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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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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Design and Analysis of Effects of Triplet Repeat Oligonucleotides in Cell Models for Myotonic Dystrophy by González-Barriga, Anchel, Mulders, Susan AM, van de Giessen, Jeroen, Hooijer, Jeroen D, Bijl, Suzanne, van Kessel, Ingeborg DG, van Beers, Josee, van Deutekom, Judith CT, Fransen, Jack AM, Wieringa, Bé, Wansink, Derick G

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Antisense transcription of the myotonic dystrophy locus yields low-abundant RNAs with and without (CAG)n repeat by Gudde, Anke E. E. G., van Heeringen, Simon J., de Oude, Amanda I., van Kessel, Ingeborg D. G., Estabrook, Joseph, Wang, Eric T., Wieringa, Bé, Wansink, Derick G.

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Trinucleotide-repeat expanded and normal DMPK transcripts contain unusually long poly(A) tails despite differential nuclear residence by Gudde, Anke E.E.G., van Kessel, Ingeborg D.G., André, Laurène M., Wieringa, Bé, Wansink, Derick G.

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