Function and regulation of phospholipid signalling in plants

CTR1, a negative regulator of the ethylene response pathway in arabidopsis, encodes a member of the Raf family of protein kinases

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Profiling Membrane Lipids in Plant Stress Responses

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Structure, Function, and Control of Phosphoinositide-Specific Phospholipase C

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Abiotic stress signalling pathways: specificity and cross-talk

Knight, H., & Knight, M. R. (2001) · Trends in Plant Science · doi:10.1016/s1360-1385(01)01946-x · Cited by 972

Cold Calcium Signaling in Arabidopsis Involves Two Cellular Pools and a Change in Calcium Signature after Acclimation

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The DEFECTIVE IN ANTHER DEHISCENCE1 Gene Encodes a Novel Phospholipase A1 Catalyzing the Initial Step of Jasmonic Acid Biosynthesis, Which Synchronizes Pollen Maturation, Anther Dehiscence, and Flower Opening in Arabidopsis

Ishiguro, S., Kawai-Oda, A., Ueda, J., Nishida, I., & Okada, K. (2001) · The Plant Cell · doi:10.1105/tpc.010192 · Cited by 878

Phosphorylation of 1-Aminocyclopropane-1-Carboxylic Acid Synthase by MPK6, a Stress-Responsive Mitogen-Activated Protein Kinase, Induces Ethylene Biosynthesis in Arabidopsis[W]

Liu, Y., & Zhang, S. (2004) · The Plant Cell · doi:10.1105/tpc.104.026609 · Cited by 875

Antagonistic Regulation of PIN Phosphorylation by PP2A and PINOID Directs Auxin Flux

Michniewicz, M., Zago, M. K., Abas, L., Weijers, D., Schweighofer, A., Meskiene, I., Heisler, M. G., Ohno, C., Zhang, J., Huang, F., et al. (2007) · Cell · doi:10.1016/j.cell.2007.07.033 · Cited by 678

Phosphoinositide Regulation of the Actin Cytoskeleton

Yin, H. L., & Janmey, P. A. (2003) · Annual Review of Physiology · doi:10.1146/annurev.physiol.65.092101.142517 · Cited by 672

Comparative transcriptional analysis of Capsicum flower buds between a sterile flower pool and a restorer flower pool provides insight into the regulation of fertility restoration

Wei, B., Wang, L., Bosland, P. W., Zhang, G., & Zhang, R. (2019) · BMC Genomics · doi:10.1186/s12864-019-6210-3 · Cited by 23

Silencing ATG6 and PI3K accelerates petal senescence and reduces flower number and shoot biomass in petunia

Lin, Y., & Jones, M. L. (2020) · Plant Science · doi:10.1016/j.plantsci.2020.110713 · Cited by 23

DWARF50 (D50), a rice (Oryza sativa L.) gene encoding inositol polyphosphate 5‐phosphatase, is required for proper development of intercalary meristem

Sato‐Izawa, K., Nakaba, S., Tamura, K., Yamagishi, Y., Nakano, Y., Nishikubo, N., KAWAI, S., Kajita, S., Ashikari, M., Funada, R., et al. (2012) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2012.02534.x · Cited by 23

Second Messengers: Central Regulators in Plant Abiotic Stress Response

Jain, M., Nagar, P., Goel, P., Singh, A. K., Kumari, S., & Mustafiz, A. (2018) · Springer eBooks · doi:10.1007/978-981-10-7479-0_2 · Cited by 23

Long-Distance Lipid Signaling and its Role in Plant Development and Stress Response

Barbaglia, A. M., & Hoffmann-Benning, S. (2016) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-3-319-25979-6_14 · Cited by 23

Impact of phenol on the glycerophospholipid turnover and potential role of circadian clock in the plant response against this pollutant in tobacco hairy roots

Alderete, L. G. S., Flor, S. A., Lucangioli, S. E., & Agostini, E. (2020) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2020.03.041 · Cited by 22

Differential gene expression patterns during gametophyte development provide insights into sex differentiation in the dioicous kelp Saccharina japonica

Zhang, J., Li, Y., Luo, S., Cao, M., Zhang, L., & Li, X. (2021) · BMC Plant Biology · doi:10.1186/s12870-021-03117-z · Cited by 25

Overexpression of a Zea mays phospholipase C1 gene enhances drought tolerance in tobacco in part by maintaining stability in the membrane lipid composition

Zhai, S., Gao, Q., Liu, X., Sui, Z., & Zhang, J. (2013) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-013-0358-3 · Cited by 22

Lipid turnover between membrane lipids and neutral lipids via inhibition of diacylglyceryl N,N,N-trimethylhomoserine synthesis in Chlamydomonas reinhardtii

Lee, J.-W., Shin, S.-Y., Kim, H.-S., Jin, E., Lee, H., & Oh, H. (2017) · Algal Research · doi:10.1016/j.algal.2017.09.001 · Cited by 21

Genomic architecture of promoters and transcriptional regulation of candidate genes in rice involved in tolerance to anaerobic germination

Mohanty, B. (2022) · Current Plant Biology · doi:10.1016/j.cpb.2022.100236 · Cited by 20

A novel-type phosphatidylinositol phosphate-interactive, Ca-binding protein PCaP1 in Arabidopsis thaliana: stable association with plasma membrane and partial involvement in stomata closure

Nagata, C., Miwa, C., Tanaka, N., Kato, M., Suito, M., Tsuchihira, A., Sato, Y., Segami, S., & Maeshima, M. (2016) · Journal of Plant Research · doi:10.1007/s10265-016-0787-2 · Cited by 21

Regulation of low phosphate stress in plants

Ceasar, S. A. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-818204-8.00007-2 · Cited by 21

Identification of novel stress-induced microRNAs and their targets in Camelina sativa using computational approach

Subburaj, S., Kim, A. Y., Lee, S., Kim, K., Suh, M. C., Kim, G.-J., & Lee, G. (2016) · Plant Biotechnology Reports · doi:10.1007/s11816-016-0395-6 · Cited by 20

Ectopic Expression of Gs5PTase8, a Soybean Inositol Polyphosphate 5-Phosphatase, Enhances Salt Tolerance in Plants

Jia, Q., Sun, S., Kong, D., Song, J., Wu, L., Yan, Z., Zuo, L., Yang, Y., Liang, K., Lin, W., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21031023 · Cited by 20

Phytohormonal Regulation of Plant Development in Response to Fluctuating Light Conditions

Razzaq, K., & Du, J. (2024) · Journal of Plant Growth Regulation · doi:10.1007/s00344-024-11568-5 · Cited by 21

Drought-Tolerant Rice at Molecular Breeding Eras: An Emerging Reality

Chengqi, Z., Ye, Y., Tian, Q., Yafan, H., Jifeng, Y., & Zhicheng, S. (2023) · Rice Science · doi:10.1016/j.rsci.2023.11.005 · Cited by 19

A transcriptional approach to unravel the connection between phospholipases A2 and D and ABA signal in citrus under water stress

Romero, P., Lafuente, M. T., & Alferez, F. M. (2014) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2014.03.014 · Cited by 19

The exogenous application of wood vinegar induces a tissue- and dose-dependent elicitation of phenolics and functional traits in onion (Allium cepa L.)

Zhang, L., García-Pérez, P., Arikan, B., Elbasan, F., Alp, F. N., Balcı, M., Zengin, G., Yıldıztugay, E., & Lucini, L. (2022) · Food Chemistry · doi:10.1016/j.foodchem.2022.134926 · Cited by 18

Abiotic Stress in Plants

Gong, Y., Rao, L., & Yu, D. (2013) · InTech eBooks · doi:10.5772/55865 · Cited by 18

Proteomics as a tool to decipher plant responses in arbuscular mycorrhizal interactions: a meta‐analysis

Domingo, G., Vannini, C., Bracale, M., & Bonfante, P. (2022) · PROTEOMICS · doi:10.1002/pmic.202200108 · Cited by 19

The action of enhancing weak light capture via phototropic growth and chloroplast movement in plants

Xin, G.-Y., Li, L.-P., Wang, P.-T., Li, X.-Y., Han, Y.-J., & Zhao, X. (2022) · Stress Biology · doi:10.1007/s44154-022-00066-x · Cited by 17

Is membrane occupation and recognition nexus domain functional in plant phosphatidylinositol phosphate kinases?

Mikami, K., Saavedra, L., & Sommarin, M. (2010) · Plant Signaling & Behavior · doi:10.4161/psb.5.10.12922 · Cited by 16

Genome-wide identification and abiotic stress responses of DGK gene family in maize

Gu, Y., Zhao, C., He, L., Yan, B., Dong, J., Li, Z., Yang, K., & Xu, J. (2017) · Journal of Plant Biochemistry and Biotechnology · doi:10.1007/s13562-017-0424-8 · Cited by 16

Arabidopsis PCaP2 Functions as a Linker Between ABA and SA Signals in Plant Water Deficit Tolerance

Wang, X., Wang, Y., Wang, L., Liu, H., Zhang, B., Cao, Q., Liu, X., Bi, S., Lv, Y., Wang, Q., et al. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.00578 · Cited by 16

A functional characterization of TaMs1 orthologs in Poaceae plants

Li, J., Wang, Z., Chang, Z., He, H., Tang, X., Ma, L., & Deng, X. W. (2021) · The Crop Journal · doi:10.1016/j.cj.2020.12.002 · Cited by 16

Expansion and Functional Divergence of Inositol Polyphosphate 5-Phosphatases in Angiosperms

Zhang, Z., Li, Y., Luo, Z., Kong, S., Zhao, Y., Zhang, C., Zhang, W., Yuan, H., & Cheng, L. Z. (2019) · Genes · doi:10.3390/genes10050393 · Cited by 15

The cold response of CBF genes in barley is regulated by distinct signaling mechanisms

Marozsán-Tóth, Z., Vashegyi, I., Galiba, G., & Tóth, B. I. (2015) · Journal of Plant Physiology · doi:10.1016/j.jplph.2015.04.002 · Cited by 15

The Arabidopsis phytohormone crosstalk network involves a consecutive metabolic route and circular control units of transcription factors that regulate enzyme-encoding genes

Yue, X., Li, X. G., Gao, X., Zhao, X., Dong, Y., & Zhou, C. (2016) · BMC Systems Biology · doi:10.1186/s12918-016-0333-9 · Cited by 15

Comparative transcriptome profile analysis of rice varieties with different tolerance to zinc deficiency

Lu, X., Liu, S., Zhi, S., Chen, J., & Ye, G. (2020) · Plant Biology · doi:10.1111/plb.13227 · Cited by 15

Metabolomic Approaches to Studying the Response to Drought Stress in Corn (Zea mays) Cobs

Gaffney, I., Sallach, J. B., Wilson, J. C., Bergström, E. T., & THOMAS‐OATES, J. E. (2021) · Metabolites · doi:10.3390/metabo11070438 · Cited by 15

Regulation of protein trafficking: Posttranslational mechanisms and the unexplored transcriptional control

Pizarro, L., & Norambuena, L. (2014) · Plant Science · doi:10.1016/j.plantsci.2014.05.004 · Cited by 15

A Bridge to the World

Xu, Z. H. (2020) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-081519-035831 · Cited by 14

The Role of Triacylglycerol in the Protection of Cells against Lipotoxicity under Drought in Lolium multiflorum/Festuca arundinacea Introgression Forms

Perlikowski, D., Lechowicz, K., Skirycz, A., Michaelis, Ä., Pawłowicz, I., & Kosmala, A. (2022) · Plant and Cell Physiology · doi:10.1093/pcp/pcac003 · Cited by 14

Role of tonoplast microdomains in plant cell protection against osmotic stress

Озолина, Н. В., Kapustina, I. S., Гурина, В. В., & Nurminsky, V. N. (2022) · Planta · doi:10.1007/s00425-021-03800-3 · Cited by 14

Lipidomic study reveals the effect of morphological variation and other metabolite interactions on the lipid composition in various cultivars of Bok choy

Khan, W. A., Hou, X., Han, K., Khan, N., Huijie, D., Saqib, M., Zhang, Z., Naseri, E., & Hu, C. (2018) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2018.04.112 · Cited by 14

Novel Molecular Signatures in the PIP4K/PIP5K Family of Proteins Specific for Different Isozymes and Subfamilies Provide Important Insights into the Evolutionary Divergence of this Protein Family

Khadka, B., & Gupta, R. S. (2019) · Genes · doi:10.3390/genes10040312 · Cited by 14

Overexpression of the Phosphatidylcholine: Diacylglycerol Cholinephosphotransferase (PDCT) gene increases carbon flux toward triacylglycerol (TAG) synthesis in Camelina sativa seeds

Abdullah, H., Pang, N., Chilcoat, B., Shachar‐Hill, Y., Schnell, D. J., & Dhankher, O. P. (2024) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2024.108470 · Cited by 13

Contributions of the dark septate endophyte extracellular metabolites to plant growth, metabolism and root-associated microbial community structure

Bi, Y., Wang, S., Song, Y., Tan, H. S., & Christie, P. (2024) · Plant and Soil · doi:10.1007/s11104-024-06980-5 · Cited by 13

Phosphorus in Soils and Plants [Working Title]

Anjum, N. A., Masood, A., Umar, S., & Khan, N. A. (2023) · IntechOpen eBooks · doi:10.5772/intechopen.107701 · Cited by 12

Comparative Metabolic Profiling of Two Contrasting Date Palm Genotypes Under Salinity

Kharusi, L. A., Jana, G. A., Patankar, H. V., & Yaish, M. W. F. (2020) · Plant Molecular Biology Reporter · doi:10.1007/s11105-020-01255-6 · Cited by 12

Inositolphosphorylceramide synthases, OsIPCSs, regulate plant height in rice

Wang, X., Zhang, Z., Peng, W., Huang, J., Yan, X., Yao, W., Ouyang, J., & Li, S. (2023) · Plant Science · doi:10.1016/j.plantsci.2023.111798 · Cited by 11

Lipid remodelling and the conversion of lipids into sugars associated with tolerance to cadmium toxicity during white clover seed germination

Lin, L., Lin, J., Zhou, M., Yuan, Y., & Li, Z. (2024) · Physiologia Plantarum · doi:10.1111/ppl.14433 · Cited by 11

A mutation in Arabidopsis SAL1 alters its in vitro activity against IP3 and delays developmental leaf senescence in association with lower ROS levels

Shirzadian-Khorramabad, R., Moazzenzadeh, T., Sajedi, R. H., Jing, H., Hille, J., & Dijkwel, P. P. (2022) · Plant Molecular Biology · doi:10.1007/s11103-022-01245-0 · Cited by 11

Phosphatidylinositol 4,5-bisphosphate regulates plant K+ channels

Wigoda, N., Ma, X., & Moran, N. (2010) · Biochemical Society Transactions · doi:10.1042/bst0380705 · Cited by 11

Sustainable Management of Phosphorus in Agriculture for Environmental Conservation

Hoque, T. S., Sarkar, D., Datta, R., Kibria, M. G., Ullah, R., Ahmed, N., Hossain, M. A., Masood, A., & Anjum, N. A. (2023) · IntechOpen eBooks · doi:10.5772/intechopen.113086 · Cited by 10

Phenol modulates lipid kinase activities in Vicia sativa plants

Ibáñez, S. G., Villasuso, A. L., Racagni, G. E., Agostini, E., & Medina, M. I. (2015) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2015.09.005 · Cited by 10

Metabolism and roles of phosphatidylinositol 3-phosphate in pollen development and pollen tube growth in Arabidopsis

Gao, X., & Zhang, X. S. (2012) · Plant Signaling & Behavior · doi:10.4161/psb.18743 · Cited by 10

Mechanisms of drought resistance in introgression forms of Lolium multiflorum/Festuca arundinacea

Perlikowski, D., & Kosmala, A. (2020) · Biologia Plantarum · doi:10.32615/bp.2020.076 · Cited by 10

Expression Profiling of Candidate Genes in Sugar Beet Leaves Treated with Leonardite-Based Biostimulant

Hajizadeh, H. S., Heidari, B., Bertoldo, G., Lucia, M. C. D., Magro, F., Broccanello, C., Baglieri, A., Puglisi, I., Squartini, A., Campagna, G., et al. (2019) · Microarrays · doi:10.3390/ht8040018 · Cited by 9

Salivary proteins of Phloeomyzus passerinii, a plant-manipulating aphid, and their impact on early gene responses of susceptible and resistant poplar genotypes

Lemus, L. P., Tricard, J., Duclercq, J., Coulette, Q., Giron, D., Hano, C., Huguet, E., Lamblin, F., Cherqui, A., & Sallé, A. (2020) · Plant Science · doi:10.1016/j.plantsci.2020.110468 · Cited by 9

Salvianolic Acid Modulates Physiological Responses and Stress-Related Genes That Affect Osmotic Stress Tolerance in Glycine max and Zea mays

Kazerooni, E. A., Al-Sadi, A. M., Rashid, U., Kim, I., Kang, ⋅.-M., & Lee, I. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.904037 · Cited by 9

Soybean Inositol Polyphosphate 5‐Phosphatase 8 Confers Salt Tolerance by Reducing Sodium Influx Through Inositol 1,4,5‐Trisphosphate Signalling

Jia, Q., Chen, Y., Kong, D., Fan, H., Sun, S., Liu, Y. J., Fu, J., Li, M., Wong, F., Qing-hua, L., et al. (2025) · Plant Cell & Environment · doi:10.1111/pce.70071 · Cited by 8

Investment in plant research and development bears fruit in China

Chong, K., & Xu, Z. H. (2014) · Plant Cell Reports · doi:10.1007/s00299-014-1587-6 · Cited by 8

Integrated Analysis of Single-Molecule Real-Time Sequencing and Next-Generation Sequencing Eveals Insights into Drought Tolerance Mechanism of Lolium multiflorum

Liu, Q., Wang, F., Yang, S., Huang, L., & Zhang, X. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23147921 · Cited by 8

Cytoskeleton and Root Hair Growth

Park, E., & Nebenführ, A. (2010) · Advances in plant biology · doi:10.1007/978-1-4419-0987-9_12 · Cited by 8

Revealing the effects of two DNA methyltransferase inhibitors on DNA methylation and carotenoid metabolism in Chlamydomonas reinhardtii by comparative transcriptome and physiological analysis

Dai, J.-L., Chen, H., Liang, M., & Jiang, J. (2024) · Algal Research · doi:10.1016/j.algal.2024.103739 · Cited by 7

Biochemical characterization of phospholipases C from Coffea arabica in response to aluminium stress

González-Mendoza, V. M., Sanchez‐Sandoval, E., Munnik, T., & Hernández‐Sotomayor, S. M. T. (2019) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2019.110951 · Cited by 7

Importance of inositols and their derivatives in cowpea under root dehydration: An omics perspective

Ferreira‐Neto, J. R. C., da Silva, M. D., Rodrigues, F. A., Nepomuceno, A. L., Pandolfi, V., Morais, D. A. D. L., Kido, É. A., & Benko‐Iseppon, A. M. (2020) · Physiologia Plantarum · doi:10.1111/ppl.13292 · Cited by 7

Phosphatidic acids mediate transport of Ca2+ and H+ through plant cell membranes

Medvedev, S. S., Voronina, O., Tankelyun, O. V., Bilova, T. E., Suslov, D. V., Bankin, M., Mackievic, V. S., Makavitskaya, M., Shishova, M. F., Martinec, J., et al. (2019) · Functional Plant Biology · doi:10.1071/fp18242 · Cited by 7

Comparative phytohormone profiles, lipid kinase and lipid phosphatase activities in barley aleurone, coleoptile, and root tissues

Meringer, M. V., Villasuso, A. L., Pasquaré, S. J., Giusto, N. M., Machado, E. E., & Racagni, G. E. (2012) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2012.06.013 · Cited by 7

Roles of plastid-located phosphate transporters in carotenoid accumulation

Hao, D., Zhou, J., Huang, Y., Wang, H., Li, X., Guo, H., & Liu, J. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.1059536 · Cited by 6

Circadian rhythms synchronise intracellular calcium dynamics and ATP production for facilitatingArabidopsispollen tube growth

Yue, X., Gao, X., & Zhang, X. S. (2015) · Plant Signaling & Behavior · doi:10.1080/15592324.2015.1017699 · Cited by 6

Overexpression of Two Upstream Phospholipid Signaling Genes Improves Cold Stress Response and Hypoxia Tolerance, but Leads to Developmental Abnormalities in Barley

Gierczik, K., Székely, A., Ahres, M., Marozsán-Tóth, Z., Vashegyi, I., Harwood, W., Tóth, B. I., Galiba, G., Soltész, A., & Vágújfalvi, A. (2019) · Plant Molecular Biology Reporter · doi:10.1007/s11105-019-01154-5 · Cited by 6

Lipid trafficking and signaling in plants

Koenig, A. M., Christoph Benning, A., & Hoffmann-Benning, S. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819404-1.00002-6 · Cited by 6

Membrane Rigidity and Phosphatidic Acid (PtdOH) Signal: Two Important Events in Acinetobacter guillouiae SFC 500‐1A Exposed to Chromium(VI) and Phenol

Fernández, M., Paulucci, N. S., Margutti, M. P., Biasutti, A., Racagni, G. E., Villasuso, A. L., Agostini, E., & González, P. S. (2019) · Lipids · doi:10.1002/lipd.12187 · Cited by 6

Structural divergence and loss of phosphoinositide-specific phospholipase C signaling components during the evolution of the green plant lineage: implications from structural characteristics of algal components

Mikami, K. (2014) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00380 · Cited by 6

The Potential of PIP3 in Enhancing Wound Healing

Blitsman, Y., Hollander, E., Benafsha, C., Yegodayev, K. M., Hadad, U., Goldbart, R., Traitel, T., Rudich, A., Elkabets, M., & Kost, J. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25031780 · Cited by 5

Phosphatidylinositol pathway-associated genes adjust the rice growth and stress signaling: A global assay of the 5PTase family in the Oryza sativa genome

Faraji, S., Chari, G., & Najafi-Zarrini, H. (2020) · Plant Gene · doi:10.1016/j.plgene.2020.100244 · Cited by 5

Diurnal rhythms in durum wheat triggered by Rhopalosiphum padi (bird cherry-oat aphid)

Goldstein, Y., Han, J., Kunk, D., Batushansky, A., Nalam, V. J., & Tzin, V. (2025) · BMC Plant Biology · doi:10.1186/s12870-025-06100-0 · Cited by 5

Understanding low-phosphate stress responses in plants: Opportunities for genome editing to improve phosphorous use efficiency (PUE)

Ceasar, S. A., Ebeed, H. T., Ramakrishnan, M., García‐Caparrós, P., & Savarimuthu Ignacimuthu, S. J. (2025) · Biotechnology Advances · doi:10.1016/j.biotechadv.2025.108686 · Cited by 4

Photosynthesis-dependent Ca2+influx and functional diversity between phospholipases in the formation of cell polarity in migrating cells of red algae

Mikami, K., Li, L., Takahashi, M., & Saga, N. (2009) · Plant Signaling & Behavior · doi:10.4161/psb.4.9.9534 · Cited by 4

Mammalian Neurotransmitter Are Important Signals Mediating Plant Morphogenesis

Erland, L. A. E., & Saxena, P. K. (2019) · Springer eBooks · doi:10.1007/978-981-13-8922-1_16 · Cited by 4

Phospholipids of Embryogenic and Non-embryogenic Cell Lines of Larixsibirica Ledeb.

Semenova, N. V., Шмаков, В. Н., Konstantinov, Y. M., & Дударева, Л. В. (2020) · Russian Journal of Plant Physiology · doi:10.1134/s1021443720060151 · Cited by 4

Sterol Composition of Lichen Peltigera canina When Exposed to Unfavorable Temperatures

Valitova, Y. N., Khabibrakhmanova, V. R., Babaev, V. M., Uvaeva, V. L., Khairullina, A. F., Rakhmatullina, D. F., Galeeva, E. I., Swid, M. A., & Minibayeva, F. V. (2023) · Russian Journal of Plant Physiology · doi:10.1134/s1021443723603154 · Cited by 4

Palm Phospholipids

Panpipat, W., & Chaijan, M. (2015) · Elsevier eBooks · doi:10.1016/b978-1-63067-044-3.50008-x · Cited by 4

PI3K is involved in nucleolar structure and function on root-tip meristematic cells of Triticum aestivum L.

Ni, X., & Zhang, F. (2014) · Acta Histochemica · doi:10.1016/j.acthis.2014.02.004 · Cited by 4

Chlorination treatment actuated structural reconstitution and aggravated toxicity of molybdenum disulfide nanosheets to freshwater algae

Wang, Q., Li, R., Zhang, X., Li, T., Jin, C., Zou, W., & Cao, Z. (2025) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2025.137919 · Cited by 3

Temperature Stress and Redox Homeostasis: The Synergistic Network of Redox and Chaperone System in Response to Stress in Plants

Wu, H.-C., Vignols, F., & Jinn, T.-L. (2019) · Heat shock proteins · doi:10.1007/978-3-030-03952-3_4 · Cited by 3

Alterations in the proteome of wheat primary roots after wortmannin application during seed germination

Cao, H., Ni, X., Zhang, C., Shi, W., Xu, Y., Yan, Y., & Zhang, F. (2017) · Acta Physiologiae Plantarum · doi:10.1007/s11738-017-2511-9 · Cited by 3

Salicylic Acid and Phospholipid Signaling

Rodas-Junco, B. A., Muñoz-Sánchez, J. A., & Hernández‐Sotomayor, S. M. T. (2013) · Springer eBooks · doi:10.1007/978-94-007-6428-6_3 · Cited by 2

Transcriptome Analysis of Stigmas of Vicia faba L. Flowers

Casimiro-Soriguer, I., Aguilar-Benitez, D., Gutiérrez, N., & Torres, A. M. (2024) · Plants · doi:10.3390/plants13111443 · Cited by 2

Comparative Genomic View of The Inositol-1,4,5-Trisphosphate Receptor in Plants

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Phosphoinositide Signaling in Root Hair Tip Growth

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