Antisense suppression of donor splice site mutations in the dystrophin gene transcript

Por Fletcher, Sue, Meloni, Penny L, Johnsen, Russell D, Wong, Brenda L, Muntoni, Francesco, Wilton, Stephen D
Publicado em 2013

Deletion of Dystrophin In-Frame Exon 5 Leads to a Severe Phenotype: Guidance for Exon Skipping Strategies

Por Toh, Zhi Yon Charles, Thandar Aung-Htut, May, Pinniger, Gavin, Adams, Abbie M., Krishnaswarmy, Sudarsan, Wong, Brenda L., Fletcher, Sue, Wilton, Steve D.
Publicado no PLoS One (2016)

Myocardial Fibrosis Burden Predicts Left Ventricular Ejection Fraction and Is Associated With Age and Steroid Treatment Duration in Duchenne Muscular Dystrophy

Por Tandon, Animesh, Villa, Chet R., Hor, Kan N., Jefferies, John L., Gao, Zhiqian, Towbin, Jeffrey A., Wong, Brenda L., Mazur, Wojciech, Fleck, Robert J., Sticka, Joshua J., Benson, D. Woodrow, Taylor, Michael D.
Publicado no J Am Heart Assoc (2015)

Clinical and Genetic Characterization of Manifesting Carriers of DMD Mutations

Por Soltanzadeh, Payam, Friez, Michael J., Dunn, Diane, von Niederhausern, Andrew, Gurvich, Olga L., Swoboda, Kathryn J., Sampson, Jacinda B., Pestronk, Alan, Connolly, Anne M., Florence, Julaine M., Finkel, Richard S., Bönnemann, Carsten G., Medne, Livija, Mendell, Jerry R., Mathews, Katherine D., Wong, Brenda L., Sussman, Michael D., Zonana, Jonathan, Kovak, Karen, Gospe, Sidney M., Gappmaier, Eduard, Taylor, Laura E., Howard, Michael T., Weiss, Robert B., Flanigan, Kevin M.
Publicado em 2010