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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.Molecular Therapy. Oncology|April 6, 2026
Identification of small molecules that enhance aminoglycoside-mediated suppression of CFTR and NF1 nonsense mutationsJoshua Sammons, Jianguo Chen, Kari Thrasher, et al.Journal of Thrombosis and Haemostasis : JTH|February 8, 2024
Pharmacologic targeting of coagulation factors XII and XI by monoclonal antibodies reduces thrombosis in nitinol stents under flowNovella M Keeling, Michael Wallisch, Jennifer Johnson, et al.British Journal of Haematology|March 10, 2005
The prevalence of the cysteine1584 variant of von Willebrand factor is increased in type 1 von Willebrand disease: co-segregation with increased susceptibility to ADAMTS13 proteolysis but not clinical phenotypeDerrick J Bowen, Peter W Collins, Will Lester, 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.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 7, 2014
Rapamycin nanoparticles target defective autophagy in muscular dystrophy to enhance both strength and cardiac functionKristin P Bibee, Ya-Jian Cheng, James K Ching, 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.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 13