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mutations nonsense
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Curated Studies
Most Correlated Studies
Nonsense-mediated mRNA decay-inhibited LCLs from families predisposed to breast cancer
NIH3T3 cells expressing the wild type or nonsense mutant PreS/S gene of HBV
Brain cancer H4 and 42-MG-BA and colorectal cancer HCT 116 cells deficient for STAG2
HPFH and mutant KLF1 (p.K288X)-associated erythroid progenitor cell gene expression
Monocytes from moleculary heterogeneous acute myeloid leukemias
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Literature
Most Relevant Literature
Suppression of premature termination codons as a therapeutic approach.
Allele-specific therapy: suppression of nonsense mutations by readthrough inducers].
Pharmaceutical therapies to recode nonsense mutations in inherited diseases.
SMRT compounds correct nonsense mutations in primary immunodeficiency and other genetic models.
When a ribosome encounters a premature termination codon.
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Clinical Trials
Most Relevant Clinical Trials
Ataluren for Nonsense Mutation in CDKL5 and Dravet Syndrome
Ataluren for Nonsense Mutation Methylmalonic Acidemia
Study of Ataluren in Nonsense Mutation Cystic Fibrosis (ACT CF)
Correction of Nonsense Mutations in Cystic Fibrosis
Efficacy of Topical Gentamycin for Hereditary Hypotrichosis Simplex Caused by Nonsense Mutations in …
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