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Featured researches published by C.H. van Os.


European Journal of Clinical Investigation | 1996

Physiology and pathophysiology of aquaporins

S.M. Mulders; A.F. van Lieburg; L.A.H. Monnens; N.V.A.M. Knoers; P.M.T. Deen; C.H. van Os

The biophysical properties of water-filled pores in biological membranes have been studied for decades, and this has cumulated in an accurate description of water channel properties [1]. In spite of all this knowledge, the molecular identification of water channels resulted from a serendipitous discovery. Denker et al. [2] copurified a 28-kD protein together with a 32-kD Rhesus antigen from human red blood cells, and this discovery led to the cloning of the first molecular water channel, CHIP28 [3]. CHIP28 appeared to be a member of the major intrinsic protein (MIP) family of intrinsic membrane proteins, named after the first cloned protein of this family, the major intrinsic protein of lens fibre cells [4]. The molecular fingerprint of MIP family members consists of two repeats, presumably the result of an ancient gene duplication event [5]. Each repeat is characterized by a very conserved region in which an NPA box (asparagine–proline–alanine) is unchanged from bacteria to mammals (Fig.1). Owing to this property, new family members were discovered by homology cloning using reverse transcription–polymerase chain reaction (RT–PCR) and primers corresponding to these conserved sequences [6–12]. It is now clear that genes coding for MIP proteins are ubiquitous in nature. For the functional characterization of water channels, theXenopus oocyte expression system has played a dominant role, merely because the osmotic swelling test of oocytes expressing water channels is of appealing simplicity. For MIP family members that were proven to be water selective, a new more appropriate name was chosen and since then water channels discovered in mammalian tissues have been rebaptized as aquaporins 0 to 5, in the rank order of their discovery [13]. In this review, we will focus on publications that appeared in 1994 and 1995 and we restrict ourselves to mam-malian aquaporins. A number of excellent reviews on water channels have recently been published, reflecting the excitement which surrounds the discovery of aquaporins and their role in water homeostasis of the body [14–17].


Science | 1994

Requirement of human renal water channel aquaporin-2 for vasopressin-dependent concentration of urine

Peter M. T. Deen; Marian Verdijk; N.V.A.M. Knoers; B. Wieringa; L.A.H. Monnens; C.H. van Os; Ba van Oost


Journal of Biological Chemistry | 1995

Water channel properties of major intrinsic protein of lens

S.M. Mulders; Gregory M. Preston; Peter M. T. Deen; William B. Guggino; C.H. van Os; Peter Agre


Journal of The American Society of Nephrology | 1997

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

S.M. Mulders; N.V.A.M. Knoers; A.F. van Lieburg; L.A.H. Monnens; E.P. Leumann; E. Wühl; E. Schober; J.P.L. Rijss; C.H. van Os; P.M.T. Deen


Journal of The American Society of Nephrology | 1997

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

P.M.T. Deen; J.P.L. Rijss; S.M. Mulders; R. J. Errington; J. van Baal; C.H. van Os


Science | 1997

Aquaporins and ion conductance.

Peter Agre; Myungken Lee; S. Devidas; William B. Guggino; Sei Sasaki; Shinichi Uchida; Michio Kuwahara; Kiyohide Fushimi; Fumiaki Marumo; A. S. Verkman; B. Yang; Peter M. T. Deen; S.M. Mulders; S.M. Kansen; C.H. van Os; Jorge Fischbarg; K. Kuang; J. Li; P. Iserovich; Q. Wen; R. V. Patil; Z. Han; M. B. Wax; J. W. Regan; W. D. Stamer; Andrea J. Yool


Journal of The American Society of Nephrology | 1998

Glycosylation is not essential for vasopressin-dependent routing of aquaporin-2 in transfected Madin-Darby canine kidney cells.

Ruben Baumgarten; M. H. J. Van De Pol; Jack F.M. Wetzels; C.H. van Os; P.M.T. Deen


American Journal of Physiology-renal Physiology | 1999

Hormone-stimulated Ca2+transport in rabbit kidney: multiple sites of inhibition by exogenous ATP

J. van Baal; Joost G. J. Hoenderop; M.R. Groenendijk; C.H. van Os; R.J.M. Bindels; Peter H. G. M. Willems


Science | 1997

Technical comments. Aquaporins and ion conductance

P.M.T. Deen; S.M. Mulders; S.M. Kansen; C.H. van Os


Journal of The American Society of Nephrology | 1997

Glycosylation of aquaporin-2 is not essential for routing and functioning in mammalian cells

Ruben Baumgarten; Jack F.M. Wetzels; C.H. van Os; P.M.T. Deen

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A.F. van Lieburg

Radboud University Nijmegen

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L.A.H. Monnens

Radboud University Nijmegen

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S.M. Mulders

Radboud University Nijmegen

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J.P.L. Rijss

Radboud University Nijmegen

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R.J.M. Bindels

Radboud University Nijmegen

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B.A. van Oost

The Catholic University of America

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J. van Baal

Radboud University Nijmegen

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Jack F.M. Wetzels

Radboud University Nijmegen

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Peter M. T. Deen

Radboud University Nijmegen

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