles of cilia in vertebrate kidney developmentGenome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental diseaseSusceptibility to metanephric apoptosis in bradykinin B2 receptor null mice via the p53-Bax pathwayThe ureteric bud epithelium: morphogenesis and roles in metanephric kidney patterning.Chronic unilateral ureteral obstruction in the neonatal mouse delays maturation of both kidneys and leads to late formation of atubular glomeruliAngiotensin II AT2 receptor regulates ureteric bud morphogenesis.Autophagy is a component of epithelial cell fate in obstructive uropathy.Renal malformations associated with mutations of developmental genes: messages from the clinic.Genome-wide analysis of gestational gene-environment interactions in the developing kidneyA retrotransposon insertion in the 5' regulatory domain of Ptf1a results in ectopic gene expression and multiple congenital defects in Danforth's short tail mouse.Ciliopathies: an expanding disease spectrum.Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33Matrilysin (MMP-7) inhibition of BMP-7 induced renal tubular branching morphogenesis suggests a role in the pathogenesis of human renal dysplasia.How have the past 5 years of research changed clinical practice in paediatric nephrology?Mutations of HNF-1beta inhibit epithelial morphogenesis through dysregulation of SOCS-3.Polycystin-2 immunolocalization and function in zebrafishTranscriptional control of terminal nephron differentiation.Fetal development of regulatory mechanisms for body fluid homeostasis.Cystic renal disease in the domestic ferret.Histochemical analysis of renal dysplasia with ureteral atresia.Unilateral multicystic dysplastic kidney: a meta-analysis of observational studies on the incidence, associated urinary tract malformations and the contralateral kidney.Inactivation of Notch signaling in the renal collecting duct causes nephrogenic diabetes insipidus in mice.Genetics of renal hypoplasia: insights into the mechanisms controlling nephron endowment.Postnatal management of congenital bilateral renal hypodysplasia.Pediatric magnetic resonance urography.Congenital anomalies of the kidney and urinary tract genetics in mice and men.Renal dysplasia in the neonateGenetics of Congenital Anomalies of the Kidney and Urinary Tract: The Current State of Play.Diagnostic accuracy of mid-trimester antenatal ultrasound for multicystic dysplastic kidneys.Fluid mechanics as a driver of tissue-scale mechanical signaling in organogenesis.Downregulation of Spry-1, an inhibitor of GDNF/Ret, causes angiotensin II-induced ureteric bud branching.Microarray interrogation of human metanephric mesenchymal cells highlights potentially important molecules in vivo.Genetics of kidney development: pathogenesis of renal anomalies.Beta-catenin is necessary to keep cells of ureteric bud/Wolffian duct epithelium in a precursor state.Esrrg functions in early branch generation of the ureteric bud and is essential for normal development of the renal papilla.Long-term risk of chronic kidney disease in unilateral multicystic dysplastic kidney.
P2860
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P2860
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Evolving concepts in human renal dysplasia.
@ast
Evolving concepts in human renal dysplasia.
@en
type
label
Evolving concepts in human renal dysplasia.
@ast
Evolving concepts in human renal dysplasia.
@en
prefLabel
Evolving concepts in human renal dysplasia.
@ast
Evolving concepts in human renal dysplasia.
@en
P50
P1476
Evolving concepts in human renal dysplasia.
@en
P2093
Paul J D Winyard
P304
P356
10.1097/01.ASN.0000113778.06598.6F
P577
2004-04-01T00:00:00Z