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Seminars in Cell and Developmental Biology, ISSN 1084-9521, 07/2019, Volume 91, pp. 104 - 110
Congenital abnormalities of the kidney and urinary tract (CAKUT) form the leading cause of pediatric end-stage renal disease. Knowledge on the molecular... 
Kidney disease | Genetics | CAKUT | Etiology | Next generation sequencing | URINARY-TRACT MALFORMATIONS | RENAL ABNORMALITIES | CANDIDATE GENES | KIDNEY DEVELOPMENT | DEVELOPMENTAL BIOLOGY | MICE LACKING | CHILDREN | CELL BIOLOGY | RENIN-ANGIOTENSIN SYSTEM | MONOGENIC CONGENITAL-ANOMALIES | DISEASE | MUTATIONS | Chronic kidney failure | Development and progression
Journal Article
Kidney International, ISSN 0085-2538, 05/2018, Volume 93, Issue 5, pp. 1142 - 1153
Congenital abnormalities of the kidney and the urinary tract (CAKUT) belong to the most common birth defects in human, but the molecular basis for the majority... 
nephron | kidney induction | Sox11 | CAKUT | duplex kidneys | RET | CELLS | MOUSE | BRANCHING MORPHOGENESIS | CRYPTORCHIDISM | MAMMALIAN KIDNEY | RENAL DEVELOPMENT | BUD | TRANSCRIPTION FACTOR SOX11 | UROLOGY & NEPHROLOGY | DIFFERENTIATION | Vesico-Ureteral Reflux - genetics | Cell Proliferation | Cadherins - metabolism | Humans | Male | Morphogenesis | Glial Cell Line-Derived Neurotrophic Factor - metabolism | Kidney - metabolism | Gene Expression Regulation, Developmental | Female | Urogenital Abnormalities - metabolism | Vesico-Ureteral Reflux - metabolism | Cadherins - genetics | SOXC Transcription Factors - deficiency | Ureter - metabolism | Disease Models, Animal | Genetic Predisposition to Disease | SOXC Transcription Factors - genetics | Genetic Association Studies | Ureter - abnormalities | Risk Factors | Glial Cell Line-Derived Neurotrophic Factor - genetics | Mice, Knockout | Phenotype | Urogenital Abnormalities - pathology | Animals | Kidney - abnormalities | Vesico-Ureteral Reflux - pathology | Mutation | Urogenital Abnormalities - genetics | Glial cell line-derived neurotrophic factor | Congenital diseases | Kidneys | Mesenchyme | Congenital defects | Genes | Whites | Urinary tract | Kinases | Embryos | Defects | Clonal deletion | Developmental stages | Protocadherin | Gene disruption | Urogenital system
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 07/2017, Volume 54, Issue 7, pp. 502 - 510
Journal Article