Prader–Willi syndrome (PWS) is a neurodevelopmental disorder characterized by hypothalamic dysfunction, developmental delay, hyperphagia, and cognitive impairment, yet the cellular mechanisms underlying circuit abnormalities remain unclear. Here, we show that loss of the imprinted gene Magel2 remodels microglial state...
Jemima Helen, M. C. Wimmer, Berkan Kanmaz et al.· bioRxiv· 0 citations
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder caused by loss of expression from the active paternal allele at an imprinted cluster on chromosome 15. Current treatments address individual symptoms rather than the underlying cause of disease. Because all patients preserve a normal but epigenetically silenc...
Megan Iminitoff, Anna Le Fevre, Tamara Cameron et al.· Science Advances· 0 citations
It is revealed that DNA binding constrains SMCHD1 mobility and supports maintenance, rather than initial recruitment, of chromatin-bound SMCHD1 both during interphase and mitosis both during interphase and mitosis.
Rui-Feng Hu, Julissa J. Sánchez-Velásquez, Jieqiong Lou et al.· bioRxiv· 0 citations
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