On the public citation graph
Plant Responses to Biotic Stress: Old Memories Matter
0 signed · 174 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-3-030-75805-9_7openalex-snapshot
Jasmonate: A Versatile Messenger in Plants
inferredcites →https://doi.org/10.1007/978-981-15-7094-0_14openalex-snapshot
ROS Signaling Under Oxidative Stress in Plants
inferredcites →https://doi.org/10.1007/s00344-021-10446-8openalex-snapshot
Roles of Nitric Oxide in Conferring Multiple Abiotic Stress Tolerance in Plants and Crosstalk with Other Plant Growth Regulators
inferredcites →https://doi.org/10.1007/s11033-022-08074-wopenalex-snapshot
Epigenetic malleability at core promoter initiates tobacco PR-1a expression post salicylic acid treatment
inferredcites →https://doi.org/10.1007/s11105-018-1067-1openalex-snapshot
Salicylic Acid Regulates Systemic Defense Signaling in Chickpea During Fusarium oxysporum f. sp. ciceri Race 1 Infection
inferredcites →https://doi.org/10.1007/s12041-021-01300-7openalex-snapshot
Eighty years of gene-for-gene relationship and its applications in identification and utilization of R genes
inferredcites →https://doi.org/10.1007/s40502-020-00557-xopenalex-snapshot
Epigenetics and transgenerational memory in plants under heat stress
inferredcites →https://doi.org/10.1007/s40626-020-00181-yopenalex-snapshot
Yes, plants do have memory
inferredcites →https://doi.org/10.1016/b978-0-12-817892-8.00016-7openalex-snapshot
Molecular mechanisms regulating priming and stress memory
inferredcites →https://doi.org/10.1016/j.coi.2019.12.007openalex-snapshot
Plant NLR-triggered immunity: from receptor activation to downstream signaling
inferredcites →https://doi.org/10.1016/j.conb.2020.08.011openalex-snapshot
Cognitive epigenetic priming: leveraging histone acetylation for memory amelioration
inferredcites →https://doi.org/10.1016/j.febslet.2015.05.016openalex-snapshot
A brief review of nucleosome structure
inferredcites →https://doi.org/10.1016/j.gene.2021.145905openalex-snapshot
Auxin drives tomato spotted wilt virus (TSWV) resistance through epigenetic regulation of auxin response factor ARF8 expression in tomato
inferredcites →https://doi.org/10.1016/j.molp.2014.12.022openalex-snapshot
Signaling Mechanisms in Pattern-Triggered Immunity (PTI)
inferredcites →https://doi.org/10.1016/j.pbi.2021.102040openalex-snapshot
Polymorphisms in plants to restrict losses to pathogens: From gene family expansions to complex network evolution
inferredcites →https://doi.org/10.1016/j.plantsci.2021.110834openalex-snapshot
Priming of seeds with INA and its transgenerational effect in common bean (Phaseolus vulgaris L.) plants
inferredcites →https://doi.org/10.1016/j.plantsci.2021.111082openalex-snapshot
Epigenetic responses to Phytophthora citrophthora gummosis in citrus
inferredcites →https://doi.org/10.1016/j.pmpp.2020.101527openalex-snapshot
Transcription factors controlling biotic stress response in potato plants
inferredcites →https://doi.org/10.1016/j.smim.2016.05.006openalex-snapshot
Innate immune memory in plants
inferredcites →https://doi.org/10.1016/j.tig.2019.12.001openalex-snapshot
Small RNAs in the Transgenerational Inheritance of Epigenetic Information
inferredcites →https://doi.org/10.1016/s0168-9525(99)01901-0openalex-snapshot
Eukaryotic transcriptional control
inferredcites →https://doi.org/10.1016/s0968-0004(99)01489-9openalex-snapshot
Eukaryotic transcriptional control
inferredcites →https://doi.org/10.1016/s1360-1385(00)01839-2openalex-snapshot
Histone acetylation: lessons from the plant kingdom
inferredcites →https://doi.org/10.1038/37918openalex-snapshot
The origin and early evolution of plants on land
inferredcites →https://doi.org/10.1038/embor.2010.186openalex-snapshot
Chromatin modification acts as a memory for systemic acquired resistance in the plant stress response
inferredcites →https://doi.org/10.1038/nature05999openalex-snapshot
A flagellin-induced complex of the receptor FLS2 and BAK1 initiates plant defence
inferredcites →https://doi.org/10.1038/nrm.2017.7openalex-snapshot
Biomolecular condensates: organizers of cellular biochemistry
inferredcites →https://doi.org/10.1038/s41477-019-0425-9openalex-snapshot
A resistosome-activated ‘death switch’
inferredcites →https://doi.org/10.1038/s41477-020-0605-7openalex-snapshot
Integrated multi-omics framework of the plant response to jasmonic acid
inferredcites →https://doi.org/10.1038/s41598-018-32448-5openalex-snapshot
The relationship between transgenerational acquired resistance and global DNA methylation in Arabidopsis
inferredcites →https://doi.org/10.1038/srep12165openalex-snapshot
Rice Xa21 primed genes and pathways that are critical for combating bacterial blight infection
inferredcites →https://doi.org/10.1039/d0ra01396jopenalex-snapshot
Comprehensive in silico modeling of the rice plant PRR Xa21 and its interaction with RaxX21-sY and OsSERK2
inferredcites →https://doi.org/10.1080/21541264.2016.1187550openalex-snapshot
HSFA2 orchestrates transcriptional dynamics after heat stress inArabidopsis thaliana
inferredcites →https://doi.org/10.1086/394440openalex-snapshot
The Problem of Acquired Physiological Immunity in Plants
inferredcites →https://doi.org/10.1093/jxb/eraa007openalex-snapshot
Evo-physio: on stress responses and the earliest land plants
inferredcites →https://doi.org/10.1093/jxb/eraa072openalex-snapshot
Reprogramming and remodeling: transcriptional and epigenetic regulation of salicylic acid-mediated plant defense
inferredcites →https://doi.org/10.1093/jxb/erm300openalex-snapshot
HDA6 is required for jasmonate response, senescence and flowering in Arabidopsis
inferredcites →https://doi.org/10.1093/plcell/koab240openalex-snapshot
The emerging role of biomolecular condensates in plant immunity
inferredcites →https://doi.org/10.1093/plphys/kiab166openalex-snapshot
The mobile SAR signal N-hydroxypipecolic acid induces NPR1-dependent transcriptional reprogramming and immune priming
inferredcites →https://doi.org/10.1101/2021.07.24.453639openalex-snapshot
Epigenetic Malleability at Core Promoter Regulates Tobacco PR-1a Expression after Salicylic Acid Treatment
inferredcites →https://doi.org/10.1101/cshperspect.a019471openalex-snapshot
Epigenetic Regulation in Plant Responses to the Environment
inferredcites →https://doi.org/10.1105/tpc.104.028514openalex-snapshot
HISTONE DEACETYLASE19 Is Involved in Jasmonic Acid and Ethylene Signaling of Pathogen Response in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.108.062158openalex-snapshot
Mitogen-Activated Protein Kinases 3 and 6 Are Required for Full Priming of Stress Responses inArabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.110.082602openalex-snapshot
Of PAMPs and Effectors: The Blurred PTI-ETI Dichotomy
inferredcites →https://doi.org/10.1105/tpc.114.131938openalex-snapshot
Salicylic Acid Regulates Arabidopsis Microbial Pattern Receptor Kinase Levels and Signaling
inferredcites →https://doi.org/10.1111/j.1365-313x.2012.04977.xopenalex-snapshot
HDA19 is required for the repression of salicylic acid biosynthesis and salicylic acid‐mediated defense responses in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1574-6976.2012.00350.xopenalex-snapshot
Host-selective toxins produced by the plant pathogenic fungusAlternaria alternata
inferredcites →https://doi.org/10.1111/mpp.13005openalex-snapshot
Priming for enhanced ARGONAUTE2 activation accompanies induced resistance to cucumber mosaic virus in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/mpp.13091openalex-snapshot
ARGONAUTE 2 increases rice susceptibility to rice black‐streaked dwarf virus infection by epigenetically regulating HEXOKINASE 1 expression
inferredcites →https://doi.org/10.1111/nph.16515openalex-snapshot
The Arabidopsis exocyst subunits EXO70B1 and EXO70B2 regulate FLS2 homeostasis at the plasma membrane
inferredcites →https://doi.org/10.1111/pbi.13499openalex-snapshot
The celery genome sequence reveals sequential paleo‐polyploidizations, karyotype evolution and resistance gene reduction in apiales
inferredcites →https://doi.org/10.1111/pce.13526openalex-snapshot
Stress priming, memory, and signalling in plants
inferredcites →https://doi.org/10.1111/pce.14118openalex-snapshot
The plasma membrane–associated Ca 2+ ‐binding protein, PCaP1, is required for oligogalacturonide and flagellin‐induced priming and immunity
inferredcites →https://doi.org/10.1111/pce.14192openalex-snapshot
The Arabidopsis thaliana LysM‐containing Receptor‐Like Kinase 2 is required for elicitor‐induced resistance to pathogens
inferredcites →https://doi.org/10.1111/ppl.13563openalex-snapshot
Comparative proteomics of Pinus–Fusarium circinatum interactions reveal metabolic clues to biotic stress resistance
inferredcites →https://doi.org/10.1111/tpj.12557openalex-snapshot
The A rabidopsis L ec RK ‐ VI .2 associates with the pattern‐recognition receptor FLS 2 and primes N icotiana benthamiana pattern‐triggered immunity
inferredcites →https://doi.org/10.1111/tpj.15124openalex-snapshot
Multiple levels of crosstalk in hormone networks regulating plant defense
inferredcites →https://doi.org/10.1126/science.270.5243.1804openalex-snapshot
A Receptor Kinase-Like Protein Encoded by the Rice Disease Resistance Gene, Xa21
inferredcites →https://doi.org/10.1128/aem.62.11.4039-4043.1996openalex-snapshot
Production of fusaric acid by Fusarium species
inferredcites →https://doi.org/10.1146/annurev.pharmtox.42.082701.145401openalex-snapshot
Molecular Psychology: Roles for the ERK MAP Kinase Cascade in Memory
inferredcites →https://doi.org/10.1186/1471-2229-13-209openalex-snapshot
Vernalization treatment induces site-specific DNA hypermethylation at the VERNALIZATION-A1 (VRN-A1) locus in hexaploid winter wheat
inferredcites →https://doi.org/10.1371/journal.pone.0070226openalex-snapshot
Contamination of Bananas with Beauvericin and Fusaric Acid Produced by Fusarium oxysporum f. sp. cubense
inferredcites →https://doi.org/10.1371/journal.pone.0073163openalex-snapshot
Fusarium oxysporum f.sp. ciceri Race 1 Induced Redox State Alterations Are Coupled to Downstream Defense Signaling in Root Tissues of Chickpea (Cicer arietinum L.)
inferredcites →https://doi.org/10.15252/msb.20177819openalex-snapshot
Lysine acetylome profiling uncovers novel histone deacetylase substrate proteins in Arabidopsis
inferredcites →https://doi.org/10.19540/j.cnki.cjcmm.20210123.103openalex-snapshot
[Preliminary study on memory function of Sorbus aucuparia suspension cell to biotic stress].
inferredcites →https://doi.org/10.25781/kaust-p6c13openalex-snapshot
Investigating the Role of the Arabidopsis Homologue of the Human G3BP in RNA Metabolism, Cellular Stress Responses and Innate Immunity
inferredcites →https://doi.org/10.3389/fpls.2012.00169openalex-snapshot
MAP Kinase Cascades in Arabidopsis Innate Immunity
inferredcites →https://doi.org/10.3389/fpls.2016.01201openalex-snapshot
Epigenetic Control of Defense Signaling and Priming in Plants
inferredcites →https://doi.org/10.3389/fpls.2018.00355openalex-snapshot
Modify the Histone to Win the Battle: Chromatin Dynamics in Plant–Pathogen Interactions
inferredcites →https://doi.org/10.3389/fpls.2018.01447openalex-snapshot
DNA Methylation and the Evolution of Developmental Complexity in Plants
inferredcites →https://doi.org/10.3389/fpls.2019.00102openalex-snapshot
The NONEXPRESSOR OF PATHOGENESIS-RELATED GENES 1 (NPR1) and Related Family: Mechanistic Insights in Plant Disease Resistance
inferredcites →https://doi.org/10.3389/fpls.2019.00800openalex-snapshot
Mechanisms of ROS Regulation of Plant Development and Stress Responses
inferredcites →https://doi.org/10.3389/fpls.2020.00277openalex-snapshot
Arabidopsis SDG8 Potentiates the Sustainable Transcriptional Induction of the Pathogenesis-Related Genes PR1 and PR2 During Plant Defense Response
inferredcites →https://doi.org/10.3389/fpls.2020.603380openalex-snapshot
Role of Chromatin Architecture in Plant Stress Responses: An Update
inferredcites →https://doi.org/10.3389/fpls.2021.688003openalex-snapshot
Two Arabidopsis Homologs of Human Lysine-Specific Demethylase Function in Epigenetic Regulation of Plant Defense Responses
inferredcites →https://doi.org/10.3390/agronomy11071383openalex-snapshot
Evaluation of Calcium Application Methods on Delaying Plant Wilting under Water Deficit in Bedding Plants
inferredcites →https://doi.org/10.3390/cells8040339openalex-snapshot
Histone Methylation and Memory of Environmental Stress
inferredcites →https://doi.org/10.3390/epigenomes3010003openalex-snapshot
Biotic Stress-Induced Priming and De-Priming of Transcriptional Memory in Arabidopsis and Apple
inferredcites →https://doi.org/10.3390/f12010100openalex-snapshot
Transgenerational Induction of Resistance to Phytophthora cinnamomi in Holm Oak
inferredcites →https://doi.org/10.3390/ijms21155197openalex-snapshot
Epigenetic Regulation of Verticillium dahliae Virulence: Does DNA Methylation Level Play A Role?
inferredcites →https://doi.org/10.3390/ijms22042013openalex-snapshot
Multifaceted Chromatin Structure and Transcription Changes in Plant Stress Response
inferredcites →https://doi.org/10.3390/ijms22137118openalex-snapshot
Deciphering the Epigenetic Alphabet Involved in Transgenerational Stress Memory in Crops
inferredcites →https://doi.org/10.3390/microorganisms9051036openalex-snapshot
The Coevolution of Plants and Microbes Underpins Sustainable Agriculture
inferredcites →https://doi.org/10.3390/plants9030300openalex-snapshot
The Histone Marks Signature in Exonic and Intronic Regions Is Relevant in Early Response of Tomato Genes to Botrytis cinerea and in miRNA Regulation
inferredcites →https://doi.org/10.4161/psb.2.2.4176openalex-snapshot
Calcium Signaling Network in Plants
inferredcites →https://doi.org/10.4161/psb.29658openalex-snapshot
Exogenous application of histone demethylase inhibitor trans-2-phenylcyclopropylamine mimicsFLDloss-of-function phenotype in terms of systemic acquired resistance inArabidopsis thaliana
inferredcites →https://doi.org/10.7554/elife.69508openalex-snapshot
A novel bivalent chromatin associates with rapid induction of camalexin biosynthesis genes in response to a pathogen signal in Arabidopsis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4536475openalex-extracted
Guardians of Wheat: Unleashing Transgenerational Immune Priming with Trichoderma Against Spot Blotch
inferred← citeshttps://doi.org/10.1002/9781394261499.ch14openalex-snapshot
Benefits of Si/SiO 2 Nanoparticles in Developing Climate Resilient Crop Plants: Opportunities and Challenges
inferred← citeshttps://doi.org/10.1007/978-1-0716-4650-2_3openalex-snapshot
Method for the Measurement of Ethylene During Pathogen Infection in Arabidopsis
inferred← citeshttps://doi.org/10.1007/978-1-0716-4981-7_9openalex-snapshot
iTRAQ-Based Proteomic Approach to Study Stress Memory Responses in Plants
inferred← citeshttps://doi.org/10.1007/978-981-95-7844-3_11openalex-snapshot
Strategic Manipulation of Pathogen Recognition Receptors in Plants for Efficient Perception of Fungal Pathogens: Benefits and Risks
inferred← citeshttps://doi.org/10.1007/978-981-99-3334-1_18openalex-snapshot
Plant Phenolics Production: A Strategy for Biotic Stress Management
inferred← citeshttps://doi.org/10.1007/s00425-023-04088-1openalex-snapshot
Plants detect and respond to sounds
inferred← citeshttps://doi.org/10.1007/s00425-023-04136-wopenalex-snapshot
Advances in the study of the function and mechanism of the action of flavonoids in plants under environmental stresses
inferred← citeshttps://doi.org/10.1007/s00438-024-02195-6openalex-snapshot
Full-length transcriptome characterization and analysis of Carrizo Citrange and molecular insights into pathogen defense
inferred← citeshttps://doi.org/10.1007/s10142-025-01623-zopenalex-snapshot
CRISPR/Cas9-mediated editing of jasmonic acid pathways to enhance biotic & abiotic stress tolerance: An overview & prospects
inferred← citeshttps://doi.org/10.1007/s10343-025-01183-zopenalex-snapshot
Beyond Survival: The Role of Secondary Metabolites in Plant Defense Mechanisms
inferred← citeshttps://doi.org/10.1007/s11033-026-11601-8openalex-snapshot
Editorial: Molecular mechanisms of plant responses to pathogens and pests in a changing climate
inferred← citeshttps://doi.org/10.1007/s11240-026-03446-7openalex-snapshot
Copper quantum dots as nano-elicitors: modulating physiological and biochemical responses and mediating phytochemical enhancement in Calotropis procera callus cultures
inferred← citeshttps://doi.org/10.1007/s12298-024-01422-zopenalex-snapshot
Revisiting plant stress memory: mechanisms and contribution to stress adaptation
inferred← citeshttps://doi.org/10.1007/s12304-026-09665-xopenalex-snapshot
Intelligence From Within: Exploring Endosemiosis, Recognition, Goal-directedness and Crowd Wisdom Inside the Organism
inferred← citeshttps://doi.org/10.1007/s13237-022-00399-yopenalex-snapshot
Memory of plants: present understanding
inferred← citeshttps://doi.org/10.1007/s44281-023-00018-zopenalex-snapshot
Genome-wide identification of trihelix transcription factor family genes in pear (Pyrus bretschneideri) and functional characterization of PbrGT15 in black spot resistance
inferred← citeshttps://doi.org/10.1016/b978-0-443-13490-6.00002-3openalex-snapshot
Reprograming stress memory in plants: primeomics
inferred← citeshttps://doi.org/10.1016/b978-0-443-16082-0.00011-4openalex-snapshot
Plant response–driven fertilizer nutrient development
inferred← citeshttps://doi.org/10.1016/b978-0-443-27324-7.00017-3openalex-snapshot
Latest molecular and biochemical approaches for mitigating the effects of biotic stresses
inferred← citeshttps://doi.org/10.1016/j.bbagen.2024.130580openalex-snapshot
Epigenetic regulation influenced by soil microbiota and nutrients: Paving road to epigenome editing in plants
inferred← citeshttps://doi.org/10.1016/j.compag.2024.109227openalex-snapshot
Current trends in the use of thermal imagery in assessing plant stresses: A review
inferred← citeshttps://doi.org/10.1016/j.funbio.2024.101525openalex-snapshot
Effect of Pinus pinaster and Pinus radiata resin on biomass growth of Fusarium circinatum
inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111954openalex-snapshot
Understanding plant stress memory traits can provide a way for sustainable agriculture
inferred← citeshttps://doi.org/10.1016/j.pmpp.2025.102586openalex-snapshot
Plant-mediated bioinspired iron nanoparticles as an alternative to enhance crop resistance against biotic and abiotic stress; a review
inferred← citeshttps://doi.org/10.1016/j.sajb.2024.04.037openalex-snapshot
Guardians of wheat: Unleashing transgenerational immune priming with Trichoderma against spot blotch
inferred← citeshttps://doi.org/10.1016/j.stress.2023.100133openalex-snapshot
Physiological responses to water stress and stress memory in Argania spinosa
inferred← citeshttps://doi.org/10.1016/j.stress.2023.100239openalex-snapshot
Nanotechnology based precision agriculture for alleviating biotic and abiotic stress in plants
inferred← citeshttps://doi.org/10.1016/j.stress.2024.100427openalex-snapshot
Salicylic acid (SA)-mediated plant immunity against biotic stresses: An insight on molecular components and signaling mechanism
inferred← citeshttps://doi.org/10.1016/j.virol.2026.110950openalex-snapshot
RNA viruses are an integral part in evolution of all organisms
inferred← citeshttps://doi.org/10.1021/acs.jafc.6c05085openalex-snapshot
Chromatography-Free Ultrasensitive Profiling of Multiclass Plant Hormones via One-Pot Dual–Channel Derivatization Coupled with Acoustic Ejection Mass Spectrometry
inferred← citeshttps://doi.org/10.1093/oso/9780198873211.002.0005openalex-snapshot
Prologue: Setting the Stage
inferred← citeshttps://doi.org/10.1093/oso/9780198873211.002.0008openalex-snapshot
Advanced Praise for The Sentient Cell: The Cellular Foundations of Consciousness
inferred← citeshttps://doi.org/10.1093/oso/9780198873211.003.0001openalex-snapshot
The Cellular Basis of Consciousness (CBC)
inferred← citeshttps://doi.org/10.1093/oso/9780198873211.003.0002openalex-snapshot
It’s Cells All the Way Down
inferred← citeshttps://doi.org/10.1093/oso/9780198873211.003.0003openalex-snapshot
What Is Life? The Vitalism–Mechanism Debate and the Origins of Life
inferred← citeshttps://doi.org/10.1093/oso/9780198873211.003.0004openalex-snapshot
Emergence and Evolution of Cells
inferred← citeshttps://doi.org/10.1093/oso/9780198873211.003.0005openalex-snapshot
The Structural and Bioelectrical Basis of Cells
inferred← citeshttps://doi.org/10.1093/oso/9780198873211.003.0006openalex-snapshot
The Biophysical Basis of Cellular Sentience
inferred← citeshttps://doi.org/10.1093/oso/9780198873211.003.0007openalex-snapshot
The Biological Information Cycle
inferred← citeshttps://doi.org/10.1093/oso/9780198873211.003.0008openalex-snapshot
Genes Are Tools of Intelligent Cells
inferred← citeshttps://doi.org/10.1093/oso/9780198873211.003.0009openalex-snapshot
The N-Space Episenome
inferred← citeshttps://doi.org/10.1093/oso/9780198873211.003.0010openalex-snapshot
Anaesthetics and Their Cellular Targets
inferred← citeshttps://doi.org/10.1093/oso/9780198873211.003.0012openalex-snapshot
Issues of Ethics and Morality
inferred← citeshttps://doi.org/10.1093/oso/9780198873211.005.0001openalex-snapshot
An Exercise in Lexicography: Defining(?) Consciousness
inferred← citeshttps://doi.org/10.1093/oso/9780198873211.005.0002openalex-snapshot
Glossary of Technical Terms in the Biological Sciences
inferred← citeshttps://doi.org/10.1111/ppl.14399openalex-snapshot
Decoding the molecular mechanism underlying salicylic acid ( SA )‐mediated plant immunity: an integrated overview from its biosynthesis to the mode of action
inferred← citeshttps://doi.org/10.1186/s12866-025-04158-2openalex-snapshot
Trichoderma: a multifunctional agent in plant health and microbiome interactions
inferred← citeshttps://doi.org/10.1186/s12870-024-05503-9openalex-snapshot
Flagellin Induced GABA-shunt improves Drought stress tolerance in Brassica napus L
inferred← citeshttps://doi.org/10.1360/ssv-2025-0173openalex-snapshot
Plant immune plasticity and epibreeding
inferred← citeshttps://doi.org/10.14293/s2199-1006.1.sop-.ppunr6c.v1openalex-snapshot
Plant Stress Memory: Struggle of Getting Better Each Time
inferred← citeshttps://doi.org/10.15377/2409-9813.2023.10.1openalex-snapshot
Priming Bean Seedlings to Boost Natural Plant Defenses Against Common Bacterial Wilt: Salicylic Acid Responses to Chemical Primers (Part 1)
inferred← citeshttps://doi.org/10.15377/2409-9813.2023.10.2openalex-snapshot
Priming Bean Seedlings to Boost Natural Plant Defenses Against Common Bacterial Wilt: Gas Exchange, and Fluorescence Results (Part 2)
inferred← citeshttps://doi.org/10.15377/2409-9813.2023.10.3openalex-snapshot
Priming Bean Seedlings to Boost Natural Plant Defenses Against Common Bacterial Wilt: Leaf Architecture, Leaf area, Foliage Water Content, and Plant Biomass Results (Part 3)
inferred← citeshttps://doi.org/10.2174/9789815322675125010009openalex-snapshot
Environmental Factors Influencing Phytochemical Production for Enhanced Phytochemical Defense
inferred← citeshttps://doi.org/10.2174/9789815324150125010005openalex-snapshot
Decoding the Role of Rhizosphere and Phyllosphere Microbiome in Biotic Stress: A Treasure Trove of Nature
inferred← citeshttps://doi.org/10.3389/fgene.2022.1052191openalex-snapshot
Genome-wide analysis of NBS-LRR genes in Rosaceae species reveals distinct evolutionary patterns
inferred← citeshttps://doi.org/10.3389/fpls.2022.1040958openalex-snapshot
Herbicide resistance in grass weeds: Epigenetic regulation matters too
inferred← citeshttps://doi.org/10.3389/fpls.2022.1083409openalex-snapshot
TIR1/AFB proteins: Active players in abiotic and biotic stress signaling
inferred← citeshttps://doi.org/10.3389/fpls.2022.958350openalex-snapshot
Will epigenetics be a key player in crop breeding?
inferred← citeshttps://doi.org/10.3389/fpls.2023.1135845openalex-snapshot
Calcium signalling in weeds under herbicide stress: An outlook
inferred← citeshttps://doi.org/10.3389/fpls.2023.1138252openalex-snapshot
The captivating role of calcium in plant-microbe interaction
inferred← citeshttps://doi.org/10.3389/fpls.2024.1456414openalex-snapshot
Unveiling the role of epigenetic mechanisms and redox signaling in alleviating multiple abiotic stress in plants
inferred← citeshttps://doi.org/10.3389/fpls.2025.1558349openalex-snapshot
IMNM: integrated multi-network model for identifying pepper leaf diseases
inferred← citeshttps://doi.org/10.3389/fpls.2025.1716996openalex-snapshot
Dancing with the enemy: symbiotic relationships between plant RNA viruses and their hosts
inferred← citeshttps://doi.org/10.3390/agronomy14061131openalex-snapshot
Effect of Drought and Seed Tuber Size on Agronomical Traits of Potato (Solanum tuberosum L.) under In Vivo Conditions
inferred← citeshttps://doi.org/10.3390/ijms25116124openalex-snapshot
Genome-Wide Transcriptomic and Metabolomic Analyses Unveiling the Defence Mechanisms of Populus tremula against Sucking and Chewing Insect Herbivores
inferred← citeshttps://doi.org/10.3390/metabo13060716openalex-snapshot
Plant Secondary Metabolites: The Weapons for Biotic Stress Management
inferred← citeshttps://doi.org/10.3390/mi14010195openalex-snapshot
Optical Sensing Technologies to Elucidate the Interplay between Plant and Microbes
inferred← citeshttps://doi.org/10.3390/physiologia3010011openalex-snapshot
Linking Phyllosphere and Rhizosphere Microbiome to the Plant–Insect Interplay: The New Dimension of Tripartite Interaction
inferred← citeshttps://doi.org/10.3390/plants11040502openalex-snapshot
Meta-Analysis of Common and Differential Transcriptomic Responses to Biotic and Abiotic Stresses in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/plants11212858openalex-snapshot
Identification and Expression Analysis of the Solanum tuberosum StATG8 Family Associated with the WRKY Transcription Factor
inferred← citeshttps://doi.org/10.3390/plants12233951openalex-snapshot
Emphasizing the Role of Long Non-Coding RNAs (lncRNA), Circular RNA (circRNA), and Micropeptides (miPs) in Plant Biotic Stress Tolerance
inferred← citeshttps://doi.org/10.3390/plants13121686openalex-snapshot
Recruitment and Aggregation Capacity of Tea Trees to Rhizosphere Soil Characteristic Bacteria Affects the Quality of Tea Leaves
inferred← citeshttps://doi.org/10.3390/plants13152029openalex-snapshot
The Ability of Different Tea Tree Germplasm Resources in South China to Aggregate Rhizosphere Soil Characteristic Fungi Affects Tea Quality
inferred← citeshttps://doi.org/10.3390/plants14071070openalex-snapshot
Plant Signaling Hormones and Transcription Factors: Key Regulators of Plant Responses to Growth, Development, and Stress
inferred← citeshttps://doi.org/10.47836/pjtas.48.3.20openalex-snapshot
Brown Plant Hopper Resistance in Promising Doubled Haploid Rice Lines Selected by MGIDI and FAI-BLUP Index
inferred← citeshttps://doi.org/10.55250/jo.vnuf.15.1.2026.010-021openalex-snapshot
Phân tích chức năng của các gene biểu hiện khác biệt ở giống sắn (Manihot esculenta) mẫn cảm khi nhiễm bệnh sọc nâu virus
inferred← citeshttps://doi.org/10.5772/intechopen.1006319openalex-snapshot
Cultivating Resilience: Exploring Biotic Stressors and Plant Immune Responses
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.