Results 211 to 219 of about 418,363 (219)

Aminoglycosides are efficient reagents to induce readthrough of premature termination codon in mutant B4GALNT1 genes found in families of hereditary spastic paraplegia

Journal of Biochemistry, 2020
Koichi Furukawa, Tetsuya Okajima, Keiko Furukawa   +2 more
exaly  

A novel mutation within intron 17 of the CUL7 gene results in appearance of premature termination codon

Clinica Chimica Acta, 2020
Hong-Dan Wang, Lin Liu, Xiaoye Jin
exaly  

T‐cell receptor sequences that elicit strong down‐regulation of premature termination codon‐bearing transcripts

EMBO Journal, 2002
Miles F Wilkinson
exaly  

eRF1 mediates codon usage effects on mRNA translation efficiency through premature termination at rare codons

Nucleic Acids Research, 2019
Cheng Wu, Fangzhou Zhao, Matthew S. Sachs   +2 more
exaly  

A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy

Journal of Neurology, 2005
Gian Nicola Gallus, Alessandra Rufa, Antonio Federico   +2 more
exaly  

Molecular Characterization of Hb Hamilton Hill (HBA2: c.388delC), a Novel HBA2 Variant Generating a Premature Termination Codon and Truncated HBA2 Chain

Hemoglobin, 2015
Reza Ghassemifar, Talal Qadah, Jill Finlayson   +2 more
exaly  

Sense from nonsense: therapies for premature stop codon diseases

Trends in Molecular Medicine, 2012
Olivier Namy, Laure Bidou, Jean-Pierre Rousset   +2 more
exaly  

Cell models for McArdle disease and aminoglycoside-induced read-through of a premature termination codon

Neuromuscular Disorders, 2013
Glenn E Morris
exaly  

The selective chemical modification of the 6-amino group of adenosine of the premature termination codon induces readthrough to produce full-length peptide in the reconstituted translation system

Bioorganic and Medicinal Chemistry
Yosuke Taniguchi, Shigeki Sasaki
exaly