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Most Correlated Studies
- Eyes from E12.5 PXDN T3816A homozygous mutants
- Gene expression in hematopoietic stem cells in Apcmin mutant mice
- Orthotopic breast cancer MDA-MB-231 cells from NSG mice with hypoxia driven reporter expression
- Myoblasts from limb-girdle muscular dystrophy D2 patient with TNPO3 mutation or correction
- Neural tube defect susceptibilty related to gene expression in 2 mouse strains with mutant Cecr1
Most Relevant Literature
- A novel function for eukaryotic elongation factor 3: Inhibition of stop codon readthrough in yeast.
- Dual stop codon suppression in mammalian cells with genomically integrated genetic code expansion ma…
- HLA-DQA1*05:01:11, a novel HLA-DQA1 allele with an ochre stop codon.
- Environment modulates protein heterogeneity through transcriptional and translational stop codon rea…
- Why Is the UAG (Amber) Stop Codon Almost Absent in Highly Expressed Bacterial Genes?
Most Relevant Clinical Trials
- Six Month Study of Gentamicin in Duchenne Muscular Dystrophy With Stop Codons
- Azithromycin Treatment for Readthrough of APC Gene Stop Codon Mutations in Familial Adenomatous Poly…
- Erythromycin Treatment for Readthrough of APC Gene Stop Codon Mutations in Familial Adenomatous Poly…
- Erythromycin Treatment for Readthrough of APC Gene Stop Codon Mutation in Familial Adenomatous Polyp…
- Rare CFTR Mutation Cell Collection Protocol (RARE)
