Lentiviral Vector Engineering
Lentiviral Vector Engineering is a methodological framework within ex vivo gene therapy that involves the design and modification of replication-deficient lentiviral vectors to achieve efficient, stable, and targeted integration of therapeutic transgenes into the host genome.
520
Publications
28.3K
Citations
3.4K
Authors
886
Institutions
Publications per year
2017–2026
123
Parents
520
F. Xiao‐Feng Qin, Dong Sung An, Irvin S. Y. Chen et al. · Proceedings of the National Academy of Sciences · 2002 · 704 citations · Full text
Gene Therapy in a Patient with Sickle Cell Disease
Jean‐Antoine Ribeil, Salima Hacein‐Bey‐Abina, Emmanuel Payen et al. · New England Journal of Medicine · 2017 · 669 citations · Full text
Medicine, Genetics, Hematology +17
A public genome-scale lentiviral expression library of human ORFs
Xiaoping Yang, Jesse S. Boehm, Xinping Yang et al. · Nature Methods · 2011 · 588 citations · Full text
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The San Raffaele Telethon Institute for Gene Therapy, Italy
11 publications · 1.3K citations
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886
Inserm
Paris, France
23 h-index
169 publications
27.4K citations
Medizinische Hochschule Hannover
Hanover, Germany
18 h-index
87 publications
4.9K citations
Harvard University
Cambridge, United States
17 h-index
47 publications
9.2K citations
University College London
London, United Kingdom
16 h-index
108 publications
7.2K citations

Centre National de la Recherche Scientifique
Paris, France
14 h-index
83 publications
5.4K citations
University of California, Los Angeles
Los Angeles, United States
13 h-index
62 publications
7.9K citations
National Institutes of Health
Bethesda, United States
13 h-index
51 publications
4.3K citations
University of Southern California
Los Angeles, United States
13 h-index
55 publications
2.8K citations
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48 publications · 3.3K citations
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19 publications · 827 citations
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15 publications · 889 citations
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