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Second-strand synthesis is a rate-limiting step for efficient transduction by recombinant adeno-associated virus vectors
Open accessAbstract
The ability of recombinant adeno-associated virus (AAV) to transduce cells with a marker gene in vitro was found to be substantially increased by the presence of adenovirus. Transfection experiments with adenovirus genomic DNA suggest that this increase is not facilitated by adenovirus-mediated viral uptake but is instead dependent on adenovirus gene expression. Using various adenovirus mutants, we were able to map this function to early-region E4 open reading frame 6. Plasmid expression of open reading frame 6 protein in cells infected with recombinant AAV increased transduction between 100- and 1,000-fold. The increase in transduction was not dependent on the recombinant AAV gene cassette but instead appeared to involve an immediate early step of the AAV life cycle. Chemical and physical agents that have been shown to induce helper-free replication of wild-type AAV were also able to stimulate recombinant AAV transduction, suggesting that the phenomenon might affect AAV DNA replication. Further experiments showed that viral uncoating was not affected and that the rate-limiting step involved synthesis of a second strand on the single-stranded genomic AAV DNA. These data suggest that the adenovirus E4 region, as well as chemical and physical agents, can play an essential role in an immediate-early step of the AAV life cycle, specifically in second-strand synthesis, and have important implications for the use of AAV vectors in gene therapy protocols.
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“Second strand synthesis after capsid uncoating in nucleus is long-recognized as the rate-limiting step of rAAV transduction (89); an improvement in such efficacy could allow rAAV administration at lower dose.”
From Immunomodulation in Administration of RAAV: Preclinical and Clinical Adjuvant Pharmacotherapies (2021) · cites this paper as [89]
Citations
Cites
Molecular Cloning: A Laboratory Manual
Sambrook, J., Fritsch, E., & Maniatis, T. (1989) · UCLA - Biblioteca de Ciencias de la Salud · Cited by 133,589
Characteristics of a human cell line transformed by DNA from human adenovirus type 5
Graham, F. L., Russell, W. C., Smiley, J., & Nairn, R. (1977) · Journal of General Virology · doi:10.1099/0022-1317-36-1-59 · Cited by 4,793
Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia
Charache, S., Terrin, M. L., Moore, R. D., Dover, G. J., Barton, F. B., Eckert, S. V., McMahon, R. P., & Bonds, D. R. (1995) · New England Journal of Medicine · doi:10.1056/nejm199505183322001 · Cited by 2,340
Use of a recombinant retrovirus to study post‐implantation cell lineage in mouse embryos.
Sanes, J. R., Rubenstein, J. L. R., & Nicolas, J. F. (1986) · The EMBO Journal · doi:10.1002/j.1460-2075.1986.tb04620.x · Cited by 1,116
(1952) · Cancer Research · Cited by 987
Site-specific integration by adeno-associated virus.
Kotin, R. M., Siniscalco, M., Samulski, R. J., Zhu, X. D., Hunter, L., Laughlin, C. A., McLaughlin, S., Muzyczka, N., Rocchi, M., & Berns, K. I. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.6.2211 · Cited by 906
Self-citationSite-specific integration by adeno-associated virus.
Linden, R. M., Ward, P., Giraud, C., Winocour, E., & Berns, K. I. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.21.11288 · Cited by 805
Jones, N. C., & Shenk, T. E. (1979) · Cell · doi:10.1016/0092-8674(79)90275-7 · Cited by 784
Self-citationTargeted integration of adeno‐associated virus (AAV) into human chromosome 19.
Samulski, R. J., Zhu, X., Xiao, X., Brook, J. D., Housman, D. E., Epstein, N., & Hunter, L. A. (1991) · The EMBO Journal · doi:10.1002/j.1460-2075.1991.tb04964.x · Cited by 783
Self-citationSamulski, R. J., Chang, L., & Shenk, T. E. (1989) · Journal of Virology · doi:10.1128/jvi.63.9.3822-3828.1989 · Cited by 742
Self-citation
Cited by
Sorted by citations
Items 201–300 of 758
Ponnazhagan, S., Mahendra, G., Curiel, D. T., & Shaw, D. R. (2001) · Journal of Virology · doi:10.1128/jvi.75.19.9493-9501.2001 · Cited by 84
Malik, P., McQuiston, S. A., Yu, X., Pepper, K. A., Krall, W. J., Podsakoff, G. M., Kurtzman, G. J., & Kohn, D. B. (1997) · Journal of Virology · doi:10.1128/jvi.71.3.1776-1783.1997 · Cited by 83
Jiang, Q., & Engelhardt, J. F. (1998) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5200158 · Cited by 83
Role of the Adenovirus DNA-Binding Protein in In Vitro Adeno-Associated Virus DNA Replication
Ward, P., Dean, F. B., O’Donnell, M. E., & Berns, K. I. (1998) · Journal of Virology · doi:10.1128/jvi.72.1.420-427.1998 · Cited by 83
Cloning and Characterization of a Bovine Adeno-Associated Virus
Schmidt, M., Katano, H., Bossis, I., & Chiorini, J. A. (2004) · Journal of Virology · doi:10.1128/jvi.78.12.6509-6516.2004 · Cited by 83
Adeno-associated virus for cancer gene therapy.
Ponnazhagan, S., Curiel, D. T., Shaw, D. R., Alvarez, R. D., & Siegal, G. P. (2001) · PubMed · Cited by 82
Liver induced transgene tolerance with AAV vectors
Keeler, G. D., Markusic, D. M., & Hoffman, B. E. (2019) · Cellular Immunology · doi:10.1016/j.cellimm.2017.12.002 · Cited by 81
Gene therapy for retinal disease
McClements, M. E., & MacLaren, R. E. (2013) · Translational Research · doi:10.1016/j.trsl.2012.12.007 · Cited by 80
Ma, H., Guo, P., Li, J., Lin, S. Z., Chiang, Y. H., Xiao, X., & Cheng, S.-Y. (2002) · PubMed · Cited by 79
Cellular transduction mechanisms of adeno-associated viral vectors
Berry, G. E., & Asokan, A. (2016) · Current Opinion in Virology · doi:10.1016/j.coviro.2016.08.001 · Cited by 90
Systemic gene delivery to the central nervous system using Adeno-associated virus
Bourdenx, M., Dutheil, N., Bézard, E., & Dehay, B. (2014) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2014.00050 · Cited by 84
Evaluation of recombinant adeno-associated virus as a gene transfer vector for the retina
Grant, C. A., Ponnazhagan, S., Wang, X.-S., Srivastava, A., & Li, T. (1997) · Current Eye Research · doi:10.1076/ceyr.16.9.949.5046 · Cited by 79
The Interaction of Heparin Sulfate and Adeno-Associated Virus 2
Qiu, J., Handa, A., Kirby, M., & Brown, K. E. (2000) · Virology · doi:10.1006/viro.2000.0205 · Cited by 79
Lovric, J., Mano, M., Zentilin, L., Eulalio, A., Zacchigna, S., & Giacca, M. (2012) · Molecular Therapy · doi:10.1038/mt.2012.144 · Cited by 77
Chowdhury, E. A., Meno‐Tetang, G. M. L., Chang, H. Y., Wu, S., Huang, H. W., Jamier, T., Chandran, J. S., & Shah, D. K. (2021) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2021.01.017 · Cited by 80
Franz, C. K., Federici, T., Yang, J., Backus, C., Oh, S. S., Teng, Q., Carlton, E. F., Bishop, K. M., Gasmi, M., Bartus, R. T., et al. (2008) · Neurobiology of Disease · doi:10.1016/j.nbd.2008.12.003 · Cited by 77
Gene therapy for Mucopolysaccharidoses
Sawamoto, K., Chen, H.-H., Alméciga-Díaz, C. J., Mason, R. W., & Tomatsu, S. (2017) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2017.12.434 · Cited by 78
The impact of pre-existing immunity on the non-clinical pharmacodynamics of AAV5-based gene therapy
Long, B. R., Sandza, K., Holcomb, J., Crockett, L., Hayes, G. M., Arens, J., Fonck, C., Tsuruda, L. S., Schweighardt, B., O’Neill, C. A., et al. (2019) · Molecular Therapy - Methods & Clinical Development · doi:10.1016/j.omtm.2019.03.006 · Cited by 75
Expression of Human Factor VIII by Splicing between Dimerized AAV Vectors
Chao, H., Sun, L., Bruce, A., Xiao, X., & Walsh, C. E. (2002) · Molecular Therapy · doi:10.1006/mthe.2002.0607 · Cited by 75
Igarashi, T., Miyake, K., Kato, K., Watanabe, A., Ishizaki, M., Ohara, K., & Shimada, T. (2003) · Gene Therapy · doi:10.1038/sj.gt.3301878 · Cited by 75
Pernet, V., Hauswirth, W. W., & Polo, A. D. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03002.x · Cited by 76
Bals, R., Xiao, W., Sang, N., Weiner, D. J., Meegalla, R. L., & Wilson, J. M. (1999) · Journal of Virology · doi:10.1128/jvi.73.7.6085-6088.1999 · Cited by 74
Salganik, M., Aydemir, F., Nam, H.-J., McKENNA, R. V., Agbandje‐McKenna, M., & Muzyczka, N. (2013) · Journal of Virology · doi:10.1128/jvi.02093-13 · Cited by 73
Allen, J. M., Halbert, C. L., & Miller, A. D. (2000) · Molecular Therapy · doi:10.1006/mthe.1999.0010 · Cited by 73
Ding, W., Yan, Z., Žák, R., Saavedra, M. T., Rodman, D. M., & Engelhardt, J. F. (2003) · Journal of Virology · doi:10.1128/jvi.77.13.7361-7366.2003 · Cited by 72
Teramoto, S., Bartlett, J. S., McCarty, D. M., Xiao, X., Samulski, R. J., & Boucher, R. C. (1998) · Journal of Virology · doi:10.1128/jvi.72.11.8904-8912.1998 · Cited by 73
Self-citationVihinen‐Ranta, M., Yuan, W., & Parrish, C. R. (2000) · Journal of Virology · doi:10.1128/jvi.74.10.4853-4859.2000 · Cited by 72
Kay, J. D., Gouze, E., Oligino, T., Gouze, J.-N., Watson, R., Levings, P. P., Bush, M. L., Dacanay, A., Nickerson, D. M., Robbins, P. D., et al. (2009) · The Journal of Gene Medicine · doi:10.1002/jgm.1334 · Cited by 72
Adeno-associated Virus: A Key to the Human Genome?
Henckaerts, E., & Linden, R. M. (2010) · Future Virology · doi:10.2217/fvl.10.48 · Cited by 71
Chen, H., McCarty, D. M., Bruce, A. T., Suzuki, K., & Suzuki, K. (1999) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19990215)55:4 · Cited by 71
Gene Therapy for Lung Disease: Hype or Hope?
Albelda, S. Μ., Wiewrodt, R. G., & Zuckerman, J. B. (2000) · Annals of Internal Medicine · doi:10.7326/0003-4819-132-8-200004180-00008 · Cited by 71
The next step in gene delivery: Molecular engineering of adeno-associated virus serotypes
Wang, J., Faust, S. M., & Rabinowitz, J. E. (2010) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2010.10.017 · Cited by 69
Near-perfect infectivity of wild-type AAV as benchmark for infectivity of recombinant AAV vectors
Zeltner, N., Kohlbrenner, E., Clément, N., Weber, T., & Linden, R. M. (2010) · Gene Therapy · doi:10.1038/gt.2010.27 · Cited by 75
Gene Delivery in Renal Tubular Epithelial Cells Using Recombinant Adeno-Associated Viral Vectors
Chen, S., Agarwal, A., Glushakova, O. Y., Scott-Jorgensen, M., Salgar, S. K., Poirier, A. E., Flotte, T. R., Croker, B. P., Madsen, K., Atkinson, M. A., et al. (2003) · Journal of the American Society of Nephrology · doi:10.1097/01.asn.0000057858.45649.f7 · Cited by 70
Hybrid vector designs to control the delivery, fate and expression of transgenes
Lam, P. Y. P., & Breakefield, X. O. (2000) · The Journal of Gene Medicine · doi:10.1002/1521-2254(200011/12)2:6 · Cited by 29
Zhao, W., Li, Z., Wu, J., Chen, L., Qing, K., Weigel-Kelley, K. A., Larsen, S. H., Shou, W., Warrington, K. H., & Srivastava, A. (2006) · Virology · doi:10.1016/j.virol.2006.04.042 · Cited by 67
Retinal gene delivery by adeno-associated virus (AAV) vectors: Strategies and applications
Schön, C., Biel, M., & Michalakis, S. (2015) · European Journal of Pharmaceutics and Biopharmaceutics · doi:10.1016/j.ejpb.2015.01.009 · Cited by 72
The Role of DNA-PKcs and Artemis in Opening Viral DNA Hairpin Termini in Various Tissues in Mice
Inagaki, K., Ma, C., Storm, T. A., Kay, M. A., & Nakai, H. (2007) · Journal of Virology · doi:10.1128/jvi.01225-07 · Cited by 70
Stracker, T. H., Cassell, G. D., Ward, P., Loo, Y., van Breukelen, B., Carrington-Lawrence, S. D., Hamatake, R. K., van der Vliet, P. C., Weller, S. K., Melendy, T., et al. (2003) · Journal of Virology · doi:10.1128/jvi.78.1.441-453.2004 · Cited by 67
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Tal, J. (2000) · Journal of Biomedical Science · doi:10.1007/bf02253246 · Cited by 67
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Critical assessment of current adeno-associated viral vector production and quantification methods
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Cardiac gene therapy with SERCA2a: From bench to bedside
Gwathmey, J. K., Yerevanian, A. I., & Hajjar, R. J. (2010) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2010.11.011 · Cited by 66
Qing, K., Li, W., Li, Z., Tan, M., Hansen, J. J., Weigel-Kelley, K. A., Chen, L., Yöder, M. C., & Srivastava, A. (2003) · Journal of Virology · doi:10.1128/jvi.77.4.2741-2746.2003 · Cited by 62
Mitchell, A. M., & Samulski, R. J. (2013) · Journal of Virology · doi:10.1128/jvi.01826-13 · Cited by 63
Self-citationIn Vitro Packaging of Adeno-Associated Virus DNA
Zhou, X., & Muzyczka, N. (1998) · Journal of Virology · doi:10.1128/jvi.72.4.3241-3247.1998 · Cited by 63
Hargrove, P. W., Vanin, E. F., Kurtzman, G. J., & Nienhuis, A. W. (1997) · Blood · doi:10.1182/blood.v89.6.2167 · Cited by 63
Direct Gene Therapy for Bone Regeneration: Gene Delivery, Animal Models, and Outcome Measures
Pelled, G., Ben‐Arav, A., Hock, C., Reynolds, D. G., Yazıcı, C., Zilberman, Y., Gazit, Z., Awad, H. A., Gazit, D., & Schwarz, E. M. (2010) · Tissue Engineering Part B Reviews · doi:10.1089/ten.teb.2009.0156 · Cited by 62
Safety of adeno-associated virus gene therapy vectors: a current evaluation
Monahan, P. E., Jooss, K. U., & Sands, M. S. (2002) · Expert Opinion on Drug Safety · doi:10.1517/14740338.1.1.79 · Cited by 61
Adeno-Associated Virus Site-Specific Integration and AAVS1 Disruption
Hamilton, H., Gomos, J. B., Berns, K. I., & Falck-Pedersen, E. (2004) · Journal of Virology · doi:10.1128/jvi.78.15.7874-7882.2004 · Cited by 67
Homologous recombination is required for AAV-mediated gene targeting
Vasileva, A. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl455 · Cited by 62
Şanlıoğlu, S., Benson, P. K., & Engelhardt, J. F. (2000) · Virology · doi:10.1006/viro.1999.0137 · Cited by 61
Nuclear Export of Adenovirus RNA
Dobner, T., & Kzhyshkowska, J. G. (2001) · Current topics in microbiology and immunology · doi:10.1007/978-3-642-56597-7_2 · Cited by 61
Native Molecular State of Adeno-Associated Viral Vectors Revealed by Single-Molecule Sequencing
Kapranov, P., Chen, L., Dederich, D. A., Dong, B., He, J., Steinmann, K. E., Moore, A. R., Thompson, J. F., Milos, P. M., & Xiao, W. (2011) · Human Gene Therapy · doi:10.1089/hum.2011.160 · Cited by 58
Ren, R., Li, Y., Liu, Z., Liu, K., & He, S. (2012) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.11-8484 · Cited by 60
Şanlıoğlu, S., Duan, D., & Engelhardt, J. F. (1999) · Human Gene Therapy · doi:10.1089/10430349950018661 · Cited by 60
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Kotin, R. M., & Snyder, R. O. (2017) · Human Gene Therapy · doi:10.1089/hum.2017.042 · Cited by 59
Li, Z., Li, W., Yang, Z., Qing, K., Tan, M., Hansen, J. J., Li, Y., Chen, L., Chan, R. J., Bischof, D., et al. (2004) · Human Gene Therapy · doi:10.1089/hum.2004.15.1207 · Cited by 56
Ocular gene transfer with self-complementary AAV vectors
Yokoi, K., Kachi, S., Zhang, H. S., Gregory, P. D., Spratt, S. K., Samulski, R. J., & Campochiaro, P. A. (2007) · Investigative Opthalmology & Visual Science · doi:10.1167/iovs.06-1306 · Cited by 58
Self-citationLópez-Gordo, E., Chamberlain, K., Riyad, J. M., Kohlbrenner, E., & Weber, T. (2024) · Viruses · doi:10.3390/v16030442 · Cited by 68
Cheng, B., Ling, C., Dai, Y., Lu, Y., Glushakova, L. G., Gee, S. W. Y., McGoogan, K. E., Aslanidi, G., Park, M., Stacpoole, P. W., et al. (2011) · Gene Therapy · doi:10.1038/gt.2011.105 · Cited by 59
Sarra, G., Stephens, C., Schlichtenbrede, F. C., Bainbridge, J. W., Thrasher, A. J., Luthert, P. J., & Ali, R. R. (2002) · Vision Research · doi:10.1016/s0042-6989(01)00230-9 · Cited by 58
The Role of Recombinant AAV in Precise Genome Editing
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Herzog, R. W. (2015) · Frontiers in bioscience · doi:10.2741/4324 · Cited by 56
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Song, L., Li, X., Jayandharan, G. R., Wang, Y., Aslanidi, G., Ling, C., Li, Z., Gao, G., Yöder, M. C., Ling, C., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0058757 · Cited by 55
Rittiner, J. E., Moncalvo, M., Chiba‐Falek, O., & Kantor, B. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.00148 · Cited by 53
Su, H., Huang, Y.-W., Takagawa, J., Bárcena, A., Arakawa-Hoyt, J. S., Ye, J., Grossman, W., & Kan, Y. W. (2006) · Gene Therapy · doi:10.1038/sj.gt.3302787 · Cited by 51
Mouw, M. B., & Pintel, D. J. (2000) · Journal of Virology · doi:10.1128/jvi.74.21.9878-9888.2000 · Cited by 53
Nakai, H., Montini, E., Fuess, S., Storm, T. A., Meuse, L., Finegold, M., Grompe, M., & Kay, M. A. (2003) · Molecular Therapy · doi:10.1016/s1525-0016(02)00023-0 · Cited by 52
Kong, F., Li, W., Li, X., Zheng, Q., Dai, X., Zhou, X., Boye, S. L., Hauswirth, W. W., Qu, J., & Pang, J. (2010) · Experimental Eye Research · doi:10.1016/j.exer.2010.01.011 · Cited by 52
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Self-citationRecent advances in recombinant adeno-associated virus vector production
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Stilwell, J. L., & Samulski, R. J. (2003) · BioTechniques · doi:10.2144/03341dd01 · Cited by 52
Self-citationWang, M., Sun, J., Crosby, A. J., Woodard, K., Hirsch, M. L., Samulski, R. J., & Li, C. (2016) · Gene Therapy · doi:10.1038/gt.2016.75 · Cited by 52
Self-citationTransduction of human neural progenitor cells using recombinant adeno-associated viral vectors
Wu, P., Ye, Y., & Svendsen, C. (2002) · Gene Therapy · doi:10.1038/sj.gt.3301646 · Cited by 51
François, A., Bouzelha, M., Lecomte, E., Broucque, F., Penaud-Budloo, M., Adjali, O., Moullier, P., Blouin, V., & Ayuso, E. (2018) · Molecular Therapy - Methods & Clinical Development · doi:10.1016/j.omtm.2018.07.004 · Cited by 50
Adeno-Associated Virus Mediated Gene Therapy for Corneal Diseases
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Hennig, A. K., Ogilvie, J. M., Ohlemiller, K. K., Timmers, A. M., Hauswirth, W. W., & Sands, M. S. (2004) · Molecular Therapy · doi:10.1016/j.ymthe.2004.03.018 · Cited by 49
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Li, Z., Qing, K., Si, Y. C., Chen, L., Tan, M., & Srivastava, A. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m310548200 · Cited by 48
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Lentz, T. B., & Samulski, R. J. (2015) · Journal of Virology · doi:10.1128/jvi.01990-14 · Cited by 48
Self-citationNicolson, S. C., Li, C., Hirsch, M. L., Setola, V., & Samulski, R. J. (2016) · Journal of Virology · doi:10.1128/jvi.02953-15 · Cited by 48
Self-citationSchreiber, C. A., Sakuma, T., Izumiya, Y., Holditch, S. J., Hickey, R., Bressin, R. K., Basu, U., Koide, K., Asokan, A., & Ikeda, Y. (2015) · PLoS Pathogens · doi:10.1371/journal.ppat.1005082 · Cited by 49
Molecular correction of Duchenne muscular dystrophy by splice modulation and gene editing
Hanson, B., Wood, M. J. A., & Roberts, T. C. (2021) · RNA Biology · doi:10.1080/15476286.2021.1874161 · Cited by 49
Johnson, J. S., Gentzsch, M., Zhang, L., Ribeiro, C. M. P., Kantor, B., Kafri, T., Pickles, R. J., & Samulski, R. J. (2011) · PLoS Pathogens · doi:10.1371/journal.ppat.1002053 · Cited by 49
Self-citationKinetics of Recombinant Adeno-Associated Virus-Mediated Gene Transfer
Malik, A. K., Monahan, P. E., Allen, D. L., Chen, B.-G., Samulski, R. J., & Kurachi, K. (2000) · Journal of Virology · doi:10.1128/jvi.74.8.3555-3565.2000 · Cited by 48
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Qian, C., Droździk, M., Caselmann, W. H., & Prìeto, J. (2000) · Journal of Hepatology · doi:10.1016/s0168-8278(00)80082-3 · Cited by 48
Ling, C., Wang, Y., Lu, Y., Wang, L., Jayandharan, G. R., Aslanidi, G. V., Li, B., Cheng, B., Ma, W., Lentz, T., et al. (2015) · Journal of Virology · doi:10.1128/jvi.02581-14 · Cited by 47
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Ito, H., Goater, J. J., Tiyapatanaputi, P., Rubery, P. T., O'Keefe, R. J., & Schwarz, E. (2003) · Gene Therapy · doi:10.1038/sj.gt.3302102 · Cited by 47
Byrne, B. J., Smith, B. K., Mah, C. S., Lawson, L. A., Islam, S., Corti, M., Martin, D., Dobija, N., Irwin, M. V., Conlon, T. J., et al. (2014) · Human Gene Therapy Clinical Development · doi:10.1089/humc.2014.2514 · Cited by 45
Metadata
- Authors
- Ferrari, F. K., Samulski, T., Shenk, T., & Samulski, R. J.
- Affiliations
- University of North Carolina at Chapel Hill (US)
- ORCID
- Shenk, T
- Venue
- Journal of Virology
- Publisher
- American Society for Microbiology
- Published
- 1996-05
- Volume
- 70
- Issue
- 5
- Pages
- 3227-3234
- ISSN
- 0022-538X (ISSN-L)
- 1098-5514
- PMC
- PMC190186
- OpenAlex
- W2165815741
- Cited by
- 761
- References
- 46
- Citations by year
- 2026: 13 · 2025: 16 · 2024: 16 · 2023: 17 · 2022: 13 · 2021: 15 · 2020: 25 · 2019: 17 · 2018: 15 · 2017: 10 · 2016: 22 · 2015: 27 · 2014: 21 · 2013: 17 · 2012: 27
- FWCI
- 24.99
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of Virology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5r01dk042701-06)
- National Heart, Lung, and Blood Institute (HL48327, P01HL051818, HL51818)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK 42701)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Virus-based gene therapy research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
- Life Sciences › Immunology and Microbiology › Virology › Bacteriophages and microbial interactions
- Keywords
- recombinant adeno-associated virus vectors, viral uncoating, gene therapy vectors
- MeSH terms
- Dependovirus, Adenoviridae, beta-Galactosidase, Cell Line, DNA, Viral, Genetic Vectors, HeLa Cells, Humans, Kinetics, Plasmids, Recombinant Proteins, Recombination, Genetic, Transduction, Genetic, Transfection, Ultraviolet Rays, X-Rays, Gene Expression, Mutagenesis, Open Reading Frames
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