Serum matrix metalloproteinase-9 (MMP-9) as a biomarker for monitoring disease progression in Duchenne muscular dystrophy (DMD) von Nadarajah, V.D, van Putten, M, Chaouch, A, Garrood, P, Straub, V, Lochmüller, H, Ginjaar, H.B, Aartsma-Rus, A.M, van Ommen, G.J.B, den Dunnen, J.T, t Hoen, P.A.C

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Relative power and sample size analysis on gene expression profiling data von Iterson, M. van, Hoen, P.A.C. 't, Pedotti, P, Hooiveld, G.J.E.J, Dunnen, J.T. den, Ommen, G.J.B. van, Boer, J.M, Menezes, R.X

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Literature-based priors for gene regulatory networks von Steele, E., Tucker, A., Hoen, P.A.C. 't, Schuemie, M.J.

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Despite differential gene expression profiles pediatric MDS derived mesenchymal stromal cells display functionality in vitro von Calkoen, F.G.J., Vervat, C., van Pel, M., de Haas, V., Vijfhuizen, L.S., Eising, E., Kroes, W.G.M., 't Hoen, P.A.C., van den Heuvel-Eibrink, M.M., Egeler, R.M., van Tol, M.J.D., Ball, L.M.

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T.P.26 Low dystrophin levels increase survival and improve pathology and motor function in dystrophin/utrophin double knockout mice von van Putten, M, Hulsker, M, Young, C, Nadarajah, V.D, Heemskerk, H, t Hoen, P.A.C, van Ommen, G.J.B, Aartsma-Rus, A.M

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O.10 Effect of combined treatment with soluble activin receptor IIB and AAV-U7-mediated dystrophin exon skipping on muscle function in mdx mice von Hoogaars, W.M.H, Mouisel, E, Relizani, K, Pasternack, A, Hourde, C, Precigout, G, Ferry, A, Garcia, L, Kemaladewi, D.U, Aartsma-Rus, A, Ritvos, O, t Hoen, P.A.C, Amthor, H

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P1.49 Mass spectrometry based clinical proteomics for biomarker discovery in Duchenne muscular dystrophy von Martin, F.C, Oonk, S, t Hoen, P.A.C, Nadarajah, V.D, Chaouch, A, Lochmüller, H, Dalebout, H, der Burgt, Y.E.M, Palmblad, M, Deelder, A.M

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O.13 Interference of myostatin and TGF-beta signaling by antisense-mediated exon skipping in ALK4/5 receptors von Kemaladewi, D.U, van Heiningen, S.H, Aartsma-Rus, A, van Ommen, G.J.B, ten Dijke, P, t Hoen, P.A.C, Hoogaars, W.M.H

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P2.44 Accelerated skeletal muscle ageing is a molecular signature in OPMD von Venema, A, Anvar, S.A, t’ Hoen, P.A.C, van der Sluijs, B, van Engelen, B, van der Maarel, S.M, Raz, V

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P4.29 Differential tissue expression and decay of dystrophin mRNA and protein von Spitali, P, van Putten, M, Vossen, R.H, den Dunnen, J.T, van Ommen, G.J.B, t Hoen, P.A.C, Aartsma-Rus, A

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P1.23 The effects of low dystrophin levels on muscle function and pathology von van Putten, M, Hulsker, M.A, van Heiningen, S.H, van Huizen, E, van Iterson, M, Admiraal, P, Messemaker, T, Dunnen, J.T. den, Nadarajah, V.D, t Hoen, P.A.C, Aartsma-Rus, A.M

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P1.48 Serum matrix metalloproteinase-9 (MMP-9) as a biomarker for monitoring Duchenne muscular dystrophy (DMD) disease progression von t Hoen, P.A.C, Nadarajah, V.D, van Putten, M, Chaouch, A, Garrood, P, Straub, V, Ginjaar, H.B, Aartsma-Rus, A.M, van Ommen, G.J.B, Dunnen, J.T. den, Lochmüller, H

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P1.44 Development of heart failure in mice with low dystrophin levels von van der Pijl, E.M, van Putten, M, Nadarajah, V.D, van Opstal, A.M, Hulsker, M.A, t Hoen, P.A.C, van der Weerd, L, Aartsma-Rus, A.M

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Recommendations for the analysis of gene expression data to identify intrinsic differences between similar tissues von Abbassi-Daloii, Tooba, Kan, Hermien E., Raz, Vered, 't Hoen, P.A.C.

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G.O.2 A primary sequence motif underlying calpain 3 substrate cleavage von de Morrée, A, Hulsik, D. Lutje, Impagliazzo, A, van Haagen, H.H.B, de Galan, P, van Remoortere, A, t Hoen, P.A.C, Frants, R.R, van der Maarel, S.M

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T.P.1.04 Dual exon skipping in myostatin and dystrophin as a potential therapy for Duchenne muscular dystrophy von Kemaladewi, D.U, Hoogaars, W.M.H, van Heiningen, S.H, van Deutekom, J.C.T, den Dunnen, J.T, van Ommen, G.J.B, Aartsma-Rus, A.R, ten Dijke, P, t Hoen, P.A.C

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Cell type-specific changes in transcriptomic profiles of endothelial cells, iPSC-derived neurons and astrocytes cultured on microfluidic chips von Middelkamp, H. H. T., Verboven, A. H. A., De Sá Vivas, A. G., Schoenmaker, C., Klein Gunnewiek, T. M., Passier, R., Albers, C. A., ‘t Hoen, P. A. C., Nadif Kasri, N., van der Meer, A. D.

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D15 - Timing and localization of human dystrophin isoform expression provide insights into the cognitive phenotype of Duchenne muscular dystrophy von Doorenweerd, N., Mahfouz, A., van Putten, M., Kaliyaperumal, R., ’t Hoen, P.A.C., Hendriksen, J.G.M., Aartsma-Rus, A., Verschuuren, J.J.G.M., Niks, E.H., Reinders, M.J.T., Kan, H.E., Lelieveldt, B.P.F.

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Timing and localization of human dystrophin isoform expression provide insights into the cognitive phenotype of Duchenne muscular dystrophy von Doorenweerd, N., Mahfouz, A., van Putten, M., Kaliyaperumal, R., ’t Hoen, P.A.C., Hendriksen, J.G.M., Aartsma-Rus, A., Verschuuren, J.J.G.M., Niks, E.H., Reinders, M.J.T., Kan, H.E., Lelieveldt, B.P.F.

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Deep sequencing of RNA from immune cell-derived vesicles uncovers the selective incorporation of small non-coding RNA biotypes with potential regulatory functions von Nolte-'t Hoen, E.N.M, Buermans, H.P, Waasdorp, M, Stoorvogel, W, Wauben, M.H.M, t Hoen, P.A.C

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