Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like protein

von van Wijk, Erwin, Kersten, Ferry F.J., Kartono, Aileen, Mans, Dorus A., Brandwijk, Kim, Letteboer, Stef J.F., Peters, Theo A., Märker, Tina, Yan, Xiumin, Cremers, Cor W.R.J., Cremers, Frans P.M., Wolfrum, Uwe, Roepman, Ronald, Kremer, Hannie
Veröffentlicht 2009

Cathepsin B as a potential cystatin M/E target in the mouse hair follicle

von Oortveld, Merel A. W., van Vlijmen-Willems, Ivonne M. J. J., Kersten, Ferry F. J., Cheng, Tsing, Verdoes, Martijn, van Erp, Piet E. J., Verbeek, Sjef, Reinheckel, Thomas, Hendriks, Wiljan J. A. J., Schalkwijk, Joost, Zeeuwen, Patrick L. J. M.
Veröffentlicht in FASEB J (2017)

Renal Ca(2+) wasting, hyperabsorption, and reduced bone thickness in mice lacking TRPV5

von Hoenderop, Joost G.J., van Leeuwen, Johannes P.T.M., van der Eerden, Bram C.J., Kersten, Ferry F.J., van derKemp, Annemiete W.C.M., Mérillat, Anne-Marie, Waarsing, Jan H., Rossier, Bernard C., Vallon, Volker, Hummler, Edith, Bindels, René J.M.
Veröffentlicht 2003