-
1
-
-
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, et al. (1997) Crx, a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes. Neuron 19(5): 1017-30.
-
(1997)
Neuron
, vol.19
, Issue.5
, pp. 1017-1030
-
-
Chen, S.1
Wang, Q.L.2
Nie, Z.3
Sun, H.4
Lennon, G.5
-
2
-
-
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
-
3
-
-
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 (4):: 466-470.
-
(1999)
Nat Genet
, vol.23
, Issue.4
, pp. 466-470
-
-
Furukawa, T.1
Morrow, E.M.2
Li, T.3
Davis, F.C.4
Cepko, C.L.5
-
4
-
-
0034711293
-
Functional domains of the cone-rod homeobox (CRX) transcription factor
-
Chau KY, Chen S, Zack DJ, Ono SJ, (2000) Functional domains of the cone-rod homeobox (CRX) transcription factor. The Journal of biological chemistry 275 (47):: 37264-70.
-
(2000)
The Journal of Biological Chemistry
, vol.275
, Issue.47
, pp. 37264-37270
-
-
Chau, K.Y.1
Chen, S.2
Zack, D.J.3
Ono, S.J.4
-
5
-
-
0033977329
-
Both PCE-1/RX and OTX/CRX Interactions Are Necessary for Photoreceptor-specific Gene Expression
-
Kimura A, Singh D, Wawrousek E, Kikuchi M, Nakamura M, et al. (2000) Both PCE-1/RX and OTX/CRX Interactions Are Necessary for Photoreceptor-specific Gene Expression. J Biol Chem 275: 1152-1160.
-
(2000)
J Biol Chem
, vol.275
, pp. 1152-1160
-
-
Kimura, A.1
Singh, D.2
Wawrousek, E.3
Kikuchi, M.4
Nakamura, M.5
-
6
-
-
56649114571
-
CRX controls retinal expression of the X-linked juvenile retinoschisis (RS1) gene
-
Langmann T, Lai CCL, Weigelt K, Tam BM, Warneke-Wittstock R, et al. (2008) CRX controls retinal expression of the X-linked juvenile retinoschisis (RS1) gene. Nucleic acids research 36 (20):: 6523-34.
-
(2008)
Nucleic Acids Research
, vol.36
, Issue.20
, pp. 6523-6534
-
-
Langmann, T.1
Lai, C.C.L.2
Weigelt, K.3
Tam, B.M.4
Warneke-Wittstock, R.5
-
7
-
-
34848832380
-
Crx activates opsin transcription by recruiting HAT-containing co-activators and promoting histone acetylation
-
Peng GH, Chen S, (2007) Crx activates opsin transcription by recruiting HAT-containing co-activators and promoting histone acetylation. Hum Mol Genet 16 (20):: 2433-2452.
-
(2007)
Hum Mol Genet
, vol.16
, Issue.20
, pp. 2433-2452
-
-
Peng, G.H.1
Chen, S.2
-
8
-
-
38849100921
-
Regulation of photoreceptor gene expression by Crx-associated transcription factor network
-
Hennig AK, Peng GH, Chen S, (2008) Regulation of photoreceptor gene expression by Crx-associated transcription factor network. Brain Res 1192: 114-133.
-
(2008)
Brain Res
, vol.1192
, pp. 114-133
-
-
Hennig, A.K.1
Peng, G.H.2
Chen, S.3
-
9
-
-
80055071058
-
Active opsin loci adopt intrachromosomal loops that depend on the photoreceptor transcription factor network
-
Peng GH, Chen S, (2011) Active opsin loci adopt intrachromosomal loops that depend on the photoreceptor transcription factor network. Proc Natl Acad Sci USA 108 (43):: 17821-6.
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, Issue.43
, pp. 17821-17826
-
-
Peng, G.H.1
Chen, S.2
-
10
-
-
0033831273
-
Nuclear trafficking of photoreceptor protein crx: the targeting sequence and pathologic implications
-
Fei Y, Hughes TE, (2000) Nuclear trafficking of photoreceptor protein crx: the targeting sequence and pathologic implications. Investigative ophthalmology & visual science 41 (10):: 2849-56.
-
(2000)
Investigative Ophthalmology & Visual Science
, vol.41
, Issue.10
, pp. 2849-2856
-
-
Fei, Y.1
Hughes, T.E.2
-
11
-
-
0034703019
-
The leucine zipper of NRL interacts with the CRX homeodomain. A possible mechanism of transcriptional synergy in rhodopsin regulation
-
Mitton KP, Swain PK, Chen S, Xu S, Zack DJ, et al. (2000) The leucine zipper of NRL interacts with the CRX homeodomain. A possible mechanism of transcriptional synergy in rhodopsin regulation. J Biol Chem 275 (38):: 29794-9.
-
(2000)
J Biol Chem
, vol.275
, Issue.38
, pp. 29794-29799
-
-
Mitton, K.P.1
Swain, P.K.2
Chen, S.3
Xu, S.4
Zack, D.J.5
-
12
-
-
77952688503
-
Two novel CRX mutant proteins causing autosomal dominant Leber congenital amaurosis interact differently with NRL
-
Nichols LL, Alur RP, Boobalan E, Sergeev YV, Caruso RC, et al. (2010) Two novel CRX mutant proteins causing autosomal dominant Leber congenital amaurosis interact differently with NRL. Human mutation 31 (6):: E1472-83.
-
(2010)
Human Mutation
, vol.31
, Issue.6
-
-
Nichols, L.L.1
Alur, R.P.2
Boobalan, E.3
Sergeev, Y.V.4
Caruso, R.C.5
-
13
-
-
15544371180
-
The photoreceptor-specific nuclear receptor Nr2e3 interacts with Crx and exerts opposing effects on the transcription of rod versus cone genes
-
Peng GH, Ahmad O, Ahmad F, Liu J, Chen S, (2005) The photoreceptor-specific nuclear receptor Nr2e3 interacts with Crx and exerts opposing effects on the transcription of rod versus cone genes. Hum Mol Genet 14: 747-764.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 747-764
-
-
Peng, G.H.1
Ahmad, O.2
Ahmad, F.3
Liu, J.4
Chen, S.5
-
14
-
-
70350716547
-
Mutations in the DNA-binding domain of NR2E3 affect in vivo dimerization and interaction with CRX
-
Roduit R, Escher P, Schorderet DF, (2009) Mutations in the DNA-binding domain of NR2E3 affect in vivo dimerization and interaction with CRX. PLoS ONE 4 (10):: e7379.
-
(2009)
PLoS ONE
, vol.4
, Issue.10
-
-
Roduit, R.1
Escher, P.2
Schorderet, D.F.3
-
15
-
-
0019364889
-
Absence of receptor outer segments in the retina of rds mutant mice
-
Sanyal S, Jansen HG, (1981) Absence of receptor outer segments in the retina of rds mutant mice. Neurosci Lett 21: 23-26.
-
(1981)
Neurosci Lett
, vol.21
, pp. 23-26
-
-
Sanyal, S.1
Jansen, H.G.2
-
16
-
-
0031045876
-
Retinopathy induced in mice by targeted disruption of the rhodopsin gene
-
Humphries MH, Rancourt D, Farrar GJ, Kenna P, Hazel M, et al. (1997) Retinopathy induced in mice by targeted disruption of the rhodopsin gene. Nature Genet 15: 216-219.
-
(1997)
Nature Genet
, vol.15
, pp. 216-219
-
-
Humphries, M.H.1
Rancourt, D.2
Farrar, G.J.3
Kenna, P.4
Hazel, M.5
-
17
-
-
26444469568
-
Synaptogenesis and outer segment formation are perturbed in the neural retina of Crx mutant mice
-
Morrow EM, Furukawa T, Raviola E, Cepko CL, (2005) Synaptogenesis and outer segment formation are perturbed in the neural retina of Crx mutant mice. BMC Neurosci 6: 5.
-
(2005)
BMC Neurosci
, vol.6
, pp. 5
-
-
Morrow, E.M.1
Furukawa, T.2
Raviola, E.3
Cepko, C.L.4
-
18
-
-
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 (6):: 301-310.
-
(2000)
Curr Biol
, vol.10
, Issue.6
, pp. 301-310
-
-
Livesey, F.J.1
Furukawa, T.2
Steffen, M.A.3
Church, G.M.4
Cepko, C.L.5
-
19
-
-
39449091111
-
The cis-regulatory logic of the mammalian photoreceptor transcriptional network
-
Hsiau TH, Diaconu C, Myers CA, Lee J, Cepko CL, et al. (2007) The cis-regulatory logic of the mammalian photoreceptor transcriptional network. PLoS ONE 2 (7):: 2e643.
-
(2007)
PLoS ONE
, vol.2
, Issue.7
-
-
Hsiau, T.H.1
Diaconu, C.2
Myers, C.A.3
Lee, J.4
Cepko, C.L.5
-
20
-
-
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 (5):: 579-589.
-
(2001)
Cell
, vol.107
, Issue.5
, pp. 579-589
-
-
Blackshaw, S.1
Fraioli, R.E.2
Furukawa, T.3
Cepko, C.L.4
-
21
-
-
77956394013
-
CRX ChIP-seq reveals the cis-regulatory architecture of mouse photoreceptors
-
Corbo JC, Lawrence KA, Karlstetter M, Myers CA, Abdelaziz M, et al. (2010) CRX ChIP-seq reveals the cis-regulatory architecture of mouse photoreceptors. Genome Research 20 (11):: 1512-1525.
-
(2010)
Genome Research
, vol.20
, Issue.11
, pp. 1512-1525
-
-
Corbo, J.C.1
Lawrence, K.A.2
Karlstetter, M.3
Myers, C.A.4
Abdelaziz, M.5
-
22
-
-
0035206015
-
Dominant Leber congenital amaurosis, cone-rod degeneration, and retinitis pigmentosa caused by mutant versions of the transcription factor CRX
-
Rivolta C, Berson EL, Dryja TP, (2001) Dominant Leber congenital amaurosis, cone-rod degeneration, and retinitis pigmentosa caused by mutant versions of the transcription factor CRX. Human mutation 18 (6):: 488-98.
-
(2001)
Human Mutation
, vol.18
, Issue.6
, pp. 488-498
-
-
Rivolta, C.1
Berson, E.L.2
Dryja, T.P.3
-
23
-
-
0032231603
-
A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene
-
Sohocki MM, Sullivan LS, Mintz-Hittner HA, Birch D, Heckenlively JR, et al. (1998) A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene. Am J Hum Genet 63 (5):: 1307-1315.
-
(1998)
Am J Hum Genet
, vol.63
, Issue.5
, pp. 1307-1315
-
-
Sohocki, M.M.1
Sullivan, L.S.2
Mintz-Hittner, H.A.3
Birch, D.4
Heckenlively, J.R.5
-
24
-
-
0031790083
-
Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) gene
-
Jacobson SG, Cideciyan AV, Huang Y, Hanna DB, Freund CL, et al. (1998) Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) gene. Invest Ophthalmol Vis Sci 39 (12):: 2417-2426.
-
(1998)
Invest Ophthalmol Vis Sci
, vol.39
, Issue.12
, pp. 2417-2426
-
-
Jacobson, S.G.1
Cideciyan, A.V.2
Huang, Y.3
Hanna, D.B.4
Freund, C.L.5
-
25
-
-
11144356431
-
Leber congenital amaurosis: comprehensive survey of the genetic heterogeneity, refinement of the clinical definition, and genotype-phenotype correlations as a strategy for molecular diagnosis
-
Hanein S, Perrault I, Gerber S, Tanguy G, Barbet F, et al. (2004) Leber congenital amaurosis: comprehensive survey of the genetic heterogeneity, refinement of the clinical definition, and genotype-phenotype correlations as a strategy for molecular diagnosis. Human mutation 23: 306-317.
-
(2004)
Human Mutation
, vol.23
, pp. 306-317
-
-
Hanein, S.1
Perrault, I.2
Gerber, S.3
Tanguy, G.4
Barbet, F.5
-
26
-
-
0033747042
-
Mutational analysis and clinical correlation in Leber congenital amaurosis
-
Dharmaraj SR, Silva ER, Pina a L, Li YY, Yang JM, et al. (2000) Mutational analysis and clinical correlation in Leber congenital amaurosis. Ophthalmic genetics 21: 135-150.
-
(2000)
Ophthalmic Genetics
, vol.21
, pp. 135-150
-
-
Dharmaraj, S.R.1
Silva, E.R.2
Pina, L.3
Li, Y.Y.4
Yang, J.M.5
-
27
-
-
26844436412
-
Evaluation of genotype-phenotype associations in Leber Congenital Amaurosis
-
Galvin JA, Fishman GA, Stone EM, Koenekoop RK, (2005) Evaluation of genotype-phenotype associations in Leber Congenital Amaurosis. Retina 25 (7):: 919-29.
-
(2005)
Retina
, vol.25
, Issue.7
, pp. 919-929
-
-
Galvin, J.A.1
Fishman, G.A.2
Stone, E.M.3
Koenekoop, R.K.4
-
28
-
-
0041706612
-
Evidence of autosomal dominant Leber congenital amaurosis (LCA) underlain by a CRX heterozygous null allele
-
Perrault I, Hanein S, Gerber S, Barbet F, Dufier JL, et al. (2003) Evidence of autosomal dominant Leber congenital amaurosis (LCA) underlain by a CRX heterozygous null allele. J Med Genet 40 (7):: e90.
-
(2003)
J Med Genet
, vol.40
, Issue.7
-
-
Perrault, I.1
Hanein, S.2
Gerber, S.3
Barbet, F.4
Dufier, J.L.5
-
29
-
-
0036741031
-
Novel De Novo Mutation in CRX Gene in a Japanese Patient with Leber Congenital Amaurosis
-
Nakamura M, Ito S, Miyake Y, (1998) Novel De Novo Mutation in CRX Gene in a Japanese Patient with Leber Congenital Amaurosis. American Journal of Ophthalmology 24: 465-467.
-
(1998)
American Journal of Ophthalmology
, vol.24
, pp. 465-467
-
-
Nakamura, M.1
Ito, S.2
Miyake, Y.3
-
30
-
-
0034834684
-
Screening for CRX gene mutations in Chinese patients with Leber congenital amaurosis and mutational phenotype
-
Zhang Q, Li S, Guo X, Guo L, Xiao X, et al. (2001) Screening for CRX gene mutations in Chinese patients with Leber congenital amaurosis and mutational phenotype. 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
-
31
-
-
0034127482
-
Mutation analysis of 3 genes in patients with Leber congenital amaurosis
-
Lotery AJ, Namperumalsamy P, Jacobson SG, Weleber RG, Fishman GA, et al. (2000) Mutation analysis of 3 genes in patients with Leber congenital amaurosis. Archives of ophthalmology 118 (4):: 538-43.
-
(2000)
Archives of Ophthalmology
, vol.118
, Issue.4
, pp. 538-543
-
-
Lotery, A.J.1
Namperumalsamy, P.2
Jacobson, S.G.3
Weleber, R.G.4
Fishman, G.A.5
-
32
-
-
34548016106
-
Further evidence of autosomal-dominant Leber congenital amaurosis caused by heterozygous CRX mutation
-
Wang P, Guo X, Zhang Q, (2007) Further evidence of autosomal-dominant Leber congenital amaurosis caused by heterozygous CRX mutation. Graefe's archive for clinical and experimental ophthalmology 245: 1401-1402.
-
(2007)
Graefe's Archive for Clinical and Experimental Ophthalmology
, vol.245
, pp. 1401-1402
-
-
Wang, P.1
Guo, X.2
Zhang, Q.3
-
33
-
-
84867225009
-
CRX variants in cone-rod dystrophy and mutation overview
-
Huang L, Xiao X, Li S, Jia X, Wang P, et al. (2012) CRX variants in cone-rod dystrophy and mutation overview. Biochemical and biophysical research communications 426 (4):: 498-503.
-
(2012)
Biochemical and Biophysical Research Communications
, vol.426
, Issue.4
, pp. 498-503
-
-
Huang, L.1
Xiao, X.2
Li, S.3
Jia, X.4
Wang, P.5
-
34
-
-
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, et al. (2001) Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX gene. Investigative ophthalmology & visual science 42: 1319-1327.
-
(2001)
Investigative Ophthalmology & Visual Science
, vol.42
, pp. 1319-1327
-
-
Tzekov, R.T.1
Liu, Y.2
Sohocki, M.M.3
Zack, D.J.4
Daiger, S.P.5
-
35
-
-
0036202254
-
Mutation report Visual improvement in Leber congenital amaurosis and the CRX genotype
-
Koenekoop RK, Loyer M, Dembinska O, Beneish R, (2002) Mutation report Visual improvement in Leber congenital amaurosis and the CRX genotype. Ophthalmic Genet 23: 49-60.
-
(2002)
Ophthalmic Genet
, vol.23
, pp. 49-60
-
-
Koenekoop, R.K.1
Loyer, M.2
Dembinska, O.3
Beneish, R.4
-
36
-
-
34347217878
-
Genotype-phenotype correlation in a German family with a novel complex CRX mutation extending the open reading frame
-
Paunescu K, Preising MN, Janke B, Wissinger B, Lorenz B, (2007) Genotype-phenotype correlation in a German family with a novel complex CRX mutation extending the open reading frame. Ophthalmology 114: 1348-1357.e1.
-
(2007)
Ophthalmology
, vol.114
, pp. 1348-1357
-
-
Paunescu, K.1
Preising, M.N.2
Janke, B.3
Wissinger, B.4
Lorenz, B.5
-
37
-
-
0033890760
-
Visual phenotype in patients with Arg41Gln and ala196+1 bp mutations in the CRX gene
-
Tzekov RT, Sohocki MM, Daiger SP, Birch DG, (2000) Visual phenotype in patients with Arg41Gln and ala196+1 bp mutations in the CRX gene. Ophthalmic genetics 21 (2):: 89-99.
-
(2000)
Ophthalmic Genetics
, vol.21
, Issue.2
, pp. 89-99
-
-
Tzekov, R.T.1
Sohocki, M.M.2
Daiger, S.P.3
Birch, D.G.4
-
38
-
-
77952889862
-
Visual acuity in patients with Leber's congenital amaurosis and early childhood-onset retinitis pigmentosa
-
Walia S, Fishman GA, Jacobson SG, Aleman TS, Koenekoop RK, et al. (2010) Visual acuity in patients with Leber's congenital amaurosis and early childhood-onset retinitis pigmentosa. Ophthalmology 117: 1190-1198.
-
(2010)
Ophthalmology
, vol.117
, pp. 1190-1198
-
-
Walia, S.1
Fishman, G.A.2
Jacobson, S.G.3
Aleman, T.S.4
Koenekoop, R.K.5
-
39
-
-
48449085738
-
Leber congenital amaurosis: genes, proteins and disease mechanisms
-
den Hollander AI, Roepman R, Koenekoop RK, Cremers FPM, (2008) Leber congenital amaurosis: genes, proteins and disease mechanisms. Progress in retinal and eye research 27: 391-419.
-
(2008)
Progress in Retinal and Eye Research
, vol.27
, pp. 391-419
-
-
den Hollander, A.I.1
Roepman, R.2
Koenekoop, R.K.3
Cremers, F.P.M.4
-
40
-
-
0030669568
-
Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor
-
Freund CL, Gregory-Evans CY, Furukawa T, Papaioannou M, Looser J, et al. (1997) Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor. Cell 91 (4):: 543-553.
-
(1997)
Cell
, vol.91
, Issue.4
, pp. 543-553
-
-
Freund, C.L.1
Gregory-Evans, C.Y.2
Furukawa, T.3
Papaioannou, M.4
Looser, J.5
-
41
-
-
0032037626
-
De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis
-
Freund C, Wang QL, Chen S, Muskat B, Wiles C, et al. (1998) De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis. Nature genetics 18 (4):: 311-312.
-
(1998)
Nature Genetics
, vol.18
, Issue.4
, pp. 311-312
-
-
Freund, C.1
Wang, Q.L.2
Chen, S.3
Muskat, B.4
Wiles, C.5
-
42
-
-
0031447030
-
Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration
-
Swain PK, Chen S, Wang QL, Affatigato LM, Coats CL, et al. (1997) Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration. Neuron 19 (6):: 1329-36.
-
(1997)
Neuron
, vol.19
, Issue.6
, pp. 1329-1336
-
-
Swain, P.K.1
Chen, S.2
Wang, Q.L.3
Affatigato, L.M.4
Coats, C.L.5
-
44
-
-
0033949797
-
A CRX null mutation is associated with both Leber congenital amaurosis and a normal ocular phenotype
-
Silva E, Yang JM, Li Y, Darmaraj S, Oh S, et al. (2000) A CRX null mutation is associated with both Leber congenital amaurosis and a normal ocular phenotype. Invest Ophthalmol Vis Sci 41: 2076-2079.
-
(2000)
Invest Ophthalmol Vis Sci
, vol.41
, pp. 2076-2079
-
-
Silva, E.1
Yang, J.M.2
Li, Y.3
Darmaraj, S.4
Oh, S.5
-
45
-
-
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, et al. (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 (2):: 299-305.
-
(1999)
Hum Mol Genet
, vol.8
, Issue.2
, pp. 299-305
-
-
Swaroop, A.1
Wang, Q.L.2
Wu, W.3
Cook, J.4
Coats, C.5
-
46
-
-
83655166997
-
OTX2 and CRX rescue overlapping and photoreceptor-specific functions in the Drosophila eye
-
Terrell D, Xie B, Workman M, Mahato S, Zelhof A, et al. (2012) OTX2 and CRX rescue overlapping and photoreceptor-specific functions in the Drosophila eye. Developmental dynamics: an official publication of the American Association of Anatomists 241: 215-228.
-
(2012)
Developmental Dynamics: An Official Publication of the American Association of Anatomists
, vol.241
, pp. 215-228
-
-
Terrell, D.1
Xie, B.2
Workman, M.3
Mahato, S.4
Zelhof, A.5
-
47
-
-
0037091102
-
Functional analysis of cone-rod homeobox (CRX) mutations associated with retinal dystrophy
-
Chen S, Wang QL, Xu S, Liu I, Li L, et al. (2002) Functional analysis of cone-rod homeobox (CRX) mutations associated with retinal dystrophy. Hum Mol Genet 11 (8):: 873-884.
-
(2002)
Hum Mol Genet
, vol.11
, Issue.8
, pp. 873-884
-
-
Chen, S.1
Wang, Q.L.2
Xu, S.3
Liu, I.4
Li, L.5
-
48
-
-
4043070783
-
Efficient gene modulation in mouse epiblast using a Sox2Cre transgenic mouse strain
-
Hayashi S, Lewis P, Pevny L, McMahon AP, (2002) Efficient gene modulation in mouse epiblast using a Sox2Cre transgenic mouse strain. Mech Dev (Suppl 1): pp. S97-S101.
-
(2002)
Mech Dev
, Issue.SUPPL. 1
-
-
Hayashi, S.1
Lewis, P.2
Pevny, L.3
McMahon, A.P.4
-
49
-
-
0344442834
-
Homeobox gene controls retinal photoreceptor cell fate and pineal gland development
-
Nishida A, Furukawa A, Koike C, Tano Y, Aizawa S, et al. (2003) Homeobox gene controls retinal photoreceptor cell fate and pineal gland development. Nature Neuroscience 6 (12):: 1255-1263.
-
(2003)
Nature Neuroscience
, vol.6
, Issue.12
, pp. 1255-1263
-
-
Nishida, A.1
Furukawa, A.2
Koike, C.3
Tano, Y.4
Aizawa, S.5
-
50
-
-
0038336001
-
Electrophysiological analysis of visual function in mutant mice. Documenta ophthalmologica
-
Peachey NS, Ball SL, (2003) Electrophysiological analysis of visual function in mutant mice. Documenta ophthalmologica. Advances in ophthalmology 107 (1):: 13-36.
-
(2003)
Advances in Ophthalmology
, vol.107
, Issue.1
, pp. 13-36
-
-
Peachey, N.S.1
Ball, S.L.2
-
52
-
-
0037121627
-
Characterization of calbindin-positive cones in primates
-
Chiquet C, Dkhissi-Benyahya O, Chounlamountri N, Szel A, Degrip WJ, et al. (2002) Characterization of calbindin-positive cones in primates. Neuroscience 115 (4):: 1323-33.
-
(2002)
Neuroscience
, vol.115
, Issue.4
, pp. 1323-1333
-
-
Chiquet, C.1
Dkhissi-Benyahya, O.2
Chounlamountri, N.3
Szel, A.4
Degrip, W.J.5
-
53
-
-
0030665993
-
Migration and synaptogenesis of cone photoreceptors in the developing mouse retina
-
Rich KA, Zhan Y, Blanks JC, (1997) Migration and synaptogenesis of cone photoreceptors in the developing mouse retina. The Journal of comparative neurology 388 (1):: 47-63.
-
(1997)
The Journal of Comparative Neurology
, vol.388
, Issue.1
, pp. 47-63
-
-
Rich, K.A.1
Zhan, Y.2
Blanks, J.C.3
-
54
-
-
0025822614
-
Rod and cone specific domains in the interphotoreceptor matrix
-
Mieziewska KE, Van Veen T, Murray JM, Aguirre GD, (1991) Rod and cone specific domains in the interphotoreceptor matrix. The Journal of Comparative Neurology 308 (3):: 371-80.
-
(1991)
The Journal of Comparative Neurology
, vol.308
, Issue.3
, pp. 371-380
-
-
Mieziewska, K.E.1
Van Veen, T.2
Murray, J.M.3
Aguirre, G.D.4
-
55
-
-
0030471288
-
Distribution of cone photoreceptors in the mammalian retina
-
Szél A, Röhlich P, Caffé AR, Van Veen T, (1996) Distribution of cone photoreceptors in the mammalian retina. Microscopy research and technique 35 (6):: 445-62.
-
(1996)
Microscopy Research and Technique
, vol.35
, Issue.6
, pp. 445-462
-
-
Szél, A.1
Röhlich, P.2
Caffé, A.R.3
Van Veen, T.4
-
56
-
-
0033714873
-
The murine cone photoreceptor: a single cone type expresses both S and M opsins with retinal spatial patterning
-
Applebury ML, Antoch MP, Baxter LC, Chun LL, Falk JD, et al. (2000) The murine cone photoreceptor: a single cone type expresses both S and M opsins with retinal spatial patterning. Neuron 27: 513-523.
-
(2000)
Neuron
, vol.27
, pp. 513-523
-
-
Applebury, M.L.1
Antoch, M.P.2
Baxter, L.C.3
Chun, L.L.4
Falk, J.D.5
-
57
-
-
0036522977
-
The mouse Crx 5′-upstream transgene sequence directs cell-specific and developmentally regulated expression in retinal photoreceptor cells
-
Furukawa A, Koike C, Lippincott P, Cepko CL, Furukawa T, (2002) The mouse Crx 5′-upstream transgene sequence directs cell-specific and developmentally regulated expression in retinal photoreceptor cells. The Journal of Neuroscience 22 (5):: 1640-7.
-
(2002)
The Journal of Neuroscience
, vol.22
, Issue.5
, pp. 1640-1647
-
-
Furukawa, A.1
Koike, C.2
Lippincott, P.3
Cepko, C.L.4
Furukawa, T.5
-
58
-
-
24644470128
-
Retinoid X receptor (gamma) is necessary to establish the S-opsin gradient in cone photoreceptors of the developing mouse retina
-
Roberts MR, Hendrickson A, McGuire CR, Reh TA, (2005) Retinoid X receptor (gamma) is necessary to establish the S-opsin gradient in cone photoreceptors of the developing mouse retina. Investigative ophthalmology & visual science 46 (8):: 2897-904.
-
(2005)
Investigative Ophthalmology & Visual Science
, vol.46
, Issue.8
, pp. 2897-2904
-
-
Roberts, M.R.1
Hendrickson, A.2
McGuire, C.R.3
Reh, T.A.4
-
59
-
-
33646583234
-
Making the gradient: thyroid hormone regulates cone opsin expression in the developing mouse retina
-
Roberts MR, Srinivas M, Forrest D, Morreale de Escobar G, Reh TA, (2006) Making the gradient: thyroid hormone regulates cone opsin expression in the developing mouse retina. Proc Natl Acad Sci USA 103 (16):: 6218-23.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, Issue.16
, pp. 6218-6223
-
-
Roberts, M.R.1
Srinivas, M.2
Forrest, D.3
Morreale de Escobar, G.4
Reh, T.A.5
-
60
-
-
77953267163
-
Mutation discovered in a feline model of human congenital retinal blinding disease
-
Menotti-Raymond M, Deckman KH, David VA, Myrkalo J, O'Brien SJ, et al. (2010) Mutation discovered in a feline model of human congenital retinal blinding disease. Invest Ophthalmol Vis Sci 51 (6):: 2852-9.
-
(2010)
Invest Ophthalmol Vis Sci
, vol.51
, Issue.6
, pp. 2852-2859
-
-
Menotti-Raymond, M.1
Deckman, K.H.2
David, V.A.3
Myrkalo, J.4
O'Brien, S.J.5
-
61
-
-
0023064044
-
An Early-Onset Retinal Dystrophy With Dominant Inheritance in the Abyssinian Cat
-
Curtis R, Barnett K, Leon A, (1987) An Early-Onset Retinal Dystrophy With Dominant Inheritance in the Abyssinian Cat. IOVS 28: 131-139.
-
(1987)
IOVS
, vol.28
, pp. 131-139
-
-
Curtis, R.1
Barnett, K.2
Leon, A.3
-
62
-
-
79955936417
-
Analysis of transcriptional regulatory pathways of photoreceptor genes by expression profiling of the Otx2-deficient retina
-
Omori Y, Katoh K, Sato S, Muranishi Y, Chaya T, et al. (2011) Analysis of transcriptional regulatory pathways of photoreceptor genes by expression profiling of the Otx2-deficient retina. PloS one 6 (5):: e19685.
-
(2011)
PloS One
, vol.6
, Issue.5
-
-
Omori, Y.1
Katoh, K.2
Sato, S.3
Muranishi, Y.4
Chaya, T.5
-
63
-
-
36849048682
-
Functional roles of Otx2 transcription factor in postnatal mouse retinal development
-
Koike C, Nishida A, Ueno S, Saito H, Sanuki R, et al. (2007) Functional roles of Otx2 transcription factor in postnatal mouse retinal development. Mol Cell Biol 27 (23):: 8318-8329.
-
(2007)
Mol Cell Biol
, vol.27
, Issue.23
, pp. 8318-8329
-
-
Koike, C.1
Nishida, A.2
Ueno, S.3
Saito, H.4
Sanuki, R.5
-
64
-
-
58049200677
-
Transplantation of human embryonic stem cell-derived photoreceptors restores some visual function in Crx-deficient mice
-
Lamba DA, Gust J, Reh TA, (2009) Transplantation of human embryonic stem cell-derived photoreceptors restores some visual function in Crx-deficient mice. Cell stem cell 4 (1):: 73-9.
-
(2009)
Cell Stem Cell
, vol.4
, Issue.1
, pp. 73-79
-
-
Lamba, D.A.1
Gust, J.2
Reh, T.A.3
-
65
-
-
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, et al. (2009) Improved retinal function in a mouse model of dominant retinitis pigmentosa following AAV-delivered gene therapy. Molecular therapy: the journal of the American Society of Gene Therapy 17 (4):: 593-9.
-
(2009)
Molecular Therapy: The Journal of the American Society of Gene Therapy
, vol.17
, Issue.4
, pp. 593-599
-
-
Chadderton, N.1
Millington-Ward, S.2
Palfi, A.3
O'Reilly, M.4
Tuohy, G.5
-
66
-
-
34347246364
-
RNA interference-mediated suppression and replacement of human rhodopsin in vivo
-
O'Reilly M, Palfi A, Chadderton N, Millington-Ward S, Ader M, et al. (2007) RNA interference-mediated suppression and replacement of human rhodopsin in vivo. American journal of human genetics 81 (1):: 127-35.
-
(2007)
American Journal of Human Genetics
, vol.81
, Issue.1
, pp. 127-135
-
-
O'Reilly, M.1
Palfi, A.2
Chadderton, N.3
Millington-Ward, S.4
Ader, M.5
-
67
-
-
18644386771
-
Barrier to autointegration factor interacts with the cone-rod homeobox and represses its transactivation function
-
Wang X, Xu S, Rivolta C, Li LY, Peng GH, et al. (2002) Barrier to autointegration factor interacts with the cone-rod homeobox and represses its transactivation function. The Journal of Biological Chemistry 277 (45):: 43288-300.
-
(2002)
The Journal of Biological Chemistry
, vol.277
, Issue.45
, pp. 43288-43300
-
-
Wang, X.1
Xu, S.2
Rivolta, C.3
Li, L.Y.4
Peng, G.H.5
-
68
-
-
0347287040
-
Interference of Crx-dependent transcription by ataxin-7 involves interaction between the glutamine regions and requires the ataxin-7 carboxy-terminal region for nuclear localization
-
Chen S, Peng GH, Wang X, Smith AC, Grote SK, et al. (2004) Interference of Crx-dependent transcription by ataxin-7 involves interaction between the glutamine regions and requires the ataxin-7 carboxy-terminal region for nuclear localization. Hum Molec Genet 13: 53-67.
-
(2004)
Hum Molec Genet
, vol.13
, pp. 53-67
-
-
Chen, S.1
Peng, G.H.2
Wang, X.3
Smith, A.C.4
Grote, S.K.5
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