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880 related items for PubMed ID: 17266784

  • 1. The transcription factor Nr2e3 functions in retinal progenitors to suppress cone cell generation.
    Haider NB, Demarco P, Nystuen AM, Huang X, Smith RS, McCall MA, Naggert JK, Nishina PM.
    Vis Neurosci; 2006; 23(6):917-29. PubMed ID: 17266784
    [Abstract] [Full Text] [Related]

  • 2. Distinct functions of photoreceptor cell-specific nuclear receptor, thyroid hormone receptor beta2 and CRX in one photoreceptor development.
    Yanagi Y, Takezawa S, Kato S.
    Invest Ophthalmol Vis Sci; 2002 Nov; 43(11):3489-94. PubMed ID: 12407160
    [Abstract] [Full Text] [Related]

  • 3. Physiological function of S-cone system is not enhanced in rd7 mice.
    Ueno S, Kondo M, Miyata K, Hirai T, Miyata T, Usukura J, Nishizawa Y, Miyake Y.
    Exp Eye Res; 2005 Dec; 81(6):751-8. PubMed ID: 16005871
    [Abstract] [Full Text] [Related]

  • 4. Expression of photoreceptor-specific nuclear receptor NR2E3 in rod photoreceptors of fetal human retina.
    Bumsted O'Brien KM, Cheng H, Jiang Y, Schulte D, Swaroop A, Hendrickson AE.
    Invest Ophthalmol Vis Sci; 2004 Aug; 45(8):2807-12. PubMed ID: 15277507
    [Abstract] [Full Text] [Related]

  • 5. Dual role of Nr2e3 in photoreceptor development and maintenance.
    Webber AL, Hodor P, Thut CJ, Vogt TF, Zhang T, Holder DJ, Petrukhin K.
    Exp Eye Res; 2008 Jul; 87(1):35-48. PubMed ID: 18547563
    [Abstract] [Full Text] [Related]

  • 6. Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.
    Haider NB, Jacobson SG, Cideciyan AV, Swiderski R, Streb LM, Searby C, Beck G, Hockey R, Hanna DB, Gorman S, Duhl D, Carmi R, Bennett J, Weleber RG, Fishman GA, Wright AF, Stone EM, Sheffield VC.
    Nat Genet; 2000 Feb; 24(2):127-31. PubMed ID: 10655056
    [Abstract] [Full Text] [Related]

  • 7. Excess cones in the retinal degeneration rd7 mouse, caused by the loss of function of orphan nuclear receptor Nr2e3, originate from early-born photoreceptor precursors.
    Cheng H, Khan NW, Roger JE, Swaroop A.
    Hum Mol Genet; 2011 Nov 01; 20(21):4102-15. PubMed ID: 21813656
    [Abstract] [Full Text] [Related]

  • 8. In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal development.
    Cheng H, Aleman TS, Cideciyan AV, Khanna R, Jacobson SG, Swaroop A.
    Hum Mol Genet; 2006 Sep 01; 15(17):2588-602. PubMed ID: 16868010
    [Abstract] [Full Text] [Related]

  • 9. Connexin 36 in photoreceptor cells: studies on transgenic rod-less and cone-less mouse retinas.
    Dang L, Pulukuri S, Mears AJ, Swaroop A, Reese BE, Sitaramayya A.
    Mol Vis; 2004 May 11; 10():323-7. PubMed ID: 15152186
    [Abstract] [Full Text] [Related]

  • 10. Excess cone cell proliferation due to lack of a functional NR2E3 causes retinal dysplasia and degeneration in rd7/rd7 mice.
    Haider NB, Naggert JK, Nishina PM.
    Hum Mol Genet; 2001 Aug 01; 10(16):1619-26. PubMed ID: 11487564
    [Abstract] [Full Text] [Related]

  • 11. Novel NR2E3 mutations (R104Q, R334G) associated with a mild form of enhanced S-cone syndrome demonstrate compound heterozygosity.
    Hayashi T, Gekka T, Goto-Omoto S, Takeuchi T, Kubo A, Kitahara K.
    Ophthalmology; 2005 Dec 01; 112(12):2115. PubMed ID: 16225923
    [Abstract] [Full Text] [Related]

  • 12. Rod differentiation factor NRL activates the expression of nuclear receptor NR2E3 to suppress the development of cone photoreceptors.
    Oh EC, Cheng H, Hao H, Jia L, Khan NW, Swaroop A.
    Brain Res; 2008 Oct 21; 1236():16-29. PubMed ID: 18294621
    [Abstract] [Full Text] [Related]

  • 13. Effects of L1 retrotransposon insertion on transcript processing, localization and accumulation: lessons from the retinal degeneration 7 mouse and implications for the genomic ecology of L1 elements.
    Chen J, Rattner A, Nathans J.
    Hum Mol Genet; 2006 Jul 01; 15(13):2146-56. PubMed ID: 16723373
    [Abstract] [Full Text] [Related]

  • 14. 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.
    Hum Mol Genet; 2005 Mar 15; 14(6):747-64. PubMed ID: 15689355
    [Abstract] [Full Text] [Related]

  • 15. Impaired opsin targeting and cone photoreceptor migration in the retina of mice lacking the cyclic nucleotide-gated channel CNGA3.
    Michalakis S, Geiger H, Haverkamp S, Hofmann F, Gerstner A, Biel M.
    Invest Ophthalmol Vis Sci; 2005 Apr 15; 46(4):1516-24. PubMed ID: 15790924
    [Abstract] [Full Text] [Related]

  • 16. Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration.
    Jacobson SG, Sumaroka A, Aleman TS, Cideciyan AV, Schwartz SB, Roman AJ, McInnes RR, Sheffield VC, Stone EM, Swaroop A, Wright AF.
    Hum Mol Genet; 2004 Sep 01; 13(17):1893-902. PubMed ID: 15229190
    [Abstract] [Full Text] [Related]

  • 17. Leukemia inhibitory factor blocks expression of Crx and Nrl transcription factors to inhibit photoreceptor differentiation.
    Graham DR, Overbeek PA, Ash JD.
    Invest Ophthalmol Vis Sci; 2005 Jul 01; 46(7):2601-10. PubMed ID: 15980254
    [Abstract] [Full Text] [Related]

  • 18. Cone neurite sprouting: an early onset abnormality of the cone photoreceptors in the retinal degeneration mouse.
    Fei Y.
    Mol Vis; 2002 Aug 27; 8():306-14. PubMed ID: 12355062
    [Abstract] [Full Text] [Related]

  • 19. Migration and synaptogenesis of cone photoreceptors in the developing mouse retina.
    Rich KA, Zhan Y, Blanks JC.
    J Comp Neurol; 1997 Nov 10; 388(1):47-63. PubMed ID: 9364238
    [Abstract] [Full Text] [Related]

  • 20. Morphological characterization of the retinal degeneration in three strains of mice carrying the rd-3 mutation.
    Linberg KA, Fariss RN, Heckenlively JR, Farber DB, Fisher SK.
    Vis Neurosci; 2005 Nov 10; 22(6):721-34. PubMed ID: 16469183
    [Abstract] [Full Text] [Related]

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