Ribonuclear foci at the neuromuscular junction in myotonic dystrophy type 1
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference38 articles.
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3. Expansion of a CUG trinucleotide repeat in the 3′ untranslated region of myotonic dystrophy protein kinase transcripts results in nuclear retention of transcripts;Davis;Proc Natl Acad Sci USA,1997
4. Foci of trinucleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues;Taneja;J Cell Biol,1995
5. Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy;Miller;EMBO J,2000
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1. CaMKIIβ deregulation contributes to neuromuscular junction destabilization in Myotonic Dystrophy type I;Skeletal Muscle;2024-05-21
2. Resistance Exercise Training Rescues Mitochondrial Dysfunction in Skeletal Muscle of Patients with Myotonic Dystrophy Type 1;Journal of Neuromuscular Diseases;2023-11-07
3. Destabilization of neuromuscular junctions and deregulation of activity-dependent signalling pathways in Myotonic Dystrophy type I;2023-03-10
4. Strength training rescues mitochondrial dysfunction in skeletal muscle of patients with myotonic dystrophy type 1;2023-01-23
5. MBNL‐dependent impaired development within the neuromuscular system in myotonic dystrophy type 1;Neuropathology and Applied Neurobiology;2023-01-17
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