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The American Journal of Pathology|March 25, 2018
Long-Term Treatment of Tamoxifen and Raloxifene Alleviates Dystrophic Phenotype and Enhances Muscle Functions of FKRP DystroglycanopathyBo Wu, Sapana N Shah, Peijuan Lu, et al.The American Journal of Pathology|June 12, 2012
Long-term rescue of dystrophin expression and improvement in muscle pathology and function in dystrophic mdx mice by peptide-conjugated morpholinoBo Wu, Peijuan Lu, Caryn Cloer, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|January 21, 2010
Guanine analogues enhance antisense oligonucleotide-induced exon skipping in dystrophin gene in vitro and in vivoYihong Hu, Bo Wu, Allen Zillmer, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|December 24, 2010
One-year treatment of morpholino antisense oligomer improves skeletal and cardiac muscle functions in dystrophic mdx miceBo Wu, Bin Xiao, Caryn Cloer, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|July 23, 2014
Muscle and heart function restoration in a limb girdle muscular dystrophy 2I (LGMD2I) mouse model by systemic FKRP gene deliveryChunping Qiao, Chi-Hsien Wang, Chunxia Zhao, et al.The American Journal of Pathology|January 13, 2011
Post-Natal knockdown of fukutin-related protein expression in muscle by long-termRNA interference induces dystrophic pathology [corrected]Chi-Hsien Wang, Yiumo Michael Chan, Ru-Hang Tang, et al.Proceedings of the National Academy of Sciences of the United States of America|September 23, 2008
Effective rescue of dystrophin improves cardiac function in dystrophin-deficient mice by a modified morpholino oligomerBo Wu, Hong M Moulton, Patrick L Iversen, et al.The American Journal of Pathology|April 26, 2016
Glucocorticoid Steroid and Alendronate Treatment Alleviates Dystrophic Phenotype with Enhanced Functional Glycosylation of α-Dystroglycan in Mouse Model of Limb-Girdle Muscular Dystrophy with FKRPP448L MutationBo Wu, Sapana N Shah, Peijuan Lu, et al.Pageof 3