Congenital progressive hydronephrosis (cph) is caused by an S256L mutation in aquaporin-2 that affects its phosphorylation and apical membrane accumulation-Reference-Cited by-同舟云学术

Congenital progressive hydronephrosis (cph) is caused by an S256L mutation in aquaporin-2 that affects its phosphorylation and apical membrane accumulation

Published:2006-04-25 Issue:18 Volume:103 Page:6952-6957
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

McDill B. W.,Li S.-Z.,Kovach P. A.,Ding L.,Chen F.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference28 articles.

1. Molecular and cellular pathophysiology of obstructive nephropathy

2. Primary, Nonsyndromic Vesicoureteric Reflux and Its Nephropathy Is Genetically Heterogeneous, with a Locus on Chromosome 1

3. Familial Vesicoureteral Reflux

4. Animal models of fetal renal disease

Cited by 120 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Implications of Genetic Factors Underlying Mouse Hydronephrosis: Cautionary Considerations on Phenotypic Interpretation in Genetically Engineered Mice;International Journal of Molecular Sciences;2024-06-29

2. Rab35 Is Required for Embryonic Development and Kidney and Ureter Homeostasis through Regulation of Epithelial Cell Junctions;Journal of the American Society of Nephrology;2024-03-26

3. Aquaporins in Diabetes Insipidus;Advances in Experimental Medicine and Biology;2023

4. Exploratory phosphoproteomics profiling of Aedes aegypti Malpighian tubules during blood meal processing reveals dramatic transition in function;PLOS ONE;2022-07-08

5. Pediatric Obstructive Uropathy;Pediatric Nephrology;2022