Novel perspectives for investigating congenital anomalies of the kidney and urinary tract (CAKUT)
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Title
Novel perspectives for investigating congenital anomalies of the kidney and urinary tract (CAKUT)
Authors
Keywords
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Journal
NEPHROLOGY DIALYSIS TRANSPLANTATION
Volume 26, Issue 12, Pages 3843-3851
Publisher
Oxford University Press (OUP)
Online
2011-11-26
DOI
10.1093/ndt/gfr655
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Note: Only part of the references are listed.- Paper 4: EUROCAT statistical monitoring: Identification and investigation of ten year trends of congenital anomalies in Europe
- (2011) Maria Loane et al. BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
- RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects
- (2011) C. Jeanpierre et al. JOURNAL OF MEDICAL GENETICS
- Long-term risk of chronic kidney disease in unilateral multicystic dysplastic kidney
- (2011) Omer Mansoor et al. PEDIATRIC NEPHROLOGY
- Exome Sequencing Identifies WDR35 Variants Involved in Sensenbrenner Syndrome
- (2010) Christian Gilissen et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Maternal diabetes and renal agenesis/dysgenesis
- (2010) Erin M. Davis et al. BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
- Systematic review of the effectiveness of antenatal intervention for the treatment of congenital lower urinary tract obstruction
- (2010) RK Morris et al. BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY
- Spectrum of HNF1B Mutations in a Large Cohort of Patients Who Harbor Renal Diseases
- (2010) L. Heidet et al. Clinical Journal of the American Society of Nephrology
- Effect of Drugs on Renal Development
- (2010) M. F. Schreuder et al. Clinical Journal of the American Society of Nephrology
- Genomic characterization of Wilms' tumor suppressor 1 targets in nephron progenitor cells during kidney development
- (2010) S. Hartwig et al. DEVELOPMENT
- Massively parallel sequencing of ataxia genes after array-based enrichment
- (2010) Alexander Hoischen et al. HUMAN MUTATION
- Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract
- (2010) Stefania Gimelli et al. HUMAN MUTATION
- Early recognition and prevention of chronic kidney disease
- (2010) Matthew T James et al. LANCET
- Genetic kidney diseases
- (2010) Friedhelm Hildebrandt LANCET
- Cardiovascular risk in the peritoneal dialysis patient
- (2010) Raymond T. Krediet et al. Nature Reviews Nephrology
- Mapping candidate regions and genes for congenital anomalies of the kidneys and urinary tract (CAKUT) by array-based comparative genomic hybridization
- (2010) Stefanie Weber et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- HNF1B alterations associated with congenital anomalies of the kidney and urinary tract
- (2010) Makiko Nakayama et al. PEDIATRIC NEPHROLOGY
- Molecular anatomy of the kidney: what have we learned from gene expression and functional genomics?
- (2010) Bree Rumballe et al. PEDIATRIC NEPHROLOGY
- Sequencing of 50 Human Exomes Reveals Adaptation to High Altitude
- (2010) X. Yi et al. SCIENCE
- Methods for Genomic Partitioning
- (2009) Emily H. Turner et al. Annual Review of Genomics and Human Genetics
- Plumbing in the embryo: developmental defects of the urinary tracts
- (2009) N Uetani et al. CLINICAL GENETICS
- Mapping of the fate of cell lineages generated from cells that express the Wnt4 gene by time-lapse during kidney development☆
- (2009) Jingdong Shan et al. DIFFERENTIATION
- Whole-Genome Linkage and Association Scan in Primary, Nonsyndromic Vesicoureteric Reflux
- (2009) H. J. Cordell et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- A Recessive Gene for Primary Vesicoureteral Reflux Maps to Chromosome 12p11-q13
- (2009) P. L. Weng et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Children’s toxicology from bench to bed - Drug-induced Renal Injury (1): The toxic effects of ARB/ACEI on fetal kidney development
- (2009) Takashi Sekine et al. JOURNAL OF TOXICOLOGICAL SCIENCES
- Renal outcome in patients with congenital anomalies of the kidney and urinary tract
- (2009) Simone Sanna-Cherchi et al. KIDNEY INTERNATIONAL
- Dissociation of embryonic kidneys followed by reaggregation allows the formation of renal tissues
- (2009) Mathieu Unbekandt et al. KIDNEY INTERNATIONAL
- ChIP-seq accurately predicts tissue-specific activity of enhancers
- (2009) Axel Visel et al. NATURE
- Mapping of a new locus for congenital anomalies of the kidney and urinary tract on chromosome 8q24
- (2009) S. Ashraf et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Absence of mutations in the HOXA11 and HOXD11 genes in children with congenital renal malformations
- (2009) Ioanna Bouba et al. PEDIATRIC NEPHROLOGY
- Renal Aplasia in Humans Is Associated with RET Mutations
- (2008) Michael A. Skinner et al. AMERICAN JOURNAL OF HUMAN GENETICS
- ROBO2 Gene Variants Are Associated with Familial Vesicoureteral Reflux
- (2008) A. M. Bertoli-Avella et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- SIX2 and BMP4 Mutations Associate With Anomalous Kidney Development
- (2008) S. Weber et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Mutation analysis of the Uromodulin gene in 96 individuals with urinary tract anomalies (CAKUT)
- (2008) Matthias T. F. Wolf et al. PEDIATRIC NEPHROLOGY
- Management and etiology of the unilateral multicystic dysplastic kidney: a review
- (2008) David S. Hains et al. PEDIATRIC NEPHROLOGY
- Renal tract malformations: perspectives for nephrologists
- (2008) Larissa Kerecuk et al. Nature clinical practice. Nephrology
- Dysplastic kidneys
- (2007) Paul Winyard et al. Seminars in Fetal & Neonatal Medicine
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