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

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

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

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

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

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

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

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

Molecular physiology of higher plant sucrose transporters

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

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

Key Regulators of Sucrose Metabolism Identified through Comprehensive Comparative Transcriptome Analysis in Peanuts

Li, W., Huang, L., Liu, N., Pandey, M. K., Chen, Y., Cheng, L., Guo, J., Yu, B., Luo, H., Zhou, X., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22147266 · Cited by 39

Multilayered regulation of developmentally programmed pre-anthesis tip degeneration of the barley inflorescence

Shanmugaraj, N., Rajaraman, J., Kale, S. M., Kamal, R., Huang, Y., Thirulogachandar, V., Garibay‐Hernández, A., Budhagatapalli, N., Moya, Y. A. T., Hajirezaei, M., et al. (2023) · The Plant Cell · doi:10.1093/plcell/koad164 · Cited by 38

Transcriptome Profiling of Taproot Reveals Complex Regulatory Networks during Taproot Thickening in Radish (Raphanus sativus L.)

Yu, R., Wang, J., Xu, L., Wang, Y., Wang, R., Zhu, X., Sun, X., Luo, X., Xie, Y., Muleke, E. M., et al. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.01210 · Cited by 39

Phosphorus and Carbohydrate Metabolism in Green Bean Plants Subjected to Increasing Phosphorus Concentration in the Nutrient Solution

García‐Caparrós, P., Lao, M. T., Preciado-Rangel, P., & Sánchez, E. (2021) · Agronomy · doi:10.3390/agronomy11020245 · Cited by 38

New Insights on Plant Cell Elongation: A Role for Acetylcholine

Sansebastiano, G. P. D., Fornaciari, S., Barozzi, F., Piro, G., & Arru, L. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms15034565 · Cited by 37

Sucrose synthase in unicellular cyanobacteria and its relationship with salt and hypoxic stress

Kolman, M. D. L. A., Torres, L. L., Martin, M. L., & Salerno, G. L. (2011) · Planta · doi:10.1007/s00425-011-1542-5 · Cited by 37

Metabolomics approach for understanding geographical dependence of soybean leaf metabolome

Yun, D.-Y., Kang, Y., Kim, E., Kim, M., Park, N. H., Choi, H., Go, G. H., Lee, J. H., Park, J. S., & Hong, Y. (2018) · Food Research International · doi:10.1016/j.foodres.2018.01.061 · Cited by 36

Heterologous expression of AtPAP2 in transgenic potato influences carbon metabolism and tuber development

Zhang, Y., Sun, F., Fettke, J., Schöttler, M. A., Ramsden, L., Fernie, A. R., & Lim, B. L. (2014) · FEBS Letters · doi:10.1016/j.febslet.2014.08.019 · Cited by 36

Transcriptome profiling identifies ABA mediated regulatory changes towards storage filling in developing seeds of castor bean (Ricinus communis L.)

Chandrasekaran, U., Xu, W. F., & Liu, A. (2014) · Cell & Bioscience · doi:10.1186/2045-3701-4-33 · Cited by 35

Silicon Stimulates Plant Growth and Metabolism in Rice Plants under Conventional and Osmotic Stress Conditions

Ramírez-Olvera, S. M., Trejo‐Téllez, L. I., Gómez‐Merino, F. C., Ruíz-Posadas, L. D. M., Alcántar-González, E. G., & Saucedo-Veloz, C. (2021) · Plants · doi:10.3390/plants10040777 · Cited by 34

The changes in C/N, carbohydrate, and amino acid content in leaves during female flower bud differentiation of Juglans sigillata

Zhang, W., Li, J., Zhang, W., Njie, A., & Pan, X. (2022) · Acta Physiologiae Plantarum · doi:10.1007/s11738-021-03328-9 · Cited by 34

Transcriptome analysis in oak uncovers a strong impact of endogenous rhythmic growth on the interaction with plant-parasitic nematodes

Maboreke, H., Feldhahn, L. M., Bönn, M., Tarkka, M. T., Buscot, F., Herrmann, S., Menzel, R., & Rueß, L. (2016) · BMC Genomics · doi:10.1186/s12864-016-2992-8 · Cited by 33

Sugar Metabolism and Transcriptome Analysis Reveal Key Sugar Transporters during Camellia oleifera Fruit Development

He, Y., Chen, R., Yang, Y., Liang, G., Zhang, H., Deng, X., & Xi, R. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23020822 · Cited by 33

Exogenous sucrose can enhance tolerance of Arabidopsis thaliana seedlings to salt stress

Qiu, Z., Wang, Y. F., Zhu, A., Peng, F., & Wang, L. S. (2014) · Biologia Plantarum · doi:10.1007/s10535-014-0444-3 · Cited by 33

Effect of Waterlogging on Carbohydrate Metabolism and the Quality of Fiber in Cotton (Gossypium hirsutum L.)

Kuai, J., Chen, Y., Wang, Y., Meng, Y., Chen, B., Zhao, W., & Zhou, Z. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.00877 · Cited by 32

Physico-chemical properties of longan fruit during development and ripening

Shi, S., Wang, W., Liu, L., Shu, B., Wei, Y., Jue, D., Fu, J., Xie, J., & Liu, C. (2016) · Scientia Horticulturae · doi:10.1016/j.scienta.2016.05.026 · Cited by 31

Mass spectrometry imaging of low molecular weight metabolites in strawberry fruit (Fragaria x ananassa Duch.) cv. Primoris with 109Ag nanoparticle enhanced target

Nizioł, J., Misiorek, M., & Ruman, T. (2018) · Phytochemistry · doi:10.1016/j.phytochem.2018.11.014 · Cited by 31

Agrobacteria reprogram virulence gene expression by controlled release of host-conjugated signals

Wang, C., Ye, F., Chang, C., Liu, X., Wang, J., Wang, J., Yan, X., Fu, Q., Zhou, J., Chen, S., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1903695116 · Cited by 31

Characterization of Sucrose transporter alleles and their association with seed yield-related traits in Brassica napus L

Li, F., Ma, C., Wang, X., Gao, C., Zhang, J., Wang, Y., Cong, N., Li, X., Wen, J., Yi, B., et al. (2011) · BMC Plant Biology · doi:10.1186/1471-2229-11-168 · Cited by 31

Proteomics Wants cRacker: Automated Standardized Data Analysis of LC–MS Derived Proteomic Data

Zauber, H., & Schulze, W. X. (2012) · Journal of Proteome Research · doi:10.1021/pr300413v · Cited by 31

Polyethylene glycol effects on somatic embryogenesis of papaya hybrid UENF/CALIMAN 01 seeds

Heringer, Â. S., Vale, E. M., Barroso, T., Santa‐Catarina, C., & Silveira, V. (2013) · Theoretical and Experimental Plant Physiology · doi:10.1590/s2197-00252013000200004 · Cited by 36

Production of Novel Antibiotics Zeamines through Optimizing Dickeya zeae Fermentation Conditions

Liao, L., Cheng, Y., Liu, S., Zhou, J., An, S., Lv, M., Chen, Y., Gu, Y., Chen, S., & Zhang, L. (2014) · PLoS ONE · doi:10.1371/journal.pone.0116047 · Cited by 31

Carbon: Nitrogen Interaction Regulates Expression of Genes Involved in N-Uptake and Assimilation in Brassica juncea L.

Goel, P., Bhuria, M., Kaushal, M., & Singh, A. K. (2016) · PLoS ONE · doi:10.1371/journal.pone.0163061 · Cited by 31

Zinc sulfate spray increases activity of carbohydrate metabolic enzymes and regulates endogenous hormone levels in apple fruit

Zhang, Y., Yan, Y., Fu, C., Li, M., & Wang, Y. (2016) · Scientia Horticulturae · doi:10.1016/j.scienta.2016.09.024 · Cited by 31

Sugar composition and transcriptome analysis in developing ‘Fengtang’ plum (Prunus salicina Lindl.) reveal candidate genes regulating sugar accumulation

Nie, X., Chen, H., Wang, Q., Lu, M., & An, H. (2023) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2023.107955 · Cited by 30

A Review of the Diverse Genes and Molecules Involved in Sucrose Metabolism and Innovative Approaches to Improve Sucrose Content in Sugarcane

Khan, Q., Qin, Y., Guo, D.-J., Yang, L., Song, X., Xing, Y., & Li, Y. (2023) · Agronomy · doi:10.3390/agronomy13122957 · Cited by 32

A re‐assessment of sucrose signaling involved in cluster‐root formation and function in phosphate‐deficient white lupin (Lupinus albus)

Wang, Z., Shen, J., Ludewig, U., & Neumann, G. (2014) · Physiologia Plantarum · doi:10.1111/ppl.12311 · Cited by 30

Sugar Transporter Protein 1 (STP1) contributes to regulation of the genes involved in shoot branching via carbon partitioning in Arabidopsis

Otori, K., Tanabe, N., Tamoi, M., & Shigeoka, S. (2018) · Bioscience Biotechnology and Biochemistry · doi:10.1080/09168451.2018.1550355 · Cited by 29

Effects of abscisic acid and an osmoticum on the maturation, starch accumulation and germination of Picea spp. somatic embryos

Hazubska-Przybył, T., Kalemba, E. M., Ratajczak, E., & Bojarczuk, K. (2016) · Acta Physiologiae Plantarum · doi:10.1007/s11738-016-2078-x · Cited by 30

An ABC transporter complex encoded by Aluminum Sensitive 3 and NAP3 is required for phosphate deficiency responses in Arabidopsis

Belal, R., Tang, R., Li, Y., Mabrouk, Y. M., Badr, E. A., & Luan, S. (2015) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2015.05.009 · Cited by 29

Modeling the diversion of primary carbon flux into secondary metabolism under variable nitrate and light/dark conditions

Larbat, R., Robin, C., Lillo, C., Drengstig, T., & Ruoff, P. (2016) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2016.05.008 · Cited by 29

Proteomic Analysis of Aphid-Resistant and -Sensitive Rose (Rosa Hybrida) Cultivars at Two Developmental Stages

Muneer, S., Jeong, H. K., Park, Y. G., & Jeong, B. R. (2018) · Proteomes · doi:10.3390/proteomes6020025 · Cited by 28

An Allelopathic Role for Garlic Root Exudates in the Regulation of Carbohydrate Metabolism in Cucumber in a Hydroponic Co-Culture System

Ding, H., Ali, A., & Cheng, Z. (2019) · Plants · doi:10.3390/plants9010045 · Cited by 28

Sugar Transporter, CmSWEET17, Promotes Bud Outgrowth in Chrysanthemum Morifolium

Liu, W., Peng, B., Song, A., Jiang, J., & Chen, F. (2019) · Genes · doi:10.3390/genes11010026 · Cited by 28

Aberrant phenotype and transcriptome expression during fiber cell wall thickening caused by the mutation of the Im gene in immature fiber (im) mutant in Gossypium hirsutum L

Wang, C., Lv, Y., Wen-tin, X., Zhang, T., & Guo, W. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-94 · Cited by 28

A NAC transcription factor and a MADS-box protein antagonistically regulate sucrose accumulation in strawberry receptacles

Xiao, K., Fan, J., Bi, X., Tu, X., Li, X., Cao, M., Liu, Z., Lin, A., Wang, C., Xu, P., et al. (2025) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiaf043 · Cited by 27

Modification of starch metabolism in transgenic Arabidopsis thaliana increases plant biomass and triples oilseed production

Liu, F., Zhao, Q., Mano, N. A., Ahmed, Z., Nitschké, F., Cai, Y., Chapman, K. D., Steup, M., Tetlow, I. J., & Emes, M. J. (2015) · Plant Biotechnology Journal · doi:10.1111/pbi.12453 · Cited by 27

The functions of cucumber sucrose phosphate synthases 4 (CsSPS4) in carbon metabolism and transport in sucrose- and stachyose-transporting plants

Li, X., Du, J., Guo, J., Wang, H., Ma, S., Lü, J., Sui, X., & Zhang, Z. (2018) · Journal of Plant Physiology · doi:10.1016/j.jplph.2018.05.013 · Cited by 27

Model-assisted comparison of sugar accumulation patterns in ten fleshy fruits highlights differences between herbaceous and woody species

Cakpo, C. B., Vercambre, G., Baldazzi, V., Roch, L., Dai, Z., Valsesia, P., Memah, M.-M., Colombié, S., Moing, A., Gibon, Y., et al. (2020) · Annals of Botany · doi:10.1093/aob/mcaa082 · Cited by 26

Transcriptome Analysis of Low- and High-Sucrose Pear Cultivars Identifies Key Regulators of Sucrose Biosynthesis in Fruits

Lü, J., Tao, X., Yao, G., Zhang, S., & Zhang, H. (2020) · Plant and Cell Physiology · doi:10.1093/pcp/pcaa068 · Cited by 26

Signalling and regulation of plant development by carbon/nitrogen balance

Fañanás‐Pueyo, I., Carrera‐Castaño, G., Pernas, M., & Oñate‐Sánchez, L. (2025) · Physiologia Plantarum · doi:10.1111/ppl.70228 · Cited by 31

Serendipita indica changes host sugar and defense status in Arabidopsis thaliana: cooperation or exploitation?

Opitz, M. W., Daneshkhah, R., Lorenz, C., Ludwig, R., Steinkellner, S., & Wieczorek, K. (2021) · Planta · doi:10.1007/s00425-021-03587-3 · Cited by 25

Exogenous sucrose alleviates salt stress in sunflower (Helianthus annuus L.) and canola (Brassica napus L.) by modulating osmotic adjustment and antioxidant defense system

Sevgi, B., & Leblebici, S. (2025) · Physiology and Molecular Biology of Plants · doi:10.1007/s12298-025-01571-9 · Cited by 26

Transgenic alfalfa (Medicago sativa) with increased sucrose phosphate synthase activity shows enhanced growth when grown under N2-fixing conditions

Gebril, S., Seger, M., Muro-Villanueva, F., Ortega, J. L., Bagga, S., & Sengupta‐Gopalan, C. (2015) · Planta · doi:10.1007/s00425-015-2342-0 · Cited by 24

Intronic Sequence Regulates Sugar-Dependent Expression of Arabidopsis thaliana Production of Anthocyanin Pigment-1/MYB75

Broeckling, B., Watson, R. A., Steinwand, B., & Bush, D. R. (2016) · PLoS ONE · doi:10.1371/journal.pone.0156673 · Cited by 24

Lateral root growth in Arabidopsis is controlled by short and long distance signaling through the LRR RLKs XIP1/CEPR1 and CEPR2

Dimitrov, I., & Tax, F. E. (2018) · Plant Signaling & Behavior · doi:10.1080/15592324.2018.1489667 · Cited by 24

Metabolic variation and cooking qualities of millet cultivars grown both organically and conventionally

Liang, K., Liang, S., Lu, L., Zhu, D., Zhu, H. M., Liu, P., & Zhang, M. (2018) · Food Research International · doi:10.1016/j.foodres.2018.01.023 · Cited by 23

Sucrose signaling function on the formation and swelling of bulblets of Lilium sargentiae E.H. Wilson

Gao, S., Zhu, Y., Zhou, L., Fu, X., Lei, T., Chen, Q., Yu, X., Zhou, Y., Li, W., Hu, J., et al. (2018) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-018-1451-4 · Cited by 23

Involvement of polyamines in sucrose-induced tolerance to atrazine-mediated chemical stress in Arabidopsis thaliana

Amrani, A. E., Couée, I., Berthomé, R., Ramel, F., Gouesbet, G., & Sulmon, C. (2019) · Journal of Plant Physiology · doi:10.1016/j.jplph.2019.04.012 · Cited by 23

Co-crystal Structure of Thermosynechococcus elongatus Sucrose Phosphate Synthase With UDP and Sucrose-6-Phosphate Provides Insight Into Its Mechanism of Action Involving an Oxocarbenium Ion and the Glycosidic Bond

Li, Y., Yao, Y., Yang, G., Tang, J. H., Ayala, G. J., Li, X., Zhang, W., Han, Q., Yang, T., Wang, H., et al. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.01050 · Cited by 22

Physical, biochemical, and sensory properties of strawberries grown in high-altitude tropical climate

Pinheiro, D. F., de Resende, J. T. V., Constantino, L. V., Hata, F. T., Hata, N. N. Y., & Lustosa, S. B. C. (2021) · Ciência e Agrotecnologia · doi:10.1590/1413-7054202145008221 · Cited by 22

Soil drought decreases oil synthesis and increases protein synthesis in cottonseed kernel during the flowering and boll formation of cotton

Li, Y., Hu, W., Setter, T. L., He, J., Zou, J., Zhu, H., Zheng, G., Zhao, W., Wang, Y., Chen, B., et al. (2022) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2022.104964 · Cited by 21

Genome‐wide binding analysis reveals that ANAC060 directly represses sugar‐induced transcription of ABI5 in Arabidopsis

Yu, B., Wang, Y. J., Zhou, H., Li, P., Liu, C., Chen, S., Peng, Y., Zhang, Y., & Teng, S. (2020) · The Plant Journal · doi:10.1111/tpj.14777 · Cited by 21

Regulation of sugar metabolism genes in the nitrogen-dependent susceptibility of tomato stems to Botrytis cinerea

Lacrampe, N., Lopez, F., Lugan, R., Colombié, S., Olivares, J., Nicot, P. C., & Lecompte, F. (2020) · Annals of Botany · doi:10.1093/aob/mcaa155 · Cited by 20

Effects of Combined Application of Potassium Silicate and Salicylic Acid on the Defense Response of Hydroponically Grown Tomato Plants to Ralstonia solanacearum Infection

Jiang, N.-H., & Zhang, S. (2021) · Sustainability · doi:10.3390/su13073750 · Cited by 20

COP1 controls salt stress tolerance by modulating sucrose content

Kim, J. Y., Lee, S. J., Min, W. K., Cha, S., Song, J. T., & Seo, H. S. (2022) · Plant Signaling & Behavior · doi:10.1080/15592324.2022.2096784 · Cited by 20

Arabidopsis thaliana Sucrose Phosphate Synthase A2 Affects Carbon Partitioning and Drought Response

Bagnato, L., Tosato, E., Gurrieri, L., Trost, P., Forlani, G., & Sparla, F. (2023) · Biology · doi:10.3390/biology12050685 · Cited by 20

Overexpression of the sucrose transporter gene NtSUT1 alleviates aluminum-induced inhibition of root elongation in tobacco (Nicotiana tabacum L.)

Kariya, K., Sameeullah, M., Sasaki, T., & Yamamoto, Y. (2017) · Soil Science & Plant Nutrition · doi:10.1080/00380768.2017.1283646 · Cited by 20

Sucrose and methyl jasmonate modulate the expression of anthocyanin biosynthesis genes and increase the frequency of flower-color mutants in chrysanthemum

Kim, S. H., Kim, Y., Jo, Y. D., Kang, S., Ahn, J., Kang, B., & Kim, J. (2019) · Scientia Horticulturae · doi:10.1016/j.scienta.2019.108602 · Cited by 20

Transcriptomic exploration of a high sucrose mutant in comparison with the low sucrose mother genotype in sugarcane during sugar accumulating stage

Khan, Q., Chen, J., Zeng, X.-P., Qin, Y., Guo, D., Mahmood, A., Yang, L., Liang, Q., Song, X., Xing, Y., et al. (2021) · GCB Bioenergy · doi:10.1111/gcbb.12868 · Cited by 20

Genome‐wide identification of invertases in Fabaceae , focusing on transcriptional regulation of Pisum sativum invertases in seed subjected to drought

Morin, A., Kadi, F., Porcheron, B., Vriet, C., Maurousset, L., Lemoine, R., Pourtau, N., & Doidy, J. (2022) · Physiologia Plantarum · doi:10.1111/ppl.13673 · Cited by 20

Colligative Effects of Solutions of Low-Molecular Sugars and Their Role in Plants under Hypothermia

Deryabin, A. N., & Trunova, T. I. (2021) · Biology Bulletin · doi:10.1134/s1062359021060042 · Cited by 19

Effects of soil drought on cottonseed kernel carbohydrate metabolism and kernel biomass accumulation

Li, Y., Hu, W., Zou, J., He, J., Zhu, H., Zhao, W., Wang, Y., Chen, B., Meng, Y., Wang, S., et al. (2023) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2022.12.020 · Cited by 19

Impact of nanopesticide CuO-NPs and nanofertilizer CeO2-NPs on wheat Triticum aestivum under global warming scenarios

Xu, X., Qiu, H., van Gestel, C. A. M., Gong, B., & He, E. (2023) · Chemosphere · doi:10.1016/j.chemosphere.2023.138576 · Cited by 19

Changes in carbohydrate distribution in cotton photosynthetic organs and increase in boll weight reduce yield loss under high temperature

Yang, L., Duan, J., Liu, Y., Hu, W., Liu, X., Wang, Y., Zhou, Z., & Zhao, W. (2024) · Journal of Experimental Botany · doi:10.1093/jxb/erae122 · Cited by 19

Low temperature differentially affects tillering in spring and winter wheat in association with changes in plant carbon status

Lorenzo, M., Assuero, S. G., & Tognetti, J. (2014) · Annals of Applied Biology · doi:10.1111/aab.12177 · Cited by 19

Rapid Effect of Nitrogen Supply for Soybean at the Beginning Flowering Stage on Biomass and Sucrose Metabolism

Zhou, H., Yao, X., Zhao, Q., Zhang, W., Zhang, B., & Xie, F. (2019) · Scientific Reports · doi:10.1038/s41598-019-52043-6 · Cited by 19

Proteomic analysis and interactions network in leaves of mycorrhizal and nonmycorrhizal sorghum plants under water deficit

Olalde‐Portugal, V., Cabrera‐Ponce, J. L., Gastélum-Arellánez, A., Guerrero‐Rangel, A., Winkler, R., & Valdés‐Rodríguez, S. (2020) · PeerJ · doi:10.7717/peerj.8991 · Cited by 19

Neuroanatomie des Morbus Parkinson

Braak, H., Rüb, U., & Braak, E. (2000) · Der Nervenarzt · doi:10.1007/s001150050607 · Cited by 20

Seasonal below‐ground metabolism in switchgrass

Palmer, N. A., Saathoff, A. J., Scully, E. D., Tobias, C. M., Twigg, P. G., Madhavan, S., Schmer, M. R., Cahoon, R. E., Sattler, S. E., Edmé, S. J., et al. (2017) · The Plant Journal · doi:10.1111/tpj.13742 · Cited by 19

A Quantitative Proteomics View on the Function of Qfhb1, a Major QTL for Fusarium Head Blight Resistance in Wheat

Eldakak, M., Das, A., Zhuang, Y., Rohila, J. S., Glover, K. D., & Yen, Y. (2018) · Pathogens · doi:10.3390/pathogens7030058 · Cited by 18

Involvement of oligosaccharides and sucrose-related genes on sucrose retention in strawberries from ripening to shelf-life

del Olmo, I., Blanch, M., Romero, I., Vázquez-Hernández, M., Sánchez-Ballesta, M. T., Escribano, M. I., & Merodio, C. (2020) · Postharvest Biology and Technology · doi:10.1016/j.postharvbio.2020.111301 · Cited by 18

Comparative Transcriptome Sequencing of Taro Corm Development With a Focus on the Starch and Sucrose Metabolism Pathway

Dong, W., He, F., HuiPing, J., Liu, L., & Qiu, Z. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.771081 · Cited by 18

Plant Adaptation to Environmental Stress: Drought, Chilling, Heat, and Salinity

Ncama, K., Aremu, O. A., & Sithole, N. J. (2021) · Springer eBooks · doi:10.1007/978-3-030-71571-7_5 · Cited by 18

Low night temperature-induced feedback inhibition of photosynthesis through sucrose accumulation in sugar beet (Beta vulgaris L.) leaves

Wang, L., Zhai, Y., Wu, J., Stevanato, P., Sha, S., Geng, G., Xu, Y., Yu, L., & Wang, Y. (2022) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2022.105083 · Cited by 18

How extreme summer weather may limit control ofFestuca paniculataby mowing in subalpine grasslands

Benot, M., Saccone, P., Vicente, R., Pautrat, E., Morvan‐Bertrand, A., Decau, M.-L., Grigulis, K., Prudhomme, M. P., & Lavorel, S. (2013) · Plant Ecology & Diversity · doi:10.1080/17550874.2013.784818 · Cited by 18

Metabotyping of rice (Oryza sativa L.) for understanding its intrinsic physiology and potential eating quality

Song, E.-H., Jeong, J., Park, C. Y., Kim, H.-Y., Kim, E., Bang, E., & Hong, Y. (2018) · Food Research International · doi:10.1016/j.foodres.2018.05.003 · Cited by 18

Soluble Carbohydrates Regulate Auxin Biosynthesis via PIF Proteins in Arabidopsis

cík, Ikeda, A., BrianJones, cGöranSandberg, & andKarinLjunga, B. (2012) · Cited by 18

Transcriptome Analysis Reveals Roles of Sucrose in Anthocyanin Accumulation in ‘Kuerle Xiangli’ (Pyrus sinkiangensis Yü)

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Plasticity in the Morphology of Growing Bamboo: A Bayesian Analysis of Exogenous Treatment Effects on Plant Height, Internode Length, and Internode Numbers

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