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    Results: 1 to 20 of 97

    1.

    Cellular origin of fundus autofluorescence in patients and mice with a defective NR2E3 gene.

    Wang NK, Fine HF, Chang S, Chou CL, Cella W, Tosi J, Lin CS, Nagasaki T, Tsang SH.

    Br J Ophthalmol. 2009 Sep;93(9):1234-40. Epub 2009 May 7.PMID: 19429590 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    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 1;10(16):1619-26.PMID: 11487564 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    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 Nov-Dec;23(6):917-29.PMID: 17266784 [PubMed - indexed for MEDLINE]Related articles

    4.

    A novel mutation in Prph2, a gene regulated by Nr2e3, causes retinal degeneration and outer-segment defects similar to Nr2e3 ( rd7/rd7 ) retinas.

    Nystuen AM, Sachs AJ, Yuan Y, Heuermann L, Haider NB.

    Mamm Genome. 2008 Sep;19(9):623-33. Epub 2008 Sep 3.PMID: 18763016 [PubMed - indexed for MEDLINE]Related articles

    5.

    Mapping of genetic modifiers of Nr2e3 rd7/rd7 that suppress retinal degeneration and restore blue cone cells to normal quantity.

    Haider NB, Zhang W, Hurd R, Ikeda A, Nystuen AM, Naggert JK, Nishina PM.

    Mamm Genome. 2008 Mar;19(3):145-54. Epub 2008 Feb 20.PMID: 18286335 [PubMed - indexed for MEDLINE]Related articles

    6.

    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;112(12):2115. Epub 2005 Oct 12.PMID: 16225923 [PubMed - indexed for MEDLINE]Related articles

    7.

    Nr2e3-directed transcriptional regulation of genes involved in photoreceptor development and cell-type specific phototransduction.

    Haider NB, Mollema N, Gaule M, Yuan Y, Sachs AJ, Nystuen AM, Naggert JK, Nishina PM.

    Exp Eye Res. 2009 Sep;89(3):365-72. Epub 2009 Apr 18. Review.PMID: 19379737 [PubMed - indexed for MEDLINE]Related articles

    8.

    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.PMID: 10655056 [PubMed - indexed for MEDLINE]Related articles

    9.

    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. Epub 2005 Jul 11.PMID: 16005871 [PubMed - indexed for MEDLINE]Related articles

    10.

    Phenotypic features of patients with NR2E3 mutations.

    Pachydaki SI, Klaver CC, Barbazetto IA, Roy MS, Gouras P, Allikmets R, Yannuzzi LA.

    Arch Ophthalmol. 2009 Jan;127(1):71-5.PMID: 19139342 [PubMed - indexed for MEDLINE]Related articles

    11.

    Enhanced S-cone syndrome in a Japanese family with a nonsense NR2E3 mutation (Q350X).

    Nakamura Y, Hayashi T, Kozaki K, Kubo A, Omoto S, Watanabe A, Toda K, Takeuchi T, Gekka T, Kitahara K.

    Acta Ophthalmol Scand. 2004 Oct;82(5):616-22.PMID: 15453866 [PubMed - indexed for MEDLINE]Related articles

    12.

    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. Epub 2005 Feb 2.PMID: 15689355 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    Mutations in NR2E3 can cause dominant or recessive retinal degenerations in the same family.

    Escher P, Gouras P, Roduit R, Tiab L, Bolay S, Delarive T, Chen S, Tsai CC, Hayashi M, Zernant J, Merriam JE, Mermod N, Allikmets R, Munier FL, Schorderet DF.

    Hum Mutat. 2009 Mar;30(3):342-51.PMID: 19006237 [PubMed - indexed for MEDLINE]Related articles

    14.

    Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration.

    Sharon D, Sandberg MA, Caruso RC, Berson EL, Dryja TP.

    Arch Ophthalmol. 2003 Sep;121(9):1316-23.PMID: 12963616 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degeneration.

    Milam AH, Rose L, Cideciyan AV, Barakat MR, Tang WX, Gupta N, Aleman TS, Wright AF, Stone EM, Sheffield VC, Jacobson SG.

    Proc Natl Acad Sci U S A. 2002 Jan 8;99(1):473-8. Epub 2002 Jan 2.PMID: 11773633 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    Phenotypic variation in enhanced S-cone syndrome.

    Audo I, Michaelides M, Robson AG, Hawlina M, Vaclavik V, Sandbach JM, Neveu MM, Hogg CR, Hunt DM, Moore AT, Bird AC, Webster AR, Holder GE.

    Invest Ophthalmol Vis Sci. 2008 May;49(5):2082-93.PMID: 18436841 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    Cone deactivation kinetics and GRK1/GRK7 expression in enhanced S cone syndrome caused by mutations in NR2E3.

    Cideciyan AV, Jacobson SG, Gupta N, Osawa S, Locke KG, Weiss ER, Wright AF, Birch DG, Milam AH.

    Invest Ophthalmol Vis Sci. 2003 Mar;44(3):1268-74.PMID: 12601058 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Atypical mild enhanced S-cone syndrome with novel compound heterozygosity of the NR2E3 gene.

    Lam BL, Goldberg JL, Hartley KL, Stone EM, Liu M.

    Am J Ophthalmol. 2007 Jul;144(1):157-9.PMID: 17601449 [PubMed - indexed for MEDLINE]Related articles

    19.

    The rod photoreceptor-specific nuclear receptor Nr2e3 represses transcription of multiple cone-specific genes.

    Chen J, Rattner A, Nathans J.

    J Neurosci. 2005 Jan 5;25(1):118-29.PMID: 15634773 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    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. Epub 2008 Apr 25.PMID: 18547563 [PubMed - indexed for MEDLINE]Related articles

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