| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0014-5793(97)00311-6 |
| P698 | PubMed publication ID | 9141485 |
| P2093 | author name string | Han L | |
| Hermonat PL | |||
| Quirk JG | |||
| Bishop BM | |||
| P2860 | cites work | Site-specific integration by adeno-associated virus | Q24558738 |
| Adeno-associated virus (AAV) Rep proteins mediate complex formation between AAV DNA and its integration site in human DNA | Q24562760 | ||
| Detection of specific sequences among DNA fragments separated by gel electrophoresis | Q25939003 | ||
| Selective extraction of polyoma DNA from infected mouse cell cultures | Q29547500 | ||
| Integration of the adeno-associated virus genome into cellular DNA in latently infected human Detroit 6 cells | Q33914608 | ||
| Isolation of a lentivirus from a macaque with lymphoma: comparison with HTLV-III/LAV and other lentiviruses. | Q33927613 | ||
| DNA synthesis and topoisomerase inhibitors increase transduction by adeno-associated virus vectors | Q34251868 | ||
| Site-specific integration by adeno-associated virus is directed by a cellular DNA sequence | Q35829692 | ||
| Targeted integration of adeno-associated virus (AAV) into human chromosome 19 | Q35936149 | ||
| Cloning of adeno-associated virus into pBR322: rescue of intact virus from the recombinant plasmid in human cells | Q36288360 | ||
| Adeno-associated virus vector for high-frequency integration, expression, and rescue of genes in mammalian cells | Q36425596 | ||
| Adeno-associated virus general transduction vectors: analysis of proviral structures | Q36868692 | ||
| Genetics of adeno-associated virus: isolation and preliminary characterization of adeno-associated virus type 2 mutants | Q36893013 | ||
| Use of adeno-associated virus as a mammalian DNA cloning vector: transduction of neomycin resistance into mammalian tissue culture cells | Q37573696 | ||
| Adeno-associated virus: a vector system for efficient introduction and integration of DNA into a variety of mammalian cell types | Q40660263 | ||
| High-efficiency transfer of the T cell co-stimulatory molecule B7-2 to lymphoid cells using high-titer recombinant adeno-associated virus vectors | Q41263327 | ||
| High prevalence of adeno-associated virus (AAV) type 2 rep DNA in cervical materials: AAV may be sexually transmitted | Q45767111 | ||
| The regulatory rep protein of adeno-associated virus binds to sequences within the c-H-ras promoter | Q45782486 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | gene therapy | Q213901 |
| vector-borne disease | Q2083837 | ||
| P304 | page(s) | 78-84 | |
| P577 | publication date | 1997-04-01 | |
| P1433 | published in | FEBS Letters | Q1388051 |
| P1476 | title | The packaging capacity of adeno-associated virus (AAV) and the potential for wild-type-plus AAV gene therapy vectors | |
| P478 | volume | 407 |
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| Q55000684 | Guiding Lights in Genome Editing for Inherited Retinal Disorders: Implications for Gene and Cell Therapy. |
| Q33729610 | Harnessing the Potential of Human Pluripotent Stem Cells and Gene Editing for the Treatment of Retinal Degeneration |
| Q54981136 | High-throughput screening identifies kinase inhibitors that increase dual AAV vectors transduction in vitro and in mouse retina. |
| Q27300915 | Homologous recombination mediates functional recovery of dysferlin deficiency following AAV5 gene transfer |
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| Q45735544 | Quantitative comparison of expression with adeno-associated virus (AAV-2) brain-specific gene cassettes. |
| Q45734168 | Rapid induction of cytotoxic T-cell response against cervical cancer cells by human papillomavirus type 16 E6 antigen gene delivery into human dendritic cells by an adeno-associated virus vector |
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