| Literature DB >> 20421843 |
Jason E Cain1, Valeria Di Giovanni, Joanna Smeeton, Norman D Rosenblum.
Abstract
Renal hypoplasia, defined as abnormally small kidneys with normal morphology and reduced nephron number, is a common cause of pediatric renal failure and adult-onset disease. Genetic studies performed in humans and mutant mice have implicated a number of critical genes, in utero environmental factors and molecular mechanisms that regulate nephron endowment and kidney size. Here, we review current knowledge regarding the genetic contributions to renal hypoplasia with particular emphasis on the mechanisms that control nephron endowment in humans and mice.Entities:
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Year: 2010 PMID: 20421843 DOI: 10.1203/PDR.0b013e3181e35a88
Source DB: PubMed Journal: Pediatr Res ISSN: 0031-3998 Impact factor: 3.756