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Department of Microbiology and Immunology School of Medicine
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Hematopoietic-specific lentiviral vectors circumvent cellular toxicity due to ectopic expression of Wiskott-Aldrich syndrome protein.
Human gene therapy Feb, 2008 | Pubmed ID: 18240968
In vivo delivery of lentiviral vectors expressing vasoactive intestinal peptide complementary DNA as gene therapy for collagen-induced arthritis.
Arthritis and rheumatism Apr, 2008 | Pubmed ID: 18383372
Safer vectors for gene therapy of primary immunodeficiencies.
Current gene therapy Aug, 2009 | Pubmed ID: 19534652
Was cDNA sequences modulate transgene expression of was promoter-driven lentiviral vectors.
Human gene therapy Nov, 2009 | Pubmed ID: 19630517
Dendritic cells transduced with lentiviral vectors expressing VIP differentiate into VIP-secreting tolerogenic-like DCs.
Molecular therapy : the journal of the American Society of Gene Therapy May, 2010 | Pubmed ID: 20068554
Docosahexaenoic acid prevents dendritic cell maturation and in vitro and in vivo expression of the IL-12 cytokine family.
Lipids in health and disease , 2010 | Pubmed ID: 20122166
Development of an all-in-one lentiviral vector system based on the original TetR for the easy generation of Tet-ON cell lines.
PloS one , 2011 | Pubmed ID: 21876765
Temple University
Miguel G. Toscano1,
Doina Ganea1,
Ana M. Gamero2
1Department of Microbiology and Immunology School of Medicine, Temple University ,
2Department of Biochemistry, School of Medicine, Temple University
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