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Position of premature termination codons determines susceptibility of hERG mutations to nonsense-mediated mRNA decay in long QT syndrome
Authors:Qiuming Gong  Matthew R. StumpZhengfeng Zhou
Affiliation:Knight Cardiovascular Institute, Oregon Health & Science University, Portland, OR, USA
Abstract:
Keywords:CHX, cycloheximide   EJC, exon junction complex   hERG, human ether-a-go-go-related gene   HPH, hygromycin B phosphotransferase   LQT2, long QT syndrome type 2   MO, morpholino oligonucleotide   NMD, nonsense-mediated mRNA decay   nt, nucleotide   PTC, premature termination codon   RPA, RNase protection assay   shRNA, short hairpin RNA   UPF1, up-frameshift protein 1   WT, wild-type
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