Year: 2018
Type: editorial
Abstract: The gateway to the promised land of gene therapy has been obstructed by the problem of accurate and efficient delivery of therapeutic agents to their target sites. This is true both of constructs d...
Institutions: Children's National, George Washington University
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: bronze
Funders: Foundation to Eradicate Duchenne, Muscular Dystrophy Association, Parent Project Muscular Dystrophy, Children’s Hospital of Wisconsin Research Institute, Duchenne Parent Project, National Institutes of Health, Intellectual and Developmental Disabilities Research Center, National Institute on Aging, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institute of Child Health and Human Development, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: G2236418009, G3566964489, District of Columbia Intellectual and Developmental Disabilities Research Center, Understanding the mechanism and role of cell membrane repair in Miyoshi Myopathy, G4851748564, G5329615806, Cellular and genomic measures of stem cell function in age-related human muscle atrophy, G6437397297, Genetics and Genomics of Muscle Postdoctoral Training Program, G8133036495
OpenAlex ID: W2805701934