Results 171 to 179 of about 7,802 (179)
Some of the next articles are maybe not open access.
Mammalian proteome expansion by stop codon readthrough
Wiley Interdisciplinary Reviews RNA, 2023Anumeha Singh +2 more
exaly
[Readthrough on transcription factor NKX2.5 premature stop codon by tRNA suppressors].
Yi chuan = Hereditas, 2015Human 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
L-MPZ, a Novel Isoform of Myelin P0, Is Produced by Stop Codon Readthrough
Journal of Biological Chemistry, 2012Yoshihide Yamaguchi +2 more
exaly
Readthrough of the premature stop codon beta039-thalassemia
2012SALVATORI, Francesca +13 more
openaire +1 more source
Evaluation of gentamycin for stop codon readthrough therapy in Fabry disease
2016BİBEROĞLU, GÜRSEL +6 more
openaire +1 more source

