| scholarly article | Q13442814 |
| P2093 | author name string | Inoue N | |
| Russell DW | |||
| Hirata RK | |||
| P2860 | cites work | High-fidelity gene targeting in embryonic stem cells by using sequence replacement vectors | Q24630186 |
| Targeted mutation of the Hprt gene in mouse embryonic stem cells | Q24645320 | ||
| Rapid and efficient site-specific mutagenesis without phenotypic selection | Q27860628 | ||
| Integration specificity of retrotransposons and retroviruses | Q28253755 | ||
| Packaging cells based on inducible gene amplification for the production of adeno-associated virus vectors | Q33783728 | ||
| Characterization of a newly derived human sarcoma cell line (HT-1080). | Q34202593 | ||
| Use of Adeno-Associated Virus as a General Transduction Vector for Mammalian Cells | Q35228018 | ||
| Recombinant adeno-associated virus-mediated high-efficiency, transient expression of the murine cationic amino acid transporter (ecotropic retroviral receptor) permits stable transduction of human HeLa cells by ecotropic retroviral vectors. | Q35869915 | ||
| Adeno-associated virus vector integration junctions. | Q35898429 | ||
| Rapid detection of homologous recombinants in nontransformed human cells | Q35949400 | ||
| Cellular recombination pathways and viral terminal repeat hairpin structures are sufficient for adeno-associated virus integration in vivo and in vitro. | Q36548752 | ||
| Construction and properties of retrovirus packaging cells based on gibbon ape leukemia virus | Q36688368 | ||
| Functional genomics in mice by tagged sequence mutagenesis | Q36873978 | ||
| Integration of retroviral DNA. | Q37950645 | ||
| Gene targeting with a replication-defective adenovirus vector. | Q39872000 | ||
| Human gene targeting by viral vectors | Q41480639 | ||
| Therapeutic gene targeting | Q41760437 | ||
| Bypass of senescence after disruption of p21CIP1/WAF1 gene in normal diploid human fibroblasts | Q42815554 | ||
| Distribution of targets for avian retrovirus DNA integration in vivo | Q72718786 | ||
| P433 | issue | 9 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | vector-borne disease | Q2083837 |
| P304 | page(s) | 7376-7380 | |
| P577 | publication date | 1999-09-01 | |
| P1433 | published in | Journal of Virology | Q1251128 |
| P1476 | title | High-fidelity correction of mutations at multiple chromosomal positions by adeno-associated virus vectors | |
| P478 | volume | 73 |
| Q33432320 | A comparison of synthetic oligodeoxynucleotides, DNA fragments and AAV-1 for targeted episomal and chromosomal gene repair |
| Q35510498 | A genome-wide map of adeno-associated virus-mediated human gene targeting |
| Q37085601 | AAV-mediated gene targeting methods for human cells |
| Q35566831 | Adeno-associated viral vectors for retinal gene transfer. |
| Q35105022 | Adeno-associated virus gene repair corrects a mouse model of hereditary tyrosinemia in vivo. |
| Q24624120 | Adeno-associated virus vector integration |
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| Q36445805 | An experimental system for the evaluation of retroviral vector design to diminish the risk for proto-oncogene activation |
| Q33922429 | Chromosomal position effects on AAV-mediated gene targeting |
| Q33804483 | Design and packaging of adeno-associated virus gene targeting vectors |
| Q39787525 | Efficient gene targeting mediated by adeno-associated virus and DNA double-strand breaks |
| Q33930075 | Engineering of human pluripotent stem cells by AAV-mediated gene targeting |
| Q34114590 | Gene targeting in livestock: a preview |
| Q45413871 | Gene targeting in vivo by adeno-associated virus vectors. |
| Q24298392 | Gene targeting of mutant COL1A2 alleles in mesenchymal stem cells from individuals with osteogenesis imperfecta |
| Q36149196 | Gene targeting with viral vectors |
| Q34186665 | Gene therapy: trials and tribulations |
| Q36675277 | Genome Engineering Using Adeno-associated Virus: Basic and Clinical Research Applications |
| Q35148796 | Human Gene Targeting by Adeno-Associated Virus Vectors Is Enhanced by DNA Double-Strand Breaks |
| Q34132693 | Human gene targeting favors insertions over deletions |
| Q33409740 | Indexing TNF-alpha gene expression using a gene-targeted reporter cell line |
| Q33870310 | Involvement of cellular double-stranded DNA break binding proteins in processing of the recombinant adeno-associated virus genome. |
| Q59349832 | Nuclease-free Adeno-Associated Virus-Mediated Il2rg Gene Editing in X-SCID Mice |
| Q36302317 | Precise hit: adeno-associated virus in gene targeting |
| Q28271767 | Production of CFTR-null and CFTR-DeltaF508 heterozygous pigs by adeno-associated virus-mediated gene targeting and somatic cell nuclear transfer |
| Q36953325 | Recombinant adeno-associated virus transduction and integration |
| Q42860274 | Self-complementary AAV mediates gene targeting and enhances endonuclease delivery for double-strand break repair |
| Q37092798 | Targeted correction of single-base-pair mutations with adeno-associated virus vectors under nonselective conditions |
| Q50657873 | Targeted genome modifications using integrase-deficient lentiviral vectors. |
| Q44387426 | Targeted transgene insertion into human chromosomes by adeno-associated virus vectors |
| Q35012925 | The application of DNA repair vectors to gene therapy |
| Q37631839 | The effects of polymorphisms on human gene targeting |
| Q74381897 | Validation of AAV-mediated gene targeting |
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