Sucrose: metabolite and signaling molecule

Sucrose metabolism: regulatory mechanisms and pivotal roles in sugar sensing and plant development

Koch, K. E. (2004) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2004.03.014 · Cited by 1,487 · see citing works

Function and regulation of plant invertases: sweet sensations

Roitsch, T. G., & González, M. (2004) · Trends in Plant Science · doi:10.1016/j.tplants.2004.10.009 · Cited by 932 · see citing works

Sucrose-Specific Induction of the Anthocyanin Biosynthetic Pathway in Arabidopsis

Solfanelli, C., Poggi, A., Loreti, E., Alpi, A., & Pierdomenico Perata, A. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.072579 · Cited by 879 · see citing works

Sucrose-Specific Induction of Anthocyanin Biosynthesis in Arabidopsis Requires the MYB75/PAP1 Gene

Teng, S., Keurentjes, J. J. B., Bentsink, L., Koornneef, M., & SMEEKENS, S. C. M. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.066688 · Cited by 715 · see citing works

Control of plant development and gene expression by sugar signaling

Gibson, S. I. (2004) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2004.11.003 · Cited by 697 · see citing works

Suppression of Sucrose Synthase Gene Expression Represses Cotton Fiber Cell Initiation, Elongation, and Seed Development

Ruan, Y., Llewellyn, D. J., & Furbank, R. T. (2003) · The Plant Cell · doi:10.1105/tpc.010108 · Cited by 502 · see citing works

Phloem Transport: Cellular Pathways and Molecular Trafficking

Turgeon, R., & Wolf, S. (2008) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.043008.092045 · Cited by 451 · see citing works

Normal growth of Arabidopsis requires cytosolic invertase but not sucrose synthase

Barratt, D. H. P., Derbyshire, P., Findlay, K., Pike, M. J., Wellner, N., Lunn, J. E., Feil, R., Simpson, C. E., Maule, A. J., & Smith, A. M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900689106 · Cited by 432 · see citing works

Molecular physiology of higher plant sucrose transporters

Sauer, N. (2007) · FEBS Letters · doi:10.1016/j.febslet.2007.03.048 · Cited by 423 · see citing works

Evidence for an essential role of the sucrose transporter in phloem loading and assimilate partitioning.

Riesmeier, J. W., Willmitzer, L., & Frommer, W. B. (1994) · The EMBO Journal · doi:10.1002/j.1460-2075.1994.tb06229.x · Cited by 419 · see citing works

Genetic evidence for the in planta role of phloem-specific plasma membrane sucrose transporters

Gottwald, J. R., Krysan, P. J., Young, J. C., Evert, R. F., & Sussman, M. R. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.250473797 · Cited by 411 · see citing works

SUT2, a Putative Sucrose Sensor in Sieve Elements

Barker, L., Kühn, C., Weise, A., Schulz, A., Gebhardt, C., Hirner, B., Hellmann, H. A., Schulze, W. X., Ward, J. M., & Frommer, W. B. (2000) · The Plant Cell · doi:10.1105/tpc.12.7.1153 · Cited by 357 · see citing works

Antisense repression of vacuolar and cell wall invertase in transgenic carrot alters early plant development and sucrose partitioning

Tang, G.-Q., Lüscher, M., & Sturm, A. (1999) · The Plant Cell · doi:10.1105/tpc.11.2.177 · Cited by 347 · see citing works

Analysis of the sucrose synthase gene family in Arabidopsis

Bieniawska, Z., Barratt, D. H. P., Garlick, A., Thole, V., Kruger, N. J., Martin, C. R., Zrenner, R. M., & Smith, A. M. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2006.03011.x · Cited by 328 · see citing works

Sucrose transporter1 functions in phloem loading in maize leaves

Slewinski, T. L., Meeley, R. B., & Braun, D. M. (2009) · Journal of Experimental Botany · doi:10.1093/jxb/ern335 · Cited by 293 · see citing works

Sucrose‐specific signalling represses translation of the Arabidopsis ATB2 bZIP transcription factor gene

Rook, F., Gerrits, N., Kortstee, A. J., van Kampen, M. D., Borrias, M., Weisbeek, P. J., & SMEEKENS, S. C. M. (1998) · The Plant Journal · doi:10.1046/j.1365-313x.1998.00205.x · Cited by 279 · see citing works

Phosphate starvation responses are mediated by sugar signaling in Arabidopsis

Karthikeyan, A. S., Varadarajan, D. K., Jain, A., Held, M., Carpita, N. C., & Raghothama, K. G. (2006) · Planta · doi:10.1007/s00425-006-0408-8 · Cited by 250 · see citing works

The sucrose regulated transcription factor bZIP11 affects amino acid metabolism by regulating the expression of ASPARAGINE SYNTHETASE1 and PROLINE DEHYDROGENASE2

Hanson, J., Hanssen, M., Wiese‐Klinkenberg, A., Hendriks, M. M. W. B., & SMEEKENS, S. C. M. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03385.x · Cited by 243 · see citing works

Transgenic tobacco plants expressing yeast-derived invertase in either the cytosol, vacuole or apoplast: a powerful tool for studying sucrose metabolism and sink/source interactions.

Sonnewald, U., Brauer, M., von Schaewen, A., Stitt, M., & Willmitzer, L. (1991) · The Plant Journal · doi:10.1111/j.1365-313x.1991.00095.x · Cited by 243 · see citing works

A Conserved Upstream Open Reading Frame Mediates Sucrose-Induced Repression of Translation[W]

Wiese‐Klinkenberg, A., Elzinga, N., Wobbes, B., & SMEEKENS, S. C. M. (2004) · The Plant Cell · doi:10.1105/tpc.019349 · Cited by 238 · see citing works

Sucrose-mediated transcriptional regulation of sucrose symporter activity in the phloem

Vaughn, M. W., Harrington, G. N., & Bush, D. R. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.172198599 · Cited by 227 · see citing works

Enhancing Sucrose Synthase Activity in Transgenic Potato (Solanum tuberosum L.) Tubers Results in Increased Levels of Starch, ADPglucose and UDPglucose and Total Yield

Baroja‐Fernández, E., Muñoz, F. J., Montero, M., Etxeberria, E., Sesma, M. T., Ovečka, M., Bahaji, A., Ezquer, I., Li, J., Prat, S., et al. (2009) · Plant and Cell Physiology · doi:10.1093/pcp/pcp108 · Cited by 215 · see citing works

Functional Characterization of the Arabidopsis AtSUC2 Sucrose/H+ Symporter by Tissue-Specific Complementation Reveals an Essential Role in Phloem Loading But Not in Long-Distance Transport

Srivastava, A. C., Ganesan, S., Ismail, I. O., & Ayre, B. G. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.124776 · Cited by 214 · see citing works

Origin of sucrose metabolism in higher plants: when, how and why?

Salerno, G. (2003) · Trends in Plant Science · doi:10.1016/s1360-1385(02)00029-8 · Cited by 202 · see citing works

Sucrose Control of Translation Mediated by an Upstream Open Reading Frame-Encoded Peptide

Rahmani, F., Hummel, M., Schuurmans, J. A. M. J., Wiese‐Klinkenberg, A., SMEEKENS, S. C. M., & Hanson, J. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.136036 · Cited by 178 · see citing works

Expression patterns within the Arabidopsis C/S1 bZIP transcription factor network: availability of heterodimerization partners controls gene expression during stress response and development

Weltmeier, F., Rahmani, F., Ehlert, A., Dietrich, K., Schütze, K., Wang, X., Chaban, C., Hanson, J., Teige, M., Harter, K., et al. (2008) · Plant Molecular Biology · doi:10.1007/s11103-008-9410-9 · Cited by 171 · see citing works

Root System Architecture in Arabidopsis Grown in Culture Is Regulated by Sucrose Uptake in the Aerial Tissues

MacGregor, D. R., Deak, K. I., Ingram, P. A., & Malamy, J. E. (2008) · The Plant Cell · doi:10.1105/tpc.107.055475 · Cited by 152 · see citing works

Transcriptional regulation of a patatin-1 gene in potato

Jefferson, R., Goldsbrough, A. P., & Bevan, M. W. (1990) · Plant Molecular Biology · doi:10.1007/bf00019396 · Cited by 150 · see citing works

Altered photosynthesis, flowering, and fruiting in transgenic tomato plants that have an increased capacity for sucrose synthesis

Micallef, B. J., Haskins, K., Vanderveer, P. J., Roh, K.-S., Shewmaker, C. K., & Sharkey, T. D. (1995) · Planta · doi:10.1007/bf00201392 · Cited by 147 · see citing works

Functional analysis of LjSUT4, a vacuolar sucrose transporter from Lotus japonicus

Reinders, A., Sivitz, A. B., Starker, C. G., Gantt, J. S., & Ward, J. M. (2008) · Plant Molecular Biology · doi:10.1007/s11103-008-9370-0 · Cited by 144 · see citing works

Apple Sucrose Transporter SUT1 and Sorbitol Transporter SOT6 Interact with Cytochrome b5 to Regulate Their Affinity for Substrate Sugars

Fan, R., Peng, C., Xu, Y., Wang, X., Li, Y., Shang, Y., Du, S., Zhao, R., Zhang, X., Zhang, L., et al. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.141374 · Cited by 134 · see citing works

CELL WALL INVERTASE 4 is required for nectar production in Arabidopsis

Ruhlmann, J. M., Kram, B. W., & Carter, C. J. (2009) · Journal of Experimental Botany · doi:10.1093/jxb/erp309 · Cited by 122 · see citing works

Cell wall invertase expression at the apical meristem alters floral, architectural, and reproductive traits in Arabidopsis thaliana

Heyer, A. G., Raap, M., Schroeer, B., Marty, B., & Willmitzer, L. (2004) · The Plant Journal · doi:10.1111/j.1365-313x.2004.02124.x · Cited by 118 · see citing works

AtCYT-INV1, a neutral invertase, is involved in osmotic stress-induced inhibition on lateral root growth in Arabidopsis

Qi, X., Wu, Z., Li, J., Mo, X., Wu, S., Chu, J., & Wu, P. (2007) · Plant Molecular Biology · doi:10.1007/s11103-007-9177-4 · Cited by 117 · see citing works

Evolution of Sucrose Synthesis

Lunn, J. E. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.010898 · Cited by 116 · see citing works

Miniature1-Encoded Cell Wall Invertase Is Essential for Assembly and Function of Wall-in-Growth in the Maize Endosperm Transfer Cell

Kang, B., Xiong, Y., Williams, D. S., Pozueta‐Romero, D., & Chourey, P. S. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.142331 · Cited by 112 · see citing works

A cytosolic invertase is required for normal growth and cell development in the model legume, Lotus japonicus

Welham, T., Pike, J., Horst, I., Flemetakis, E., Katinakis, P. K., Kaneko, T., Sato, S., Tabata, S., Perry, J. A., Parniske, M., et al. (2009) · Journal of Experimental Botany · doi:10.1093/jxb/erp169 · Cited by 111 · see citing works

Over-expression of an arabidopsis family A sucrose phosphate synthase (SPS) gene alters plant growth and fibre development

Park, J. Y., Canam, T., Kang, K., Ellis, D. D., & Mansfield, S. D. (2007) · Transgenic Research · doi:10.1007/s11248-007-9090-2 · Cited by 105 · see citing works

A feedback control element near the transcription start site of the maize Shrunken gene determines promoter activity.

Maas, C., Schaal, S., & Werr, W. (1990) · The EMBO Journal · doi:10.1002/j.1460-2075.1990.tb07552.x · Cited by 105 · see citing works

Decreased sucrose-6-phosphate phosphatase level in transgenic tobacco inhibits photosynthesis, alters carbohydrate partitioning, and reduces growth

Chen, D., Hajirezaei, M. R., Peisker, M., Tschiersch, H., Sonnewald, U., & Börnke, F. A. J. (2005) · Planta · doi:10.1007/s00425-004-1458-4 · Cited by 101 · see citing works

Sucrose-regulated expression of a chimeric potato tuber gene in leaves of transgenic tobacco plants

Wenzler, H., Mignery, G. A., Fisher, L. M., & Park, W. (1989) · Plant Molecular Biology · doi:10.1007/bf00015546 · Cited by 99 · see citing works

Transport and Sorting of the Solanum tuberosum Sucrose Transporter SUT1 Is Affected by Posttranslational Modification

Krügel, U., Veenhoff, L. M., Langbein, J. E., Wiederhold, E., Liesche, J., Friedrich, T., Grimm, B., Martinoia, E., Poolman, B., & Kühn, C. (2008) · The Plant Cell · doi:10.1105/tpc.108.058271 · Cited by 94 · see citing works

Identification and characterization of bZIP‐type transcription factors involved in carrot (Daucus carota L.) somatic embryogenesis

Guan, Y., Ren, H., Xie, H., Ma, Z., & Chen, F. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.03948.x · Cited by 84 · see citing works

Sucrose Metabolism in Plastids

Gerrits, N., Turk, S. C. H. J., van Dun, K. M. P., Hulleman, S. H. D., Visser, R. G. F., Weisbeek, P. J., & SMEEKENS, S. C. M. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.125.2.926 · Cited by 80 · see citing works

Sucrose Represses the Developmentally Controlled Transient Activation of the Plastocyanin Gene in Arabidopsis thaliana Seedlings

Dijkwel, P. P., Kock, P., Bezemer, R., Weisbeek, P. J., & SMEEKENS, S. C. M. (1996) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.2.455 · Cited by 74 · see citing works

Downregulating the sucrose transporter VpSUT1 in Verbascum phoeniceum does not inhibit phloem loading

Zhang, C., & Turgeon, R. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0904189106 · Cited by 59 · see citing works

Sucrose utilization during somatic embryo development in black spruce: involvement of apoplastic invertase in the tissue and of extracellular invertase in the medium

Iraqi, D., Le, V. Q., Lamhamedi, M. S., & Tremblay, F. M. (2005) · Journal of Plant Physiology · doi:10.1016/j.jplph.2003.06.001 · Cited by 33 · see citing works

Sucrose Regulates Elongation of Carrot Somatic Embryo Radicles as a Signal Molecule

Yang, Z., Zhang, L., Diao, F., Huang, M., & Wu, N. (2004) · Plant Molecular Biology · doi:10.1023/b:plan.0000036375.40006.d3 · Cited by 30 · see citing works

Demonstration of an intramitochondrial invertase activity and the corresponding sugar transporters of the inner mitochondrial membrane in Jerusalem artichoke (Helianthus tuberosus L.) tubers

Szarka, A., Horemans, N., Passarella, S., Tarcsay, Á., Örsi, F., Salgó, A., & Bánhegyi, G. (2008) · Planta · doi:10.1007/s00425-008-0778-1 · Cited by 24 · see citing works

Differential expression of putative floral genes in Pharbitis nil shoot apices cultured on glucose compared with sucrose

Parfitt, D. (2004) · Journal of Experimental Botany · doi:10.1093/jxb/erh234 · Cited by 15 · see citing works

How Sweet It Is: Identification of Vacuolar Sucrose Transporters

Grennan, A. K., & Gragg, J. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.900295 · Cited by 5 · see citing works

Sugar signals and the control of plant growth and development

Lastdrager, J., Hanson, J., & SMEEKENS, S. C. M. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/ert474 · Cited by 638 · see citing works

Carbohydrates in plant immunity and plant protection: roles and potential application as foliar sprays

Trouvelot, S., Héloir, M., Poinssot, B., Gauthier, A., Paris, F., Guillier, C., Combier, M., Trdá, L., Daire, X., & Adrian, M. (2014) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00592 · Cited by 415 · see citing works

Drought stress condition increases root to shoot ratio via alteration of carbohydrate partitioning and enzymatic activity in rice seedlings

Xu, W., Cui, K., Xu, A., Nie, L., Huang, J., & Peng, S. (2015) · Acta Physiologiae Plantarum · doi:10.1007/s11738-014-1760-0 · Cited by 410 · see citing works

Sugars and plant innate immunity

Moghaddam, M. R. B., & den Ende, W. V. (2012) · Journal of Experimental Botany · doi:10.1093/jxb/ers129 · Cited by 386 · see citing works

The role of sugar signaling in plant defense responses against fungal pathogens

Morkunas, I., & Ratajczak, L. (2014) · Acta Physiologiae Plantarum · doi:10.1007/s11738-014-1559-z · Cited by 364 · see citing works

Sucrose functions as a signal involved in the regulation of strawberry fruit development and ripening

Jia, H., Wang, Y., Sun, M., Li, B., Han, Y., Zhao, Y., Li, X., Ding, N., Li, C., Ji, W., et al. (2013) · New Phytologist · doi:10.1111/nph.12176 · Cited by 339 · see citing works

Sucrose and invertases, a part of the plant defense response to the biotic stresses

Tauzin, A. S., & Giardina, T. (2014) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00293 · Cited by 335 · see citing works

Plant Hormone-Mediated Regulation of Heat Tolerance in Response to Global Climate Change

Li, N., Euring, D., Cha, J. Y., Lin, Z., Lu, M.-Z., Huang, L., & Kim, W. Y. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2020.627969 · Cited by 332 · see citing works

Sucrose signaling in higher plants

Yoon, J., Cho, L., Tun, W., Jeon, J., & An, G. (2020) · Plant Science · doi:10.1016/j.plantsci.2020.110703 · Cited by 325 · see citing works

Salt stress resilience in plants mediated through osmolyte accumulation and its crosstalk mechanism with phytohormones

Singh, P., Choudhary, K. K., Chaudhary, N., Gupta, S. K., Sahu, M., Tejaswini, B., & Sarkar, S. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.1006617 · Cited by 276 · see citing works

The Sugar-Signaling Hub: Overview of Regulators and Interaction with the Hormonal and Metabolic Network

Sakr, S., Wang, M., Dédaldéchamp, F., Pérez-Garcia, M.-D., Ogé, L., Hamama, L., & Atanassova, R. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19092506 · Cited by 268 · see citing works

Metabolic engineering of sugars and simple sugar derivatives in plants

Patrick, J. W., Botha, F. C., & Birch, R. G. (2012) · Plant Biotechnology Journal · doi:10.1111/pbi.12002 · Cited by 260 · see citing works

Sugar Signaling During Fruit Ripening

Durán-Soria, S., Pott, D. M., Osorio, S., & Vallarino, J. G. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.564917 · Cited by 257 · see citing works

Soluble Carbohydrates Regulate Auxin Biosynthesis via PIF Proteins in Arabidopsis

Sairanen, I., Novák, O., Pěnčík, A., Ikeda, Y., Jones, B. J., Sandberg, G., & Ljung, K. (2012) · The Plant Cell · doi:10.1105/tpc.112.104794 · Cited by 255 · see citing works

Photosynthetic sucrose acts as cotyledon-derived long-distance signal to control root growth during early seedling development in Arabidopsis

Kircher, S., & Schöpfer, P. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1203746109 · Cited by 251 · see citing works

Sucrose signaling in plants: A world yet to be explored

Pontis, H. G., & Martínez-Noël, G. M. A. (2013) · Plant Signaling & Behavior · doi:10.4161/psb.23316 · Cited by 250 · see citing works

Soybean (Glycine max) SWEET gene family: insights through comparative genomics, transcriptome profiling and whole genome re-sequence analysis

Patil, G., Valliyodan, B., Deshmukh, R. K., Prince, S., Nicander, B., Zhao, M., Sonah, H., Song, L., Lin, L., Chaudhary, J., et al. (2015) · BMC Genomics · doi:10.1186/s12864-015-1730-y · Cited by 244 · see citing works

Master regulators in plant glucose signaling networks

Sheen, J. (2014) · Journal of Plant Biology · doi:10.1007/s12374-014-0902-7 · Cited by 237 · see citing works

Plant adaptations to severely phosphorus-impoverished soils

Lambers, H., Martinoia, E., & Renton, M. (2015) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2015.04.002 · Cited by 228 · see citing works

Identification and characterization of fructose 1,6-bisphosphate aldolase genes in Arabidopsis reveal a gene family with diverse responses to abiotic stresses

Lü, W., Tang, X., Huo, Y., Xu, R., Qi, S., Huang, J., Zheng, C., & Wu, C. (2012) · Gene · doi:10.1016/j.gene.2012.04.042 · Cited by 215 · see citing works

Metabolic pathways regulated by γ-aminobutyric acid (GABA) contributing to heat tolerance in creeping bentgrass (Agrostis stolonifera)

Li, Z., Yu, J., Peng, Y., & Huang, B. (2016) · Scientific Reports · doi:10.1038/srep30338 · Cited by 202 · see citing works

Sugar Signaling in Root Responses to Low Phosphorus Availability

Hammond, J. P., & White, P. J. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.175380 · Cited by 203 · see citing works

Metabolite transport and associated sugar signalling systems underpinning source/sink interactions

Griffiths, C. A., Paul, M. J., & Foyer, C. H. (2016) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2016.07.007 · Cited by 170 · see citing works

Allantoin, a stress-related purine metabolite, can activate jasmonate signaling in a MYC2-regulated and abscisic acid-dependent manner

Takagi, H., Ishiga, Y., Watanabe, S., Konishi, T., Egusa, M., Akiyoshi, N., Matsuura, T., Mori, I. C., Hirayama, T., Kaminaka, H., et al. (2016) · Journal of Experimental Botany · doi:10.1093/jxb/erw071 · Cited by 154 · see citing works

Ready, steady, go! A sugar hit starts the race to shoot branching

Barbier, F. F., Lunn, J. E., & Beveridge, C. A. (2015) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2015.04.004 · Cited by 153 · see citing works

Insight into the Role of Sugars in Bud Burst Under Light in the Rose

Rabot, A., Henry, C., Baaziz, K. B., Mortreau, E., Azri, W., Lothier, J., Hamama, L., Boummaza, R., Leduc, N., Pelleschi, S., et al. (2012) · Plant and Cell Physiology · doi:10.1093/pcp/pcs051 · Cited by 143 · see citing works

Cell‐wall invertases, key enzymes in the modulation of plant metabolism during defence responses

Proels, R. K., & Hückelhoven, R. (2014) · Molecular Plant Pathology · doi:10.1111/mpp.12139 · Cited by 142 · see citing works

Comparative metabolomic profiling in the roots and leaves in contrasting genotypes reveals complex mechanisms involved in post-anthesis drought tolerance in wheat

Kang, Z., Babar, M. A., Khan, N., Guo, J. X., Khan, J., Islam, S., Shrestha, S., & Shahi, D. (2019) · PLoS ONE · doi:10.1371/journal.pone.0213502 · Cited by 139 · see citing works

Sugars, the clock and transition to flowering

Moghaddam, M. R. B., & den Ende, W. V. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00022 · Cited by 137 · see citing works

Photoreceptor effects on plant biomass, resource allocation, and metabolic state

Yang, D., Seaton, D. D., Krahmer, J., & Halliday, K. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1601309113 · Cited by 137 · see citing works

Soybean GmbZIP123 gene enhances lipid content in the seeds of transgenic Arabidopsis plants

Song, Q., Li, Q., Liu, Y.-F., Zhang, F.-X., Ma, B., Zhang, W.-K., Man, W., Du, W.-G., Wang, G., Chen, S.-Y., et al. (2013) · Journal of Experimental Botany · doi:10.1093/jxb/ert238 · Cited by 134 · see citing works

Fructose sensitivity is suppressed in Arabidopsis by the transcription factor ANAC089 lacking the membrane-bound domain

Li, P., Wind, J. J., Shi, X., Zhang, H., Hanson, J., SMEEKENS, S. C. M., & Teng, S. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1018665108 · Cited by 131 · see citing works

Emerging Roles of SWEET Sugar Transporters in Plant Development and Abiotic Stress Responses

Gautam, T., Dutta, M., Jaiswal, V., Zinta, G., Gahlaut, V., & Kumar, S. (2022) · Cells · doi:10.3390/cells11081303 · Cited by 128 · see citing works

Ethylene involvement in the regulation of heat stress tolerance in plants

Poór, P., Nawaz, K., Gupta, R., Ashfaque, F., & Khan, M. I. R. (2021) · Plant Cell Reports · doi:10.1007/s00299-021-02675-8 · Cited by 130 · see citing works

Effect of exogenous sucrose on anthocyanin synthesis in postharvest strawberry fruit

Li, D., Zhang, X., Xu, Y., Li, L., Aghdam, M. S., & Luo, Z. (2019) · Food Chemistry · doi:10.1016/j.foodchem.2019.03.042 · Cited by 126 · see citing works

Sweet immunity in the plant circadian regulatory network

Moghaddam, M. R. B., & den Ende, W. V. (2013) · Journal of Experimental Botany · doi:10.1093/jxb/ert046 · Cited by 118 · see citing works

Regulation of fruit and seed response to heat and drought by sugars as nutrients and signals

Liu, Y., Offler, C. E., & Ruan, Y. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00282 · Cited by 116 · see citing works

Aluminum toxicity in plant cells: Mechanisms of cell death and inhibition of cell elongation

Yamamoto, Y. (2018) · Soil Science & Plant Nutrition · doi:10.1080/00380768.2018.1553484 · Cited by 115 · see citing works

Sugar enhances waterlogging‐induced adventitious root formation in cucumber by promoting auxin transport and signalling

Qi, X., Li, Q., Shen, J., Qian, C., Xu, X., Xu, Q., & Chen, X. (2020) · Plant Cell & Environment · doi:10.1111/pce.13738 · Cited by 112 · see citing works

Comparison of Sugar Profile between Leaves and Fruits of Blueberry and Strawberry Cultivars Grown in Organic and Integrated Production System

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Overexpression of Sucrose Phosphate Synthase Enhanced Sucrose Content and Biomass Production in Transgenic Sugarcane

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