242 related articles for article (PubMed ID: 16624856)
1. Senseless physically interacts with proneural proteins and functions as a transcriptional co-activator.
Acar M; Jafar-Nejad H; Giagtzoglou N; Yallampalli S; David G; He Y; Delidakis C; Bellen HJ
Development; 2006 May; 133(10):1979-89. PubMed ID: 16624856
[TBL] [Abstract][Full Text] [Related]
2. Senseless and Daughterless confer neuronal identity to epithelial cells in the Drosophila wing margin.
Jafar-Nejad H; Tien AC; Acar M; Bellen HJ
Development; 2006 May; 133(9):1683-92. PubMed ID: 16554363
[TBL] [Abstract][Full Text] [Related]
3. The SUMO pathway promotes basic helix-loop-helix proneural factor activity via a direct effect on the Zn finger protein senseless.
Powell LM; Chen A; Huang YC; Wang PY; Kemp SE; Jarman AP
Mol Cell Biol; 2012 Jul; 32(14):2849-60. PubMed ID: 22586269
[TBL] [Abstract][Full Text] [Related]
4. Senseless acts as a binary switch during sensory organ precursor selection.
Jafar-Nejad H; Acar M; Nolo R; Lacin H; Pan H; Parkhurst SM; Bellen HJ
Genes Dev; 2003 Dec; 17(23):2966-78. PubMed ID: 14665671
[TBL] [Abstract][Full Text] [Related]
5. Senseless, a Zn finger transcription factor, is necessary and sufficient for sensory organ development in Drosophila.
Nolo R; Abbott LA; Bellen HJ
Cell; 2000 Aug; 102(3):349-62. PubMed ID: 10975525
[TBL] [Abstract][Full Text] [Related]
6. Neural precursor-specific expression of multiple Drosophila genes is driven by dual enhancer modules with overlapping function.
Miller SW; Rebeiz M; Atanasov JE; Posakony JW
Proc Natl Acad Sci U S A; 2014 Dec; 111(48):17194-9. PubMed ID: 25404315
[TBL] [Abstract][Full Text] [Related]
7. Proneural and abdominal Hox inputs synergize to promote sensory organ formation in the Drosophila abdomen.
Gutzwiller LM; Witt LM; Gresser AL; Burns KA; Cook TA; Gebelein B
Dev Biol; 2010 Dec; 348(2):231-43. PubMed ID: 20875816
[TBL] [Abstract][Full Text] [Related]
8. Klumpfuss is involved in the determination of sensory organ precursors in Drosophila.
Kaspar M; Schneider M; Chia W; Klein T
Dev Biol; 2008 Dec; 324(2):177-91. PubMed ID: 18831969
[TBL] [Abstract][Full Text] [Related]
9. Proneural proteins Achaete and Scute associate with nuclear actin to promote formation of external sensory organs.
Hsiao YL; Chen YJ; Chang YJ; Yeh HF; Huang YC; Pi H
J Cell Sci; 2014 Jan; 127(Pt 1):182-90. PubMed ID: 24190881
[TBL] [Abstract][Full Text] [Related]
10. Robust specification of sensory neurons by dual functions of charlatan, a Drosophila NRSF/REST-like repressor of extramacrochaetae and hairy.
Yamasaki Y; Lim YM; Niwa N; Hayashi S; Tsuda L
Genes Cells; 2011 Aug; 16(8):896-909. PubMed ID: 21762412
[TBL] [Abstract][Full Text] [Related]
11. Specificity of Atonal and Scute bHLH factors: analysis of cognate E box binding sites and the influence of Senseless.
Powell LM; Deaton AM; Wear MA; Jarman AP
Genes Cells; 2008 Sep; 13(9):915-29. PubMed ID: 18681894
[TBL] [Abstract][Full Text] [Related]
12. phyllopod is a target gene of proneural proteins in Drosophila external sensory organ development.
Pi H; Huang SK; Tang CY; Sun YH; Chien CT
Proc Natl Acad Sci U S A; 2004 Jun; 101(22):8378-83. PubMed ID: 15148389
[TBL] [Abstract][Full Text] [Related]
13. The proneural proteins Atonal and Scute regulate neural target genes through different E-box binding sites.
Powell LM; Zur Lage PI; Prentice DR; Senthinathan B; Jarman AP
Mol Cell Biol; 2004 Nov; 24(21):9517-26. PubMed ID: 15485919
[TBL] [Abstract][Full Text] [Related]
14. cato encodes a basic helix-loop-helix transcription factor implicated in the correct differentiation of Drosophila sense organs.
Goulding SE; White NM; Jarman AP
Dev Biol; 2000 May; 221(1):120-31. PubMed ID: 10772796
[TBL] [Abstract][Full Text] [Related]
15. Role of the Sc C terminus in transcriptional activation and E(spl) repressor recruitment.
Giagtzoglou N; Koumbanakis KA; Fullard J; Zarifi I; Delidakis C
J Biol Chem; 2005 Jan; 280(2):1299-305. PubMed ID: 15507447
[TBL] [Abstract][Full Text] [Related]
16. Senseless is required for pupal retinal development in Drosophila.
Frankfort BJ; Pepple KL; Mamlouk M; Rose MF; Mardon G
Genesis; 2004 Apr; 38(4):182-94. PubMed ID: 15083519
[TBL] [Abstract][Full Text] [Related]
17. The HLH domain of a zebrafish HE12 homologue can partially substitute for functions of the HLH domain of Drosophila DAUGHTERLESS.
Wülbeck C; Fromental-Ramain C; Campos-Ortega JA
Mech Dev; 1994 May; 46(2):73-85. PubMed ID: 7918099
[TBL] [Abstract][Full Text] [Related]
18. Hairy function as a DNA-binding helix-loop-helix repressor of Drosophila sensory organ formation.
Ohsako S; Hyer J; Panganiban G; Oliver I; Caudy M
Genes Dev; 1994 Nov; 8(22):2743-55. PubMed ID: 7958930
[TBL] [Abstract][Full Text] [Related]
19. Restricted expression of a novel murine atonal-related bHLH protein in undifferentiated neural precursors.
Gradwohl G; Fode C; Guillemot F
Dev Biol; 1996 Nov; 180(1):227-41. PubMed ID: 8948587
[TBL] [Abstract][Full Text] [Related]
20. Histone deacetylase-associating Atrophin proteins are nuclear receptor corepressors.
Wang L; Rajan H; Pitman JL; McKeown M; Tsai CC
Genes Dev; 2006 Mar; 20(5):525-30. PubMed ID: 16481466
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]