Center-Authored Papers

Filters: Author is Jagannathan, Sujatha  [Clear All Filters]
Journal Article
Jagannathan S, Bradley RK.  2017.  Congenital myotonic dystrophy-an RNA-mediated disease across a developmental continuum.. Genes & development. 31(11):1067-1068. Abstract
Shadle SC, Zhong JW, Campbell AE, Conerly ML, Jagannathan S, Wong C-J, Morello TD, van der Maarel SM, Tapscott SJ.  2017.  DUX4-induced dsRNA and MYC mRNA stabilization activate apoptotic pathways in human cell models of facioscapulohumeral dystrophy.. PLoS genetics. 13(3):e1006658. Abstract
Feng Q, Snider L, Jagannathan S, Tawil R, van der Maarel SM, Tapscott SJ, Bradley RK.  2015.  A feedback loop between nonsense-mediated decay and the retrogene DUX4 in facioscapulohumeral muscular dystrophy.. eLife. 4 Abstract
Jagannathan S, Shadle S, Resnick R, Snider L, Tawil RN, van der Maarel SM, Bradley RK, Tapscott SJ.  2016.  Model systems of DUX4 expression recapitulate the transcriptional profile of FSHD cells.. Human molecular genetics. Abstract
Campbell AE, Shadle SC, Jagannathan S, Lim J-W, Resnick R, Tawil R, van der Maarel SM, Tapscott SJ.  2018.  NuRD and CAF-1-mediated silencing of the D4Z4 array is modulated by DUX4-induced MBD3L proteins.. eLife. 7 Abstract
Jagannathan S, Ogata Y, Gafken PR, Tapscott SJ, Bradley RK.  2019.  Quantitative proteomics reveals key roles for post-transcriptional gene regulation in the molecular pathology of FSHD.. eLife. 8 Abstract
Feng Q, Jagannathan S, Bradley RK.  2017.  The RNA Surveillance Factor UPF1 Represses Myogenesis via Its E3 Ubiquitin Ligase Activity.. Molecular cell. Abstract
Jagannathan S, Bradley RK.  2016.  Translational plasticity facilitates the accumulation of nonsense genetic variants in the human population.. Genome research. Abstract