|
XB-GENEPAGE-485800
Papers associated with nr2e3
???pagination.result.count???
???pagination.result.page??? 1
Sort Newest To Oldest | Sort Oldest To Newest |
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. February 1, 2000; 24 (2): 127-31. |
|
The Xenopus ortholog of the nuclear hormone receptor Nr2e3 is primarily expressed in developing photoreceptors., Martinez-De Luna RI, El-Hodiri HM., Int J Dev Biol. January 1, 2007; 51 (3): 235-40. |
|
Nr2e3 and Nrl can reprogram retinal precursors to the rod fate in Xenopus retina., McIlvain VA, Knox BE., Dev Dyn. July 1, 2007; 236 (7): 1970-9. |
|
CRX controls retinal expression of the X-linked juvenile retinoschisis (RS1) gene., Langmann T, Lai CC, Weigelt K, Tam BM, Warneke-Wittstock R, Moritz OL, Weber BH., Nucleic Acids Res. November 1, 2008; 36 (20): 6523-34. |
|
SUMO weighs in on a photoreceptor finish., LaBonne C., Dev Cell. February 1, 2009; 16 (2): 165-6. |
|
Characterization of three synuclein genes in Xenopus laevis., Wang C, Wang C, Wang C, Liu Y, Chan WY, Chan SO, Grunz H, Zhao H., Dev Dyn. August 1, 2011; 240 (8): 2028-33. |
???pagination.result.page??? 1