These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
206 related articles for article (PubMed ID: 17012604)
21. FHY3 promotes shoot branching and stress tolerance in Arabidopsis in an AXR1-dependent manner. Stirnberg P; Zhao S; Williamson L; Ward S; Leyser O Plant J; 2012 Sep; 71(6):907-20. PubMed ID: 22540368 [TBL] [Abstract][Full Text] [Related]
22. Gating of the rapid shade-avoidance response by the circadian clock in plants. Salter MG; Franklin KA; Whitelam GC Nature; 2003 Dec; 426(6967):680-3. PubMed ID: 14668869 [TBL] [Abstract][Full Text] [Related]
23. ELF4 is a phytochrome-regulated component of a negative-feedback loop involving the central oscillator components CCA1 and LHY. Kikis EA; Khanna R; Quail PH Plant J; 2005 Oct; 44(2):300-13. PubMed ID: 16212608 [TBL] [Abstract][Full Text] [Related]
24. Transposase-derived proteins FHY3/FAR1 interact with PHYTOCHROME-INTERACTING FACTOR1 to regulate chlorophyll biosynthesis by modulating HEMB1 during deetiolation in Arabidopsis. Tang W; Wang W; Chen D; Ji Q; Jing Y; Wang H; Lin R Plant Cell; 2012 May; 24(5):1984-2000. PubMed ID: 22634759 [TBL] [Abstract][Full Text] [Related]
25. FAR-RED ELONGATED HYPOCOTYLS3 negatively regulates shade avoidance responses in Arabidopsis. Ma L; Li Y; Li X; Xu D; Lin X; Liu M; Li G; Qin X Plant Cell Environ; 2019 Dec; 42(12):3280-3292. PubMed ID: 31351015 [TBL] [Abstract][Full Text] [Related]
26. Phytochrome-interacting factor 4 and 5 (PIF4 and PIF5) activate the homeobox ATHB2 and auxin-inducible IAA29 genes in the coincidence mechanism underlying photoperiodic control of plant growth of Arabidopsis thaliana. Kunihiro A; Yamashino T; Nakamichi N; Niwa Y; Nakanishi H; Mizuno T Plant Cell Physiol; 2011 Aug; 52(8):1315-29. PubMed ID: 21666227 [TBL] [Abstract][Full Text] [Related]
27. FAR-RED ELONGATED HYPOCOTYL3 activates SEPALLATA2 but inhibits CLAVATA3 to regulate meristem determinacy and maintenance in Arabidopsis. Li D; Fu X; Guo L; Huang Z; Li Y; Liu Y; He Z; Cao X; Ma X; Zhao M; Zhu G; Xiao L; Wang H; Chen X; Liu R; Liu X Proc Natl Acad Sci U S A; 2016 Aug; 113(33):9375-80. PubMed ID: 27469166 [TBL] [Abstract][Full Text] [Related]
28. Arabidopsis thaliana TERMINAL FLOWER2 is involved in light-controlled signalling during seedling photomorphogenesis. Valdés AE; Rizzardi K; Johannesson H; Para A; Sundås-Larsson A; Landberg K Plant Cell Environ; 2012 Jun; 35(6):1013-25. PubMed ID: 22145973 [TBL] [Abstract][Full Text] [Related]
29. Arabidopsis FHY3 defines a key phytochrome A signaling component directly interacting with its homologous partner FAR1. Wang H; Deng XW EMBO J; 2002 Mar; 21(6):1339-49. PubMed ID: 11889039 [TBL] [Abstract][Full Text] [Related]
30. Arabidopsis FHY3 and FAR1 Regulate Light-Induced myo-Inositol Biosynthesis and Oxidative Stress Responses by Transcriptional Activation of MIPS1. Ma L; Tian T; Lin R; Deng XW; Wang H; Li G Mol Plant; 2016 Apr; 9(4):541-57. PubMed ID: 26714049 [TBL] [Abstract][Full Text] [Related]
31. The circadian clock regulates the photoperiodic response of hypocotyl elongation through a coincidence mechanism in Arabidopsis thaliana. Niwa Y; Yamashino T; Mizuno T Plant Cell Physiol; 2009 Apr; 50(4):838-54. PubMed ID: 19233867 [TBL] [Abstract][Full Text] [Related]
32. Phytochrome A is an irradiance-dependent red light sensor. Franklin KA; Allen T; Whitelam GC Plant J; 2007 Apr; 50(1):108-17. PubMed ID: 17346261 [TBL] [Abstract][Full Text] [Related]
33. Nuclear accumulation of the phytochrome A photoreceptor requires FHY1. Hiltbrunner A; Viczián A; Bury E; Tscheuschler A; Kircher S; Tóth R; Honsberger A; Nagy F; Fankhauser C; Schäfer E Curr Biol; 2005 Dec; 15(23):2125-30. PubMed ID: 16332538 [TBL] [Abstract][Full Text] [Related]
34. Dual role of TOC1 in the control of circadian and photomorphogenic responses in Arabidopsis. Más P; Alabadí D; Yanovsky MJ; Oyama T; Kay SA Plant Cell; 2003 Jan; 15(1):223-36. PubMed ID: 12509533 [TBL] [Abstract][Full Text] [Related]
35. The Arabidopsis pseudo-response regulators, PRR5 and PRR7, coordinately play essential roles for circadian clock function. Nakamichi N; Kita M; Ito S; Sato E; Yamashino T; Mizuno T Plant Cell Physiol; 2005 Apr; 46(4):609-19. PubMed ID: 15695441 [TBL] [Abstract][Full Text] [Related]
37. Functional characterization of phytochrome interacting factor 3 for the Arabidopsis thaliana circadian clockwork. Viczián A; Kircher S; Fejes E; Millar AJ; Schäfer E; Kozma-Bognár L; Nagy F Plant Cell Physiol; 2005 Oct; 46(10):1591-602. PubMed ID: 16055924 [TBL] [Abstract][Full Text] [Related]
38. Expression profiling of phyB mutant demonstrates substantial contribution of other phytochromes to red-light-regulated gene expression during seedling de-etiolation. Tepperman JM; Hudson ME; Khanna R; Zhu T; Chang SH; Wang X; Quail PH Plant J; 2004 Jun; 38(5):725-39. PubMed ID: 15144375 [TBL] [Abstract][Full Text] [Related]
39. The nuclear localization signal and the C-terminal region of FHY1 are required for transmission of phytochrome A signals. Zeidler M; Zhou Q; Sarda X; Yau CP; Chua NH Plant J; 2004 Nov; 40(3):355-65. PubMed ID: 15469493 [TBL] [Abstract][Full Text] [Related]
40. FHY3 interacts with phytochrome B and regulates seed dormancy and germination. Liu S; Yang L; Li J; Tang W; Li J; Lin R Plant Physiol; 2021 Sep; 187(1):289-302. PubMed ID: 33764465 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]