378 related articles for article (PubMed ID: 36015231)
1. Lentiviral Vectors for Ocular Gene Therapy.
Arsenijevic Y; Berger A; Udry F; Kostic C
Pharmaceutics; 2022 Jul; 14(8):. PubMed ID: 36015231
[TBL] [Abstract][Full Text] [Related]
2. Ocular gene delivery using lentiviral vectors.
Balaggan KS; Ali RR
Gene Ther; 2012 Feb; 19(2):145-53. PubMed ID: 22052240
[TBL] [Abstract][Full Text] [Related]
3. Hereditary Retinal Dystrophy.
Hohman TC
Handb Exp Pharmacol; 2017; 242():337-367. PubMed ID: 28035529
[TBL] [Abstract][Full Text] [Related]
4. Republished review: Gene therapy for ocular diseases.
Liu MM; Tuo J; Chan CC
Postgrad Med J; 2011 Jul; 87(1029):487-95. PubMed ID: 21705775
[TBL] [Abstract][Full Text] [Related]
5. Gene therapy for inherited retinal diseases: progress and possibilities.
Hu ML; Edwards TL; O'Hare F; Hickey DG; Wang JH; Liu Z; Ayton LN
Clin Exp Optom; 2021 May; 104(4):444-454. PubMed ID: 33689657
[TBL] [Abstract][Full Text] [Related]
6. Gene therapy for neurodegenerative and ocular diseases using lentiviral vectors.
Ralph GS; Binley K; Wong LF; Azzouz M; Mazarakis ND
Clin Sci (Lond); 2006 Jan; 110(1):37-46. PubMed ID: 16336203
[TBL] [Abstract][Full Text] [Related]
7. Gene therapy for ocular diseases.
Liu MM; Tuo J; Chan CC
Br J Ophthalmol; 2011 May; 95(5):604-12. PubMed ID: 20733027
[TBL] [Abstract][Full Text] [Related]
8. Treatment of ocular disorders by gene therapy.
Solinís MÁ; del Pozo-Rodríguez A; Apaolaza PS; Rodríguez-Gascón A
Eur J Pharm Biopharm; 2015 Sep; 95(Pt B):331-42. PubMed ID: 25536112
[TBL] [Abstract][Full Text] [Related]
9. AAV-mediated gene supply for treatment of degenerative and neovascular retinal diseases.
Colella P; Auricchio A
Curr Gene Ther; 2010 Oct; 10(5):371-80. PubMed ID: 20712580
[TBL] [Abstract][Full Text] [Related]
10. Strategies for retargeted gene delivery using vectors derived from lentiviruses.
Bartosch B; Cosset FL
Curr Gene Ther; 2004 Dec; 4(4):427-43. PubMed ID: 15578992
[TBL] [Abstract][Full Text] [Related]
11. Lentiviral gene transfer of RPE65 rescues survival and function of cones in a mouse model of Leber congenital amaurosis.
Bemelmans AP; Kostic C; Crippa SV; Hauswirth WW; Lem J; Munier FL; Seeliger MW; Wenzel A; Arsenijevic Y
PLoS Med; 2006 Oct; 3(10):e347. PubMed ID: 17032058
[TBL] [Abstract][Full Text] [Related]
12. Evaluation of tolerance to lentiviral LV-RPE65 gene therapy vector after subretinal delivery in non-human primates.
Matet A; Kostic C; Bemelmans AP; Moulin A; Rosolen SG; Martin S; Mavilio F; Amirjanians V; Stieger K; Lorenz B; Behar-Cohen F; Arsenijevic Y
Transl Res; 2017 Oct; 188():40-57.e4. PubMed ID: 28754419
[TBL] [Abstract][Full Text] [Related]
13. Gene therapy for leber congenital amaurosis caused by RPE65 mutations: safety and efficacy in 15 children and adults followed up to 3 years.
Jacobson SG; Cideciyan AV; Ratnakaram R; Heon E; Schwartz SB; Roman AJ; Peden MC; Aleman TS; Boye SL; Sumaroka A; Conlon TJ; Calcedo R; Pang JJ; Erger KE; Olivares MB; Mullins CL; Swider M; Kaushal S; Feuer WJ; Iannaccone A; Fishman GA; Stone EM; Byrne BJ; Hauswirth WW
Arch Ophthalmol; 2012 Jan; 130(1):9-24. PubMed ID: 21911650
[TBL] [Abstract][Full Text] [Related]
14. Production of lentiviral vectors for transducing cells from the central nervous system.
Li M; Husic N; Lin Y; Snider BJ
J Vis Exp; 2012 May; (63):e4031. PubMed ID: 22664962
[TBL] [Abstract][Full Text] [Related]
15. Gene therapy in inherited retinal degenerative diseases, a review.
Takahashi VKL; Takiuti JT; Jauregui R; Tsang SH
Ophthalmic Genet; 2018 Oct; 39(5):560-568. PubMed ID: 30040511
[TBL] [Abstract][Full Text] [Related]
16. Gene therapy for Leber congenital amaurosis: advances and future directions.
Hufnagel RB; Ahmed ZM; Corrêa ZM; Sisk RA
Graefes Arch Clin Exp Ophthalmol; 2012 Aug; 250(8):1117-28. PubMed ID: 22644094
[TBL] [Abstract][Full Text] [Related]
17. [Viral vectors for gene delivery to corneal endothelial cells].
Fuchsluger TA; Jurkunas U; Kazlauskas A; Dana R
Klin Monbl Augenheilkd; 2011 Jun; 228(6):498-503. PubMed ID: 21656431
[TBL] [Abstract][Full Text] [Related]
18. Gene therapy using self-complementary Y733F capsid mutant AAV2/8 restores vision in a model of early onset Leber congenital amaurosis.
Ku CA; Chiodo VA; Boye SL; Goldberg AF; Li T; Hauswirth WW; Ramamurthy V
Hum Mol Genet; 2011 Dec; 20(23):4569-81. PubMed ID: 21880665
[TBL] [Abstract][Full Text] [Related]
19. The Role of Gene Therapy in the Treatment of Retinal Diseases: A Review.
Campa C; Gallenga CE; Bolletta E; Perri P
Curr Gene Ther; 2017; 17(3):194-213. PubMed ID: 29149824
[TBL] [Abstract][Full Text] [Related]
20. Recent breakthroughs in gene therapy for inherited retinal degeneration.
Revere KE; Chung DC
Discov Med; 2009 Oct; 8(42):125-9. PubMed ID: 19833058
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]