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The Journal of Biological Chemistry|April 14, 1995
Water channel properties of major intrinsic protein of lensS M Mulders, G M Preston, P M Deen, et al.
The American Journal of Physiology|October 10, 1997
Importance of the mercury-sensitive cysteine on function and routing of AQP1 and AQP2 in oocytesS M Mulders, J P Rijss, A Hartog, et al.
Journal of the American Society of Nephrology : JASN|October 23, 1997
Aquaporin-2 transfection of Madin-Darby canine kidney cells reconstitutes vasopressin-regulated transcellular osmotic water transportP M Deen, J P Rijss, S M Mulders, et al.
Endocrinology|September 8, 2011
Prevention of the onset of ovarian hyperstimulation syndrome (OHSS) in the rat after ovulation induction with a low molecular weight agonist of the LH receptor compared with hCG and rec-LHRuud van de Lagemaat, B C Raafs, C van Koppen, et al.
The Journal of Biological Chemistry|March 25, 1994
GP-3, a newly characterized glycoprotein on the inner surface of the zymogen granule membrane, undergoes regulated secretionA C Wagner, M J Wishart, S M Mulders, et al.
Pflugers Archiv : European Journal of Physiology|July 31, 1998
The exchange of functional domains among aquaporins with different transport characteristicsS M Mulders, A J van der Kemp, S A Terlouw, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Localization of the human gene for aquaporin 3 (AQP3) to chromosome 9, region p21-->p12, using fluorescent in situ hybridizationS M Mulders, D Olde Weghuis, J A van Boxtel, et al.
Reproduction (Cambridge, England)|September 21, 2011
Contraception by induction of luteinized unruptured follicles with short-acting low molecular weight FSH receptor agonists in female animal modelsR van de Lagemaat, C J van Koppen, M A M Krajnc-Franken, et al.
Journal of the American Society of Nephrology : JASN|February 1, 1997
New mutations in the AQP2 gene in nephrogenic diabetes insipidus resulting in functional but misrouted water channelsS M Mulders, N V Knoers, A F Van Lieburg, et al.
The Journal of Clinical Investigation|July 3, 1998
An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complexS M Mulders, D G Bichet, J P Rijss, et al.
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