Readthrough compounds for nonsense mutations: bridging the translational gap-Reference-Cited by-同舟云学术

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Readthrough compounds for nonsense mutations: bridging the translational gap

Published:2023-04 Issue:4 Volume:29 Page:297-314
ISSN:1471-4914
Container-title:Trends in Molecular Medicine
language:en
Short-container-title:Trends in Molecular Medicine

Author:

Spelier Sacha,van Doorn Eveline P.M.,van der Ent Cornelis K.,Beekman Jeffrey M.,Koppens Martijn A.J.

Funder

Nederlandse Cystic Fibrosis Stichting

Gilead Sciences

Teva Pharmaceutical Industries

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference109 articles.

1. A meta-analysis of nonsense mutations causing human genetic disease;Mort;Hum. Mutat.,2008

2. The broader sense of nonsense;Karousis;Trends Biochem. Sci.,2022

3. Estimating cumulative point prevalence of rare diseases: analysis of the Orphanet database;Nguengang Wakap;Eur. J. Hum. Genet.,2022

4. The antimalarial drug mefloquine enhances TP53 premature termination codon readthrough by aminoglycoside G418;Ferguson;PLoS One,2019

5. A global analysis of the reconstitution of PTEN function by translational readthrough of PTEN pathogenic premature termination codons;Luna;Hum. Mutat.,2021

Cited by 24 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Ataluren-mediated nonsense variant readthrough in D-bifunctional protein deficiency: A case report;Molecular Genetics and Metabolism Reports;2024-12

2. Protein isoform-centric therapeutics: expanding targets and increasing specificity;Nature Reviews Drug Discovery;2024-09-04

3. Genome-scale quantification and prediction of pathogenic stop codon readthrough by small molecules;Nature Genetics;2024-08-22

4. Potentiation by Protein Synthesis Inducers of Translational Readthrough of Pathogenic Premature Termination Codons in PTEN Isoforms;Cancers;2024-08-13

5. mRNA-specific readthrough of nonsense codons by antisense oligonucleotides (R-ASOs);Nucleic Acids Research;2024-07-16

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