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Full Text	Issue Date	Title	Author(s)
	2011	Myotonic dystrophy type 2 (DM2) and related disorders report of the 180th ENMC workshop including guidelines on diagnostics and management 3-5 December 2010, Naarden, The Netherlands.	Udd, B.; Meola, G.; Krahe, R.; Wansink, D.G.; Bassez, G.; Kress, W.; Schoser, B.; Moxley, R.
	2011	The mouse mismatch repair protein, MSH3, is a nucleoplasmic protein that aggregates into denser nuclear bodies under conditions of stress.	Holt, I.; Thanh Lam, L.; Tome, S.; Wansink, D.G.; Riele, H. te; Gourdon, G.; Morris, G.E.
	2011	Abnormal actomyosin assembly in proliferating and differentiating myoblasts upon expression of a cytosolic DMPK isoform	Mulders, S.A.M.; Horssen, R. van; Gerrits, L.; Bennink, M.B.; Pluk, W.L.L.P.; Boer-van Huizen, R.T. de; Croes, H.J.E.; Wijers, M.J.P.; Loo, F.A. van de; Fransen, J.; Wieringa, B.; Wansink, D.G.
	2010	Molecular therapy in myotonic dystrophy: focus on RNA gain-of-function.	Mulders, S.A.M.; Engelen, B.G.M. van; Wieringa, B.; Wansink, D.G.
	2009	DMPK protein isoforms are differentially expressed in myogenic and neural cell lineages.	Oude Ophuis, R.J.A.; Mulders, S.A.M.; Herpen, R.E.M.A. van; Vorstenbosch, R.A. van de; Wieringa, B.; Wansink, D.G.
	2009	Triplet-repeat oligonucleotide-mediated reversal of RNA toxicity in myotonic dystrophy.	Mulders, S.A.M.; Broek, W.J.A.A. van den; Wheeler, T.M.; Croes, H.J.E.; Kuik-Romeijn, P. van; Kimpe, S.J. de; Furling, D.; Platenburg, G.J.; Gourdon, G.; Thornton, C.A.; Wieringa, B.; Wansink, D.G.
	2009	A tail-anchored myotonic dystrophy protein kinase isoform induces perinuclear clustering of mitochondria, autophagy, and apoptosis.	Oude Ophuis, R.J.A.; Wijers-Rouw, M.J.P.; Bennink, M.B.; Loo, F.A.J. van de; Fransen, J.; Wieringa, B.; Wansink, D.G.
	2007	Somatic CTG*CAG repeat instability in a mouse model for myotonic dystrophy type 1 is associated with changes in cell nuclearity and DNA ploidy.	Broek, W.J.A.A. van den; Wansink, D.G.; Wieringa, B.
	2007	Chromosome-wide nucleosome replacement and H3.3 incorporation during mammalian meiotic sex chromosome inactivation.	Heijden, G.W. van der; Derijck, A.H.A.; Posfai, E.; Giele, M.M.; Pelczar, P.; Ramos, L.; Wansink, D.G.; Vlag, J. van der; Peters, A.H.; Boer, P. de
	2006	Fen1 does not control somatic hypermutability of the (CTG)(n)*(CAG)(n) repeat in a knock-in mouse model for DM1.	Broek, W.J.A.A. van den; Nelen, M.R.; Heijden, G.W. van der; Wansink, D.G.; Wieringa, B.
	2006	Coiled-coil interactions modulate multimerization, mitochondrial binding and kinase activity of myotonic dystrophy protein kinase splice isoforms.	Herpen, R.E.M.A. van; Tjeertes, J.V.; Mulders, S.A.M.; Oude Ophuis, R.J.A.; Wieringa, B.; Wansink, D.G.
	2005	Divergent mitochondrial and endoplasmic reticulum association of DMPK splice isoforms depends on unique sequence arrangements in tail anchors.	Herpen, R.E.M.A. van; Oude Ophuis, R.J.A.; Wijers-Rouw, M.J.P.; Bennink, M.B.; Loo, F.A.J. van de; Fransen, J.; Wieringa, B.; Wansink, D.G.
	2004	Mild impairment of motor nerve repair in mice lacking PTP-BL tyrosine phosphatase activity.	Wansink, D.G.; Peters, W.J.M; Schaafsma, I.; Sutmuller, R.P.M.; Oerlemans, F.T.J.J.; Adema, G.J.; Wieringa, B.; Zee, C.E.E.M. van der; Hendriks, W.J.A.J.
	2004	Transgenic overexpression of human DMPK accumulates into hypertrophic cardiomyopathy, myotonic myopathy and hypotension traits of myotonic dystrophy.	O'Cochlain, D.F.; Perez-Terzic, C.; Reyes, S.; Kane, G.C.; Behfar, A.; Hodgson, D.M.; Strommen, J.A.; Liu, X.K.; Broek, W.J.A.A. van den; Wansink, D.G.; Wieringa, B.; Terzic, A.
	1995	Synthesis of 2,9-Carbonyl-4-Brendenes, Strained Half-Cage Systems with Orthogonal Pi-Bonds in Close Proximity	Klunder, A.J.H.; Depre, H.L.E.; Aar, M.P.M. van; Waals, A.C.L.M. van der; Wansink, D.G.; Swanenburg, B.

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