A mutation in NRL is associated with autosomal dominant retinitis pigmentosa

[1] RETINAL PHOTORECEPTOR DYSTROPHIES LL-EDWARD-JACKSON-MEMORIAL-LECTURE [J]. AMERICAN JOURNAL OF OPHTHALMOLOGY, 1995, 119 (05) : 543 - 562

[2] Crx, a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes [J]. NEURON, 1997, 19 (05) : 1017 - 1030

[3] Human bZIP transcription factor gene NRL: Structure, genomic sequence, and fine linkage mapping at 14q11.2 and negative mutation analysis in patients with retinal degeneration [J]. GENOMICS, 1997, 45 (02) : 395 - 401

[4] De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis [J]. NATURE GENETICS, 1998, 18 (04) : 311 - 312

[5] Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor [J]. CELL, 1997, 91 (04) : 543 - 553

[6] Retinopathy induced in mice by targeted disruption of the rhodopsin gene [J]. NATURE GENETICS, 1997, 15 (02) : 216 - 219

[7] A COMPLETED SCREEN FOR MUTATIONS OF THE RHODOPSIN GENE IN A PANEL OF PATIENTS WITH AUTOSOMAL DOMINANT RETINITIS-PIGMENTOSA [J]. HUMAN MOLECULAR GENETICS, 1992, 1 (01) : 41 - 45

[8] Kaufman R. J., 1992, Gene amplification in mammalian cells: a comprehensive guide., P315

[9] KEEN J, 1991, TRENDS GENET, V7, P5

[10] The bZIP transcription factor Nrl stimulates rhodopsin promoter activity in primary retinal cell cultures [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (47) : 29612 - 29618

[1] RETINAL PHOTORECEPTOR DYSTROPHIES LL-EDWARD-JACKSON-MEMORIAL-LECTURE [J]. AMERICAN JOURNAL OF OPHTHALMOLOGY, 1995, 119 (05) : 543 - 562

[2] Crx, a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes [J]. NEURON, 1997, 19 (05) : 1017 - 1030

[3] Human bZIP transcription factor gene NRL: Structure, genomic sequence, and fine linkage mapping at 14q11.2 and negative mutation analysis in patients with retinal degeneration [J]. GENOMICS, 1997, 45 (02) : 395 - 401

[4] De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis [J]. NATURE GENETICS, 1998, 18 (04) : 311 - 312

[5] Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor [J]. CELL, 1997, 91 (04) : 543 - 553

[6] Retinopathy induced in mice by targeted disruption of the rhodopsin gene [J]. NATURE GENETICS, 1997, 15 (02) : 216 - 219

[7] A COMPLETED SCREEN FOR MUTATIONS OF THE RHODOPSIN GENE IN A PANEL OF PATIENTS WITH AUTOSOMAL DOMINANT RETINITIS-PIGMENTOSA [J]. HUMAN MOLECULAR GENETICS, 1992, 1 (01) : 41 - 45

[8] Kaufman R. J., 1992, Gene amplification in mammalian cells: a comprehensive guide., P315

[9] KEEN J, 1991, TRENDS GENET, V7, P5

[10] The bZIP transcription factor Nrl stimulates rhodopsin promoter activity in primary retinal cell cultures [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (47) : 29612 - 29618