Aquaporin1–3 expression in normal and hydronephrotic kidneys in the human fetus-Reference-Cited by-同舟云学术

Aquaporin1–3 expression in normal and hydronephrotic kidneys in the human fetus

Published:2019-07-01 Issue:5 Volume:86 Page:595-602
ISSN:0031-3998
Container-title:Pediatric Research
language:en
Short-container-title:Pediatr Res

Author:

Feng Jinjin,Yan Shaohua,Chen Yan,Han Liping,Wen Lu,Guo Xi,Wen Yibo,Li Yunlong,He Xiangfei,Han Zhongjiang,Ren Chuanchuan,Jia Zhiming,Guo Zhan,Zhai Rongqun,Wu Junwei,Wen Jianguo

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Link

http://www.nature.com/articles/s41390-019-0485-6.pdf

Reference35 articles.

1. Shimada, K. et al. Urological emergency in neonates with congential hydronephrosis. Int. J. Urol. 14, 388–392 (2007).

2. Chevalier, R. L. Molecular and cellular pathophysiology of obstructive nephropathy. Pediatr. Nephrol. 13, 612–619 (1999).

3. McDill, BradleyW. et al. Congenital progressive hydronephrosis (cph) is caused by an S256L mutation in aquaporin-2 that affects its phosphorylation and apical membrane accumulation. Proc. Natl. Acad. Sci. USA 103, 6952–6957 (2006).

4. Ardissino, G. et al. Epidemiology of chronic renal failure in children: data from the ItalKid project. Pediatrics 111, e382–e387 (2003).

5. Wen, J. G. et al. Expression of renal aquaporins is down-regulated in children with congenital hydronephrosis. Scand. J. Urol. Nephrol. 43, 486–493 (2009).

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