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One or more keywords matched the following items that are connected to Tai, Phillip
Item TypeName
Concept Genetic Therapy
Academic Article Adeno-associated virus vector as a platform for gene therapy delivery.
Academic Article Circumventing cellular immunity by miR142-mediated regulation sufficiently supports rAAV-delivered OVA expression without activating humoral immunity.
Academic Article A Safe and Reliable Technique for CNS Delivery of AAV Vectors in the Cisterna Magna.
Academic Article Overcoming innate immune barriers that impede AAV gene therapy vectors.
Academic Article Engineering adeno-associated viral vectors to evade innate immune and inflammatory responses.
Academic Article Viral vector platforms within the gene therapy landscape.
Academic Article Large-scale molecular epidemiological analysis of AAV in a cancer patient population.
Academic Article Novel Combinatorial MicroRNA-Binding Sites in AAV Vectors Synergistically Diminish Antigen Presentation and Transgene Immunity for Efficient and Stable Transduction.
Academic Article Rational engineering of a functional CpG-free ITR for AAV gene therapy.
Academic Article Self-inactivating, all-in-one AAV vectors for precision Cas9 genome editing via homology-directed repair in vivo.
Academic Article AAV gene therapy for Tay-Sachs disease.
Academic Article Querying Recombination Junctions of Replication-Competent Adeno-Associated Viruses in Gene Therapy Vector Preparations with Single Molecule, Real-Time Sequencing.
Academic Article Integration of Gene Therapy Vectors: A Risk Factor for Tumorigenesis or Another Commensal Property of Adeno-Associated Viruses That Benefits Long-Term Transgene Expression?
Academic Article Improved gene therapy for spinal muscular atrophy in mice using codon-optimized hSMN1 transgene and hSMN1 gene-derived promotor.
Academic Article The AAV2.7m8 capsid packages a higher degree of heterogeneous vector genomes than AAV2.
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  • Gene therapy