HNF1B alterations associated with congenital anomalies of the kidney and urinary tract-Reference-Cited by-同舟云学术

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HNF1B alterations associated with congenital anomalies of the kidney and urinary tract

Published:2010-02-13 Issue:6 Volume:25 Page:1073-1079
ISSN:0931-041X
Container-title:Pediatric Nephrology
language:en
Short-container-title:Pediatr Nephrol

Author:

Nakayama Makiko,Nozu Kandai,Goto Yuki,Kamei Koichi,Ito Shuichi,Sato Hidenori,Emi Mitsuru,Nakanishi Koichi,Tsuchiya Shigeru,Iijima Kazumoto

Publisher

Springer Science and Business Media LLC

Subject

Nephrology,Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00467-010-1454-9.pdf

Reference32 articles.

1. Pope JC 4th, Brock JW 3rd, Adams MC, Stephens FD, Ichikawa I (1999) How they begin and how they end: classic and new theories for the development and deterioration of congenital anomalies of the kidney and urinary tract, CAKUT. J Am Soc Nephrol 10:2018–2028

2. Woolf AS (2000) A molecular and genetic view of human renal and urinary tract malformations. Kidney Int 58:500–512

3. Nakanishi K, Yoshikawa N (2003) Genetic disorders of human congenital anomalies of the kidney and urinary tract (CAKUT). Pediatr Int 45:610–616

4. Schedl A (2007) Renal abnormalities and their developmental origin. Nat Rev Genet 8:791–802

5. Cereghini S (1996) Liver-enriched transcription factors and hepatocyte differentiation. FASEB J 10:267–282

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