The naive T-cell receptor repertoire has an extremely broad distribution of clone sizes von de Greef, Peter C, Oakes, Theres, Gerritsen, Bram, Ismail, Mazlina, Heather, James M, Hermsen, Rutger, Chain, Benjamin, de Boer, Rob J

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On the feasibility of using TCR sequencing to follow a vaccination response - lessons learned von de Greef, Peter C, Lanfermeijer, Josien, Hendriks, Marion, Cevirgel, Alper, Vos, Martijn, Borghans, José A M, van Baarle, Debbie, de Boer, Rob J

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Cytoskeletal disorganization underlies PABPN1-mediated myogenic disability von Olie, Cyriel Sebastiaan, van der Wal, Erik, Cikes, Domagoj, Maton, Loes, de Greef, Jessica C., Lin, I.-Hsuan, Chen, Yi-Fan, Kareem, Elsayad, Penninger, Josef M., Kessler, Benedikt M., Raz, Vered

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Author Correction: Cytoskeletal disorganization underlies PABPN1-mediated myogenic disability von Olie, Cyriel Sebastiaan, van der Wal, Erik, Cikes, Domagoj, Maton, Loes, de Greef, Jessica C., Lin, I.-Hsuan, Chen, Yi-Fan, Kareem, Elsayad, Penninger, Josef M., Kessler, Benedikt M., Raz, Vered

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Clinical features of facioscapulohumeral muscular dystrophy 2 von DE GREEF, J. C, LEMMERS, R. J. L. F, DESNUELLE, C, SPULER, S, TARNOPOLSKY, M, VENANCE, S. L, FRANTS, R. R, VAN DER MAAREL, S. M, TAWIL, R, CAMANO, P, DAY, J. W, SACCONI, S, DUNAND, M, VAN ENGELEN, B. G. M, KIURU-ENARI, S, PADBERG, G. W, ROSA, A. L

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Facioscapulohumeral muscular dystrophy: the road to targeted therapies von Tihaya, Mara S., Mul, Karlien, Balog, Judit, de Greef, Jessica C., Tapscott, Stephen J., Tawil, Rabi, Statland, Jeffrey M., van der Maarel, Silvère M.

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Mouse models for muscular dystrophies: an overview von van Putten, Maaike, Lloyd, Erin M, de Greef, Jessica C, Raz, Vered, Willmann, Raffaella, Grounds, Miranda D

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USP18 is an essential regulator of muscle cell differentiation and maturation von Olie, Cyriel Sebastiaan, Pinto-Fernández, Adán, Damianou, Andreas, Vendrell, Iolanda, Mei, Hailiang, den Hamer, Bianca, van der Wal, Erik, de Greef, Jessica C., Raz, Vered, Kessler, Benedikt M.

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SMCHD1 has separable roles in chromatin architecture and gene silencing that could be targeted in disease von Tapia del Fierro, Andres, den Hamer, Bianca, Benetti, Natalia, Jansz, Natasha, Chen, Kelan, Beck, Tamara, Vanyai, Hannah, Gurzau, Alexandra D., Daxinger, Lucia, Xue, Shifeng, Ly, Thanh Thao Nguyen, Wanigasuriya, Iromi, Iminitoff, Megan, Breslin, Kelsey, Oey, Harald, Krom, Yvonne D., van der Hoorn, Dinja, Bouwman, Linde F., Johanson, Timothy M., Ritchie, Matthew E., Gouil, Quentin A., Reversade, Bruno, Prin, Fabrice, Mohun, Timothy, van der Maarel, Silvère M., McGlinn, Edwina, Murphy, James M., Keniry, Andrew, de Greef, Jessica C., Blewitt, Marnie E.

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Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHD von DE GREEF, J. C, WOHLGEMUTH, M, CHAN, O. A, HANSSON, K. B, SMEETS, D, FRANTS, R. R, WEEMAES, C. M, PADBERG, G. W, VAN DER MAAREL, S. M

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Meeting report: the 2021 FSHD International Research Congress von Jagannathan, Sujatha, de Greef, Jessica C, Hayward, Lawrence J, Yokomori, Kyoko, Gabellini, Davide, Mul, Karlien, Sacconi, Sabrina, Arjomand, Jamshid, Kinoshita, June, Harper, Scott Q

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Common epigenetic changes of D4Z4 in contraction-dependent and contraction-independent FSHD von de Greef, Jessica C, Lemmers, Richard J.L.F, van Engelen, Baziel G.M, Sacconi, Sabrina, Venance, Shannon L, Frants, Rune R, Tawil, Rabi, van der Maarel, Silvère M

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Systemic delivery of a DUX4-targeting antisense oligonucleotide to treat facioscapulohumeral muscular dystrophy von Bouwman, Linde F., den Hamer, Bianca, van den Heuvel, Anita, Franken, Marnix, Jackson, Michaela, Dwyer, Chrissa A., Tapscott, Stephen J., Rigo, Frank, van der Maarel, Silvère M., de Greef, Jessica C.

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A knock down strategy for rapid, generic, and versatile modelling of muscular dystrophies in 3D-tissue-engineered-skeletal muscle von In 't Groen, Stijn L M, Franken, Marnix, Bock, Theresa, Krüger, Marcus, de Greef, Jessica C, Pijnappel, W W M Pim

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Mutations in ZBTB24 Are Associated with Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome Type 2 von DE GREEF, Jessica C, JUN WANG, GENNERY, Andrew R, GIMELLI, Giorgio, REISLI, Ismail, SCHUETZ, Catharina, SCHULZ, Ansgar, SMEETS, Dominique F. C. M, SZNAJER, Yves, WIJMENGA, Cisca, VAN EGGERMOND, Marja C, VAN OSTAIJEN-TEN DAM, Monique M, BALOG, Judit, LANKESTER, Arjan C, VAN TOL, Maarten J. D, VAN DEN ELSEN, Peter J, WEEMAES, Corry M, VAN DER MAAREL, Silvere M, DEN DUNNEN, Johan T, FRANTS, Rune R, STRAASHEIJM, Kirsten R, AYTEKIN, Caner, VAN DER BURG, Mirjam, DUPREZ, Laurence, FERSTER, Alina

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Dnmt3b regulates DUX4 expression in a tissue-dependent manner in transgenic D4Z4 mice von Bouwman, Linde F, den Hamer, Bianca, Verveer, Elwin P, Lerink, Lente J S, Krom, Yvonne D, van der Maarel, Silvère M, de Greef, Jessica C

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Generation of genetically matched hiPSC lines from two mosaic facioscapulohumeral dystrophy type 1 patients von van der Wal, Erik, den Hamer, Bianca, van der Vliet, Patrick J., Tok, Merve, Brands, Tom, Eussen, Bert, Lemmers, Richard J.L.F., Freund, Christian, de Klein, Annelies, Buijsen, Ronald A.M., van Roon-Mom, Willeke M.C., Tawil, Rabi, van der Maarel, Silvère M., de Greef, Jessica C.

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TCRβ rearrangements without a D segment are common, abundant, and public von de Greef, Peter C., de Boer, Rob J.

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Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2 von Lemmers, Richard J L F, Tawil, Rabi, Petek, Lisa M, Balog, Judit, Block, Gregory J, Santen, Gijs W E, Amell, Amanda M, van der Vliet, Patrick J, Almomani, Rowida, Straasheijm, Kirsten R, Krom, Yvonne D, Klooster, Rinse, Sun, Yu, den Dunnen, Johan T, Helmer, Quinta, Donlin-Smith, Colleen M, Padberg, George W, van Engelen, Baziel G M, de Greef, Jessica C, Aartsma-Rus, Annemieke M, Frants, Rune R, de Visser, Marianne, Desnuelle, Claude, Sacconi, Sabrina, Filippova, Galina N, Bakker, Bert, Bamshad, Michael J, Tapscott, Stephen J, Miller, Daniel G, van der Maarel, Silvère M

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Mutations in CDCA7 and HELLS cause immunodeficiency–centromeric instability–facial anomalies syndrome von Thijssen, Peter E., Ito, Yuya, Grillo, Giacomo, Wang, Jun, Velasco, Guillaume, Nitta, Hirohisa, Unoki, Motoko, Yoshihara, Minako, Suyama, Mikita, Sun, Yu, Lemmers, Richard J. L. F., de Greef, Jessica C., Gennery, Andrew, Picco, Paolo, Kloeckener-Gruissem, Barbara, Güngör, Tayfun, Reisli, Ismail, Picard, Capucine, Kebaili, Kamila, Roquelaure, Bertrand, Iwai, Tsuyako, Kondo, Ikuko, Kubota, Takeo, van Ostaijen-Ten Dam, Monique M., van Tol, Maarten J. D., Weemaes, Corry, Francastel, Claire, van der Maarel, Silvère M., Sasaki, Hiroyuki

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