Remodeling and spacing factor 1 (RSF1) deposits centromere proteins at DNA double-strand breaks to promote non-homologous end-joining

Yazar: Helfricht, Angela, Wiegant, Wouter W, Thijssen, Peter E, Vertegaal, Alfred C, Luijsterburg, Martijn S, van Attikum, Haico
Baskı/Yayın Bilgisi 2013

DUX4 promotes transcription of FRG2 by directly activating its promoter in facioscapulohumeral muscular dystrophy

Yazar: Thijssen, Peter E, Balog, Judit, Yao, Zizhen, Pham, Tan Phát, Tawil, Rabi, Tapscott, Stephen J, Van der Maarel, Silvère M
Yayımlandı Skelet Muscle (2014)

The de-ubiquitylating enzymes USP26 and USP37 regulate homologous recombination by counteracting RAP80

Yazar: Typas, Dimitris, Luijsterburg, Martijn S., Wiegant, Wouter W., Diakatou, Michaela, Helfricht, Angela, Thijssen, Peter E., van de Broek, Bram, Mullenders, Leon H., van Attikum, Haico
Yayımlandı Nucleic Acids Res (2015)

The de-ubiquitylating enzymes USP26 and USP37 regulate homologous recombination by counteracting RAP80

Yazar: Typas, Dimitris, Luijsterburg, Martijn S., Wiegant, Wouter W., Diakatou, Michaela, Helfricht, Angela, Thijssen, Peter E., van den Broek, Bram, Mullenders, Leon H., van Attikum, Haico
Yayımlandı Nucleic Acids Res (2016)

Correlation analysis of clinical parameters with epigenetic modifications in the DUX4 promoter in FSHD

Yazar: Balog, Judit, Thijssen, Peter E., de Greef, Jessica C., Shah, Bharati, van Engelen, Baziel G.M., Yokomori, Kyoko, Tapscott, Stephen J., Tawil, Rabi, van der Maarel, Silvère M.
Baskı/Yayın Bilgisi 2012

Chromatin remodeling of human subtelomeres and TERRA promoters upon cellular senescence: Commonalities and differences between chromosomes

Yazar: Thijssen, Peter E., Tobi, Elmar W., Balog, Judit, Schouten, Suzanne G., Kremer, Dennis, El Bouazzaoui, Fatiha, Henneman, Peter, Putter, Hein, Eline Slagboom, P., Heijmans, Bastiaan T., Van der Maarel, Silvère M.
Baskı/Yayın Bilgisi 2013

MuSK IgG4 autoantibodies cause myasthenia gravis by inhibiting binding between MuSK and Lrp4

Yazar: Huijbers, Maartje G., Zhang, Wei, Klooster, Rinse, Niks, Erik H., Friese, Matthew B., Straasheijm, Kirsten R., Thijssen, Peter E., Vrolijk, Hans, Plomp, Jaap J., Vogels, Pauline, Losen, Mario, Van der Maarel, Silvère M., Burden, Steven J., Verschuuren, Jan J.
Baskı/Yayın Bilgisi 2013

DNA methylation signatures link prenatal famine exposure to growth and metabolism

Yazar: Tobi, Elmar W., Goeman, Jelle J., Monajemi, Ramin, Gu, Hongcang, Putter, Hein, Zhang, Yanju, Slieker, Roderick C., Stok, Arthur P., Thijssen, Peter E., Müller, Fabian, van Zwet, Erik W., Bock, Christoph, Meissner, Alexander, Lumey, L. H., Eline Slagboom, P., Heijmans, Bastiaan T.
Yayımlandı Nat Commun (2014)

Increased DUX4 expression during muscle differentiation correlates with decreased SMCHD1 protein levels at D4Z4

Yazar: Balog, Judit, Thijssen, Peter E., Shadle, Sean, Straasheijm, Kirsten R., van der Vliet, Patrick J., Krom, Yvonne D., van den Boogaard, Marlinde L., de Jong, Annika, F Lemmers, Richard J. L., Tawil, Rabi, Tapscott, Stephen J., van der Maarel, Silvère M.
Yayımlandı Epigenetics (2015)

Corrigendum: DNA methylation signatures link prenatal famine exposure to growth and metabolism

Yazar: Tobi, Elmar W., Goeman, Jelle J., Monajemi, Ramin, Gu, Hongcang, Putter, Hein, Zhang, Yanju, Slieker, Roderick C., Stok, Arthur P., Thijssen, Peter E., Müller, Fabian, van Zwet, Erik W., Bock, Christoph, Meissner, Alexander, Lumey, L. H., Eline Slagboom, P., Heijmans, Bastiaan T.
Yayımlandı Nat Commun (2015)

Gene set analysis of GWAS data for human longevity highlights the relevance of the insulin/IGF-1 signaling and telomere maintenance pathways

Yazar: Deelen, Joris, Uh, Hae-Won, Monajemi, Ramin, van Heemst, Diana, Thijssen, Peter E., Böhringer, Stefan, van den Akker, Erik B., de Craen, Anton J. M., Rivadeneira, Fernando, Uitterlinden, André G., Westendorp, Rudi G. J., Goeman, Jelle J., Slagboom, P. Eline, Houwing-Duistermaat, Jeanine J., Beekman, Marian
Baskı/Yayın Bilgisi 2011

Intrinsic Epigenetic Regulation of the D4Z4 Macrosatellite Repeat in a Transgenic Mouse Model for FSHD

Yazar: Krom, Yvonne D., Thijssen, Peter E., Young, Janet M., den Hamer, Bianca, Balog, Judit, Yao, Zizhen, Maves, Lisa, Snider, Lauren, Knopp, Paul, Zammit, Peter S., Rijkers, Tonnie, van Engelen, Baziel G. M., Padberg, George W., Frants, Rune R., Tawil, Rabi, Tapscott, Stephen J., van der Maarel, Silvère M.
Baskı/Yayın Bilgisi 2013

Leukocyte telomere length associates with prospective mortality independent of immune-related parameters and known genetic markers

Yazar: Deelen, Joris, Beekman, Marian, Codd, Veryan, Trompet, Stella, Broer, Linda, Hägg, Sara, Fischer, Krista, Thijssen, Peter E, Suchiman, H Eka D, Postmus, Iris, Uitterlinden, André G, Hofman, Albert, de Craen, Anton J M, Metspalu, Andres, Pedersen, Nancy L, van Duijn, Cornelia M, Wouter Jukema, J, Houwing-Duistermaat, Jeanine J, Samani, Nilesh J, Eline Slagboom, P
Baskı/Yayın Bilgisi 2014

Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defects

Yazar: Weemaes, Corry MR, van Tol, Maarten JD, Wang, Jun, van Ostaijen-ten Dam, Monique M, van Eggermond, Marja CJA, Thijssen, Peter E, Aytekin, Caner, Brunetti-Pierri, Nicola, van der Burg, Mirjam, Graham Davies, E, Ferster, Alina, Furthner, Dieter, Gimelli, Giorgio, Gennery, Andy, Kloeckener-Gruissem, Barbara, Meyn, Stephan, Powell, Cynthia, Reisli, Ismail, Schuetz, Catharina, Schulz, Ansgar, Shugar, Andrea, van den Elsen, Peter J, van der Maarel, Silvère M
Baskı/Yayın Bilgisi 2013

Mutations in CDCA7 and HELLS cause immunodeficiency–centromeric instability–facial anomalies syndrome

Yazar: 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
Yayımlandı Nat Commun (2015)

Corrigendum: Mutations in CDCA7 and HELLS cause immunodeficiency–centromeric instability–facial anomalies syndrome

Yazar: 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
Yayımlandı Nat Commun (2016)

Loss of ZBTB24 impairs nonhomologous end-joining and class-switch recombination in patients with ICF syndrome

Yazar: Helfricht, Angela, Thijssen, Peter E., Rother, Magdalena B., Shah, Rashmi G., Du, Likun, Takada, Sanami, Rogier, Mélanie, Moritz, Jacques, IJspeert, Hanna, Stoepker, Chantal, van Ostaijen-ten Dam, Monique M., Heyer, Vincent, Luijsterburg, Martijn S., de Groot, Anton, Jak, Rianca, Grootaers, Gwendolynn, Wang, Jun, Rao, Pooja, Vertegaal, Alfred C.O., van Tol, Maarten J.D., Pan-Hammarström, Qiang, Reina-San-Martin, Bernardo, Shah, Girish M., van der Burg, Mirjam, van der Maarel, Silvère M., van Attikum, Haico
Yayımlandı J Exp Med (2020)