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Articles (47)

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1-10 of 47 results for nonsense codon

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Select article: Read-Through Strategies for Suppression of Nonsense Mutations in Duchenne/ Becker Muscular Dystrophy: Aminoglycosides and Ataluren (PTC124)

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Other

First published 2010-9

Read-Through Strategies for Suppression of Nonsense Mutations in Duchenne/ Becker Muscular Dystrophy: Aminoglycosides and Ataluren (PTC124)

Richard S. Finkel

Journal of Child Neurology

Select article: A Chinese boy with familial Duchenne muscular dystrophy owing to a novel hemizygous nonsense mutation (c.6283C>T) in an exon of the DMD gene

Open access

Case report

First published 2022

A Chinese boy with familial Duchenne muscular dystrophy owing to a novel hemizygous nonsense mutation (c.6283C>T) in an exon of the DMD gene

Xing-Chuan Li, Song Wang, Jia-Rui Zhu [...]

Sage Open Medical Case Reports

Select article: Conserved Nonsense-Prone CpG Sites in Apoptosis-Regulatory Genes: Conditional Stop Signs on the Road to cell Death

Open access

Research article

First published 2013

Conserved Nonsense-Prone CpG Sites in Apoptosis-Regulatory Genes: Conditional Stop Signs on the Road to cell Death

Yongzhong Zhao, Richard J. Epstein

Evolutionary Bioinformatics

Select article: A Splice-Site Mutation that Induces Exon Skipping and Reduction in Lysyl Hydroxylase mRNA Levels but Does Not Create a Nonsense Codon in Ehlers-Danlos Syndrome Type VI

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Research article

First published 1998-02

A Splice-Site Mutation that Induces Exon Skipping and Reduction in Lysyl Hydroxylase mRNA Levels but Does Not Create a Nonsense Codon in Ehlers-Danlos Syndrome Type VI

L. Pajunen, M. Suokas, T. Hautala [...]

DNA and Cell Biology

Select article: Suppression of Single and Double Nonsense Mutations Introduced into the Diphtheria Toxin A-Chain Gene: A Potential Binary System for Toxin Gene Therapy

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Research article

First published 1995-02

Suppression of Single and Double Nonsense Mutations Introduced into the Diphtheria Toxin A-Chain Gene: A Potential Binary System for Toxin Gene Therapy

Donald F. Robinson, Ian H. Maxwell

Human Gene Therapy

Select article: Aminoglycoside-induced mutation suppression (stop codon readthrough) as a therapeutic strategy for Duchenne muscular dystrophy

Free access

Review article

First published 2010-11

Aminoglycoside-induced mutation suppression (stop codon readthrough) as a therapeutic strategy for Duchenne muscular dystrophy

Vinod Malik, Louise R. Rodino-Klapac, Laurence Viollet [...]

Therapeutic Advances in Neurological Disorders

Select article: Targeting translational read-through of premature termination mutations in BMPR2 with PTC124 for pulmonary arterial hypertension

Open access

Research article

First published 2020-7

Targeting translational read-through of premature termination mutations in BMPR2 with PTC124 for pulmonary arterial hypertension

Lu Long, Xudong Yang, Mark Southwood [...]

Pulmonary Circulation

Select article: Sequence Verification of Mutant Codon Assignments in trpA of Escherichia coli

Retricted access

Research article

First published 1986-04

Sequence Verification of Mutant Codon Assignments in trpA of Escherichia coli

Stanley D. Tucker, Emanuel J. Murgola

DNA and Cell Biology

Select article: Expression of a novel versican variant in dorsal root ganglia from spared nerve injury rats

Open access

Research article

First published 2019

Expression of a novel versican variant in dorsal root ganglia from spared nerve injury rats

Oliver Bogen, Olaf Bender, Pedro Alvarez [...]

Molecular Pain

Select article: Targeting Translation Termination Machinery with Antisense Oligonucleotides for Diseases Caused by Nonsense Mutations

Open access

Research article

First published 2019-08

Targeting Translation Termination Machinery with Antisense Oligonucleotides for Diseases Caused by Nonsense Mutations

Lulu Huang, Mariam Aghajan, Tianna Quesenberry [...]

Nucleic Acid Therapeutics

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