![The TOP vector: a new high-titer lentiviral construct for delivery of sgRNAs and transgenes to primary T cells: Molecular Therapy - Methods & Clinical Development The TOP vector: a new high-titer lentiviral construct for delivery of sgRNAs and transgenes to primary T cells: Molecular Therapy - Methods & Clinical Development](https://els-jbs-prod-cdn.jbs.elsevierhealth.com/cms/attachment/766ca309-467d-4cb4-a1ce-c502735cc18f/fx1_lrg.jpg)
The TOP vector: a new high-titer lentiviral construct for delivery of sgRNAs and transgenes to primary T cells: Molecular Therapy - Methods & Clinical Development
![Novel lentiviral vectors with mutated reverse transcriptase for mRNA delivery of TALE nucleases | Scientific Reports Novel lentiviral vectors with mutated reverse transcriptase for mRNA delivery of TALE nucleases | Scientific Reports](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fsrep06409/MediaObjects/41598_2014_Article_BFsrep06409_Fig1_HTML.jpg)
Novel lentiviral vectors with mutated reverse transcriptase for mRNA delivery of TALE nucleases | Scientific Reports
![A trans-lentiviral packaging cell line for high-titer conditional self-inactivating HIV-1 vectors: Molecular Therapy A trans-lentiviral packaging cell line for high-titer conditional self-inactivating HIV-1 vectors: Molecular Therapy](https://els-jbs-prod-cdn.jbs.elsevierhealth.com/cms/attachment/2083937873/2073368459/gr1.jpg)
A trans-lentiviral packaging cell line for high-titer conditional self-inactivating HIV-1 vectors: Molecular Therapy
![A Guide to Approaching Regulatory Considerations for Lentiviral-Mediated Gene Therapies | Human Gene Therapy Methods A Guide to Approaching Regulatory Considerations for Lentiviral-Mediated Gene Therapies | Human Gene Therapy Methods](https://www.liebertpub.com/cms/10.1089/hgtb.2017.096/asset/images/medium/figure1.gif)
A Guide to Approaching Regulatory Considerations for Lentiviral-Mediated Gene Therapies | Human Gene Therapy Methods
![Targeting microglia with lentivirus and AAV: Recent advances and remaining challenges - ScienceDirect Targeting microglia with lentivirus and AAV: Recent advances and remaining challenges - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0304394019303842-gr2.jpg)
Targeting microglia with lentivirus and AAV: Recent advances and remaining challenges - ScienceDirect
![Production of Retroviral and Lentiviral Gene Therapy Vectors: Challenges in the Manufacturing of Lipid Enveloped Virus | IntechOpen Production of Retroviral and Lentiviral Gene Therapy Vectors: Challenges in the Manufacturing of Lipid Enveloped Virus | IntechOpen](https://www.intechopen.com/media/chapter/16776/media/image4.png)
Production of Retroviral and Lentiviral Gene Therapy Vectors: Challenges in the Manufacturing of Lipid Enveloped Virus | IntechOpen
![Eliminating HIV-1 Packaging Sequences from Lentiviral Vector Proviruses Enhances Safety and Expedites Gene Transfer for Gene Therapy: Molecular Therapy Eliminating HIV-1 Packaging Sequences from Lentiviral Vector Proviruses Enhances Safety and Expedites Gene Transfer for Gene Therapy: Molecular Therapy](https://els-jbs-prod-cdn.jbs.elsevierhealth.com/cms/attachment/efce18df-4339-4959-be14-efdf084fa578/gr1_lrg.jpg)
Eliminating HIV-1 Packaging Sequences from Lentiviral Vector Proviruses Enhances Safety and Expedites Gene Transfer for Gene Therapy: Molecular Therapy
![Development of a replication-competent lentivirus assay for dendritic cell-targeting lentiviral vectors: Molecular Therapy - Methods & Clinical Development Development of a replication-competent lentivirus assay for dendritic cell-targeting lentiviral vectors: Molecular Therapy - Methods & Clinical Development](https://els-jbs-prod-cdn.jbs.elsevierhealth.com/cms/attachment/ba083c2b-fc39-489c-9158-ab774335d923/gr1_lrg.jpg)
Development of a replication-competent lentivirus assay for dendritic cell-targeting lentiviral vectors: Molecular Therapy - Methods & Clinical Development
![Experimental design for stable genetic manipulation in mammalian cell lines: lentivirus and alternatives - Shearer - 2015 - Genes to Cells - Wiley Online Library Experimental design for stable genetic manipulation in mammalian cell lines: lentivirus and alternatives - Shearer - 2015 - Genes to Cells - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/d8bbca5a-86fe-474a-a03b-2f97fa19658c/gtc12183-fig-0001-m.jpg)
Experimental design for stable genetic manipulation in mammalian cell lines: lentivirus and alternatives - Shearer - 2015 - Genes to Cells - Wiley Online Library
![Manufacture of Third-Generation Lentivirus for Preclinical Use, with Process Development Considerations for Translation to Good Manufacturing Practice | Human Gene Therapy Methods Manufacture of Third-Generation Lentivirus for Preclinical Use, with Process Development Considerations for Translation to Good Manufacturing Practice | Human Gene Therapy Methods](https://www.liebertpub.com/cms/10.1089/hgtb.2017.098/asset/images/medium/figure1.gif)