Cellular fate of truncated slow skeletal muscle troponin T produced by Glu¹⁸⁰ nonsense mutation in amish nemaline myopathy

Medicine & Life Sciences

• Nemaline myopathy 5 100%
• Troponin T 55%
• Nonsense Codon 52%
• Skeletal Muscle 36%
• Myofibrils 7%
• Messenger RNA 6%
• Muscle Cells 5%
• Muscles 5%
• Complementary DNA 4%
• Nemaline Myopathies 4%
• Proteins 4%
• RNA Splicing 4%
• Myoblasts 3%
• Skeletal Muscle Fibers 3%
• RNA Stability 3%
• Eukaryotic Cells 3%
• Codon 2%
• Proteolysis 2%
• Exons 2%
• Nucleotides 2%
• Binding Sites 2%
• Escherichia coli 2%
• Peptides 1%
• Mutation 1%
• Genes 1%

Chemical Compounds

• Mutation 38%
• Protein 15%
• Protein Hydrolysis 9%
• Complementary DNA 9%
• Protective 7%
• Polypeptide 7%
• Nucleotide 7%
• Amount 3%