On the public citation graph
1O2-Mediated and EXECUTER-Dependent Retrograde Plastid-to-Nucleus Signaling in Norflurazon-Treated Seedlings of Arabidopsis thaliana
0 signed · 127 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known work and none has been retracted — and get a dated CiteStamped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/10.1002/9780470133361.ch1openalex-snapshot
Type II Photooxygenation Reactions in Solution
inferredcites →https://doi.org/10.1006/jmbi.2001.4573openalex-snapshot
Effects of chlorophyll a, chlorophyll b, and xanthophylls on the in vitro assembly kinetics of the major light-harvesting chlorophyll a/b complex, LHCIIb11Edited by G. von Heijne
inferredcites →https://doi.org/10.1007/bf00016069openalex-snapshot
The molecular basis of resistance to the herbicide norflurazon
inferredcites →https://doi.org/10.1007/bf00390180openalex-snapshot
The effect of light on the biosynthesis of the light-harvesting chlorophyll a/b protein
inferredcites →https://doi.org/10.1007/bf00409141openalex-snapshot
Photooxidative destruction of chloroplasts and its consequences for cytosolic enzyme levels and plant development
inferredcites →https://doi.org/10.1007/s11103-009-9491-0openalex-snapshot
Arabidopsis mutants reveal multiple singlet oxygen signaling pathways involved in stress response and development
inferredcites →https://doi.org/10.1016/0003-9861(68)90654-1openalex-snapshot
Photoperoxidation in isolated chloroplasts
inferredcites →https://doi.org/10.1016/0092-8674(93)90459-4openalex-snapshot
Signal transduction mutants of arabidopsis uncouple nuclear CAB and RBCS gene expression from chloroplast development
inferredcites →https://doi.org/10.1016/0306-3623(91)90478-oopenalex-snapshot
Free radicals in biology and medicine
inferredcites →https://doi.org/10.1016/j.cub.2011.04.004openalex-snapshot
Heme Synthesis by Plastid Ferrochelatase I Regulates Nuclear Gene Expression in Plants
inferredcites →https://doi.org/10.1016/j.jplph.2010.10.016openalex-snapshot
Transient accumulation of Mg-protoporphyrin IX regulates expression of PhANGs – New evidence for the signaling role of tetrapyrroles in mature Arabidopsis plants
inferredcites →https://doi.org/10.1016/j.tig.2003.08.001openalex-snapshot
Chloroplast-to-nucleus signalling: a role for Mg-protoporphyrin
inferredcites →https://doi.org/10.1016/s0021-9258(18)34446-6openalex-snapshot
Biosynthesis of chlorophyll a/b-binding polypeptides in wild type and the chlorina f2 mutant of barley.
inferredcites →https://doi.org/10.1016/s0031-9422(00)83147-7openalex-snapshot
Singlet oxygen and plants
inferredcites →https://doi.org/10.1016/s0168-9452(00)00273-9openalex-snapshot
Antioxidative parameters in the seedlings of pigeonpea (Cajanus cajan (L.) Millspaugh) in response to Zn and Ni stresses
inferredcites →https://doi.org/10.1038/nature01204openalex-snapshot
Chloroplast to nucleus communication triggered by accumulation of Mg-protoporphyrinIX
inferredcites →https://doi.org/10.1073/pnas.0609063103openalex-snapshot
Cross-talk between singlet oxygen- and hydrogen peroxide-dependent signaling of stress responses in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.0702061104openalex-snapshot
EXECUTER1- and EXECUTER2-dependent transfer of stress-related signals from the plastid to the nucleus of Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.0803054105openalex-snapshot
Tetrapyrrole profiling in Arabidopsis seedlings reveals that retrograde plastid nuclear signaling is not due to Mg-protoporphyrin IX accumulation
inferredcites →https://doi.org/10.1073/pnas.0803245105openalex-snapshot
The steady-state level of Mg-protoporphyrin IX is not a determinant of plastid-to-nucleus signaling in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0901315106openalex-snapshot
1 O 2 -mediated retrograde signaling during late embryogenesis predetermines plastid differentiation in seedlings by recruiting abscisic acid
inferredcites →https://doi.org/10.1073/pnas.1115982109openalex-snapshot
Carotenoid oxidation products are stress signals that mediate gene responses to singlet oxygen in plants
inferredcites →https://doi.org/10.1073/pnas.221252798openalex-snapshot
FLU: A negative regulator of chlorophyll biosynthesis in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.84.1.146openalex-snapshot
Reconstitution of chlorophyll a/b light-harvesting complexes: Xanthophyll-dependent assembly and energy transfer
inferredcites →https://doi.org/10.1073/pnas.98.2.771openalex-snapshot
The Arabidopsis- accelerated cell death gene ACD2 encodes red chlorophyll catabolite reductase and suppresses the spread of disease symptoms
inferredcites →https://doi.org/10.1073/pnas.98.4.2053openalex-snapshot
Arabidopsis genomes uncoupled 5 ( GUN5 ) mutant reveals the involvement of Mg-chelatase H subunit in plastid-to-nucleus signal transduction
inferredcites →https://doi.org/10.1074/jbc.274.7.4231openalex-snapshot
Expression of Uroporphyrinogen Decarboxylase or Coproporphyrinogen Oxidase Antisense RNA in Tobacco Induces Pathogen Defense Responses Conferring Increased Resistance to Tobacco Mosaic Virus
inferredcites →https://doi.org/10.1080/09553009014552071openalex-snapshot
Free Radicals in Biology and Medicine
inferredcites →https://doi.org/10.1093/jexbot/52.365.2375openalex-snapshot
Comparison of two methods used to analyse lipid peroxidation from Vaccinium myrtillus (L.) during snow removal, reacclimation and cold acclimation
inferredcites →https://doi.org/10.1093/jxb/erj181openalex-snapshot
Imaging the production of singlet oxygen in vivo using a new fluorescent sensor, Singlet Oxygen Sensor Green(R)
inferredcites →https://doi.org/10.1093/jxb/erq186openalex-snapshot
The Arabidopsis plastid-signalling mutant gun1 (genomes uncoupled1) shows altered sensitivity to sucrose and abscisic acid and alterations in early seedling development
inferredcites →https://doi.org/10.1104/pp.108.125690openalex-snapshot
Singlet Oxygen Is the Major Reactive Oxygen Species Involved in Photooxidative Damage to Plants
inferredcites →https://doi.org/10.1104/pp.70.5.1277openalex-snapshot
Nature of Photooxidative Events in Leaves Treated with Chlorosis-Inducing Herbicides
inferredcites →https://doi.org/10.1104/pp.94.4.1663openalex-snapshot
Effects of High Light Stress on Carotenoid-Deficient Chloroplasts in Pisum sativum
inferredcites →https://doi.org/10.1105/tpc.010446openalex-snapshot
Signal Transduction between the Chloroplast and the Nucleus
inferredcites →https://doi.org/10.1105/tpc.014662openalex-snapshot
Rapid Induction of Distinct Stress Responses after the Release of Singlet Oxygen in Arabidopsis[W]
inferredcites →https://doi.org/10.1105/tpc.015008openalex-snapshot
Substrate-Dependent and Organ-Specific Chloroplast Protein Import in Planta
inferredcites →https://doi.org/10.1105/tpc.10.7.1095openalex-snapshot
A Porphyrin Pathway Impairment Is Responsible for the Phenotype of a Dominant Disease Lesion Mimic Mutant of Maize
inferredcites →https://doi.org/10.1105/tpc.106.048744openalex-snapshot
In Vivo Visualization of Mg-ProtoporphyrinIX, a Coordinator of Photosynthetic Gene Expression in the Nucleus and the Chloroplast
inferredcites →https://doi.org/10.1105/tpc.107.054312openalex-snapshot
Plastid Signals Remodel Light Signaling Networks and Are Essential for Efficient Chloroplast Biogenesis inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.107.054809openalex-snapshot
General Detoxification and Stress Responses Are Mediated by Oxidized Lipids through TGA Transcription Factors inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.100479openalex-snapshot
Chloroplasts of Arabidopsis Are the Source and a Primary Target of a Plant-Specific Programmed Cell Death Signaling Pathway
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02262.xopenalex-snapshot
Concurrent interactions of heme and FLU with Glu tRNA reductase (HEMA1), the target of metabolic feedback inhibition of tetrapyrrole biosynthesis, in dark‐ and light‐grown Arabidopsis plants
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03409.xopenalex-snapshot
Enzymatic, but not non‐enzymatic, 1O2‐mediated peroxidation of polyunsaturated fatty acids forms part of the EXECUTER1‐dependent stress response program in the flu mutant of Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04454.xopenalex-snapshot
‘ happy on norflurazon ’ ( hon ) mutations implicate perturbance of plastid homeostasis with activating stress acclimatization and changing nuclear gene expression in norflurazon‐treated seedlings
inferredcites →https://doi.org/10.1111/j.1399-3054.2009.01343.xopenalex-snapshot
In‐depth analysis of the distinctive effects of norflurazon implies that tetrapyrrole biosynthesis, organellar gene expression and ABA cooperate in the GUN‐type of plastid signalling
inferredcites →https://doi.org/10.1111/j.1432-1033.1984.tb08433.xopenalex-snapshot
Carotenoid‐deficient maize seedlings fail to accumulate light‐harvesting chlorophyll a/b binding protein (LHCP) mRNA
inferredcites →https://doi.org/10.1111/j.1432-1033.1986.tb09444.xopenalex-snapshot
The implication of a plastid‐derived factor in the transcriptional control of nuclear genes encoding the light‐harvesting chlorophyll a/b protein
inferredcites →https://doi.org/10.1111/j.1751-1097.1999.tb01944.xopenalex-snapshot
Environmental Significance of Anthocyanins in Plant Stress Responses
inferredcites →https://doi.org/10.1126/science.1079978openalex-snapshot
GUN4, a Regulator of Chlorophyll Synthesis and Intracellular Signaling
inferredcites →https://doi.org/10.1126/science.1103178openalex-snapshot
The Genetic Basis of Singlet OxygenInduced Stress Responses of Arabidopsis thaliana
inferredcites →https://doi.org/10.1126/science.1140516openalex-snapshot
Signals from chloroplasts converge to regulate nuclear gene expression.
inferredcites →https://doi.org/10.1146/annurev.arplant.55.031903.141701openalex-snapshot
REACTIVE OXYGEN SPECIES: Metabolism, Oxidative Stress, and Signal Transduction
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105310openalex-snapshot
PLASTID-TO-NUCLEUS RETROGRADE SIGNALING
inferredcites →https://doi.org/10.1146/annurev.arplant.58.032806.103844openalex-snapshot
Sensing and Responding to Excess Light
inferredcites →https://doi.org/10.1186/1471-2229-9-28openalex-snapshot
Differential patterns of reactive oxygen species and antioxidative mechanisms during atrazine injury and sucrose-induced tolerance in Arabidopsis thaliana plantlets
inferredcites →https://doi.org/10.1562/2006-02-06-ra-797openalex-snapshot
Singlet Oxygen in Plants—Its Significance and Possible Detection with Double (Fluorescent and Spin) Indicator Reagents
inferredcites →https://doi.org/10.3389/fpls.2012.00135openalex-snapshot
Retrograde signaling in plants: from simple to complex scenarios
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.4753300openalex-extracted
Redox Regulation of Autophagy in Arabidopsis: Reactive Oxygen Species Differential Effects
inferred← citeshttps://doi.org/10.1002/9781119324928.ch17openalex-snapshot
Role of Reactive Oxygen Species Signaling in Cell Proliferation and Differentiation
inferred← citeshttps://doi.org/10.1007/978-1-4614-7570-5_10openalex-snapshot
Chloroplast Signaling in Plants
inferred← citeshttps://doi.org/10.1007/978-1-4939-0263-7_10-1openalex-snapshot
Cytoplasm: Chloroplast Signaling
inferred← citeshttps://doi.org/10.1007/978-981-13-8922-1_18openalex-snapshot
Plastid Retrograde Signals: More to Discover
inferred← citeshttps://doi.org/10.1007/s00425-015-2384-3openalex-snapshot
The roles of tetrapyrroles in plastid retrograde signaling and tolerance to environmental stresses
inferred← citeshttps://doi.org/10.1007/s11120-013-9876-4openalex-snapshot
Singlet oxygen-mediated signaling in plants: moving from flu to wild type reveals an increasing complexity
inferred← citeshttps://doi.org/10.1007/s40626-019-00157-7openalex-snapshot
Genome uncoupled (gun) phenotype is associated with root growth repression in Arabidopsis seedlings grown on lincomycin
inferred← citeshttps://doi.org/10.1016/bs.abr.2022.08.023openalex-snapshot
Singlet oxygen in plants: From genesis to signaling
inferred← citeshttps://doi.org/10.1016/j.bbabio.2016.03.017openalex-snapshot
Retrograde signaling: Organelles go networking
inferred← citeshttps://doi.org/10.1016/j.bbagen.2014.12.020openalex-snapshot
ROS-mediated redox signaling during cell differentiation in plants
inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.01.142openalex-snapshot
Perturbations in carotenoid and porphyrin status result in differential photooxidative stress signaling and antioxidant responses
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2023.115388openalex-snapshot
Resilient and sustainable production of peanut (Arachis hypogaea) in phosphorus-limited environment by using exogenous gamma-aminobutyric acid to sustain photosynthesis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2014.06.021openalex-snapshot
Mechanisms of oxidative stress in plants: From classical chemistry to cell biology
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2024.04.233openalex-snapshot
What can reactive oxygen species (ROS) tell us about the action mechanism of herbicides and other phytotoxins?
inferred← citeshttps://doi.org/10.1016/j.jbc.2023.105481openalex-snapshot
Singlet oxygen induces cell wall thickening and stomatal density reducing by transcriptome reprogramming
inferred← citeshttps://doi.org/10.1016/j.molp.2016.06.008openalex-snapshot
PTOX Mediates Novel Pathways of Electron Transport in Etioplasts of Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.pbi.2015.04.006openalex-snapshot
Metabolites and chloroplast retrograde signaling
inferred← citeshttps://doi.org/10.1016/j.pbi.2019.06.005openalex-snapshot
Chloroplast stress signals: regulation of cellular degradation and chloroplast turnover
inferred← citeshttps://doi.org/10.1016/j.plaphy.2015.02.001openalex-snapshot
Enhanced excision repair and lack of PSII activity contribute to higher UV survival of Chlamydomonas reinhardtii cells in dark
inferred← citeshttps://doi.org/10.1016/j.plaphy.2019.04.039openalex-snapshot
Acquiring control: The evolution of ROS-Induced oxidative stress and redox signaling pathways in plant stress responses
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108813openalex-snapshot
Plastid dynamism integrates development and environment
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109800openalex-snapshot
Redox regulation of autophagy in Arabidopsis: The different ROS effects
inferred← citeshttps://doi.org/10.1016/j.tplants.2024.09.007openalex-snapshot
The interplay of singlet oxygen and ABI4 in plant growth regulation
inferred← citeshttps://doi.org/10.1016/j.xplc.2022.100411openalex-snapshot
Tetrapyrrole biosynthesis pathway regulates plastid-to-nucleus signaling by controlling plastid gene expression in plants
inferred← citeshttps://doi.org/10.1089/ars.2013.5662openalex-snapshot
Specificity in ROS Signaling and Transcript Signatures
inferred← citeshttps://doi.org/10.1089/ars.2017.7392openalex-snapshot
Piecing the Puzzle Together: The Central Role of Reactive Oxygen Species and Redox Hubs in Chloroplast Retrograde Signaling
inferred← citeshttps://doi.org/10.1093/bbb/zbad024openalex-snapshot
Chemical and genetic carotenoid deficiency delays growth in dark-grownEuglena gracilis
inferred← citeshttps://doi.org/10.1093/jxb/erv018openalex-snapshot
An Arabidopsis soluble chloroplast proteomic analysis reveals the participation of the Executer pathway in response to increased light conditions
inferred← citeshttps://doi.org/10.1093/jxb/erw136openalex-snapshot
Novel connections in plant organellar signalling link different stress responses and signalling pathways
inferred← citeshttps://doi.org/10.1093/jxb/erx383openalex-snapshot
A novel tetratricopeptide repeat protein, WHITE TO GREEN1, is required for early chloroplast development and affects RNA editing in chloroplasts
inferred← citeshttps://doi.org/10.1093/jxb/ery168openalex-snapshot
ROS and redox balance as multifaceted players of cross-tolerance: epigenetic and retrograde control of gene expression
inferred← citeshttps://doi.org/10.1093/plphys/kiad001openalex-snapshot
Zeaxanthin is required for eyespot formation and phototaxis inEuglena gracilis
inferred← citeshttps://doi.org/10.1098/rstb.2013.0232openalex-snapshot
Influence of plastids on light signalling and development
inferred← citeshttps://doi.org/10.1101/798900openalex-snapshot
Impact of small RNAs in retrograde signalling pathways in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1104/pp.114.236380openalex-snapshot
Singlet Oxygen Signatures Are Detected Independent of Light or Chloroplasts in Response to Multiple Stresses
inferred← citeshttps://doi.org/10.1104/pp.18.00772openalex-snapshot
genome uncoupled1 Mutants Are Hypersensitive to Norflurazon and Lincomycin
inferred← citeshttps://doi.org/10.1104/pp.18.00982openalex-snapshot
The genomes uncoupled Mutants Are More Sensitive to Norflurazon Than Wild Type
inferred← citeshttps://doi.org/10.1105/tpc.19.00751openalex-snapshot
Light Activates the Translational Regulatory Kinase GCN2 via Reactive Oxygen Species Emanating from the Chloroplast
inferred← citeshttps://doi.org/10.1111/nph.14223openalex-snapshot
Singlet oxygen initiates a plastid signal controlling photosynthetic gene expression
inferred← citeshttps://doi.org/10.1111/nph.19717openalex-snapshot
Activating plant immunity: the hidden dance of intracellular Ca2+ stores
inferred← citeshttps://doi.org/10.1111/pbi.12356openalex-snapshot
Tetrapyrrole‐based drought stress signalling
inferred← citeshttps://doi.org/10.1111/pbi.14548openalex-snapshot
Characterization of a tomato chlh mis‐sense mutant reveals a new function of ChlH in fruit ripening
inferred← citeshttps://doi.org/10.1111/pce.12462openalex-snapshot
Blocking the QB ‐binding site of photosystem II by tenuazonic acid, a non–host‐specific toxin of A lternaria alternata, activates singlet oxygen‐mediated and EXECUTER ‐dependent signalling in Arabidopsis
inferred← citeshttps://doi.org/10.1111/pce.14162openalex-snapshot
Attenuation of cytosolic translation by RNA oxidation is involved in singlet oxygen‐mediated transcriptomic responses
inferred← citeshttps://doi.org/10.1111/ppl.14144openalex-snapshot
Diethyl ether anaesthesia inhibits de‐etiolation of barley seedlings by locking them in intermediate skoto‐photomorphogenetic state
inferred← citeshttps://doi.org/10.1111/tpj.14912openalex-snapshot
Identification of small non‐coding RNAs responsive to GUN1 and GUN5 related retrograde signals in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/tpj.16776openalex-snapshot
ZmPTOX1 , a plastid terminal oxidase, contributes to redox homeostasis during seed development and germination
inferred← citeshttps://doi.org/10.1146/annurev-arplant-043015-111854openalex-snapshot
Learning the Languages of the Chloroplast: Retrograde Signaling and Beyond
inferred← citeshttps://doi.org/10.1186/s12870-015-0426-4openalex-snapshot
Carotenoid accumulation affects redox status, starch metabolism, and flavonoid/anthocyanin accumulation in citrus
inferred← citeshttps://doi.org/10.1186/s12870-016-0795-3openalex-snapshot
A putative pyruvate transporter TaBASS2 positively regulates salinity tolerance in wheat via modulation of ABI4 expression
inferred← citeshttps://doi.org/10.1186/s43897-025-00153-3openalex-snapshot
Smi-miRmTERF regulates organelle development, retrograde signaling, secondary metabolism and immunity via targeting a subset of SmmTERFs in Salvia miltiorrhiza
inferred← citeshttps://doi.org/10.1371/journal.pone.0150983openalex-snapshot
Impaired Chloroplast Biogenesis in Immutans, an Arabidopsis Variegation Mutant, Modifies Developmental Programming, Cell Wall Composition and Resistance to Pseudomonas syringae
inferred← citeshttps://doi.org/10.3389/fpls.2013.00371openalex-snapshot
Thiol-based redox control of enzymes involved in the tetrapyrrole biosynthesis pathway in plants
inferred← citeshttps://doi.org/10.3389/fpls.2015.01078openalex-snapshot
Chloroplast Biogenesis-Associated Nuclear Genes: Control by Plastid Signals Evolved Prior to Their Regulation as Part of Photomorphogenesis
inferred← citeshttps://doi.org/10.3389/fpls.2016.01586openalex-snapshot
Tetrapyrrole Signaling in Plants
inferred← citeshttps://doi.org/10.3389/fpls.2021.637853openalex-snapshot
Chloroplast: The Emerging Battlefield in Plant–Microbe Interactions
inferred← citeshttps://doi.org/10.3389/fpls.2021.786208openalex-snapshot
Suppression of the Lycopene Cyclase Gene Causes Downregulation of Ascorbate Peroxidase Activity and Decreased Glutathione Pool Size, Leading to H2O2 Accumulation in Euglena gracilis
inferred← citeshttps://doi.org/10.3389/fpls.2022.850504openalex-snapshot
Impact of Porphyrin Binding to GENOMES UNCOUPLED 4 on Tetrapyrrole Biosynthesis in planta
inferred← citeshttps://doi.org/10.3389/fpls.2023.1331346openalex-snapshot
A genetic screen for dominant chloroplast reactive oxygen species signaling mutants reveals life stage-specific singlet oxygen signaling networks
inferred← citeshttps://doi.org/10.3390/ijms23041995openalex-snapshot
How to Cope with the Challenges of Environmental Stresses in the Era of Global Climate Change: An Update on ROS Stave off in Plants
inferred← citeshttps://doi.org/10.3390/ijms25158458openalex-snapshot
Singlet-Oxygen-Mediated Regulation of Photosynthesis-Specific Genes: A Role for Reactive Electrophiles in Signal Transduction
inferred← citeshttps://doi.org/10.3390/plants10020196openalex-snapshot
The Role of Tetrapyrrole- and GUN1-Dependent Signaling on Chloroplast Biogenesis
inferred← citeshttps://doi.org/10.3390/plants14233659openalex-snapshot
Physiological Responses of Paulownia fortunei to Leaf Herbivory by Epicauta ruficeps: Nitrogen Assimilation, Porphyrin Metabolism, and ROS-Driven Antioxidant and Phenylpropanoid Responses
inferred← citeshttps://doi.org/10.4141/cjps-2014-294openalex-snapshot
Proteome response of wild wheat relative Kengyilia thoroldiana to drought stress
inferred← citeshttps://doi.org/10.4161/15592324.2014.976150openalex-snapshot
Shedding light on the chloroplast as a remote control of nuclear gene expression
inferred← citeshttps://doi.org/10.70675/254c9ffbz7842z4148zbeddz06e38bc460a7openalex-snapshot
Functional analysis of catalase mutants and their application to the analysis of NADPH-linked pathways in oxidative signaling in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.70675/a5e169f3z7d6dz4723z8605z40c5a18b145copenalex-snapshot
Singlet Oxygen Signaling and Acclimation of Plants to Environmental Constraints
inferred← citeshttps://doi.org/10.7287/peerj.preprints.827openalex-snapshot
An ecological implication of glandular trichome-sequestered artemisinin: as a sink of biotic/abiotic stress-triggered singlet oxygen
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.