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First published online March 15, 2004
doi: 10.1242/10.1242/dev.01089
Review |

Departments of Pediatrics, Medicine, and Cellular and Molecular Medicine, University of California, San Diego, CA 92093-0693, USA
Author for correspondence (e-mail:
snigam{at}ucsd.edu)
SUMMARY
Branching morphogenesis in the kidney is a tightly regulated, complex process and its disruption potentially can lead to a broad spectrum of diseases, ranging from rare hereditary syndromes to common conditions such as hypertension and chronic kidney failure. This review synthesizes data on branching during kidney development derived from in vitro and in vivo rodent studies and to apply them to human diseases. It discusses how the broad organization of molecular interactions during kidney development might provide a mechanistic framework for understanding disorders related to aberrant branching.
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