On the public citation graph
Influence of cultivation practices on the metabolism of cytokinin and its correlation in rice production
0 signed · 192 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.
1 of the 173 references listed on this page is in the Retraction Watch database as retracted (export 2026-11-04): 10.3389/fgene.2022.943025 (notice 2024-03-18).
Dataset join, best-effort; this page does not check the publisher record. Retraction Watch data via Crossref Labs, used with credit; OpenCitations Index (CC0) and Meta (CC BY 4.0); dataset doi:10.7910/DVN/WT8VOA (CC BY 4.0).
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known work and none has been retracted — and get a dated CiteStamped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/pbc.24713openalex-snapshot
Long‐term results of the combination of the N7 induction chemotherapy and the busulfan‐melphalan high dose chemotherapy
inferredcites →https://doi.org/10.1007/978-3-642-74545-4_33openalex-snapshot
Cytokinin Oxidase and the Degradative Metabolism of Cytokinins
inferredcites →https://doi.org/10.1007/s00299-019-02500-3openalex-snapshot
Cytokinin oxidase PpCKX1 plays regulatory roles in development and enhances dehydration and salt tolerance in Physcomitrella patens
inferredcites →https://doi.org/10.1007/s00425-021-03810-1openalex-snapshot
On the biological activity of cytokinin free bases and their ribosides
inferredcites →https://doi.org/10.1007/s11103-008-9391-8openalex-snapshot
Rice DREB1B promoter shows distinct stress-specific responses, and the overexpression of cDNA in tobacco confers improved abiotic and biotic stress tolerance
inferredcites →https://doi.org/10.1007/s11103-013-0013-8openalex-snapshot
Plant senescence and crop productivity
inferredcites →https://doi.org/10.1007/s11103-016-0463-xopenalex-snapshot
Hormones and nitrate: a two-way connection
inferredcites →https://doi.org/10.1007/s11627-000-0021-7openalex-snapshot
Cytokinins: Biosynthesis metabolism and perception
inferredcites →https://doi.org/10.1007/s11738-021-03235-zopenalex-snapshot
High-affinity ammonium transport by Arabidopsis thaliana AMT1;4
inferredcites →https://doi.org/10.1007/s13593-016-0361-2openalex-snapshot
Lower global warming potential and higher yield of wet direct-seeded rice in Central China
inferredcites →https://doi.org/10.1016/bs.ircmb.2016.01.001openalex-snapshot
Cytokinin Synthesis, Signaling, and Function—Advances and New Insights
inferredcites →https://doi.org/10.1016/j.cub.2011.04.049openalex-snapshot
Phloem-Transported Cytokinin Regulates Polar Auxin Transport and Maintains Vascular Pattern in the Root Meristem
inferredcites →https://doi.org/10.1016/j.devcel.2013.10.004openalex-snapshot
Side-Chain Modification of Cytokinins Controls Shoot Growth in Arabidopsis
inferredcites →https://doi.org/10.1016/j.fcr.2017.02.021openalex-snapshot
Canopy light and nitrogen distributions are related to grain yield and nitrogen use efficiency in rice
inferredcites →https://doi.org/10.1016/j.fcr.2019.107635openalex-snapshot
High nitrogen input causes poor grain filling of spikelets at the panicle base of super hybrid rice
inferredcites →https://doi.org/10.1016/j.fcr.2021.108257openalex-snapshot
Roles of canopy architecture and nitrogen distribution in the better performance of an aerobic than a lowland rice cultivar under water deficit
inferredcites →https://doi.org/10.1016/j.jgg.2016.11.001openalex-snapshot
The OsAMT1.1 gene functions in ammonium uptake and ammonium–potassium homeostasis over low and high ammonium concentration ranges
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.pbi.2009.07.002openalex-snapshot
Cytokinin action in plant development
inferredcites →https://doi.org/10.1016/j.pbi.2017.05.010openalex-snapshot
Plant nitrogen nutrition: sensing and signaling
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.2011.02.004openalex-snapshot
A framework integrating plant growth with hormones and nutrients
inferredcites →https://doi.org/10.1016/j.tplants.2012.04.006openalex-snapshot
Uptake, allocation and signaling of nitrate
inferredcites →https://doi.org/10.1016/s0168-9452(00)00261-2openalex-snapshot
Cloning and in vitro expression of the cDNA encoding a putative nucleoside transporter from Arabidopsis thaliana
inferredcites →https://doi.org/10.1023/a:1006356125418openalex-snapshot
Grain filling pattern and cytokinin content in the grains and roots of rice plants
inferredcites →https://doi.org/10.1023/a:1022808711970openalex-snapshot
Dynamics of expression and distribution of cytokinin oxidase/dehydrogenase in developing maize kernels
inferredcites →https://doi.org/10.1038/35059117openalex-snapshot
Identification of CRE1 as a cytokinin receptor from Arabidopsis
inferredcites →https://doi.org/10.1038/ncomms4274openalex-snapshot
Arabidopsis ABCG14 protein controls the acropetal translocation of root-synthesized cytokinins
inferredcites →https://doi.org/10.1038/ncomms5983openalex-snapshot
Shoot-derived cytokinins systemically regulate root nodulation
inferredcites →https://doi.org/10.1038/nplants.2017.112openalex-snapshot
Systemic transport of trans-zeatin and its precursor have differing roles in Arabidopsis shoots
inferredcites →https://doi.org/10.1038/s41467-020-14440-8openalex-snapshot
Shoot-to-root mobile CEPD-like 2 integrates shoot nitrogen status to systemically regulate nitrate uptake in Arabidopsis
inferredcites →https://doi.org/10.1038/s41598-017-02338-3openalex-snapshot
The rice production practices of high yield and high nitrogen use efficiency in Jiangsu, China
inferredcites →https://doi.org/10.1038/s41598-017-10026-5openalex-snapshot
Shade Inhibits Leaf Size by Controlling Cell Proliferation and Enlargement in Soybean
inferredcites →https://doi.org/10.1038/s41598-017-18766-0openalex-snapshot
Canopy nitrogen distribution is optimized to prevent photoinhibition throughout the canopy during sun flecks
inferredcites →https://doi.org/10.1038/s41598-018-29398-3openalex-snapshot
Interleukin-27 controls basal pain threshold in physiological and pathological conditions
inferredcites →https://doi.org/10.1038/s41598-020-80223-2openalex-snapshot
Characterization of CHARK, an unusual cytokinin receptor of rice
inferredcites →https://doi.org/10.1038/s41598-021-04585-xopenalex-snapshot
Effects of water saving and nitrogen reduction on the yield, quality, water and nitrogen use efficiency of Isatis indigotica in Hexi Oasis
inferredcites →https://doi.org/10.1038/s41598-021-96747-0openalex-snapshot
Effects of water and nitrogen coupling on the photosynthetic characteristics, yield, and quality of Isatis indigotica
inferredcites →https://doi.org/10.1038/srep07962openalex-snapshot
AtNPF5.5, a nitrate transporter affecting nitrogen accumulation in Arabidopsis embryo
inferredcites →https://doi.org/10.1042/bj20040389openalex-snapshot
Characterization of three novel members of the Arabidopsis thaliana equilibrative nucleoside transporter (ENT) family
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00408.xopenalex-snapshot
Cytokinin oxidase from Zea mays: purification, cDNA cloning and expression in moss protoplasts
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01700.xopenalex-snapshot
Transport of cytokinins mediated by purine transporters of the PUP family expressed in phloem, hydathodes, and pollen of Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01945.xopenalex-snapshot
Expression of cytokinin biosynthetic isopentenyltransferase genes in Arabidopsis : tissue specificity and regulation by auxin, cytokinin, and nitrate
inferredcites →https://doi.org/10.1071/fp02223openalex-snapshot
Root-derived trans -zeatin riboside and abscisic acid in drought-stressed and rewatered sunflower plants: interaction in the control of leaf diffusive resistance?
inferredcites →https://doi.org/10.1073/pnas.0505150103openalex-snapshot
Cytokinin-mediated control of leaf longevity by AHK3 through phosphorylation of ARR2 in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0603522103openalex-snapshot
Roles of Arabidopsis ATP/ADP isopentenyltransferases and tRNA isopentenyltransferases in cytokinin biosynthesis
inferredcites →https://doi.org/10.1073/pnas.0805619105openalex-snapshot
Cytokinins are central regulators of cambial activity
inferredcites →https://doi.org/10.1073/pnas.101128798openalex-snapshot
A maize cytokinin gene encoding an O -glucosyltransferase specific to cis -zeatin
inferredcites →https://doi.org/10.1073/pnas.1321519111openalex-snapshot
Arabidopsis ABCG14 is essential for the root-to-shoot translocation of cytokinin
inferredcites →https://doi.org/10.1073/pnas.1702275114openalex-snapshot
Neighbor detection at the leaf tip adaptively regulates upward leaf movement through spatial auxin dynamics
inferredcites →https://doi.org/10.1073/pnas.171304098openalex-snapshot
Regulation of plant growth by cytokinin
inferredcites →https://doi.org/10.1074/jbc.m304768200openalex-snapshot
Equilibrative Nucleoside Transporters of Arabidopsis thaliana
inferredcites →https://doi.org/10.1074/mcp.m114.038075openalex-snapshot
O-Glycosylation of the N-terminal Region of the Serine-rich Adhesin Srr1 of Streptococcus agalactiae Explored by Mass Spectrometry
inferredcites →https://doi.org/10.1074/mcp.m600250-mcp200openalex-snapshot
A Proteomics Dissection of Arabidopsis thaliana Vacuoles Isolated from Cell Culture
inferredcites →https://doi.org/10.1079/bjn20041260openalex-snapshot
Hypoglycaemic and anorexigenic activities of an α-amylase inhibitor from white kidney beans (Phaseolus vulgaris) in Wistar rats
inferredcites →https://doi.org/10.1080/17429145.2022.2037763openalex-snapshot
Signal molecules controlling nitrate uptake by roots
inferredcites →https://doi.org/10.1093/aob/mcf198openalex-snapshot
Correlation of Cytokinin Levels in the Endosperms and Roots with Cell Number and Cell Division Activity during Endosperm Development in Rice
inferredcites →https://doi.org/10.1093/aob/mcg189openalex-snapshot
Maclean, J.L., Dawe, D.C., Hardy, B. and Hettel, G.P. (eds) Rice almanac. 3rd edn
inferredcites →https://doi.org/10.1093/aob/mci050openalex-snapshot
Leaf Canopy as a Dynamic System: Ecophysiology and Optimality in Leaf Turnover
inferredcites →https://doi.org/10.1093/aob/mcq028openalex-snapshot
Nitrogen uptake, assimilation and remobilization in plants: challenges for sustainable and productive agriculture
inferredcites →https://doi.org/10.1093/aob/mcw099openalex-snapshot
A meta-analysis of leaf nitrogen distribution within plant canopies
inferredcites →https://doi.org/10.1093/glycob/cwaa042openalex-snapshot
Deducing the N- and O-glycosylation profile of the spike protein of novel coronavirus SARS-CoV-2
inferredcites →https://doi.org/10.1093/jxb/eraa033openalex-snapshot
Signaling pathways underlying nitrogen-dependent changes in root system architecture: from model to crop species
inferredcites →https://doi.org/10.1093/jxb/erg276openalex-snapshot
Cytokinin levels in leaves, leaf exudate and shoot apical meristem of Arabidopsis thaliana during floral transition
inferredcites →https://doi.org/10.1093/jxb/eri107openalex-snapshot
Root-derived cytokinins as long-distance signals for NO3--induced stimulation of leaf growth
inferredcites →https://doi.org/10.1093/jxb/erl179openalex-snapshot
Biochemical characteristics and ligand-binding properties of Arabidopsis cytokinin receptor AHK3 compared to CRE1/AHK4 as revealed by a direct binding assay
inferredcites →https://doi.org/10.1093/jxb/erm157openalex-snapshot
Regulation of cytokinin biosynthesis, compartmentalization and translocation
inferredcites →https://doi.org/10.1093/jxb/ern364openalex-snapshot
Redundant roles of photoreceptors and cytokinins in regulating photosynthetic acclimation to canopy density
inferredcites →https://doi.org/10.1093/jxb/erp348openalex-snapshot
Grain-filling problem in ‘super’ rice
inferredcites →https://doi.org/10.1093/jxb/erq409openalex-snapshot
From the soil to the seeds: the long journey of nitrate in plants
inferredcites →https://doi.org/10.1093/jxb/erq410openalex-snapshot
Hormonal control of nitrogen acquisition: roles of auxin, abscisic acid, and cytokinin
inferredcites →https://doi.org/10.1093/jxb/err263openalex-snapshot
Post-anthesis alternate wetting and moderate soil drying enhances activities of key enzymes in sucrose-to-starch conversion in inferior spikelets of rice
inferredcites →https://doi.org/10.1093/jxb/eru001openalex-snapshot
Nitrate transport and signalling in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/eru522openalex-snapshot
Plant membrane assays with cytokinin receptors underpin the unique role of free cytokinin bases as biologically active ligands
inferredcites →https://doi.org/10.1093/jxb/erv461openalex-snapshot
Cytokinin: a key driver of seed yield
inferredcites →https://doi.org/10.1093/jxb/erv575openalex-snapshot
Cytokinin delays dark-induced senescence in rice by maintaining the chlorophyll cycle and photosynthetic complexes
inferredcites →https://doi.org/10.1093/jxb/erx013openalex-snapshot
How do plants sense their nitrogen status?
inferredcites →https://doi.org/10.1093/jxb/erx086openalex-snapshot
Ammonium as a signal for physiological and morphological responses in plants
inferredcites →https://doi.org/10.1093/jxb/erx426openalex-snapshot
Antibody-mediated modulation of cytokinins in tobacco: organ-specific changes in cytokinin homeostasis
inferredcites →https://doi.org/10.1093/pcp/pce112openalex-snapshot
Identification of Plant Cytokinin Biosynthetic Enzymes as Dimethylallyl Diphosphate:ATP/ADP Isopentenyltransferases
inferredcites →https://doi.org/10.1093/pcp/pch119openalex-snapshot
AtIPT3 is a Key Determinant of Nitrate-Dependent Cytokinin Biosynthesis in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pct127openalex-snapshot
Nitrogen-Dependent Regulation of De Novo Cytokinin Biosynthesis in Rice: The Role of Glutamine Metabolism as an Additional Signal
inferredcites →https://doi.org/10.1104/pp.011494openalex-snapshot
The Arabidopsis AtIPT8/PGA22 Gene Encodes an Isopentenyl Transferase That Is Involved in De Novo Cytokinin Biosynthesis
inferredcites →https://doi.org/10.1104/pp.017210openalex-snapshot
O-Glucosylation of cis-Zeatin in Maize. Characterization of Genes, Enzymes, and Endogenous Cytokinins
inferredcites →https://doi.org/10.1104/pp.105.060137openalex-snapshot
Functional Characterization and Expression Analysis of a Gene, OsENT2, Encoding an Equilibrative Nucleoside Transporter in Rice Suggest a Function in Cytokinin Transport
inferredcites →https://doi.org/10.1104/pp.106.091223openalex-snapshot
Dissection of the AtNRT2.1 : AtNRT2.2 Inducible High-Affinity Nitrate Transporter Gene Cluster
inferredcites →https://doi.org/10.1104/pp.106.094631openalex-snapshot
Cytokinin Import Rate as a Signal for Photosynthetic Acclimation to Canopy Light Gradients
inferredcites →https://doi.org/10.1104/pp.109.139188openalex-snapshot
Unraveling the Evolution of Cytokinin Signaling
inferredcites →https://doi.org/10.1104/pp.112.202853openalex-snapshot
Proteome Analysis in Arabidopsis Reveals Shoot- and Root-Specific Targets of Cytokinin Action and Differential Regulation of Hormonal Homeostasis
inferredcites →https://doi.org/10.1104/pp.113.224667openalex-snapshot
A Novel Protective Function for Cytokinin in the Light Stress Response Is Mediated by the ARABIDOPSIS HISTIDINE KINASE2 and ARABIDOPSIS HISTIDINE KINASE3 Receptors
inferredcites →https://doi.org/10.1104/pp.113.227702openalex-snapshot
Stress-Induced Cytokinin Synthesis Increases Drought Tolerance through the Coordinated Regulation of Carbon and Nitrogen Assimilation in Rice
inferredcites →https://doi.org/10.1104/pp.113.230599openalex-snapshot
Glucose Elevates NITRATE TRANSPORTER2.1 Protein Levels and Nitrate Transport Activity Independently of Its HEXOKINASE1-Mediated Stimulation of NITRATE TRANSPORTER2.1 Expression
inferredcites →https://doi.org/10.1105/tpc.014928openalex-snapshot
Cytokinin-Deficient Transgenic Arabidopsis Plants Show Multiple Developmental Alterations Indicating Opposite Functions of Cytokinins in the Regulation of Shoot and Root Meristem Activity
inferredcites →https://doi.org/10.1105/tpc.107.052662openalex-snapshot
Cytokinin Regulates Type-A Arabidopsis Response Regulator Activity and Protein Stability via Two-Component Phosphorelay
inferredcites →https://doi.org/10.1105/tpc.109.067603openalex-snapshot
The Arabidopsis Nitrate Transporter NRT1.7, Expressed in Phloem, Is Responsible for Source-to-Sink Remobilization of Nitrate
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.111.083618openalex-snapshot
Arabidopsis Nitrate Transporter NRT1.9 Is Important in Phloem Nitrate Transport
inferredcites →https://doi.org/10.1105/tpc.18.00011openalex-snapshot
Responses to Systemic Nitrogen Signaling in Arabidopsis Roots Involve trans -Zeatin in Shoots
inferredcites →https://doi.org/10.1105/tpc.19.00748openalex-snapshot
Nitrate in 2020: Thirty Years from Transport to Signaling Networks
inferredcites →https://doi.org/10.1111/j.1365-3040.2011.02335.xopenalex-snapshot
Rice OsNAR2.1 interacts with OsNRT2.1, OsNRT2.2 and OsNRT2.3a nitrate transporters to provide uptake over high and low concentration ranges
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03502.xopenalex-snapshot
Cytokinins negatively regulate the root iron uptake machinery in Arabidopsis through a growth‐dependent pathway
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04584.xopenalex-snapshot
The specificity of cytokinin signalling in Arabidopsis thaliana is mediated by differing ligand affinities and expression profiles of the receptors
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04795.xopenalex-snapshot
Arabidopsis lonely guy (LOG) multiple mutants reveal a central role of the LOG‐dependent pathway in cytokinin activation
inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04094.xopenalex-snapshot
Nitrate transport capacity of the Arabidopsis thaliana NRT2 family members and their interactions with AtNAR2.1
inferredcites →https://doi.org/10.1111/j.1744-7909.2005.00104.xopenalex-snapshot
Arabidopsis SOI33/AtENT8 Gene Encodes a Putative Equilibrative Nucleoside Transporter That Is Involved in Cytokinin Transport In Planta
inferredcites →https://doi.org/10.1111/jipb.12101openalex-snapshot
Characterization of a Purine Permease Family Gene Os PUP 7 Involved in Growth and Development Control in Rice
inferredcites →https://doi.org/10.1111/jipb.12727openalex-snapshot
Big Grain3, encoding a purine permease, regulates grain size via modulating cytokinin transport in rice
inferredcites →https://doi.org/10.1111/pbi.13305openalex-snapshot
Cytokinin dehydrogenase: a genetic target for yield improvement in wheat
inferredcites →https://doi.org/10.1111/pbi.13603openalex-snapshot
Isopentenyltransferases as master regulators of crop performance: their function, manipulation, and genetic potential for stress adaptation and yield improvement
inferredcites →https://doi.org/10.1111/pce.12291openalex-snapshot
Optimal nitrogen distribution within a leaf canopy under direct and diffuse light
inferredcites →https://doi.org/10.1111/plb.13044openalex-snapshot
Orchid seed sensitivity to nitrate reflects habitat preferences and soil nitrate content
inferredcites →https://doi.org/10.1126/science.1113373openalex-snapshot
Cytokinin Oxidase Regulates Rice Grain Production
inferredcites →https://doi.org/10.1126/scisignal.aaa4829openalex-snapshot
Nitrate sensing and uptake in Arabidopsis are enhanced by ABI2, a phosphatase inactivated by the stress hormone abscisic acid
inferredcites →https://doi.org/10.1134/s0006297912120024openalex-snapshot
Cytokinin oxidase is key enzyme of cytokinin degradation
inferredcites →https://doi.org/10.1134/s1021443715060151openalex-snapshot
Effects of nitrate and ammonium on growth of Arabidopsis thaliana plants transformed with the ARR5::GUS construct and a role for cytokinins in suppression of disturbances induced by the presence of ammonium
inferredcites →https://doi.org/10.1146/annurev-arplant-042811-105532openalex-snapshot
Plant Nitrogen Assimilation and Use Efficiency
inferredcites →https://doi.org/10.1146/annurev-arplant-042817-040056openalex-snapshot
Nitrate Transport, Signaling, and Use Efficiency
inferredcites →https://doi.org/10.1146/annurev.arplant.52.1.89openalex-snapshot
C YTOKININ M ETABOLISM AND A CTION
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105231openalex-snapshot
CYTOKININS: Activity, Biosynthesis, and Translocation
inferredcites →https://doi.org/10.1186/s12284-019-0333-7openalex-snapshot
The Initiation of Inferior Grain Filling is Affected by Sugar Translocation Efficiency in Large Panicle Rice
inferredcites →https://doi.org/10.1186/s12870-019-1657-6openalex-snapshot
Root enhancement in cytokinin-deficient oilseed rape causes leaf mineral enrichment, increases the chlorophyll concentration under nutrient limitation and enhances the phytoremediation capacity
inferredcites →https://doi.org/10.1186/s12915-015-0214-5openalex-snapshot
Q&A: How do plants respond to cytokinins and what is their importance?
inferredcites →https://doi.org/10.1186/s43170-022-00117-3openalex-snapshot
Optimization of photosynthesis for sustainable crop production
inferredcites →https://doi.org/10.1186/s43897-021-00006-9openalex-snapshot
Leaf senescence: progression, regulation, and application
inferredcites →https://doi.org/10.1210/jc.2015-1991openalex-snapshot
Reversible Albumin-Binding GH Possesses a Potential Once-Weekly Treatment Profile in Adult Growth Hormone Deficiency
inferredcites →https://doi.org/10.1242/dev.149344openalex-snapshot
Cytokinin signaling in plant development
inferredcites →https://doi.org/10.1371/journal.pone.0008236openalex-snapshot
AtSOFL1 and AtSOFL2 Act Redundantly as Positive Modulators of the Endogenous Content of Specific Cytokinins in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pone.0072126openalex-snapshot
The Nitrate Transporter (NRT) Gene Family in Poplar
inferredcites →https://doi.org/10.1371/journal.pone.0196086openalex-snapshot
Fluorescent reporter lines for auxin and cytokinin signalling in barley (Hordeum vulgare)
inferredcites →https://doi.org/10.1371/journal.pone.0233055openalex-snapshot
Response of cytokinins and nitrogen metabolism in the fronds of Pteris sp. under arsenic stress
inferredcites →https://doi.org/10.1371/journal.pone.0248796openalex-snapshot
Evidence that synergism between potassium and nitrate enhances the alleviation of ammonium toxicity in rice seedling roots
inferredcites →https://doi.org/10.3389/fgene.2022.900324openalex-snapshot
Chickpea Biofortification for Cytokinin Dehydrogenase via Genome Editing to Enhance Abiotic-Biotic Stress Tolerance and Food Security
inferredcites →https://doi.org/10.3389/fgene.2022.943025openalex-snapshot
RETRACTED: Cytokinin and abiotic stress tolerance -What has been accomplished and the way forward?
inferredcites →https://doi.org/10.3389/fmicb.2022.1035586openalex-snapshot
Antibacterial activity of bioactive compounds extracted from red kidney bean (Phaseolus vulgaris L.) seeds against multidrug-resistant Enterobacterales
inferredcites →https://doi.org/10.3389/fpls.2013.00334openalex-snapshot
Photosynthetic acclimation responses of maize seedlings grown under artificial laboratory light gradients mimicking natural canopy conditions
inferredcites →https://doi.org/10.3389/fpls.2014.00443openalex-snapshot
Nucleobase and nucleoside transport and integration into plant metabolism
inferredcites →https://doi.org/10.3389/fpls.2015.01060openalex-snapshot
Behavior of Leaf Meristems and Their Modification
inferredcites →https://doi.org/10.3389/fpls.2016.00310openalex-snapshot
AtHD2D Gene Plays a Role in Plant Growth, Development, and Response to Abiotic Stresses in Arabidopsis thaliana
inferredcites →https://doi.org/10.3389/fpls.2017.01697openalex-snapshot
Dancing with Hormones: A Current Perspective of Nitrate Signaling and Regulation in Arabidopsis
inferredcites →https://doi.org/10.3389/fpls.2017.02039openalex-snapshot
Arbuscular Mycorrhizal Fungus Enhances Lateral Root Formation in Poncirus trifoliata (L.) as Revealed by RNA-Seq Analysis
inferredcites →https://doi.org/10.3389/fpls.2018.01150openalex-snapshot
Local and Systemic Effect of Cytokinins on Soybean Nodulation and Regulation of Their Isopentenyl Transferase (IPT) Biosynthesis Genes Following Rhizobia Inoculation
inferredcites →https://doi.org/10.3389/fpls.2019.00384openalex-snapshot
NRT1.1 Regulates Nitrate Allocation and Cadmium Tolerance in Arabidopsis
inferredcites →https://doi.org/10.3389/fpls.2019.01103openalex-snapshot
Can Ammonium Stress Be Positive for Plant Performance?
inferredcites →https://doi.org/10.3389/fpls.2019.01285openalex-snapshot
Improved Wheat Growth and Yield by Delayed Leaf Senescence Using Developmentally Regulated Expression of a Cytokinin Biosynthesis Gene
inferredcites →https://doi.org/10.3389/fpls.2019.01802openalex-snapshot
Estimation of Vertical Leaf Nitrogen Distribution Within a Rice Canopy Based on Hyperspectral Data
inferredcites →https://doi.org/10.3389/fpls.2020.00741openalex-snapshot
New Insights Into the Metabolism and Role of Cytokinin N-Glucosides in Plants
inferredcites →https://doi.org/10.3389/fpls.2020.604489openalex-snapshot
Cytokinin Signaling Downstream of the His-Asp Phosphorelay Network: Cytokinin-Regulated Genes and Their Functions
inferredcites →https://doi.org/10.3389/fpls.2020.628366openalex-snapshot
Targeting Nitrogen Metabolism and Transport Processes to Improve Plant Nitrogen Use Efficiency
inferredcites →https://doi.org/10.3389/fpls.2021.613488openalex-snapshot
The Cytokinin Status of the Epidermis Regulates Aspects of Vegetative and Reproductive Development in Arabidopsis thaliana
inferredcites →https://doi.org/10.3389/fpls.2021.677585openalex-snapshot
Cytokinin Regulation of Source-Sink Relationships in Plant-Pathogen Interactions
inferredcites →https://doi.org/10.3389/fpls.2021.729021openalex-snapshot
Super Rice With High Sink Activities Has Superior Adaptability to Low Filling Stage Temperature
inferredcites →https://doi.org/10.3389/fpls.2022.851562openalex-snapshot
Integrated Crop Management Practices Improve Grain Yield and Resource Use Efficiency of Super Hybrid Rice
inferredcites →https://doi.org/10.3389/fpls.2022.894840openalex-snapshot
Carbon and Nitrogen Metabolism Are Jointly Regulated During Shading in Roots and Leaves of Camellia Sinensis
inferredcites →https://doi.org/10.3390/biom10121658openalex-snapshot
Cytokinin-Regulated Expression of Arabidopsis thaliana PAP Genes and Its Implication for the Expression of Chloroplast-Encoded Genes
inferredcites →https://doi.org/10.3390/ijms19030853openalex-snapshot
Impairment of Meristem Proliferation in Plants Lacking the Mitochondrial Protease AtFTSH4
inferredcites →https://doi.org/10.3390/ijms20082043openalex-snapshot
AHK3-Mediated Cytokinin Signaling Is Required for the Delayed Leaf Senescence Induced by SSPP
inferredcites →https://doi.org/10.3390/ijms20092349openalex-snapshot
An Integrated Analysis of the Rice Transcriptome and Metabolome Reveals Differential Regulation of Carbon and Nitrogen Metabolism in Response to Nitrogen Availability
inferredcites →https://doi.org/10.3390/ijms20236008openalex-snapshot
Cytokines in Inflammatory Disease
inferredcites →https://doi.org/10.3390/ijms21239124openalex-snapshot
Amino Acid and Carbohydrate Metabolism Are Coordinated to Maintain Energetic Balance during Drought in Sugarcane
inferredcites →https://doi.org/10.3390/ijms22010318openalex-snapshot
Recent Advances in Carbon and Nitrogen Metabolism in C3 Plants
inferredcites →https://doi.org/10.3390/ijms23147770openalex-snapshot
Moderate Soil Drying-Induced Alternative Splicing Provides a Potential Novel Approach for the Regulation of Grain Filling in Rice Inferior Spikelets
inferredcites →https://doi.org/10.3390/nu14071495openalex-snapshot
Cytokinins: Wide-Spread Signaling Hormones from Plants to Humans with High Medical Potential
inferredcites →https://doi.org/10.3390/plants11050685openalex-snapshot
Micro-RNA-Regulated SQUAMOSA-PROMOTER BINDING PROTEIN-LIKE (SPL) Gene Expression and Cytokinin Accumulation Distinguish Early-Developing Male and Female Inflorescences in Oil Palm (Elaeis guineensis)
inferredcites →https://doi.org/10.3390/plants11182344openalex-snapshot
Crosstalk of Cytokinin with Ethylene and Auxin for Cell Elongation Inhibition and Boron Transport in Arabidopsis Primary Root under Boron Deficiency
inferredcites →https://doi.org/10.3390/plants8030077openalex-snapshot
Root-growth Characteristics Contributing to Genotypic Variation in Nitrogen Efficiency of Bottle Gourd and Rootstock Potential for Watermelon
inferredcites →https://doi.org/10.3390/plants9101303openalex-snapshot
Light-Independent Nitrogen Assimilation in Plant Leaves: Nitrate Incorporation into Glutamine, Glutamate, Aspartate, and Asparagine Traced by 15N
inferredcites →https://doi.org/10.3390/rs8100789openalex-snapshot
Estimating the Total Nitrogen Concentration of Reed Canopy with Hyperspectral Measurements Considering a Non-Uniform Vertical Nitrogen Distribution
inferredcites →https://doi.org/10.3390/toxics10080446openalex-snapshot
Alleviation of Ammonium Toxicity in Salvia splendens ‘Vista Red’ with Silicon Supplementation
inferredcites →https://doi.org/10.4161/psb.3.5.5375openalex-snapshot
Phosphorylation of A-type ARR to function as negative regulator of cytokinin signal transduction
inferredcites →https://doi.org/10.5194/isprs-archives-xlii-4-w19-241-2019openalex-snapshot
THE RICE PLANTING WINDOW IN THE PHILIPPINES: AN ANALYSIS USING MULTI-TEMPORAL SAR IMAGERY
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/978-3-031-63149-8_2openalex-snapshot
Phytostimulator Microorganisms
inferred← citeshttps://doi.org/10.1007/s11104-024-07160-1openalex-snapshot
Comparative study on the application of straw, biochar, dimethylpyrazole phosphate, and polyaspartic acid on nitrogen cycle, soil properties, and yield of potted rice
inferred← citeshttps://doi.org/10.1016/b978-0-443-30244-2.00002-6openalex-snapshot
Signal transduction pathways mediated by membrane-bound and endoplasmic reticulum-localized cytokinin receptors
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.121362openalex-snapshot
Regulation of the cytokinin metabolic spectrum and morphogenesis in Quercus robur (L.) in vitro by exogenous cytokinins and activated charcoal
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110739openalex-snapshot
In-field assessment of foliar cytokinin timing and dosage effects on morphological traits, photosynthesis, yield and quality in common wheat
inferred← citeshttps://doi.org/10.1016/j.plgene.2025.100498openalex-snapshot
Differential expression of genes related to tillering in lowland rice varieties cultivated under upland condition
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2024.113084openalex-snapshot
BrARR10 contributes to 6-BA-delayed leaf senescence in Chinese flowering cabbage by activating genes related to CTK, GA and ABA metabolism
inferred← citeshttps://doi.org/10.1016/j.rhisph.2026.101427openalex-snapshot
AMF and PGPR enhance Suaeda salsa phytoremediation of heavy metals-contaminated saline soils: Metabolic reprogramming and rhizosphere microbiome remodeling
inferred← citeshttps://doi.org/10.1080/17429145.2024.2327378openalex-snapshot
Impact of cis-zeatin and lovastatin on antioxidant systems and growth parameters in Zea mays seedlings under phytohormonal crosstalks
inferred← citeshttps://doi.org/10.1371/journal.pone.0317536openalex-snapshot
Mowing management favors primary productivity and carbon sequestration without changing species diversity in a temperate hayfield in Central Interior British Columbia, Canada
inferred← citeshttps://doi.org/10.29303/jbt.v24i1.6387openalex-snapshot
Induksi Kalus dari Hipokotil Belimbing Merah (Baccaurea angulata) dengan Penambahan 2,4-D (Dichlorophenoxy Acetic Acid) dan BAP (6-Benzyl Amino Purin)
inferred← citeshttps://doi.org/10.32604/phyton.2025.061776openalex-snapshot
From Cell Division to Stress Tolerance: The Versatile Roles of Cytokinins in Plants
inferred← citeshttps://doi.org/10.3390/agronomy14010041openalex-snapshot
Agronomic and Physiological Performance of the Indica Rice Varieties Differing in Tolerance to Low Phosphorus
inferred← citeshttps://doi.org/10.3390/ijms25105518openalex-snapshot
Differential Transcription Profiling Reveals the MicroRNAs Involved in Alleviating Damage to Photosynthesis under Drought Stress during the Grain Filling Stage in Wheat
inferred← citeshttps://doi.org/10.3390/nitrogen5010013openalex-snapshot
Cytokinin Biosynthesis Is Affected by Selenium and Nitrate Availabilities to Regulate Shoot and Root Growth in Rice Seedlings
inferred← citeshttps://doi.org/10.3390/plants14142193openalex-snapshot
The Research Progress on the Effects of Phytohormones on Nitrogen Use Efficiency in Rice
inferred← citeshttps://doi.org/10.3390/plants14233567openalex-snapshot
Meta-Topolin as an Aromatic Cytokinin for In Vitro Propagation of Thymus vulgaris L.
inferred← citeshttps://doi.org/10.7717/peerj.21457openalex-snapshot
Plant growth regulator applications and mechanisms for boosting rice productivity
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.