Results 171 to 179 of about 7,802 (179)
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Mammalian proteome expansion by stop codon readthrough

Wiley Interdisciplinary Reviews RNA, 2023
Anumeha Singh   +2 more
exaly  

[Readthrough on transcription factor NKX2.5 premature stop codon by tRNA suppressors].

Yi chuan = Hereditas, 2015
Human NKX2.5 (NK2 homeobox 5) premature stop codon (PTC) mutations cause congenital heart diseases such as atrial septal defect and atrioventricular block. At present, eight NKX2.5 PTC mutations were reported as E109X, Q149X, Q170X, Q187X, Q198X, Y256X, Y259X and C264X. To observe the ability of tRNA suppressors to read through NKX2.5 PTC mutations and
Ping, Ouyang   +8 more
openaire   +1 more source

Influence of negamycin-derived stop codon readthrough agents on physiological readthrough event in vivo

Journal of the Neurological Sciences, 2017
H. Baba   +5 more
openaire   +1 more source

L-MPZ, a Novel Isoform of Myelin P0, Is Produced by Stop Codon Readthrough

Journal of Biological Chemistry, 2012
Yoshihide Yamaguchi   +2 more
exaly  

Readthrough of the premature stop codon beta039-thalassemia

2012
SALVATORI, Francesca   +13 more
openaire   +1 more source

Evaluation of gentamycin for stop codon readthrough therapy in Fabry disease

2016
BİBEROĞLU, GÜRSEL   +6 more
openaire   +1 more source

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