197 related articles for article (PubMed ID: 19898638)
1. A comprehensive analysis of sequence variants and putative disease-causing mutations in photoreceptor-specific nuclear receptor NR2E3.
Kanda A; Swaroop A
Mol Vis; 2009 Oct; 15():2174-84. PubMed ID: 19898638
[TBL] [Abstract][Full Text] [Related]
2. Differential dimerization of variants linked to enhanced S-cone sensitivity syndrome (ESCS) located in the NR2E3 ligand-binding domain.
von Alpen D; Tran HV; Guex N; Venturini G; Munier FL; Schorderet DF; Haider NB; Escher P
Hum Mutat; 2015 Jun; 36(6):599-610. PubMed ID: 25703721
[TBL] [Abstract][Full Text] [Related]
3. 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; 13(15):1563-75. PubMed ID: 15190009
[TBL] [Abstract][Full Text] [Related]
4. Mutations in the DNA-binding domain of NR2E3 affect in vivo dimerization and interaction with CRX.
Roduit R; Escher P; Schorderet DF
PLoS One; 2009 Oct; 4(10):e7379. PubMed ID: 19823680
[TBL] [Abstract][Full Text] [Related]
5. 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; 14(6):747-64. PubMed ID: 15689355
[TBL] [Abstract][Full Text] [Related]
6. 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; 15(17):2588-602. PubMed ID: 16868010
[TBL] [Abstract][Full Text] [Related]
7. 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; 1236():16-29. PubMed ID: 18294621
[TBL] [Abstract][Full Text] [Related]
8. The crystal structure of the orphan nuclear receptor NR2E3/PNR ligand binding domain reveals a dimeric auto-repressed conformation.
Tan MH; Zhou XE; Soon FF; Li X; Li J; Yong EL; Melcher K; Xu HE
PLoS One; 2013; 8(9):e74359. PubMed ID: 24069298
[TBL] [Abstract][Full Text] [Related]
9. The loss of transcriptional inhibition by the photoreceptor-cell specific nuclear receptor (NR2E3) is not a necessary cause of enhanced S-cone syndrome.
Fradot M; Lorentz O; Wurtz JM; Sahel JA; Léveillard T
Mol Vis; 2007 Apr; 13():594-601. PubMed ID: 17438525
[TBL] [Abstract][Full Text] [Related]
10. Retinopathy mutations in the bZIP protein NRL alter phosphorylation and transcriptional activity.
Kanda A; Friedman JS; Nishiguchi KM; Swaroop A
Hum Mutat; 2007 Jun; 28(6):589-98. PubMed ID: 17335001
[TBL] [Abstract][Full Text] [Related]
11. The leucine zipper of NRL interacts with the CRX homeodomain. A possible mechanism of transcriptional synergy in rhodopsin regulation.
Mitton KP; Swain PK; Chen S; Xu S; Zack DJ; Swaroop A
J Biol Chem; 2000 Sep; 275(38):29794-9. PubMed ID: 10887186
[TBL] [Abstract][Full Text] [Related]
12. 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; 20(21):4102-15. PubMed ID: 21813656
[TBL] [Abstract][Full Text] [Related]
13. Sumoylation of bZIP transcription factor NRL modulates target gene expression during photoreceptor differentiation.
Roger JE; Nellissery J; Kim DS; Swaroop A
J Biol Chem; 2010 Aug; 285(33):25637-44. PubMed ID: 20551322
[TBL] [Abstract][Full Text] [Related]
14. Different effects of valproic acid on photoreceptor loss in Rd1 and Rd10 retinal degeneration mice.
Mitton KP; Guzman AE; Deshpande M; Byrd D; DeLooff C; Mkoyan K; Zlojutro P; Wallace A; Metcalf B; Laux K; Sotzen J; Tran T
Mol Vis; 2014; 20():1527-44. PubMed ID: 25489226
[TBL] [Abstract][Full Text] [Related]
15. Association of NR2E3 but not NRL mutations with retinitis pigmentosa in the Chinese population.
Yang Y; Zhang X; Chen LJ; Chiang SW; Tam PO; Lai TY; Chan CK; Wang N; Lam DS; Pang CP
Invest Ophthalmol Vis Sci; 2010 Apr; 51(4):2229-35. PubMed ID: 19933183
[TBL] [Abstract][Full Text] [Related]
16. 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
[TBL] [Abstract][Full Text] [Related]
17. NR2E3 mutations in enhanced S-cone sensitivity syndrome (ESCS), Goldmann-Favre syndrome (GFS), clumped pigmentary retinal degeneration (CPRD), and retinitis pigmentosa (RP).
Schorderet DF; Escher P
Hum Mutat; 2009 Nov; 30(11):1475-85. PubMed ID: 19718767
[TBL] [Abstract][Full Text] [Related]
18. Heterodimers of photoreceptor-specific nuclear receptor (PNR/NR2E3) and peroxisome proliferator-activated receptor-γ (PPARγ) are disrupted by retinal disease-associated mutations.
Fulton J; Mazumder B; Whitchurch JB; Monteiro CJ; Collins HM; Chan CM; Clemente MP; Hernandez-Quiles M; Stewart EA; Amoaku WM; Moran PM; Mongan NP; Persson JL; Ali S; Heery DM
Cell Death Dis; 2017 Mar; 8(3):e2677. PubMed ID: 28300834
[TBL] [Abstract][Full Text] [Related]
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; 25(1):118-29. PubMed ID: 15634773
[TBL] [Abstract][Full Text] [Related]
20. The cis-regulatory logic of the mammalian photoreceptor transcriptional network.
Hsiau TH; Diaconu C; Myers CA; Lee J; Cepko CL; Corbo JC
PLoS One; 2007 Jul; 2(7):e643. PubMed ID: 17653270
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
