Congenital anomalies of the kidney and urinary tract: a genetic disorder?
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Integrin alpha 8 recessive mutations are responsible for bilateral renal agenesis in humansMulti-modality imaging review of congenital abnormalities of kidney and upper urinary tractSingle-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humansRenal progenitors: Roles in kidney disease and regenerationThe prevalence and epidemiology of genetic renal disease amongst adults with chronic kidney disease in Australia.Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract.Congenital Anomalies of the Kidney and the Urinary Tract (CAKUT)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).Incidence and Risks of Congenital Anomalies of Kidney and Urinary Tract in Newborns: A Population-Based Case-Control Study in TaiwanGenetic Basis of Ureterocele.Estimation of the relationship between the polymorphisms of selected genes: ACE, AGTR1, TGFβ1 and GNB3 with the occurrence of primary vesicoureteral reflux.Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association.MicroRNAs: potential regulators of renal development genes that contribute to CAKUT.Ectopic liver tissue in the kidney: case report and literature review.Congenital anomalies of the kidney and urinary tract: an embryogenetic review.Transcriptome-wide based identification of miRs in congenital anomalies of the kidney and urinary tract (CAKUT) in children: the significant upregulation of tissue miR-144 expression.Whole exome sequencing: a state-of-the-art approach for defining (and exploring!) genetic landscapes in pediatric nephrology.Genetics of Congenital Anomalies of the Kidney and Urinary Tract: The Current State of Play.Genetics of vesicoureteral reflux and congenital anomalies of the kidney and urinary tract.Fetal anomalies associated with HNF1B mutations: report of 20 autopsy cases.AT2 R deficiency mediated podocyte loss via activation of ectopic hedgehog interacting protein (Hhip) gene expression.Copy-number variation associated with congenital anomalies of the kidney and urinary tract.Renal complications in 6p duplication syndrome: microarray-based investigation of the candidate gene(s) for the development of congenital anomalies of the kidney and urinary tract (CAKUT) and focal segmental glomerular sclerosis (FSGS).Association of angiotensin type 2 receptor gene polymorphisms with ureteropelvic junction obstruction in Brazilian patientsPAX2 polymorphisms and congenital abnormalities of the kidney and urinary tract in a Brazilian pediatric population: evidence for a role in vesicoureteral refluxPlanar Cell Polarity Pathway in Kidney Development and Function
P2860
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P2860
Congenital anomalies of the kidney and urinary tract: a genetic disorder?
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Congenital anomalies of the kidney and urinary tract: a genetic disorder?
@ast
Congenital anomalies of the kidney and urinary tract: a genetic disorder?
@en
type
label
Congenital anomalies of the kidney and urinary tract: a genetic disorder?
@ast
Congenital anomalies of the kidney and urinary tract: a genetic disorder?
@en
prefLabel
Congenital anomalies of the kidney and urinary tract: a genetic disorder?
@ast
Congenital anomalies of the kidney and urinary tract: a genetic disorder?
@en
P2860
P356
P1476
Congenital anomalies of the kidney and urinary tract: a genetic disorder?
@en
P2093
Ihor V Yosypiv
P2860
P304
P356
10.1155/2012/909083
P577
2012-05-20T00:00:00Z