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Volumn 10, Issue 2, 2014, Pages

Mechanistically Distinct Mouse Models for CRX-Associated Retinopathy

Author keywords

[No Author keywords available]

Indexed keywords

CONE OPSIN; CONE ROD HOMEOBOX PROTEIN; DNA; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG; HOMEODOMAIN PROTEIN; TRANSACTIVATOR PROTEIN;

EID: 84901741997     PISSN: 15537390     EISSN: 15537404     Source Type: Journal    
DOI: 10.1371/journal.pgen.1004111     Document Type: Article
Times cited : (44)

References (68)
  • 1
    • 0030781996 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 7
    • 34848832380 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 32
    • 34548016106 scopus 로고    scopus 로고
    • 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
  • 35
    • 0036202254 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 40
    • 0030669568 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 47
    • 0037091102 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 53
    • 0030665993 scopus 로고    scopus 로고
    • 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
  • 56
    • 0033714873 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 61
    • 0023064044 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 67
    • 18644386771 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.