536 related articles for article (PubMed ID: 17335001)
21. 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]
22. A point mutation of the rhodopsin gene in one form of retinitis pigmentosa.
Dryja TP; McGee TL; Reichel E; Hahn LB; Cowley GS; Yandell DW; Sandberg MA; Berson EL
Nature; 1990 Jan; 343(6256):364-6. PubMed ID: 2137202
[TBL] [Abstract][Full Text] [Related]
23. Novel mutations in the NRL gene and associated clinical findings in patients with dominant retinitis pigmentosa.
DeAngelis MM; Grimsby JL; Sandberg MA; Berson EL; Dryja TP
Arch Ophthalmol; 2002 Mar; 120(3):369-75. PubMed ID: 11879142
[TBL] [Abstract][Full Text] [Related]
24. The bZIP transcription factor Nrl stimulates rhodopsin promoter activity in primary retinal cell cultures.
Kumar R; Chen S; Scheurer D; Wang QL; Duh E; Sung CH; Rehemtulla A; Swaroop A; Adler R; Zack DJ
J Biol Chem; 1996 Nov; 271(47):29612-8. PubMed ID: 8939891
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. 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]
27. RETINA-specific expression of Kcnv2 is controlled by cone-rod homeobox (Crx) and neural retina leucine zipper (Nrl).
Aslanidis A; Karlstetter M; Walczak Y; Jägle H; Langmann T
Adv Exp Med Biol; 2014; 801():31-41. PubMed ID: 24664678
[TBL] [Abstract][Full Text] [Related]
28. Autosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesterase.
Huang SH; Pittler SJ; Huang X; Oliveira L; Berson EL; Dryja TP
Nat Genet; 1995 Dec; 11(4):468-71. PubMed ID: 7493036
[TBL] [Abstract][Full Text] [Related]
29. Altered expression of the transcription factor Mef2c during retinal degeneration in Rpe65-/- mice.
Escher P; Schorderet DF; Cottet S
Invest Ophthalmol Vis Sci; 2011 Jul; 52(8):5933-40. PubMed ID: 21715356
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families.
Riazuddin SA; Zulfiqar F; Zhang Q; Sergeev YV; Qazi ZA; Husnain T; Caruso R; Riazuddin S; Sieving PA; Hejtmancik JF
Invest Ophthalmol Vis Sci; 2005 Jul; 46(7):2264-70. PubMed ID: 15980210
[TBL] [Abstract][Full Text] [Related]
32. Leukemia inhibitory factor blocks expression of Crx and Nrl transcription factors to inhibit photoreceptor differentiation.
Graham DR; Overbeek PA; Ash JD
Invest Ophthalmol Vis Sci; 2005 Jul; 46(7):2601-10. PubMed ID: 15980254
[TBL] [Abstract][Full Text] [Related]
33. Mechanisms of cell death in rhodopsin retinitis pigmentosa: implications for therapy.
Mendes HF; van der Spuy J; Chapple JP; Cheetham ME
Trends Mol Med; 2005 Apr; 11(4):177-85. PubMed ID: 15823756
[TBL] [Abstract][Full Text] [Related]
34. Neural retina leucine-zipper regulates the expression of Ppp2r5c, the regulatory subunit of protein phosphatase 2A, in photoreceptor development.
Kim JW; Jang SM; Kim CH; An JH; Kang EJ; Choi KH
FEBS J; 2010 Dec; 277(24):5051-60. PubMed ID: 21078119
[TBL] [Abstract][Full Text] [Related]
35. Different amino acid substitutions at the same position in rhodopsin lead to distinct phenotypes.
Neidhardt J; Barthelmes D; Farahmand F; Fleischhauer JC; Berger W
Invest Ophthalmol Vis Sci; 2006 Apr; 47(4):1630-5. PubMed ID: 16565402
[TBL] [Abstract][Full Text] [Related]
36. Expression of the bZIP transcription factor gene Nrl in the developing nervous system.
Liu Q; Ji X; Breitman ML; Hitchcock PF; Swaroop A
Oncogene; 1996 Jan; 12(1):207-11. PubMed ID: 8552394
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. [Genetic analysis of rhodopsin and peripherin genes in patients with autosomal dominant retinitis pigmentosa (adRP) in Polish families].
Brzeziańska E; Zdzieszyńska M; Goś R; Lewiński A
Klin Oczna; 2004; 106(6):743-8. PubMed ID: 15787173
[TBL] [Abstract][Full Text] [Related]
39. The retinitis pigmentosa-mutated RP2 protein exhibits exonuclease activity and translocates to the nucleus in response to DNA damage.
Yoon JH; Qiu J; Cai S; Chen Y; Cheetham ME; Shen B; Pfeifer GP
Exp Cell Res; 2006 May; 312(8):1323-34. PubMed ID: 16457815
[TBL] [Abstract][Full Text] [Related]
40. Transcriptional activity of neural retina leucine zipper (Nrl) is regulated by c-Jun N-terminal kinase and Tip60 during retina development.
Kim JW; Jang SM; Kim CH; An JH; Choi KH
Mol Cell Biol; 2012 May; 32(9):1720-32. PubMed ID: 22354990
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
