-
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, Copeland NG, Gilbert DJ, Jenkins NA, Zack DJ. Crx, a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes. Neuron 1997; 19:1017-30.
-
(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
-
2
-
-
0030725687
-
Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation
-
Furukawa T, Morrow EM, Cepko CL. Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation. Cell 1997; 91:531-41.
-
(1997)
Cell
, vol.91
, pp. 531-541
-
-
Furukawa, T.1
Morrow, E.M.2
Cepko, C.L.3
-
3
-
-
0035878559
-
Temporal and spatial expression patterns of the CRX transcription factor and its downstream targets. Critical differences during human and mouse eye development
-
Bibb LC, Holt JK, Tarttelin EE, Hodges MD, Gregory-Evans K, Rutherford A, Lucas RJ, Sowden JC, Gregory-Evans CY. Temporal and spatial expression patterns of the CRX transcription factor and its downstream targets. Critical differences during human and mouse eye development. Hum Mol Genet 2001; 10:1571-9.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 1571-1579
-
-
Bibb, L.C.1
Holt, J.K.2
Tarttelin, E.E.3
Hodges, M.D.4
Gregory-Evans, K.5
Rutherford, A.6
Lucas, R.J.7
Sowden, J.C.8
Gregory-Evans, C.Y.9
-
4
-
-
0035140924
-
Isolation and characterization of a zebrafish homologue of the cone rod homeobox gene
-
Liu Y, Shen Y, Rest JS, Raymond PA, Zack DJ. Isolation and characterization of a zebrafish homologue of the cone rod homeobox gene. Invest Ophthalmol Vis Sci 2001; 42:481-7.
-
(2001)
Invest. Ophthalmol. Vis. Sci.
, vol.42
, pp. 481-487
-
-
Liu, Y.1
Shen, Y.2
Rest, J.S.3
Raymond, P.A.4
Zack, D.J.5
-
5
-
-
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, Brady KD, Fishman GA, Jacobson SG, Swaroop A, Stone E, Sieving PA, Zack DJ. Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration. Neuron 1997; 19:1329-36.
-
(1997)
Neuron
, vol.19
, pp. 1329-1336
-
-
Swain, P.K.1
Chen, S.2
Wang, Q.L.3
Affatigato, L.M.4
Coats, C.L.5
Brady, K.D.6
Fishman, G.A.7
Jacobson, S.G.8
Swaroop, A.9
Stone, E.10
Sieving, P.A.11
Zack, D.J.12
-
6
-
-
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, Ploder L, Bellingham J, Ng D, Herbrick JA, Duncan A, Scherer SW, Tsui LC, Loutradis-Anagnostou A, Jacobson SG, Cepko CL, Bhattacharya SS, McInnes RR. Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor. Cell 1997; 91:543-53.
-
(1997)
Cell
, vol.91
, pp. 543-553
-
-
Freund, C.L.1
Gregory-Evans, C.Y.2
Furukawa, T.3
Papaioannou, M.4
Looser, J.5
Ploder, L.6
Bellingham, J.7
Ng, D.8
Herbrick, J.A.9
Duncan, A.10
Scherer, S.W.11
Tsui, L.C.12
Loutradis-Anagnostou, A.13
Jacobson, S.G.14
Cepko, C.L.15
Bhattacharya, S.S.16
McInnes, R.R.17
-
7
-
-
0031790083
-
Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) gene
-
Jacobson SG, Cideciyan AV, Huang Y, Hanna DB, Freund CL, Affatigato LM, Carr RE, Zack DJ, Stone EM, McInnes RR. Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) gene. Invest Ophthalmol Vis Sci 1998; 39:2417-26.
-
(1998)
Invest. Ophthalmol. Vis. Sci.
, vol.39
, pp. 2417-2426
-
-
Jacobson, S.G.1
Cideciyan, A.V.2
Huang, Y.3
Hanna, D.B.4
Freund, C.L.5
Affatigato, L.M.6
Carr, R.E.7
Zack, D.J.8
Stone, E.M.9
McInnes, R.R.10
-
8
-
-
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, Freund CL, McInnes RR, Daiger SP. A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene. Am J Hum Genet 1998; 63:1307-15.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 1307-1315
-
-
Sohocki, M.M.1
Sullivan, L.S.2
Mintz-Hittner, H.A.3
Birch, D.4
Heckenlively, J.R.5
Freund, C.L.6
McInnes, R.R.7
Daiger, S.P.8
-
10
-
-
0032037626
-
De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis
-
Freund CL, Wang QL, Chen S, Muskat BL, Wiles CD, Sheffield VC, Jacobson SG, McInnes RR, Zack DJ, Stone EM. De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis. Nat Genet 1998; 18:311-2.
-
(1998)
Nat. Genet.
, vol.18
, pp. 311-312
-
-
Freund, C.L.1
Wang, Q.L.2
Chen, S.3
Muskat, B.L.4
Wiles, C.D.5
Sheffield, V.C.6
Jacobson, S.G.7
McInnes, R.R.8
Zack, D.J.9
Stone, E.M.10
-
11
-
-
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. 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 1999; 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
-
12
-
-
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. Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX gene. Invest Ophthalmol Vis Sci 2001; 42:1319-27.
-
(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
-
13
-
-
0032749223
-
Retinopathy and attenuated circadian entrainment in Crx-deficient mice
-
Furukawa T, Morrow EM, Li T, Davis FC, Cepko CL. Retinopathy and attenuated circadian entrainment in Crx-deficient mice. Nat Genet 1999; 23:466-70.
-
(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
-
14
-
-
0942298092
-
Inner retinal abnormalities in a mouse model of Leber's congenital amaurosis
-
Pignatelli V, Cepko CL, Strettoi E. Inner retinal abnormalities in a mouse model of Leber's congenital amaurosis. J Comp Neurol 2004; 469:351-9.
-
(2004)
J. Comp. Neurol.
, vol.469
, pp. 351-359
-
-
Pignatelli, V.1
Cepko, C.L.2
Strettoi, E.3
-
15
-
-
1842766142
-
Zebrafish cone-rod (crx) homeobox gene promotes retinogenesis
-
Shen YC, Raymond PA. Zebrafish cone-rod (crx) homeobox gene promotes retinogenesis. Dev Biol 2004; 269:237-51.
-
(2004)
Dev. Biol.
, vol.269
, pp. 237-251
-
-
Shen, Y.C.1
Raymond, P.A.2
-
17
-
-
0036177470
-
Forward and reverse genetic approaches to the analysis of eye development in zebrafish
-
Malicki JJ, Pujic Z, Thisse C, Thisse B, Wei X. Forward and reverse genetic approaches to the analysis of eye development in zebrafish. Vision Res 2002; 42:527-33.
-
(2002)
Vision Res.
, vol.42
, pp. 527-533
-
-
Malicki, J.J.1
Pujic, Z.2
Thisse, C.3
Thisse, B.4
Wei, X.5
-
18
-
-
0037004902
-
Analysis of gene function in the zebrafish retina
-
Malicki J, Jo H, Wei X, Hsiung M, Pujic Z. Analysis of gene function in the zebrafish retina. Methods 2002; 28:427-38.
-
(2002)
Methods
, vol.28
, pp. 427-438
-
-
Malicki, J.1
Jo, H.2
Wei, X.3
Hsiung, M.4
Pujic, Z.5
-
19
-
-
0037326951
-
The zebrafish as a tool for understanding the biology of visual disorders
-
Goldsmith P, Harris WA. The zebrafish as a tool for understanding the biology of visual disorders. Semin Cell Dev Biol 2003; 14:11-8.
-
(2003)
Semin. Cell Dev. Biol.
, vol.14
, pp. 11-18
-
-
Goldsmith, P.1
Harris, W.A.2
-
20
-
-
0028306801
-
Early eye morphogenesis in the zebrafish, Brachydanio rerio
-
Schmitt EA, Dowling JE. Early eye morphogenesis in the zebrafish, Brachydanio rerio. J Comp Neurol 1994; 344:532-42.
-
(1994)
J. Comp. Neurol.
, vol.344
, pp. 532-542
-
-
Schmitt, E.A.1
Dowling, J.E.2
-
21
-
-
0033559665
-
Retinal neurogenesis: The formation of the initial central patch of postmitotic cells
-
Hu M, Easter SS. Retinal neurogenesis: the formation of the initial central patch of postmitotic cells. Dev Biol 1999; 207:309-21.
-
(1999)
Dev. Biol.
, vol.207
, pp. 309-321
-
-
Hu, M.1
Easter, S.S.2
-
22
-
-
0031307279
-
The development of eye movements in the zebrafish (Danio rerio)
-
Easter SS Jr, Nicola GN. The development of eye movements in the zebrafish (Danio rerio). Dev Psychobiol 1997; 31:267-76.
-
(1997)
Dev. Psychobiol.
, vol.31
, pp. 267-276
-
-
Easter Jr., S.S.1
Nicola, G.N.2
-
23
-
-
12644295051
-
Mutations affecting development of the zebrafish retina
-
Malicki J, Neuhauss SC, Schier AF, Solnica-Krezel L, Stemple DL, Stainier DY, Abdelilah S, Zwartkruis F, Rangini Z, Driever W. Mutations affecting development of the zebrafish retina. Development 1996; 123:263-73.
-
(1996)
Development
, vol.123
, pp. 263-273
-
-
Malicki, J.1
Neuhauss, S.C.2
Schier, A.F.3
Solnica-Krezel, L.4
Stemple, D.L.5
Stainier, D.Y.6
Abdelilah, S.7
Zwartkruis, F.8
Rangini, Z.9
Driever, W.10
-
24
-
-
0035666825
-
Genetic analysis of photoreceptor cell development in the zebrafish retina
-
Doerre G, Malicki J. Genetic analysis of photoreceptor cell development in the zebrafish retina. Mech Dev 2002; 110:125-38.
-
(2002)
Mech. Dev.
, vol.110
, pp. 125-138
-
-
Doerre, G.1
Malicki, J.2
-
25
-
-
0035449746
-
A mutation of early photoreceptor development, mikre oko, reveals cell-cell interactions involved in the survival and differentiation of zebrafish photoreceptors
-
Doerre G, Malicki J. A mutation of early photoreceptor development, mikre oko, reveals cell-cell interactions involved in the survival and differentiation of zebrafish photoreceptors. J Neurosci 2001; 21:6745-57.
-
(2001)
J. Neurosci.
, vol.21
, pp. 6745-6757
-
-
Doerre, G.1
Malicki, J.2
-
28
-
-
0036431293
-
Characterization of the genomic and transcriptional structure of the CRX gene: Substantial differences between human and mouse
-
Hodges MD, Vieira H, Gregory-Evans K, Gregory-Evans CY. Characterization of the genomic and transcriptional structure of the CRX gene: substantial differences between human and mouse. Genomics 2002; 80:531-42.
-
(2002)
Genomics
, vol.80
, pp. 531-542
-
-
Hodges, M.D.1
Vieira, H.2
Gregory-Evans, K.3
Gregory-Evans, C.Y.4
-
29
-
-
0347928918
-
Cloning and characterization of the canine photoreceptor specific cone-rod homeobox (CRX) gene and evaluation as a candidate for early onset photoreceptor diseases in the dog
-
Akhmedov NB, Baldwin VJ, Zangerl B, Kijas JW, Hunter L, Minoofar KD, Mellersh C, Ostrander EA, Acland GM, Farber DB, Aguirre GD. Cloning and characterization of the canine photoreceptor specific cone-rod homeobox (CRX) gene and evaluation as a candidate for early onset photoreceptor diseases in the dog. Mol Vis 2002; 8:79-84.
-
(2002)
Mol. Vis.
, vol.8
, pp. 79-84
-
-
Akhmedov, N.B.1
Baldwin, V.J.2
Zangerl, B.3
Kijas, J.W.4
Hunter, L.5
Minoofar, K.D.6
Mellersh, C.7
Ostrander, E.A.8
Acland, G.M.9
Farber, D.B.10
Aguirre, G.D.11
-
30
-
-
1442280669
-
Dynamic mutation and human disorders: The spinocerebellar ataxias
-
(review)
-
Costa Lima MA, Pimentel MM. Dynamic mutation and human disorders: the spinocerebellar ataxias (review). Int J Mol Med 2004; 13:299-302.
-
(2004)
Int. J. Mol. Med.
, vol.13
, pp. 299-302
-
-
Costa Lima, M.A.1
Pimentel, M.M.2
-
31
-
-
0035800434
-
Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9
-
Liquori CL, Ricker K, Moseley ML, Jacobsen JF, Kress W, Naylor SL, Day JW, Ranum LP. Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9. Science 2001; 293:864-7.
-
(2001)
Science
, vol.293
, pp. 864-867
-
-
Liquori, C.L.1
Ricker, K.2
Moseley, M.L.3
Jacobsen, J.F.4
Kress, W.5
Naylor, S.L.6
Day, J.W.7
Ranum, L.P.8
-
32
-
-
2442687762
-
Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10
-
Matsuura T, Fang P, Lin X, Khajavi M, Tsuji K, Rasmussen A, Grewal RP, Achari M, Alonso ME, Pulst SM, Zoghbi HY, Nelson DL, Roa BB, Ashizawa T. Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10. Am J Hum Genet 2004; 74:1216-24.
-
(2004)
Am. J. Hum. Genet.
, vol.74
, pp. 1216-1224
-
-
Matsuura, T.1
Fang, P.2
Lin, X.3
Khajavi, M.4
Tsuji, K.5
Rasmussen, A.6
Grewal, R.P.7
Achari, M.8
Alonso, M.E.9
Pulst, S.M.10
Zoghbi, H.Y.11
Nelson, D.L.12
Roa, B.B.13
Ashizawa, T.14
-
33
-
-
0033564291
-
Zebrafish genetic map with 2000 microsatellite markers
-
Shimoda N, Knapik EW, Ziniti J, Sim C, Yamada E, Kaplan S, Jackson D, de Sauvage F, Jacob H, Fishman MC. Zebrafish genetic map with 2000 microsatellite markers. Genomics 1999; 58:219-32.
-
(1999)
Genomics
, vol.58
, pp. 219-232
-
-
Shimoda, N.1
Knapik, E.W.2
Ziniti, J.3
Sim, C.4
Yamada, E.5
Kaplan, S.6
Jackson, D.7
de Sauvage, F.8
Jacob, H.9
Fishman, M.C.10
|