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Article

Aminoglycoside-mediated suppression of nonsensemutations in late infantile neuronal ceroid lipofuscinosis

1 Jan 2001

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 11589009
DOI: 10.1053/ejpn.2000.0436

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Aminoglycoside-mediated suppression of nonsensemutations in late infantile neuronal ceroid lipofuscinosisPMID 11589009Read ↗

Repairing faulty genes by aminoglycosides: Development of new derivatives of geneticin (G418) with enhanced suppression of diseases-causing nonsense mutationsSemantic proximity Read ↗

Survival advantage of neonatal CNS gene transfer for late infantile neuronal ceroid lipofuscinosisSemantic proximity Read ↗

Residual levels of tripeptidyl-peptidase I activity dramatically ameliorate disease in late-infantile neuronal ceroid lipofuscinosisSemantic proximity Read ↗

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Suppression of aminoglycoside-induced premature termination codon readthrough by the TRP channel inhibitor AC1903Semantic proximity Read ↗

Tissue‐specific variation in nonsense mutant transcript level and drug‐induced read‐through efficiency in the Cln1R151X mouse model of INCLSemantic proximity Read ↗

Characterization of new-generation aminoglycoside promoting premature termination codon readthrough in cancer cells.Semantic proximity Read ↗

The novel Cln1R151X mouse model of infantile neuronal ceroid lipofuscinosis (INCL) for testing nonsense suppression therapySemantic proximity Read ↗

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