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Sj Howe

University College London

139

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Foamy Virus Vectors Transduce Visceral Organs and Hippocampal Structures following In Vivo Delivery to Neonatal Mice

2018 Molecular therapy. Nucleic acids
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Molecular Evidence of Genome Editing in a Mouse Model of Immunodeficiency

2018 Scientific Reports
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Enhancement of mouse hematopoietic stem/progenitor cell function via transient gene delivery using integration-deficient lentiviral vectors

2018 Experimental Hematology
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Eliminating HIV-1 Packaging Sequences from Lentiviral Vector Proviruses Enhances Safety and Expedites Gene Transfer for Gene Therapy

2017 Molecular Therapy
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BMI-1 extends proliferative potential of human bronchial epithelial cells while retaining their mucociliary differentiation capacity

2017 American Journal of Physiology-lung Cellular and Molecular Physiology
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Lentiviral vectors can be used for full-length dystrophin gene therapy

2017 Scientific Reports
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Molecular Evidence of Ex Vivo Gene Editing in a Mouse Model of Immunodeficiency

2017
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Erratum: Lentiviral vectors can be used for full-length dystrophin gene therapy

2017 Scientific Reports
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Barriers to Effective Genome Editing of Haematopoietic Stem Cells

2016 Stem cell reports
- Sj Howe
- Michael D. Milsom
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Site- and allele-specific polycomb dysregulation in T-cell leukaemia

2015 Nature Communications
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Citations (35)