Search Results - "Mitrophanous, K"
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Oviduct-specific expression of two therapeutic proteins in transgenic hens
Published in Proceedings of the National Academy of Sciences - PNAS (06-02-2007)“…Recent advances in avian transgenesis have led to the possibility of utilizing the laying hen as a production platform for the large-scale synthesis of…”
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Enhancing titres of therapeutic viral vectors using the transgene repression in vector production (TRiP) system
Published in Nature communications (27-03-2017)“…A key challenge in the field of therapeutic viral vector/vaccine manufacturing is maximizing production. For most vector platforms, the ‘benchmark’ vector…”
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Optogenetic Tractography for anatomo-functional characterization of cortico-subcortical neural circuits in non-human primates
Published in Scientific reports (20-02-2018)“…Dissecting neural circuitry in non-human primates (NHP) is crucial to identify potential neuromodulation anatomical targets for the treatment of…”
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Stable gene transfer to the nervous system using a non-primate lentiviral vector
Published in Gene therapy (01-11-1999)“…We have constructed a non-primate lentiviral vector system based on the equine infectious anaemia virus (EIAV). This system is able to transduce both dividing…”
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Hsp40 Molecules That Target to the Ubiquitin-proteasome System Decrease Inclusion Formation in Models of Polyglutamine Disease
Published in Molecular therapy (01-06-2007)“…We studied the ability of heat shock, DnaJ-like-1 (HSJ1) proteins (which contain DnaJ and ubiquitin-interacting motifs) to reduce polyglutamine-mediated…”
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Gene transduction efficiency in cells of different species by HIV and EIAV vectors
Published in Gene therapy (01-07-2002)“…The ability of human immunodeficiency virus (HIV)- and equine infectious anaemia virus (EIAV)-based vectors to transduce cell lines from a range of species was…”
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Hsp40 Molecules That Target to the Ubiquitin-proteasome System Decrease Inclusion Formation in Models of Polyglutamine Disease
Published in Molecular therapy (01-06-2007)“…We studied the ability of heat shock, DnaJ-like-1 (HSJ1) proteins (which contain DnaJ and ubiquitin-interacting motifs) to reduce polyglutamine-mediated…”
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Potential oncogene activity of the woodchuck hepatitis post-transcriptional regulatory element (WPRE)
Published in Gene therapy (01-01-2005)Get full text
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Development of inducible EIAV-based lentiviral vector packaging and producer cell lines
Published in Gene therapy (01-06-2009)“…Large-scale production of gene therapeutics comprising equine infectious anaemia virus (EIAV) -based lentiviral vectors (LVs) would benefit from the…”
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Analysis of factor VIII mediated suppression of lentiviral vector titres
Published in Gene therapy (01-02-2008)“…Effective gene therapy for haemophilia A necessitates a vector system that is not subject to a pre-existing immune response, has adequate coding capacity,…”
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Long-term transgene expression by administration of a lentivirus-based vector to the fetal circulation of immuno-competent mice
Published in Gene therapy (01-08-2003)“…Inefficient gene transfer, inaccessibility of stem cell compartments, transient gene expression, and adverse immune and inflammatory reactions to vector and…”
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Multiple gene products from a single vector: 'self-cleaving' 2A peptides
Published in Gene therapy (01-12-2004)Get full text
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Highly efficient EIAV-mediated in utero gene transfer and expression in the major muscle groups affected by Duchenne muscular dystrophy
Published in Gene therapy (01-07-2004)“…Gene therapy for Duchenne muscular dystrophy has so far not been successful because of the difficulty in achieving efficient and permanent gene transfer to the…”
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Rabies virus glycoprotein pseudotyping of lentiviral vectors enables retrograde axonal transport and access to the nervous system after peripheral delivery
Published in Human molecular genetics (15-09-2001)“…In this report it is demonstrated for the first time that rabies-G envelope of the rabies virus is sufficient to confer retrograde axonal transport to a…”
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In vivo evaluation of an EIAV vector for the systemic genetic delivery of therapeutic antibodies
Published in Gene therapy (01-06-2005)“…Lentiviral-based vectors hold great promise as gene delivery vehicles for the treatment of a wide variety of diseases. We have previously reported the…”
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A replication competent lentivirus (RCL) assay for equine infectious anaemia virus (EIAV)-based lentiviral vectors
Published in Gene therapy (01-02-2006)“…Lentiviral vectors are being developed to satisfy a wide range of currently unmet medical needs. Vectors destined for clinical evaluation have been rendered…”
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A Rev-independent human immunodeficiency virus type 1 (HIV-1)-based vector that exploits a codon-optimized HIV-1 gag-pol gene
Published in Journal of virology (01-05-2000)“…The human immunodeficiency virus (HIV) genome is AU rich, and this imparts a codon bias that is quite different from the one used by human genes. The codon…”
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THE TETRAVECTA™ SYSTEM: A NEW TOOL KIT ENHANCING LENTIVIRAL VECTOR PRODUCTION FOR THE NEXT GENERATION OF GENE THERAPIES
Published in Cytotherapy (Oxford, England) (01-06-2024)“…The use of HIV-1 based lentiviral vectors (LVs) remains the most established and efficient means to deliver transgenes to non-/dividing cells, achieving…”
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Growth factor enhanced retroviral gene transfer to the adult central nervous system
Published in Gene therapy (01-07-2000)“…The use of viral vectors for gene delivery into mammalian cells provides a new approach in the treatment of many human diseases. The first viral vector…”
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