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New generation adenoviral vectors improve gene transfer by coxsackie and adenoviral receptor-independent cell entry

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Year: 2002
Type: review
Source: Kidney International
DOI: 10.1046/j.1523-1755.2002.0610s1024.x
Authors: Paul N. Reynolds, David T. Curiel
Institution: University of Alabama at Birmingham
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: bronze

Funders: National Heart, Lung, and Blood Institute, National Cancer Institute, National Institute of Diabetes and Digestive and Kidney Diseases
Awards: G1558878478, ADENOVIRAL MEDIATED TARGETED GENE DELIVERY, GENE THERAPY FOR OVARIAN CANCER, CYSTIC FIBROSIS GENE THERAPY CORE CENTER, G8091858967, G8816007083, TARGETED VECTORS FOR CYSTIC FIBROSIS GENE THERAPY
OpenAlex ID: W2050631740
FWCI: 0.201
Cites: 78
Cited by: 8
Related to: 10
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