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Construction of a Fully Retargeted Herpes Simplex Virus 1 Recombinant Capable of Entering Cells Solely via Human Epidermal Growth Factor Receptor 2.pdf

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Construction of a Fully Retargeted Herpes Simplex Virus 1 Recombinant Capable of Entering Cells Solely via Human Epidermal Growth Factor Receptor 2.pdf
PDF 4 years ago 459.12 kB
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Cell penetrating peptides - overview and applications to the delivery of oligonucleotides.pdf
PDF 4 years ago 391.96 kB
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Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1.pdf
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Cancer regression in patients after transfer of genetically engineered lymphocytes.pdf
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Current status of nonviral vectors for gene therapy in China - 2017.pdf
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CNS-restricted transduction and CRISPR-Cas9-mediated gene deletion with an engineered AAV vector - 2016.pdf
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Delivery technologies for genome editing - 2017.pdf
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CAV-2 - why a canine virus is a neurobiologist's best friend - 2015.pdf
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Ectopic Catalase Expression in Mitochondria by Adeno-Associated Virus Enhances Exercise Performance in Mice.pdf
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A single-molecule view of genome editing proteins: Biophysical mechanisms for TALEs and CRISPR-cas9 - 2017.pdf
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Effective depletion of pre-existing anti-AAV antibodies requires broad immune targeting - 2017.pdf
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A sight on the current nanoparticle-based gene delivery vectors - 2014.pdf
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Efficient gene delivery to the adult and fetal CNS using pseudotyped non-integrating lentiviral vectors.pdf
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Adeno-associated virus vectors and neurological gene therapy - review - 2014.pdf
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Efficient siRNA delivery into primary cells by a peptide transduction domain-dsRNA binding domain fusion protein.pdf
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Adeno-associated virus serotypes - vector toolkit for human gene therapy - 2006.pdf
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Emerging issues in AAV-mediated in vivo gene therapy - 2018.pdf
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A 10 patient case report on the impact of plasmapheresis upon neutralizing factors against adeno-associated virus (AAV) types 1, 2, 6, and 8 - 2011.pdf
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Endogenous microRNA regulation suppresses transgene expression in hematopoietic lineages and enables stable gene transfer.pdf
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Engineering adeno-associated viruses for clinical gene therapy - 2015.pdf
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