Research on plant abiotic stress responses in the post‐genome era: past, present and future

Europe-wide reduction in primary productivity caused by the heat and drought in 2003

Ciais, P., Reichstein, M., Viovy, N., Granier, A., Ogée, J., Allard, V., Aubinet, M., Buchmann, N., Bernhofer, C., Carrara, A., et al. (2005) · Nature · doi:10.1038/nature03972 · Cited by 4,153

Abiotic stress, the field environment and stress combination

Mittler, R. (2006) · Trends in Plant Science · doi:10.1016/j.tplants.2005.11.002 · Cited by 3,083

Abscisic Acid Inhibits Type 2C Protein Phosphatases via the PYR/PYL Family of START Proteins

Park, S., Fung, P., Nishimura, N., Jensen, D. R., Fujii, H., Zhao, Y., Lumba, S., Santiago, J., Rodrigues, A., Chow, T.-F. F., et al. (2009) · Science · doi:10.1126/science.1173041 · Cited by 2,986

TRANSCRIPTIONAL REGULATORY NETWORKS IN CELLULAR RESPONSES AND TOLERANCE TO DEHYDRATION AND COLD STRESSES

Yamaguchi‐Shinozaki, K., & Shinozaki, K. (2006) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.57.032905.105444 · Cited by 2,935

Salinity tolerance in halophytes*

Flowers, T. J., & Colmer, T. D. (2008) · New Phytologist · doi:10.1111/j.1469-8137.2008.02531.x · Cited by 2,789

The complex language of chromatin regulation during transcription

Berger, S. L. (2007) · Nature · doi:10.1038/nature05915 · Cited by 2,768

MicroRNAs AND THEIR REGULATORY ROLES IN PLANTS

Jones-Rhoades, M. W., Bartel, D. P., & Bartel, B. (2006) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.57.032905.105218 · Cited by 2,720

Gene networks involved in drought stress response and tolerance

Shinozaki, K., & Yamaguchi‐Shinozaki, K. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erl164 · Cited by 2,641

Drought and Salt Tolerance in Plants

Bartels, D., & Sunkar, R. (2005) · Critical Reviews in Plant Sciences · doi:10.1080/07352680590910410 · Cited by 2,611

Regulators of PP2C Phosphatase Activity Function as Abscisic Acid Sensors

Ma, Y., Szostkiewicz, I., Korte, A., Moes, D., Yang, Y., Christmann, A., & Grill, E. (2009) · Science · doi:10.1126/science.1172408 · Cited by 2,467

Genetic response of growth phases for abiotic environmental stress tolerance in cereal crop plants

Ali, Q., & Malik, A. (2021) · Genetika · doi:10.2298/gensr2101419a · Cited by 28

Water deficiency induces evolutionary tradeoff between stress tolerance and chemical defense allocation that may help explain range limits in plants

Siemens, D. H., Duvall‐Jisha, J., Jacobs, J., Manthey, J. D., Haugen, R. H., & Matzner, S. L. (2012) · Oikos · doi:10.1111/j.1600-0706.2011.19944.x · Cited by 28

Plant Metabolomics in a Changing World: Metabolite Responses to Abiotic Stress Combinations

Jorge, T. F., & António, C. (2018) · InTech eBooks · doi:10.5772/intechopen.71769 · Cited by 30

PncStress: a manually curated database of experimentally validated stress-responsive non-coding RNAs in plants

Wu, W., Wu, Y. R., Hu, D., Zhou, Y., Hu, Y., Chen, Y., & Chen, M. (2020) · Database · doi:10.1093/database/baaa001 · Cited by 28

Evolution and Expression of the Membrane Attack Complex and Perforin Gene Family in the Poaceae

Yu, L., Liu, D., Chen, S., Dai, Y., Guo, W., Zhang, X., Wang, L., Ma, S., Xiao, M., Qi, H., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21165736 · Cited by 28

Remodeling of the cell wall as a drought-tolerance mechanism of a soybean genotype revealed by global gene expression analysis

Coutinho, F. S., Rodrigues, J. M., Lima, L. L., Mesquita, R. O., Carpinetti, P. A., Machado, J. P., Vital, C. E., Vidigal, P. M. P., Ramos, M. E. S., Maximiano, M. R., et al. (2021) · aBIOTECH · doi:10.1007/s42994-021-00043-4 · Cited by 28

Genome-Wide Analysis of Late Embryogenesis Abundant Protein Gene Family in Vigna Species and Expression of VrLEA Encoding Genes in Vigna glabrescens Reveal Its Role in Heat Tolerance

SINGH, C. M., Kumar, M., Pratap, A., Tripathi, A., Singh, S., Mishra, A., Kumar, H., Nair, R. M., & Singh, N. P. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.843107 · Cited by 28

Calcium and nitric oxide signaling in plant cadmium stress tolerance: A cross talk

Mir, I. R., Gautam, H., Anjum, N. A., Masood, A., & Khan, N. A. (2022) · South African Journal of Botany · doi:10.1016/j.sajb.2022.07.039 · Cited by 28

CAMTAs, a family of calmodulin-binding transcription factors, are versatile regulators of biotic and abiotic stress responses in plants

Abdel‐Hameed, A. A. E., Liao, W., Prasad, K. V. S. K., & Reddy, A. S. N. (2024) · Critical Reviews in Plant Sciences · doi:10.1080/10407782.2024.2302671 · Cited by 29

Comparative physiological and metabolomic responses of four Brachypodium distachyon varieties contrasting in drought stress resistance

Shi, H., Ye, T., Song, B., Qi, X., & Chan, Z. (2015) · Acta Physiologiae Plantarum · doi:10.1007/s11738-015-1873-0 · Cited by 28

Physiological, biochemical and genetic responses of Caucasian tea (Camellia sinensis(L.) Kuntze) genotypes under cold and frost stress

Samarina, L. S., Malyukova, L. S., Efremov, A. M., Simonyan, T. A., Matskiv, A. O., Koninskaya, N. G., Rakhmangulov, R. S., Gvasaliya, M. V., Malyarovskaya, V. I., Ryndin, A. V., et al. (2020) · PeerJ · doi:10.7717/peerj.9787 · Cited by 28

Genome-wide association study presents insights into the genetic architecture of drought tolerance in maize seedlings under field water-deficit conditions

Chen, S., Dang, D., Liu, Y., Ji, S., Zheng, H., Zhao, C., Dong, X., Li, C., Guan, Y., Zhang, A., et al. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2023.1165582 · Cited by 27

Comprehensive Identification and Expression Analysis of the Multidrug and Toxic Compound Extrusion (MATE) Gene Family in Brachypodium distachyon

Ma, S., Guo, Y., Zhang, T., Liu, D., Wang, L., Hu, R., Zhou, D., Zhou, Y., Chen, Q., & Yu, L. (2024) · Plants · doi:10.3390/plants13182586 · Cited by 27

Recent advancement in mass based plant metabolomics: techniques, tools, and analytical approaches

Kumar, N., Bharat, J. S., Kumar, A., & Jaitak, V. (2024) · Phytochemistry Reviews · doi:10.1007/s11101-024-10028-y · Cited by 27

Genome-wide survey and expression analysis of the calcium-dependent protein kinase gene family in cassava

Hu, W., Hou, X., Xia, Z., Yan, Y., Wei, Y., Wang, L., Zou, M., Lu, C., Wang, W., & Peng, M. (2015) · Molecular Genetics and Genomics · doi:10.1007/s00438-015-1103-x · Cited by 27

Responsive Proteins in Wheat Cultivars with Contrasting Nitrogen Efficiencies under the Combined Stress of High Temperature and Low Nitrogen

Yousuf, P. Y., Allah, E. F. A., Nauman, M., Asif, A., Hashem, A., Alqarawi, A. A., & Ahmad, A. (2017) · Genes · doi:10.3390/genes8120356 · Cited by 27

Engineering cereal crops for enhanced abiotic stress tolerance

Lata, C., & Shivhare, R. (2021) · Proceedings of the Indian National Science Academy · doi:10.1007/s43538-021-00006-9 · Cited by 27

Sugarcane Transcriptomics in Response to Abiotic and Biotic Stresses: A Review

Manimekalai, R., Suresh, G., & Singaravelu, B. (2022) · Sugar Tech · doi:10.1007/s12355-021-01098-9 · Cited by 27

Genome-wide identification of Tomato Golden 2-Like transcription factors and abiotic stress related members screening

Wang, Z.-Y., Zhao, S., Liu, J., Zhao, H.-Y., Sun, X.-Y., Wu, T.-R., Pei, T., Wang, Y., Liu, Q., Yang, H., et al. (2022) · BMC Plant Biology · doi:10.1186/s12870-022-03460-9 · Cited by 27

Effects of drought and high temperature on physiological and biochemical processes, and productivity of plants nanochelates

Kiriziy, D. A., & Стасик, О. О. (2022) · Fiziologia rastenij i genetika · doi:10.15407/frg2022.02.095 · Cited by 27

Mechanisms of Kale (Brassica oleracea var. acephala) Tolerance to Individual and Combined Stresses of Drought and Elevated Temperature

Bauer, N., Tkalec, M., Major, N., Vasari, A. T., Tokić, M., Vitko, S., Ban, D., Ban, S. G., & Salopek‐Sondi, B. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231911494 · Cited by 27

StMAPKK5 Positively Regulates Response to Drought and Salt Stress in Potato

Luo, Y., Wang, K., Zhu, L., Zhang, N., & Si, H. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25073662 · Cited by 27

Biochemical characterization of the Arabidopsis KS-type dehydrin protein, whose gene expression is constitutively abundant rather than stress dependent

Hara, M., Shinoda, Y., Kubo, M., Kashima, D., Takahashi, I., Kato, T., Horiike, T., & Kuboi, T. (2011) · Acta Physiologiae Plantarum · doi:10.1007/s11738-011-0749-1 · Cited by 29

Engineering plants to tolerate abiotic stresses

Chen, M., Lung, S., Du, Z., & Chye, M. (2013) · Biocatalysis and Agricultural Biotechnology · doi:10.1016/j.bcab.2013.09.010 · Cited by 27

Carbon dots-mediated plant adaptive responses to abiotic stress

Chen, F., Shen, Z., Shi, R., Zhang, X., Zhang, H., Li, W., & Lei, B. (2024) · Materials Research Bulletin · doi:10.1016/j.materresbull.2024.113137 · Cited by 26

Epigenetic modifications in plant abiotic stress adaptation: towards climate-resilient and sustainable crop improvement

Qadir, M., Kaur, N., Rahman, F. U., Nabi, F., Ahmed, Z. F. R., & Wu, J. (2026) · Frontiers in Plant Science · doi:10.3389/fpls.2026.1738299 · Cited by 26

Systems biology approaches to abscisic acid signaling

Umezawa, T. (2011) · Journal of Plant Research · doi:10.1007/s10265-011-0418-x · Cited by 26

Arabidopsis Acyl-Coenzyme-A-Binding Protein ACBP1 interacts with AREB1 and mediates salt and osmotic signaling in seed germination and seedling growth

Chen, M., Hu, T., Xue, Y., Zhu, F., Du, Z., Lo, C., & Chye, M. (2018) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2018.09.007 · Cited by 26

Genome-wide characterization of a SRO gene family involved in response to biotic and abiotic stresses in banana (Musa spp.)

Zhang, L., Zhou, D., Hu, H., Li, W., Hu, Y., Xie, J., Huang, S., & Wang, W. (2019) · BMC Plant Biology · doi:10.1186/s12870-019-1807-x · Cited by 26

Effect of High-Temperature Stress on Crop Productivity

Bhattacharya, A. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-817562-0.00001-x · Cited by 26

Comprehensive Bioinformatics and Expression Analysis of TCP Transcription Factors in Liriodendron chinense Reveals Putative Abiotic Stress Regulatory Roles

Hwarari, D., Guan, Y., Li, R., Movahedi, A., Chen, J., & Yang, L. (2022) · Forests · doi:10.3390/f13091401 · Cited by 26

Mechanism of Reactive Oxygen Species Regulation in Plants

Shehzad, J., & Mustafa, G. (2023) · Springer eBooks · doi:10.1007/978-981-19-9794-5_2 · Cited by 26

Maize ZmBES1/BZR1-1 transcription factor negatively regulates drought tolerance

Feng, W., Zhang, H., Cao, Y., Liu, Y., Zhao, Y., Sun, F., Yang, Q., Zhang, X., Zhang, Y., Wang, Y., et al. (2023) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2023.108188 · Cited by 26

Molecular and functional characterization of the HbSRPP promoter in response to hormones and abiotic stresses

Guo, D., Li, H.-L., Tang, X., & Peng, S.-Q. (2013) · Transgenic Research · doi:10.1007/s11248-013-9753-0 · Cited by 26

Isolation and characterization of a rice glutathione S-transferase gene promoter regulated by herbicides and hormones

Hu, T., He, S., Yang, G., Zeng, H., Wang, G., Chen, Z., & Huang, X. (2010) · Plant Cell Reports · doi:10.1007/s00299-010-0964-z · Cited by 26

Changes in RNA Splicing in Developing Soybean (Glycine max) Embryos

Aghamirzaie, D., Nabiyouni, M., Fang, Y., Klumas, C., Heath, L. S., Grene, R., & Collakova, E. (2013) · Biology · doi:10.3390/biology2041311 · Cited by 26

De Novo Assembly of Expressed Transcripts and Global Transcriptomic Analysis from Seedlings of the Paper Mulberry (Broussonetia kazinoki x Broussonetia papyifera)

Xianjun, P., Teng, L., Xiaoman, W., Yucheng, W., & Shihua, S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0097487 · Cited by 26

RNA-seq Analysis Reveals Ethylene-Mediated Reproductive Organ Development and Abscission in Soybean (Glycine max L. Merr.)

Cheng, Y., Liu, J., Yang, X., Ma, R., Liu, C., & Liu, Q. (2012) · Plant Molecular Biology Reporter · doi:10.1007/s11105-012-0533-4 · Cited by 27

Comparative Transcriptomic Profiling of Vitis vinifera Under High Light Using a Custom-Made Array and the Affymetrix GeneChip

Carvalho, L. C., Vilela, B., Mullineaux, P. M., & Amâncio, S. (2011) · Molecular Plant · doi:10.1093/mp/ssr027 · Cited by 26

Identification of salt-stress responsive microRNAs from Solanum lycopersicum and Solanum pimpinellifolium

Zhao, G., Yu, H., Liu, M., Lu, Y., & Ouyang, B. (2017) · Plant Growth Regulation · doi:10.1007/s10725-017-0289-9 · Cited by 26

Menadione sodium bisulphite (MSB): Beyond seed-soaking. Root pretreatment with MSB primes salt stress tolerance in tomato plants

Jiménez-Árias, D., García-Machado, F. J., Morales-Sierra, S., Suárez, E., Pérez, J. A. P., Luis, J., Garrido-Orduña, C., Herrera, A. J., Valdés, F., Sandalio, L. M., et al. (2018) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2018.10.009 · Cited by 26

Overexpression of OsLea14-A improves the tolerance of rice and increases Hg accumulation under diverse stresses

Hu, T., Liu, Y., Zhu, S., Qin, J., Li, W., & Zhou, N. (2019) · Environmental Science and Pollution Research · doi:10.1007/s11356-019-04464-z · Cited by 26

Reactive Oxygen Species

Choudhary, K. K., Chaudhary, N., Agrawal, S. B., & Agrawal, M. (2017) · Wiley eBooks · doi:10.1002/9781119324928.ch5 · Cited by 26

The suppressed expression of a stress responsive gene 'OsDSR2' enhances rice tolerance in drought and salt stress

Luo, C., Akhtar, M., Min, W., Alam, Y. S. J., Ma, T., Shi, Y., She, Y., & Lu, X. (2023) · Journal of Plant Physiology · doi:10.1016/j.jplph.2023.153927 · Cited by 25

Arabidopsis thaliana: Model Plant for the Study of Abiotic Stress Responses

Raza, A., Charagh, S., Sadaqat, N., & Jin, W. (2020) · Springer eBooks · doi:10.1007/978-981-15-6345-4_3 · Cited by 25

ROS Regulation Mechanism for Mitigation of Abiotic Stress in Plants

Kumari, A., Bhinda, M. S., Sharma, S., Chitara, M. K., Debnath, A., Maharana, C., Parihar, M., & Sharma, B. (2021) · Biochemistry · doi:10.5772/intechopen.99845 · Cited by 25

Indole-3-acetic acid, a hormone potentially involved in chilling-induced seed browning of pepper (Capsicum annuum L.) fruit during cold storage

Seo, J., Lee, J. G., Kang, B., Lim, S., & Lee, E. J. (2023) · Postharvest Biology and Technology · doi:10.1016/j.postharvbio.2023.112299 · Cited by 25

Potential Role of Beneficial Soil Microorganisms in Plant Tolerance to Abiotic Stress Factors

Balestrini, R., Chitarra, W., Fotopoulos, V., & Ruocco, M. (2017) · Springer eBooks · doi:10.1007/978-3-319-63336-7_12 · Cited by 25

Molecular cloning and characterization of novel WIN1/SHN1 ethylene responsive transcription factor HvSHN1 in barley (Hordeum vulgare L.)

Djemal, R., Mila, I., Bouzayen, M., Pirrello, J., & Khoudi, H. (2018) · Journal of Plant Physiology · doi:10.1016/j.jplph.2018.04.019 · Cited by 25

AlNAC4 Transcription Factor From Halophyte Aeluropus lagopoides Mitigates Oxidative Stress by Maintaining ROS Homeostasis in Transgenic Tobacco

Khedia, J., Agarwal, P., & Agarwal, P. K. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.01522 · Cited by 25

Exogenous Abscisic Acid Can Influence Photosynthetic Processes in Peas through a Decrease in Activity of H+-ATP-ase in the Plasma Membrane

Yudina, L., Sukhova, E., Николаевна, Ш. О., Grinberg, M. A., Ladeynova, M. M., Vodeneev, V., & Sukhov, V. (2020) · Biology · doi:10.3390/biology9100324 · Cited by 25

Identification and Expression of the Multidrug and Toxic Compound Extrusion (MATE) Gene Family in Capsicum annuum and Solanum tuberosum

Chen, Q., Wang, L., Liu, D., Ma, S., Dai, Y., Zhang, X., Wang, Y., Hu, T., Xiao, M., Zhou, Y., et al. (2020) · Plants · doi:10.3390/plants9111448 · Cited by 25

Transcriptome Expression Profiling in Response to Drought Stress in Paulownia australis

Dong, Y., Fan, G., Zhao, Z., & Deng, M. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms15034583 · Cited by 24

Response of Tea Plants to Drought Stress

Qian, W., Hu, J., Zhang, X., Zhao, L., Wang, Y., & Ding, Z. (2018) · Springer eBooks · doi:10.1007/978-981-13-2140-5_4 · Cited by 24

The BTB-TAZ protein MdBT2 negatively regulates the drought stress response by interacting with the transcription factor MdNAC143 in apple

Ji, X., Li, H., Qiao, Z., Zhang, J.-C., Sun, W.-J., Wang, C., Yang, K., You, C., & Hao, Y. (2020) · Plant Science · doi:10.1016/j.plantsci.2020.110689 · Cited by 25

Regulation of rose petal dehydration tolerance and senescence by RhNAP transcription factor via the modulation of cytokinin catabolism

Zou, J., Lü, P., Jiang, L., Liu, K., Zhang, T., Chen, J., Yao, Y., Cui, Y., Gao, J., & Zhang, C. (2021) · Molecular Horticulture · doi:10.1186/s43897-021-00016-7 · Cited by 24

Structured patterns in geographic variability of metabolic phenotypes in Arabidopsis thaliana

Kleeßen, S., António, C., Sulpice, R., Laitinen, R. A. E., Fernie, A. R., Stitt, M., & Nikoloski, Z. (2012) · Nature Communications · doi:10.1038/ncomms2333 · Cited by 24

Molecular switch for cold acclimation — anatomy of the cold-inducible promoter in plants

Jiang, Y., Peng, D., Bai, L.-P., Ma, H., Chen, L., Zhao, M., Xu, Z., & Guo, Z. (2013) · Biochemistry (Moscow) · doi:10.1134/s0006297913040032 · Cited by 24

An Integrated Approach of Proteomics and Computational Genetic Modification Effectiveness Analysis to Uncover the Mechanisms of Flood Tolerance in Soybeans

Wang, X., Sakata, K., & Komatsu, S. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19051301 · Cited by 24

Heterologous expression of Brassica juncea annexin, AnnBj2 confers salt tolerance and ABA insensitivity in transgenic tobacco seedlings

Ahmed, I., Yadav, D., Shukla, P., & Kirti, P. B. (2018) · Functional & Integrative Genomics · doi:10.1007/s10142-018-0614-z · Cited by 24

Understanding the function and regulation of plant secondary metabolism through metabolomics approaches

Delfin, J. C., Watanabe, M., & Tohge, T. (2018) · Theoretical and Experimental Plant Physiology · doi:10.1007/s40626-018-0126-1 · Cited by 24

PnSAG1, an E3 ubiquitin ligase of the Antarctic moss Pohlia nutans, enhanced sensitivity to salt stress and ABA

Wang, J., Liu, S., Liu, H., Chen, K., & Zhang, P. (2019) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2019.06.002 · Cited by 24

Calcium Signaling in Plants Under Drought

Aliniaeifard, S., Shomali, A., Seifikalhor, M., & Lastochkina, O. V. (2020) · Signaling and communication in plants · doi:10.1007/978-3-030-40277-8_10 · Cited by 24

Molecular characterization, expression and functional analysis of acyl-CoA-binding protein gene family in maize (Zea mays)

Zhu, J., Li, W., Zhou, Y., Pei, L., Liu, J., Xia, X., Che, R., & Li, H. (2021) · BMC Plant Biology · doi:10.1186/s12870-021-02863-4 · Cited by 24

Controlled Over-Expression of AtDREB1A Enhances Tolerance against Drought and Salinity in Rice

Raveendran, M., Ramanathan, V., Shillak, A. B., Pralhad, S. M., Shankarrao, C. N., Rahman, H., Kambale, R., Nallathambi, J., Tamilselvan, S., & Parani, M. (2021) · Agronomy · doi:10.3390/agronomy11010159 · Cited by 23

Roles of Mangroves in Combating the Climate Change

Kumari, A., & Rathore, M. S. (2021) · Springer eBooks · doi:10.1007/978-981-16-2494-0_10 · Cited by 23

Non-Coding RNAs in Glioma Microenvironment and Angiogenesis

Li, D., Zhang, Z., Xia, C., Niu, C., & Zhou, W. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.763610 · Cited by 24

Comparative transcriptomic and metabolic profiling provides insight into the mechanism by which the autophagy inhibitor 3-MA enhances salt stress sensitivity in wheat seedlings

Yue, J., Wang, Y., Jiao, J., & Wang, H. (2021) · BMC Plant Biology · doi:10.1186/s12870-021-03351-5 · Cited by 23

Genome-wide analysis and functional characterization of CHYR gene family associated with abiotic stress tolerance in bread wheat (Triticum aestivum L.)

Liu, H., Yang, W., Zhao, X., Kang, G., Li, N., & Xu, H. (2022) · BMC Plant Biology · doi:10.1186/s12870-022-03589-7 · Cited by 23

G protein controls stress readiness by modulating transcriptional and metabolic homeostasis in Arabidopsis thaliana and Marchantia polymorpha

Wu, T., Krishnamoorthi, S., Boonyaves, K., Al‐Darabsah, I., Leong, R., Jones, A. M., Ishizaki, K., Liao, K., & Urano, D. (2022) · Molecular Plant · doi:10.1016/j.molp.2022.10.020 · Cited by 23

Epigenomics: a new tool for the generation of climate resilient grapevines

Tan, J. W., & Lopez, C. M. R. (2023) · Frontiers in Horticulture · doi:10.3389/fhort.2023.1116866 · Cited by 23

Transcriptome profiling of Eucalyptus nitens reveals deeper insight into the molecular mechanism of cold acclimation and deacclimation process

Gaete-Loyola, J., Lagos, C., Beltrán, M. F., Valenzuela, S., Emhart, V., & Férnandez, M. (2017) · Tree Genetics & Genomes · doi:10.1007/s11295-017-1121-4 · Cited by 23

Investigating the molecular basis for heterophylly in the aquatic plant Potamogeton octandrus (Potamogetonaceae) with comparative transcriptomics

He, D., Guo, P., Gugger, P. F., Guo, Y., Liu, X., & Chen, J. (2018) · PeerJ · doi:10.7717/peerj.4448 · Cited by 23

The Role of Long Noncoding RNAs in Plant Stress Tolerance

Song, Y., & Zhang, D. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-7136-7_3 · Cited by 23

Abiotic Stress Signaling in Plants–An Overview

Gill, S. S., Anjum, N. A., Gill, R., & Tuteja, N. (2016) · Wiley eBooks · doi:10.1002/9783527694570.ch1 · Cited by 23

Protein kinase SnRK2.6 phosphorylates transcription factor bHLH3 to regulate anthocyanin homeostasis during strawberry fruit ripening

Huang, F., Sun, M., Yao, Z., Zhou, J., Bai, Q., Chen, X., Huang, Y., & Shen, Y. (2024) · Journal of Experimental Botany · doi:10.1093/jxb/erae250 · Cited by 23

Genome-wide identification of major transcription factor superfamilies in rice identifies key candidates involved in abiotic stress dynamism

Muthuramalingam, P., Krishnan, S. R., Saravanan, K., Mareeswaran, N., Kumar, R., & Ramesh, M. (2018) · Journal of Plant Biochemistry and Biotechnology · doi:10.1007/s13562-018-0440-3 · Cited by 22

Transcriptomic profiling and identification of candidate genes in two Phoebe bournei ecotypes with contrasting cold stress responses

Zhang, J., Zhu, Y., Pan, Y., Huang, H., Li, C., Li, G., & Tong, Z. (2018) · Trees · doi:10.1007/s00468-018-1713-0 · Cited by 22

Identification and expression profiling of proline metabolizing genes in Arabidopsis thaliana and Oryza sativa to reveal their stress-specific transcript alteration

Arabia, S., Shah, M. N. A., Sami, A. A., Ghosh, A., & Islam, T. (2021) · Physiology and Molecular Biology of Plants · doi:10.1007/s12298-021-01023-0 · Cited by 22

The C4 protein of tomato yellow leaf curl Sardinia virus primes drought tolerance in tomato through morphological adjustments

Pagliarani, C., Moine, A., Chitarra, W., Nerva, L., Catoni, M., Tavazza, R., Matić, S., Vallino, M., Secchi, F., & Noris, E. (2022) · Horticulture Research · doi:10.1093/hr/uhac164 · Cited by 22

Natural variation of Alfin‐like family affects seed size and drought tolerance in rice

Yang, Y., Ma, X., Xia, H., Wang, L., Chen, S., Xu, K., Yang, F., Zou, Y., Wang, Y., Zhu, J., et al. (2022) · The Plant Journal · doi:10.1111/tpj.16003 · Cited by 22

Semi-embedded flexible multifunctional sensor for on-site continuous monitoring of plant microclimate

Qu, C., Sun, W., Hu, D., Yang, C., Zhao, T., Wang, Q., & He, Z. (2023) · Computers and Electronics in Agriculture · doi:10.1016/j.compag.2023.108521 · Cited by 22

GIGANTEA Unveiled: Exploring Its Diverse Roles and Mechanisms

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