Hepatocyte-targeted expression by integrase-defective lentiviral vectors induces antigen-specific tolerance in mice with low genotoxic risk
Mátrai, Janka, Cantore, Alessio, Bartholomae, Cynthia C., Annoni, Andrea, Wang, Wei, Acosta-Sanchez, Abel, Samara-Kuko, Ermira, De Waele, Liesbeth +12 more·2011·Hepatology
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- Identification of hepatocyte-primed cholangiocytes in the homeostatic liver by in vivo lentiviral gene transfer to mice and non-human primatesMichela Milani, Francesco Starinieri, Anna Fabiano, Stefano Beretta, Tiziana Plati, Cesare Canepari, Mauro Biffi, Fabio Russo, Valeria Berno, Rossana Norata et al. · 2025 · Cell Reports
- Erosion of the pump mechanism of an inflatable penile prosthesis through the scrotum in a diabetic patient.Ihor S. Sawczuk, Michael E. Wechsler · 1985 · PubMed Central
- Cell and gene therapeutic approaches in non-alcoholic fatty liver diseaseMohadeseh Poudineh, Fatemeh Mohammadyari, Negin Parsamanesh, Tananz Jamialahmadi, Prashant Kesharwani, Amirhossein Sahebkar · 2025 · Gene
- Hitting the Target Without Pulling the TriggerThierry VandenDriessche, Marinee Chuah · 2015 · Molecular Therapy
- Genetic and Epigenetic Modification of Rat Liver Progenitor Cells via HNF4α Transduction and 5’ Azacytidine Treatment: An Integrated miRNA and mRNA Expression Profile AnalysisJennifer Bolleyn, Matthias Rombaut, Nisha Nair, Steven Branson, Anja Heymans, Marinee Chuah, Thierry VandenDriessche, Vera Rogiers, Joery De Kock, Tamara Vanhaecke · 2020 · Genes
- Regulatory T Cells in Autoimmune DiabetesVitalijs Ovcinnikovs, Lucy S. K. Walker · 2015 · Progress in molecular biology and translational science
- Platelet‐directed gene therapy overcomes inhibitory antibodies to factor VIIIMarinee Chuah, Thierry VandenDriessche · 2012 · Journal of Thrombosis and Haemostasis
- Gene Therapy for Liver DiseaseRajagopal N. Aravalli · 2017 · Elsevier eBooks
- Development of viral & non-viral episomal vectors for gene therapy applicationsHanna Kymäläinen · 2012 · OpenGrey (Institut de l'Information Scientifique et Technique)
- Recent Advances and Future Perspectives in Lentiviral Gene Therapy for Hemophilia A and BJanka Mátrai, Marinee Chuah, Thierry VandenDriessche · 2012 · Journal of Genetic Syndromes & Gene Therapy
- GENE THERAPY FOR HAEMOPHILIAA Asghar, Zarafshan Asjad, H Tahir, Z Maheen, S Hanif · 2021 · Pakistan Journal of Intensive Care Medicine
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- Assessing the potential of non-integrating lentiviral vectors for cardiovascular gene therapyHelen Elizabeth Chick · 2011 · Enlighten: Theses (The University of Glasgow)
- Strategies for the Gene Modification of Megakaryopoiesis and PlateletsLisette J. Latorre-Rey, Ute Modlich · 2016 · Springer eBooks
- MDS1/EVI1 and PRDM16 deregulation in hematopoiesis after experimental and clinical gene transferWang, Wei · 2012 · heiDOK (Heidelberg University)
- Insights into the mechanisms of HIV-1 cis elements and trans factors required for RNA encapsidation and transductionAdam S. Cockrell · 2019 · Carolina Digital Repository (University of North Carolina at Chapel Hill)
- Controlling Transgene Expression in the Central Nervous System For MRI-Guided Focused Ultrasound Delivery of Adeno-Associated VirusDanielle Weber‐Adrian · 2017 · TSpace (University of Toronto)
- A study of mechanisms of genotoxicity in mammalian cells by retrovirus vectors intended for gene therapySafia Reja · 2013 · Brunel University Research Archive (BURA) (Brunel University London)
- Faculty Opinions recommendation of Efficient In Vivo Liver-Directed Gene Editing Using CRISPR/Cas9.Irina M. Conboy · 2018 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
- Identification of Hepatocyte-Primed Biliary Epithelial Cells in the Homeostatic Liver by in vivo Lentiviral Gene Transfer to Mice and Non-Human PrimatesMichela Milani, Francesco Starinieri, Stefano Beretta, Anna Fabiano, Tiziana Plati, Cesare Canepari, Mauro Biffi, Fabio Russo, Rossana Norata, Francesca Sanvito et al. · 2023 · SSRN Electronic Journal
- Cell of origin epigenetic priming determines susceptibility to Tet2 mutationGiulia Schiroli, Vinay K. Kartha, Fabiana M. Duarte, Trine Ahn Kristiansen, Christina Mayerhofer, Rojesh Shrestha, Andrew Earl, Yan Hu, Tristan Tay, Catherine Rhee et al. · 2023 · bioRxiv (Cold Spring Harbor Laboratory)
- LSpECifying transgene expressionAndrea Annoni, Alessio Cantore · 2024 · Molecular Therapy — Nucleic Acids
- In vivo delivery and clinical advances of RNA therapeutics and vaccinesTingting Zhao, Shuai Guo, Yuanyu Huang · 2026 · Scientia Sinica Vitae
- Stealthy lentiviral vectors: Breaking the barriers to systemic in vivo gene deliveryAmy L. Keating, Robert C. Carlisle, Kyriacos A. Mitrophanous, L. W. Seymour, Kerry D. Fisher · 2026 · Molecular Therapy Advances