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gene-therapy

Home / Discover /diyhpl.us/~bryan/papers2/gene-therapy/

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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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A sight on the current nanoparticle-based gene delivery vectors - 2014.pdf
PDF 4 years ago 654.17 kB
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A single-molecule view of genome editing proteins: Biophysical mechanisms for TALEs and CRISPR-cas9 - 2017.pdf
PDF 4 years ago 3.55 MB
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Adeno-associated virus serotypes - vector toolkit for human gene therapy - 2006.pdf
PDF 4 years ago 234.79 kB
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Adeno-associated virus vectors and neurological gene therapy - review - 2014.pdf
PDF 4 years ago 55.91 kB
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CAV-2 - why a canine virus is a neurobiologist's best friend - 2015.pdf
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CNS-restricted transduction and CRISPR-Cas9-mediated gene deletion with an engineered AAV vector - 2016.pdf
PDF 4 years ago 5.18 MB
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Cancer regression in patients after transfer of genetically engineered lymphocytes.pdf
PDF 4 years ago 571.71 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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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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Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1.pdf
PDF 4 years ago 1.16 MB
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Current status of nonviral vectors for gene therapy in China - 2017.pdf
PDF 4 years ago 359.73 kB
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Delivery technologies for genome editing - 2017.pdf
PDF 4 years ago 893.12 kB
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Ectopic Catalase Expression in Mitochondria by Adeno-Associated Virus Enhances Exercise Performance in Mice.pdf
PDF 4 years ago 698.28 kB
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Effective depletion of pre-existing anti-AAV antibodies requires broad immune targeting - 2017.pdf
PDF 4 years ago 2.32 MB
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Efficient gene delivery to the adult and fetal CNS using pseudotyped non-integrating lentiviral vectors.pdf
PDF 4 years ago 1.00 MB
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Efficient siRNA delivery into primary cells by a peptide transduction domain-dsRNA binding domain fusion protein.pdf
PDF 4 years ago 438.03 kB
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Emerging issues in AAV-mediated in vivo gene therapy - 2018.pdf
PDF 4 years ago 1.53 MB
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Endogenous microRNA regulation suppresses transgene expression in hematopoietic lineages and enables stable gene transfer.pdf
PDF 4 years ago 673.88 kB
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Engineering adeno-associated viruses for clinical gene therapy - 2015.pdf
PDF 4 years ago 624.99 kB
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Engineering targeted viral vectors for gene therapy - 2007.pdf
PDF 4 years ago 528.61 kB
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FDA Public Workshop on Cell and Gene Therapy - Agenda - November 2010.pdf
PDF 4 years ago 178.61 kB
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Flushing out antibodies to make AAV gene therapy available to more patients - 2013.pdf
PDF 4 years ago 1.20 MB
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Gene doping - a review of performance-enhancing genetics.pdf
PDF 4 years ago 326.92 kB
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Gene therapy clinical trials worldwide 1989-2004.pdf
PDF 4 years ago 106.37 kB
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Gene therapy clinical trials worldwide to 2007—an update.pdf
PDF 4 years ago 573.85 kB
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Gene therapy for red-green color blindness in adult primates - 2009.pdf
PDF 4 years ago 1.08 MB
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Gene therapy using adeno-associated virus vectors - 2008.pdf
PDF 4 years ago 969.53 kB
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Gene transfer in humans using a conditionally replicating lentiviral vector.pdf
PDF 4 years ago 648.13 kB
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Genome-editing technologies for gene and cell therapy - 2016.pdf
PDF 4 years ago 927.09 kB
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How to name and classify your phage: an informal guide - 2017.pdf
PDF 4 years ago 310.08 kB
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Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics.pdf
PDF 4 years ago 934.43 kB
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Immune responses to AAV vectors: overcoming barriers to successful gene therapy - 2013.pdf
PDF 4 years ago 1.53 MB
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In vivo selection yields AAV-B1 capsid for central nervous system and muscle gene therapy - 2016.pdf
PDF 4 years ago 3.22 MB
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Intensive pharmacological immunosuppression allows for repetitive liver gene transfer with recombinant adenovirus in nonhuman primates - 2010.pdf
PDF 4 years ago 1.22 MB
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Long-term gene expression and phenotypic correction using adeno-associated virus vectors in the mammalian brain - 1994.pdf
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Mechanisms and strategies for effective delivery of antisense and siRNA - 2008.pdf
PDF 4 years ago 1.26 MB
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Nanoparticles as a tool for transfection and transgenesis - A review - 2016.pdf
PDF 4 years ago 253.15 kB
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Naturally enveloped AAV vectors for shielding neutralizing antibodies and robust gene delivery in vivo - 2014.pdf
PDF 4 years ago 1.77 MB
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Non-viral nucleic acid delivery strategies to the central nervous system - 2016.pdf
PDF 4 years ago 1.60 MB
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Non-viral vectors for gene-based therapy - review - 2014.pdf
PDF 4 years ago 2.78 MB
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Optimization of PAMAM-gold nanoparticle conjugation for gene therapy - 2015.pdf
PDF 4 years ago 4.08 MB
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Overcoming preexisting humoral immunity to AAV using capsid decoys - 2013.pdf
PDF 4 years ago 1.53 MB
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Overview of gene therapy and viral vectors for CNS applications - Martha Bohn - 2005.pdf
PDF 4 years ago 319.40 kB
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Pharmacological modulation of humoral immunity in a nonhuman primate model of AAV gene transfer for hemophilia B - 2012.pdf
PDF 4 years ago 231.41 kB
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Pre-existing anti-adeno-associated virus antibodies as a challenge in AAV gene therapy - 2013.pdf
PDF 4 years ago 273.16 kB
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Programmable genome editing tools and their regulation for efficient genome engineering - 2017.pdf
PDF 4 years ago 1.07 MB
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Progress towards in vivo use of siRNAs.pdf
PDF 4 years ago 355.43 kB
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