Articles with "fshd2 muscle" as a keyword



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Small noncoding RNAs in FSHD2 muscle cells reveal both DUX4- and SMCHD1-specific signatures

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Published in 2018 at "Human Molecular Genetics"

DOI: 10.1093/hmg/ddy173

Abstract: Facioscapulohumeral muscular dystrophy (FSHD) is caused by insufficient epigenetic repression of D4Z4 macrosatellite repeat where DUX4, an FSHD causing gene is embedded. There are two forms of FSHD, FSHD1 with contraction of D4Z4 repeat and… read more here.

Keywords: small noncoding; muscle; muscle cells; noncoding rnas ... See more keywords