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Journal of Molecular Medicine (Berlin, Germany)|September 13, 2002
Aminoglycoside suppression of a premature stop mutation in a Cftr-/- mouse carrying a human CFTR-G542X transgeneMing Du, Julie R Jones, Jessica Lanier, et al.American Journal of Respiratory Cell and Molecular Biology|November 21, 2013
Synthetic aminoglycosides efficiently suppress cystic fibrosis transmembrane conductance regulator nonsense mutations and are enhanced by ivacaftorXiaojiao Xue, Venkateshwar Mutyam, Liping Tang, et al.Molecular Therapy. Oncology|April 6, 2026
Identification of small molecules that enhance aminoglycoside-mediated suppression of <i>CFTR</i> and <i>NF1</i> nonsense mutationsJoshua Sammons, Jianguo Chen, Kari Thrasher, et al.Proceedings of the National Academy of Sciences of the United States of America|October 6, 2016
Ataluren stimulates ribosomal selection of near-cognate tRNAs to promote nonsense suppressionBijoyita Roy, Westley J Friesen, Yuki Tomizawa, et al.American Journal of Respiratory and Critical Care Medicine|April 23, 2016
Discovery of Clinically Approved Agents That Promote Suppression of Cystic Fibrosis Transmembrane Conductance Regulator Nonsense MutationsVenkateshwar Mutyam, Ming Du, Xiaojiao Xue, et al.International Journal of Molecular Sciences|March 11, 2023
Triamterene Functions as an Effective Nonsense Suppression Agent for MPS I-H (Hurler Syndrome)Amna Siddiqui, Halil Dundar, Jyoti Sharma, et al.Plos One|March 11, 2014
Characterization of defects in ion transport and tissue development in cystic fibrosis transmembrane conductance regulator (CFTR)-knockout ratsKatherine L Tuggle, Susan E Birket, Xiaoxia Cui, et al.Nature Communications|July 17, 2021
A small molecule that induces translational readthrough of CFTR nonsense mutations by eRF1 depletionJyoti Sharma, Ming Du, Eric Wong, et al.Pageof 5