Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequency von Kiezun, Adam, Pulit, Sara L, Francioli, Laurent C, van Dijk, Freerk, Swertz, Morris, Boomsma, Dorret I, van Duijn, Cornelia M, Slagboom, P Eline, van Ommen, G J B, Wijmenga, Cisca, de Bakker, Paul I W, Sunyaev, Shamil R

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Muscle regeneration in dystrophin-deficient mdx mice studied by gene expression profiling von Turk, R, Sterrenburg, E, de Meijer, E J, van Ommen, G-J B, den Dunnen, J T, 't Hoen, P A C

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Deletion of the Caenorhabditis elegans homologues of the CLN3 gene, involved in human juvenile neuronal ceroid lipofuscinosis, causes a mild progeric phenotype von Voer, G., Bent, P., Rodrigues, A. J. G., Ommen, G.‐J. B., Peters, D. J. M., Taschner, P. E. M.

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Limb-girdle muscular dystrophy in the Netherlands : Gene defect identified in half the families von VAN DER KOOI, A. J, FRANKHUIZEN, W. S, BAKKER, E, GINJAAR, H. B, BARTH, P. G, HOWELER, C. J, PADBERG, G. W, SPAANS, F, WINTZEN, A. R, WOKKE, J. H. J, VAN OMMEN, G.-J. B, DE VISSER, M

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Comparative analysis of antisense oligonucleotide analogs for targeted DMD exon 46 skipping in muscle cells von AARTSMA-RUS, A, KAMAN, W. E, BREMMER-BOUT, M, JANSON, A. A. M, DEN DUNNEN, J. T, VAN OMMEN, G-Jb, VAN DEUTEKOM, J. C. T

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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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WHSC1, a 90 kb SET Domain-Containing Gene, Expressed in Early Development and Homologous to a Drosophila Dysmorphy Gene Maps in the Wolf-Hirschhorn Syndrome Critical Region and is... von Stec, Ingrid, Wright, Tracy J., van Ommen, Gert-Jan B., de Boer, Piet A. J., van Haeringen, Arie, Moorman, Antoon F. M., Altherr, Michael R., den Dunnen, Johan T.

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Fluorescent labelling of cRNA for microarray applications von ’t Hoen, Peter A. C., de Kort, Floor, van Ommen, G. J. B., den Dunnen, Johan T.

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Therapeutic Modulation of DMD Splicing by Blocking Exonic Splicing Enhancer Sites with Antisense Oligonucleotides von AARTSMA-RUS, A., JANSON, A.A.M., HEEMSKERK, J.A., DE WINTER, C.L., VAN OMMEN, G.-J.B., VAN DEUTEKOM, J.C.T.

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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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The Human Genome Project and the future of diagnostics, treatment and prevention von Ommen, G.‐J. B.

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Detection of CBP rearrangements in acute myelogenous leukemia with t(8;16) von GILES, R. H, DAUWERSE, J. G, VAN OMMEN, G.-J. B, HAGEMEIJER, A, VAN DER REIJDEN, B. A, BREUNING, M. H, HIGGINS, C, PETRIJ, F, WESSELS, J. W, BEVERSTOCK, G. C, DÖHNER, H, JOTTERAND-BELLOMO, M, FALKENBURG, J. H. F, SLATER, R. M

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Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease von AZIZ, N. A, JURGENS, C. K, LANDWEHRMEYER, G. B, VAN ROON-MOM, W. M. C, VAN OMMEN, G. J. B, STIJNEN, T, ROOS, R. A. C

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Common pathological mechanisms in mouse models for muscular dystrophies von Turk, R, Sterrenburg, E, van der Wees, C. G. C, de Meijer, E. J, de Menezes, R. X, Groh, S, Campbell, K. P, Noguchi, S, van Ommen, G. J. B, den Dunnen, J. T, t Hoen, P. A. C

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The peripheral myelin gene PMP-22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1A von Valentijn, L. J, Bolhuis, P. A, Zorn, I, Hoogendijk, J. E, van den Bosch, N, Hensels, G. W, Stanton, V. P, Housman, D. E, Fischbeck, K. H, Ross, D. A, Nicholson, G. A, Meershoek, E. J, Dauwerse, H. G, van Ommen, G. -J. B, Baas, F

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Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP von Petrif, Fred, Giles, Rachel H, Dauwerse, Hans G, Saris, Jasper J, Hennekam, Raoul C. M, Masuno, Mitsuo, Tommerup, Niels, van Ommen, Gert-Jan B, Goodman, Richard H, Peters, Dorien J. M, Breuning, Martijn H

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Genome-wide assessment of differential roles for p300 and CBP in transcription regulation von Ramos, Y. F. M., Hestand, M. S., Verlaan, M., Krabbendam, E., Ariyurek, Y., van Galen, M., van Dam, H., van Ommen, G.-J. B., den Dunnen, J. T., Zantema, A., 't Hoen, P. A. C.

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Screening for BRCA2 mutations in 81 Dutch breast-ovarian cancer families von PEELEN, T, VAN VLIET, M, DEVILEE, P, BOSCH, A, BIGNELL, G, VASEN, H. F. A, KLIJN, J. G. M, MEIJERS-HEIJBOER, H, STRATTON, M, VAN OMMEN, G.-J, CORNELISSE, C. J

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High-resolution DNA Fiber-FISH for genomic DNA mapping and colour bar-coding of large genes von Florijn, Ralpha J., Bonden, A. J., Vrolijk, Hans, Wiegant, Joop, Vaandrager, Jan-Willem, Bass, Frank, den Dunnen, Johan T., Tanke, Hans J., van Ommen, Gert-Jan B., Raap, Anton K.

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FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit von Deutekom, Judith C.T.Van, Wljmenga, Cisca, Tlenhoven, Esther A.E.Van, Gruter, Anne-Marie, Hewitt, Jane E., Padberg, George W., Ommen, Gert-Jan. B.van, Hofker, Marten H., Fronts, Rune R.

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