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Oliver Muhlemann et al.
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Effectiveness of PTC124 treatment of cystic fibrosis caused by nonsense mutations: a prospective phase II trial
Eitan Kerem et al.
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Ming Du et al.
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Olaf Isken et al.
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PTC124 targets genetic disorders caused by nonsense mutations
Ellen M. Welch et al.
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Unproductive splicing of SR genes associated with highly conserved and ultraconserved DNA elements
Liana F. Lareau et al.
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Liat Linde et al.
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Gene-expression variation within and among human populations
John D. Storey et al.
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Exogenous control of mammalian gene expression via modulation of translational termination
George J. Murphy et al.
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Holly A. Kuzmiak et al.
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Functions of hUpf3a and hUpf3b in nonsense-mediated mRNA decay and translation
Joachim B. Kunz et al.
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Exon-junction complex components specify distinct routes of nonsense-mediated mRNA decay with differential cofactor requirements
NH Gehring et al.
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DHCR7 nonsense mutations and characterisation of mRNA nonsense mediated decay in Smith-Lemli-Opitz syndrome
LS Correa-Cerro et al.
JOURNAL OF MEDICAL GENETICS (2005)
Characterization of novel airway submucosal gland cell models for cystic fibrosis studies
AC da Paula et al.
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Premature stop codons involved in muscular dystrophies show a broad spectrum of readthrough efficiencies in response to gentamicin treatment
L Bidou et al.
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The pioneer translation initiation complex is functionally distinct from but structurally overlaps with the steady-state translation initiation complex
SY Chin et al.
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The major 5 ' determinant in stop codon read-through involves two adjacent adenines
S Tork et al.
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Evidence for a pioneer round of mRNA translation: mRNAs subject to nonsense-mediated decay in mammalian cells are bound by CBP80 and CBP20
Y Ishigaki et al.
CELL (2001)
Impact of the six nucleotides downstream of the stop codon on translation termination
O Namy et al.
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SC35 autoregulates its expression by promoting splicing events that destabilize its mRNAs
A Sureau et al.
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Human Upf proteins target an mRNA for nonsense-mediated decay when bound downstream of a termination codon
J Lykke-Andersen et al.
CELL (2000)
Assembly of the dystrophin-associated protein complex does not require the dystrophin COOH-terminal domain
GE Crawford et al.
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