CRISPR/Cas9-Induced (CTG⋅CAG)n Repeat Instability in the Myotonic Dystrophy Type 1 Locus: Implications for Therapeutic Genome Editing by van Agtmaal, Ellen L., André, Laurène M., Willemse, Marieke, Cumming, Sarah A., van Kessel, Ingeborg D.G., van den Broek, Walther J.A.A., Gourdon, Geneviève, Furling, Denis, Mouly, Vincent, Monckton, Darren G., Wansink, Derick G., Wieringa, Bé

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Triplet-repeat oligonucleotide-mediated reversal of RNA toxicity in myotonic dystrophy by Mulders, Susan A.M, van den Broek, Walther J.A.A, Wheeler, Thurman M, Croes, Huib J.E, van Kuik-Romeijn, Petra, de Kimpe, Sjef J, Furling, Denis, Platenburg, Gerard J, Gourdon, Geneviève, Thornton, Charles A, Wieringa, Bé, Wansink, Derick G

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Differentiation shifts from a reversible to an irreversible heterochromatin state at the DM1 locus by Handal, Tayma, Juster, Sarah, Abu Diab, Manar, Yanovsky-Dagan, Shira, Zahdeh, Fouad, Aviel, Uria, Sarel-Gallily, Roni, Michael, Shir, Bnaya, Ester, Sebban, Shulamit, Buganim, Yosef, Drier, Yotam, Mouly, Vincent, Kubicek, Stefan, van den Broek, Walther J. A. A., Wansink, Derick G., Epsztejn-Litman, Silvina, Eiges, Rachel

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A low absolute number of expanded transcripts is involved in myotonic dystrophy type 1 manifestation in muscle by Gudde, Anke E E G, González-Barriga, Anchel, van den Broek, Walther J A A, Wieringa, Bé, Wansink, Derick G

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Cell membrane integrity in myotonic dystrophy type 1: implications for therapy by González-Barriga, Anchel, Kranzen, Julia, Croes, Huib J E, Bijl, Suzanne, van den Broek, Walther J A A, van Kessel, Ingeborg D G, van Engelen, Baziel G M, van Deutekom, Judith C T, Wieringa, Bé, Mulders, Susan A M, Wansink, Derick G

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Somatic expansion behaviour of the (CTG)n repeat in myotonic dystrophy knock-in mice is differentially affected by Msh3 and Msh6 mismatch-repair proteins by VAN DEN BROEK, Walther J. A. A, NELEN, Marcel R, WANSINK, Derick G, COERWINKEL, Marga M, TE RIELE, Hein, GROENEN, Patricia J. T. A, WIERINGA, Bé

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Fen1 does not control somatic hypermutability of the (CTG) n · (CAG) n repeat in a knock-in mouse model for DM1 by van den Broek, Walther J.A.A., Nelen, Marcel R., van der Heijden, Godfried W., Wansink, Derick G., Wieringa, Bé

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Somatic CTG•CAG repeat instability in a mouse model for myotonic dystrophy type 1 is associated with changes in cell nuclearity and DNA ploidy by van den Broek, Walther JAA, Wansink, Derick G, Wieringa, Bé

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Atypical xanthomatosis in apolipoprotein E-deficient mice after cholesterol feeding by van Ree, Janine H., Gijbels, Marion J.J., van den Broek, Walther J.A.A., Hofker, Marten H., Havekes, Louis M.

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Variability in cholesterol content in serum and aortic tissue in apolipoprotein E-deficient mice is comparable in inbred (129/Sv) and outbred (mixed 129/Sv and C57BL/6) mice by van Ree, Janine H., van den Broek, Walther J.A.A., Dahlmans, Vivian E.H., Wieringa, Bé, Frants, Rune R., Havekes, Louis M., Hofker, Marten H.

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