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Items: 15

1.

Expression and functional analysis of Nr2e3, a photoreceptor-specific nuclear receptor, suggest common mechanisms in retinal development between avians and mammals.

Kobayashi M, Hara K, Yu RT, Yasuda K.

Dev Genes Evol. 2008 Aug;218(8):439-44. doi: 10.1007/s00427-008-0232-1. Epub 2008 Jul 1.

2.

Analysis of the involvement of the NR2E3 gene in autosomal recessive retinal dystrophies.

Bernal S, Solans T, Gamundi MJ, Hernan I, de Jorge L, Carballo M, Navarro R, Tizzano E, Ayuso C, Baiget M.

Clin Genet. 2008 Apr;73(4):360-6. doi: 10.1111/j.1399-0004.2008.00963.x. Epub 2008 Feb 20.

PMID:
18294254
3.

The Gly56Arg mutation in NR2E3 accounts for 1-2% of autosomal dominant retinitis pigmentosa.

Gire AI, Sullivan LS, Bowne SJ, Birch DG, Hughbanks-Wheaton D, Heckenlively JR, Daiger SP.

Mol Vis. 2007 Oct 17;13:1970-5.

PMID:
17982421
4.

Recurrent mutation in the first zinc finger of the orphan nuclear receptor NR2E3 causes autosomal dominant retinitis pigmentosa.

Coppieters F, Leroy BP, Beysen D, Hellemans J, De Bosscher K, Haegeman G, Robberecht K, Wuyts W, Coucke PJ, De Baere E.

Am J Hum Genet. 2007 Jul;81(1):147-57. Epub 2007 May 24.

5.

A cell cycle-dependent co-repressor mediates photoreceptor cell-specific nuclear receptor function.

Takezawa S, Yokoyama A, Okada M, Fujiki R, Iriyama A, Yanagi Y, Ito H, Takada I, Kishimoto M, Miyajima A, Takeyama K, Umesono K, Kitagawa H, Kato S.

EMBO J. 2007 Feb 7;26(3):764-74. Epub 2007 Jan 25. Retraction in: EMBO J. 2014 Dec 1;33(23):2881.

6.

Development of the high throughput screening assay for identification of agonists of an orphan nuclear receptor.

Kapitskaya M, Cunningham ME, Lacson R, Kornienko O, Bednar B, Petrukhin K.

Assay Drug Dev Technol. 2006 Jun;4(3):253-62.

PMID:
16834531
7.

The nuclear receptor superfamily: a rosetta stone for physiology.

Evans RM.

Mol Endocrinol. 2005 Jun;19(6):1429-38. No abstract available.

PMID:
15914712
8.
9.

Photoreceptor-specific nuclear receptor NR2E3 functions as a transcriptional activator in rod photoreceptors.

Cheng H, Khanna H, Oh EC, Hicks D, Mitton KP, Swaroop A.

Hum Mol Genet. 2004 Aug 1;13(15):1563-75. Epub 2004 Jun 9.

10.

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
11.

Activation of nuclear receptors: a perspective from structural genomics.

Li Y, Lambert MH, Xu HE.

Structure. 2003 Jul;11(7):741-6. Review.

12.
13.

The photoreceptor cell-specific nuclear receptor gene (PNR) accounts for retinitis pigmentosa in the Crypto-Jews from Portugal (Marranos), survivors from the Spanish Inquisition.

Gerber S, Rozet JM, Takezawa SI, dos Santos LC, Lopes L, Gribouval O, Penet C, Perrault I, Ducroq D, Souied E, Jeanpierre M, Romana S, Fr├ęzal J, Ferraz F, Yu-Umesono R, Munnich A, Kaplan J.

Hum Genet. 2000 Sep;107(3):276-84.

PMID:
11071390
14.

A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse.

Akhmedov NB, Piriev NI, Chang B, Rapoport AL, Hawes NL, Nishina PM, Nusinowitz S, Heckenlively JR, Roderick TH, Kozak CA, Danciger M, Davisson MT, Farber DB.

Proc Natl Acad Sci U S A. 2000 May 9;97(10):5551-6.

15.

Orphan nuclear receptors: shifting endocrinology into reverse.

Kliewer SA, Lehmann JM, Willson TM.

Science. 1999 Apr 30;284(5415):757-60. Review.

PMID:
10221899
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