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Hydrogen sulfide modulates actin-dependent auxin transport via regulating ABPs results in changing of root development 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/10.1002/j.1460-2075.1987.tb02730.xopenalex-snapshot
GUS fusions: beta‐glucuronidase as a sensitive and versatile gene fusion marker in higher plants.
inferredcites →https://doi.org/10.1007/s00299-012-1349-2openalex-snapshot
Overexpression of profilin 3 affects cell elongation and F-actin organization in Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/s00709-013-0592-xopenalex-snapshot
Hydrogen sulfide is involved in maintaining ion homeostasis via regulating plasma membrane Na+/H+ antiporter system in the hydrogen peroxide-dependent manner in salt-stress Arabidopsis thaliana root
inferredcites →https://doi.org/10.1007/s10534-012-9551-9openalex-snapshot
Roles of hydrogen sulfide and nitric oxide in the alleviation of cadmium-induced oxidative damage in alfalfa seedling roots
inferredcites →https://doi.org/10.1007/s11104-011-0936-2openalex-snapshot
Hydrogen sulfide enhances alfalfa (Medicago sativa) tolerance against salinity during seed germination by nitric oxide pathway
inferredcites →https://doi.org/10.1007/s11104-012-1275-7openalex-snapshot
Hydrogen sulfide alleviates aluminum toxicity in barley seedlings
inferredcites →https://doi.org/10.1016/0003-2697(77)90043-4openalex-snapshot
A simplification of the protein assay method of Lowry et al. which is more generally applicable
inferredcites →https://doi.org/10.1016/0003-2697(77)90413-4openalex-snapshot
Determination of hydrogen sulfide with 5,5′-dithiobis-(2-nitrobenzoic acid), N-ethylmaleimide, and parachloromercuribenzoate
inferredcites →https://doi.org/10.1016/j.cell.2009.03.001openalex-snapshot
Auxin: A Trigger for Change in Plant Development
inferredcites →https://doi.org/10.1016/j.cub.2006.04.029openalex-snapshot
High-Affinity Auxin Transport by the AUX1 Influx Carrier Protein
inferredcites →https://doi.org/10.1016/j.cub.2013.03.064openalex-snapshot
An Auxin Transport Mechanism Restricts Positive Orthogravitropism in Lateral Roots
inferredcites →https://doi.org/10.1016/j.devcel.2012.04.008openalex-snapshot
Role of Actin Cytoskeleton in Brassinosteroid Signaling and in Its Integration with the Auxin Response in Plants
inferredcites →https://doi.org/10.1016/j.febslet.2005.08.061openalex-snapshot
MDR‐like ABC transporter AtPGP4 is involved in auxin‐mediated lateral root and root hair development
inferredcites →https://doi.org/10.1016/j.jmb.2006.10.102openalex-snapshot
Actin Filament Severing by Cofilin
inferredcites →https://doi.org/10.1016/j.neuint.2009.08.008openalex-snapshot
Hydrogen sulfide: A novel signaling molecule in the central nervous system
inferredcites →https://doi.org/10.1016/j.plantsci.2012.06.002openalex-snapshot
Arabidopsis actin capping protein (AtCP) subunits have different expression patterns, and downregulation of AtCPB confers increased thermotolerance of Arabidopsis after heat shock stress
inferredcites →https://doi.org/10.1016/j.plaphy.2013.02.014openalex-snapshot
cGMP modulates Arabidopsis lateral root formation through regulation of polar auxin transport
inferredcites →https://doi.org/10.1016/j.plaphy.2013.12.024openalex-snapshot
Auxin-induced hydrogen sulfide generation is involved in lateral root formation in tomato
inferredcites →https://doi.org/10.1016/j.tplants.2009.05.002openalex-snapshot
Arabidopsis lateral root development: an emerging story
inferredcites →https://doi.org/10.1016/s0092-8674(00)81535-4openalex-snapshot
An Auxin-Dependent Distal Organizer of Pattern and Polarity in the Arabidopsis Root
inferredcites →https://doi.org/10.1016/s0092-8674(03)00924-3openalex-snapshot
Local, Efflux-Dependent Auxin Gradients as a Common Module for Plant Organ Formation
inferredcites →https://doi.org/10.1038/emboj.2010.181openalex-snapshot
The march of the PINs: developmental plasticity by dynamic polar targeting in plant cells
inferredcites →https://doi.org/10.1038/nature02085openalex-snapshot
Efflux-dependent auxin gradients establish the apical–basal axis of Arabidopsis
inferredcites →https://doi.org/10.1038/nature03184openalex-snapshot
The PIN auxin efflux facilitator network controls growth and patterning in Arabidopsis roots
inferredcites →https://doi.org/10.1073/pnas.0711414105openalex-snapshot
Auxin transport inhibitors impair vesicle motility and actin cytoskeleton dynamics in diverse eukaryotes
inferredcites →https://doi.org/10.1073/pnas.0712307105openalex-snapshot
Auxin acts as a local morphogenetic trigger to specify lateral root founder cells
inferredcites →https://doi.org/10.1073/pnas.1108644108openalex-snapshot
Nitric oxide causes root apical meristem defects and growth inhibition while reducing PIN-FORMED 1 (PIN1)-dependent acropetal auxin transport
inferredcites →https://doi.org/10.1073/pnas.91.4.1510openalex-snapshot
Dynamic actin structures stabilized byprofilin.
inferredcites →https://doi.org/10.1074/jbc.m113.483594openalex-snapshot
Arabidopsis CROLIN1, a Novel Plant Actin-binding Protein, Functions in Cross-linking and Stabilizing Actin Filaments
inferredcites →https://doi.org/10.1074/jbc.m306670200openalex-snapshot
Arabidopsis Capping Protein (AtCP) Is a Heterodimer That Regulates Assembly at the Barbed Ends of Actin Filaments
inferredcites →https://doi.org/10.1091/mbc.e05-09-0840openalex-snapshot
Heterodimeric Capping Protein from Arabidopsis Is Regulated by Phosphatidic Acid
inferredcites →https://doi.org/10.1093/aob/mci083openalex-snapshot
Auxin: Regulation, Action, and Interaction
inferredcites →https://doi.org/10.1093/jxb/erp033openalex-snapshot
Nitric oxide modulates dynamic actin cytoskeleton and vesicle trafficking in a cell type-specific manner in root apices
inferredcites →https://doi.org/10.1093/jxb/ert055openalex-snapshot
Hydrogen sulfide induces systemic tolerance to salinity and non-ionic osmotic stress in strawberry plants through modification of reactive species biosynthesis and transcriptional regulation of multiple defence pathways
inferredcites →https://doi.org/10.1093/pcp/pcg158openalex-snapshot
An Arabidopsis ACT2 Dominant-Negative Mutation, which Disturbs F-actin Polymerization, Reveals its Distinctive Function in Root Development
inferredcites →https://doi.org/10.1096/fj.03-1052fjeopenalex-snapshot
Hydrogen sulfide induces calcium waves in astrocytes
inferredcites →https://doi.org/10.1101/cshperspect.a001594openalex-snapshot
Approaching Cellular and Molecular Resolution of Auxin Biosynthesis and Metabolism
inferredcites →https://doi.org/10.1104/pp.103.034900openalex-snapshot
Interactions between Auxin Transport and the Actin Cytoskeleton in Developmental Polarity of Fucus distichus Embryos in Response to Light and Gravity
inferredcites →https://doi.org/10.1104/pp.122.2.481openalex-snapshot
Basipetal Auxin Transport Is Required for Gravitropism in Roots of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.61.2.184openalex-snapshot
Light-dependent Emission of Hydrogen Sulfide from Plants
inferredcites →https://doi.org/10.1105/tpc.020313openalex-snapshot
The transparent testa4 Mutation Prevents Flavonoid Synthesis and Alters Auxin Transport and the Response of Arabidopsis Roots to Gravity and Light[W]
inferredcites →https://doi.org/10.1105/tpc.106.042770openalex-snapshot
Subcellular Trafficking of the Arabidopsis Auxin Influx Carrier AUX1 Uses a Novel Pathway Distinct from PIN1
inferredcites →https://doi.org/10.1105/tpc.108.061960openalex-snapshot
A Single Vegetative Actin Isovariant Overexpressed under the Control of Multiple Regulatory Sequences Is Sufficient for NormalArabidopsisDevelopment
inferredcites →https://doi.org/10.1105/tpc.109.066480openalex-snapshot
An Auxin Gradient and Maximum in the Arabidopsis Root Apex Shown by High-Resolution Cell-Specific Analysis of IAA Distribution and Synthesis
inferredcites →https://doi.org/10.1105/tpc.110.076257openalex-snapshot
ArabidopsisVILLIN5, an Actin Filament Bundling and Severing Protein, Is Necessary for Normal Pollen Tube Growth
inferredcites →https://doi.org/10.1105/tpc.140230openalex-snapshot
An Emerging Model of Auxin Transport Regulation
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02369.xopenalex-snapshot
Complex regulation of Arabidopsis AGR1/PIN2‐mediated root gravitropic response and basipetal auxin transport by cantharidin‐sensitive protein phosphatases
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03068.xopenalex-snapshot
Auxin, actin and growth of the Arabidopsis thaliana primary root
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03465.xopenalex-snapshot
Hydrogen sulphide, a novel gasotransmitter involved in guard cell signalling
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03757.xopenalex-snapshot
Auxin minimum defines a developmental window for lateral root initiation
inferredcites →https://doi.org/10.1111/j.1744-7909.2008.00769.xopenalex-snapshot
Hydrogen Sulfide Promotes Wheat Seed Germination and Alleviates Oxidative Damage against Copper Stress
inferredcites →https://doi.org/10.1111/j.1744-7909.2009.00885.xopenalex-snapshot
Hydrogen Sulfide Promotes Root Organogenesis in Ipomoea batatas, Salix matsudana and Glycine max
inferredcites →https://doi.org/10.1111/pce.12092openalex-snapshot
Hydrogen sulphide may be a novel downstream signal molecule in nitric oxide‐induced heat tolerance of maize ( Z ea mays L .) seedlings
inferredcites →https://doi.org/10.1126/science.1121356openalex-snapshot
Polar PIN Localization Directs Auxin Flow in Plants
inferredcites →https://doi.org/10.1126/science.1175862openalex-snapshot
Actin, a Central Player in Cell Shape and Movement
inferredcites →https://doi.org/10.1146/annurev.arplant.51.1.257openalex-snapshot
S IGNALING TO THE A CTIN C YTOSKELETON IN P LANTS
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105206openalex-snapshot
CONTROL OF THE ACTIN CYTOSKELETON IN PLANT CELL GROWTH
inferredcites →https://doi.org/10.1242/dev.00926openalex-snapshot
Partial loss-of-function alleles reveal a role forGNOMin auxin transport-related, post-embryonic development ofArabidopsis
inferredcites →https://doi.org/10.1242/dev.124.1.33openalex-snapshot
Organization and cell differentiation in lateral roots of Arabidopsis thaliana
inferredcites →https://doi.org/10.1371/journal.pone.0062048openalex-snapshot
Increased Growth and Germination Success in Plants following Hydrogen Sulfide Administration
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.4480360openalex-extracted
Synergism of Vesicle Trafficking and Cytoskeleton During Regulation of Plant Growth and Development: A Mechanistic Outlook
inferred← citeshttps://doi.org/10.1007/978-3-030-73678-1_1openalex-snapshot
Hydrogen Sulfide on the Crossroad of Regulation, Protection, Interaction and Signaling in Plant Systems Under Different Environmental Conditions
inferred← citeshttps://doi.org/10.1007/978-3-030-73678-1_10openalex-snapshot
A Transcriptomic and Proteomic View of Hydrogen Sulfide Signaling in Plant Abiotic Stress
inferred← citeshttps://doi.org/10.1007/978-3-030-73678-1_4openalex-snapshot
Hydrogen Sulfide and Redox Homeostasis for Alleviation of Heavy Metal Stress
inferred← citeshttps://doi.org/10.1007/978-3-030-77477-6_7openalex-snapshot
Recent Insights into Auxin-Mediated Molecular Cross Talk Events Associated with Regulation of Root Growth and Architecture During Abiotic Stress in Plants
inferred← citeshttps://doi.org/10.1007/978-3-031-43029-9_1openalex-snapshot
Role of Gasotransmitters in Hormonal Responses of Plants to Abiotic Stress
inferred← citeshttps://doi.org/10.1007/978-3-031-43029-9_9openalex-snapshot
Interaction of Hydrogen Sulfide with Phytohormones During Plant Physiological and Stress Conditions
inferred← citeshttps://doi.org/10.1007/978-3-032-03608-7_6openalex-snapshot
Plant Responses Under Combined Effect of Atmospheric Hydrogen Sulfide and Tropospheric Ozone
inferred← citeshttps://doi.org/10.1007/978-3-319-40713-5_2openalex-snapshot
Hydrogen Sulfide in Plant Biology
inferred← citeshttps://doi.org/10.1007/978-981-16-0917-6_24openalex-snapshot
Sulfur in Soil: Abiotic Stress Signaling, Transmission and Induced Physiological Responses in Plants
inferred← citeshttps://doi.org/10.1007/s00299-016-1952-8openalex-snapshot
Putrescine protects hulless barley from damage due to UV-B stress via H2S- and H2O2-mediated signaling pathways
inferred← citeshttps://doi.org/10.1007/s00299-026-03726-8openalex-snapshot
Imperative roles of auxin signaling in reprogramming of drought tolerance in plants
inferred← citeshttps://doi.org/10.1007/s00344-018-9817-8openalex-snapshot
Identification of Wheat d-Cysteine Desulfhydrase (TaD-CDes) Required for Abscisic Acid Regulation of Seed Germination, Root Growth, and Stomatal Closure in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00344-020-10284-0openalex-snapshot
Hydrogen Sulfide: A Novel Gaseous Molecule for Plant Adaptation to Stress
inferred← citeshttps://doi.org/10.1007/s00344-021-10350-1openalex-snapshot
Hydrogen Sulfide–Phytohormone Interaction in Plants Under Physiological and Stress Conditions
inferred← citeshttps://doi.org/10.1007/s00344-026-12376-9openalex-snapshot
Climate-associated Variation in the Response of Bermudagrass (Cynodon dactylon) to Exogenous Hydrogen Sulfide Under Shade Stress
inferred← citeshttps://doi.org/10.1007/s00425-019-03334-9openalex-snapshot
Hydrogen sulfide acts downstream of jasmonic acid to inhibit stomatal development in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s10725-018-0454-9openalex-snapshot
Interaction between hydrogen sulfide and hormones in plant physiological responses
inferred← citeshttps://doi.org/10.1007/s10725-021-00693-wopenalex-snapshot
H2S action in plant life cycle
inferred← citeshttps://doi.org/10.1007/s10725-022-00887-wopenalex-snapshot
Hydrogen Sulfide: A new warrior in assisting seed germination during adverse environmental conditions
inferred← citeshttps://doi.org/10.1007/s11104-020-04471-xopenalex-snapshot
The role of hydrogen sulfide in plant alleviates heavy metal stress
inferred← citeshttps://doi.org/10.1007/s11105-019-01181-2openalex-snapshot
Cloning and Characterization of a gene Encoding True D-cysteine Desulfhydrase from Oryza sativa
inferred← citeshttps://doi.org/10.1007/s11356-024-33298-7openalex-snapshot
The role of exogenous hydrogen sulfide in mitigating cadmium toxicity in plants: A comprehensive meta-analysis
inferred← citeshttps://doi.org/10.1007/s12192-017-0854-1openalex-snapshot
Gene encoding vesicle-associated membrane protein-associated protein from Triticum aestivum (TaVAP) confers tolerance to drought stress
inferred← citeshttps://doi.org/10.1007/s12230-026-10041-1openalex-snapshot
Hydrogen Sulfide Released by Dibutyl Dithiophosphate Increases Potato Growth and Yield
inferred← citeshttps://doi.org/10.1007/s42994-021-00035-4openalex-snapshot
Hydrogen sulfide (H2S) signaling in plant development and stress responses
inferred← citeshttps://doi.org/10.1016/b978-0-323-85862-5.00009-9openalex-snapshot
Hydrogen sulfide and phytohormones crosstalk in plant defense against abiotic stress
inferred← citeshttps://doi.org/10.1016/b978-0-323-85862-5.00010-5openalex-snapshot
General view on H2S and abiotic stress tolerance in plants
inferred← citeshttps://doi.org/10.1016/b978-0-323-85862-5.00013-0openalex-snapshot
Regulation of metal stress toxicity in plants by the hydrogen sulfide
inferred← citeshttps://doi.org/10.1016/b978-0-323-85862-5.00014-2openalex-snapshot
Gene regulation by H2S in plants
inferred← citeshttps://doi.org/10.1016/b978-0-323-91886-2.00015-xopenalex-snapshot
Interplay between phytohormones and hydrogen sulfide regulates plant growth and development under normal and abiotic stresses
inferred← citeshttps://doi.org/10.1016/b978-0-323-99035-6.00001-4openalex-snapshot
Role of H2S in nutrient excesses and deficiencies
inferred← citeshttps://doi.org/10.1016/b978-0-323-99035-6.00006-3openalex-snapshot
The role of H2S in plant defense against pathogens and herbivores
inferred← citeshttps://doi.org/10.1016/b978-0-323-99035-6.00013-0openalex-snapshot
Role of hydrogen sulfide in regulating postharvest horticultural crops quality
inferred← citeshttps://doi.org/10.1016/b978-0-323-99035-6.00015-4openalex-snapshot
Is H2S a lead or supporting player in plant development and growth?
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116879openalex-snapshot
Hydrogen sulfide persulfidates OAS-A1 to balance cysteine levels in regulating Arabidopsis stomatal development
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2020.127999openalex-snapshot
Hydrogen sulfide mitigates cadmium induced toxicity in Brassica rapa by modulating physiochemical attributes, osmolyte metabolism and antioxidative machinery
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2020.104365openalex-snapshot
Transcriptome and metabolome analyses reveal the pivotal role of hydrogen sulfide in promoting submergence tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105354openalex-snapshot
Hydrogen sulfide alleviates salt stress through auxin signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.fgb.2019.04.014openalex-snapshot
Hydrogen sulfide, a novel small molecule signalling agent, participates in the regulation of ganoderic acids biosynthesis induced by heat stress in Ganoderma lucidum
inferred← citeshttps://doi.org/10.1016/j.foodcont.2025.111914openalex-snapshot
Hydrogen sulfide maintains banana postharvest quality by antagonizing ethylene and enhancing antioxidant properties in Musa nana Lour
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e21976openalex-snapshot
RETRACTED: Synergism of vesicle trafficking and cytoskeleton during regulation of plant growth and development: A mechanistic outlook
inferred← citeshttps://doi.org/10.1016/j.jare.2020.03.011openalex-snapshot
H2S signaling in plants and applications in agriculture
inferred← citeshttps://doi.org/10.1016/j.jgg.2026.07.011openalex-snapshot
Current landscape of Cys-OxiPTMs in plants: from hormone signaling to phenotypic control and their potential in sustainable agriculture
inferred← citeshttps://doi.org/10.1016/j.molp.2020.01.004openalex-snapshot
Hydrogen Sulfide Positively Regulates Abscisic Acid Signaling through Persulfidation of SnRK2.6 in Guard Cells
inferred← citeshttps://doi.org/10.1016/j.molp.2021.07.002openalex-snapshot
Persulfidation-induced structural change in SnRK2.6 establishes intramolecular interaction between phosphorylation and persulfidation
inferred← citeshttps://doi.org/10.1016/j.niox.2023.09.001openalex-snapshot
Exploring the potential role of hydrogen sulfide and jasmonic acid in plants during heavy metal stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2016.02.033openalex-snapshot
Hydrogen sulfide mediates nicotine biosynthesis in tobacco (Nicotiana tabacum) under high temperature conditions
inferred← citeshttps://doi.org/10.1016/j.plaphy.2018.08.028openalex-snapshot
Hydrogen sulphide trapeze: Environmental stress amelioration and phytohormone crosstalk
inferred← citeshttps://doi.org/10.1016/j.plaphy.2018.12.015openalex-snapshot
Hydrogen sulfide directs metabolic flux towards the lignan biosynthesis in Linum album hairy roots
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.04.038openalex-snapshot
Gibberellic acid-induced generation of hydrogen sulfide alleviates boron toxicity in tomato (Solanum lycopersicum L.) plants
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.08.020openalex-snapshot
Crosstalk among hydrogen sulfide (H2S), nitric oxide (NO) and carbon monoxide (CO) in root-system development and its rhizosphere interactions: A gaseous interactome
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.09.020openalex-snapshot
Hydrogen sulfide regulates the activity of antioxidant enzymes through persulfidation and improves the resistance of tomato seedling to Copper Oxide nanoparticles (CuO NPs)-induced oxidative stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.11.045openalex-snapshot
Hydrogen sulfide: A versatile gaseous molecule in plants
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.12.018openalex-snapshot
Regulation of growth in peach roots by exogenous hydrogen sulfide based on RNA-Seq
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.03.006openalex-snapshot
Recent advances and mechanistic interactions of hydrogen sulfide with plant growth regulators in relation to abiotic stress tolerance in plants
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108730openalex-snapshot
Unraveling the potential of hydrogen sulfide as a signaling molecule for plant development and environmental stress responses: A state-of-the-art review
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2021.111520openalex-snapshot
Hydrogen sulfide reduced colour change in Lanzhou lily-bulb scales
inferred← citeshttps://doi.org/10.1016/j.redox.2024.103227openalex-snapshot
Hydrogen sulfide maintains mitochondrial homeostasis and regulates ganoderic acids biosynthesis by SQR under heat stress in Ganoderma lucidum
inferred← citeshttps://doi.org/10.1016/j.sajb.2022.11.029openalex-snapshot
Exogenous calcium (Ca2+) and verapamil-sensitive Ca2+ channel activity differentially modulates melatonin-mediated regulation of endogenous hydrogen sulphide (H2S) homeostasis, and L-cysteine desulfhydrase (L-DES) activity in NaCl-stressed etiolated sunflower seedlings
inferred← citeshttps://doi.org/10.1016/j.sajb.2024.01.068openalex-snapshot
Auxin and hydrogen peroxide (H2O2) interaction differentially regulate seedling growth, Na+/K+ ratio and H2S homeostasis accompanying NaCl stress in etiolated sunflower (Helianthus annuus L. cv. Microgreen) seedling roots and cotyledons
inferred← citeshttps://doi.org/10.1016/j.scienta.2020.109802openalex-snapshot
Cloning of cucumber LCD and DES gene and their response to abiotic stress
inferred← citeshttps://doi.org/10.1016/j.scienta.2021.110366openalex-snapshot
H2S improves growth of tomato seedlings involving the MAPK signaling
inferred← citeshttps://doi.org/10.1016/j.scienta.2023.112356openalex-snapshot
D-cysteine desulfhydrase silence influences the level of sugar, organic acid, carotenoids, and polyphenols in tomato fruit
inferred← citeshttps://doi.org/10.1016/j.tplants.2021.07.016openalex-snapshot
Nitric oxide and hydrogen sulfide: an indispensable combination for plant functioning
inferred← citeshttps://doi.org/10.1016/j.watres.2024.122197openalex-snapshot
Use of reclaimed municipal wastewater in agriculture: Comparison of present practice versus an emerging paradigm of anaerobic membrane bioreactor treatment coupled with hydroponic controlled environment agriculture
inferred← citeshttps://doi.org/10.1038/s41598-017-01046-2openalex-snapshot
Hydrogen sulfide toxicity inhibits primary root growth through the ROS-NO pathway
inferred← citeshttps://doi.org/10.1038/s41598-017-02872-0openalex-snapshot
Functional analysis of the role of hydrogen sulfide in the regulation of dark-induced leaf senescence in Arabidopsis
inferred← citeshttps://doi.org/10.1038/srep39702openalex-snapshot
Hydrogen sulfide - cysteine cycle system enhances cadmium tolerance through alleviating cadmium-induced oxidative stress and ion toxicity in Arabidopsis roots
inferred← citeshttps://doi.org/10.1039/9781788013000-00235openalex-snapshot
Gasotransmitters in Plants
inferred← citeshttps://doi.org/10.1080/01904167.2022.2160743openalex-snapshot
Excess boron stress and alleviation of its toxicity in plants: mechanisms and strategies
inferred← citeshttps://doi.org/10.1080/07388551.2018.1472551openalex-snapshot
VOCs-mediated hormonal signaling and crosstalk with plant growth promoting microbes
inferred← citeshttps://doi.org/10.1080/07388551.2021.1924113openalex-snapshot
Plant phospholipase D: novel structure, regulatory mechanism, and multifaceted functions with biotechnological application
inferred← citeshttps://doi.org/10.1080/15592324.2015.1055433openalex-snapshot
Roles of H2S in adaptation of alpine plants Lamiophlomis rotata to altitude gradients
inferred← citeshttps://doi.org/10.1080/17435390.2019.1678693openalex-snapshot
Copper oxide nanoparticles alter cellular morphology via disturbing the actin cytoskeleton dynamics inArabidopsisroots
inferred← citeshttps://doi.org/10.1093/hr/uhaf273openalex-snapshot
From odor to order: unveiling the crucial role of hydrogen sulfide in plant life
inferred← citeshttps://doi.org/10.1093/jxb/eraa318openalex-snapshot
Hydrogen sulfide promotes hypocotyl elongation via increasing cellulose content and changing the arrangement of cellulose fibrils in alfalfa
inferred← citeshttps://doi.org/10.1093/jxb/erab239openalex-snapshot
Hydrogen sulfide signaling in plant adaptations to adverse conditions: molecular mechanisms
inferred← citeshttps://doi.org/10.1093/jxb/erz225openalex-snapshot
Signaling by hydrogen sulfide and cyanide through post-translational modification
inferred← citeshttps://doi.org/10.1093/plphys/kiag603openalex-snapshot
miR169a-MhNF-YA2 module modulates H2S dosage-dependent lateral root formation via MhPIN1 and MhCYCB1;2 in Malus hupehensis
inferred← citeshttps://doi.org/10.1104/pp.17.01636openalex-snapshot
Hydrogen Sulfide Increases Production of NADPH Oxidase-Dependent Hydrogen Peroxide and Phospholipase D-Derived Phosphatidic Acid in Guard Cell Signaling
inferred← citeshttps://doi.org/10.1104/pp.18.00838openalex-snapshot
Hydrogen Sulfide Disturbs Actin Polymerization via S-Sulfhydration Resulting in Stunted Root Hair Growth
inferred← citeshttps://doi.org/10.1104/pp.19.01504openalex-snapshot
WRKY13 Enhances Cadmium Tolerance by Promoting D-CYSTEINE DESULFHYDRASE and Hydrogen Sulfide Production
inferred← citeshttps://doi.org/10.1111/nph.20122openalex-snapshot
Hydrogen sulfide antagonizes cytokinin to change root system architecture through persulfidation of CKX2 in Arabidopsis
inferred← citeshttps://doi.org/10.1111/pbi.70245openalex-snapshot
Hydrogen sulfide promotes lateral root formation in peach through persulfidation of SnRK1α kinase
inferred← citeshttps://doi.org/10.1111/pce.13011openalex-snapshot
Effects of discrete bioactive microbial volatiles on plants and fungi
inferred← citeshttps://doi.org/10.1111/pce.14531openalex-snapshot
H 2 O 2 , NO, and H 2 S networks during root development and signalling under physiological and challenging environments: Beneficial or toxic?
inferred← citeshttps://doi.org/10.1111/pce.15110openalex-snapshot
Hydrogen sulphide alleviates root growth inhibition induced by phosphate starvation
inferred← citeshttps://doi.org/10.1111/pce.15309openalex-snapshot
Hydrogen Sulphide: A Key Player in Plant Development and Stress Resilience
inferred← citeshttps://doi.org/10.1111/pce.70520openalex-snapshot
Hydrogen Sulphide Signalling in Plants: From Persulfidation to Metabolic Regulation and Stress Response
inferred← citeshttps://doi.org/10.1111/plb.13368openalex-snapshot
Hydrogen sulfide: an emerging component against abiotic stress in plants
inferred← citeshttps://doi.org/10.1111/plb.13372openalex-snapshot
Harnessing the power of hydrogen sulphide (H 2 S) for improving fruit quality traits
inferred← citeshttps://doi.org/10.1111/plb.13417openalex-snapshot
Hydrogen sulphide (H 2 S) in the hidden half: Role in root growth, stress signalling and rhizospheric interactions
inferred← citeshttps://doi.org/10.1111/tpj.13627openalex-snapshot
The Ca2+/calmodulin2‐binding transcription factor TGA 3 elevates LCD expression and H2S production to bolster Cr6+ tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1111/tpj.16073openalex-snapshot
Multi‐omics analyses reveal stone cell distribution pattern in pear fruit
inferred← citeshttps://doi.org/10.1111/tpj.16198openalex-snapshot
Hydrogen sulfide alleviates osmotic stress‐induced root growth inhibition by promoting auxin homeostasis
inferred← citeshttps://doi.org/10.1186/s12870-015-0637-8openalex-snapshot
Proline affects the size of the root meristematic zone in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2017.00232openalex-snapshot
Cadmium Disrupts the Balance between Hydrogen Peroxide and Superoxide Radical by Regulating Endogenous Hydrogen Sulfide in the Root Tip of Brassica rapa
inferred← citeshttps://doi.org/10.3389/fpls.2018.01172openalex-snapshot
Hydrogen Sulfide: A Gaseous Molecule in Postharvest Freshness
inferred← citeshttps://doi.org/10.3389/fpls.2018.01404openalex-snapshot
Central Role of Adenosine 5′-Phosphosulfate Reductase in the Control of Plant Hydrogen Sulfide Metabolism
inferred← citeshttps://doi.org/10.3389/fpls.2018.01517openalex-snapshot
Ethylene-Induced Hydrogen Sulfide Negatively Regulates Ethylene Biosynthesis by Persulfidation of ACO in Tomato Under Osmotic Stress
inferred← citeshttps://doi.org/10.3389/fpls.2020.00108openalex-snapshot
Improving Photosynthetic Capacity, Alleviating Photosynthetic Inhibition and Oxidative Stress Under Low Temperature Stress With Exogenous Hydrogen Sulfide in Blueberry Seedlings
inferred← citeshttps://doi.org/10.3389/fpls.2025.1653008openalex-snapshot
Ion toxicity in waterlogged soils: mechanisms of root response and adaptive strategies
inferred← citeshttps://doi.org/10.3390/agriculture10010012openalex-snapshot
Hydrogen Sulfide Affects the Root Development of Strawberry During Plug Transplant Production
inferred← citeshttps://doi.org/10.3390/antiox9070621openalex-snapshot
Hydrogen Sulfide: From a Toxic Molecule to a Key Molecule of Cell Life
inferred← citeshttps://doi.org/10.3390/biology9070172openalex-snapshot
Impact of the Static Magnetic Field on Growth, Pigments, Osmolytes, Nitric Oxide, Hydrogen Sulfide, Phenylalanine Ammonia-Lyase Activity, Antioxidant Defense System, and Yield in Lettuce
inferred← citeshttps://doi.org/10.3390/biom12050678openalex-snapshot
The Functional Interplay between Ethylene, Hydrogen Sulfide, and Sulfur in Plant Heat Stress Tolerance
inferred← citeshttps://doi.org/10.3390/ijms21134593openalex-snapshot
Crosstalk between Hydrogen Sulfide and Other Signal Molecules Regulates Plant Growth and Development
inferred← citeshttps://doi.org/10.3390/ijms23031024openalex-snapshot
The Role of Hydrogen Sulfide in Plant Roots during Development and in Response to Abiotic Stress
inferred← citeshttps://doi.org/10.3390/ijms23084272openalex-snapshot
The Interplay between Hydrogen Sulfide and Phytohormone Signaling Pathways under Challenging Environments
inferred← citeshttps://doi.org/10.3390/ijms23126435openalex-snapshot
A NAC Transcription Factor from ‘Sea Rice 86′ Enhances Salt Tolerance by Promoting Hydrogen Sulfide Production in Rice Seedlings
inferred← citeshttps://doi.org/10.3390/ijms232315107openalex-snapshot
Biological Functions of Hydrogen Sulfide in Plants
inferred← citeshttps://doi.org/10.3390/ijms25073978openalex-snapshot
Sulfate Availability and Hormonal Signaling in the Coordination of Plant Growth and Development
inferred← citeshttps://doi.org/10.3390/nitrogen4020016openalex-snapshot
Isoenzymatic Pattern of Hydrogen Sulfide (H2S)-Generating L-Cysteine Desulfhydrase (LCD) in Arabidopsis thaliana Seedlings: Effect of Nitric Oxide (NO) and H2S
inferred← citeshttps://doi.org/10.3390/plants10091928openalex-snapshot
Hydrogen Sulfide Enhances Plant Tolerance to Waterlogging Stress
inferred← citeshttps://doi.org/10.36921/kos.2019_2609openalex-snapshot
SIARKOWODÓR JAKO CZĄSTECZKA REGULATOROWA W KOMÓRKACH ROŚLINNYCH
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.