J.P.L. Rijss

An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complex.

S.M. Mulders, Daniel G. Bichet, J.P.L. Rijss et al. · Journal of Clinical Investigation · 1998 · 260 citations · Full text

Biology, Molecular Physiology, Signal Transduction +14

An impaired routing of wild-type aquaporin-2 after tetramerization with an aquaporin-2 mutant explains dominant nephrogenic diabetes insipidus

Erik-Jan Kamsteeg, Thera A.M. Wormhoudt, J.P.L. Rijss et al. · The EMBO Journal · 1999 · 208 citations · Full text

Biology, Natural Sciences, Aquaporin-2 Mutant +6

The human AQP4 gene: definition of the locus encoding two water channel polypeptides in brain.

Meiling Lü, M D Lee, Bradley Smith et al. · Proceedings of the National Academy of Sciences · 1996 · 198 citations · Full text

New mutations in the AQP2 gene in nephrogenic diabetes insipidus resulting in functional but misrouted water channels.

S.M. Mulders, Nine V.A.M. Knoers, A.F. van Lieburg et al. · Journal of the American Society of Nephrology · 1997 · 175 citations

Protein Secretion, Genetics, Molecular Biology +19

Aquaporin-2 transfection of Madin-Darby canine kidney cells reconstitutes vasopressin-regulated transcellular osmotic water transport.

Peter M.T. Deen, J.P.L. Rijss, S.M. Mulders et al. · Journal of the American Society of Nephrology · 1997 · 109 citations · Full text

Cytoskeleton, Ddavp Admission, Cellular Physiology +18