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Sense and Antisense DMPK RNA Foci Accumulate in DM1 Tissues during Development

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Aggregation-prone c9FTD/ALS poly(GA) RAN-translated proteins cause neurotoxicity by inducing ER stress

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Antisense Proline-Arginine RAN Dipeptides Linked to C9ORF72-ALS/FTD Form Toxic Nuclear Aggregates that Initiate In Vitro and In Vivo Neuronal Death

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Age of Onset of RNA Toxicity Influences Phenotypic Severity: Evidence from an Inducible Mouse Model of Myotonic Dystrophy (DM1)

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Molecular, Physiological, and Motor Performance Defects in DMSXL Mice Carrying >1,000 CTG Repeats from the Human DM1 Locus

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Mutant Human Embryonic Stem Cells Reveal Neurite and Synapse Formation Defects in Type 1 Myotonic Dystrophy

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DMPK protein isoforms are differentially expressed in myogenic and neural cell lineages

(2009) Ralph J. A. Oude Ophuis et al.   MUSCLE & NERVE

Satellite cell dysfunction contributes to the progressive muscle atrophy in myotonic dystrophy type 1

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Reversal of RNA Dominance by Displacement of Protein Sequestered on Triplet Repeat RNA

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Myotonic dystrophy protein kinase is expressed in embryonic myocytes and is required for myotube formation

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