Cited by 382

The DOI matches its Crossref record; 162 of the 162 references it cites were found in a registry or an index.

Shade Avoidance

Open access

Casal, Jorge J.·2012·The Arabidopsis Book

Open this paper in CoChat — free account

Abstract

The presence of neighboring vegetation modifies the light environment experienced by plants, generating signals that are perceived by phytochromes and cryptochromes. These signals cause large changes in plant body form and function, including enhanced growth of the hypocotyl and petioles, a more erect position of the leaves and early flowering in Arabidopsis thaliana. Collectively, these so-called shade-avoidance responses tend to reduce the degree of current or future shade by neighbors. Shade light signals increase the abundance of PHYTOCHROME INTERACTING FACTOR 4 (PIF4) and PIF5 proteins, promote the synthesis and redirection of auxin, favor the degradation of DELLA proteins and increase the expression of auxin, gibberellins and brassinosteroid-promoted genes, among other events downstream the photoreceptors. Selectively disrupting these events by genetic or pharmacological approaches affects shade-avoidance responses with an intensity that depends on the developmental context and the environment. Shade-avoidance responses provide a model to investigate the signaling networks used by plants to take advantage of the cues provided by the environment to adjust to the challenges imposed by the environment itself.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1199/tab.0157

Cites

162 of 162 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Growth of the plant cell wall
Cosgrove, D. J. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1746 · Cited by 3,308
FT Protein Movement Contributes to Long-Distance Signaling in Floral Induction of Arabidopsis
Corbesier, L., Vincent, C., Jang, S., Fornara, F., Fan, Q., Searle, I., Giakountis, A., Farrona, S., Gissot, L., Turnbull, C., et al. (2007) · Science · doi:10.1126/science.1141752 · Cited by 2,253
The F-box protein TIR1 is an auxin receptor
Dharmasiri, N., Dharmasiri, S., & Estelle, M. (2005) · Nature · doi:10.1038/nature03543 · Cited by 2,083
FLOWERING LOCUS C Encodes a Novel MADS Domain Protein That Acts as a Repressor of Flowering
Michaels, S. D., & Amasino, R. M. (1999) · The Plant Cell · doi:10.1105/tpc.11.5.949 · Cited by 1,992
The Arabidopsis F-box protein TIR1 is an auxin receptor
Kepinski, S., & Leyser, O. (2005) · Nature · doi:10.1038/nature03542 · Cited by 1,714
CONSTANS mediates between the circadian clock and the control of flowering in Arabidopsis
Suárez-López, P., Wheatley, K., Robson, F., Onouchi, H., Valverde, F., & Coupland, G. (2001) · Nature · doi:10.1038/35074138 · Cited by 1,463
Lateral relocation of auxin efflux regulator PIN3 mediates tropism in Arabidopsis
Friml, J., Wiśniewska, J., Benková, E., Mendgen, K., & Palme, K. (2002) · Nature · doi:10.1038/415806a · Cited by 1,426
A molecular framework for light and gibberellin control of cell elongation
de Lucas, M., Davière, J.-M., Rodríguez-Falcón, M., Pontin, M., Iglesias-Pedraz, J. M., Lorrain, S., Fankhauser, C., Blázquez, M. A., Titarenko, E., & Prat, S. (2008) · Nature · doi:10.1038/nature06520 · Cited by 1,319
Photoreceptor Regulation of CONSTANS Protein in Photoperiodic Flowering
Valverde, F., Mouradov, A., Soppe, W., Ravenscroft, D., Samach, A., & Coupland, G. (2004) · Science · doi:10.1126/science.1091761 · Cited by 1,309
A Role for Flavin Monooxygenase-Like Enzymes in Auxin Biosynthesis
Zhao, Y., Christensen, S. K., Fankhauser, C., Cashman, J. R., Cohen, J. D., Weigel, D., & Chory, J. (2001) · Science · doi:10.1126/science.291.5502.306 · Cited by 1,225
Perception of UV-B by the Arabidopsis UVR8 Protein
Rizzini, L., Favory, J.-J., Cloix, C., Faggionato, D., O’Hara, A., Kaiserli, E., Baumeister, R., Schäfer, E., Nagy, F., Jenkins, G. I., et al. (2011) · Science · doi:10.1126/science.1200660 · Cited by 1,134
Coordinated regulation of Arabidopsis thaliana development by light and gibberellins
Feng, S., Martinez, C., Gusmaroli, G., Wang, Y., Zhou, J., Wang, F., Chen, L., Yu, L., Iglesias-Pedraz, J. M., Kircher, S., et al. (2008) · Nature · doi:10.1038/nature06448 · Cited by 1,115
Rapid Synthesis of Auxin via a New Tryptophan-Dependent Pathway Is Required for Shade Avoidance in Plants
Tao, Y., Ferrer, J.-L., Ljung, K., Pojer, F., Hong, F., Long, J. A., Li, L., Moreno, J. E., Bowman, M. E., Ivans, L. J., et al. (2008) · Cell · doi:10.1016/j.cell.2008.01.049 · Cited by 1,059
PIFs: pivotal components in a cellular signaling hub
Leivar, P., & Quail, P. H. (2011) · Trends in Plant Science · doi:10.1016/j.tplants.2010.08.003 · Cited by 972
Mutations in the gene for the red/far-red light receptor phytochrome B alter cell elongation and physiological responses throughout Arabidopsis development.
Reed, J. W., Nagpal, P., Poole, D. S., Furuya, M., & Chory, J. (1993) · The Plant Cell · doi:10.1105/tpc.5.2.147 · Cited by 943
The ELF4–ELF3–LUX complex links the circadian clock to diurnal control of hypocotyl growth
Nusinow, D. A., Helfer, A., Hamilton, E. E., King, J. J., Imaizumi, T., Schultz, T. F., Farré, E. M., & Kay, S. A. (2011) · Nature · doi:10.1038/nature10182 · Cited by 907
Arabidopsis BRANCHED1 Acts as an Integrator of Branching Signals within Axillary Buds
Aguilar-Martínez, J. A., Poza-Carrión, C., & Cubas, P. (2007) · The Plant Cell · doi:10.1105/tpc.106.048934 · Cited by 883
Cloning of the Arabidopsis Clock Gene TOC1 , an Autoregulatory Response Regulator Homolog
Strayer, C., Oyama, T., Schultz, T. F., Raman, R., Somers, D. E., Más, P., Panda, S., Kreps, J. A., & Kay, S. A. (2000) · Science · doi:10.1126/science.289.5480.768 · Cited by 849
BRI1 is a critical component of a plasma-membrane receptor for plant steroids
Wang, Z.-Y., Seto, H., Fujioka, S., Yoshida, S., & Chory, J. (2001) · Nature · doi:10.1038/35066597 · Cited by 846
Signal integration in the control of shoot branching
Domagalska, M. A., & Leyser, O. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3088 · Cited by 835
The Arabidopsis HY5 gene encodes a bZIP protein that regulates stimulus-induced development of root and hypocotyl
Oyama, T., Shimura, Y., & Okada, K. (1997) · Genes & Development · doi:10.1101/gad.11.22.2983 · Cited by 833
Phytochrome‐mediated inhibition of shade avoidance involves degradation of growth‐promoting bHLH transcription factors
Lorrain, S., Allen, T., Duek, P. D., Whitelam, G. C., & Fankhauser, C. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03341.x · Cited by 812
Phototropins 1 and 2: versatile plant blue-light receptors
Briggs, W. R., & Christie, J. M. (2002) · Trends in Plant Science · doi:10.1016/s1360-1385(02)02245-8 · Cited by 785 · cited 1×
“Canopies are heterogeneous and create horizontal gradients that can be perceived by phototropins (Briggs and Christie, 2002).”
Cytokinin action in plant development
Werner, T., & Schmülling, T. (2009) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2009.07.002 · Cited by 763
Molecular basis of seasonal time measurement in Arabidopsis
Yanovsky, M. J., & Kay, S. A. (2002) · Nature · doi:10.1038/nature00996 · Cited by 689
Far-Red Radiation Reflected from Adjacent Leaves: An Early Signal of Competition in Plant Canopies
Ballaré, C. L., Scopel, A. L., & Sánchez, R. A. (1990) · Science · doi:10.1126/science.247.4940.329 · Cited by 657
LHY and CCA1 Are Partially Redundant Genes Required to Maintain Circadian Rhythms in Arabidopsis
Mizoguchi, T., Wheatley, K., Hanzawa, Y., Wright, L., Mizoguchi, M., Song, H.-R., Carré, I. A., & Coupland, G. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00170-3 · Cited by 638
Towards an understanding of photosynthetic acclimation
Walters, R. G. (2004) · Journal of Experimental Botany · doi:10.1093/jxb/eri060 · Cited by 630
Multiple Phytochrome-Interacting bHLH Transcription Factors Repress Premature Seedling Photomorphogenesis in Darkness
Leivar, P., Monte, E., Oka, Y., Liu, T., Carle, C., Castillon, A., Huq, E., & Quail, P. H. (2008) · Current Biology · doi:10.1016/j.cub.2008.10.058 · Cited by 603
Phytochrome Signaling Mechanisms
Li, J., Li, G., Wang, H., & Wang Deng, X. (2011) · The Arabidopsis Book · doi:10.1199/tab.0148 · Cited by 561
Action spectra for phytochrome A- and B-specific photoinduction of seed germination in Arabidopsis thaliana.
Shinomura, T., Nagatani, A., Hanzawa, H., Kubota, M., Watanabe, M., & Furuya, M. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.15.8129 · Cited by 545
Regulation of flowering time by light quality
Cerdán, P. D., & Chory, J. (2003) · Nature · doi:10.1038/nature01636 · Cited by 543
A Repressor Complex Governs the Integration of Flowering Signals in Arabidopsis
Li, D., Liu, C., Shen, L., Wu, Y., Chen, H., Robertson, M., Helliwell, C. A., Ito, T., Meyerowitz, E., & Yu, H. (2008) · Developmental Cell · doi:10.1016/j.devcel.2008.05.002 · Cited by 522
Phytochromes promote seedling light responses by inhibiting four negatively-acting phytochrome-interacting factors
Shin, J., Kim, K., Kang, H., Zulfugarov, I. S., Bae, G., Lee, C.-H., Lee, D., & Choi, G. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0812219106 · Cited by 516
AXR2 Encodes a Member of the Aux/IAA Protein Family
Nagpal, P., Walker, L. M., Young, J. C., Sonawala, A., Timpte, C., Estelle, M., & Reed, J. W. (2000) · Plant Physiology · doi:10.1104/pp.123.2.563 · Cited by 470
Constitutive Photomorphogenesis 1 and Multiple Photoreceptors Control Degradation of Phytochrome Interacting Factor 3, a Transcription Factor Required for Light Signaling in Arabidopsis
Bauer, D., Viczián, A., Kircher, S., Nobis, T., Nitschke, R., Kunkel, T., Panigrahi, K. C. S., Ádám, É., Fejes, E., Schäfer, E., et al. (2004) · The Plant Cell · doi:10.1105/tpc.021568 · Cited by 443
Cryptochrome Blue Light Photoreceptors Are Activated through Interconversion of Flavin Redox States
Bouly, J.-P., Schleicher, E., Dionisio-Sese, M., Vandenbussche, F., Van Der Straeten, D., Bakrim, N., Meier, S., Batschauer, A., Galland, P., Bittl, R., et al. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m609842200 · Cited by 441
Early detection of neighbour plants by phytochrome perception of spectral changes in reflected sunlight
BALLARÉ, C. L., SÁNCHEZ, R. A., SCOPEL, A. L., CASAL, J. J., & GHERSA, C. M. (1987) · Plant, Cell & Environment · doi:10.1111/1365-3040.ep11604091 · Cited by 438
Self-citation
COP1 and ELF3 Control Circadian Function and Photoperiodic Flowering by Regulating GI Stability
Yu, J.-W., Rubio, V., Lee, N.-Y., Bai, S., Lee, S.-Y., Kim, S.-S., Liu, L., Zhang, Y., Irigoyen, M. L., Sullivan, J. A., et al. (2008) · Molecular Cell · doi:10.1016/j.molcel.2008.09.026 · Cited by 425
Seed Dormancy and Germination
Bentsink, L., & Koornneef, M. (2008) · The Arabidopsis Book · doi:10.1199/tab.0119 · Cited by 422
The Arabidopsis Phytochrome-Interacting Factor PIF7, Together with PIF3 and PIF4, Regulates Responses to Prolonged Red Light by Modulating phyB Levels
Leivar, P., Monte, E., Al-Sady, B., Carle, C., Storer, A., Alonso, J. M., Ecker, J. R., & Quail, P. H. (2008) · The Plant Cell · doi:10.1105/tpc.107.052142 · Cited by 418
Genetic and molecular analysis of an allelic series of cop1 mutants suggests functional roles for the multiple protein domains.
McNellis, T. W., von Arnim, A. G., Araki, T., Komeda, Y., Miséra, S., & Deng, X. W. (1994) · The Plant Cell · doi:10.1105/tpc.6.4.487 · Cited by 413
Integration of auxin and brassinosteroid pathways by Auxin Response Factor 2
Vert, G., Walcher, C. L., Chory, J., & Nemhauser, J. L. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0803996105 · Cited by 406
Inhibition of the shade avoidance response by formation of non‐DNA binding bHLH heterodimers
Hornitschek, P., Lorrain, S., Zoete, V., Michielin, O., & Fankhauser, C. (2009) · The EMBO Journal · doi:10.1038/emboj.2009.306 · Cited by 405
The Cryptochrome Blue Light Receptors
Yu, X., Liu, H., Klejnot, J., & Lin, C. (2010) · The Arabidopsis Book · doi:10.1199/tab.0135 · Cited by 338
Shade avoidance responses are mediated by the ATHB-2 HD-Zip protein, a negative regulator of gene expression
Steindler, C., Matteucci, A., Sessa, G., Weimar, T., Ohgishi, M., Aoyama, T., Morelli, G., & Ruberti, I. (1999) · Development · doi:10.1242/dev.126.19.4235 · Cited by 336
cis-Regulatory Elements and Chromatin State Coordinately Control Temporal and Spatial Expression of FLOWERING LOCUS T in Arabidopsis
Adrian, J., Farrona, S., Reimer, J. J., Albani, M. C., Coupland, G., & Turck, F. (2010) · The Plant Cell · doi:10.1105/tpc.110.074682 · Cited by 336
Phytochrome E Influences Internode Elongation and Flowering Time in Arabidopsis
Devlin, P. F., Patel, S. R., & Whitelam, G. C. (1998) · The Plant Cell · doi:10.1105/tpc.10.9.1479 · Cited by 334
Gating of the rapid shade-avoidance response by the circadian clock in plants
Salter, M. G., Franklin, K. A., & Whitelam, G. C. (2003) · Nature · doi:10.1038/nature02174 · Cited by 328
Interaction of the Response Regulator ARR4 with Phytochrome B in Modulating Red Light Signaling
Sweere, U., Eichenberg, K., Lohrmann, J., Mira-Rodado, V., Bäurle, I., Kudla, J., Nagy, F., Schäfer, E., & Harter, K. (2001) · Science · doi:10.1126/science.1065022 · Cited by 325
Phytochrome control of flowering is temperature sensitive and correlates with expression of the floral integrator FT
Halliday, K. J., Salter, M. G., Thingnaes, E., & Whitelam, G. C. (2003) · The Plant Journal · doi:10.1046/j.1365-313x.2003.01674.x · Cited by 323
A Test of the Adaptive Plasticity Hypothesis Using Transgenic and Mutant Plants Disabled in Phytochrome-Mediated Elongation Responses to Neighbors
Schmitt, J., McCormac, A. C., & Smith, H. (1995) · The American Naturalist · doi:10.1086/285832 · Cited by 318
Gibberellin Metabolism, Perception and Signaling Pathways in Arabidopsis
Sun, T.-P. (2008) · The Arabidopsis Book · doi:10.1199/tab.0103 · Cited by 299
Cryptochromes, Phytochromes, and COP1 Regulate Light-Controlled Stomatal Development in Arabidopsis
Kang, C.-Y., Lian, H.-L., Wang, F.-F., Huang, J.-R., & Yang, H.-Q. (2009) · The Plant Cell · doi:10.1105/tpc.109.069765 · Cited by 298
Jasmonate-induced defenses: a tale of intelligence, collaborators and rascals
Ballaré, C. L. (2011) · Trends in Plant Science · doi:10.1016/j.tplants.2010.12.001 · Cited by 295
A systematic relationship between phytochrome-controlled development and species habitat, for plants grown in simulated natural radiation
Morgan, D. C., & Smith, H. (1979) · Planta · doi:10.1007/bf00454449 · Cited by 291
The Arabidopsis DIMINUTO/DWARF1 Gene Encodes a Protein Involved in Steroid Synthesis
Klahre, U., Noguchi, T., Fujioka, S., Takatsuto, S., Yokota, T., Nomura, T., Yoshida, S., & Chua, N.-H. (1998) · The Plant Cell · doi:10.1105/tpc.10.10.1677 · Cited by 289
Auxin transport through PIN-FORMED 3 (PIN3) controls shade avoidance and fitness during competition
Keuskamp, D. H., Pollmann, S., Voesenek, L. A. C. J., Peeters, A. J. M., & Pierik, R. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1013457108 · Cited by 284
Ecological modulation of plant defense via phytochrome control of jasmonate sensitivity
Moreno, J. E., Tao, Y., Chory, J., & Ballaré, C. L. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900701106 · Cited by 283
Phytochrome B Represses Teosinte Branched1 Expression and Induces Sorghum Axillary Bud Outgrowth in Response to Light Signals
Kebrom, T. H., Burson, B. L., & Finlayson, S. A. (2006) · Plant Physiology · doi:10.1104/pp.105.074856 · Cited by 280
Phytochromes B, D, and E Act Redundantly to Control Multiple Physiological Responses in Arabidopsis
Franklin, K. A., Praekelt, U., Stoddart, W. M., Billingham, O. E., Halliday, K. J., & Whitelam, G. C. (2003) · Plant Physiology · doi:10.1104/pp.102.015487 · Cited by 280
A Genomic Analysis of the Shade Avoidance Response in Arabidopsis
Devlin, P. F., Yanovsky, M. J., & Kay, S. A. (2003) · Plant Physiology · doi:10.1104/pp.103.034397 · Cited by 275
Phytochrome signalling modulates the SA‐perceptive pathway in Arabidopsis
Genoud, T., Buchala, A. J., Chua, N., & Métraux, J. (2002) · The Plant Journal · doi:10.1046/j.1365-313x.2002.01338.x · Cited by 271
BIG: a calossin-like protein required for polar auxin transport in Arabidopsis
Gil, P., Dewey, E., Friml, J., Zhao, Y., Snowden, K. C., Putterill, J., Palme, K., Estelle, M., & Chory, J. (2001) · Genes & Development · doi:10.1101/gad.905201 · Cited by 269
Phytochrome D Acts in the Shade-Avoidance Syndrome in Arabidopsis by Controlling Elongation Growth and Flowering Time1
Devlin, P. F., Robson, P. R. H., Patel, S. R., Goosey, L., Sharrock, R. A., & Whitelam, G. C. (1999) · Plant Physiology · doi:10.1104/pp.119.3.909 · Cited by 266
Spectral Distribution of Light in a Tobacco Canopy and Effects of End-of-Day Light Quality on Growth and Development
Kasperbauer, M. J. (1971) · Plant Physiology · doi:10.1104/pp.47.6.775 · Cited by 264
The Signaling State of Arabidopsis Cryptochrome 2 Contains Flavin Semiquinone
Banerjee, R., Schleicher, E., Meier, S., Viana, R. M., Pokorny, R., Ahmad, M., Bittl, R., & Batschauer, A. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m700616200 · Cited by 262
DELLA protein function in growth responses to canopy signals
Djakovic‐Petrovic, T., Wit, M. D., Voesenek, L. A. C. J., & Pierik, R. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03122.x · Cited by 258
Cryptochrome 1 and phytochrome B control shade‐avoidance responses in Arabidopsis via partially independent hormonal cascades
Keller, M. M., Jaillais, Y., Pedmale, U. V., Moreno, J. E., Chory, J., & Ballaré, C. L. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04598.x · Cited by 257
A dynamic balance between gene activation and repression regulates the shade avoidance response in Arabidopsis
Sessa, G., Carabelli, M., Sassi, M., Ciolfi, A., Possenti, M., Mittempergher, F., Becker, J., Morelli, G., & Ruberti, I. (2005) · Genes & Development · doi:10.1101/gad.364005 · Cited by 256
The ROTUNDIFOLIA3 gene of Arabidopsis thaliana encodes a new member of the cytochrome P-450 family that is required for the regulated polar elongation of leaf cells
Kim, G.-T., Tsukaya, H., & Uchimiya, H. (1998) · Genes & Development · doi:10.1101/gad.12.15.2381 · Cited by 254
Cryptochrome as a Sensor of the Blue/Green Ratio of Natural Radiation in Arabidopsis
Sellaro, R., Crepy, M., Trupkin, S. A., Karayekov, E., Buchovsky, A. S., Rossi, C., & Casal, J. J. (2010) · Plant Physiology · doi:10.1104/pp.110.160820 · Cited by 249
Self-citation
Arabidopsis TEOSINTE BRANCHED1-LIKE 1 Regulates Axillary Bud Outgrowth and is Homologous to Monocot TEOSINTE BRANCHED1
Finlayson, S. A. (2007) · Plant and Cell Physiology · doi:10.1093/pcp/pcm044 · Cited by 242
Phytochrome regulation of branching in Arabidopsis
Finlayson, S. A., Krishnareddy, S. R., Kebrom, T. H., & Casal, J. J. (2010) · Plant Physiology · doi:10.1104/pp.109.148833 · Cited by 240
Self-citation
Tillering Responses to Enrichment of Red Light Beneath the Canopy in a Humid Natural Grassland
Deregibus, V. A., Sánchez, R. A., Casal, J. J., et al. (1985) · Journal of Applied Ecology · doi:10.2307/2403337 · Cited by 234
Self-citation
Interaction of shade avoidance and auxin responses: a role for two novel atypical bHLH proteins
Roig‐Villanova, I., Bou‐Torrent, J., Galstyan, A., Carretero‐Paulet, L., Portolés, S., Rodríguez‐Concepción, M., & Martínez‐García, J. F. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601890 · Cited by 226
Photoreversible Control of Elongation of Pinto Beans and Other Plants under Normal Conditions of Growth
Downs, R. J., Hendricks, S. B., & Borthwick, H. A. (1957) · Botanical Gazette · doi:10.1086/335946 · Cited by 223
Linear relationship between phytochrome photoequilibrium and growth in plants under simulated natural radiation
MORGAN, D. C., & SMITH, H. (1976) · Nature · doi:10.1038/262210a0 · Cited by 217
Canopy shade causes a rapid and transient arrest in leaf development through auxin-induced cytokinin oxidase activity
Carabelli, M., Possenti, M., Sessa, G., Ciolfi, A., Sassi, M., Morelli, G., & Ruberti, I. (2007) · Genes & Development · doi:10.1101/gad.432607 · Cited by 216
Phytochrome B and at Least One Other Phytochrome Mediate the Accelerated Flowering Response of Arabidopsis thaliana L. to Low Red/Far-Red Ratio
Halliday, K. J., Koornneef, M., & Whitelam, G. C. (1994) · Plant Physiology · doi:10.1104/pp.104.4.1311 · Cited by 214
The function, action and adaptive significance of phytochrome in light‐grown plants
CASAL, J. J., & SMITH, H. (1989) · Plant, Cell & Environment · doi:10.1111/j.1365-3040.1989.tb01966.x · Cited by 212
Self-citation
Variations in Tiller Dynamics and Morphology in Lolium multiflorum Lam.Vegetative and Reproductive Plants as affected by Differences in Red/Far-Red Irradiation
CASAL, J. J., DEREGIBUS, V. A., & SÁNCHEZ, R. A. (1985) · Annals of Botany · doi:10.1093/oxfordjournals.aob.a087040 · Cited by 211
Self-citation
Phytochrome A Mediates the Promotion of Seed Germination by Very Low Fluences of Light and Canopy Shade Light in Arabidopsis
Botto, J. F., Sanchez, R. A., Whitelam, G. C., & Casal, J. J. (1996) · Plant Physiology · doi:10.1104/pp.110.2.439 · Cited by 210
Self-citation
Phytochrome‐mediated development in land plants: red light sensing evolves to meet the challenges of changing light environments
MATHEWS, S. (2006) · Molecular Ecology · doi:10.1111/j.1365-294x.2006.03051.x · Cited by 205
Involvement of Auxin and Brassinosteroid in the Regulation of Petiole Elongation under the Shade
Kozuka, T., Kobayashi, J., Horiguchi, G., Demura, T., Sakakibara, H., Tsukaya, H., & Nagatani, A. (2010) · Plant Physiology · doi:10.1104/pp.110.156802 · Cited by 200
The HAT2 gene, a member of the HD‐Zip gene family, isolated as an auxin inducible gene by DNA microarray screening, affects auxin response in Arabidopsis
Sawa, S., Ohgishi, M., Goda, H., Higuchi, K., Shimada, Y., Yoshida, S., & Koshiba, T. (2002) · The Plant Journal · doi:10.1046/j.1365-313x.2002.01488.x · Cited by 199
Auxin and Ethylene Regulate Elongation Responses to Neighbor Proximity Signals Independent of Gibberellin and DELLA Proteins in Arabidopsis
Pierik, R., Djakovic-Petrovic, T., Keuskamp, D. H., de Wit, M., & Voesenek, L. A. C. J. (2009) · Plant Physiology · doi:10.1104/pp.108.133496 · Cited by 197
Light Quality-Mediated Petiole Elongation in Arabidopsis during Shade Avoidance Involves Cell Wall Modification by Xyloglucan Endotransglucosylase/Hydrolases
Sasidharan, R., Chinnappa, C. C., Staal, M., Elzenga, J. T. M., Yokoyama, R., Nishitani, K., Voesenek, L. A. C. J., & Pierik, R. (2010) · Plant Physiology · doi:10.1104/pp.110.162057 · Cited by 196
The Involvement of Gibberellin 20-Oxidase Genes in Phytochrome-Regulated Petiole Elongation of Arabidopsis
Hisamatsu, T., King, R. W., Helliwell, C. A., & Koshioka, M. (2005) · Plant Physiology · doi:10.1104/pp.104.059055 · Cited by 194
Effects of Light Quality on Tiller Production in Lolium spp.
Deregibus, V. A., Sanchez, R. A., & Casal, J. J. (1983) · Plant Physiology · doi:10.1104/pp.72.3.900 · Cited by 192
Self-citation
THE FUNCTION OF PHYTOCHROME IN THE NATURAL ENVIRONMENT—III. MEASUREMENT AND CALCULATION OF PHYTOCHROME PHOTOEQUILIBRIA
Smth, H., & Holmes, M. G. (1977) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1977.tb09126.x · Cited by 189
Ethylene and Auxin Control the Arabidopsis Response to Decreased Light Intensity
Vandenbussche, F., Vriezen, W. H., Smalle, J., Laarhoven, L. J. J., Harren, F. J. M., & Van Der Straeten, D. (2003) · Plant Physiology · doi:10.1104/pp.103.022665 · Cited by 188
Blue‐light‐mediated shade avoidance requires combined auxin and brassinosteroid action in Arabidopsis seedlings
Keuskamp, D. H., Sasidharan, R., Vos, I., Peeters, A. J. M., Voesenek, L. A. C. J., & Pierik, R. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04597.x · Cited by 186
Remote sensing of future competitors: Impacts on plant defenses
Izaguirre, M. M., Mazza, C. A., Biondini, M., Baldwin, I. T., & Ballaré, C. L. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0509805103 · Cited by 185
Photocontrol of stem elongation in plant neighbourhoods: effects of photon fluence rate under natural conditions of radiation
BALLARÉ, C. L., SCOPEL, A. L., & SÁNCHEZ, R. A. (1991) · Plant, Cell & Environment · doi:10.1111/j.1365-3040.1991.tb01371.x · Cited by 184
Phytochrome B Enhances Photosynthesis at the Expense of Water-Use Efficiency in Arabidopsis
Boccalandro, H. E., Rugnone, M. L., Moreno, J. E., Ploschuk, E. L., Serna, L., Yanovsky, M. J., & Casal, J. J. (2009) · Plant Physiology · doi:10.1104/pp.109.135509 · Cited by 184
Self-citation
Green Light Induces Shade Avoidance Symptoms
Zhang, T., Maruhnich, S. A., & Folta, K. M. (2011) · Plant Physiology · doi:10.1104/pp.111.180661 · Cited by 183
Shade Avoidance Responses. Driving Auxin along Lateral Routes
Morelli, G., & Ruberti, I. (2000) · Plant Physiology · doi:10.1104/pp.122.3.621 · Cited by 183
Arabidopsis thaliana life without phytochromes
Strasser, B., Sánchez-Lamas, M., Yanovsky, M. J., Casal, J. J., & Cerdán, P. D. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0910446107 · Cited by 182
Self-citation
Maize Leaves Turn Away from Neighbors
Maddonni, G. A., Otegui, M. E., Andrieu, B., Chelle, M., & Casal, J. J. (2002) · Plant Physiology · doi:10.1104/pp.009738 · Cited by 177
Self-citation
Photoconversion and Nuclear Trafficking Cycles Determine Phytochrome A's Response Profile to Far-Red Light
Rausenberger, J., Tscheuschler, A., Nordmeier, W., Wüst, F., Timmer, J., Schäfer, E., Fleck, C., & Hiltbrunner, A. (2011) · Cell · doi:10.1016/j.cell.2011.07.023 · Cited by 174
The Arabidopsis Athb‐2 and ‐4 genes are strongly induced by far‐red‐rich light
Carabelli, M., Sessa, G., Baima, S., Morelli, G., & Ruberti, I. (1993) · The Plant Journal · doi:10.1046/j.1365-313x.1993.04030469.x · Cited by 172
Searching for a photocycle of the cryptochrome photoreceptors
Liu, B., Liu, H., Zhong, D., & Lin, C. (2010) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2010.09.005 · Cited by 169
Light and shade in the photocontrol of Arabidopsis growth
Morelli, G., & Ruberti, I. (2002) · Trends in Plant Science · doi:10.1016/s1360-1385(02)02314-2 · Cited by 164
Phytochrome A, phytochrome B and HY4 are involved in hypocotyl growth responses to natural radiation in Arabidopsis: weak de‐etiolation of the phyA mutant under dense canopies
YANOVSKY, M. J., CASAL, J. J., & WHITELAM, G. C. (1995) · Plant, Cell & Environment · doi:10.1111/j.1365-3040.1995.tb00582.x · Cited by 160
Self-citation
Phytochrome B Is Not Detectable in the hy3 Mutant of Arabidopsis, Which Is Deficient in Responding to End-of-Day Far-Red Light Treatments
Nagatani, A., Chory, J., & Furuya, M. (1991) · Plant and Cell Physiology · doi:10.1093/oxfordjournals.pcp.a078177 · Cited by 153
Identification of Primary Target Genes of Phytochrome Signaling. Early Transcriptional Control during Shade Avoidance Responses in Arabidopsis
Roig‐Villanova, I., Bou‐Torrent, J., Sorin, C., Devlin, P. F., & Martínez‐García, J. F. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.076331 · Cited by 153
ATHB4, a regulator of shade avoidance, modulates hormone response in Arabidopsis seedlings
Sorin, C., Salla‐Martret, M., Bou‐Torrent, J., Roig‐Villanova, I., & Martínez‐García, J. F. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.03866.x · Cited by 146
The Arabidopsis thaliana myo-Inositol 1-Phosphate Synthase (EC 5.5.1.4)
Johnson, M. D. (1994) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.3.1023 · Cited by 141
Phytochrome degradation
Clough, R. C., & Vierstra, R. D. (1997) · Plant Cell & Environment · doi:10.1046/j.1365-3040.1997.d01-107.x · Cited by 138
The fall and rise of apical dominance
Leyser, O. (2005) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2005.06.010 · Cited by 135
Selected Components of the Shade-Avoidance Syndrome Are Displayed in a Normal Manner in Mutants of Arabidopsis thaliana and Brassica rapa Deficient in Phytochrome B
Robson, P. R. H., Whitelam, G. C., & Smith, H. (1993) · PLANT PHYSIOLOGY · doi:10.1104/pp.102.4.1179 · Cited by 135
AtBBX21 and COP1 genetically interact in the regulation of shade avoidance: B-box zinc finger proteins and shade avoidance
Crocco, C. D., Holm, M., Yanovsky, M. J., & Botto, J. F. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04360.x · Cited by 134
Rapid photomodulation of stem extension in light-grownSinapis alba L. Studies on kinetics, site of perception and photoreceptor
Morgan, D. C., O'Brien, T., & Smith, H. (1980) · Planta · doi:10.1007/bf00582351 · Cited by 127
Phytochromes Regulate SA and JA Signaling Pathways in Rice and Are Required for Developmentally Controlled Resistance to Magnaporthe grisea
Xie, X., Xue, Y., Zhou, J., Zhang, B., Chang, H., & Takano, M. (2011) · Molecular Plant · doi:10.1093/mp/ssr005 · Cited by 127
Phytochrome B Affects Responsiveness to Gibberellins in Arabidopsis
Reed, J. W., Foster, K. R., Morgan, P. W., & Chory, J. (1996) · PLANT PHYSIOLOGY · doi:10.1104/pp.112.1.337 · Cited by 126
Phenotypic characterization of a photomorphogenic mutant
Fankhauser, C., & Casal, J. J. (2004) · The Plant Journal · doi:10.1111/j.1365-313x.2004.02148.x · Cited by 125
Self-citation
Acceleration of Flowering during Shade Avoidance in Arabidopsis Alters the Balance betweenFLOWERING LOCUS C-Mediated Repression and Photoperiodic Induction of Flowering
Wollenberg, A. C., Strasser, B., Cerdán, P. D., & Amasino, R. M. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.125468 · Cited by 125
Post-transcriptional control of the Arabidopsis auxin efflux carrier EIR1 requires AXR1
Sieberer, T., Seifert, G. J., Hauser, M., Grisafi, P. L., Fink, G. R., & Luschnig, C. (2000) · Current Biology · doi:10.1016/s0960-9822(00)00861-7 · Cited by 120
Network Analysis Identifies ELF3 as a QTL for the Shade Avoidance Response in Arabidopsis
Jiménez‐Gómez, J. M., Wallace, A. D., & Maloof, J. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1001100 · Cited by 119
CRYPTOCHROME 1 Is Implicated in Promoting R Protein-Mediated Plant Resistance to Pseudomonas syringae in Arabidopsis
Wu, L., & Yang, H. (2010) · Molecular Plant · doi:10.1093/mp/ssp107 · Cited by 118
Lotus japonicus nodulation is photomorphogenetically controlled by sensing the red/far red (R/FR) ratio through jasmonic acid (JA) signaling
Suzuki, A., Suriyagoda, L. D. B., Shigeyama, T., Tominaga, A., Sasaki, M., Hiratsuka, Y., Yoshinaga, A., Arima, S., Agarie, S., Sakai, T., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1105892108 · Cited by 118
The rosette habit of Arabidopsis thaliana is dependent upon phytochrome action: novel phytochromes control internode elongation and flowering time
Devlin, P. F., Halliday, K., Harberd, N. P., & Whitelam, G. C. (1996) · The Plant Journal · doi:10.1046/j.1365-313x.1996.10061127.x · Cited by 115
Far-red enrichment and photosynthetically active radiation level influence leaf senescence in field-grown sunflower
Rousseaux, M. C., Hall, A. J., & Sánchez, R. A. (1996) · Physiologia Plantarum · doi:10.1034/j.1399-3054.1996.960208.x · Cited by 114
Shade avoidance and the regulation of leaf inclination in Arabidopsis
Mullen, J. L., Weinig, C., & Hangarter, R. P. (2006) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2005.01484.x · Cited by 108
Differential genetic variation in adaptive strategies to a common environmental signal in Arabidopsis accessions: phytochrome‐mediated shade avoidance
Botto, J. F., & Smith, H. (2002) · Plant Cell & Environment · doi:10.1046/j.0016-8025.2001.00812.x · Cited by 106
Modulation of leaf elongation, tiller appearance and tiller senescence in spring barley by far‐red light
Skinner, R. H., & Simmons, S. R. (1993) · Plant Cell & Environment · doi:10.1111/j.1365-3040.1993.tb00903.x · Cited by 104
The shade avoidance syndrome in Arabidopsis: a fundamental role for atypical basic helix–loop–helix proteins as transcriptional cofactors
Galstyan, A., Cifuentes‐Esquivel, N., Bou‐Torrent, J., & Martínez‐García, J. F. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04485.x · Cited by 101
Mutations in the huge Arabidopsis gene BIG affect a range of hormone and light responses
Kanyuka, K., Praekelt, U. M., Franklin, K. A., Billingham, O. E., Hooley, R., Whitelam, G. C., & Halliday, K. (2003) · The Plant Journal · doi:10.1046/j.1365-313x.2003.01779.x · Cited by 97
A Constitutive Shade-Avoidance Mutant Implicates TIR-NBS-LRR Proteins inArabidopsisPhotomorphogenic Development
Soverna, A. F., Harmon, F. G., Storani, L., Karayekov, E., Staneloni, R. J., Gassmann, W., Más, P., Casal, J. J., Kay, S. A., & Yanovsky, M. J. (2006) · The Plant Cell · doi:10.1105/tpc.105.038810 · Cited by 96
Self-citation
Low red/far-red ratios delay spike and stem growth in wheat
Ugarte, C. C., Trupkin, S. A., Ghiglione, H., Slafer, G. A., & Casal, J. J. (2010) · Journal of Experimental Botany · doi:10.1093/jxb/erq140 · Cited by 94
Self-citation
Tillering Responses ofLolium multiflorumPlants to Changes of Red/Far-Red Ratio Typical of Sparse Canopies
Casal, J. J., SÁCHEZ, R. A., & Deregibus, V. A. (1987) · Journal of Experimental Botany · doi:10.1093/jxb/38.9.1432 · Cited by 92
Self-citation
Phytochrome signalling in plant canopies: testing its population‐level implications with photoreceptor mutants of Arabidopsis
Ballaré, C. L., & Scopel, A. L. (1997) · Functional Ecology · doi:10.1046/j.1365-2435.1997.00108.x · Cited by 92
On the opportunity cost of the photosynthate invested in stem elongation reactions mediated by phytochrome
Ballaré, C. L., Scopel, A. L., & Sánchez, R. A. (1991) · Oecologia · doi:10.1007/bf00318323 · Cited by 92
Brassinosteroid Mutants Uncover Fine Tuning of Phytochrome Signaling
Luccioni, L. G., Oliverio, K. A., Yanovsky, M. J., Boccalandro, H. E., & Casal, J. J. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.010668 · Cited by 90
Self-citation
Automated analysis of hypocotyl growth dynamics during shade avoidance in Arabidopsis
Cole, B., Kay, S. A., & Chory, J. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04476.x · Cited by 88
Differential petiole growth in Arabidopsis thaliana: photocontrol and hormonal regulation
Millenaar, F. F., van Zanten, M., Cox, M. C. H., Pierik, R., Voesenek, L. A. C. J., & Peeters, A. J. M. (2009) · New Phytologist · doi:10.1111/j.1469-8137.2009.02921.x · Cited by 85
RESPONSES OF LIGHT‐GROWN WILD‐TYPE and LONG‐HYPOCOTYL MUTANT CUCUMBER SEEDLINGS TO NATURAL and SIMULATED SHADE LIGHT*
Ballaré, C. L., Casal, J. J., & Kendrick, R. E. (1991) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1991.tb02096.x · Cited by 84
Self-citation
Phytochrome A is an irradiance‐dependent red light sensor
Franklin, K. A., Allen, T., & Whitelam, G. C. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03036.x · Cited by 81
Biochemical Characterization of Arabidopsis Wild-Type and Mutant Phytochrome B Holoproteins
Elich, T. D., & Chory, J. (1997) · The Plant Cell · doi:10.1105/tpc.9.12.2271 · Cited by 79
The significance of changes in the red/far‐red ratio, associated with either neighbour plants or twilight, for tillering in Lolium multiflorum Lam.
Casal, J. J., Sánchez, R. A., & GIBSON, D. (1990) · New Phytologist · doi:10.1111/j.1469-8137.1990.tb00540.x · Cited by 77
Self-citation
Antagonistic but Complementary Actions of Phytochromes A and B Allow Optimum Seedling De-Etiolation
Smith, H., Xu, Y., & Quail, P. H. (1997) · PLANT PHYSIOLOGY · doi:10.1104/pp.114.2.637 · Cited by 76
Genes affecting phenotypic plasticity in Arabidopsis: pleiotropic effects and reproductive fitness of photomorphogenic mutants
Pigliucci, & Schmitt (1999) · Journal of Evolutionary Biology · doi:10.1046/j.1420-9101.1999.00057.x · Cited by 75
Repression of shade‐avoidance reactions by sunfleck induction of HY5 expression in Arabidopsis
Sellaro, R., Yanovsky, M. J., & Casal, J. J. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04745.x · Cited by 73
Self-citation
Light quality effects on the appearance of tillers of different order in wheat (Triticum aestivum)
Casal, J. J. (1988) · Annals of Applied Biology · doi:10.1111/j.1744-7348.1988.tb02052.x · Cited by 73
Self-citation
Hierarchical coupling of phytochromes and cryptochromes reconciles stability and light modulation ofArabidopsisdevelopment
Mazzella, M. A., Cerdán, P. D., Staneloni, R. J., & Casal, J. J. (2001) · Development · doi:10.1242/dev.128.12.2291 · Cited by 69
Self-citation
Dual effect of phytochrome A on hypocotyl growth under continuous red light
Mazzella, M. A., Magliano, T. M. A., & Casal, J. J. (1997) · Plant Cell & Environment · doi:10.1046/j.1365-3040.1997.d01-62.x · Cited by 68
Self-citation
Photomodulation of Axis Extension in Sparse Canopies
Ballaré, C. L., Scopel, A. L., & Sánchez, R. A. (1989) · PLANT PHYSIOLOGY · doi:10.1104/pp.89.4.1324 · Cited by 66
Phototropism: Mechanism and Outcomes
Pedmale, U. V., Celaya, R. B., & Liscum, E. (2010) · The Arabidopsis Book · doi:10.1199/tab.0125 · Cited by 66
Regulation of phytochrome B signaling by phytochrome A and FHY1 in Arabidopsis thaliana
Cerdán, P. D., Yanovsky, M. J., Reymundo, F. C., Nagatani, A., Staneloni, R. J., Whitelam, G. C., & Casal, J. J. (1999) · The Plant Journal · doi:10.1046/j.1365-313x.1999.00475.x · Cited by 63
Self-citation
Temperature-dependent internode elongation in vegetative plants of Arabidopsis thaliana lacking phytochrome B and cryptochrome 1
Mazzella, M. A., Bertero, D., & Casal, J. J. (2000) · Planta · doi:10.1007/pl00008157 · Cited by 60
Self-citation
Photosynthetic photon flux density and phytochrome B interact to regulate branching in Arabidopsis
Su, H., Abernathy, S. D., White, R. H., & Finlayson, S. A. (2011) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2011.02393.x · Cited by 56
Anatomy, Growth and Survival of a Long-hypocotyl Mutant of Cucumis sativus Deficient in Phytochrome B
Casal, J. J. (1994) · Annals of Botany · doi:10.1006/anbo.1994.1071 · Cited by 55
Self-citation
The Arabidopsis Myb genes MYR1 and MYR2 are redundant negative regulators of flowering time under decreased light intensity
Zhao, C., Hanada, A., Yamaguchi, S., Kamiya, Y., & Beers, E. P. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04508.x · Cited by 54
Genetic mapping of natural variation in a shade avoidance response: ELF3 is the candidate gene for a QTL in hypocotyl growth regulation
COLUCCIO, M. P., Sánchez, S. E., Kasulin, L., Yanovsky, M. J., & Botto, J. F. (2010) · Journal of Experimental Botany · doi:10.1093/jxb/erq253 · Cited by 52
Phytochrome A Enhances the Promotion of Hypocotyl Growth Caused by Reductions in Levels of Phytochrome B in Its Far-Red-Light-Absorbing Form in Light-Grown Arabidopsis thaliana
Casal, J. J. (1996) · PLANT PHYSIOLOGY · doi:10.1104/pp.112.3.965 · Cited by 49
Self-citation
PHYTOCHROME KINASE SUBSTRATE4 Modulates Phytochrome-Mediated Control of Hypocotyl Growth Orientation
Schepens, I., Boccalandro, H. E., Kami, C., Casal, J. J., & Fankhauser, C. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.118166 · Cited by 49
Self-citation
Far-red light as a suppressor of side shoot growth in the tomato
Tucker, D. J. (1975) · Plant Science Letters · doi:10.1016/0304-4211(75)90053-x · Cited by 41
Genes underlying quantitative variation in ecologically important traits:PIF4(PHYTOCHROME INTERACTING FACTOR 4) is associated with variation in internode length, flowering time, and fruit set inArabidopsis thaliana
Brock, M. T., Maloof, J., & Weinig, C. (2010) · Molecular Ecology · doi:10.1111/j.1365-294x.2010.04538.x · Cited by 41
Variation in dynamics of phytochrome A inArabidopsisecotypes and mutants
Eichenberg, K., Hennig, L., Martin, A. E., & Schäfer, E. (2000) · Plant Cell & Environment · doi:10.1046/j.1365-3040.2000.00550.x · Cited by 33
Interactive signalling by phytochromes and cryptochromes generates de‐etiolation homeostasis inArabidopsis thaliana
Mazzella, M. A., & Casal, J. J. (2001) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2001.00653.x · Cited by 31
Self-citation
Balancing forces in the photoperiodic control of flowering
Sánchez, S. E., Cagnola, J. I., Crepy, M., Yanovsky, M. J., & Casal, J. J. (2010) · Photochemical & Photobiological Sciences · doi:10.1039/c0pp00252f · Cited by 14
Self-citation

Photoreceptor Signaling Networks in Plant Responses to Shade
Casal, J. J. (2013) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-050312-120221 · Cited by 865
Self-citation
Light Regulation of Plant Defense
Ballaré, C. L. (2014) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-050213-040145 · Cited by 560
Shade avoidance: phytochrome signalling and other aboveground neighbour detection cues
Pierik, R., & de Wit, M. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/ert389 · Cited by 298
From physics to fixtures to food: current and potential LED efficacy
Kusuma, P., Pattison, P. M., & Bugbee, B. (2020) · Horticulture Research · doi:10.1038/s41438-020-0283-7 · Cited by 283
BRANCHED1 Promotes Axillary Bud Dormancy in Response to Shade in Arabidopsis
González-Grandío, E., Poza-Carrión, C., Sorzano, C. O. S., & Cubas, P. (2013) · The Plant Cell · doi:10.1105/tpc.112.108480 · Cited by 272

See all 382

Authors: Casal, J. J.
Venue: The Arabidopsis Book
Publisher: BioOne
Published: 2012-01
Volume: 10
Pages: e0157
ISSN: 1543-8120 (ISSN-L)
DOI: 10.1199/tab.0157
OpenAlex: W4210709242
Cited by: 382
References: 162
FWCI: 15.30
Type: journal article
Language: en
Open access: bronze

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.

Shade Avoidance

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Self-check

Citations

Cites

Cited by

Metadata

Record

About these checks

Data sources