Insulin receptor splicing alteration in myotonic dystrophy type 2

Keyphrases

• Myotonic Dystrophy 100%
• Myotonic Dystrophy Type 2 100%
• Insulin Receptor 100%
• Splicing Alteration 100%
• Repeat Expansion 40%
• Diabetes 20%
• Mouse Model 20%
• Dysregulation 20%
• Nonmuscle 20%
• RNA-binding Protein 20%
• Species Differences 20%
• Muscle Pathology 20%
• 3′-untranslated Region (3′-UTR) 20%
• Chromosome 3 20%
• DMPK Gene 20%
• Insulin Deficiency 20%
• RNA Splicing 20%
• Chromosome 19 20%
• ZNF9 20%
• Tetranucleotide Repeats 20%
• Splicing Abnormality 20%
• CTG Expansion 20%
• Pathogenic Effects 20%

Neuroscience

• Myotonic Dystrophy 100%
• Insulin Receptor 100%
• Untranslated Region 33%
• Alternative Splicing 33%
• Histopathology 33%
• Intron 33%
• Chromosome 19 33%
• Chromosome 3 33%
• RNA-binding Protein 33%
• Nucleus 33%

Biochemistry, Genetics and Molecular Biology

• Insulin Receptor 100%
• Isoform 33%
• Mouse Model 33%
• RNA 33%
• RNA-binding Protein 33%
• Insulin Sensitivity 33%
• Intron 33%
• Chromosome 3 33%
• Untranslated Region 33%
• Alternative Splicing 33%
• Species Difference 33%
• Chromosome 19 33%