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204th ENMC International Workshop on Biomarkers in Duchenne Muscular Dystrophy 24-26 January 2014, Naarden, The NetherlandsConserved regions of the DMD 3' UTR regulate translation and mRNA abundance in cultured myotubesLong-term efficacy of systemic multiexon skipping targeting dystrophin exons 45-55 with a cocktail of vivo-morpholinos in mdx52 miceGenome-wide association study to identify potential genetic modifiers in a canine model for Duchenne muscular dystrophyDigital Droplet PCR for the Absolute Quantification of Exon Skipping Induced by Antisense Oligonucleotides in (Pre-)Clinical Development for Duchenne Muscular Dystrophy.Dp412e: a novel human embryonic dystrophin isoform induced by BMP4 in early differentiated cells.Genetic myostatin decrease in the golden retriever muscular dystrophy model does not significantly affect the ubiquitin proteasome system despite enhancing the severity of disease.Dystrophin insufficiency causes selective muscle histopathology and loss of dystrophin-glycoprotein complex assembly in pig skeletal muscle.The Dynamics of Compound, Transcript, and Protein Effects After Treatment With 2OMePS Antisense Oligonucleotides in mdx Mice.A novel canine model for Duchenne muscular dystrophy (DMD): single nucleotide deletion in DMD gene exon 20.Tracking disease progression non-invasively in Duchenne and Becker muscular dystrophies
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DMD transcript imbalance determines dystrophin levels.
@en
DMD transcript imbalance determines dystrophin levels.
@nl
type
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DMD transcript imbalance determines dystrophin levels.
@en
DMD transcript imbalance determines dystrophin levels.
@nl
prefLabel
DMD transcript imbalance determines dystrophin levels.
@en
DMD transcript imbalance determines dystrophin levels.
@nl
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DMD transcript imbalance determines dystrophin levels.
@en
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Anneke A M Janson
Beatrijs Wokke
Janneke C van den Bergen
Johan T den Dunnen
Rani van den Eijnde
P304
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10.1096/FJ.13-232025
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P577
2013-08-23T00:00:00Z