About: Quantitative analysis of CAPN3 and DMD transcripts: Involvement of nonsense-mediated mRNA decay     Goto   Sponge   NotDistinct   Permalink

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  • Duchenne and Becker muscular dystrophy (DMD/BMD) are associated with mutations in the DMD gene (Xp21); limb girdle muscular dystrophy type 2A (LGMD2A) with mutations in the CAPN3 gene (15q15). Pathological mutations connected with these phenotypes frequently disrupt the translational reading frame, giving rise to truncated proteins. Nonsense-mediated mRNA decay (NMD) is a type of quality control mechanism that selectively degrades mRNAs with premature termination codons (PTCs). Using real-time PCR, we performed quantitative analysis of DMD and CAPN3 transcripts carrying various mutated alleles and examined mRNA degradation by reason of NMD.
  • Duchenne and Becker muscular dystrophy (DMD/BMD) are associated with mutations in the DMD gene (Xp21); limb girdle muscular dystrophy type 2A (LGMD2A) with mutations in the CAPN3 gene (15q15). Pathological mutations connected with these phenotypes frequently disrupt the translational reading frame, giving rise to truncated proteins. Nonsense-mediated mRNA decay (NMD) is a type of quality control mechanism that selectively degrades mRNAs with premature termination codons (PTCs). Using real-time PCR, we performed quantitative analysis of DMD and CAPN3 transcripts carrying various mutated alleles and examined mRNA degradation by reason of NMD. (en)
Title
  • Quantitative analysis of CAPN3 and DMD transcripts: Involvement of nonsense-mediated mRNA decay
  • Quantitative analysis of CAPN3 and DMD transcripts: Involvement of nonsense-mediated mRNA decay (en)
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  • Quantitative analysis of CAPN3 and DMD transcripts: Involvement of nonsense-mediated mRNA decay
  • Quantitative analysis of CAPN3 and DMD transcripts: Involvement of nonsense-mediated mRNA decay (en)
skos:notation
  • RIV/00216224:14310/08:00027360!RIV10-MSM-14310___
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  • P(LC06023), Z(MSM0021622415)
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  • RIV/00216224:14310/08:00027360
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  • Duchenne muscular dystrophy; limb girdle muscular dystrophy type 2A; Nonsense-mediated mRNA decay; real-time PCR; premature termination codon (en)
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  • [0413303AC361]
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  • Fajkusová, Lenka
  • Hermanová, Markéta
  • Sedláčková, Jana
  • Vondráček, Petr
  • Stehlíková, K.
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  • 14310
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