-
1
-
-
0035032662
-
Gene therapy restores vision in a canine model of childhood blindness
-
Acland GM, Aguirre GD, Ray J, Zhang Q, Aleman TS, Cideciyan AV, Pearce-Kelling SE, Anand V, Zeng Y, Maguire AM, Jacobson SG, Hauswirth WW, Bennett J. 2001. Gene therapy restores vision in a canine model of childhood blindness. Nat Genet 28:92-95.
-
(2001)
Nat Genet
, vol.28
, pp. 92-95
-
-
Acland, G.M.1
Aguirre, G.D.2
Ray, J.3
Zhang, Q.4
Aleman, T.S.5
Cideciyan, A.V.6
Pearce-Kelling, S.E.7
Anand, V.8
Zeng, Y.9
Maguire, A.M.10
Jacobson, S.G.11
Hauswirth, W.W.12
Bennett, J.13
-
2
-
-
0035977135
-
Comprehensive analysis of photoreceptor gene expression and the identification of candidate retinal disease genes
-
Blackshaw S, Fraioli RE, Furukawa T, Cepko CL. 2001. Comprehensive analysis of photoreceptor gene expression and the identification of candidate retinal disease genes. Cell 107:579-589.
-
(2001)
Cell
, vol.107
, pp. 579-589
-
-
Blackshaw, S.1
Fraioli, R.E.2
Furukawa, T.3
Cepko, C.L.4
-
3
-
-
0030781996
-
Crx, a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes
-
Chen S, Wang QL, Nie Z, Sun H, Lennon G, Copeland NG, Gilbert DJ, Jenkins NA, Zack DJ. 1997. Crx, a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes. Neuron 19:1017-1030.
-
(1997)
Neuron
, vol.19
, pp. 1017-1030
-
-
Chen, S.1
Wang, Q.L.2
Nie, Z.3
Sun, H.4
Lennon, G.5
Copeland, N.G.6
Gilbert, D.J.7
Jenkins, N.A.8
Zack, D.J.9
-
4
-
-
0035722135
-
Leber's congenital amaurosis with anterior keratoconus in Pakistani families is caused by the Trp278X mutation in the AIPL1 gene on 17p
-
Damji KF, Sohocki MM, Khan R, Gupta SK, Rahim M, Loyer M, Hussein N, Karim N, Ladak SS, Jamal A, Bulman D, Koenekoop RK. 2001. Leber's congenital amaurosis with anterior keratoconus in Pakistani families is caused by the Trp278X mutation in the AIPL1 gene on 17p. Can J Ophthalmol 36:252-259.
-
(2001)
Can J Ophthalmol
, vol.36
, pp. 252-259
-
-
Damji, K.F.1
Sohocki, M.M.2
Khan, R.3
Gupta, S.K.4
Rahim, M.5
Loyer, M.6
Hussein, N.7
Karim, N.8
Ladak, S.S.9
Jamal, A.10
Bulman, D.11
Koenekoop, R.K.12
-
6
-
-
0034717512
-
Shared and unique roles of CAP23 and GAP43 in actin regulation, neurite outgrowth, and anatomical plasticity
-
Frey D, Laux T, Xu L, Schneider C, Caroni P. 2000. Shared and unique roles of CAP23 and GAP43 in actin regulation, neurite outgrowth, and anatomical plasticity. J Cell Biol 149:1443-1454.
-
(2000)
J Cell Biol
, vol.149
, pp. 1443-1454
-
-
Frey, D.1
Laux, T.2
Xu, L.3
Schneider, C.4
Caroni, P.5
-
7
-
-
0030725687
-
Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation
-
Furukawa T, Morrow EM, Cepko CL. 1997. Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation. Cell 91:531-541.
-
(1997)
Cell
, vol.91
, pp. 531-541
-
-
Furukawa, T.1
Morrow, E.M.2
Cepko, C.L.3
-
8
-
-
0032749223
-
Retinopathy and attenuated circadian entrainment in Crx-deficient mice
-
Furukawa T, Morrow EM, Li T, Davis FC, Cepko CL. 1999. Retinopathy and attenuated circadian entrainment in Crx-deficient mice. Nat Genet 23:466-470.
-
(1999)
Nat Genet
, vol.23
, pp. 466-470
-
-
Furukawa, T.1
Morrow, E.M.2
Li, T.3
Davis, F.C.4
Cepko, C.L.5
-
9
-
-
0031255068
-
Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy
-
Gu SM, Thompson DA, Srikumari CR, Lorenz B, Finckh U, Nicoletti A, Murthy KR, Rathmann M, Kumaramanickavel G, Denton MJ, Gal A. 1997. Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy. Nat Genet 17:194-197.
-
(1997)
Nat Genet
, vol.17
, pp. 194-197
-
-
Gu, S.M.1
Thompson, D.A.2
Srikumari, C.R.3
Lorenz, B.4
Finckh, U.5
Nicoletti, A.6
Murthy, K.R.7
Rathmann, M.8
Kumaramanickavel, G.9
Denton, M.J.10
Gal, A.11
-
10
-
-
0030970420
-
Control of dopamine release in the retina: A transgenic approach to neural networks
-
Gustincich S, Feigenspan A, Wu DK, Koopman LJ, Raviola E. 1997. Control of dopamine release in the retina: a transgenic approach to neural networks. Neuron 18:723-736.
-
(1997)
Neuron
, vol.18
, pp. 723-736
-
-
Gustincich, S.1
Feigenspan, A.2
Wu, D.K.3
Koopman, L.J.4
Raviola, E.5
-
11
-
-
0031853033
-
Artificial vision
-
Humayun MS, de Juan E Jr. 1998. Artificial vision. Eye 12(Pt 3b):605-607.
-
(1998)
Eye
, vol.12
, Issue.PART 3B
, pp. 605-607
-
-
Humayun, M.S.1
De Juan Jr., E.2
-
12
-
-
0032212151
-
The major cell populations of the mouse retina
-
Jeon CJ, Strettoi E, Masland RH. 1998. The major cell populations of the mouse retina. J Neurosci 18:8936-8946.
-
(1998)
J Neurosci
, vol.18
, pp. 8936-8946
-
-
Jeon, C.J.1
Strettoi, E.2
Masland, R.H.3
-
13
-
-
0042867290
-
Retinal remodeling triggered by photoreceptor degenerations
-
Jones BW, Watt CB, Frederick JM, Baehr W, Chen CK, Levine EM, Milam AH, LaVail MM, Marc RE. 2003. Retinal remodeling triggered by photoreceptor degenerations. J Comp Neurol 464:1-16.
-
(2003)
J Comp Neurol
, vol.464
, pp. 1-16
-
-
Jones, B.W.1
Watt, C.B.2
Frederick, J.M.3
Baehr, W.4
Chen, C.K.5
Levine, E.M.6
Milam, A.H.7
LaVail, M.M.8
Marc, R.E.9
-
14
-
-
0034704768
-
Microarray analysis of the transcriptional network controlled by the photoreceptor homeobox gene Crx
-
Livesey FJ, Furukawa T, Steffen MA, Church GM, Cepko CL. 2000. Microarray analysis of the transcriptional network controlled by the photoreceptor homeobox gene Crx. Curr Biol 10:301-310.
-
(2000)
Curr Biol
, vol.10
, pp. 301-310
-
-
Livesey, F.J.1
Furukawa, T.2
Steffen, M.A.3
Church, G.M.4
Cepko, C.L.5
-
15
-
-
0035090259
-
Mutations in the CRB1 gene cause Leber congenital amaurosis
-
Lotery AJ, Jacobson SG, Fishman GA, Weleber RG, Fulton AB, Namperumalsamy P, Heon E, Levin AV, Grover S, Rosenow JR, Kopp KK, Sheffield VC, Stone EM. 2001. Mutations in the CRB1 gene cause Leber congenital amaurosis. Arch Ophthalmol 119:415-420.
-
(2001)
Arch Ophthalmol
, vol.119
, pp. 415-420
-
-
Lotery, A.J.1
Jacobson, S.G.2
Fishman, G.A.3
Weleber, R.G.4
Fulton, A.B.5
Namperumalsamy, P.6
Heon, E.7
Levin, A.V.8
Grover, S.9
Rosenow, J.R.10
Kopp, K.K.11
Sheffield, V.C.12
Stone, E.M.13
-
16
-
-
0034982881
-
Cell transplantation as a treatment for retinal disease
-
Lund RD, Kwan AS, Keegan DJ, Sauve Y, Coffey PJ, Lawrence JM. 2001. Cell transplantation as a treatment for retinal disease. Prog Retin Eye Res 20:415-449.
-
(2001)
Prog Retin Eye Res
, vol.20
, pp. 415-449
-
-
Lund, R.D.1
Kwan, A.S.2
Keegan, D.J.3
Sauve, Y.4
Coffey, P.J.5
Lawrence, J.M.6
-
17
-
-
0028218968
-
Developmentally regulated postsynaptic localization of a metabotropic glutamate receptor in rat rod bipolar cells
-
Nomura A, Shigemoto R, Nakamura Y, Okamoto N, Mizuno N, Nakanishi S. 1994. Developmentally regulated postsynaptic localization of a metabotropic glutamate receptor in rat rod bipolar cells. Cell 77:361-369.
-
(1994)
Cell
, vol.77
, pp. 361-369
-
-
Nomura, A.1
Shigemoto, R.2
Nakamura, Y.3
Okamoto, N.4
Mizuno, N.5
Nakanishi, S.6
-
18
-
-
0028425892
-
Morphological types of horizontal cell in rodent retinae: A comparison of rat, mouse, gerbil, and guinea pig
-
Peichl L, Gonzalez-Soriano J. 1994. Morphological types of horizontal cell in rodent retinae: a comparison of rat, mouse, gerbil, and guinea pig. Vis Neurosci 11:501-517.
-
(1994)
Vis Neurosci
, vol.11
, pp. 501-517
-
-
Peichl, L.1
Gonzalez-Soriano, J.2
-
19
-
-
16144363583
-
Retinal-specific guanylate cyclase gene mutations in Leber's congenital amaurosis
-
Perrault I, Rozet JM, Calvas P, Gerber S, Camuzat A, Dollfus H, Chatelin S, Souied E, Ghazi I, Leowski C, Bonnemaison M, Le Paslier D, Frezal J, Dufier JL, Pittler S, Munnich A, Kaplan J. 1996. Retinal-specific guanylate cyclase gene mutations in Leber's congenital amaurosis. Nat Genet 14:461-464.
-
(1996)
Nat Genet
, vol.14
, pp. 461-464
-
-
Perrault, I.1
Rozet, J.M.2
Calvas, P.3
Gerber, S.4
Camuzat, A.5
Dollfus, H.6
Chatelin, S.7
Souied, E.8
Ghazi, I.9
Leowski, C.10
Bonnemaison, M.11
Le Paslier, D.12
Frezal, J.13
Dufier, J.L.14
Pittler, S.15
Munnich, A.16
Kaplan, J.17
-
20
-
-
0035651286
-
Novel frameshift mutations in CRX associated with Leber congenital amaurosis
-
Rivolta C, Peck NE, Fulton AB, Fishman GA, Berson EL, Dryja TP. 2001. Novel frameshift mutations in CRX associated with Leber congenital amaurosis. Hum Mutat 18:550-551.
-
(2001)
Hum Mutat
, vol.18
, pp. 550-551
-
-
Rivolta, C.1
Peck, N.E.2
Fulton, A.B.3
Fishman, G.A.4
Berson, E.L.5
Dryja, T.P.6
-
23
-
-
0033985972
-
Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis
-
Sohocki MM, Bowne SJ, Sullivan LS, Blackshaw S, Cepko CL, Payne AM, Bhattacharya SS, Khaliq S, Qasim Mehdi S, Birch DG, Harrison WR, Elder FF, Heckenlively JR, Daiger SP. 2000. Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis. Nat Genet 24:79-83.
-
(2000)
Nat Genet
, vol.24
, pp. 79-83
-
-
Sohocki, M.M.1
Bowne, S.J.2
Sullivan, L.S.3
Blackshaw, S.4
Cepko, C.L.5
Payne, A.M.6
Bhattacharya, S.S.7
Khaliq, S.8
Qasim Mehdi, S.9
Birch, D.G.10
Harrison, W.R.11
Elder, F.F.12
Heckenlively, J.R.13
Daiger, S.P.14
-
24
-
-
0034718480
-
Modifications of retinal neurons in a mouse model of retinitis pigmentosa
-
Strettoi E, Pignatelli V. 2000. Modifications of retinal neurons in a mouse model of retinitis pigmentosa. Proc Natl Acad Sci U S A 97:11020-11025.
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 11020-11025
-
-
Strettoi, E.1
Pignatelli, V.2
-
25
-
-
0036662776
-
Morphological and functional abnormalities in the inner retina of the rd/rd mouse
-
Strettoi E, Porciatti V, Falsini B, Pignatelli V, Rossi C. 2002. Morphological and functional abnormalities in the inner retina of the rd/rd mouse. J Neurosci 22:5492-5504.
-
(2002)
J Neurosci
, vol.22
, pp. 5492-5504
-
-
Strettoi, E.1
Porciatti, V.2
Falsini, B.3
Pignatelli, V.4
Rossi, C.5
-
26
-
-
0032929074
-
Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: Direct evidence for the involvement of CRX in the development of photoreceptor function
-
Swaroop A, Wang QL, Wu W, Cook J, Coats C, Xu S, Chen S, Zack DJ, Sieving PA. 1999. Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function. Hum Mol Genet 8:299-305.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 299-305
-
-
Swaroop, A.1
Wang, Q.L.2
Wu, W.3
Cook, J.4
Coats, C.5
Xu, S.6
Chen, S.7
Zack, D.J.8
Sieving, P.A.9
-
27
-
-
0035037746
-
Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX gene
-
Tzekov RT, Liu Y, Sohocki MM, Zack DJ, Daiger SP, Heckenlively JR, Birch DG. 2001. Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX gene. Invest Ophthalmol Vis Sci 42:1319-1327.
-
(2001)
Invest Ophthalmol Vis Sci
, vol.42
, pp. 1319-1327
-
-
Tzekov, R.T.1
Liu, Y.2
Sohocki, M.M.3
Zack, D.J.4
Daiger, S.P.5
Heckenlively, J.R.6
Birch, D.G.7
-
28
-
-
0026026006
-
Differential localization of protein kinase C isozymes in retinal neurons
-
Usuda N, Kong Y, Hagiwara M, Uchida C, Terasawa M, Nagata T, Hidaka H. 1991. Differential localization of protein kinase C isozymes in retinal neurons. J Cell Biol 112:1241-1247.
-
(1991)
J Cell Biol
, vol.112
, pp. 1241-1247
-
-
Usuda, N.1
Kong, Y.2
Hagiwara, M.3
Uchida, C.4
Terasawa, M.5
Nagata, T.6
Hidaka, H.7
-
29
-
-
0032565442
-
Alpha subunit of Go localizes in the dendritic tips of ON bipolar cells
-
Vardi N. 1998. Alpha subunit of Go localizes in the dendritic tips of ON bipolar cells. J Comp Neurol 395:43-52.
-
(1998)
J Comp Neurol
, vol.395
, pp. 43-52
-
-
Vardi, N.1
-
30
-
-
0036680477
-
Meaningless minis? Mechanisms of neurotransmitter-receptor clustering
-
Verstreken P, Bellen HJ. 2002. Meaningless minis? Mechanisms of neurotransmitter-receptor clustering. Trends Neurosci 25:383-385.
-
(2002)
Trends Neurosci
, vol.25
, pp. 383-385
-
-
Verstreken, P.1
Bellen, H.J.2
-
31
-
-
0034834684
-
Screening for CRX gene mutations in Chinese patients with Leber congenital amaurosis and mutational phenotype. PG-89-96
-
Zhang Q, Li S, Guo X, Guo L, Xiao X, Jia X, Kuang Z. 2001. Screening for CRX gene mutations in Chinese patients with Leber congenital amaurosis and mutational phenotype. PG-89-96. Ophthalmic Genet 22:89-96.
-
(2001)
Ophthalmic Genet
, vol.22
, pp. 89-96
-
-
Zhang, Q.1
Li, S.2
Guo, X.3
Guo, L.4
Xiao, X.5
Jia, X.6
Kuang, Z.7
|