Pathogenesis of nephrogenic diabetes insipidus by aquaporin-2 C-terminus mutations
- 1 July 2003
- journal article
- Published by Elsevier in Kidney International
- Vol. 64 (1) , 2-10
- https://doi.org/10.1046/j.1523-1755.2003.00049.x
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Heteroligomerization of an Aquaporin-2 mutant with wild-type Aquaporin-2 and their misrouting to late endosomes/lysosomes explains dominant nephrogenic diabetes insipidus.Human Molecular Genetics, 2002
- Aquaporins in the Kidney: From Molecules to MedicinePhysiological Reviews, 2002
- Three Families with Autosomal Dominant Nephrogenic Diabetes Insipidus Caused by Aquaporin-2 Mutations in the C-TerminusAmerican Journal of Human Genetics, 2001
- Nephrogenic Diabetes InsipidusAnnual Review of Physiology, 2001
- Multicolour imaging of post-Golgi sorting and trafficking in live cellsNature Cell Biology, 2001
- An impaired routing of wild-type aquaporin-2 after tetramerization with an aquaporin-2 mutant explains dominant nephrogenic diabetes insipidusThe EMBO Journal, 1999
- An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complex.Journal of Clinical Investigation, 1998
- Requirement of Human Renal Water Channel Aquaporin-2 for Vasopressin-dependent Concentration of UrineScience, 1994
- Cloning and expression of apical membrane water channel of rat kidney collecting tubuleNature, 1993
- Transport and metabolic functions in cultured renal tubule cellsKidney International, 1986