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GNC and CGA1 Modulate Chlorophyll Biosynthesis and Glutamate Synthase (GLU1/Fd-GOGAT) Expression in Arabidopsis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-94-007-1579-0_3openalex-snapshot
Chlorophyll Biosynthesis in Higher Plants
inferredcites →https://doi.org/10.1007/bf03030443openalex-snapshot
Chlorophyll biosynthesis in higher plants. Regulatory aspects of 5-aminolevulinate formation
inferredcites →https://doi.org/10.1007/s00425-005-0013-2openalex-snapshot
Expression of a ferredoxin-dependent glutamate synthase gene in mesophyll and vascular cells and functions of the enzyme in ammonium assimilation in Nicotiana tabacum (L.)
inferredcites →https://doi.org/10.1007/s00726-009-0303-2openalex-snapshot
Analysis of glutamate homeostasis by overexpression of Fd-GOGAT gene in Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/s11103-004-2331-3openalex-snapshot
Recent advances in chlorophyll biosynthesis and breakdown in higher plants
inferredcites →https://doi.org/10.1007/s11103-007-9194-3openalex-snapshot
HEMA RNAi silencing reveals a control mechanism of ALA biosynthesis on Mg chelatase and Fe chelatase
inferredcites →https://doi.org/10.1007/s11103-007-9241-0openalex-snapshot
Genome-wide analysis of Arabidopsis responsive transcriptome to nitrogen limitation and its regulation by the ubiquitin ligase gene NLA
inferredcites →https://doi.org/10.1007/s11103-008-9407-4openalex-snapshot
Interactions between circadian and hormonal signalling in plants
inferredcites →https://doi.org/10.1007/s11103-009-9582-yopenalex-snapshot
Arabidopsis protochlorophyllide oxidoreductase A (PORA) restores bulk chlorophyll synthesis and normal development to a porB porC double mutant
inferredcites →https://doi.org/10.1016/j.jplph.2009.05.007openalex-snapshot
Cytokinin-induced changes of nitrogen remobilization and chloroplast ultrastructure in wheat (Triticum aestivum)
inferredcites →https://doi.org/10.1016/j.jplph.2009.05.010openalex-snapshot
The bZIP transcription factors HY5 and HYH are positive regulators of the main nitrate reductase gene in Arabidopsis leaves, NIA2, but negative regulators of the nitrate uptake gene NRT1.1
inferredcites →https://doi.org/10.1016/j.pbi.2009.07.010openalex-snapshot
Time for circadian rhythms: plants get synchronized
inferredcites →https://doi.org/10.1016/j.pbi.2010.08.006openalex-snapshot
Cytokinin signaling and transcriptional networks
inferredcites →https://doi.org/10.1016/j.plantsci.2008.12.013openalex-snapshot
The stay-green revolution: Recent progress in deciphering the mechanisms of chlorophyll degradation in higher plants
inferredcites →https://doi.org/10.1016/j.tplants.2006.07.004openalex-snapshot
Interactions between nitrogen and cytokinin in the regulation of metabolism and development
inferredcites →https://doi.org/10.1016/j.tplants.2007.11.005openalex-snapshot
Cytokinin signaling: two-components and more
inferredcites →https://doi.org/10.1016/j.tplants.2010.08.003openalex-snapshot
PIFs: pivotal components in a cellular signaling hub
inferredcites →https://doi.org/10.1016/s0168-6445(02)00071-2openalex-snapshot
Transmitting the signal of excess nitrogen in Saccharomyces cerevisiae from the Tor proteins to the GATA factors: connecting the dots
inferredcites →https://doi.org/10.1016/s0960-9822(02)00815-1openalex-snapshot
Critical Role for CCA1 and LHY in Maintaining Circadian Rhythmicity in Arabidopsis
inferredcites →https://doi.org/10.1016/s0981-9428(02)01453-5openalex-snapshot
Role of gibberellins and of the RGA and GAI genes in controlling nitrate assimilation in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/s1002-0160(07)60071-xopenalex-snapshot
New Insights into the Nitrogen Form Effect on Photosynthesis and Photorespiration
inferredcites →https://doi.org/10.1016/s1360-1385(98)01311-9openalex-snapshot
Molecular and physiological aspects of nitrate uptake in plants
inferredcites →https://doi.org/10.1016/s1360-1385(99)01433-8openalex-snapshot
Plant sugar sensing and signaling – a complex reality
inferredcites →https://doi.org/10.1016/s1369-5266(00)00168-0openalex-snapshot
Carbon and nitrogen sensing and signaling in plants: emerging ‘matrix effects’
inferredcites →https://doi.org/10.1016/s1369-5266(01)00219-9openalex-snapshot
Seed dormancy and germination
inferredcites →https://doi.org/10.1016/s1369-5266(02)00011-0openalex-snapshot
Shedding light on the circadian clock and the photoperiodic control of flowering
inferredcites →https://doi.org/10.1016/s1369-5274(00)00063-1openalex-snapshot
The fungal GATA factors
inferredcites →https://doi.org/10.1021/bi050240xopenalex-snapshot
Structural and Biochemical Characterization of Gun4 Suggests a Mechanism for Its Role in Chlorophyll Biosynthesis,
inferredcites →https://doi.org/10.1023/a:1005842812321openalex-snapshot
Footprinting of the spinach nitrite reductase gene promoter reveals the preservation of nitrate regulatory elements between fungi and higher plants
inferredcites →https://doi.org/10.1038/22307openalex-snapshot
‘Green revolution’ genes encode mutant gibberellin response modulators
inferredcites →https://doi.org/10.1038/416701aopenalex-snapshot
A mutant gibberellin-synthesis gene in rice
inferredcites →https://doi.org/10.1038/nature05946openalex-snapshot
Rhythmic growth explained by coincidence between internal and external cues
inferredcites →https://doi.org/10.1038/nature06448openalex-snapshot
Coordinated regulation of Arabidopsis thaliana development by light and gibberellins
inferredcites →https://doi.org/10.1042/bst0330269openalex-snapshot
Sugar sensing and signalling networks in plants
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.0402887101openalex-snapshot
In planta functions of the Arabidopsis cytokinin receptor family
inferredcites →https://doi.org/10.1073/pnas.0404388101openalex-snapshot
Nitrate assimilation in plant shoots depends on photorespiration
inferredcites →https://doi.org/10.1073/pnas.0407107101openalex-snapshot
The phytochrome-interacting transcription factor, PIF3, acts early, selectively, and positively in light-induced chloroplast development
inferredcites →https://doi.org/10.1073/pnas.0800211105openalex-snapshot
Systems approach identifies an organic nitrogen-responsive gene network that is regulated by the master clock control gene CCA1
inferredcites →https://doi.org/10.1073/pnas.0803611105openalex-snapshot
PIF1 directly and indirectly regulates chlorophyll biosynthesis to optimize the greening process in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0811684106openalex-snapshot
PIF3 is a repressor of chloroplast development
inferredcites →https://doi.org/10.1073/pnas.0812219106openalex-snapshot
Phytochromes promote seedling light responses by inhibiting four negatively-acting phytochrome-interacting factors
inferredcites →https://doi.org/10.1073/pnas.0914428107openalex-snapshot
Direct regulation of phytoene synthase gene expression and carotenoid biosynthesis by phytochrome-interacting factors
inferredcites →https://doi.org/10.1073/pnas.1101050108openalex-snapshot
Circadian oscillation of gibberellin signaling in Arabidopsis
inferredcites →https://doi.org/10.1074/jbc.m109.025205openalex-snapshot
Porphyrins Promote the Association of GENOMES UNCOUPLED 4 and a Mg-chelatase Subunit with Chloroplast Membranes
inferredcites →https://doi.org/10.1074/jbc.m109.085712openalex-snapshot
Distinct Phosphatase Requirements and GATA Factor Responses to Nitrogen Catabolite Repression and Rapamycin Treatment in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1093/aob/mcl249openalex-snapshot
Plastid Division: Evolution, Mechanism and Complexity
inferredcites →https://doi.org/10.1093/jexbot/53.370.971openalex-snapshot
Multiple routes communicating nitrogen availability from roots to shoots: a signal transduction pathway mediated by cytokinin
inferredcites →https://doi.org/10.1093/jxb/erm097openalex-snapshot
The challenge of improving nitrogen use efficiency in crop plants: towards a more central role for genetic variability and quantitative genetics within integrated approaches
inferredcites →https://doi.org/10.1093/jxb/ern148openalex-snapshot
Adaptation of Arabidopsis to nitrogen limitation involves induction of anthocyanin synthesis which is controlled by the NLA gene
inferredcites →https://doi.org/10.1093/mp/ssp072openalex-snapshot
GUN4 Is Required for Posttranslational Control of Plant Tetrapyrrole Biosynthesis
inferredcites →https://doi.org/10.1093/mp/ssq049openalex-snapshot
Metabolic and Signaling Aspects Underpinning the Regulation of Plant Carbon Nitrogen Interactions
inferredcites →https://doi.org/10.1093/pcp/pce009openalex-snapshot
Nitrogen-Dependent Accumulation of Cytokinins in Root and theTranslocation to Leaf: Implication of Cytokinin Species that Induces GeneExpression of Maize ResponseRegulator
inferredcites →https://doi.org/10.1093/pcp/pci033openalex-snapshot
Combinatorial Microarray Analysis Revealing Arabidopsis Genes Implicated in Cytokinin Responses through the His→Asp Phosphorelay Circuitry
inferredcites →https://doi.org/10.1093/pcp/pci141openalex-snapshot
Contribution of Gibberellins to the Formation of Arabidopsis Seed Coat Through Starch Degradation
inferredcites →https://doi.org/10.1093/pcp/pcm063openalex-snapshot
Genetic Linkages Between Circadian Clock-Associated Components and Phytochrome-Dependent Red Light Signal Transduction in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/treephys/23.8.553openalex-snapshot
Leaf chlorophyll, net gas exchange and chloroplast ultrastructure in citrus leaves of different nitrogen status
inferredcites →https://doi.org/10.1101/gad.11.23.3194openalex-snapshot
The Arabidopsis GAI gene defines a signaling pathway that negatively regulates gibberellin responses
inferredcites →https://doi.org/10.1101/gad.594910openalex-snapshot
The GATA-type transcription factors GNC and GNL/CGA1 repress gibberellin signaling downstream from DELLA proteins and PHYTOCHROME-INTERACTING FACTORS
inferredcites →https://doi.org/10.1104/pp.103.037788openalex-snapshot
The GATA Family of Transcription Factors in Arabidopsis and Rice
inferredcites →https://doi.org/10.1104/pp.104.047019openalex-snapshot
Genome-Wide Reprogramming of Primary and Secondary Metabolism, Protein Synthesis, Cellular Growth Processes, and the Regulatory Infrastructure of Arabidopsis in Response to Nitrogen
inferredcites →https://doi.org/10.1104/pp.106.090761openalex-snapshot
Conservation, Convergence, and Divergence of Light-Responsive, Circadian-Regulated, and Tissue-Specific Expression Patterns during Evolution of the Arabidopsis GATA Gene Family
inferredcites →https://doi.org/10.1104/pp.107.100370openalex-snapshot
Mechanisms of Cross Talk between Gibberellin and Other Hormones
inferredcites →https://doi.org/10.1104/pp.107.115634openalex-snapshot
Two GATA Transcription Factors Are Downstream Effectors of Floral Homeotic Gene Action in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.108.130195openalex-snapshot
Increasing Crop Productivity to Meet Global Needs for Feed, Food, and Fuel
inferredcites →https://doi.org/10.1104/pp.118.3.773openalex-snapshot
Overexpression of 20-Oxidase Confers a Gibberellin-Overproduction Phenotype in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.122.1.49openalex-snapshot
Antisense HEMA1 RNA Expression Inhibits Heme and Chlorophyll Biosynthesis in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.125.1.61openalex-snapshot
Nitrogen and Carbon Nutrient and Metabolite Signaling in Plants
inferredcites →https://doi.org/10.1104/pp.125.4.1554openalex-snapshot
The Nitrate Reductase Circadian System. The Central Clock Dogma Contra Multiple Oscillatory Feedback Loops
inferredcites →https://doi.org/10.1104/pp.77.2.483openalex-snapshot
Extinction Coefficients of Chlorophyll a and b in N,N -Dimethylformamide and 80% Acetone
inferredcites →https://doi.org/10.1105/tpc.10.5.741openalex-snapshot
Arabidopsis gls Mutants and Distinct Fd-GOGAT Genes: Implications for Photorespiration and Primary Nitrogen Assimilation
inferredcites →https://doi.org/10.1105/tpc.104.028472openalex-snapshot
Cross Talk between Gibberellin and Cytokinin: The Arabidopsis GA Response Inhibitor SPINDLY Plays a Positive Role in Cytokinin Signaling
inferredcites →https://doi.org/10.1105/tpc.105.035071openalex-snapshot
Two Types of FtsH Protease Subunits Are Required for Chloroplast Biogenesis and Photosystem II Repair in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.105.037796openalex-snapshot
ArabidopsisCytokinin Receptor Mutants Reveal Functions in Shoot Growth, Leaf Senescence, Seed Size, Germination, Root Development, and Cytokinin Metabolism
inferredcites →https://doi.org/10.1105/tpc.106.045484openalex-snapshot
PDV1 and PDV2 Mediate Recruitment of the Dynamin-Related Protein ARC5 to the Plastid Division Site
inferredcites →https://doi.org/10.1105/tpc.107.050153openalex-snapshot
PIL5, a Phytochrome-Interacting bHLH Protein, Regulates Gibberellin Responsiveness by Binding Directly to theGAIandRGAPromoters inArabidopsisSeeds
inferredcites →https://doi.org/10.1105/tpc.107.053074openalex-snapshot
Returning to Our Roots: Making Plant Biology Research Relevant to Future Challenges in Agriculture
inferredcites →https://doi.org/10.1105/tpc.108.061440openalex-snapshot
Arabidopsis ARC6 Coordinates the Division Machineries of the Inner and Outer Chloroplast Membranes through Interaction with PDV2 in the Intermembrane Space
inferredcites →https://doi.org/10.1105/tpc.108.064691openalex-snapshot
Genome-Wide Analysis of Genes Targeted by PHYTOCHROME INTERACTING FACTOR 3-LIKE5 during Seed Germination inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.109.067785openalex-snapshot
The PLASTID DIVISION1 and 2 Components of the Chloroplast Division Machinery Determine the Rate of Chloroplast Division in Land Plant Cell Differentiation
inferredcites →https://doi.org/10.1105/tpc.109.070672openalex-snapshot
Definition of Early Transcriptional Circuitry Involved in Light-Induced Reversal of PIF-Imposed Repression of Photomorphogenesis in YoungArabidopsisSeedlings
inferredcites →https://doi.org/10.1105/tpc.110.079079openalex-snapshot
Cytokinin Regulates the Activity of Reproductive Meristems, Flower Organ Size, Ovule Formation, and Thus Seed Yield in Arabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.111.085233openalex-snapshot
DELLAs Regulate Chlorophyll and Carotenoid Biosynthesis to Prevent Photooxidative Damage during Seedling Deetiolation in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.5.8.887openalex-snapshot
Mutations at the SPINDLY Locus of Arabidopsis Alter Gibberellin Signal Transduction
inferredcites →https://doi.org/10.1105/tpc.9.1.5openalex-snapshot
Hexokinase as a Sugar Sensor in Higher Plants
inferredcites →https://doi.org/10.1111/j.1365-2443.2006.01026.xopenalex-snapshot
Multiple phytohormones influence distinct parameters of the plant circadian clock
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02437.xopenalex-snapshot
The Botany Array Resource: e‐Northerns, Expression Angling, and promoter analyses
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02530.xopenalex-snapshot
Immediate‐early and delayed cytokinin response genes of Arabidopsis thaliana identified by genome‐wide expression profiling reveal novel cytokinin‐sensitive processes and suggest cytokinin action through transcriptional cascades
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02568.xopenalex-snapshot
Genetic analysis of Arabidopsis GATA transcription factor gene family reveals a nitrate‐inducible member important for chlorophyll synthesis and glucose sensitivity
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02681.xopenalex-snapshot
The Arabidopsis co‐expression tool ( act ): a WWW‐based tool and database for microarray‐based gene expression analysis
inferredcites →https://doi.org/10.1111/j.1467-7652.2010.00584.xopenalex-snapshot
Cytokinin‐mediated source/sink modifications improve drought tolerance and increase grain yield in rice under water‐stress
inferredcites →https://doi.org/10.1111/j.1742-4658.2009.07114.xopenalex-snapshot
Assimilation of excess ammonium into amino acids and nitrogen translocation in Arabidopsis thaliana– roles of glutamate synthases and carbamoylphosphate synthetase in leaves
inferredcites →https://doi.org/10.1111/j.1744-7909.2010.00980.xopenalex-snapshot
Arabidopsis Chloroplast FtsH, var2 and Suppressors of var2 Leaf Variegation: a Review
inferredcites →https://doi.org/10.1126/science.1080585openalex-snapshot
Role of the Arabidopsis Glucose Sensor HXK1 in Nutrient, Light, and Hormonal Signaling
inferredcites →https://doi.org/10.1126/science.1099728openalex-snapshot
PHYTOCHROME-INTERACTING FACTOR 1 Is a Critical bHLH Regulator of Chlorophyll Biosynthesis
inferredcites →https://doi.org/10.1126/science.1113373openalex-snapshot
Cytokinin Oxidase Regulates Rice Grain Production
inferredcites →https://doi.org/10.1126/science.290.5499.2110openalex-snapshot
Orchestrated Transcription of Key Pathways in Arabidopsis by the Circadian Clock
inferredcites →https://doi.org/10.1126/stke.4072007cm5openalex-snapshot
Arabidopsis Cytokinin Signaling Pathway
inferredcites →https://doi.org/10.1146/annurev.arplant.47.1.569openalex-snapshot
THE MOLECULAR-GENETICS OF NITROGEN ASSIMILATION INTO AMINO ACIDS IN HIGHER PLANTS
inferredcites →https://doi.org/10.1186/1471-2164-11-190openalex-snapshot
Transcriptional profiling of an Fd-GOGAT1/GLU1 mutant in Arabidopsis thaliana reveals a multiple stress response and extensive reprogramming of the transcriptome
inferredcites →https://doi.org/10.1186/1752-0509-3-85openalex-snapshot
From gene expression to gene regulatory networks in Arabidopsis thaliana
inferredcites →https://doi.org/10.1242/dev.005017openalex-snapshot
Integration of cytokinin and gibberellin signalling byArabidopsistranscription factors GIS, ZFP8 and GIS2 in the regulation of epidermal cell fate
inferredcites →https://doi.org/10.1271/bbb.60692openalex-snapshot
Characterization of a Unique GATA Family Gene That Responds to Both Light and Cytokinin inArabidopsis thaliana
inferredcites →https://doi.org/10.1371/journal.pone.0000718openalex-snapshot
An “Electronic Fluorescent Pictograph” Browser for Exploring and Analyzing Large-Scale Biological Data Sets
inferredcites →https://doi.org/10.1371/journal.pone.0019894openalex-snapshot
PIF Genes Mediate the Effect of Sucrose on Seedling Growth Dynamics
inferredcites →https://doi.org/10.1387/ijdb.051997elopenalex-snapshot
Plastids unleashed: their development and their integration in plant development
inferredcites →https://doi.org/10.2134/agronj2000.925875xopenalex-snapshot
Use of Chlorophyll Meter Sufficiency Indices for Nitrogen Management of Irrigated Rice in Asia
inferredcites →https://doi.org/10.2134/agronj2005.0070openalex-snapshot
Chlorophyll Meter Readings Can Predict Nitrogen Need and Yield Response of Corn in the North‐Central USA
inferredcites →https://doi.org/10.2307/3870661openalex-snapshot
Arabidopsis gls Mutants and Distinct Fd-GOGAT Genes: Implications for Photorespiration and Primary Nitrogen Assimilation
inferredcites →https://doi.org/10.4161/psb.5.2.10461openalex-snapshot
The evolution of the regulatory mechanism of chloroplast division
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.4753282openalex-extracted
Functional-Urea Nanofertilizer to Promote Nitrogen Availability in Plant
inferred← citeshttps://doi.org/10.1002/pld3.16openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/pld3.483openalex-snapshot
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Genetic diversity for nitrogen use efficiency in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00438-016-1275-zopenalex-snapshot
The ferredoxin-dependent glutamate synthase (OsFd-GOGAT) participates in leaf senescence and the nitrogen remobilization in rice
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Transcriptome-wide investigation and functional characterization reveal a terpene synthase involved in γ-terpinene biosynthesis in Monarda citriodora
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Transcriptomic insights into nitrogen-regulated cadmium absorption and accumulation in Spirodela polyrhiza: Toward enhanced phytoremediation strategies for cadmium-polluted environments
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An integrative gene regulatory network identifies transcriptional hubs governing the photosynthetic apparatus in rice
inferred← citeshttps://doi.org/10.1016/j.jplph.2013.11.016openalex-snapshot
Nitrogen metabolism and gas exchange parameters associated with zinc stress in tobacco expressing an ipt gene for cytokinin synthesis
inferred← citeshttps://doi.org/10.1016/j.molp.2016.09.004openalex-snapshot
Rice Ferredoxin-Dependent Glutamate Synthase Regulates Nitrogen–Carbon Metabolomes and Is Genetically Differentiated between japonica and indica Subspecies
inferred← citeshttps://doi.org/10.1016/j.plantsci.2017.07.013openalex-snapshot
NSR1/MYR2 is a negative regulator of ASN1 expression and its possible involvement in regulation of nitrogen reutilization in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2022.111238openalex-snapshot
Glutamate: A multifunctional amino acid in plants
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112586openalex-snapshot
The MYB transcription factor ClPC modulates petal color and chlorophyll accumulation in watermelon
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113378openalex-snapshot
TaGATA5 acts as a positive regulator of drought tolerance in wheat
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113409openalex-snapshot
Contrasting redox-related physiological responses associated with HaGATA23 and HaGATA36 during Orobanche cumana parasitism in sunflower (Helianthus annuus L.)
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.08.031openalex-snapshot
5-Aminolevulinic acid and hydrogen sulphide alleviate chilling stress in pepper (Capsicum annuum L.) seedlings by enhancing chlorophyll synthesis pathway
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111402openalex-snapshot
Altered cytokinin signaling drives plant drought resilience through lipid remodeling, nutrient homeostasis, cell wall reinforcement, and modulation of biotic stress–associated pathways
inferred← citeshttps://doi.org/10.1016/j.rhisph.2025.101129openalex-snapshot
Physiological and metabolic effects of a transposon-mediated mutation in the glutamate synthase gene, gltB, of plant-beneficial, cytokinin-producing Pseudomonas hormoni G20-18T
inferred← citeshttps://doi.org/10.1016/j.scienta.2026.114954openalex-snapshot
Organic–synthetic fertilization strategies and biochar amendment sustain yield and nutritional quality in Butternut Squash (Cucurbita moschata Duch.)
inferred← citeshttps://doi.org/10.1038/ncomms1926openalex-snapshot
Chloroplast-mediated activation of plant immune signalling in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41598-021-83689-wopenalex-snapshot
Genome wide association analyses to understand genetic basis of flowering and plant height under three levels of nitrogen application in Brassica juncea (L.) Czern & Coss
inferred← citeshttps://doi.org/10.1038/s41598-021-95940-5openalex-snapshot
Genome-wide comparative analyses of GATA transcription factors among seven Populus genomes
inferred← citeshttps://doi.org/10.1038/srep27795openalex-snapshot
Overexpression of Arabidopsis NLP7 improves plant growth under both nitrogen-limiting and -sufficient conditions by enhancing nitrogen and carbon assimilation
inferred← citeshttps://doi.org/10.1038/srep45492openalex-snapshot
ATHB17 enhances stress tolerance by coordinating photosynthesis associated nuclear gene and ATSIG5 expression in response to abiotic stress
inferred← citeshttps://doi.org/10.1042/ebc20170047openalex-snapshot
Non-photosynthetic plastids as hosts for metabolic engineering
inferred← citeshttps://doi.org/10.1073/pnas.2012245117openalex-snapshot
Maize ANT1 modulates vascular development, chloroplast development, photosynthesis, and plant growth
inferred← citeshttps://doi.org/10.1080/07352689.2017.1355661openalex-snapshot
Environmental Adaptation of the Heterotrophic-to-Autotrophic Transition: The Developmental Plasticity of Seedling Establishment
inferred← citeshttps://doi.org/10.1080/15592324.2017.1338999openalex-snapshot
Simultaneous but spatially different regulation of non-photosynthetic callus formation and photosynthetic root development after shoot removal
inferred← citeshttps://doi.org/10.1093/jxb/erab430openalex-snapshot
The chromatin remodelling ATPase BRAHMA interacts with GATA-family transcription factor GNC to regulate flowering time in Arabidopsis
inferred← citeshttps://doi.org/10.1093/jxb/erac190openalex-snapshot
The transcription factor GNC optimizes nitrogen use efficiency and growth by up-regulating the expression of nitrate uptake and assimilation genes in poplar
inferred← citeshttps://doi.org/10.1093/jxb/erac281openalex-snapshot
MAX2-dependent competence for callus formation and shoot regeneration from Arabidopsis thaliana root explants
inferred← citeshttps://doi.org/10.1093/jxb/eraf530openalex-snapshot
Regulation of chloroplast biogenesis and differentiation
inferred← citeshttps://doi.org/10.1093/jxb/ert183openalex-snapshot
Sequence variations of the partially dominant DELLA gene Rht-B1c in wheat and their functional impacts
inferred← citeshttps://doi.org/10.1093/jxb/eru193openalex-snapshot
Was low CO2 a driving force of C4 evolution: Arabidopsis responses to long-term low CO2 stress
inferred← citeshttps://doi.org/10.1093/jxb/eru236openalex-snapshot
The challenges of commercializing second-generation transgenic crop traits necessitate the development of international public sector research infrastructure
inferred← citeshttps://doi.org/10.1093/jxb/erv132openalex-snapshot
Regulation of chloroplast development and function by cytokinin
inferred← citeshttps://doi.org/10.1093/jxb/erx101openalex-snapshot
Nitrogen use efficiency in crops: lessons from Arabidopsis and rice
inferred← citeshttps://doi.org/10.1093/jxb/erz564openalex-snapshot
The GATA transcription factor GNC plays an important role in photosynthesis and growth in poplar
inferred← citeshttps://doi.org/10.1093/pcp/pcv184openalex-snapshot
Asparagine Metabolic Pathways in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plphys/kiad029openalex-snapshot
Shade represses photosynthetic genes by disrupting the DNA binding of GOLDEN2-LIKE1
inferred← citeshttps://doi.org/10.1093/plphys/kiad055openalex-snapshot
Withdrawn as duplicate: Shade represses photosynthetic genes by disrupting the DNA binding of GOLDEN2-LIKE1
inferred← citeshttps://doi.org/10.1093/plphys/kiae273openalex-snapshot
Transcriptional landscape and dynamics involved in sugar and acid accumulation during apple fruit development
inferred← citeshttps://doi.org/10.1093/plphys/kiaf108openalex-snapshot
Increased chloroplast area in the rice bundle sheath through cell-specific perturbation of brassinosteroid signaling
inferred← citeshttps://doi.org/10.1093/plphys/kiaf475openalex-snapshot
FAR1-RELATED SEQUENCE 5 prevents photobleaching under short days by balancing chlorophyll biosynthetic gene expression
inferred← citeshttps://doi.org/10.1094/mpmi-08-24-0095-scopenalex-snapshot
Contrasting Roles of Plant GATA21/22 Transcriptional Regulators in Defense Against Fungal and Bacterial Pathogens
inferred← citeshttps://doi.org/10.1101/040501openalex-snapshot
Arabidopsis ATHB17 coordinates nuclear and plastidic photosynthesis gene expression in response to abiotic stress
inferred← citeshttps://doi.org/10.1101/2020.06.21.163725openalex-snapshot
NMR spectroscopy analysis reveals an altered metabolic homeostasis in Arabidopsis seedlings treated with a cytokinesis inhibitor
inferred← citeshttps://doi.org/10.1101/2025.05.29.656866openalex-snapshot
GNC is a regulator of metabolic and productivity responses to elevated CO 2 in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1104/pp.112.198705openalex-snapshot
Functional Characterization of the GATA Transcription Factors GNC and CGA1 Reveals Their Key Role in Chloroplast Development, Growth, and Division in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.113.215996openalex-snapshot
AtWRKY40 and AtWRKY63 Modulate the Expression of Stress-Responsive Nuclear Genes Encoding Mitochondrial and Chloroplast Proteins
inferred← citeshttps://doi.org/10.1104/pp.113.217026openalex-snapshot
Identification of Cytokinin-Responsive Genes Using Microarray Meta-Analysis and RNA-Seq in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.113.217265openalex-snapshot
Rice Cytokinin GATA Transcription Factor1 Regulates Chloroplast Development and Plant Architecture
inferred← citeshttps://doi.org/10.1104/pp.113.219238openalex-snapshot
Cross-Repressive Interactions between SOC1 and the GATAs GNC and GNL/CGA1 in the Control of Greening, Cold Tolerance, and Flowering Time in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.114.246660openalex-snapshot
Functional Diversification within the Family of B-GATA Transcription Factors through the Leucine-Leucine-Methionine Domain
inferred← citeshttps://doi.org/10.1104/pp.114.256180openalex-snapshot
GROWTH REGULATING FACTOR5 Stimulates Arabidopsis Chloroplast Division, Photosynthesis, and Leaf Longevity
inferred← citeshttps://doi.org/10.1104/pp.16.00640openalex-snapshot
Cytokinin Regulates the Etioplast-Chloroplast Transition through the Two-Component Signaling System and Activation of Chloroplast-Related Genes
inferred← citeshttps://doi.org/10.1104/pp.16.01368openalex-snapshot
Shoot Removal Induces Chloroplast Development in Roots via Cytokinin Signaling
inferred← citeshttps://doi.org/10.1104/pp.18.00414openalex-snapshot
Coordination of Chloroplast Development through the Action of the GNC and GLK Transcription Factor Families
inferred← citeshttps://doi.org/10.1104/pp.19.00489openalex-snapshot
GATA and Phytochrome Interacting Factor Transcription Factors Regulate Light-Induced Vindoline Biosynthesis in Catharanthus roseus
inferred← citeshttps://doi.org/10.1105/tpc.114.134908openalex-snapshot
Sulfur-Responsive Elements in the 3′-Nontranscribed Intergenic Region Are Essential for the Induction of SULFATE TRANSPORTER 2;1 Gene Expression in Arabidopsis Roots under Sulfur Deficiency
inferred← citeshttps://doi.org/10.1105/tpc.15.00783openalex-snapshot
LLM-Domain B-GATA Transcription Factors Promote Stomatal Development Downstream of Light Signaling Pathways in Arabidopsis thaliana Hypocotyls
inferred← citeshttps://doi.org/10.1105/tpc.17.00947openalex-snapshot
LLM-Domain B-GATA Transcription Factors Play Multifaceted Roles in Controlling Greening in Arabidopsis
inferred← citeshttps://doi.org/10.1111/jipb.13437openalex-snapshot
The GATA transcription factor TaGATA1 recruits demethylase TaELF6‐A1 and enhances seed dormancy in wheat by directly regulating TaABI5
inferred← citeshttps://doi.org/10.1111/nph.17074openalex-snapshot
The molecular–physiological functions of mineral macronutrients and their consequences for deficiency symptoms in plants
inferred← citeshttps://doi.org/10.1111/nph.17839openalex-snapshot
Chloroplast development in green plant tissues: the interplay between light, hormone, and transcriptional regulation
inferred← citeshttps://doi.org/10.1111/nph.70887openalex-snapshot
B‐ GATA factors are required for nitrogen‐responsive growth in Physcomitrium patens and Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/pbi.13660openalex-snapshot
Engineering chloroplast development in rice through cell‐specific control of endogenous genetic circuits
inferred← citeshttps://doi.org/10.1111/pce.12147openalex-snapshot
Replication protein A subunit 3 and the iron efficiency response in soybean
inferred← citeshttps://doi.org/10.1111/ppl.70315openalex-snapshot
Crosstalk Between Auxin Signalling and Growth Regulating Factor 5: Implications for Chloroplast Division and Leaf Development
inferred← citeshttps://doi.org/10.1111/tpj.12753openalex-snapshot
Accumulation of the NON ‐ YELLOW COLORING 1 protein of the chlorophyll cycle requires chlorophyll b in A rabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/tpj.16425openalex-snapshot
Multi‐environment association study highlights candidate genes for robust agronomic quantitative trait loci in a novel worldwide Capsicum core collection
inferred← citeshttps://doi.org/10.1146/annurev-arplant-072221-092913openalex-snapshot
Plant GATA Factors: Their Biology, Phylogeny, and Phylogenomics
inferred← citeshttps://doi.org/10.1146/annurev-genet-102209-163450openalex-snapshot
Brassinosteroid Signaling Network and Regulation of Photomorphogenesis
inferred← citeshttps://doi.org/10.1186/s12864-021-08147-3openalex-snapshot
Interaction between Rag genes results in a unique synergistic transcriptional response that enhances soybean resistance to soybean aphids
inferred← citeshttps://doi.org/10.1186/s12864-024-10794-1openalex-snapshot
Identification of quantitative trait loci for lodging and related agronomic traits in soybean (Glycine max [L.] Merr.)
inferred← citeshttps://doi.org/10.1186/s12870-018-1507-yopenalex-snapshot
Integrated physiologic, genomic and transcriptomic strategies involving the adaptation of allotetraploid rapeseed to nitrogen limitation
inferred← citeshttps://doi.org/10.1186/s12870-020-02752-2openalex-snapshot
Genome-wide identification, phylogenetic and expression pattern analysis of GATA family genes in Brassica napus
inferred← citeshttps://doi.org/10.1186/s12870-025-06313-3openalex-snapshot
The CGA1-SNAT regulatory module potentially contributes to cytokinin-mediated melatonin biosynthesis and drought tolerance in wheat
inferred← citeshttps://doi.org/10.1186/s12870-025-07540-4openalex-snapshot
Genome-wide association mapping reveals genetic loci underlying phenotypic variation in early root vigour improvement induced by osmopriming in Brassica napus L
inferred← citeshttps://doi.org/10.1186/s12870-025-07920-wopenalex-snapshot
Genome-wide identification of the YABBY gene family and functional characterization of TaYABBY4A in wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.1242/dev.081547openalex-snapshot
Stable establishment of cotyledon identity during embryogenesis in Arabidopsis by ANGUSTIFOLIA3 and HANABA TARANU
inferred← citeshttps://doi.org/10.1371/journal.pone.0073092openalex-snapshot
The Reduced Plastid-Encoded Polymerase-Dependent Plastid Gene Expression Leads to the Delayed Greening of the Arabidopsis fln2 Mutant
inferred← citeshttps://doi.org/10.1371/journal.pone.0073291openalex-snapshot
Analysis of Essential Arabidopsis Nuclear Genes Encoding Plastid-Targeted Proteins
inferred← citeshttps://doi.org/10.1371/journal.pone.0125174openalex-snapshot
Genome-Wide Survey of the Soybean GATA Transcription Factor Gene Family and Expression Analysis under Low Nitrogen Stress
inferred← citeshttps://doi.org/10.1371/journal.pone.0208648openalex-snapshot
Genome-scale characterization of the vacuole nitrate transporter Chloride Channel (CLC) genes and their transcriptional responses to diverse nutrient stresses in allotetraploid rapeseed
inferred← citeshttps://doi.org/10.1371/journal.pone.0227303openalex-snapshot
Transcriptome analysis of Actinidia chinensis in response to Botryosphaeria dothidea infection
inferred← citeshttps://doi.org/10.1371/journal.pone.0241627openalex-snapshot
NMR spectroscopy analysis reveals differential metabolic responses in arabidopsis roots and leaves treated with a cytokinesis inhibitor
inferred← citeshttps://doi.org/10.1371/journal.pone.0252181openalex-snapshot
Genome-wide comparative analyses of GATA transcription factors among 19 Arabidopsis ecotype genomes: Intraspecific characteristics of GATA transcription factors
inferred← citeshttps://doi.org/10.1371/journal.pone.0287943openalex-snapshot
Oligosaccharide production and signaling correlate with delayed flowering in an Arabidopsis genotype grown and selected in high [CO2]
inferred← citeshttps://doi.org/10.1533/9781908818478.49openalex-snapshot
Metabolite profiling for plant research
inferred← citeshttps://doi.org/10.17474/artvinofd.1254754openalex-snapshot
Effects of salt water intrusion on biochemical components of Alder and Ash tree fresh leaves in Karacabey Coastal Forested Wetland
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1963114/v1openalex-snapshot
Genome-wide identification and expression analysis of GATA gene family in wheat
inferred← citeshttps://doi.org/10.2298/abs150608087dopenalex-snapshot
Differential regulation of GS-GOGAT gene expression by plant growth regulators in Arabidopsis seedlings
inferred← citeshttps://doi.org/10.32615/ps.2022.034openalex-snapshot
The effects of nitrogen application on the growth, photosynthesis, and antioxidant activity of Amaranthus viridis
inferred← citeshttps://doi.org/10.33540/894openalex-snapshot
Deciphering acclimation strategies to combined abiotic stresses in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3389/fenvs.2022.1020308openalex-snapshot
Integrated transcriptomic and metabolomic analyses of pak choi [Brassica pekinensis (Lour.) Rupr] response to combined stress of acid rain and cadmium-containing atmospheric fine particulate matter
inferred← citeshttps://doi.org/10.3389/fgene.2023.1012460openalex-snapshot
Mapping quantitative trait loci and predicting candidate genes for Striga resistance in maize using resistance donor line derived from Zea diploperennis
inferred← citeshttps://doi.org/10.3389/fphgy.2026.1886654openalex-snapshot
The role of light in shaping plant growth: mechanisms of photomorphogenesis and hormonal integration during seedling development
inferred← citeshttps://doi.org/10.3389/fpls.2014.00272openalex-snapshot
Transcriptional regulation of thylakoid galactolipid biosynthesis coordinated with chlorophyll biosynthesis during the development of chloroplasts in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2015.00090openalex-snapshot
B-GATA transcription factors – insights into their structure, regulation, and role in plant development
inferred← citeshttps://doi.org/10.3389/fpls.2016.01281openalex-snapshot
Transcriptome Analysis of Pepper (Capsicum annuum) Revealed a Role of 24-Epibrassinolide in Response to Chilling
inferred← citeshttps://doi.org/10.3389/fpls.2016.01811openalex-snapshot
Transcriptional Regulation of Tetrapyrrole Biosynthesis in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3389/fpls.2017.01433openalex-snapshot
Interplay between Light and Plant Hormones in the Control of Arabidopsis Seedling Chlorophyll Biosynthesis
inferred← citeshttps://doi.org/10.3389/fpls.2020.604489openalex-snapshot
Cytokinin Signaling Downstream of the His-Asp Phosphorelay Network: Cytokinin-Regulated Genes and Their Functions
inferred← citeshttps://doi.org/10.3389/fpls.2024.1346523openalex-snapshot
Dual RNA-seq of maize and H. seropedicae ZAE94 association, in different doses of nitrate, reveals novel insights into Plant-PGPB-environment relationship
inferred← citeshttps://doi.org/10.3389/fpls.2025.1539445openalex-snapshot
Integrative transcriptomic-physiological analysis deciphers nitrogen-mediated carbon reallocation balancing growth and flavonoid metabolism in Epimedium pubescens
inferred← citeshttps://doi.org/10.3389/fpls.2025.1642681openalex-snapshot
Transcriptomic and metabolomic analysis of yellow leaf mutant variation in Taxus cuspidata
inferred← citeshttps://doi.org/10.3389/fpls.2025.1661591openalex-snapshot
Genome-wide characterization and expression analysis of the GATA transcription factor family in response to salt and drought stress in barley (Hordeum vulgare L.)
inferred← citeshttps://doi.org/10.3389/fpls.2026.1901011openalex-snapshot
Cytokinin availability and chloroplast functional lifetime in senescing leaves
inferred← citeshttps://doi.org/10.3390/agronomy12040826openalex-snapshot
Effects of Cultivar, Nitrogen Rate and Biostimulant Application on the Chemical Composition of Perennial Ryegrass (Lolium perenne L.) Biomass
inferred← citeshttps://doi.org/10.3390/agronomy13071921openalex-snapshot
Identification, Characterization, and Expression Profiling of Maize GATA Gene Family in Response to Abiotic and Biotic Stresses
inferred← citeshttps://doi.org/10.3390/agronomy13092250openalex-snapshot
The Effect of Far-Red Light and Nutrient Level on the Growth and Secondary Metabolites of the In Vitro Culture of Prunella vulgaris
inferred← citeshttps://doi.org/10.3390/biom13121771openalex-snapshot
The Role of Glutamine Synthetase (GS) and Glutamate Synthase (GOGAT) in the Improvement of Nitrogen Use Efficiency in Cereals
inferred← citeshttps://doi.org/10.3390/genes13050826openalex-snapshot
Genome-Wide Association Analysis Reveals Genetic Architecture and Candidate Genes Associated with Grain Yield and Other Traits under Low Soil Nitrogen in Early-Maturing White Quality Protein Maize Inbred Lines
inferred← citeshttps://doi.org/10.3390/horticulturae10030282openalex-snapshot
Genome-Wide Prediction and Expression Characterization of the GATA Gene Family under Nitrogen and Phosphate Deficiency in Panax ginseng
inferred← citeshttps://doi.org/10.3390/horticulturae12080927openalex-snapshot
Genome-Wide Identification and Stress Response Analysis of the GATA Gene Family in Eggplant (Solanum melongena L.)
inferred← citeshttps://doi.org/10.3390/ijms19030782openalex-snapshot
Transcriptome Analysis of a Premature Leaf Senescence Mutant of Common Wheat (Triticum aestivum L.)
inferred← citeshttps://doi.org/10.3390/ijms20071708openalex-snapshot
Transcriptional Profile Corroborates that bml Mutant Plays likely Role in Premature Leaf Senescence of Rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.3390/ijms23095251openalex-snapshot
Genome-Wide Identification of the Eucalyptus urophylla GATA Gene Family and Its Diverse Roles in Chlorophyll Biosynthesis
inferred← citeshttps://doi.org/10.3390/ijms24010027openalex-snapshot
Genome-Wide Analysis of Wheat GATA Transcription Factor Genes Reveals Their Molecular Evolutionary Characteristics and Involvement in Salt and Drought Tolerance
inferred← citeshttps://doi.org/10.3390/ijms241210342openalex-snapshot
Genome-Wide Identification of GATA Family Genes in Phoebe bournei and Their Transcriptional Analysis under Abiotic Stresses
inferred← citeshttps://doi.org/10.3390/ijms242417624openalex-snapshot
The Genetic Dissection of Nitrogen Use-Related Traits in Flax (Linum usitatissimum L.) at the Seedling Stage through the Integration of Multi-Locus GWAS, RNA-seq and Genomic Selection
inferred← citeshttps://doi.org/10.3390/ijms252312961openalex-snapshot
Ubiquitin Ligase U-Box51 Positively Regulates Drought Stress in Potato (Solanum tuberosum L.)
inferred← citeshttps://doi.org/10.3390/life14040470openalex-snapshot
The Putative GATA Transcription Factor SbGATA22 as a Novel Regulator of Dhurrin Biosynthesis
inferred← citeshttps://doi.org/10.3390/life16101600openalex-snapshot
Physiological and Transcriptomic Analyses Reveal Divergent Responses of Vegetative Growth and Inflorescence Development to Temperature in Chrysanthemum × morifolium
inferred← citeshttps://doi.org/10.3390/plants10081626openalex-snapshot
Genome-Wide Identification, Phylogenetic and Expression Pattern Analysis of GATA Family Genes in Cucumber (Cucumis sativus L.)
inferred← citeshttps://doi.org/10.3390/plants11060743openalex-snapshot
5-Aminolevulinic Acid and 24-Epibrassinolide Improve the Drought Stress Resilience and Productivity of Banana Plants
inferred← citeshttps://doi.org/10.3390/plants13192759openalex-snapshot
Glutamine Synthetase and Glutamate Synthase Family Perform Diverse Physiological Functions in Exogenous Hormones and Abiotic Stress Responses in Pyrus betulifolia Bunge (P.be)
inferred← citeshttps://doi.org/10.3390/plants9081036openalex-snapshot
A GATA Transcription Factor from Soybean (Glycine max) Regulates Chlorophyll Biosynthesis and Suppresses Growth in the Transgenic Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/pr13072084openalex-snapshot
Glutamate and Its Role in the Metabolism of Plants and Animals
inferred← citeshttps://doi.org/10.4161/15592324.2014.992264openalex-snapshot
Characterization ofArabidopsis thalianaGCN2 kinase roles in seed germination and plant development
inferred← citeshttps://doi.org/10.6084/m9.figshare.17163456openalex-snapshot
Additional file 3 of Interaction between Rag genes results in a unique synergistic transcriptional response that enhances soybean resistance to soybean aphids
inferred← citeshttps://doi.org/10.70675/78900108z4663z41cdzbf26zafd5dc5f55cdopenalex-snapshot
Opening the black box of the interaction between soybean and microbial community under heat and water stresses
inferred← citeshttps://doi.org/10.70675/d9985fa0z7eddz401dzbecfz50d805b64d14openalex-snapshot
Molecular mechanisms of plant-xenobiotic interactions : involvement of stress, development and hormone signaling regulations
inferred← citeshttps://doi.org/10.70675/ea895fa4z89fbz4d1cz988ez37dd2b534c60openalex-snapshot
Effects of the Xanthomonas campestris pv campestris type III effectors on Arabidopsis physiology
inferred← citeshttps://doi.org/10.7287/peerj.12343v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Genome-wide association study and population structure analysis of seed-bound amino acids and total protein in watermelon (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.12343v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Genome-wide association study and population structure analysis of seed-bound amino acids and total protein in watermelon (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.12343v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Genome-wide association study and population structure analysis of seed-bound amino acids and total protein in watermelon (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.12343openalex-snapshot
Genome-wide association study and population structure analysis of seed-bound amino acids and total protein in watermelon
inferred← citeshttps://doi.org/10.9734/ajea/2015/13398openalex-snapshot
Exogenous Cytokinin Promotes Epipremnum aureum L. Growth through Enhanced Dry Weight Assimilation rather than through Changes in Partitioning
inferred← citeshttps://doi.org/10.9787/kjbs.2020.52.4.281openalex-snapshot
Recent Advances in Genetic Regulation of Chlorophyll Metabolism in Plants
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.