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Reengineering a receptor footprint of adeno-associated virus enables selective and systemic gene transfer to muscle

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Year: 2009
Type: article
Source: Nature Biotechnology
DOI: 10.1038/nbt.1599
Authors: Aravind Asokan, Julia C Conway, Jana L Phillips, Chengwen Li, Julia Hegge, Rebecca Sinnott, Swati Yadav, Nina DiPrimio, Hyun-Joo Nam, Mavis Agbandje-McKenna, Scott McPhee, Jon Wolff, R Jude Samulski
Institutions: University of North Carolina at Chapel Hill, Mirus Bio (United States), University of Florida, AskBio (United States)
Language: English

Topic: Virus-based gene therapy research
Subfield: Genetics
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: green

Funders: American Heart Association, National Institutes of Health, National Heart, Lung, and Blood Institute, National Institute of General Medical Sciences, National Institute of Allergy and Infectious Diseases, National Institute of Arthritis and Musculoskeletal and Skin Diseases
Awards: G110866749, Rational and Combinatorial Engineering of AAV Vectors, Senator Paul D. Wellstone Muscular Dystrophy Cooperative Research Center, Muscle-specific AAV Vectors for DMD Gene Therapy, G4443903763, G6809074, AAV capsids and their cellular interactions, Determinants of AAV Tropism
OpenAlex ID: W2061013034
FWCI: 8.903
Cites: 21
Cited by: 266
Related to: 10
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