141 related articles for article (PubMed ID: 11726636)
1. Gene transfer mediated by recombinant baculovirus into mouse eye.
Haeseleer F; Imanishi Y; Saperstein DA; Palczewski K
Invest Ophthalmol Vis Sci; 2001 Dec; 42(13):3294-300. PubMed ID: 11726636
[TBL] [Abstract][Full Text] [Related]
2. Gene therapy following subretinal AAV5 vector delivery is not affected by a previous intravitreal AAV5 vector administration in the partner eye.
Li W; Kong F; Li X; Dai X; Liu X; Zheng Q; Wu R; Zhou X; Lü F; Chang B; Li Q; Hauswirth WW; Qu J; Pang JJ
Mol Vis; 2009; 15():267-75. PubMed ID: 19190735
[TBL] [Abstract][Full Text] [Related]
3. Efficiency of lentiviral transduction during development in normal and rd mice.
Pang J; Cheng M; Haire SE; Barker E; Planelles V; Blanks JC
Mol Vis; 2006 Jul; 12():756-67. PubMed ID: 16862069
[TBL] [Abstract][Full Text] [Related]
4. Real-time, noninvasive in vivo assessment of adeno-associated virus-mediated retinal transduction.
Bennett J; Duan D; Engelhardt JF; Maguire AM
Invest Ophthalmol Vis Sci; 1997 Dec; 38(13):2857-63. PubMed ID: 9418740
[TBL] [Abstract][Full Text] [Related]
5. Intraocular route of AAV2 vector administration defines humoral immune response and therapeutic potential.
Li Q; Miller R; Han PY; Pang J; Dinculescu A; Chiodo V; Hauswirth WW
Mol Vis; 2008 Sep; 14():1760-9. PubMed ID: 18836574
[TBL] [Abstract][Full Text] [Related]
6. Sustained transduction of ocular cells with a bovine immunodeficiency viral vector.
Takahashi K; Luo T; Saishin Y; Saishin Y; Sung J; Hackett S; Brazzell RK; Kaleko M; Campochiaro PA
Hum Gene Ther; 2002 Jul; 13(11):1305-16. PubMed ID: 12162813
[TBL] [Abstract][Full Text] [Related]
7. Baculovirus is an efficient vector for the transduction of the eye: comparison of baculovirus- and adenovirus-mediated intravitreal vascular endothelial growth factor D gene transfer in the rabbit eye.
Kinnunen K; Kalesnykas G; Mähönen AJ; Laidinen S; Holma L; Heikura T; Airenne K; Uusitalo H; Ylä-Herttuala S
J Gene Med; 2009 May; 11(5):382-9. PubMed ID: 19263462
[TBL] [Abstract][Full Text] [Related]
8. Self-complementary AAV5 vector facilitates quicker transgene expression in photoreceptor and retinal pigment epithelial cells of normal mouse.
Kong F; Li W; Li X; Zheng Q; Dai X; Zhou X; Boye SL; Hauswirth WW; Qu J; Pang JJ
Exp Eye Res; 2010 May; 90(5):546-54. PubMed ID: 20138034
[TBL] [Abstract][Full Text] [Related]
9. Efficient and stable gene expression in rabbit intervertebral disc cells transduced with a recombinant baculovirus vector.
Liu X; Li K; Song J; Liang C; Wang X; Chen X
Spine (Phila Pa 1976); 2006 Apr; 31(7):732-5. PubMed ID: 16582845
[TBL] [Abstract][Full Text] [Related]
10. In vivo transcriptional targeting into the retinal vasculature using recombinant baculovirus carrying the human flt-1 promoter.
Luz-Madrigal A; Clapp C; Aranda J; Vaca L
Virol J; 2007 Sep; 4():88. PubMed ID: 17877803
[TBL] [Abstract][Full Text] [Related]
11. Direct comparison of administration routes for AAV8-mediated ocular gene therapy.
Igarashi T; Miyake K; Asakawa N; Miyake N; Shimada T; Takahashi H
Curr Eye Res; 2013 May; 38(5):569-77. PubMed ID: 23489150
[TBL] [Abstract][Full Text] [Related]
12. Ocular gene transfer with self-complementary AAV vectors.
Yokoi K; Kachi S; Zhang HS; Gregory PD; Spratt SK; Samulski RJ; Campochiaro PA
Invest Ophthalmol Vis Sci; 2007 Jul; 48(7):3324-8. PubMed ID: 17591905
[TBL] [Abstract][Full Text] [Related]
13. Intraocular adenoviral vector-mediated gene transfer in proliferative retinopathies.
Mori K; Gehlbach P; Ando A; Wahlin K; Gunther V; McVey D; Wei L; Campochiaro PA
Invest Ophthalmol Vis Sci; 2002 May; 43(5):1610-5. PubMed ID: 11980881
[TBL] [Abstract][Full Text] [Related]
14. Comparative analysis of in vivo and in vitro AAV vector transduction in the neonatal mouse retina: effects of serotype and site of administration.
Pang JJ; Lauramore A; Deng WT; Li Q; Doyle TJ; Chiodo V; Li J; Hauswirth WW
Vision Res; 2008 Feb; 48(3):377-85. PubMed ID: 17950399
[TBL] [Abstract][Full Text] [Related]
15. Comparative Study of Adeno-associated Virus, Adenovirus, Bacu lovirus and Lentivirus Vectors for Gene Therapy of the Eyes.
Kalesnykas G; Kokki E; Alasaarela L; Lesch HP; Tuulos T; Kinnunen K; Uusitalo H; Airenne K; Yla-Herttuala S
Curr Gene Ther; 2017; 17(3):235-247. PubMed ID: 28982327
[TBL] [Abstract][Full Text] [Related]
16. In vivo gene transfer to the rat retina using herpes simplex virus type 1 (HSV-1)-based amplicon vectors.
Fraefel C; Mendes-Madeira A; Mabon O; Lefebvre A; Le Meur G; Ackermann M; Moullier P; Rolling F
Gene Ther; 2005 Aug; 12(16):1283-8. PubMed ID: 15889134
[TBL] [Abstract][Full Text] [Related]
17. A Novel Method Combining Vitreous Aspiration and Intravitreal AAV2/8 Injection Results in Retina-Wide Transduction in Adult Mice.
Da Costa R; Röger C; Segelken J; Barben M; Grimm C; Neidhardt J
Invest Ophthalmol Vis Sci; 2016 Oct; 57(13):5326-5334. PubMed ID: 27784063
[TBL] [Abstract][Full Text] [Related]
18. Feline immunodeficiency virus vectors. Gene transfer to mouse retina following intravitreal injection.
Derksen TA; Sauter SL; Davidson BL
J Gene Med; 2002; 4(5):463-9. PubMed ID: 12221638
[TBL] [Abstract][Full Text] [Related]
19. Evaluation of adeno-associated virus-mediated gene transfer into the rat retina by clinical fluorescence photography.
Rolling F; Shen WY; Tabarias H; Constable I; Kanagasingam Y; Barry CJ; Rakoczy PE
Hum Gene Ther; 1999 Mar; 10(4):641-8. PubMed ID: 10094207
[TBL] [Abstract][Full Text] [Related]
20. Efficient gene transfer into retinal cells using adenoviral vectors: dependence on receptor expression.
Mallam JN; Hurwitz MY; Mahoney T; Chévez-Barrios P; Hurwitz RL
Invest Ophthalmol Vis Sci; 2004 Jun; 45(6):1680-7. PubMed ID: 15161826
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]