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Full Text	Issue Date	Title	Author(s)
	2011	New patches in the molecular understanding of renal magnesium handling	Wijst, J.A.J. van der
	2010	Effects of the EGFR Inhibitor Erlotinib on Magnesium Handling.	Dimke, H.; Wijst, J.A.J. van der; Alexander, T.; Meijer, I.M.J.; Mulder, G.M.; Goor, H. van; Tejpar, S.; Hoenderop, J.G.J.; Bindels, R.J.M.
	2010	Methionine sulfoxide reductase B1 (MsrB1) recovers TRPM6 channel activity during oxidative stress.	Cao, G.; Lee, K.P.; Wijst, J.A.J. van der; Graaf, M. van der; Kemp, A. van der; Bindels, R.J.M.; Hoenderop, J.G.J.
	2010	Functional analysis of the Kv1.1 N255D mutation associated with autosomal dominant hypomagnesemia.	Wijst, J.A.J. van der; Glaudemans, B.; Venselaar, H.; Nair, A.V.; Forst, A.L.; Hoenderop, J.G.J.; Bindels, R.J.M.
	2010	Targeted next-generation sequencing of a 12.5 Mb homozygous region reveals ANO10 mutations in patients with autosomal-recessive cerebellar ataxia.	Vermeer, S.; Hoischen, A.; Meijer, R.P.; Gilissen, C.F.H.A.; Neveling, K.; Wieskamp, N.A.W.; Brouwer, A.; Koenig, M.; Anheim, M.; Assoum, M.; Drouot, N.; Todorovic, S.; Milic-Rasic, V.; Lochmuller, H.; Stevanin, G.; Goizet, C.; David, A.; Durr, A.; Brice, A.; Kremer, B.; Warrenburg, B.P.C. van de; Schijvenaars, M.M.V.A.P.; Heister, A.; Kwint, M.P.; Arts, P.J.W.; Wijst, J.A.J. van der; Veltman, J.; Kamsteeg, E.J.; Scheffer, H.; Knoers, N.V.A.M.
	2009	Epithelial Mg2+ channel TRPM6: insight into the molecular regulation.	Wijst, J.A.J. van der; Hoenderop, J.G.J.; Bindels, R.J.M.
	2009	Rare but relevant kidney disorders.	Grünveld, J.P; Scholl, U.; Choi, M.; Liu, T.; Ramaekers, V.; Häusler, M.; Grimmer, J.; Tobe, S.; Fahri, A.; Nelson-Williams, C.; Lifton, R.P.; Bockenhauer, D.; Feather, S.; Stanescu, H.; Bandulik, S.; Zdebik, A.; Reichold, M.; Tobin, J.; Lieberer, E.; Sterner, C.; Landoure, G.; Arora, R.; Sirimanna, T.; Thompson, D.; Cross, J.; Hof, W. van 't; Al Masri, O.; Tullus, K.; Yeung, S.; Anikster, Y.; Klootwijk, E.D.; Hubank, M.; Dillon, M.; Heitzmann, D.; Arcos-Burgos, M.; Knepper, M.A.; Dobbie, A.; Gahl, W.A.; Warth, R.; Sheridan, E.; Kleta, R.; Glaudemans, B.; Wijst, J.A.J. van der; Scola, R.H.; Lorenzoni, P.J.; Heister, J.G.A.M.; Kemp, J.W.C.M. van der; Knoers, N.V.A.M.; Hoenderop, J.G.J.; Bindels, R.J.M.; Bommel, E. van; Jansen, I.J.; Hendriksz, T.; Aarnoudse, A.; Scheel, P.; Feeley, N.; Delvaeye, M.; Noris, M.; Vriese, A. de; Esmon, C.; Esmon, N.; Ferrell, G.; Del-Favero, J.; Plaisance, S.; Claes, B.; Lambrechts, D.; Remuzzi, G.; Conway, E.
	2009	A missense mutation in the Kv1.1 voltage-gated potassium channel-encoding gene KCNA1 is linked to human autosomal dominant hypomagnesemia.	Glaudemans, B.; Wijst, J.A.J. van der; Scola, R.H.; Lorenzoni, P.J.; Heister, J.G.A.M.; Kemp, J.W.C.M. van der; Slobbe-Knoers, V.V.A.M.; Hoenderop, J.G.J.; Bindels, R.J.M.
	2009	Regulation of the epithelial Mg2+ channel TRPM6 by estrogen and the associated repressor protein of estrogen receptor activity (REA).	Cao, G.; Wijst, J.A.J. van der; Kemp, A. van der; Zeeland, F. van; Bindels, R.J.M.; Hoenderop, J.G.J.
	2007	Impaired basolateral sorting of pro-EGF causes isolated recessive renal hypomagnesemia.	Groenestege, W.M.; Thebault, S.C.; Wijst, J.A.J. van der; Berg, D. Van den; Janssen, R.; Tejpar, S.; Heuvel, L.P.W.J. van den; Cutsem, E. van; Hoenderop, J.G.J.; Knoers, N.V.A.M.; Bindels, R.J.M.

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