Showing results (61-70 of 234) with videos related to
Sort By:
Pageof 24
Msphere|May 24, 2019
The Vacuolar Zinc Transporter TgZnT Protects Toxoplasma gondii from Zinc ToxicityNathan M Chasen, Andrew J Stasic, Beejan Asady, et al.American Journal of Medical Genetics|June 15, 1993
Two distinct mutations in a single dystrophin gene: identification of an altered splice-site as the primary Becker muscular dystrophy mutationS D Wilton, R D Johnsen, J R Pedretti, et al.Human Mutation|January 1, 1994
Identification of a point mutation and germinal mosaicism in a Duchenne muscular dystrophy familyS D Wilton, D C Chandler, B A Kakulas, et al.Molecular Therapy. Nucleic Acids|March 20, 2014
Targeted exon skipping to correct exon duplications in the dystrophin geneKane L Greer, Hanns Lochmüller, Kevin Flanigan, et al.International Journal of Molecular Sciences|October 21, 2020
Nonsequential Splicing Events Alter Antisense-Mediated Exon Skipping Outcome in COL7A1Kristin A Ham, May Thandar Aung-Htut, Sue Fletcher, et al.Journal of Medical Case Reports|September 22, 2007
Advanced adenoma diagnosis with FDG PET in a visibly normal mucosa: a case reportBhavya Rehani, Richard M Chasen, Yvonne Dowdy, et al.The Journal of Gene Medicine|November 20, 2002
Improved antisense oligonucleotide induced exon skipping in the mdx mouse model of muscular dystrophyChristopher J Mann, Kaite Honeyman, Graham McClorey, et al.International Journal of Molecular Sciences|November 6, 2019
Removal of the Polyglutamine Repeat of Ataxin-3 by Redirecting pre-mRNA ProcessingCraig S McIntosh, May Thandar Aung-Htut, Sue Fletcher, et al.Biomedicines|November 27, 2021
Polyglutamine Ataxias: Our Current Molecular Understanding and What the Future Holds for Antisense TherapiesCraig S McIntosh, Dunhui Li, Steve D Wilton, et al.Journal of Biomolecular Screening|November 1, 2012
A cell-based high-throughput screening assay for posttranscriptional utrophin upregulationCatherine Moorwood, Neha Soni, Gopal Patel, et al.Pageof 24