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M. Bryan Warf et al.
RNA (2007)
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C Martel et al.
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Use of minigene systems to dissect alternative splicing elements
TA Cooper
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YK Kim et al.
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HnRNP H inhibits nuclear export of mRNA containing expanded CUG repeats and a distal branch point sequence
DH Kim et al.
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Interaction of Staufen1 with the 5 ' end of mRNA facilitates translation of these RNAs
S Dugre-Brisson et al.
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NA Timchenko et al.
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Muscleblind proteins regulate alternative splicing
TH Ho et al.
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A muscleblind knockout model for myotonic dystrophy
RN Kanadia et al.
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Localization of the RNA-binding proteins Staufen1 and Staufen2 at the mammalian neuromuscular junction
G Bélanger et al.
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A Buj-Bello et al.
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M Luo et al.
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A Mankodi et al.
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N Charlet-B et al.
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H Seznec et al.
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Molecular basis for impaired muscle differentiation in myotonic dystrophy
NA Timchenko et al.
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RS Savkur et al.
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Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat
A Mankodi et al.
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B Tian et al.
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