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Generation of genetically matched hiPSC lines from two mosaic facioscapulohumeral dystrophy type 1 patients.
van der Wal E, den Hamer B, van der Vliet PJ, Tok M, Brands T, Eussen B, Lemmers RJLF, Freund C, de Klein A, Buijsen RAM, van Roon-Mom WMC, Tawil R, van der Maarel SM, de Greef JC. van der Wal E, et al. Among authors: de klein a, de greef jc. Stem Cell Res. 2019 Oct;40:101560. doi: 10.1016/j.scr.2019.101560. Epub 2019 Aug 28. Stem Cell Res. 2019. PMID: 31518905 Free article.
Mouse models for muscular dystrophies: an overview.
van Putten M, Lloyd EM, de Greef JC, Raz V, Willmann R, Grounds MD. van Putten M, et al. Among authors: de greef jc. Dis Model Mech. 2020 Feb 21;13(2):dmm043562. doi: 10.1242/dmm.043562. Dis Model Mech. 2020. PMID: 32224495 Free PMC article. Review.
Cytoskeletal disorganization underlies PABPN1-mediated myogenic disability.
Olie CS, van der Wal E, Cikes D, Maton L, de Greef JC, Lin IH, Chen YF, Kareem E, Penninger JM, Kessler BM, Raz V. Olie CS, et al. Among authors: de greef jc. Sci Rep. 2020 Oct 19;10(1):17621. doi: 10.1038/s41598-020-74676-8. Sci Rep. 2020. PMID: 33077830 Free PMC article.
USP18 is an essential regulator of muscle cell differentiation and maturation.
Olie CS, Pinto-Fernández A, Damianou A, Vendrell I, Mei H, den Hamer B, van der Wal E, de Greef JC, Raz V, Kessler BM. Olie CS, et al. Among authors: de greef jc. Cell Death Dis. 2023 Mar 31;14(3):231. doi: 10.1038/s41419-023-05725-z. Cell Death Dis. 2023. PMID: 37002195 Free PMC article.
Highly contractile 3D tissue engineered skeletal muscles from human iPSCs reveal similarities with primary myoblast-derived tissues.
van der Wal E, Iuliano A, In 't Groen SLM, Bholasing AP, Priesmann D, Sharma P, den Hamer B, Saggiomo V, Krüger M, Pijnappel WWMP, de Greef JC. van der Wal E, et al. Among authors: de greef jc. Stem Cell Reports. 2023 Oct 10;18(10):1954-1971. doi: 10.1016/j.stemcr.2023.08.014. Epub 2023 Sep 28. Stem Cell Reports. 2023. PMID: 37774701 Free PMC article.
No effect of folic acid and methionine supplementation on D4Z4 methylation in patients with facioscapulohumeral muscular dystrophy.
van der Kooi EL, de Greef JC, Wohlgemuth M, Frants RR, van Asseldonk RJ, Blom HJ, van Engelen BG, van der Maarel SM, Padberg GW. van der Kooi EL, et al. Among authors: de greef jc. Neuromuscul Disord. 2006 Nov;16(11):766-9. doi: 10.1016/j.nmd.2006.08.005. Epub 2006 Sep 26. Neuromuscul Disord. 2006. PMID: 17005397 Free article.
Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD).
Zeng W, de Greef JC, Chen YY, Chien R, Kong X, Gregson HC, Winokur ST, Pyle A, Robertson KD, Schmiesing JA, Kimonis VE, Balog J, Frants RR, Ball AR Jr, Lock LF, Donovan PJ, van der Maarel SM, Yokomori K. Zeng W, et al. Among authors: de greef jc. PLoS Genet. 2009 Jul;5(7):e1000559. doi: 10.1371/journal.pgen.1000559. Epub 2009 Jul 10. PLoS Genet. 2009. PMID: 19593370 Free PMC article.
32 results