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308 related items for PubMed ID: 28732105

  • 21. 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
    [Abstract] [Full Text] [Related]

  • 22. Arabidopsis EARLY FLOWERING 3 controls temperature responsiveness of the circadian clock independently of the evening complex.
    Zhu Z, Quint M, Anwer MU.
    J Exp Bot; 2022 Jan 27; 73(3):1049-1061. PubMed ID: 34698833
    [Abstract] [Full Text] [Related]

  • 23. The regulation of UV-B responses by the circadian clock.
    Horak E, Farré EM.
    Plant Signal Behav; 2015 Jan 27; 10(5):e1000164. PubMed ID: 26039469
    [Abstract] [Full Text] [Related]

  • 24. The ELF3 zeitnehmer regulates light signalling to the circadian clock.
    McWatters HG, Bastow RM, Hall A, Millar AJ.
    Nature; 2000 Dec 07; 408(6813):716-20. PubMed ID: 11130072
    [Abstract] [Full Text] [Related]

  • 25. PSEUDO-RESPONSE REGULATORS, PRR9, PRR7 and PRR5, together play essential roles close to the circadian clock of Arabidopsis thaliana.
    Nakamichi N, Kita M, Ito S, Yamashino T, Mizuno T.
    Plant Cell Physiol; 2005 May 07; 46(5):686-98. PubMed ID: 15767265
    [Abstract] [Full Text] [Related]

  • 26. How do phytochromes transmit the light quality information to the circadian clock in Arabidopsis?
    Yeom M, Kim H, Lim J, Shin AY, Hong S, Kim JI, Nam HG.
    Mol Plant; 2014 Nov 07; 7(11):1701-1704. PubMed ID: 25095795
    [No Abstract] [Full Text] [Related]

  • 27. Gibberellin driven growth in elf3 mutants requires PIF4 and PIF5.
    Filo J, Wu A, Eliason E, Richardson T, Thines BC, Harmon FG.
    Plant Signal Behav; 2015 Nov 07; 10(3):e992707. PubMed ID: 25738547
    [Abstract] [Full Text] [Related]

  • 28. Iron around the clock.
    Tissot N, Przybyla-Toscano J, Reyt G, Castel B, Duc C, Boucherez J, Gaymard F, Briat JF, Dubos C.
    Plant Sci; 2014 Jul 07; 224():112-9. PubMed ID: 24908512
    [Abstract] [Full Text] [Related]

  • 29. The evening complex is central to the difference between the circadian clocks of Arabidopsis thaliana shoots and roots.
    Nimmo HG, Laird J, Bindbeutel R, Nusinow DA.
    Physiol Plant; 2020 Jul 07; 169(3):442-451. PubMed ID: 32303120
    [Abstract] [Full Text] [Related]

  • 30. 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 07; 44(2):300-13. PubMed ID: 16212608
    [Abstract] [Full Text] [Related]

  • 31. Arabidopsis PSEUDO-RESPONSE REGULATOR7 is a signaling intermediate in phytochrome-regulated seedling deetiolation and phasing of the circadian clock.
    Kaczorowski KA, Quail PH.
    Plant Cell; 2003 Nov 07; 15(11):2654-65. PubMed ID: 14563930
    [Abstract] [Full Text] [Related]

  • 32. Arabidopsis FHY3 specifically gates phytochrome signaling to the circadian clock.
    Allen T, Koustenis A, Theodorou G, Somers DE, Kay SA, Whitelam GC, Devlin PF.
    Plant Cell; 2006 Oct 07; 18(10):2506-16. PubMed ID: 17012604
    [Abstract] [Full Text] [Related]

  • 33. Phenotypic characterization of a photomorphogenic mutant.
    Fankhauser C, Casal JJ.
    Plant J; 2004 Sep 07; 39(5):747-60. PubMed ID: 15315636
    [Abstract] [Full Text] [Related]

  • 34. Genomewide characterization of the light-responsive and clock-controlled output pathways in Lotus japonicus with special emphasis of its uniqueness.
    Ono N, Ishida K, Yamashino T, Nakanishi H, Sato S, Tabata S, Mizuno T.
    Plant Cell Physiol; 2010 Oct 07; 51(10):1800-14. PubMed ID: 20833628
    [Abstract] [Full Text] [Related]

  • 35. Conditional circadian regulation of PHYTOCHROME A gene expression.
    Hall A, Kozma-Bognár L, Tóth R, Nagy F, Millar AJ.
    Plant Physiol; 2001 Dec 07; 127(4):1808-18. PubMed ID: 11743124
    [Abstract] [Full Text] [Related]

  • 36. Double loss-of-function mutation in EARLY FLOWERING 3 and CRYPTOCHROME 2 genes delays flowering under continuous light but accelerates it under long days and short days: an important role for Arabidopsis CRY2 to accelerate flowering time in continuous light.
    Nefissi R, Natsui Y, Miyata K, Oda A, Hase Y, Nakagawa M, Ghorbel A, Mizoguchi T.
    J Exp Bot; 2011 May 07; 62(8):2731-44. PubMed ID: 21296763
    [Abstract] [Full Text] [Related]

  • 37. The circadian clock controls the expression pattern of the circadian input photoreceptor, phytochrome B.
    Bognár LK, Hall A, Adám E, Thain SC, Nagy F, Millar AJ.
    Proc Natl Acad Sci U S A; 1999 Dec 07; 96(25):14652-7. PubMed ID: 10588760
    [Abstract] [Full Text] [Related]

  • 38. Organ specificity in the plant circadian system is explained by different light inputs to the shoot and root clocks.
    Bordage S, Sullivan S, Laird J, Millar AJ, Nimmo HG.
    New Phytol; 2016 Oct 07; 212(1):136-49. PubMed ID: 27240972
    [Abstract] [Full Text] [Related]

  • 39. Light Perception: A Matter of Time.
    Sanchez SE, Rugnone ML, Kay SA.
    Mol Plant; 2020 Mar 02; 13(3):363-385. PubMed ID: 32068156
    [Abstract] [Full Text] [Related]

  • 40. ELF3 modulates resetting of the circadian clock in Arabidopsis.
    Covington MF, Panda S, Liu XL, Strayer CA, Wagner DR, Kay SA.
    Plant Cell; 2001 Jun 02; 13(6):1305-15. PubMed ID: 11402162
    [Abstract] [Full Text] [Related]

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