Overexpression of the Artemisia Orthologue of ABA Receptor, AaPYL9, Enhances ABA Sensitivity and Improves Artemisinin Content in Artemisia annua L

S ALT AND D ROUGHT S TRESS S IGNAL T RANSDUCTION IN P LANTS

Zhu, J. (2002) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.53.091401.143329 · Cited by 5,808 · see citing works

Significance of Inducible Defense-related Proteins in Infected Plants

van Loon, L. C., Rep, M., & Pieterse, C. M. J. (2006) · Annual Review of Phytopathology · doi:10.1146/annurev.phyto.44.070505.143425 · Cited by 3,401 · see citing works

Abscisic Acid: Emergence of a Core Signaling Network

Cutler, S. R., Rodrı́guez, P. L., Finkelstein, R. R., & Abrams, S. R. (2010) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042809-112122 · Cited by 3,169 · see citing works

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 · see citing works

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 · see citing works

Agrobacterium-mediated transformation of Arabidopsis thaliana using the floral dip method

Zhang, X., Henriques, R., Lin, S., Niu, Q., & Chua, N. (2006) · Nature Protocols · doi:10.1038/nprot.2006.97 · Cited by 2,344 · see citing works

Abscisic Acid Signaling in Seeds and Seedlings

Finkelstein, R. R., Gampala, S. S. L., & Rock, C. D. (2002) · The Plant Cell · doi:10.1105/tpc.010441 · Cited by 2,300 · see citing works

A novel cis-acting element in an Arabidopsis gene is involved in responsiveness to drought, low-temperature, or high-salt stress.

Yamaguchi‐Shinozaki, K., & Shinozaki, K. (1994) · The Plant Cell · doi:10.1105/tpc.6.2.251 · Cited by 1,996 · see citing works

Molecular Aspects of Seed Dormancy

Finkelstein, R. R., Reeves, W., Ariizumi, T., & Steber, C. M. (2008) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.59.032607.092740 · Cited by 1,389 · see citing works

In vitro reconstitution of an abscisic acid signalling pathway

Fujii, H., Chinnusamy, V., Rodrigues, A., Rubio, S., Antoni, R., Park, S., Cutler, S. R., Sheen, J., Rodrı́guez, P. L., & Zhu, J. (2009) · Nature · doi:10.1038/nature08599 · Cited by 1,347 · see citing works

ABA perception and signalling

Raghavendra, A. S., Gonugunta, V. K., Christmann, A., & Grill, E. (2010) · Trends in Plant Science · doi:10.1016/j.tplants.2010.04.006 · Cited by 1,311 · see citing works

Different Plant Hormones Regulate Similar Processes through Largely Nonoverlapping Transcriptional Responses

Nemhauser, J. L., Hong, F., & Chory, J. (2006) · Cell · doi:10.1016/j.cell.2006.05.050 · Cited by 947 · see citing works

Molecular Basis of the Core Regulatory Network in ABA Responses: Sensing, Signaling and Transport

Umezawa, T., Nakashima, K., Miyakawa, T., Kuromori, T., Tanokura, M., Shinozaki, K., & Yamaguchi‐Shinozaki, K. (2010) · Plant and Cell Physiology · doi:10.1093/pcp/pcq156 · Cited by 923 · see citing works

Abscisic acid-dependent multisite phosphorylation regulates the activity of a transcription activator AREB1

Furihata, T., Maruyama, K., Fujita, Y., Umezawa, T., Yoshida, R., Shinozaki, K., & Yamaguchi‐Shinozaki, K. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0505667103 · Cited by 849 · see citing works

Three SnRK2 Protein Kinases are the Main Positive Regulators of Abscisic Acid Signaling in Response to Water Stress in Arabidopsis

Fujita, Y., Nakashima, K., Yoshida, T., Katagiri, T., Kidokoro, S., Kanamori, N., Umezawa, T., Fujita, M., Maruyama, K., Ishiyama, K., et al. (2009) · Plant and Cell Physiology · doi:10.1093/pcp/pcp147 · Cited by 733 · see citing works

A gate–latch–lock mechanism for hormone signalling by abscisic acid receptors

Melcher, K., Ng, L.-M., Zhou, X. E., Soon, F.-F., Xu, Y., Suino-Powell, K. M., Park, S.-Y., Weiner, J. J., Fujii, H., Chinnusamy, V., et al. (2009) · Nature · doi:10.1038/nature08613 · Cited by 731 · see citing works

Abscisic Acid Plays an Important Role in the Regulation of Strawberry Fruit Ripening

Jia, H., Chai, Y., Li, C., Lu, D., Luo, J., Qin, L., & Shen, Y. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.177311 · Cited by 725 · see citing works

EXPRESSION OF CONCERN: Modulation of drought resistance by the abscisic acid receptor PYL5 through inhibition of clade A PP2Cs

Santiago, J., Rodrigues, A., Saéz, Á., Rubio, S., Antoni, R., Dupeux, F., Park, S., Márquez, J. A., Cutler, S. R., & Rodrı́guez, P. L. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.03981.x · Cited by 597 · see citing works

Arabidopsis PYR/PYL/RCAR Receptors Play a Major Role in Quantitative Regulation of Stomatal Aperture and Transcriptional Response to Abscisic Acid

González‐Guzmán, M., Pizzio, G. A., Antoni, R., Vera‐Sirera, F., Merilo, E., Bassel, G. W., Fernández, M. A., Holdsworth, M. J., Perez-Amador, M. A., Kollist, H., et al. (2012) · The Plant Cell · doi:10.1105/tpc.112.098574 · Cited by 582 · see citing works

Structural basis of abscisic acid signalling

Miyazono, K., Miyakawa, T., Sawano, Y., Kubota, K., Kang, H., Asano, A., Miyauchi, Y., Takahashi, M., Zhi, Y., Fujita, Y., et al. (2009) · Nature · doi:10.1038/nature08583 · Cited by 578 · see citing works

Effects of plant hormones and shading on the accumulation of anthocyanins and the expression of anthocyanin biosynthetic genes in grape berry skins

Jeong, S.-T., Goto‐Yamamoto, N., Kobayashi, S., & Esaka, M. (2004) · Plant Science · doi:10.1016/j.plantsci.2004.03.021 · Cited by 563 · see citing works

Microarray Expression Analyses of Arabidopsis Guard Cells and Isolation of a Recessive Abscisic Acid Hypersensitive Protein Phosphatase 2C Mutant[W]

Leonhardt, N., Kwak, J. M., Robert, N., Waner, D., Leonhardt, G., & Schroeder, J. I. (2004) · The Plant Cell · doi:10.1105/tpc.019000 · Cited by 553 · see citing works

The abscisic acid receptor PYR1 in complex with abscisic acid

Santiago, J., Dupeux, F., Round, A. R., Antoni, R., Park, S., Jamin, M., Cutler, S. R., Rodrı́guez, P. L., & Márquez, J. A. (2009) · Nature · doi:10.1038/nature08591 · Cited by 536 · see citing works

PYR/PYL/RCAR family members are major in‐vivo ABI1 protein phosphatase 2C‐interacting proteins in Arabidopsis

Nishimura, N., Sarkeshik, A., Nito, K., Park, S., Wang, A., Carvalho, P. C., Lee, S., Caddell, D. F., Cutler, S. R., Chory, J., et al. (2009) · The Plant Journal · doi:10.1111/j.1365-313x.2009.04054.x · Cited by 505 · see citing works

Structural Mechanism of Abscisic Acid Binding and Signaling by Dimeric PYR1

Nishimura, N., Hitomi, K., Arvai, A. S., Rambo, R. P., Hitomi, C., Cutler, S. R., Schroeder, J. I., & Getzoff, E. D. (2009) · Science · doi:10.1126/science.1181829 · Cited by 493 · see citing works

Gibberellins, jasmonate and abscisic acid modulate the sucrose‐induced expression of anthocyanin biosynthetic genes in Arabidopsis

Loreti, E., Povero, G., Novi, G., Solfanelli, C., Alpi, A., & Pierdomenico Perata, A. (2008) · New Phytologist · doi:10.1111/j.1469-8137.2008.02511.x · Cited by 476 · see citing works

Monitoring the expression pattern of around 7,000 Arabidopsis genes under ABA treatments using a full-length cDNA microarray

Seki, M., Ishida, J., Narusaka, M., Fujita, M., Nanjo, T., Umezawa, T., Kamiya, A., Nakajima, M., Enju, A., Sakurai, T., et al. (2002) · Functional & Integrative Genomics · doi:10.1007/s10142-002-0070-6 · Cited by 471 · see citing works

Structural insights into the mechanism of abscisic acid signaling by PYL proteins

Yin, P., Fan, H., Hao, Q., Yuan, X., Wu, D., Pang, Y., Yan, C., Li, W., Wang, J., & Yan, N. (2009) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1730 · Cited by 462 · see citing works

The AIP2 E3 ligase acts as a novel negative regulator of ABA signaling by promoting ABI3 degradationPreprint

Zhang, X., Garretón, V., & Chua, N. (2005) · Genes & Development · doi:10.1101/gad.1318705 · Cited by 438 · see citing works

Combining quantitative trait Loci analysis and an ecophysiological model to analyze the genetic variability of the responses of maize leaf growth to temperature and water deficit

Reymond, M., Muller, B., Leonardi, A., Charcosset, A., & Tardieu, F. (2003) · Plant Physiology · doi:10.1104/pp.013839 · Cited by 428 · see citing works

Breeding for water-saving and drought-resistance rice (WDR) in China

Luo, L. (2010) · Journal of Experimental Botany · doi:10.1093/jxb/erq185 · Cited by 425 · see citing works

A rice orthologue of the ABA receptor, OsPYL/RCAR5, is a positive regulator of the ABA signal transduction pathway in seed germination and early seedling growth

Kim, H.-M., Hwang, H., Hong, J.-W., Lee, Y.-N., Ahn, I. P., Yoon, I. S., Yoo, S.-D., Lee, S., Lee, S. C., & Kim, B. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err338 · Cited by 357 · see citing works

The Genetic Map of <i>Artemisia annua</i> L. Identifies Loci Affecting Yield of the Antimalarial Drug Artemisinin

Graham, I. A., Besser, K., Blumer, S., Branigan, C. A., Czechowski, T., Elias, L., Guterman, I., Harvey, D., Isaac, P. G., Khan, A. M., et al. (2010) · Science · doi:10.1126/science.1182612 · Cited by 348 · see citing works

AFP is a novel negative regulator of ABA signaling that promotes ABI5 protein degradationPreprint

Lopez‐Molina, L., Mongrand, S., Kinoshita, N., & Chua, N. (2003) · Genes & Development · doi:10.1101/gad.1055803 · Cited by 345 · see citing works

Genome-wide gene expression profiling inArabidopsis thalianareveals new targets of abscisic acid and largely impaired gene regulation in theabi1-1mutant

Hoth, S., Morgante, M., Sanchez, J.-P., Hanafey, M. K., Tingey, S. V., & Chua, N. (2002) · Journal of Cell Science · doi:10.1242/jcs.00175 · Cited by 326 · see citing works

ABA receptors: the START of a new paradigm in phytohormone signalling

Klingler, J., Batelli, G., & Zhu, J. (2010) · Journal of Experimental Botany · doi:10.1093/jxb/erq151 · Cited by 305 · see citing works

ABA‐Hypersensitive Germination1 encodes a protein phosphatase 2C, an essential component of abscisic acid signaling in Arabidopsis seed

Nishimura, N., Yoshida, T., Kitahata, N., Asami, T., Shinozaki, K., & Hirayama, T. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03107.x · Cited by 286 · see citing works

A novel role for abscisic acid emerges from underground

Smet, I. D., Zhang, H., Inzé, D., & Beeckman, T. (2006) · Trends in Plant Science · doi:10.1016/j.tplants.2006.07.003 · Cited by 284 · see citing works

Structural and functional insights into core ABA signaling

Weiner, J. J., Peterson, F. C., Volkman, B. F., & Cutler, S. R. (2010) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2010.09.007 · Cited by 271 · see citing works

The Protein Phosphatase AtPP2CA Negatively Regulates Abscisic Acid Signal Transduction in Arabidopsis, and Effects of abh1 on AtPP2CA mRNA

Kuhn, J. M., Boisson‐Dernier, A., Dizon, M. B., Maktabi, M. H., & Schroeder, J. I. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.070318 · Cited by 266 · see citing works

Jasmonate signaling involves the abscisic acid receptor PYL4 to regulate metabolic reprogramming in Arabidopsis and tobacco

Lackman, P., González‐Guzmán, M., Tilleman, S., Carqueijeiro, I., Pérez, A. C., Moses, T., Seo, M., Kanno, Y., Häkkinen, S. T., Montagu, M. C. E. V., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1103010108 · Cited by 265 · see citing works

Molecular Pharmacology and Pharmacogenomics of Artemisinin and its Derivatives in Cancer Cells

Efferth, T. (2006) · Current Drug Targets · doi:10.2174/138945006776359412 · Cited by 263 · see citing works

FaPYR1 is involved in strawberry fruit ripening

Chai, Y., Jia, H., Li, C., Dong, Q., & Shen, Y. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err207 · Cited by 252 · see citing works

Artemisinins for schistosomiasis and beyond.

Utzinger, J., Xiao, S.-H., Tanner, M., & Keiser, J. (2007) · PubMed · Cited by 232 · see citing works

Development of transgenic <i>Artemisia annua</i> (Chinese wormwood) plants with an enhanced content of artemisinin, an effective anti‐malarial drug, by hairpin‐RNA‐mediated gene silencing

Zhang, L., Jing, F., Li, F., Li, M., Wang, Y., Wang, G., Sun, X., & Tang, K. (2009) · Biotechnology and Applied Biochemistry · doi:10.1042/ba20080068 · Cited by 206 · see citing works

Common and unique elements of the ABA-regulated transcriptome of Arabidopsis guard cells

Wang, R., Pandey, S., Song, L., Gookin, T. E., Zhao, Z., Albert, R., & Assmann, S. M. (2011) · BMC Genomics · doi:10.1186/1471-2164-12-216 · Cited by 196 · see citing works

Are source and sink strengths genetically linked in maize plants subjected to water deficit? A QTL study of the responses of leaf growth and of Anthesis-Silking Interval to water deficit

Welcker, C., Boussuge, B., Bencivenni, C., Ribaut, J.-M., & Tardieu, F. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erl227 · Cited by 174 · see citing works

Identification and mechanism of ABA receptor antagonism

Melcher, K., Xu, Y., Ng, L.-M., Zhou, X. E., Soon, F.-F., Chinnusamy, V., Suino-Powell, K. M., Kovach, A., Tham, F. S., Cutler, S. R., et al. (2010) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1887 · Cited by 165 · see citing works

Functional genomics and the biosynthesis of artemisinin

Covello, P. S., Teoh, K. H., Polichuk, D. R., Reed, D. W., & Nowak, G. (2007) · Phytochemistry · doi:10.1016/j.phytochem.2007.02.016 · Cited by 152 · see citing works

The Nuclear Interactor PYL8/RCAR3 ofFagus sylvaticaFsPP2C1 Is a Positive Regulator of Abscisic Acid Signaling in Seeds and Stress

Saavedra, X., Modrego, A., Rodriݩguez, D., González‐García, M. P., Sanz, L., Nicolaݩs, G., & Lorenzo, Ó. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.146381 · Cited by 131 · see citing works

Abscisic acid (ABA) treatment increases artemisinin content in Artemisia annua by enhancing the expression of genes in artemisinin biosynthetic pathway

Jing, F., Zhang, L., Li, M., Tang, Y., Wang, Y., Wang, Y., Wang, Q., Pan, Q., Wang, G., & Tang, K. (2009) · Biologia · doi:10.2478/s11756-009-0040-8 · Cited by 123 · see citing works

Antiviral Effect of Artemisinin from Artemisia annua against a Model Member of the Flaviviridae Family, the Bovine Viral Diarrhoea Virus (BVDV)

Romero, M. R., Serrano, M. A., Vallejo, M., Efferth, T., Alvarez, M., & Marı́n, J. J. G. (2006) · Planta Medica · doi:10.1055/s-2006-947198 · Cited by 122 · see citing works

Functional Genomics and the Biosynthesis of Artemisinin

Covello, P. S., Teoh, K. H., Polichuk, D. R., Reed, D. W., & Nowak, G. (2007) · ChemInform · doi:10.1002/chin.200742266 · Cited by 121 · see citing works

Structural basis for selective activation of ABA receptors

Peterson, F. C., Burgie, E. S., Park, S., Jensen, D. R., Weiner, J. J., Bingman, C. A., Chang, C. A., Cutler, S. R., Phillips, G. N., & Volkman, B. F. (2010) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1898 · Cited by 116 · see citing works

Effects of abscisic acid treatment and night temperatures on anthocyanin composition in Pinot noir grapes

Mori, K., Sato, H., Goto‐Yamamoto, N., Kitayama, M., Kobayashi, S., Sugaya, S., Gemma, H., & Hashizume, K. (2015) · Vitis · doi:10.5073/vitis.2005.44.161-165 · Cited by 108 · see citing works

Nuclear localization of the mutant protein phosphatase abi1 is required for insensitivity towards ABA responses in Arabidopsis

Moes, D., Himmelbach, A., Korte, A., Haberer, G., & Grill, E. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03454.x · Cited by 104 · see citing works

Induction of RAB18 gene expression and activation of K+ outward rectifying channels depend on an extracellular perception of ABA in Arabidopsis thaliana suspension cells

Jeannette, E., Rona, J. P., Bardat, F., Cornel, D., Sotta, B., & Miginiac, É. (1999) · The Plant Journal · doi:10.1046/j.1365-313x.1999.00423.x · Cited by 94 · see citing works

A hypermorphic mutation in the protein phosphatase 2C HAB1 strongly affects ABA signaling inArabidopsis

Robert, N., Merlot, S., N’Guyen, V., Boisson‐Dernier, A., & Schroeder, J. I. (2006) · FEBS Letters · doi:10.1016/j.febslet.2006.07.047 · Cited by 92 · see citing works

Dude, Where's My Phenotype? Dealing with Redundancy in Signaling Networks

Cutler, S. R., & McCourt, P. (2005) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.900152 · Cited by 83 · see citing works

Responses to environmental and chemical signals for anthocyanin biosynthesis in non-chlorophyllous corn (Zea mays L.) leaf

Kim, J., Lee, B.-H., Kim, S., Oh, K.-H., & Cho, K. Y. (2006) · Journal of Plant Biology · doi:10.1007/bf03030784 · Cited by 62 · see citing works

Growth, metabolic profiling and enzymes activities of Catharanthus roseus seedlings treated with plant growth regulators

El-Sayed, M., & Verpoorte, R. (2004) · Plant Growth Regulation · doi:10.1007/s10725-004-2604-5 · Cited by 57 · see citing works

Immunoquantitative analysis of artemisinin from Artemisia annua using polyclonal antibodies

Ferreira, J., & Janick, J. (1996) · Phytochemistry · doi:10.1016/0031-9422(95)00542-0 · Cited by 54 · see citing works

Identification of the abscisic acid receptor VvPYL1 in Vitis vinifera

Li, G., Xin, H., Zheng, X., Li, S., & Hu, Z. (2011) · Plant Biology · doi:10.1111/j.1438-8677.2011.00504.x · Cited by 37 · see citing works

Simultaneous Determination of Artemisinin and Its Bioprecursors in Artemisia annua

Vandenberghe, D., Vergauwe, A., Montagu, M. V., & den Eeckhout, E. G. V. (1995) · Journal of Natural Products · doi:10.1021/np50119a027 · Cited by 36 · see citing works

A Basic Leucine Zipper Transcription Factor, AabZIP1, Connects Abscisic Acid Signaling with Artemisinin Biosynthesis in Artemisia annua

Zhang, F., Fu, X., Lv, Z., Lu, X., Shen, Q., Zhang, L., Zhu, M., Wang, G., Sun, X., Liao, Z., et al. (2015) · Molecular Plant · doi:10.1016/j.molp.2014.12.004 · Cited by 248 · see citing works

Transcriptional regulatory network of high-value active ingredients in medicinal plants

Zheng, H., Fu, X., Shao, J., Tang, Y., Yu, M., Li, L., Huang, L., & Tang, K. (2023) · Trends in Plant Science · doi:10.1016/j.tplants.2022.12.007 · Cited by 196 · see citing works

Hormonal regulation of anthocyanin biosynthesis for improved stress tolerance in plants

Li, Z., & Ahammed, G. J. (2023) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2023.107835 · Cited by 156 · see citing works

Plant Metabolic Engineering Strategies for the Production of Pharmaceutical Terpenoids

Lu, X., Tang, K., & Li, P. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.01647 · Cited by 141 · see citing works

Genome-wide identification and characterization of ABA receptor PYL gene family in rice

Yadav, S. K., Kumar, V. V. S., Verma, R. K., Yadav, P. D., Saroha, A., Wankhede, D. P., Chaudhary, B., & Chinnusamy, V. (2020) · BMC Genomics · doi:10.1186/s12864-020-07083-y · Cited by 139 · see citing works

Overexpression of a Novel NAC Domain-Containing Transcription Factor Gene (AaNAC1) Enhances the Content of Artemisinin and Increases Tolerance to Drought andBotrytis cinereainArtemisia annua

Lv, Z., Wang, S., Zhang, F., Chen, L., Hao, X., Pan, Q., Fu, X., Li, L., Sun, X., & Tang, K. (2016) · Plant and Cell Physiology · doi:10.1093/pcp/pcw118 · Cited by 133 · see citing works

Overexpression of ABA Receptor PYL10 Gene Confers Drought and Cold Tolerance to Indica Rice

Verma, R. K., Kumar, V. V. S., Yadav, S. K., Pushkar, S., Rao, M. V., & Chinnusamy, V. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.01488 · Cited by 132 · see citing works

A Review of Biotechnological Artemisinin Production in Plants

Ikram, N. K. K., & Simonsen, H. T. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.01966 · Cited by 130 · see citing works

Transgenic approach to increase artemisinin content in Artemisia annua L.

Tang, K., Shen, Q., Yan, T., & Fu, X. (2014) · Plant Cell Reports · doi:10.1007/s00299-014-1566-y · Cited by 96 · see citing works

Artemisia annua glandular secretory trichomes: the biofactory of antimalarial agent artemisinin

Ling Zhi, X. I. A. O., Tan, H., & Zhang, L. (2016) · 中国科学通报：英文版 · doi:10.1007/s11434-015-0980-z · Cited by 94 · see citing works

Metabolomics-assisted biotechnological interventions for developing plant-based functional foods and nutraceuticals

Kumar, A., Mosa, K. A., Ji, L., Kage, U., Dhokane, D., Karre, S., Madalageri, D. M., & Pathania, N. (2017) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2017.1285752 · Cited by 90 · see citing works

Enhancing artemisinin content in and delivery from Artemisia annua: a review of alternative, classical, and transgenic approaches

Wani, K. I., Choudhary, S., Zehra, A., Naeem, M., Weathers, P., & Aftab, T. (2021) · Planta · doi:10.1007/s00425-021-03676-3 · Cited by 74 · see citing works

Characterization of the ABA Receptor VlPYL1 That Regulates Anthocyanin Accumulation in Grape Berry Skin

Gao, Z., Li, Q., Li, J., Chen, Y., Luo, M., Li, H., Wang, J., Wu, Y., Duan, S., Wang, L., et al. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.00592 · Cited by 73 · see citing works

Molecular regulation of the key specialized metabolism pathways in medicinal plants

Shi, M., Siwei, Z., Zheng, Z., Maoz, I., Zhang, L., & Kai, G. (2024) · Journal of Integrative Plant Biology · doi:10.1111/jipb.13634 · Cited by 59 · see citing works

Artemisinin-based antimalarial research: application of biotechnology to the production of artemisinin, its mode of action, and the mechanism of resistance of Plasmodium parasites

Muangphrom, P., Seki, H., Fukushima, E. O., & Muranaka, T. (2016) · Journal of Natural Medicines · doi:10.1007/s11418-016-1008-y · Cited by 59 · see citing works

ARTEMISININ BIOSYNTHESIS PROMOTING KINASE 1 positively regulates artemisinin biosynthesis through phosphorylating AabZIP1

Zhang, F., Xiang, L., Yu, Q., Zhang, H., Zhang, T., Zeng, J., Chen, G., Li, L., Fu, X., Shen, Q., et al. (2017) · Journal of Experimental Botany · doi:10.1093/jxb/erx444 · Cited by 59 · see citing works

Enhancement of artemisinin content and relative expression of genes of artemisinin biosynthesis in Artemisia annua by exogenous MeJA treatment

Xiang, L., Zhu, S., Zhao, T., Zhang, M., Liu, W., Chen, M., Lan, X., & Liao, Z. (2015) · Plant Growth Regulation · doi:10.1007/s10725-014-0004-z · Cited by 52 · see citing works

A Putative PP2C-Encoding Gene Negatively Regulates ABA Signaling in Populus euphratica

Chen, J., Zhang, D., Zhang, C., Xia, X., Yin, W., & Tian, Q. (2015) · PLoS ONE · doi:10.1371/journal.pone.0139466 · Cited by 48 · see citing works

Profiling of phytohormone‐specific microRNAs and characterization of the miR160‐ARF1 module involved in glandular trichome development and artemisinin biosynthesis in Artemisia annua

Guo, Z., Hao, K., Lv, Z., Yu, L., Bu, Q., Ren, J., Zhang, H., Chen, R., & Zhang, L. (2022) · Plant Biotechnology Journal · doi:10.1111/pbi.13974 · Cited by 45 · see citing works

Transcriptional regulation of ABA core signaling component genes in sorghum (Sorghum bicolor L. Moench)

Dalal, M., & Inupakutika, M. A. (2014) · Molecular Breeding · doi:10.1007/s11032-014-0114-3 · Cited by 40 · see citing works

Overexpression of AaPIF3 promotes artemisinin production in Artemisia annua

Zhang, Q., Wu, N., Jian, D., Jiang, R., Yang, C., Lan, X., Chen, M., Zhang, F., & Liao, Z. (2019) · Industrial Crops and Products · doi:10.1016/j.indcrop.2019.111476 · Cited by 37 · see citing works

The abscisic acid receptor gene VvPYL4 positively regulates grapevine resistance to Plasmopara viticola

Liu, L., Liu, C.-Y., Wang, H., Yu, S., Guan, T., Huang, Y., & Li, R.-C. (2020) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-020-01872-9 · Cited by 36 · see citing works

AaABF3, an Abscisic Acid–Responsive Transcription Factor, Positively Regulates Artemisinin Biosynthesis in Artemisia annua

Zhong, Y., Li, L., Hao, X., Fu, X., Ma, Y., Xie, L., Shen, Q., Kayani, S., Pan, Q., Sun, X., et al. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.01777 · Cited by 30 · see citing works

Endosperm-specific OsPYL8 and OsPYL9 act as positive regulators of the ABA signaling pathway in rice seed germination

Chen, Z., Kong, L., Zhou, Y., Chen, Z., Tian, D., Lin, Y., Wang, F., & Chen, S. (2017) · Functional Plant Biology · doi:10.1071/fp16314 · Cited by 29 · see citing works

Abscisic acid induces biosynthesis of bisbibenzyls and tolerance to UV-C in the liverwort Marchantia polymorpha

Kageyama, A., Ishizaki, K., Kohchi, T., Matsuura, H., & Takahashi, K. (2015) · Phytochemistry · doi:10.1016/j.phytochem.2015.05.009 · Cited by 29 · see citing works

Exogenous abscisic acid reduces saikosaponin accumulation by inhibiting saikosaponin synthesis pathway gene expression under drought stress in Bupleurum chinense DC.

Yang, L., Li, Y., Lan, Y., Zhao, Y., Han, M., & Yang, L. (2020) · Industrial Crops and Products · doi:10.1016/j.indcrop.2020.112686 · Cited by 28 · see citing works

Transcriptome analyses revealed the ultraviolet B irradiation and phytohormone gibberellins coordinately promoted the accumulation of artemisinin in Artemisia annua L.

Ma, T., Gao, H., Zhang, D., Shi, Y., Zhang, T., Shen, X., Wu, L., Li, X., & Chen, S. (2020) · Chinese Medicine · doi:10.1186/s13020-020-00344-8 · Cited by 28 · see citing works

Genetic engineering of artemisinin biosynthesis: prospects to improve its production

Abdin, M. Z., & Alam, P. (2015) · Acta Physiologiae Plantarum · doi:10.1007/s11738-015-1771-5 · Cited by 25 · see citing works

Trihelix Transcriptional Factor GhGT26 of Cotton Enhances Salinity Tolerance in Arabidopsis

Li, Y., Hu, Z., Dong, Y., & Xie, Z. (2022) · Plants · doi:10.3390/plants11202694 · Cited by 22 · see citing works

GhPYL9-5D and GhPYR1-3 A positively regulate Arabidopsis and cotton responses to ABA, drought, high salinity and osmotic stress

Wang, Y., Zhang, G., Zhou, H., Yin, S., Li, Y., Ma, C., Chen, P., Sun, L., & Hao, F. (2023) · BMC Plant Biology · doi:10.1186/s12870-023-04330-8 · Cited by 22 · see citing works

Type 2C Phosphatase 1 of Artemisia annua L. Is a Negative Regulator of ABA Signaling

Zhang, F., Fu, X., Lv, Z., Shen, Q., Yan, T., Jiang, W., Wang, G., Sun, X., & Tang, K. (2014) · BioMed Research International · doi:10.1155/2014/521794 · Cited by 21 · see citing works

AaABCG40 Enhances Artemisinin Content and Modulates Drought Tolerance in Artemisia annua

Fu, X., Liu, H., Hassani, D., Peng, B., Yan, X., Wang, Y., Wang, C., Li, L., Pin, L., Pan, Q., et al. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.00950 · Cited by 21 · see citing works

Molecular characterization of an AtPYL1-like protein, BrPYL1, as a putative ABA receptor in Brassica rapa

Li, Y., Wang, D., Sun, C., Hu, X., Mu, X., Jing-jiang, H., Yang, Y., Zhang, Y., Xie, C., & Zhou, X. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.04.116 · Cited by 20 · see citing works

Transcriptome exploration for further understanding of the tropane alkaloids biosynthesis in Anisodus acutangulus

Cui, L., Huang, F., Zhang, D., Lin, Y., Liao, P., Zong, J., & Kai, G. (2015) · Molecular Genetics and Genomics · doi:10.1007/s00438-015-1005-y · Cited by 20 · see citing works

The Light- and Jasmonic Acid-Induced AaMYB108-like Positive Regulates the Initiation of Glandular Secretory Trichome in Artemisia annua L.

Liu, H., He, W., Yao, X., Yan, X., Wang, X., Peng, B., Zhang, Y., Shao, J., Hu, X., Miao, Q., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241612929 · Cited by 18 · see citing works

Genome-wide identification of abscisic acid (ABA) receptor pyrabactin resistance 1-like protein (PYL) family members and expression analysis of PYL genes in response to different concentrations of ABA stress in Glycyrrhiza uralensis

Cui, Y., Xu, Z., Chen, X., Li-Ping, N. I. E., Wu, L., Wang, Y., Song, J., & Yao, H. (2020) · Chinese Journal of Natural Medicines · doi:10.1016/s1875-5364(20)30072-8 · Cited by 18 · see citing works

Specialized metabolites in seeds

Corso, M., Perreau, F., Rajjou, L., Malek, R. B., Lepiniec, L., & Mouille, G. (2020) · Advances in botanical research · doi:10.1016/bs.abr.2020.11.001 · Cited by 17 · see citing works

Increased abscisic acid sensitivity and drought tolerance of Arabidopsis by overexpression of poplar abscisic acid receptors

Li, Q., Tian, Q., Zhang, Y., Niu, M., Yu, X., Lian, C., Liu, C., Wang, H., Yin, W., & Xia, X. (2022) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-021-02178-0 · Cited by 15 · see citing works

Guard Cell Transcriptome Reveals Membrane Transport, Stomatal Development and Cell Wall Modifications as Key Traits Involved in Salinity Tolerance in Halophytic Chenopodium quinoa

Rasouli, F., Kiani‐Pouya, A., Movahedi, A., Wang, Y., Li, L., Yu, M., Pourkheirandish, M., Zhou, M., Chen, Z., Zhang, H., et al. (2022) · Plant and Cell Physiology · doi:10.1093/pcp/pcac158 · Cited by 14 · see citing works

AaABI5 transcription factor mediates light and abscisic acid signaling to promote anti-malarial drug artemisinin biosynthesis in Artemisia annua

Li, Y., Yang, Y., Li, P., Sheng, M., Li, L., Ma, X., Du, Z., Tang, K., Hao, X., & Kai, G. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.127345 · Cited by 14 · see citing works

Molecular cloning, characterization, and promoter analysis of the isochorismate synthase (AaICS1) gene from Artemisia annua

Wang, L., Zhang, Y., Fu, X., Zhang, T., Ma, J., Zhang, L., Qian, H., Tang, K., Li, S., & Zhao, J. (2017) · Journal of Zhejiang University SCIENCE B · doi:10.1631/jzus.b1600223 · Cited by 13 · see citing works

MADS-box gene AaSEP4 promotes artemisinin biosynthesis in Artemisia annua

Chen, T.-T., Yao, X., Liu, H., Li, Y., Qin, W. D., Yan, X., Wang, X., Peng, B., Zhang, Y., Shao, J., et al. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.982317 · Cited by 13 · see citing works

Pathway Modulation of Medicinal and Aromatic Plants Through Metabolic Engineering Using Agrobacterium tumefaciens

Khan, S. H., & Rahman, L. U. (2017) · Reference series in phytochemistry · doi:10.1007/978-3-319-28669-3_15 · Cited by 13 · see citing works

Biosynthesis of Sesquiterpene Lactones in Plants and Metabolic Engineering for Their Biotechnological Production

Perassolo, M., Cardillo, A. B., Busto, V. D., Giulietti, A. M., & Talou, J. R. (2018) · Springer eBooks · doi:10.1007/978-3-319-78274-4_4 · Cited by 12 · see citing works

Aa PP 2C1 negatively regulates the expression of genes involved in artemisinin biosynthesis through dephosphorylating Aa APK 1

Zhang, T., Gou, Y., Bai, F., Bai, G., Chen, M., Zhang, F., & Liao, Z. (2019) · FEBS Letters · doi:10.1002/1873-3468.13350 · Cited by 10 · see citing works

Genome-Wide Analysis of Oxidosqualene Cyclase Genes in Artemisia annua: Evolution, Expression, and Potential Roles in Triterpenoid Biosynthesis

Guo, C., Xu, S., & Guo, X. (2025) · Current Issues in Molecular Biology · doi:10.3390/cimb47070545 · Cited by 7 · see citing works

ABA Receptors: Prospects for Enhancing Biotic and Abiotic Stress Tolerance of Crops

Dalal, M., & Chinnusamy, V. (2015) · Springer eBooks · doi:10.1007/978-1-4939-2211-6_10 · Cited by 6 · see citing works

Current state, strategies, and perspectives in enhancing artemisinin production

Zakariya, A. M., Saiman, M. Z., Simonsen, H. T., & Ikram, N. K. K. (2023) · Phytochemistry Reviews · doi:10.1007/s11101-023-09897-6 · Cited by 5 · see citing works

AaCOI1, Encoding a CORONATINE INSENSITIVE 1-Like Protein of Artemisia annua L., Is Involved in Development, Defense, and Anthocyanin Synthesis

Liu, R., Wang, J., Xiao, M., Gao, X., Chen, J., & Dai, Y. (2020) · Genes · doi:10.3390/genes11020221 · Cited by 5 · see citing works

T‐shaped trichome‐specific expression of monoterpene synthase ADH2 using promoter–β‐GUS fusion in transgenic Artemisia annua L.

Fu, X., Shi, P., Shen, Q., Jiang, W., Tang, Y., Lv, Z., Yan, T., Li, L., Wang, G., Sun, X., et al. (2015) · Biotechnology and Applied Biochemistry · doi:10.1002/bab.1440 · Cited by 5 · see citing works

Effects of co-overexpression of ALDH1, CYP71AV1, and iaaM on the density, length, and width of glandular secretory trichomes and the contents of artemisinin in Artemisia annua

Zhao, Y., Xiao, N., Long, Y., Luo, J., Liu, X., & Zhang, X. (2023) · Canadian Journal of Plant Science · doi:10.1139/cjps-2023-0119 · Cited by 4 · see citing works

Characterization of terpene synthase gene family in 'Artemisia annua' L.

Jia, W., Wang, Y., Yu, X., Zhang, L., Liu, S., & Huang, Z. (2014) · Plant Omics · Cited by 3 · see citing works

ABA-responsive transcription factor CbNAC63 is involved in modulating biosynthesis of triterpenoid saponins in Conyza blinii

Yuan, Y., Zhou, M., Yang, M., Wang, M., Zhan, J., Wang, T., Chen, H., & Zheng, T. (2026) · Plant Stress · doi:10.1016/j.stress.2026.101367 · Cited by 2 · see citing works

Pathway Modulation of Medicinal and Aromatic Plants Through Metabolic Engineering Using Agrobacterium tumefaciens

Khan, S. H., & Rahman, L. U. (2016) · Springer eBooks · doi:10.1007/978-3-319-27490-4_15-1 · Cited by 2 · see citing works

Sustainable Metabolic Engineering and Epigenetic Modulation

Saurabh, S., Kiran, S., Pranay, K., Kumari, R., & Kumar, N. (2024) · Wiley eBooks · doi:10.1002/9781394186631.ch18 · Cited by 2 · see citing works

An ecological implication of glandular trichome-sequestered artemisinin: as a sink of biotic/abiotic stress-triggered singlet oxygenPreprint

He, J., Gao, Q., Liao, T., & Zeng, Q.-P. (2015) · doi:10.7287/peerj.preprints.827v1 · Cited by 2 · see citing works

An ecological implication of glandular trichome-sequestered artemisinin: as a sink of biotic/abiotic stress-triggered singlet oxygenPreprint

He, J., Gao, Q., Liao, T., & Zeng, Q.-P. (2015) · doi:10.7287/peerj.preprints.827 · Cited by 1 · see citing works

Antimalarial Compound Synthesis from Transgenic Cultures

Kundu, S., Mukherjee, S., & Ghosh, B. (2017) · Reference series in phytochemistry · doi:10.1007/978-3-319-28669-3_22

Antimalarial Compound Synthesis from Transgenic Cultures

Kundu, S., Mukherjee, S., & Ghosh, B. (2016) · Springer eBooks · doi:10.1007/978-3-319-27490-4_22-1

Additional file 1 of Transcriptome analyses revealed the ultraviolet B irradiation and phytohormone gibberellins coordinately promoted the accumulation of artemisinin in Artemisia annua L.

Ma, T., Gao, H., Zhang, D., Shi, Y., Zhang, T., Shen, X., Wu, L., Xiang, L., & Chen, S. (2020) · Figshare · doi:10.6084/m9.figshare.12599340

Additional file 3 of Transcriptome analyses revealed the ultraviolet B irradiation and phytohormone gibberellins coordinately promoted the accumulation of artemisinin in Artemisia annua L.

Ma, T., Gao, H., Zhang, D., Shi, Y., Zhang, T., Shen, X., Wu, L., Xiang, L., & Chen, S. (2020) · Figshare · doi:10.6084/m9.figshare.12599346

Additional file 5 of Transcriptome analyses revealed the ultraviolet B irradiation and phytohormone gibberellins coordinately promoted the accumulation of artemisinin in Artemisia annua L.

Ma, T., Gao, H., Zhang, D., Shi, Y., Zhang, T., Shen, X., Wu, L., Xiang, L., & Chen, S. (2020) · Figshare · doi:10.6084/m9.figshare.12599352

Additional file 6 of Transcriptome analyses revealed the ultraviolet B irradiation and phytohormone gibberellins coordinately promoted the accumulation of artemisinin in Artemisia annua L.

Ma, T., Gao, H., Zhang, D., Shi, Y., Zhang, T., Shen, X., Wu, L., Xiang, L., & Chen, S. (2020) · Figshare · doi:10.6084/m9.figshare.12599355

Research progress in the stress-improved medicinal plants

LÜ, B., Wang, H., & Jin, H. (2025) · Scientia Sinica Vitae · doi:10.1360/ssv-2024-0125

Additional file 1 of Genome-wide identification and characterization of ABA receptor PYL gene family in rice

Yadav, S. K., Santosh Kumar, V. V., Verma, R. K., Yadav, P., Saroha, A., Wankhede, D. P., Chaudhary, B., & Chinnusamy, V. (2020) · Figshare · doi:10.6084/m9.figshare.13031233

Additional file 4 of Transcriptome analyses revealed the ultraviolet B irradiation and phytohormone gibberellins coordinately promoted the accumulation of artemisinin in Artemisia annua L.

Ma, T., Gao, H., Zhang, D., Shi, Y., Zhang, T., Shen, X., Wu, L., Xiang, L., & Chen, S. (2020) · Figshare · doi:10.6084/m9.figshare.12599349

Additional file 8 of Transcriptome analyses revealed the ultraviolet B irradiation and phytohormone gibberellins coordinately promoted the accumulation of artemisinin in Artemisia annua L.

Ma, T., Gao, H., Zhang, D., Shi, Y., Zhang, T., Shen, X., Wu, L., Xiang, L., & Chen, S. (2020) · Figshare · doi:10.6084/m9.figshare.12599361

Additional file 4 of Genome-wide identification and characterization of ABA receptor PYL gene family in rice

Yadav, S. K., Santosh Kumar, V. V., Verma, R. K., Yadav, P., Saroha, A., Wankhede, D. P., Chaudhary, B., & Chinnusamy, V. (2020) · Figshare · doi:10.6084/m9.figshare.13031242

Additional file 1 of GhPYL9-5D and GhPYR1-3 A positively regulate Arabidopsis and cotton responses to ABA, drought, high salinity and osmotic stress

Wang, Y., Zhang, G., Zhou, H., Yin, S., Li, Y., Ma, C., Chen, P., Sun, L., & 郝福顺 (2024) · Figshare · doi:10.6084/m9.figshare.26596214

Additional file 2 of Transcriptome analyses revealed the ultraviolet B irradiation and phytohormone gibberellins coordinately promoted the accumulation of artemisinin in Artemisia annua L.

Ma, T., Gao, H., Zhang, D., Shi, Y., Zhang, T., Shen, X., Wu, L., Xiang, L., & Chen, S. (2020) · Figshare · doi:10.6084/m9.figshare.12599343

Additional file 5 of Genome-wide identification and characterization of ABA receptor PYL gene family in rice

Yadav, S. K., Santosh Kumar, V. V., Verma, R. K., Yadav, P., Saroha, A., Wankhede, D. P., Chaudhary, B., & Chinnusamy, V. (2020) · Figshare · doi:10.6084/m9.figshare.13031245

Additional file 2 of GhPYL9-5D and GhPYR1-3 A positively regulate Arabidopsis and cotton responses to ABA, drought, high salinity and osmotic stress

Wang, Y., Zhang, G., Zhou, H., Yin, S., Li, Y., Ma, C., Chen, P., Sun, L., & 郝福顺 (2024) · Figshare · doi:10.6084/m9.figshare.26596217

Additional file 7 of Transcriptome analyses revealed the ultraviolet B irradiation and phytohormone gibberellins coordinately promoted the accumulation of artemisinin in Artemisia annua L.

Ma, T., Gao, H., Zhang, D., Shi, Y., Zhang, T., Shen, X., Wu, L., Xiang, L., & Chen, S. (2020) · Figshare · doi:10.6084/m9.figshare.12599358

Additional file 12 of Genome-wide identification and characterization of ABA receptor PYL gene family in rice

Yadav, S. K., Santosh Kumar, V. V., Verma, R. K., Yadav, P., Saroha, A., Wankhede, D. P., Chaudhary, B., & Chinnusamy, V. (2020) · Figshare · doi:10.6084/m9.figshare.13031227

Additional file 2 of Genome-wide identification and characterization of ABA receptor PYL gene family in rice

Yadav, S. K., Santosh Kumar, V. V., Verma, R. K., Yadav, P., Saroha, A., Wankhede, D. P., Chaudhary, B., & Chinnusamy, V. (2020) · Figshare · doi:10.6084/m9.figshare.13031236

Additional file 13 of Genome-wide identification and characterization of ABA receptor PYL gene family in rice

Yadav, S. K., Santosh Kumar, V. V., Verma, R. K., Yadav, P., Saroha, A., Wankhede, D. P., Chaudhary, B., & Chinnusamy, V. (2020) · Figshare · doi:10.6084/m9.figshare.13031230

Additional file 3 of Genome-wide identification and characterization of ABA receptor PYL gene family in rice

Yadav, S. K., Santosh Kumar, V. V., Verma, R. K., Yadav, P., Saroha, A., Wankhede, D. P., Chaudhary, B., & Chinnusamy, V. (2020) · Figshare · doi:10.6084/m9.figshare.13031239

AaABCG40 Enhances Artemisinin Content and Modulates Drought Tolerance in Artemisia annua

Fu, X., Liu, H., Hassani, D., Peng, B., Yan, X., Wang, Y., Wang, C., Li, L., Pin, L., Pan, Q., et al. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.00950 · Cited by 21 · see citing works

Type 2C Phosphatase 1 of Artemisia annua L. Is a Negative Regulator of ABA Signaling

Zhang, F., Fu, X., Lv, Z., Shen, Q., Yan, T., Jiang, W., Wang, G., Sun, X., & Tang, K. (2014) · BioMed Research International · doi:10.1155/2014/521794 · Cited by 21 · see citing works

Increased abscisic acid sensitivity and drought tolerance of Arabidopsis by overexpression of poplar abscisic acid receptors

Li, Q., Tian, Q., Zhang, Y., Niu, M., Yu, X., Lian, C., Liu, C., Wang, H., Yin, W., & Xia, X. (2022) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-021-02178-0 · Cited by 15 · see citing works

An Engineered Abscisic Acid Receptor Enhances ABA Signaling and Improves Abiotic Stress Tolerance in Rice

Song, J., Song, I., Kim, R., Park, S., Kim, E., Lee, H., Lee, S. B., Cho, H., Lee, S., Lee, O. R., et al. (2026) · Plant Cell & Environment · doi:10.1111/pce.70488 · Cited by 2 · see citing works

Overexpression of Poplar Pyrabactin Resistance-Like Abscisic Acid Receptors Promotes Abscisic Acid Sensitivity and Drought Resistance in Transgenic Arabidopsis

Yu, J., Yang, L., Liu, X., Tang, R., Wang, Y., Ge, H., Wu, M., Zhang, J., Zhao, F., Luan, S., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0168040 · Cited by 80 · see citing works