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

Biochemistry, Genetics and Molecular Biology

• Troponin T 100%
• Mutant 31%
• Messenger RNA 31%
• Protein 25%
• Skeletal Muscle 12%
• Nonsense Mutation 12%
• Tropomyosin 12%
• TNNT1 12%
• Mutation 6%
• Nested Gene 6%
• Electric Potential 6%
• Escherichia coli 6%
• Codon 6%
• Degradation 6%
• Protein Catabolism 6%
• Binding Site 6%
• Nucleotide 6%
• Isoform 6%
• Autosomal Recessive Inheritance 6%
• RNA Splicing 6%
• C2C12 6%
• Transcription 6%
• Protein Hydrolysis 6%

INIS

• muscles 50%
• mutants 31%
• messenger-rna 31%
• proteins 25%
• mutations 18%
• patients 12%
• instability 12%
• tropomyosin 12%
• levels 6%
• rna 6%
• genes 6%
• losses 6%
• nucleotides 6%
• transcription 6%
• splicing 6%
• affinity 6%
• exons 6%
• polypeptides 6%
• escherichia coli 6%
• proteolysis 6%
• codons 6%
• myoblasts 6%