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| Open AccessNewt A1 cell-derived extracellular vesicles promote mammalian nerve growth
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| Open AccessFull-length human dystrophin on human artificial chromosome compensates for mouse dystrophin deficiency in a Duchenne muscular dystrophy mouse model
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| Open AccessA LexAop > UAS > QUAS trimeric plasmid to generate inducible and interconvertible Drosophila overexpression transgenes
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| Open AccessOptimization in the expression of ASFV proteins for the development of subunit vaccines using poxviruses as delivery vectors
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| Open AccessAluminum particles generated during millisecond electric pulse application enhance adenovirus-mediated gene transfer in L929 cells
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| Open AccessA deterministic genotyping workflow reduces waste of transgenic individuals by two-thirds
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| Open AccessHIV-1 sequences in lentiviral vector genomes can be substantially reduced without compromising transduction efficiency
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| Open AccessA double-Flp-in method for stable overexpression of two genes
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| Open AccessAdeno-associated virus-binding antibodies detected in cats living in the Northeastern United States lack neutralizing activity
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| Open AccessAbrogation of PRRSV infectivity by CRISPR-Cas13b-mediated viral RNA cleavage in mammalian cells
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| Open AccessEpisomal vectors based on S/MAR and the β-globin Replicator, encoding a synthetic transcriptional activator, mediate efficient γ-globin activation in haematopoietic cells
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| Open AccessAdeno-associated virus capsid protein expression in Escherichia coli and chemically defined capsid assembly
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| Open AccessHighly efficient ex vivo lentiviral transduction of primary human pancreatic exocrine cells
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| Open AccessNon-viral vector based gene transfection with human induced pluripotent stem cells derived cardiomyocytes
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| Open AccessConsiderations related to the use of short neuropeptide promoters in viral vectors targeting hypothalamic neurons
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| Open AccessAAV GCG-EGFP, a new tool to identify glucagon-secreting α-cells
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| Open AccessThe adeno-associated virus rh10 vector is an effective gene transfer system for chronic spinal cord injury
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| Open AccessDiphtheria Toxin A-Resistant Cell Lines Enable Robust Production and Evaluation of DTA-Encoding Lentiviruses
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| Open AccessBile-duct proliferation as an unexpected side-effect after AAV2-LDLR gene transfer to rabbit liver
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| Open AccessA note on retrograde gene transfer efficiency and inflammatory response of lentiviral vectors pseudotyped with FuG-E vs. FuG-B2 glycoproteins
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| Open AccessGene activated adipose tissue fragments as advanced autologous biomaterials for bone regeneration: osteogenic differentiation within the tissue and implications for clinical translation
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| Open AccessSynergistic and independent action of endogenous microRNAs 122a and 199a for post-transcriptional liver detargeting of gene vectors
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| Open AccessRobust Enhancement of Lentivirus Production by Promoter Activation
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| Open AccessLiposome co-incubation with cancer cells secreted exosomes (extracellular vesicles) with different proteins expressions and different uptake pathways
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| Open AccessPEGylation of polypropylenimine dendrimers: effects on cytotoxicity, DNA condensation, gene delivery and expression in cancer cells
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| Open AccessEnhanced viral-mediated cochlear gene delivery in adult mice by combining canal fenestration with round window membrane inoculation
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| Open AccessControlling AOX1 promoter strength in Pichia pastoris by manipulating poly (dA:dT) tracts
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| Open AccessRFX1 and RFX3 Transcription Factors Interact with the D Sequence of Adeno-Associated Virus Inverted Terminal Repeat and Regulate AAV Transduction
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| Open AccessAdeno-associated virus serotype rh10 is a useful gene transfer vector for sensory nerves that innervate bone in immunodeficient mice
- Sun H. Park
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| Open AccessCRISPR/Cas9 delivery with one single adenoviral vector devoid of all viral genes
- Eric Ehrke-Schulz
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| Open AccessIL-27, but not IL-35, inhibits neuroinflammation through modulating GM-CSF expression
- Giacomo Casella
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| Open AccessCRISPR/Cas9-induced transgene insertion and telomere-associated truncation of a single human chromosome for chromosome engineering in CHO and A9 cells
- Narumi Uno
- , Kei Hiramatsu
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| Open AccessDevelopment of oriC-plasmids for use in Mycoplasma hyorhinis
- Hassan Z. A. Ishag
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| Open AccessCancer-targeted Nucleic Acid Delivery and Quantum Dot Imaging Using EGF Receptor Aptamer-conjugated Lipid Nanoparticles
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