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pro vyhledávání: '"Nune Schelling-Kazaryan"'
Autor:
Celine E.F. de Esch, Mehrnaz Ghazvini, Friedemann Loos, Nune Schelling-Kazaryan, W. Widagdo, Shashini T. Munshi, Erik van der Wal, Hannie Douben, Nilhan Gunhanlar, Steven A. Kushner, W.W.M. Pim Pijnappel, Femke M.S. de Vrij, Niels Geijsen, Joost Gribnau, Rob Willemsen
Publikováno v:
Stem Cell Reports, Vol 3, Iss 4, Pp 548-555 (2014)
Silencing of the FMR1 gene leads to fragile X syndrome, the most common cause of inherited intellectual disability. To study the epigenetic modifications of the FMR1 gene during silencing in time, we used fibroblasts and induced pluripotent stem cell
Externí odkaz:
https://doaj.org/article/4bc398bc60f04d64abcc5a91b2acd30d
