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Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 8/2006, Volume 103, Issue 31, pp. 11748 - 11753
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2/2008, Volume 105, Issue 7, pp. 2646 - 2651
Severe skeletal muscle wasting is the most debilitating symptom experienced by individuals with myotonic dystrophy type 1 (DM1). We present a DM1 mouse model... 
Alternative splicing | Messenger RNA | Splicing | RNA | Myotonic dystrophy | Tissue samples | Exons | Muscles | Gene expression regulation | Skeletal muscle | CUG-binding protein 1 | Muscle atrophy | Microsatellite expansion | Muscleblind-like 1 | alternative splicing | MULTIDISCIPLINARY SCIENCES | RECEPTOR | muscleblind-like 1 | BINDING PROTEIN | CUGBP1 | PRE-MESSENGER-RNA | OVEREXPRESSION | IN-VIVO | microsatellite expansion | NUCLEAR FOCI | MICE | muscle atrophy | STRIATED-MUSCLE | TYPE-1 | Muscle, Skeletal - enzymology | Myotonin-Protein Kinase | Protein-Serine-Threonine Kinases - genetics | 3' Untranslated Regions - genetics | CELF1 Protein | Disease Progression | Gene Expression Regulation, Enzymologic | Myotonic Dystrophy - pathology | Animals | Base Sequence | RNA Splicing - genetics | Sensitivity and Specificity | Myotonic Dystrophy - genetics | Mice | Myotonic Dystrophy - enzymology | Protein-Serine-Threonine Kinases - metabolism | RNA-Binding Proteins - metabolism | Disease Models, Animal | Influence | Models | Genetic aspects | Genetic engineering | Properties | Binding proteins | Muscular dystrophy | Proteins | Musculoskeletal system | Ribonucleic acid--RNA | Rodents | Index Medicus | Myotonic Dystrophy | Protein-Serine-Threonine Kinases | Biochemistry, Molecular Biology | RNA-Binding Proteins | Life Sciences | RNA Splicing | Muscle, Skeletal | 3' Untranslated Regions | Molecular biology | Biological Sciences
Journal Article
Journal Article
Science, ISSN 0036-8075, 8/2001, Volume 293, Issue 5531, pp. 864 - 867
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 3/2012, Volume 109, Issue 11, pp. 4221 - 4226
Myotonic dystrophy type 1 (DM1) is an RNA-dominant disease caused by abnormal transcripts containing expanded CUG repeats. The CUG transcripts aggregate in the... 
Cell culture techniques | Messenger RNA | RNA | Splicing | Myotonic dystrophy | Reverse transcriptase polymerase chain reaction | Muscles | Nucleotides | Nucleic acids | Skeletal muscle | Phosphorothioate | Microsatellite expansion | Muscular dystrophy | Gapmer | PROTEIN | MULTIDISCIPLINARY SCIENCES | MOUSE | gapmer | CTG-REPEAT | MECHANISMS | REVERSAL | SKELETAL-MUSCLE | muscular dystrophy | MESSENGER-RNA | phosphorothioate | microsatellite expansion | LOCKED NUCLEIC-ACIDS | ANTISENSE OLIGONUCLEOTIDES | CPG OLIGODEOXYNUCLEOTIDE | Gene Expression Regulation, Enzymologic - drug effects | Molecular Sequence Data | RNA Stability - drug effects | RNA, Messenger - metabolism | Gene Knockdown Techniques | Myotonic Dystrophy - pathology | Base Sequence | Muscle, Skeletal - drug effects | Myotonic Dystrophy - genetics | Protein-Serine-Threonine Kinases - metabolism | Disease Models, Animal | Muscle, Skeletal - enzymology | Oligonucleotides, Antisense - pharmacology | Myotonin-Protein Kinase | Morpholinos - administration & dosage | RNA, Messenger - genetics | Cells, Cultured | Protein-Serine-Threonine Kinases - genetics | Animals | Oligonucleotides, Antisense - genetics | Muscle, Skeletal - abnormalities | Morpholinos - pharmacology | Trinucleotide Repeat Expansion - genetics | Oligonucleotides, Antisense - administration & dosage | Mice | Muscle, Skeletal - pathology | Ribonuclease H - metabolism | Oligonucleotides | Physiological aspects | Development and progression | Genetic aspects | Health aspects | Proteins | Cell culture | Ribonucleic acid--RNA | Rodents | Degradation | Alternative splicing | Residues | Animal models | Antisense oligonucleotides | regulatory proteins | Ribonuclease | Index Medicus | Biological Sciences
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 03/2017, Volume 100, Issue 3, pp. 488 - 505
Journal Article
Journal Article
CANADIAN MEDICAL ASSOCIATION JOURNAL, ISSN 0820-3946, 10/2016, Volume 188, Issue 14, pp. 1033 - 1033