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

Por 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
Publicado em 2009

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

Por 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.
Publicado no FASEB J (2017)

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

Por 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.
Publicado em 2003