310 related articles for article (PubMed ID: 22990673)
1. AAV vectors containing rDNA homology display increased chromosomal integration and transgene persistence.
Wang Z; Lisowski L; Finegold MJ; Nakai H; Kay MA; Grompe M
Mol Ther; 2012 Oct; 20(10):1902-11. PubMed ID: 22990673
[TBL] [Abstract][Full Text] [Related]
2. Ribosomal DNA integrating rAAV-rDNA vectors allow for stable transgene expression.
Lisowski L; Lau A; Wang Z; Zhang Y; Zhang F; Grompe M; Kay MA
Mol Ther; 2012 Oct; 20(10):1912-23. PubMed ID: 22990671
[TBL] [Abstract][Full Text] [Related]
3. Herpes simplex virus type 1/adeno-associated virus hybrid vectors mediate site-specific integration at the adeno-associated virus preintegration site, AAVS1, on human chromosome 19.
Heister T; Heid I; Ackermann M; Fraefel C
J Virol; 2002 Jul; 76(14):7163-73. PubMed ID: 12072516
[TBL] [Abstract][Full Text] [Related]
4. Hybrid adeno-associated viral vectors utilizing transposase-mediated somatic integration for stable transgene expression in human cells.
Zhang W; Solanki M; Müther N; Ebel M; Wang J; Sun C; Izsvak Z; Ehrhardt A
PLoS One; 2013; 8(10):e76771. PubMed ID: 24116154
[TBL] [Abstract][Full Text] [Related]
5. Isolation of recombinant adeno-associated virus vector-cellular DNA junctions from mouse liver.
Nakai H; Iwaki Y; Kay MA; Couto LB
J Virol; 1999 Jul; 73(7):5438-47. PubMed ID: 10364291
[TBL] [Abstract][Full Text] [Related]
6. Extrachromosomal recombinant adeno-associated virus vector genomes are primarily responsible for stable liver transduction in vivo.
Nakai H; Yant SR; Storm TA; Fuess S; Meuse L; Kay MA
J Virol; 2001 Aug; 75(15):6969-76. PubMed ID: 11435577
[TBL] [Abstract][Full Text] [Related]
7. Efficient integration of recombinant adeno-associated virus DNA vectors requires a p5-rep sequence in cis.
Philpott NJ; Giraud-Wali C; Dupuis C; Gomos J; Hamilton H; Berns KI; Falck-Pedersen E
J Virol; 2002 Jun; 76(11):5411-21. PubMed ID: 11991970
[TBL] [Abstract][Full Text] [Related]
8. Selection and evaluation of clinically relevant AAV variants in a xenograft liver model.
Lisowski L; Dane AP; Chu K; Zhang Y; Cunningham SC; Wilson EM; Nygaard S; Grompe M; Alexander IE; Kay MA
Nature; 2014 Feb; 506(7488):382-6. PubMed ID: 24390344
[TBL] [Abstract][Full Text] [Related]
9. A limited number of transducible hepatocytes restricts a wide-range linear vector dose response in recombinant adeno-associated virus-mediated liver transduction.
Nakai H; Thomas CE; Storm TA; Fuess S; Powell S; Wright JF; Kay MA
J Virol; 2002 Nov; 76(22):11343-9. PubMed ID: 12388694
[TBL] [Abstract][Full Text] [Related]
10. Safety of liver gene transfer following peripheral intravascular delivery of adeno-associated virus (AAV)-5 and AAV-6 in a large animal model.
Favaro P; Finn JD; Siner JI; Wright JF; High KA; Arruda VR
Hum Gene Ther; 2011 Jul; 22(7):843-52. PubMed ID: 21126217
[TBL] [Abstract][Full Text] [Related]
11. Enhancing transduction of the liver by adeno-associated viral vectors.
Nathwani AC; Cochrane M; McIntosh J; Ng CY; Zhou J; Gray JT; Davidoff AM
Gene Ther; 2009 Jan; 16(1):60-9. PubMed ID: 18701909
[TBL] [Abstract][Full Text] [Related]
12. Expressing Transgenes That Exceed the Packaging Capacity of Adeno-Associated Virus Capsids.
Chamberlain K; Riyad JM; Weber T
Hum Gene Ther Methods; 2016 Feb; 27(1):1-12. PubMed ID: 26757051
[TBL] [Abstract][Full Text] [Related]
13. [Integration of AAV vectors and insertional mutagenesis].
Rossi A; Salvetti A
Med Sci (Paris); 2016 Feb; 32(2):167-74. PubMed ID: 26936174
[TBL] [Abstract][Full Text] [Related]
14. Improved hepatic gene transfer by using an adeno-associated virus serotype 5 vector.
Mingozzi F; Schüttrumpf J; Arruda VR; Liu Y; Liu YL; High KA; Xiao W; Herzog RW
J Virol; 2002 Oct; 76(20):10497-502. PubMed ID: 12239326
[TBL] [Abstract][Full Text] [Related]
15. AAV integration in human hepatocytes.
Dalwadi DA; Calabria A; Tiyaboonchai A; Posey J; Naugler WE; Montini E; Grompe M
Mol Ther; 2021 Oct; 29(10):2898-2909. PubMed ID: 34461297
[TBL] [Abstract][Full Text] [Related]
16. Optimized adeno-associated virus (AAV)-protein phosphatase-5 helper viruses for efficient liver transduction by single-stranded AAV vectors: therapeutic expression of factor IX at reduced vector doses.
Jayandharan GR; Zhong L; Sack BK; Rivers AE; Li M; Li B; Herzog RW; Srivastava A
Hum Gene Ther; 2010 Mar; 21(3):271-83. PubMed ID: 19788390
[TBL] [Abstract][Full Text] [Related]
17. AAV serotype 2 vectors preferentially integrate into active genes in mice.
Nakai H; Montini E; Fuess S; Storm TA; Grompe M; Kay MA
Nat Genet; 2003 Jul; 34(3):297-302. PubMed ID: 12778174
[TBL] [Abstract][Full Text] [Related]
18. Cellular recombination pathways and viral terminal repeat hairpin structures are sufficient for adeno-associated virus integration in vivo and in vitro.
Yang CC; Xiao X; Zhu X; Ansardi DC; Epstein ND; Frey MR; Matera AG; Samulski RJ
J Virol; 1997 Dec; 71(12):9231-47. PubMed ID: 9371582
[TBL] [Abstract][Full Text] [Related]
19. Herpes simplex virus type 1/adeno-associated virus rep(+) hybrid amplicon vector improves the stability of transgene expression in human cells by site-specific integration.
Wang Y; Camp SM; Niwano M; Shen X; Bakowska JC; Breakefield XO; Allen PD
J Virol; 2002 Jul; 76(14):7150-62. PubMed ID: 12072515
[TBL] [Abstract][Full Text] [Related]
20. In Utero Transfer of Adeno-Associated Viral Vectors Produces Long-Term Factor IX Levels in a Cynomolgus Macaque Model.
Mattar CNZ; Gil-Farina I; Rosales C; Johana N; Tan YYW; McIntosh J; Kaeppel C; Waddington SN; Biswas A; Choolani M; Schmidt M; Nathwani AC; Chan JKY
Mol Ther; 2017 Aug; 25(8):1843-1853. PubMed ID: 28462816
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]