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213 related items for PubMed ID: 9344665

  • 1. 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.
    Farjo Q, Jackson A, Pieke-Dahl S, Scott K, Kimberling WJ, Sieving PA, Richards JE, Swaroop A.
    Genomics; 1997 Oct 15; 45(2):395-401. PubMed ID: 9344665
    [Abstract] [Full Text] [Related]

  • 2. Retinopathy mutations in the bZIP protein NRL alter phosphorylation and transcriptional activity.
    Kanda A, Friedman JS, Nishiguchi KM, Swaroop A.
    Hum Mutat; 2007 Jun 15; 28(6):589-98. PubMed ID: 17335001
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  • 3. Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL gene.
    Acar C, Mears AJ, Yashar BM, Maheshwary AS, Andreasson S, Baldi A, Sieving PA, Iannaccone A, Musarella MA, Jacobson SG, Swaroop A.
    Mol Vis; 2003 Jan 24; 9():14-7. PubMed ID: 12552256
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  • 4. NRL S50T mutation and the importance of 'founder effects' in inherited retinal dystrophies.
    Bessant DA, Payne AM, Plant C, Bird AC, Swaroop A, Bhattacharya SS.
    Eur J Hum Genet; 2000 Oct 24; 8(10):783-7. PubMed ID: 11039579
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  • 5. Nrl is required for rod photoreceptor development.
    Mears AJ, Kondo M, Swain PK, Takada Y, Bush RA, Saunders TL, Sieving PA, Swaroop A.
    Nat Genet; 2001 Dec 24; 29(4):447-52. PubMed ID: 11694879
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  • 6. Molecular characterization of the murine neural retina leucine zipper gene, Nrl.
    Farjo Q, Jackson AU, Xu J, Gryzenia M, Skolnick C, Agarwal N, Swaroop A.
    Genomics; 1993 Nov 24; 18(2):216-22. PubMed ID: 8288222
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  • 7. Expression of the bZIP transcription factor gene Nrl in the developing nervous system.
    Liu Q, Ji X, Breitman ML, Hitchcock PF, Swaroop A.
    Oncogene; 1996 Jan 04; 12(1):207-11. PubMed ID: 8552394
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  • 8. A mutation in NRL is associated with autosomal dominant retinitis pigmentosa.
    Bessant DA, Payne AM, Mitton KP, Wang QL, Swain PK, Plant C, Bird AC, Zack DJ, Swaroop A, Bhattacharya SS.
    Nat Genet; 1999 Apr 04; 21(4):355-6. PubMed ID: 10192380
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  • 11. Characterization of human retinal fascin gene (FSCN2) at 17q25: close physical linkage of fascin and cytoplasmic actin genes.
    Tubb BE, Bardien-Kruger S, Kashork CD, Shaffer LG, Ramagli LS, Xu J, Siciliano MJ, Bryan J.
    Genomics; 2000 Apr 15; 65(2):146-56. PubMed ID: 10783262
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  • 20. Expression of the ETS transcription factor ELF3 in the retinal pigment epithelium.
    Jobling AI, Fang Z, Koleski D, Tymms MJ.
    Invest Ophthalmol Vis Sci; 2002 Nov 15; 43(11):3530-7. PubMed ID: 12407165
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