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

Tekijä 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
Julkaistu 2009

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

Tekijä 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.
Julkaisussa FASEB J (2017)

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

Tekijä 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.
Julkaistu 2003