Human Molecular Genetics · 2016 · 74 citations · 51 references
Life SciencesGeneticsMolecular BiologyCell SignalingGenome EditingPharmacogeneticsInherited Retinal DystrophiesRetinal DegenerationInherited Ocular DiseaseNonsense Mutation EffectsNonsense Mutation TherapyNonsense SuppressionRetinal Degeneration MechanismsSingle-gene MutationsTranscriptional ReadthroughTranslational Readthrough
fibroblasts, there was a recovery of prenylation activity following treatment with either PTC124 (42 ± 5%) or PTC-414 (36 ± 11%), although an increase in REP1 protein was not detected in these cells, in contrast to the zebrafish model. This comprehensive study on the use of PTC124 and PTC-414 as successful nonsense suppression agents for the treatment of CHM highlights the translational potential of these drugs for inherited retinal disease.
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Stages of embryonic development of the zebrafish
Charles B. Kimmel, William W. Ballard, Seth R. Kimmel et al. · Developmental Dynamics · 1995 · 12.3K citations
PTC124 targets genetic disorders caused by nonsense mutations
Ellen Welch, Elisabeth R. Barton, Jin Zhuo et al. · Nature · 2007 · 1.1K citations