-
1
-
-
50049136340
-
The eyes have it! Ocular gene therapy trials for LCA look promising
-
Bainbridge, J.W., and Ali, R.R. (2008). The eyes have it! Ocular gene therapy trials for LCA look promising. Gene Ther. 15, 1191-1192.
-
(2008)
Gene Ther.
, vol.15
, pp. 1191-1192
-
-
Bainbridge, J.W.1
Ali, R.R.2
-
2
-
-
85047699046
-
Inhibition of retinal neovascularisation by gene transfer of soluble VEGF receptor sFlt-1
-
Bainbridge, J.W., Mistry, A., De Alwis, M., Paleolog, E., Baker, A., Thrasher, A.J., and Ali, R.R. (2002). Inhibition of retinal neovascularisation by gene transfer of soluble VEGF receptor sFlt-1. Gene Ther. 9, 320-326.
-
(2002)
Gene Ther.
, vol.9
, pp. 320-326
-
-
Bainbridge, J.W.1
Mistry, A.2
De Alwis, M.3
Paleolog, E.4
Baker, A.5
Thrasher, A.J.6
Ali, R.R.7
-
3
-
-
33746863749
-
Gene therapy progress and prospects: The eye
-
Bainbridge, J.W., Tan, M.H., and Ali, R.R. (2006). Gene therapy progress and prospects: The eye. Gene Ther. 13, 1191-1197.
-
(2006)
Gene Ther.
, vol.13
, pp. 1191-1197
-
-
Bainbridge, J.W.1
Tan, M.H.2
Ali, R.R.3
-
4
-
-
44249120315
-
Effect of gene therapy on visual function in Le-ber's congenital amaurosis
-
Bainbridge, J.W., Smith, A.J., Barker, S.S., Robbie, S., Henderson, R., Balaggan, K., Viswanathan, A., Holder, G.E., Stockman, A., Tyler, N., Petersen-Jones, S., Bhattacharya, S.S., Thrasher, A.J., Fitzke, F.W., Carter, B.J., Rubin, G.S., Moore, A.T., and Ali, R.R. (2008). Effect of gene therapy on visual function in Le-ber's congenital amaurosis. N. Engl. J. Med. 358, 2231-2239.
-
(2008)
N. Engl. J. Med.
, vol.358
, pp. 2231-2239
-
-
Bainbridge, J.W.1
Smith, A.J.2
Barker, S.S.3
Robbie, S.4
Henderson, R.5
Balaggan, K.6
Viswanathan, A.7
Holder, G.E.8
Stockman, A.9
Tyler, N.10
Petersen-Jones, S.11
Bhattacharya, S.S.12
Thrasher, A.J.13
Fitzke, F.W.14
Carter, B.J.15
Rubin, G.S.16
Moore, A.T.17
Ali, R.R.18
-
5
-
-
0036323191
-
Gene therapy for glaucoma: Treating a multifaceted, chronic disease
-
Borrás, T., Brandt, C.R., Nickells, R., and Ritch, R. (2002). Gene therapy for glaucoma: Treating a multifaceted, chronic disease. Invest. Ophthalmol. Vis. Sci. 42, 2513-2518.
-
(2002)
Invest. Ophthalmol. Vis. Sci.
, vol.42
, pp. 2513-2518
-
-
Borrás, T.1
Brandt, C.R.2
Nickells, R.3
Ritch, R.4
-
6
-
-
63949087144
-
Improved retinal function in a mouse model of dominant retinitis pigmentosa following AAV-delivered gene therapy
-
Chadderton, N., Millington-Ward, S., Palfi, A., O'Reilly, M., Tuohy, G., Humphries, M.M., Li, T., Humphries, P., Kenna, P.F., and Farrar, G.J. (2009). Improved retinal function in a mouse model of dominant retinitis pigmentosa following AAV-delivered gene therapy. Mol. Ther. 17, 593-599.
-
(2009)
Mol. Ther.
, vol.17
, pp. 593-599
-
-
Chadderton, N.1
Millington-Ward, S.2
Palfi, A.3
O'Reilly, M.4
Tuohy, G.5
Humphries, M.M.6
Li, T.7
Humphries, P.8
Kenna, P.F.9
Farrar, G.J.10
-
7
-
-
33845953595
-
Association of complement factor H polymorphisms with exudative age-related macular degeneration
-
Chen, L.J., Liu, D.T., Tam, P.O., Chan, W.M., Liu, K., Chong, K.K., Lam, D.S., and Pang, C.P. (2006). Association of complement factor H polymorphisms with exudative age-related macular degeneration. Mol. Vis. 12, 1536-1542.
-
(2006)
Mol. Vis.
, vol.12
, pp. 1536-1542
-
-
Chen, L.J.1
Liu, D.T.2
Tam, P.O.3
Chan, W.M.4
Liu, K.5
Chong, K.K.6
Lam, D.S.7
Pang, C.P.8
-
8
-
-
37849022204
-
Sub-conjunctival injection of recombinant AAV-angiostatin ameliorates alkali burn induced corneal angiogenesis
-
Cheng, H.C., Yeh, S.I., Tsao, Y.P., and Kuo, P.C. (2007). Sub-conjunctival injection of recombinant AAV-angiostatin ameliorates alkali burn induced corneal angiogenesis. Mol. Vis. 13, 2344-2352.
-
(2007)
Mol. Vis.
, vol.13
, pp. 2344-2352
-
-
Cheng, H.C.1
Yeh, S.I.2
Tsao, Y.P.3
Kuo, P.C.4
-
9
-
-
0037095710
-
TrkB gene transfer protects retinal ganglion cells from axotomy-induced death in vivo
-
Cheng, L., Sapieha, P., Kittlerová, P., Hauswirth, W.W., and Di Polo, A. (2002). TrkB gene transfer protects retinal ganglion cells from axotomy-induced death in vivo. J. Neurosci. 22, 3977-3986.
-
(2002)
J. Neurosci.
, vol.22
, pp. 3977-3986
-
-
Cheng, L.1
Sapieha, P.2
Kittlerová, P.3
Hauswirth, W.W.4
Di Polo, A.5
-
10
-
-
0037262106
-
Tetracyclin-inducible transgene expression mediated by a single AAV vector
-
Chtarto, A., Bender, H.U., Hanemann, C.O., Kemp, T., Lehtonen, E., Leviver, M., Brotchi, J., Velu, T., and Tenenbaum, L. (2003). Tetracyclin-inducible transgene expression mediated by a single AAV vector. Gene Ther. 10, 84-94.
-
(2003)
Gene Ther.
, vol.10
, pp. 84-94
-
-
Chtarto, A.1
Bender, H.U.2
Hanemann, C.O.3
Kemp, T.4
Lehtonen, E.5
Leviver, M.6
Brotchi, J.7
Velu, T.8
Tenenbaum, L.9
-
11
-
-
68849088569
-
Vision 1 year after gene therapy for Leber's congenital amaurosis
-
[correspondence]
-
Cideciyan, A.V., Hauswirth, W.W., Aleman, T.S., Kaushal, S., Schwartz, S.B., Boye, S.L., Windsor, E.A.M., Conlon, T.J., Sumaroka, A., Roman, A.J., Byrne, B.J., and Jacobson, S.G. (2009). Vision 1 year after gene therapy for Leber's congenital amaurosis [correspondence]. N. Engl. J. Med. 361, 725-727.
-
(2009)
N. Engl. J. Med.
, vol.361
, pp. 725-727
-
-
Cideciyan, A.V.1
Hauswirth, W.W.2
Aleman, T.S.3
Kaushal, S.4
Schwartz, S.B.5
Boye, S.L.6
Windsor, E.A.M.7
Conlon, T.J.8
Sumaroka, A.9
Roman, A.J.10
Byrne, B.J.11
Jacobson, S.G.12
-
12
-
-
58149484922
-
Ocular gene therapy: Current progress and future prospects
-
Colella, P., Cotugno, G., and Auricchio, A. (2008). Ocular gene therapy: Current progress and future prospects. J. Mol. Med. 15, 23-31.
-
(2008)
J. Mol. Med.
, vol.15
, pp. 23-31
-
-
Colella, P.1
Cotugno, G.2
Auricchio, A.3
-
13
-
-
27744567638
-
Adeno-associated virus-mediated expression of vascular endothelial growth factor peptides inhibits retinal neovascularization in a mouse model of oxygen-induced retinopathy
-
Deng, W.T., Yan, Z., Dinculescu, A., Pang, J., Teusner, J.T., Cortez, N.G., Berns, K.I., and Hauswirth, W.W. (2005). Adeno-associated virus-mediated expression of vascular endothelial growth factor peptides inhibits retinal neovascularization in a mouse model of oxygen-induced retinopathy. Hum. Gene Ther. 16, 1247-1254.
-
(2005)
Hum. Gene Ther.
, vol.16
, pp. 1247-1254
-
-
Deng, W.T.1
Yan, Z.2
Dinculescu, A.3
Pang, J.4
Teusner, J.T.5
Cortez, N.G.6
Berns, K.I.7
Hauswirth, W.W.8
-
14
-
-
20844442295
-
Adeno-associated virus-vectored gene therapy for retinal disease
-
DOI 10.1089/hum.2005.16.649
-
Dinculescu, A., Glushakova, L., Min, S.H., and Hauswirth, W.W. (2005). Adeno-associated virus-vectored gene therapy for retinal disease. Hum. Gene Ther. 16, 649-663. (Pubitemid 40864266)
-
(2005)
Human Gene Therapy
, vol.16
, Issue.6
, pp. 649-663
-
-
Dinculescu, A.1
Glushakova, L.2
Min, S.-H.3
Hauswirth, W.W.4
-
15
-
-
0032506235
-
Adeno-associated viral-mediated catalase expression suppresses optic neuritis in experimental allergic encephalomyelitis
-
Guy, J., Qi, X., and Hauswirth, W.W. (1998). Adeno-associated viral-mediated catalase expression suppresses optic neuritis in experimental allergic encephalomyelitis. Proc. Natl. Acad. Sci. U.S.A. 95, 13847-13852.
-
(1998)
Proc. Natl. Acad. Sci. U.S.A.
, vol.95
, pp. 13847-13852
-
-
Guy, J.1
Qi, X.2
Hauswirth, W.W.3
-
16
-
-
0036830565
-
Rescue of a mitochondrial deficiency causing Leber hereditary optic neuropathy
-
Guy, J., Qi, X., Pallotti, F., Schon, E.A., Manfredi, G., Carelli, V., Martinuzzi, A., Hauswirth, W.W., and Lewin, A.S. (2002). Rescue of a mitochondrial deficiency causing Leber hereditary optic neuropathy. Ann. Neurol. 52, 534-542.
-
(2002)
Ann. Neurol.
, vol.52
, pp. 534-542
-
-
Guy, J.1
Qi, X.2
Pallotti, F.3
Schon, E.A.4
Manfredi, G.5
Carelli, V.6
Martinuzzi, A.7
Hauswirth, W.W.8
Lewin, A.S.9
-
17
-
-
0033827451
-
Ocular gene therapy: Quo vadis? Invest
-
Hauswirth, W.W., and Beaufrere, L. (2000). Ocular gene therapy: Quo vadis? Invest. Ophthalmol. Vis. Sci. 41, 2821-2826.
-
(2000)
Ophthalmol. Vis. Sci.
, vol.41
, pp. 2821-2826
-
-
Hauswirth, W.W.1
Beaufrere, L.2
-
18
-
-
54949104686
-
Treatment of Leber congenital amaurosis due to RPE65 mutations by ocular subretinal injection of adeno-associated virus gene vector: Short-term results of a phase i trial
-
Hauswirth, W.W., Aleman, T.S., Kaushal, S., Cideciyan, A.V., Schwartz, S.B., Wang, L., Conlon, T.J., Boye, S.L., Flotte, T.R., Byrne, B.J., and Jacobson, S.G. (2008). Treatment of Leber congenital amaurosis due to RPE65 mutations by ocular subretinal injection of adeno-associated virus gene vector: Short-term results of a phase I trial. Hum. Gene Ther. 19, 979-990.
-
(2008)
Hum. Gene Ther.
, vol.19
, pp. 979-990
-
-
Hauswirth, W.W.1
Aleman, T.S.2
Kaushal, S.3
Cideciyan, A.V.4
Schwartz, S.B.5
Wang, L.6
Conlon, T.J.7
Boye, S.L.8
Flotte, T.R.9
Byrne, B.J.10
Jacobson, S.G.11
-
19
-
-
0346957021
-
Prospects for gene therapy in corneal disease
-
Jun, A.S., and Larkin, D.F.P. (2003). Prospects for gene therapy in corneal disease. Eye 17, 906-911.
-
(2003)
Eye
, vol.17
, pp. 906-911
-
-
Jun, A.S.1
Larkin, D.F.P.2
-
20
-
-
35148850085
-
AAV-mediated expression targeting of rod and cone photoreceptors with a human rhodopsin kinase promoter
-
Khani, S.C., Pawlyk, B.S., Bulgakov, O.V., Kasperek, E., Young, J.E., Adamian, M., Sun, X., Smith, A.J., Ali, R.R., and Li, T. (2007). AAV-mediated expression targeting of rod and cone photoreceptors with a human rhodopsin kinase promoter. Invest. Ophthalmol. Vis. Sci. 48, 3954-3961.
-
(2007)
Invest. Ophthalmol. Vis. Sci.
, vol.48
, pp. 3954-3961
-
-
Khani, S.C.1
Pawlyk, B.S.2
Bulgakov, O.V.3
Kasperek, E.4
Young, J.E.5
Adamian, M.6
Sun, X.7
Smith, A.J.8
Ali, R.R.9
Li, T.10
-
21
-
-
36048975465
-
Corneal gene therapy
-
Klausner, E.A., Peer, D., Chapman, R.L., Multack, R.F., and Andurkar, S.V. (2007). Corneal gene therapy. J. Control. Release 124, 107-133.
-
(2007)
J. Control. Release
, vol.124
, pp. 107-133
-
-
Klausner, E.A.1
Peer, D.2
Chapman, R.L.3
Multack, R.F.4
Andurkar, S.V.5
-
22
-
-
0033823851
-
The combined effect of brain-derived neurotrophic factor and a free radical scavenger in experimental glaucoma
-
Ko, M.L., Hu, D.N., Ritch, R., and Sharma, S.C. (2000). The combined effect of brain-derived neurotrophic factor and a free radical scavenger in experimental glaucoma. Invest. Ophthalmol. Vis. Sci. 41, 2967-2971.
-
(2000)
Invest. Ophthalmol. Vis. Sci.
, vol.41
, pp. 2967-2971
-
-
Ko, M.L.1
Hu, D.N.2
Ritch, R.3
Sharma, S.C.4
-
23
-
-
0036083592
-
Potential long-term inhibition of ocular neovascularisation by recombinant adeno-associated virus-mediated secretion gene therapy
-
Lai, Y.K., Shen, W.Y., Brankov, M., Lai, C.M., Constable, I.J., and Rakoczy, P.E. (2002). Potential long-term inhibition of ocular neovascularisation by recombinant adeno-associated virus-mediated secretion gene therapy. Gene Ther. 9, 804-813.
-
(2002)
Gene Ther.
, vol.9
, pp. 804-813
-
-
Lai, Y.K.1
Shen, W.Y.2
Brankov, M.3
Lai, C.M.4
Constable, I.J.5
Rakoczy, P.E.6
-
24
-
-
25144485909
-
Long-term evaluation of AAV-mediated sFlt-1 gene therapy for ocular neovascularizationin mice and monkeys
-
Lai, C.M., Shen, W.Y., Brankov, M., Lai, Y.K.Y., Barnett, N.L., Lee, S.Y., Yeo, I.Y.S., Mathur, R., Ho, J.E.S., Pineda, P., Barathi, A., Ang, C.L., Constable, I.J., and Rakoczy, E. (2005). Long-term evaluation of AAV-mediated sFlt-1 gene therapy for ocular neovascularizationin mice and monkeys. Mol. Ther. 12, 659-668.
-
(2005)
Mol. Ther.
, vol.12
, pp. 659-668
-
-
Lai, C.M.1
Shen, W.Y.2
Brankov, M.3
Lai, Y.K.Y.4
Barnett, N.L.5
Lee, S.Y.6
Yeo, I.Y.S.7
Mathur, R.8
Ho, J.E.S.9
Pineda, P.10
Barathi, A.11
Ang, C.L.12
Constable, I.J.13
Rakoczy, E.14
-
25
-
-
34648820406
-
Inhibition of corneal neovascularization with endostatin delivered by adeno-asso-ciated viral (AAV) vector in a mouse corneal injury model
-
Lai, L.U., Xiao, X., and Wu, J.H. (2007). Inhibition of corneal neovascularization with endostatin delivered by adeno-asso-ciated viral (AAV) vector in a mouse corneal injury model. J. Biomed. Sci. 14, 313-322.
-
(2007)
J. Biomed. Sci.
, vol.14
, pp. 313-322
-
-
Lai, L.U.1
Xiao, X.2
Wu, J.H.3
-
26
-
-
56849102958
-
Different tropism of adenoviruses and adeno-associated viruses to corneal cells: Implications for corneal gene therapy
-
Liu, J., Saghizadeh, M., Tuli, S.S., Kramerov, A.A., Lewin, A.S., Bloom, D.C., Hauswirth, W.W., Castro, M.G., Schultz, G.S., and Ljubimov, A.V. (2008). Different tropism of adenoviruses and adeno-associated viruses to corneal cells: Implications for corneal gene therapy. Mol. Vis. 14, 2087-2096.
-
(2008)
Mol. Vis.
, vol.14
, pp. 2087-2096
-
-
Liu, J.1
Saghizadeh, M.2
Tuli, S.S.3
Kramerov, A.A.4
Lewin, A.S.5
Bloom, D.C.6
Hauswirth, W.W.7
Castro, M.G.8
Schultz, G.S.9
Ljubimov, A.V.10
-
27
-
-
44249085878
-
Safety and efficacy of gene transfer for Leber's congenital amaurosis
-
Maguire, A.M., Simonelli, F., Pierce, E.A., Pugh, E.N., Jr., Min-gozzi, F., Bennicelli, J., Banfi, S., Marshall, K.A., Testa, F., Surace, E.M., Rossi, S., Lyubarsky, A., Arruda, V.R., Konkle, B., Stone, E., Sun, J., Jacobs, J., Dell'Osso, L., Hertle, R., Ma, J.X., Redmond, T.M., Zhu, X., Hauck, B., Zelenaia, O., Shindler, K.S., Maguire, M.G., Wright, J.F., Volpe, N.J., McDonnell, J.W., Auricchio, A., High, K.A., and Bennett, J. (2008). Safety and efficacy of gene transfer for Leber's congenital amaurosis. N. Engl. J. Med. 358, 2240-2248.
-
(2008)
N. Engl. J. Med.
, vol.358
, pp. 2240-2248
-
-
Maguire, A.M.1
Simonelli, F.2
Pierce, E.A.3
Pugh Jr., E.N.4
Min-Gozzi, F.5
Bennicelli, J.6
Banfi, S.7
Marshall, K.A.8
Testa, F.9
Surace, E.M.10
Rossi, S.11
Lyubarsky, A.12
Arruda, V.R.13
Konkle, B.14
Stone, E.15
Sun, J.16
Jacobs, J.17
Dell'Osso, L.18
Hertle, R.19
Ma, J.X.20
Redmond, T.M.21
Zhu, X.22
Hauck, B.23
Zelenaia, O.24
Shindler, K.S.25
Maguire, M.G.26
Wright, J.F.27
Volpe, N.J.28
McDonnell, J.W.29
Auricchio, A.30
High, K.A.31
Bennett, J.32
more..
-
28
-
-
70349971731
-
Gene therapy for red-green colour-blindness in adult primates
-
Mancuso, K., Hauswirth, W.W., Li, Q., Connor, T.B., Kuchen-becker, J.A., Mauck, M.C., Neitz, J., and Neitz, M. (2009). Gene therapy for red-green colour-blindness in adult primates. Nature 461, 784-787.
-
(2009)
Nature
, vol.461
, pp. 784-787
-
-
Mancuso, K.1
Hauswirth, W.W.2
Li, Q.3
Connor, T.B.4
Kuchen-Becker, J.A.5
Mauck, M.C.6
Neitz, J.7
Neitz, M.8
-
29
-
-
9944226710
-
Gene therapy for optic nerve disease
-
Martin, K.R.G., and Quigley, H.A. (2004). Gene therapy for optic nerve disease. Eye 18, 1049-1055.
-
(2004)
Eye
, vol.18
, pp. 1049-1055
-
-
Martin, K.R.G.1
Quigley, H.A.2
-
30
-
-
0035989022
-
Baculoviral IAP repeat-containing-4 protects optic nerve axons in a rat glaucoma model
-
McKinnon, S.J., Lehman, D.M., Tahzib, N.G., Ransom, N.L., Reitsamer, H.A., Liston, P., LaCasse, E., Li, Q., Korneluk, R.G., and Hauswirth, W.W. (2002). Baculoviral IAP repeat-containing-4 protects optic nerve axons in a rat glaucoma model. Mol. Ther. 5, 780-787.
-
(2002)
Mol. Ther.
, vol.5
, pp. 780-787
-
-
McKinnon, S.J.1
Lehman, D.M.2
Tahzib, N.G.3
Ransom, N.L.4
Reitsamer, H.A.5
Liston, P.6
Lacasse, E.7
Li, Q.8
Korneluk, R.G.9
Hauswirth, W.W.10
-
31
-
-
25144501446
-
Prolonged recovery of retinal structure and function after gene therapy in a Rs1h-deficient mouse model of human X-linked juvenile retinoschisis
-
Min, S.H., Molday, L.L., Seeliger, M.W., Dinculescu, A., Tim-mers, A.M., Janssen, A., Tonagel, F., Tanimoto, N., Weber, B.H.F., Molday, R.S., and Hauswirth, W.W. (2005). Prolonged recovery of retinal structure and function after gene therapy in a Rs1h-deficient mouse model of human X-linked juvenile retinoschisis. Mol. Ther. 12, 644-651.
-
(2005)
Mol. Ther.
, vol.12
, pp. 644-651
-
-
Min, S.H.1
Molday, L.L.2
Seeliger, M.W.3
Dinculescu, A.4
Tim-Mers, A.M.5
Janssen, A.6
Tonagel, F.7
Tanimoto, N.8
Weber, B.H.F.9
Molday, R.S.10
Hauswirth, W.W.11
-
32
-
-
0036271989
-
AAV-mediated gene transfer of pigment epithelium-derived factor inhibits choroidal neovascularization
-
Mori, K., Gehlbach, P., Yamamoto, S., Duh, E., Zack, D.J., Li, Q., Berns, K.I., Raisler, B.J., Hauswirth, W.W., and Campochiaro, P.A. (2002). AAV-mediated gene transfer of pigment epithelium-derived factor inhibits choroidal neovascularization. Invest. Ophthalmol. Vis. Sci. 43, 1994-2000.
-
(2002)
Invest. Ophthalmol. Vis. Sci.
, vol.43
, pp. 1994-2000
-
-
Mori, K.1
Gehlbach, P.2
Yamamoto, S.3
Duh, E.4
Zack, D.J.5
Li, Q.6
Berns, K.I.7
Raisler, B.J.8
Hauswirth, W.W.9
Campochiaro, P.A.10
-
33
-
-
58149141478
-
Stimulation of the insulin/mTOR pathway delays cone death in a mouse model of retinitis pigmentosa
-
Punzo, C., Kornacker, K., and Cepko, C.L. (2009). Stimulation of the insulin/mTOR pathway delays cone death in a mouse model of retinitis pigmentosa. Nat. Neurosci. 12, 44-52.
-
(2009)
Nat. Neurosci.
, vol.12
, pp. 44-52
-
-
Punzo, C.1
Kornacker, K.2
Cepko, C.L.3
-
34
-
-
38549125007
-
Long-term suppression of neurodegeneration in chronic experimental optic neuritis: Antioxidant gene therapy
-
Qi, X., Sun, L., Lewin, A.S., Hauswirth, W.W., and Guy, J. (2007a). Long-term suppression of neurodegeneration in chronic experimental optic neuritis: Antioxidant gene therapy. Invest. Ophthalmol. Vis. Sci. 48, 5360-5370.
-
(2007)
Invest. Ophthalmol. Vis. Sci.
, vol.48
, pp. 5360-5370
-
-
Qi, X.1
Sun, L.2
Lewin, A.S.3
Hauswirth, W.W.4
Guy, J.5
-
35
-
-
33846198704
-
Dual gene therapy with extracellular superoxide dismutase and catalase attenuates experimental optic neuritis
-
Qi, X., Hauswirth, W.W., and Guy, J. (2007b). Dual gene therapy with extracellular superoxide dismutase and catalase attenuates experimental optic neuritis. Mol. Vis. 13, 1-11.
-
(2007)
Mol. Vis.
, vol.13
, pp. 1-11
-
-
Qi, X.1
Hauswirth, W.W.2
Guy, J.3
-
36
-
-
31644446394
-
Mouse models of age-related mac-ular degeneration
-
Rakoczy, P.E., Yu, M.J.T., Nusinowitz, S., Chang, B., and Heckenlively, J.R. (2006). Mouse models of age-related mac-ular degeneration. Exp. Eye Res. 82, 741-752.
-
(2006)
Exp. Eye Res.
, vol.82
, pp. 741-752
-
-
Rakoczy, P.E.1
Yu, M.J.T.2
Nusinowitz, S.3
Chang, B.4
Heckenlively, J.R.5
-
37
-
-
0038392951
-
Gene therapy for ocular neo-vascularization
-
Reich, S.J., and Bennett, J. (2003). Gene therapy for ocular neo-vascularization. Curr. Opin. Genet. Dev. 13, 317-322.
-
(2003)
Curr. Opin. Genet. Dev.
, vol.13
, pp. 317-322
-
-
Reich, S.J.1
Bennett, J.2
-
38
-
-
77955499381
-
The state of gene therapy with viral vectors for AMD
-
article 102294 (accessed June 2010)
-
Salehi-Had, H., and Miller, J.W. (2008). The state of gene therapy with viral vectors for AMD. Retinal Physician November. Available at http://www.retinalphysician.com/article.aspx? article102294 (accessed June 2010
-
(2008)
Retinal Physician November
-
-
Salehi-Had, H.1
Miller, J.W.2
-
39
-
-
63449125884
-
Prospects for retinal gene replacement therapy
-
Smith, A.J., Bainbridge, J.W., and Ali, R.R. (2009). Prospects for retinal gene replacement therapy. Trends Genet. 25, 156-165.
-
(2009)
Trends Genet.
, vol.25
, pp. 156-165
-
-
Smith, A.J.1
Bainbridge, J.W.2
Ali, R.R.3
-
40
-
-
41449092949
-
Genetic models of retinal degeneration and targets for gene therapy
-
Song, B.J., Tsang, S.H., and Lin, C.S. (2007). Genetic models of retinal degeneration and targets for gene therapy. Gene Ther. Mol. Biol. 11, 229-262.
-
(2007)
Gene Ther. Mol. Biol.
, vol.11
, pp. 229-262
-
-
Song, B.J.1
Tsang, S.H.2
Lin, C.S.3
-
41
-
-
74349104948
-
Gene therapy with a promoter targeting both rods and cones rescues retinal degeneration caused by AIPL1 mutations
-
Sun, X., Pawlyk, B., Xu, X., Liu, X., Bulgakov, O.V., Adamian, M., Sandberg, M.A., Khani, S.C., Tan, M.H., Smith, A.J., Ali, R.R., and Li, T. (2009). Gene therapy with a promoter targeting both rods and cones rescues retinal degeneration caused by AIPL1 mutations. Gene Ther. 17, 117-131.
-
(2009)
Gene Ther.
, vol.17
, pp. 117-131
-
-
Sun, X.1
Pawlyk, B.2
Xu, X.3
Liu, X.4
Bulgakov, O.V.5
Adamian, M.6
Sandberg, M.A.7
Khani, S.C.8
Tan, M.H.9
Smith, A.J.10
Ali, R.R.11
Li, T.12
-
42
-
-
38749087929
-
Versatility of AAV vectors for retinal gene transfer
-
Surace, E.M., and Auricchio, A. (2008). Versatility of AAV vectors for retinal gene transfer. Vision Res. 48, 353-359.
-
(2008)
Vision Res.
, vol.48
, pp. 353-359
-
-
Surace, E.M.1
Auricchio, A.2
-
43
-
-
0036187464
-
Inducible adeno-associated virus vector-delivered transgene expression in corneal endothelium
-
Tsai, M.L., Chen, S.L., Chou, P.I., Wen, L.Y., Tsai, R.J.F., and Tsao, Y.P. (2002). Inducible adeno-associated virus vector-delivered transgene expression in corneal endothelium. Invest. Ophthalmol. Vis. Sci. 43, 751-757.
-
(2002)
Invest. Ophthalmol. Vis. Sci.
, vol.43
, pp. 751-757
-
-
Tsai, M.L.1
Chen, S.L.2
Chou, P.I.3
Wen, L.Y.4
Tsai, R.J.F.5
Tsao, Y.P.6
-
44
-
-
68749105905
-
Suppression of experimental uveitis by a recombinant adeno-associated virus vector encoding inter-leukin-1 receptor antagonist
-
Tsai, M.L., Horng, C.T., Chen. S.L., Xiao, X., Wang, C.H., and Tsao, Y.P. (2009). Suppression of experimental uveitis by a recombinant adeno-associated virus vector encoding inter-leukin-1 receptor antagonist. Mol. Vis. 15, 1542-1552.
-
(2009)
Mol. Vis.
, vol.15
, pp. 1542-1552
-
-
Tsai, M.L.1
Horng, C.T.2
Chen., S.L.3
Xiao, X.4
Wang, C.H.5
Tsao, Y.P.6
-
45
-
-
0037310001
-
AAV-mediated expression of vascular endothelial growth factor induces choroidal neovasculariza-tion in rat
-
Wang, F., Rendahl, K.G., Manning, W.C., Quiroz, D., Coyne, M., and Miller, S.S. (2003). AAV-mediated expression of vascular endothelial growth factor induces choroidal neovasculariza-tion in rat. Invest. Ophthalmol. Vis. Sci. 44, 781-790.
-
(2003)
Invest. Ophthalmol. Vis. Sci.
, vol.44
, pp. 781-790
-
-
Wang, F.1
Rendahl, K.G.2
Manning, W.C.3
Quiroz, D.4
Coyne, M.5
Miller, S.S.6
-
46
-
-
54849148000
-
Toll-like receptor 3 and geographic atrophy in age-related macular degeneration
-
Yang, Z., Stratton, C., Francis, P.J., Kleinman, M.E., Tan, P.L., Gibbs, D., Tong, Z., Chen, H., Constantine, R., Yang, X., Chen, Y., Zeng, J., Davey, L., Ma, X., Hau, V.S., Wang, C., Harmon, J., Buehler, J., Pearson, E., Patel, S., Kaminoh, Y., Watkins, S., Luo, L., Zabriskie, N.A., Bernstein, P.S., Cho, W., Schwager, A., Hinton, D.R., Klein, M.L., Hamon, S.C., Simmons, E., Yu, B., Campochiaro, B., Sunness, J.S., Campochiaro, P., Jorde, L., Par-migiani, G., Zack, D.J., Katsanis, N., Ambati, J., and Zhang, K. (2008). Toll-like receptor 3 and geographic atrophy in age-related macular degeneration. N. Engl. J. Med. 359, 1456-1463.
-
(2008)
N. Engl. J. Med.
, vol.359
, pp. 1456-1463
-
-
Yang, Z.1
Stratton, C.2
Francis, P.J.3
Kleinman, M.E.4
Tan, P.L.5
Gibbs, D.6
Tong, Z.7
Chen, H.8
Constantine, R.9
Yang, X.10
Chen, Y.11
Zeng, J.12
Davey, L.13
Ma, X.14
Hau, V.S.15
Wang, C.16
Harmon, J.17
Buehler, J.18
Pearson, E.19
Patel, S.20
Kaminoh, Y.21
Watkins, S.22
Luo, L.23
Zabriskie, N.A.24
Bernstein, P.S.25
Cho, W.26
Schwager, A.27
Hinton, D.R.28
Klein, M.L.29
Hamon, S.C.30
Simmons, E.31
Yu, B.32
Campochiaro, B.33
Sunness, J.S.34
Campochiaro, P.35
Jorde, L.36
Par-Migiani, G.37
Zack, D.J.38
Katsanis, N.39
Ambati, J.40
Zhang, K.41
more..
-
47
-
-
45549090635
-
Next generation of adeno-associated virus 2 vectors: Point mutation in tyrosines lead to high-efficiency transduction at lower doses
-
Zhong, L., Baozheng, L., Mah, C.S., Govindasamy, L., Agbandje-McKenna, M., Cooper, M., Herzog, R.W., Zolotukhin, I., Warrington, K.H. Jr., Weigel-Van Aken, K., Hobbs, J.A., Zo-lotukhin, S., Muzyczka, N., and Srivastava, A. (2008). Next generation of adeno-associated virus 2 vectors: Point mutation in tyrosines lead to high-efficiency transduction at lower doses. Proc. Natl. Acad. Sci. 105, 7827-7832.
-
(2008)
Proc. Natl. Acad. Sci.
, vol.105
, pp. 7827-7832
-
-
Zhong, L.1
Baozheng, L.2
Mah, C.S.3
Govindasamy, L.4
Agbandje-Mckenna, M.5
Cooper, M.6
Herzog, R.W.7
Zolotukhin, I.8
Warrington Jr., K.H.9
Weigel-Van Aken, K.10
Hobbs, J.A.11
Zo-Lotukhin, S.12
Muzyczka, N.13
Srivastava, A.14
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