Publications

Found 33 results
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2014
Gerhardt J, Zaninovic N, Zhan Q, Madireddy A, Nolin SL, Ersalesi N, Yan Z, Rosenwaks Z, Schildkraut CL.  2014.  Cis-acting DNA sequence at a replication origin promotes repeat expansion to fragile X full mutation.. J Cell Biol. 206(5):599-607.
Gerhardt J, Tomishima MJ, Zaninovic N, Colak D, Yan Z, Zhan Q, Rosenwaks Z, Jaffrey SR, Schildkraut CL.  2014.  The DNA replication program is altered at the FMR1 locus in fragile X embryonic stem cells.. Mol Cell. 53(1):19-31.
Colak D, Zaninovic N, Cohen MS, Rosenwaks Z, Yang W-Y, Gerhardt J, Disney MD, Jaffrey SR.  2014.  Promoter-bound trinucleotide repeat mRNA drives epigenetic silencing in fragile X syndrome.. Science. 343(6174):1002-5.
2008
Zhao X, Madden-Fuentes RJ, Lou BX, Pipas JM, Gerhardt J, Rigell CJ, Fanning E.  2008.  Ataxia telangiectasia-mutated damage-signaling kinase- and proteasome-dependent destruction of Mre11-Rad50-Nbs1 subunits in Simian virus 40-infected primate cells.. J Virol. 82(11):5316-28.
2007
Gray SJ, Gerhardt J, Doerfler W, Small LE, Fanning E.  2007.  An origin of DNA replication in the promoter region of the human fragile X mental retardation (FMR1) gene.. Mol Cell Biol. 27(2):426-37.
2006
Gerhardt J, Jafar S, Spindler M-P, Ott E, Schepers A.  2006.  Identification of new human origins of DNA replication by an origin-trapping assay.. Mol Cell Biol. 26(20):7731-46.
2003
Ritzi M, Tillack K, Gerhardt J, Ott E, Humme S, Kremmer E, Hammerschmidt W, Schepers A.  2003.  Complex protein-DNA dynamics at the latent origin of DNA replication of Epstein-Barr virus.. J Cell Sci. 116(Pt 19):3971-84.