Jessica de Greef - Dissemin

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All papers authored by Jessica de Greef

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2023 Cyriel Sebastiaan Olie, Adán Pinto-Fernández

ORCID

, Andreas Damianou, Iolanda Vendrell, Hailiang Mei, Bianca den Hamer, Bianca den Hamer, Erik van der Wal, Jessica C. de Greef

ORCID

, Eleonora Aronica, Vered Raz

ORCID

, Benedikt M. Kessler

ORCID

USP18 is an essential regulator of muscle cell differentiation and maturation

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Mara S. Tihaya

ORCID

, Karlien Mul, Judit Balog, Jessica C. de Greef

ORCID

, Stephen J. Tapscott, Rabi Tawil, Jeffrey M. Statland, Silvère M. van der Maarel

ORCID

Facioscapulohumeral muscular dystrophy: the road to targeted therapies

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2020 Cyriel Sebastiaan Olie, Erik van der Wal, Domagoj Cikes, Loes Maton, Jessica C. de Greef

ORCID

, I.-Hsuan Lin, Yi-Fan Chen, Elsayad Kareem, Josef M. Penninger, Benedikt M. Kessler, Vered Raz

Cytoskeletal disorganization underlies PABPN1-mediated myogenic disability

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Linde F. Bouwman, Bianca den Hamer, Elwin P. Verveer, Lente J. S. Lerink, Yvonne D. Krom, Silvère M. van der Maarel

ORCID

, Jessica C. de Greef

ORCID

Dnmt3b regulates DUX4 expression in a tissue-dependent manner in transgenic D4Z4 mice

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Alessandro Iuliano, Erik Wal, Claudine W. B. Ruijmbeek, Stijn L. M. in ‘t Groen, W. W. M. Pim Pijnappel

ORCID

, Jessica C. Greef

ORCID

, Vittorio Saggiomo

Coupling 3D Printing and Novel Replica Molding for In House Fabrication of Skeletal Muscle Tissue Engineering Devices

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Maaike van Putten

ORCID

, Erin M. Lloyd, Jessica C. de Greef

ORCID

ORCID

, Raffaella Willmann

ORCID

, Miranda D. Grounds

ORCID

Mouse models for muscular dystrophies: an overview

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2019 Erik van der Wal, Bianca den Hamer, Patrick J. van der Vliet, Merve Tok, Tom Brands

ORCID

, Bert Eussen, Richard J. L. F. Lemmers, Christian Freund, Annelies de Klein, Ronald A. M. Buijsen

ORCID

, Willeke M. C. van Roon-Mom, Rabi Tawil, Silvère M. van der Maarel

ORCID

, Jessica C. de Greef

ORCID

Generation of genetically matched hiPSC lines from two mosaic facioscapulohumeral dystrophy type 1 patients

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Jessica C. de Greef

ORCID

, Bram Slütter, Mary E. Anderson, Rebecca Hamlyn, Raul O’Campo Landa, Ellison J. McNutt, Yuji Hara, Lecia L. Pewe, David Venzke, Kiichiro Matsumura, Fumiaki Saito, John T. Harty, Kevin P. Campbell

ORCID

Protective role for the N-terminal domain of α-dystroglycan in Influenza A virus proliferation

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2017 Yvonne D. Krom, Jessica C. de Greef

ORCID

, Bianca den Hamer, Lauren Snider, Yosuke Hiramuki, Rob F. P. van den Akker, Kelsey Breslin, Miha Pakusch, Daniela C. F. Salvatori, Bram Slütter, Rabi Tawil, Marnie E. Blewitt, Silvère M. van der Maarel, Stephen J. Tapscott

Smchd1 haploinsufficiency exacerbates the phenotype of a transgenic FSHD1 mouse model

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2016 Peter E. Thijssen, Yuya Ito, Giacomo Grillo, Jun Wang, Guillaume Velasco, Hirohisa Nitta, Motoko Unoki, Minako Yoshihara, Mikita Suyama, Yu Sun, Richard J. L. F. Lemmers, Jessica C. de Greef

ORCID

, Andrew Gennery, Paolo Picco, Barbara Kloeckener-Gruissem and 14 other authors

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

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Jessica C. de Greef

ORCID

, Rebecca Hamlyn, Braden S. Jensen, Raul O'Campo Landa, Raul O'Campo Landa, Jennifer R. Levy, Kazuhiro Kobuke, Kevin P. Campbell

ORCID

Collagen VI deficiency reduces muscle pathology, but does not improve muscle function, in the γ-sarcoglycan-null mouse

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2015 Peter E. Thijssen, Yuya Ito, Giacomo Grillo, Jun Wang, Guillaume Velasco, Hirohisa Nitta, Motoko Unoki, Minako Yoshihara, Mikita Suyama, Yu Sun, Richard J. L. F. Lemmers, Jessica C. de Greef

ORCID

, Andrew Gennery, Paolo Picco, Barbara Kloeckener-Gruissem and 14 other authors

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

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2012 Richard J. L. F. Lemmers, Rabi Tawil, Lisa M. Petek, P. J. van der Vliet, Judit Balog, Gregory J. Block, M. de Visser, Gijs W. E. Santen, Amanda M. Amell, Patrick J. van der Vliet, Rowida Almomani, Kirsten R. Straasheijm, Yvonne D. Krom, Rinse Klooster, Yu Sun and 21 other authors

Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2

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Judit Balog, Peter E. Thijssen, Jessica C. de Greef

ORCID

, J. C. de Greef, Bharati Shah, Baziel G. M. van Engelen, B. G. M. van Engelen, Kyoko Yokomori, Stephen J. Tapscott, Rabi Tawil, Silvère M. van der Maarel

ORCID

, S. M. van der Maarel

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

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2011 Sabrina Sacconi

ORCID

, Adolfo Lopez de Munain Arregui, Pilar Camaño

ORCID

, Jessica C. de Greef

ORCID

, de Greef Jc, Richard J. L. F. Lemmers, Lemmers Rj, Leonardo Salviati, Pascal Boileau, Adolfo Lopez De Munain Arregui, Silvère M. van der Maarel

ORCID

, van der Maarel Sm, Claude Desnuelle

Patients with a phenotype consistent with facioscapulohumeral muscular dystrophy display genetic and epigenetic heterogeneity

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Jessica C. de Greef

ORCID

, Jun Wang, J. C. de Greef, Judit Balog, Johan T. den Dunnen, Rune R. Frants, Kirsten R. Straasheijm, J. T. den Dunnen, Mirjam van der Burg, Caner Aytekin, M. van der Burg, Laurence Duprez, Alina Ferster, Andrew R. Gennery, Giorgio Gimelli and 20 other authors

Mutations in ZBTB24 Are Associated with Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome Type 2

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2010 J. C. de Greef, J. C. de Greef, Rjlf J. L. F. Lemmers, Jc De Greef

ORCID

ORCID

, Jw W. Day, S. Sacconi, B. G. M. van Engelen, M. Dunand, Bgm G. M. van Engelen, S. Kiuru-Enari, Gw W. A. M. Padberg, Rosa Al, Al L. Rosa, C. Desnuelle and 7 other authors

Clinical features of facioscapulohumeral muscular dystrophy 2.

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2009 Peter S. Masny, On Ying A. Chan, Jessica C. de Greef

ORCID

, Ulla Bengtsson, Melanie Ehrlich, Rabi Tawil, Leslie F. Lock, Jane E. Hewitt, Jennifer Stocksdale, Jorge H. Martin, Silvere M. van der Maarel

ORCID

, Sara T. Winokur

Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonuclei

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Weihua Zeng, Jessica C. de Greef

ORCID

, Yen-Yun Chen, Richard Chien, Xiangduo Kong, Heather C. Gregson, Sara T. Winokur, April Pyle, Keith D. Robertson, John A. Schmiesing, Virginia E. Kimonis, Judit Balog, Rune R. Frants, Alexander R. Ball, Leslie F. Lock and 3 other authors

Specific Loss of Histone H3 Lysine 9 Trimethylation and HP1γ/Cohesin Binding at D4Z4 Repeats Is Associated with Facioscapulohumeral Dystrophy (FSHD)

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J. C. de Greef, Jessica C. de Greef

ORCID

, Richard J. L. F. Lemmers, Baziel G. M. van Engelen, B. G. M. van Engelen, Sabrina Sacconi

ORCID

, Shannon L. Venance, Rune R. Frants, Rabi Tawil, Silvère M. van der Maarel

ORCID

, S. M. van der Maarel

Common epigenetic changes of D4Z4 in contraction-dependent and contraction-independent FSHD.

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