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Dual symbiosis between Piriformospora indica and Azotobacter chroococcum enhances the artemisinin content in Artemisia annua L.

Arora, M., Saxena, P., Choudhary, D. K., Abdin, M. Z., & Varma, A. (2016) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-015-1972-5 · Cited by 59 · see citing works

Significance of Arbuscular Mycorrhizal Fungi in Mitigating Abiotic Environmental Stress in Medicinal and Aromatic Plants: A Review

Israel, A., Langrand, J., Fontaine, J., & Sahraoui, A. L. (2022) · Foods · doi:10.3390/foods11172591 · Cited by 53 · see citing works

Arbuscular mycorrhiza augments essential oil composition and antioxidant properties of Ocimum tenuiflorum L. – A popular green tea additive

Thokchom, S. D., Gupta, S., & Kapoor, R. (2020) · Industrial Crops and Products · doi:10.1016/j.indcrop.2020.112418 · Cited by 53 · see citing works

Responses of Vitis vinifera cv. Cabernet Sauvignon roots to the arbuscular mycorrhizal fungus Funneliformis mosseae and the plant growth-promoting rhizobacterium Ensifer meliloti include changes in volatile organic compounds

Velásquez, A., Vega-Celedón, P., Fiaschi, G., Agnolucci, M., Avio, L., Giovannetti, M., D’Onofrio, C., & Seeger, M. (2020) · Mycorrhiza · doi:10.1007/s00572-020-00933-3 · Cited by 53 · see citing works

Increase in Artemisia annua Plant Biomass Artemisinin Content and Guaiacol Peroxidase Activity Using the Arbuscular Mycorrhizal Fungus Rhizophagus irregularis

Domokos, E., Jakab-Farkas, L., Darkó, B., Bíró-Janka, B., Mara, G., Albert, C., & Balog, A. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.00478 · Cited by 52 · see citing works

Arbuscular mycorrhiza differentially affects synthesis of essential oils in coriander and dill

Rydlová, J., Jelínková, M., Dušek, K., Dušková, E., Vosátka, M., & Püschel, D. (2015) · Mycorrhiza · doi:10.1007/s00572-015-0652-5 · Cited by 51 · see citing works

Arbuscular mycorrhizal fungi: effects on plant terpenoid accumulation

Welling, M. T., Liu, L., Rose, T. J., Waters, D. L., & Benkendorff, K. (2015) · Plant Biology · doi:10.1111/plb.12408 · Cited by 50 · see citing works

Arbuscular mycorrhizal fungi: Effects on secondary metabolite accumulation of traditional Chinese medicines

Ran, Z., Ding, W., Cao, S., Fang, L., Zhou, J., & Zhang, Y. (2022) · Plant Biology · doi:10.1111/plb.13449 · Cited by 47 · see citing works

Combined Analysis of Pharmaceutical Active Ingredients and Transcriptomes of Glycyrrhiza uralensis Under PEG6000-Induced Drought Stress Revealed Glycyrrhizic Acid and Flavonoids Accumulation via JA-Mediated Signaling

Yao, H., Wang, F., Bi, Q., Liu, H., Liu, L., Xiao, G., Zhu, J., Shen, H., & Li, H. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.920172 · Cited by 43 · see citing works

Advanced metabolic engineering strategies for increasing artemisinin yield in Artemisia annua L.

Li, Y., Yang, Y., Li, L., Tang, K., Hao, X., & Kai, G. (2024) · Horticulture Research · doi:10.1093/hr/uhad292 · Cited by 42 · see citing works

Surface interactions of Fusarium graminearum on barley

Imboden, L. A., Afton, D., & Trail, F. (2017) · Molecular Plant Pathology · doi:10.1111/mpp.12616 · Cited by 41 · see citing works

Root Endophytic Fungi Regulate Changes in Sugar and Medicinal Compositions of Polygonum cuspidatum

Sun, R.-T., Feng, X.-C., Zhang, Z.-Z., Zhou, N., Feng, H.-D., Liu, Y., Hashem, A., Al-Arjani, A.-B. F., Allah, E. F. A., & Wu, Q. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.818909 · Cited by 39 · see citing works

Artemisinins in Combating Viral Infections Like SARS-CoV-2, Inflammation and Cancers and Options to Meet Increased Global Demand

Kalalagh, K. F., Kashkooli, A. B., Babaei, A., Rezaei, A., & van der Krol, A. R. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.780257 · Cited by 39 · see citing works

Arbuscular mycorrhizal symbiosis in Stevia rebaudiana increases trichome development, flavonoid and phenolic compound accumulation

Sarmiento-López, L. G., López‐Meyer, M., Sepúlveda‐Jiménez, G., Cárdenas, L., & Rodrı́guez-Monroy, M. (2020) · Biocatalysis and Agricultural Biotechnology · doi:10.1016/j.bcab.2020.101889 · Cited by 35 · see citing works

Mycorrhizal Fungi: Biodiversity, Ecological Significance, and Industrial Applications

Pandey, D., Kehri, H. K., Zoomi, I., Akhtar, O., & Singh, A. K. (2019) · Fungal biology · doi:10.1007/978-3-030-10480-1_5 · Cited by 34 · see citing works

Reference gene selection for quantitative real-time PCR in Solanum lycopersicum L. inoculated with the mycorrhizal fungus Rhizophagus irregularis

Fuentes, A., Ortiz, J., Saavedra, N., Salazar, L. A., Meneses, C., & Arriagada, C. (2016) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2016.01.022 · Cited by 34 · see citing works

Arbuscular Mycorrhizal Fungi and Higher Plants

Ahammed, G. J., & Hajiboland, R. (2024) · Springer eBooks · doi:10.1007/978-981-99-8220-2 · Cited by 33 · see citing works

Arbuscular mycorrhiza and vermicompost alleviate drought stress and enhance yield, total flavonoid concentration, rutin content, and antioxidant activity of buckwheat (Fagopyrum esculentum Moench)

Mohammadi, E., Fattahi, M., Barin, M., & Ashrafi-Saeidlou, S. (2022) · South African Journal of Botany · doi:10.1016/j.sajb.2022.05.020 · Cited by 33 · see citing works

Enhanced specialized metabolite, trichome density, and biosynthetic gene expression in Stevia rebaudiana (Bertoni) Bertoni plants inoculated with endophytic bacteria Enterobacter hormaechei

Oviedo-Pereira, D., López‐Meyer, M., Evangelista‐Lozano, S., Sarmiento-López, L. G., Sepúlveda‐Jiménez, G., & Rodrı́guez-Monroy, M. (2022) · PeerJ · doi:10.7717/peerj.13675 · Cited by 33 · see citing works

Practical applications of jasmonates in the biosynthesis and accumulation of secondary metabolites in plants

Ali, B. (2021) · Biocatalysis and Agricultural Biotechnology · doi:10.1016/j.bcab.2021.102205 · Cited by 30 · see citing works

Mycorrhizal inoculation as an alternative for the sustainable production of Mimosa tenuiflora seedlings with improved growth and secondary compounds content

Pedone-Bonfim, M. V. L., da Silva, D. K. A., da Silva-Batista, A. R., de Oliveira, A. P., Almeida, J. R. G. D. S., Yano‐Melo, A. M., & Maia, L. C. (2018) · Fungal Biology · doi:10.1016/j.funbio.2018.05.009 · Cited by 28 · see citing works

Complex regulation of microRNAs in roots of competitively-grown isogenic Nicotiana attenuata plants with different capacities to interact with arbuscular mycorrhizal fungi

Pandey, P., Wang, M., Baldwin, I. T., Pandey, S. P., & Groten, K. (2018) · BMC Genomics · doi:10.1186/s12864-018-5338-x · Cited by 28 · see citing works

Endophytic Fungi Accelerate Leaf Physiological Activity and Resveratrol Accumulation in Polygonum cuspidatum by Up-Regulating Expression of Associated Genes

Sun, R.-T., Zhang, Z.-Z., Feng, X.-C., Zhou, N., Feng, H.-D., Liu, Y., Harsonowati, W., Hashem, A., Allah, E. F. A., & Wu, Q. (2022) · Agronomy · doi:10.3390/agronomy12051220 · Cited by 27 · see citing works

Silencing a key gene of the common symbiosis pathway in N icotiana attenuata specifically impairs arbuscular mycorrhizal infection without influencing the root‐associated microbiome or plant growth

Groten, K., Nawaz, A., Nguyen, N. H. T., Santhanam, R., & Baldwin, I. T. (2015) · Plant Cell & Environment · doi:10.1111/pce.12561 · Cited by 25 · see citing works

An updated review on distribution, biosynthesis and pharmacological effects of artemisinin: A wonder drug

Nabi, N., Singh, S. K., & Saffeullah, P. (2023) · Phytochemistry · doi:10.1016/j.phytochem.2023.113798 · Cited by 25 · see citing works

Artemisinin production strategies for industrial scale: Current progress and future directions

Qamar, F., Ashrafi, K., Singh, A., Dash, P. K., & Abdin, M. Z. (2024) · Industrial Crops and Products · doi:10.1016/j.indcrop.2024.118937 · Cited by 24 · see citing works

Arbuscular mycorrhizal fungi enhance active ingredients of medicinal plants: a quantitative analysis

Yuan, M., Zhang, M.-H., Shi, Z., Yang, S., Zhang, M., Wang, Z., Wu, S., & Gao, J. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2023.1276918 · Cited by 23 · see citing works

Phosphate transporters, PnPht1;1 and PnPht1;2 from Panax notoginseng enhance phosphate and arsenate acquisition

Cao, G., Li, Z.-D., Wang, X., Zhang, X., Zhao, R., Gu, W., Chen, D., Yu, J., & He, S. (2020) · BMC Plant Biology · doi:10.1186/s12870-020-2316-7 · Cited by 23 · see citing works

Endophytes in Artemisia annua L.: new potential regulators for plant growth and artemisinin biosynthesis

Zheng, L. P., Li, X. P., Zhou, L. L., & Wang, J. (2021) · Plant Growth Regulation · doi:10.1007/s10725-021-00751-3 · Cited by 21 · see citing works

A review of the interaction of medicinal plants and arbuscular mycorrhizal fungi in the rhizosphere

Sun, R.-T., Zhang, Z.-Z., Zhou, N., Srivastava, A. K., Kuča, K., Allah, E. F. A., Hashem, A., & Wu, Q. (2021) · Notulae Botanicae Horti Agrobotanici Cluj-Napoca · doi:10.15835/nbha49312454 · Cited by 21 · see citing works

Interactive influence of elevated CO2 and arbuscular mycorrhizal fungi on sucrose and coumarin metabolism in Ammi majus

Mohammed, A. E., Alotaibi, M. O., & Elobeid, M. M. (2022) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2022.05.029 · Cited by 21 · see citing works

Pre-inoculation with arbuscular mycorrhizal fungi affects essential oil quality and the reproduction of root lesion nematode in Cymbopogon citratus

Silva, M. T. R. E., Calandrelli, A., Miamoto, A., Rinaldi, L. K., Moreno, B. P., da Silva, C., & Dias‐Arieira, C. R. (2021) · Mycorrhiza · doi:10.1007/s00572-021-01045-2 · Cited by 20 · see citing works

Arbuscular Mycorrhizal Fungi in Alleviation of Cold Stress in Plants

Devi, T. S., Gupta, S., & Kapoor, R. (2019) · Springer eBooks · doi:10.1007/978-981-13-9349-5_17 · Cited by 20 · see citing works

Improvement of Panax notoginseng saponin accumulation triggered by methyl jasmonate under arbuscular mycorrhizal fungi

Dai, H.-Y., Zhang, X., Bi, Y., Chen, D., Long, X.-N., Wu, Y., Cao, G., & He, S. (2024) · Frontiers in Plant Science · doi:10.3389/fpls.2024.1360919 · Cited by 19 · see citing works

Arbuscular Mycorrhizal Fungi Enhance Growth and Increase Concentrations of Anthocyanin, Phenolic Compounds, and Antioxidant Activity of Black Rice (Oryza sativa L.)

Nacoon, S., Seemakram, W., Ekprasert, J., Theerakulpisut, P., Sanitchon, J., Kuyper, T. W., & Boonlue, S. (2023) · Soil Systems · doi:10.3390/soilsystems7020044 · Cited by 19 · see citing works

An appraisal of arbuscular mycorrhiza-mediated augmentation in production of secondary metabolites in medicinal plants

Thokchom, S. D., Gupta, S., & Kapoor, R. (2023) · Journal of Applied Research on Medicinal and Aromatic Plants · doi:10.1016/j.jarmap.2023.100515 · Cited by 17 · see citing works

Arbuscular mycorrhizal fungi: Source of secondary metabolite production in medicinal plants

Kumar, S., Arora, N., & Upadhyay, H. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-821005-5.00011-9 · Cited by 17 · see citing works

Crop productivity and chemical compositions of dragonhead (Dracocephalum moldavica L.) essential oil under different cropping patterns and fertilization

Nasiri, Y. (2021) · Industrial Crops and Products · doi:10.1016/j.indcrop.2021.113920 · Cited by 18 · see citing works

Mycorrhization and phosphorus may be an alternative for increasing the production of metabolites in Myracrodruon urundeuva

da Silva, F. S. B., & Maia, L. C. (2018) · Theoretical and Experimental Plant Physiology · doi:10.1007/s40626-018-0123-4 · Cited by 16 · see citing works

A low cost alternative, using mycorrhiza and organic fertilizer, to optimize the production of foliar bioactive compounds in pomegranates

da Silva, F. S. B., & Silva, F. A. (2019) · Journal of Applied Microbiology · doi:10.1111/jam.14477 · Cited by 16 · see citing works

A review of various efforts to increase artemisinin and other antimalarial compounds in Artemisia Annua L plant

Aidah, N., Bazira, J., Tolo, C. U., & Engeu, P. O. (2018) · Cogent Biology · doi:10.1080/23312025.2018.1513312 · Cited by 16 · see citing works

Seaweed extract and arbuscular mycorrhiza co-application affect the growth responses and essential oil composition of Foeniculum vulgare L.

Rasouli, F., Nasiri, Y., Hassanpouraghdam, M. B., Asadi, M., Qaderi, T., Trifa, A., Strzemski, M., Dresler, S., & Szczepanek, M. (2023) · Scientific Reports · doi:10.1038/s41598-023-39194-3 · Cited by 15 · see citing works

Metabolome profiling of arbuscular mycorrhizal fungus treated Ocimum tenuiflorum L. provides insights into deviation in allocation of carbon compounds to secondary metabolism

Thokchom, S. D., Gupta, S., Mewar, S. K., Kumar, P., Kalra, C., & Kapoor, R. (2023) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2023.108039 · Cited by 15 · see citing works

Interactive effects of CO2 concentrations and Alternaria brassicae (Berk.) Sacc. infection on defense signalling in Brassica juncea (L.) Czern. & Coss.

Mathur, P., Singh, V. P., & Kapoor, R. (2017) · European Journal of Plant Pathology · doi:10.1007/s10658-017-1382-7 · Cited by 15 · see citing works

Mycorrhizal influence on the growth and bioactive compounds composition of two medicinal plants: Mikania glomerata Spreng. and Mikania laevigata Sch. Bip. ex Baker (Asteraceae)

Almeida, C. D. L., Sawaya, A. C. H. F., & de Andrade, S. A. L. (2018) · Revista Brasileira de Botânica · doi:10.1007/s40415-017-0436-6 · Cited by 15 · see citing works

Essential oil yield and compositions of Dracocephalum moldavica L. in intercropping with fenugreek, inoculation with mycorrhizal fungi and bacteria

Chelan, Z. A., Amini, R., & Nasab, A. D. M. (2023) · Scientific Reports · doi:10.1038/s41598-023-35156-x · Cited by 14 · see citing works

Arbuscular Mycorrhizal Fungi: Green Approach/Technology for Sustainable Agriculture and Environment

Srivastava, P., Saxena, B., & Giri, B. (2017) · Springer eBooks · doi:10.1007/978-3-319-68867-1_20 · Cited by 14 · see citing works

Arbuscular mycorrhiza alters the nutritional requirements in Salvia miltiorrhiza and low nitrogen enhances the mycorrhizal efficiency

Pu, C.-J., Yang, G., Li, P., Yang, G., Garran, T. A., Zhou, X., Shen, Y., Zheng, H., Chen, M., & Huang, L. (2022) · Scientific Reports · doi:10.1038/s41598-022-17121-2 · Cited by 13 · see citing works

Arbuscular mycorrhizal fungi-mediated rhizospheric changes: What is the impact on plant secondary metabolism?

Falcão, E. L., Wu, Q., & da Silva, F. S. B. (2024) · Rhizosphere · doi:10.1016/j.rhisph.2024.100887 · Cited by 13 · see citing works

Arbuscular Mycorrhizal Fungi, Especially Rhizophagus intraradices as a Biostimulant, Improve Plant Growth and Root Columbin Levels in Tinospora sagittata

Meng, L., Xu, F.-Q., Zhang, Z.-Z., Alqahtani, M. D., Tashkandi, M. A., & Wu, Q. (2023) · Horticulturae · doi:10.3390/horticulturae9121350 · Cited by 12 · see citing works

A Panax notoginseng phosphate transporter, PnPht1;3, greatly contributes to phosphate and arsenate uptake

Cao, G.-H., Wang, X.-F., Li, Z.-D., Zhang, X., Li, X.-G., Gu, W., Zhang, F., Yu, J., & He, S. (2022) · Functional Plant Biology · doi:10.1071/fp21218 · Cited by 12 · see citing works

Arbuscular mycorrhizal fungi as biotechnology alternative to increase concentrate of secondary metabolites in Zea mays L.

da Silva, F. A., Maia, L. C., & da Silva, F. S. B. (2018) · Revista Brasileira de Botânica · doi:10.1007/s40415-018-0508-2 · Cited by 12 · see citing works

Widely Targeted Metabolomic Analysis Reveals the Improvement in Panax notoginseng Triterpenoids Triggered by Arbuscular Mycorrhizal Fungi via UPLC–ESI–MS/MS

Zhang, X., Wu, Y., Long, X.-N., You, X.-X., Chen, D., Bi, Y., He, S., & Cao, G. (2024) · Molecules · doi:10.3390/molecules29133235 · Cited by 10 · see citing works

Paraglomus and Glomus arbuscular mycorrhizal fungi induce the green tea catechin quality index and phosphorus bioavailability in tropical soils

Yuan, P., Wang, Y., Peng, J., Chen, Y., Li, J., Eissa, M. A., Luo, G., & Tian, C. (2025) · Mycorrhiza · doi:10.1007/s00572-025-01185-9 · Cited by 10 · see citing works

Root regulation of artemisinin production in Artemisia annua: trichome and metabolite evidence

Wang, S., Towler, M. J., & Weathers, P. J. (2016) · Planta · doi:10.1007/s00425-016-2560-0 · Cited by 9 · see citing works

Arbuscular mycorrhizal symbiosis modulates the apocarotenoid biosynthetic pathway in saffron

Stelluti, S., Grasso, G., Nebauer, S. G., Alonso, G. L., Renau‐Morata, B., Caser, M., Demasi, S., Lumini, E., Gómez‐Gómez, L., Molina, R. V., et al. (2023) · Scientia Horticulturae · doi:10.1016/j.scienta.2023.112441 · Cited by 9 · see citing works

Arbuscular Mycorrhizal Fungus Rhizophagus irregularis Influences Artemisia annua Plant Parameters and Artemisinin Content under Different Soil Types and Cultivation Methods

Domokos, E., Bíró-Janka, B., Bálint, J., Molnár, K., Fazakas, C., Jakab-Farkas, L., Domokos, J., Albert, C., Mara, G., & Balog, A. (2020) · Microorganisms · doi:10.3390/microorganisms8060899 · Cited by 9 · see citing works

Impact of Phosphatic Nutrition on Growth Parameters and Artemisinin Production in Artemisia annua Plants Inoculated or Not with Funneliformis mosseae

Todeschini, V., Anastasia, F., Massa, N., Marsano, F., Cesaro, P., Bona, E., Gamalero, E., Oddi, L., & Lingua, G. (2022) · Life · doi:10.3390/life12040497 · Cited by 9 · see citing works

Transcriptomic differences in response to Metarhizium anisopliae and Trichoderma harzianum uncovers major regulative genes and pathways for establishment of beneficial relationship in peanut

Yan, D., Cai, N., Nong, X., Wang, G., Wang, Q., Ullah, H., Tu, X., & Zhang, Z. (2022) · Biological Control · doi:10.1016/j.biocontrol.2022.104964 · Cited by 9 · see citing works

Advances in the studies on symbiotic arbuscular mycorrhizal fungi of traditional Chinese medicinal plants

Yu, L., Zhang, Z., & ZHOU, L. (2022) · Biocell · doi:10.32604/biocell.2022.022825 · Cited by 8 · see citing works

Mycorrhizal Fungi Synergistically Promote the Growth and Secondary Metabolism of Cyclocarya paliurus

Zhao, T., Yu, B., Zhang, M., Chen, S., & Deng, B. (2022) · Forests · doi:10.3390/f13122188 · Cited by 7 · see citing works

Mechanism allowing biochar to aid in arbuscular mycorrhizal colonization in Panax quinquefolius L. roots and improve secondary metabolite production

Chen, X., Ran, Z., Wang, Y., Chen, T., Guo, L., Fang, L., & Zhou, J. (2025) · Mycorrhiza · doi:10.1007/s00572-025-01195-7 · Cited by 6 · see citing works

Mutualistic and Endophytic Microorganisms of Artemisia Annua: Description, Role and Use

Péterfi, O., & Domokos, E. (2018) · Acta Biologica Marisiensis · doi:10.2478/abmj-2018-0009 · Cited by 6 · see citing works

The Importance of Mycorrhizal Fungi in the Development and Secondary Metabolite Production of Echinacea purpurea and Relatives (Asteraceae): Current Research Status and Perspectives

Iakab, M., Domokos, E., Benedek, K., Molnár, K., Kentelky, E., Buta, E., & Dulf, F. V. (2022) · Horticulturae · doi:10.3390/horticulturae8121106 · Cited by 6 · see citing works

Arbuscular mycorrhizal fungi acting as biostimulants of proanthocyanidins accumulation – What is there to know?

Falcão, E. L., & da Silva, F. S. B. (2023) · Rhizosphere · doi:10.1016/j.rhisph.2023.100762 · Cited by 6 · see citing works

Arbuscular Mycorrhizal Fungi and Plant Secondary Metabolism

Rahmat, S., & Soheilikhah, Z. (2024) · Springer eBooks · doi:10.1007/978-981-99-8220-2_5 · Cited by 6 · see citing works

The Influence of Mycorrhizal Fungi on the Accumulation of Sennosides A and B in Senna alexandrina and Senna italica

Alzain, M. N., Alatar, A. A., Alqarawi, A. A., Mothana, R. A., Noman, O. M., Herqash, R. N., Al-Sheddi, E. S., Farshori, N. N., & Alam, P. (2020) · Separations · doi:10.3390/separations7040065 · Cited by 5 · 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

Is there space for arbuscular mycorrhizal fungi in the production chain of photoprotective cosmetics?

Falcão, E. L., Muniz, B. C., Barreto, C. B., da Luz, R. D. C. R., de Carvalho, J. G. L., Costa, C. A. R., & da Silva, F. S. B. (2023) · Rhizosphere · doi:10.1016/j.rhisph.2023.100811 · Cited by 5 · see citing works

TECNOLOGIA MICORRÍZICA COMO BIOINSUMO PARA PRODUÇÃO DE COMPOSTOS FENÓLICOS DE IMPORTÂNCIA À INDÚSTRIA DE FITOMEDICAMENTOS

dos Santos, E. L., Falcão, E. L., & da Silva, F. S. B. (2021) · Research Society and Development · doi:10.33448/rsd-v10i2.12856 · Cited by 5 · see citing works

Mycorrhization changes the antioxidant response and chemical profile of Lippia alba (Verbenaceae) essential oil under salinity conditions

Neto, L. P., Silva-Santos, L., de Souza, L. M., de Morais, M. B., Corte-Real, N., do Monte, I. P., da Câmara, C. A. G., de Moraes, M. M., & Ulisses, C. (2022) · South African Journal of Botany · doi:10.1016/j.sajb.2022.11.001 · Cited by 5 · see citing works

Research and Development on Artemisia annua in India

Shukla, A. K., Shasany, A. K., & Khanuja, S. P. S. (2018) · Springer eBooks · doi:10.1007/978-981-10-8291-7_2 · Cited by 5 · see citing works

Addition of Arbuscular Mycorrhizal Fungi Enhances Terpene Synthase Expression in Salvia rosmarinus Cultivars

Leggatt, E., Griffiths, A., Budge, S. P., Stead, A. D., Gange, A. C., & Devlin, P. F. (2023) · Life · doi:10.3390/life13020315 · Cited by 4 · see citing works

Metabolomic Approaches to Study Trichoderma-Plant Interactions

Mishra, N., Chauhan, P., Verma, P., Singh, S. P., & Mishra, A. (2022) · Fungal biology · doi:10.1007/978-3-030-91650-3_10 · Cited by 3 · see citing works

Annonacin accumulation in leaves of Annona muricata L. induced by mycorrhizal colonization

González-López, A. M., Quiñones-Aguilar, E. E., Guízar‐González, C., & Rincón‐Enríquez, G. (2025) · FEMS Microbiology Letters · doi:10.1093/femsle/fnaf085 · Cited by 3 · see citing works

Bark of the Stem of Libidibia Ferrea Associated with Mycorrhizal Fungi: An Alternative to Produce High Levels of Phenolic Acids

da Silva, F. A., da Silva, W. A. V., Ferreira, M. R. A., Soares, L. A. L., & da Silva, F. S. B. (2018) · The Open Microbiology Journal · doi:10.2174/1874285801812010412 · Cited by 3 · see citing works

Microbial Symbiosis and Bioactive Ingredients of Medicinal Plants

Kilam, D., Sharma, P., Agnihotri, A., Kharkwal, A. C., & Varma, A. K. (2017) · Springer eBooks · doi:10.1007/978-3-319-57849-1_16 · Cited by 3 · see citing works

Arbuscular mycorrhizal fungal consortium stabilizes physiological and metabolomic responses of Psoralea corylifolia under arsenic stress

Chowdhary, N. A., & Songachan, L. S. (2026) · Rhizosphere · doi:10.1016/j.rhisph.2026.101306 · Cited by 2 · see citing works

Combined effect of photoperiod and arbuscular mycorrhizal symbiosis on photosynthesis and specialized metabolites in Stevia rebaudiana

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