Supplemental material
Drug Delivery
Volume 24, 2017 - Issue 1
Related Research Data
Interaction between DNA–cationic liposome complexes and erythrocytes is an important factor in systemic gene transfer via the intravenous route in mice: the role of the neutral helper lipid
Source:
Springer Science and Business Media LLC
Control of protein-binding kinetics on synthetic polymer nanoparticles by tuning flexibility and inducing conformation changes of polymer chains
Source:
American Chemical Society (ACS)
Chronic systemic therapy with low-dose morpholino oligomers ameliorates the pathology and normalizes locomotor behavior in mdx mice.
Source:
Elsevier BV
Long-Term Rescue of Dystrophin Expression and Improvement in Muscle Pathology and Function in Dystrophic mdx Mice by Peptide-Conjugated Morpholino
Source:
American Society for Investigative Pathology. Published by Elsevier Inc.
Effects of complement depletion on the pharmacokinetics and gene delivery mediated by cationic lipid-DNA complexes.
Source:
Mary Ann Liebert Inc
Nuclear antisense effects of neutral, anionic and cationic oligonucleotide analogs
Source:
Oxford University Press (OUP)
Dose-dependent restoration of dystrophin expression in cardiac muscle of dystrophic mice by systemically delivered morpholino.
Source:
Springer Science and Business Media LLC
Cell-penetrating peptide-conjugated antisense oligonucleotides restore systemic muscle and cardiac dystrophin expression and function
Source:
Oxford University Press (OUP)
Effective rescue of dystrophin improves cardiac function in dystrophin-deficient mice by a modified morpholino oligomer
Source:
The University of North Carolina at Chapel Hill University Libraries
Guanine Analogues Enhance Antisense Oligonucleotide-induced Exon Skipping in Dystrophin Gene In Vitro and In Vivo
Source:
Elsevier BV
Fructose Promotes Uptake and Activity of Oligonucleotides With Different Chemistries in a Context-dependent Manner in mdx Mice
Source:
Elsevier BV
Dantrolene Enhances Antisense-Mediated Exon Skipping in Human and Mouse Models of Duchenne Muscular Dystrophy
Source:
American Association for the Advancement of Science (AAAS)
Dystrophin: The protein product of the duchenne muscular dystrophy locus
Source:
Elsevier BV
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