PubMed (OMIM) for id: 341446

Year	Number of Results
1958	1
1970	1
1974	1
1989	1
1990	1
1991	1
1995	1
1999	1
2000	5
2001	1
2002	1
2003	1
2024	0

1

[Two cases of hyaloid-retinal degeneration].

FAVRE M. FAVRE M. Ophthalmologica. 1958 May-Jun;135(5-6):604-9. doi: 10.1159/000303360. Ophthalmologica. 1958. PMID: 13553271 French. No abstract available.

2

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. Cideciyan AV, et al. Invest Ophthalmol Vis Sci. 2003 Mar;44(3):1268-74. doi: 10.1167/iovs.02-0494. Invest Ophthalmol Vis Sci. 2003. PMID: 12601058

3

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. Milam AH, et al. Proc Natl Acad Sci U S A. 2002 Jan 8;99(1):473-8. doi: 10.1073/pnas.022533099. Epub 2002 Jan 2. Proc Natl Acad Sci U S A. 2002. PMID: 11773633 Free PMC article.

4

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. Haider NB, et al. Hum Mol Genet. 2001 Aug 1;10(16):1619-26. doi: 10.1093/hmg/10.16.1619. Hum Mol Genet. 2001. PMID: 11487564

5

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, Frézal J, Ferraz F, Yu-Umesono R, Munnich A, Kaplan J. Gerber S, et al. Hum Genet. 2000 Sep;107(3):276-84. doi: 10.1007/s004390000350. Hum Genet. 2000. PMID: 11071390 Free article.

6

Assignment of the NR2E3 gene to mouse chromosome 9 and to human chromosome 15q22.33-->q23.

Rendtorff ND, Vissing H, Tümer Z, Silahtaroglu A, Tommerup N. Rendtorff ND, et al. Cytogenet Cell Genet. 2000;89(3-4):279-80. doi: 10.1159/000015635. Cytogenet Cell Genet. 2000. PMID: 10965145 No abstract available.

7

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. Akhmedov NB, et al. Proc Natl Acad Sci U S A. 2000 May 9;97(10):5551-6. doi: 10.1073/pnas.97.10.5551. Proc Natl Acad Sci U S A. 2000. PMID: 10805811 Free PMC article.

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. Haider NB, et al. Nat Genet. 2000 Feb;24(2):127-31. doi: 10.1038/72777. Nat Genet. 2000. PMID: 10655056

9

Giving in to the blues.

Cepko C. Cepko C. Nat Genet. 2000 Feb;24(2):99-100. doi: 10.1038/72887. Nat Genet. 2000. PMID: 10655045

10

Identification of a photoreceptor cell-specific nuclear receptor.

Kobayashi M, Takezawa S, Hara K, Yu RT, Umesono Y, Agata K, Taniwaki M, Yasuda K, Umesono K. Kobayashi M, et al. Proc Natl Acad Sci U S A. 1999 Apr 27;96(9):4814-9. doi: 10.1073/pnas.96.9.4814. Proc Natl Acad Sci U S A. 1999. PMID: 10220376 Free PMC article.

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