Related Posts


  1. Recent Publication
    Rbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD).
    PLoS Genet. 2013 Jan;9(1)
    Facioscapulohumeral muscular dystrophy (FSHD) is a common muscle disease whose molecular pathogenesis remains largely unknown. Over-expression of FSHD region gene 1 (FRG1) in mice, more…

  2. Recent Publication
    A repetitive elements perspective in Polycomb epigenetics.
    Front Genet. 2012;3:199.
    Repetitive elements comprise over two-thirds of the human genome. For a long time, these elements have received little attention since they were considered non-functional. more…

  3. Recent Publication
    A novel molecular mechanism in human genetic disease: A DNA repeat-derived lncRNA.
    RNA Biol. 2012 Oct 1;9(10):1211-7.
    Two thirds of the human genome is composed of repetitive sequences. Despite their prevalence, DNA repeats are largely ignored. The vast majority of our genome is transcribed to produce non protein-coding RNAs. more…

Leave a Comment

You must be logged in to post a comment.

Parse error: syntax error, unexpected '<' in /web/htdocs/ on line 2