These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
254 related articles for article (PubMed ID: 27358030)
1. Insulin Therapy Improves Adeno-Associated Virus Transduction of Liver and Skeletal Muscle in Mice and Cultured Cells. Carrig S; Bijjiga E; Wopat MJ; Martino AT Hum Gene Ther; 2016 Nov; 27(11):892-905. PubMed ID: 27358030 [TBL] [Abstract][Full Text] [Related]
2. Application of polyploid adeno-associated virus vectors for transduction enhancement and neutralizing antibody evasion. Chai Z; Sun J; Rigsbee KM; Wang M; Samulski RJ; Li C J Control Release; 2017 Sep; 262():348-356. PubMed ID: 28789965 [TBL] [Abstract][Full Text] [Related]
3. Transduction Efficiency of Adeno-Associated Virus Serotypes After Local Injection in Mouse and Human Skeletal Muscle. Muraine L; Bensalah M; Dhiab J; Cordova G; Arandel L; Marhic A; Chapart M; Vasseur S; Benkhelifa-Ziyyat S; Bigot A; Butler-Browne G; Mouly V; Negroni E; Trollet C Hum Gene Ther; 2020 Feb; 31(3-4):233-240. PubMed ID: 31880951 [TBL] [Abstract][Full Text] [Related]
4. Identification and Validation of Small Molecules That Enhance Recombinant Adeno-associated Virus Transduction following High-Throughput Screens. Nicolson SC; Li C; Hirsch ML; Setola V; Samulski RJ J Virol; 2016 Aug; 90(16):7019-7031. PubMed ID: 27147738 [TBL] [Abstract][Full Text] [Related]
5. Efficient AAV1-AAV2 hybrid vector for gene therapy of hemophilia. Hauck B; Xu RR; Xie J; Wu W; Ding Q; Sipler M; Wang H; Chen L; Wright JF; Xiao W Hum Gene Ther; 2006 Jan; 17(1):46-54. PubMed ID: 16409124 [TBL] [Abstract][Full Text] [Related]
6. Muscle-specific promoters may be necessary for adeno-associated virus-mediated gene transfer in the treatment of muscular dystrophies. Cordier L; Gao GP; Hack AA; McNally EM; Wilson JM; Chirmule N; Sweeney HL Hum Gene Ther; 2001 Jan; 12(2):205-15. PubMed ID: 11177557 [TBL] [Abstract][Full Text] [Related]
7. Muscle as a target for supplementary factor IX gene transfer. Hoffman BE; Dobrzynski E; Wang L; Hirao L; Mingozzi F; Cao O; Herzog RW Hum Gene Ther; 2007 Jul; 18(7):603-13. PubMed ID: 17594244 [TBL] [Abstract][Full Text] [Related]
8. Therapeutic levels of factor IX expression using a muscle-specific promoter and adeno-associated virus serotype 1 vector. Liu YL; Mingozzi F; Rodriguéz-Colôn SM; Joseph S; Dobrzynski E; Suzuki T; High KA; Herzog RW Hum Gene Ther; 2004 Aug; 15(8):783-92. PubMed ID: 15319035 [TBL] [Abstract][Full Text] [Related]
9. Gene transfer into skeletal muscle using novel AAV serotypes. Louboutin JP; Wang L; Wilson JM J Gene Med; 2005 Apr; 7(4):442-51. PubMed ID: 15517544 [TBL] [Abstract][Full Text] [Related]
10. Human apolipoprotein E expression from mouse skeletal muscle by electrotransfer of nonviral DNA (plasmid) and pseudotyped recombinant adeno-associated virus (AAV2/7). Evans V; Foster H; Graham IR; Foster K; Athanasopoulos T; Simons JP; Dickson G; Owen JS Hum Gene Ther; 2008 Jun; 19(6):569-78. PubMed ID: 18578629 [TBL] [Abstract][Full Text] [Related]
11. Improved cardiac gene transfer by transcriptional and transductional targeting of adeno-associated viral vectors. Müller OJ; Leuchs B; Pleger ST; Grimm D; Franz WM; Katus HA; Kleinschmidt JA Cardiovasc Res; 2006 Apr; 70(1):70-8. PubMed ID: 16448634 [TBL] [Abstract][Full Text] [Related]
12. Direct intramuscular injection with recombinant AAV vectors results in sustained expression in a dog model of hemophilia. Monahan PE; Samulski RJ; Tazelaar J; Xiao X; Nichols TC; Bellinger DA; Read MS; Walsh CE Gene Ther; 1998 Jan; 5(1):40-9. PubMed ID: 9536263 [TBL] [Abstract][Full Text] [Related]
13. Enhancing Transgene Expression from Recombinant AAV8 Vectors in Different Tissues Using Woodchuck Hepatitis Virus Post-Transcriptional Regulatory Element. Wang L; Wang Z; Zhang F; Zhu R; Bi J; Wu J; Zhang H; Wu H; Kong W; Yu B; Yu X Int J Med Sci; 2016; 13(4):286-91. PubMed ID: 27076785 [TBL] [Abstract][Full Text] [Related]
14. Cytotoxic immune response after retroviral-mediated hepatic gene transfer in rat does not preclude expression from adeno-associated virus 1 transduced muscles. Aubert D; Pichard V; Durand S; Moullier P; Ferry N Hum Gene Ther; 2003 Mar; 14(5):473-81. PubMed ID: 12691612 [TBL] [Abstract][Full Text] [Related]
16. Hyaluronidase enhances recombinant adeno-associated virus (rAAV)-mediated gene transfer in the rat skeletal muscle. Favre D; Cherel Y; Provost N; Blouin V; Ferry N; Moullier P; Salvetti A Gene Ther; 2000 Aug; 7(16):1417-20. PubMed ID: 10981669 [TBL] [Abstract][Full Text] [Related]
17. Theodore E. Woodward Award. AAV-mediated gene transfer for hemophilia. High KA Trans Am Clin Climatol Assoc; 2003; 114():337-51; discussion 351-2. PubMed ID: 12813929 [TBL] [Abstract][Full Text] [Related]
18. Potential limits of AAV-based gene therapy with the use of new transgenes expressing factor IX fusion proteins. Le Quellec S; Dane A; Enjolras N; McIntosh J; Rosales C; Negrier C; Nathwani A Haemophilia; 2019 Jan; 25(1):e11-e18. PubMed ID: 30520547 [TBL] [Abstract][Full Text] [Related]