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MicroRNAs balance growth and salt stress responses in sweet sorghum

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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/s00122-022-04130-yopenalex-snapshot
SbWRKY55 regulates sorghum response to saline environment by its dual role in abscisic acid signaling
inferredcites →https://doi.org/10.1007/s00299-013-1418-1openalex-snapshot
ABA signaling in stress-response and seed development
inferredcites →https://doi.org/10.1007/s00425-010-1104-2openalex-snapshot
Over-expression of osa-MIR396c decreases salt and alkali stress tolerance
inferredcites →https://doi.org/10.1007/s10142-015-0451-2openalex-snapshot
Plant miRNAs: biogenesis, organization and origins
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Root precursors of microRNAs in wild emmer and modern wheats show major differences in response to drought stress
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Obesity and survival in the neoadjuvant breast cancer setting: role of tumor subtype in an ethnically diverse population
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Differential regulation of microRNAs in response to osmotic, salt and cold stresses in wheat
inferredcites →https://doi.org/10.1007/s11103-005-8395-xopenalex-snapshot
Calmodulin-like Proteins from Arabidopsis and Tomato are Involved in Host Defense Against Pseudomonas syringae pv. tomato
inferredcites →https://doi.org/10.1007/s11103-010-9710-8openalex-snapshot
Bacteria-responsive microRNAs regulate plant innate immunity by modulating plant hormone networks
inferredcites →https://doi.org/10.1007/s11103-013-0124-2openalex-snapshot
Comprehensive transcriptional profiling of NaHCO3-stressed Tamarix hispida roots reveals networks of responsive genes
inferredcites →https://doi.org/10.1007/s11104-018-3736-0openalex-snapshot
Transcriptome analysis of sweet Sorghum inbred lines differing in salt tolerance provides novel insights into salt exclusion by roots
inferredcites →https://doi.org/10.1007/s11105-017-1033-3openalex-snapshot
A Novel miRNA Sponge Form Efficiently Inhibits the Activity of miR393 and Enhances the Salt Tolerance and ABA Insensitivity in Arabidopsis thaliana
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Comparative transcriptomics-based selection of suitable reference genes for normalization of RT-qPCR experiments in drought-stressed leaves of three European Quercus species
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Plant abiotic stress response and nutrient use efficiency
inferredcites →https://doi.org/10.1016/j.bbagrm.2011.08.004openalex-snapshot
AP2/ERF family transcription factors in plant abiotic stress responses
inferredcites →https://doi.org/10.1016/j.bbrc.2009.04.028openalex-snapshot
Insights into the mechanism of plant development: Interactions of miRNAs pathway with phytohormone response
inferredcites →https://doi.org/10.1016/j.cell.2005.04.004openalex-snapshot
microRNA-Directed Phasing during Trans-Acting siRNA Biogenesis in Plants
inferredcites →https://doi.org/10.1016/j.cell.2006.07.034openalex-snapshot
Activation of Glucosidase via Stress-Induced Polymerization Rapidly Increases Active Pools of Abscisic Acid
inferredcites →https://doi.org/10.1016/j.cell.2016.08.029openalex-snapshot
Abiotic Stress Signaling and Responses in Plants
inferredcites →https://doi.org/10.1016/j.cell.2017.06.002openalex-snapshot
A Sacrifice-for-Survival Mechanism Protects Root Stem Cell Niche from Chilling Stress
inferredcites →https://doi.org/10.1016/j.cub.2020.02.002openalex-snapshot
PIN-LIKES Coordinate Brassinosteroid Signaling with Nuclear Auxin Input in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.foodchem.2022.134663openalex-snapshot
Integration of transcriptome, miRNA and degradome sequencing reveals the early browning response in fresh-cut apple
inferredcites →https://doi.org/10.1016/j.molp.2015.01.013openalex-snapshot
Growth-Regulating Factors (GRFs): A Small Transcription Factor Family with Important Functions in Plant Biology
inferredcites →https://doi.org/10.1016/j.pbi.2007.08.014openalex-snapshot
Auxin response factors
inferredcites →https://doi.org/10.1016/j.pbi.2016.06.010openalex-snapshot
Integration of calcium and ABA signaling
inferredcites →https://doi.org/10.1016/j.plantsci.2015.02.008openalex-snapshot
Stress responsive miRNAs and isomiRs in cereals
inferredcites →https://doi.org/10.1016/j.plantsci.2018.11.004openalex-snapshot
The moss jasmonate ZIM-domain protein PnJAZ1 confers salinity tolerance via crosstalk with the abscisic acid signalling pathway
inferredcites →https://doi.org/10.1016/j.plantsci.2020.110801openalex-snapshot
Analysis of N6-methyladenosine reveals a new important mechanism regulating the salt tolerance of sweet sorghum
inferredcites →https://doi.org/10.1016/j.plaphy.2014.01.015openalex-snapshot
Hormone profiling and transcription analysis reveal a major role of ABA in tomato salt tolerance
inferredcites →https://doi.org/10.1016/j.tplants.2012.01.010openalex-snapshot
Functions of microRNAs in plant stress responses
inferredcites →https://doi.org/10.1016/j.tplants.2018.04.001openalex-snapshot
ABA Transport and Plant Water Stress Responses
inferredcites →https://doi.org/10.1016/j.tplants.2019.04.008openalex-snapshot
Revisiting the Basal Role of ABA – Roles Outside of Stress
inferredcites →https://doi.org/10.1016/j.tplants.2020.04.004openalex-snapshot
Emerging Connections between Small RNAs and Phytohormones
inferredcites →https://doi.org/10.1016/j.tplants.2020.05.009openalex-snapshot
Altering Plant Architecture to Improve Performance and Resistance
inferredcites →https://doi.org/10.1016/j.tplants.2020.06.008openalex-snapshot
How Plant Hormones Mediate Salt Stress Responses
inferredcites →https://doi.org/10.1016/j.tplants.2021.03.005openalex-snapshot
How roots and shoots communicate through stressful times
inferredcites →https://doi.org/10.1016/j.xplc.2020.100040openalex-snapshot
Multifaceted Signaling Networks Mediated by Abscisic Acid Insensitive 4
inferredcites →https://doi.org/10.1016/s0014-5793(04)00222-4openalex-snapshot
Analysis of GT‐3a identifies a distinct subgroup of trihelix DNA‐binding transcription factors in Arabidopsis
inferredcites →https://doi.org/10.1021/ac00056a738openalex-snapshot
Journal of Agricultural and Food Chemistry
inferredcites →https://doi.org/10.1021/acs.jafc.0c02473openalex-snapshot
miRNA and Degradome Sequencing Identify miRNAs and Their Target Genes Involved in the Browning Inhibition of Fresh-Cut Apples by Hydrogen Sulfide
inferredcites →https://doi.org/10.1023/a:1006151427889openalex-snapshot
Breast Cancer Research and Treatment
inferredcites →https://doi.org/10.1038/186124d0openalex-snapshot
Biochemical and Biophysical Research Communications
inferredcites →https://doi.org/10.1038/cr.2017.102openalex-snapshot
IPA1 functions as a downstream transcription factor repressed by D53 in strigolactone signaling in rice
inferredcites →https://doi.org/10.1038/nrm2868openalex-snapshot
MicroRNA control of signal transduction
inferredcites →https://doi.org/10.1038/s41467-018-05571-0openalex-snapshot
Gating of miRNA movement at defined cell-cell interfaces governs their impact as positional signals
inferredcites →https://doi.org/10.1038/s41467-020-14477-9openalex-snapshot
A RAF-SnRK2 kinase cascade mediates early osmotic stress signaling in higher plants
inferredcites →https://doi.org/10.1038/s41477-019-0565-yopenalex-snapshot
A HAK family Na+ transporter confers natural variation of salt tolerance in maize
inferredcites →https://doi.org/10.1038/s41586-019-1413-yopenalex-snapshot
A calmodulin-gated calcium channel links pathogen patterns to plant immunity
inferredcites →https://doi.org/10.1038/s41586-019-1679-0openalex-snapshot
Genetic strategies for improving crop yields
inferredcites →https://doi.org/10.1038/s41598-020-59981-6openalex-snapshot
Machine learning improves our knowledge about miRNA functions towards plant abiotic stresses
inferredcites →https://doi.org/10.1042/bj20091147openalex-snapshot
Breaking the code: Ca2+ sensors in plant signalling
inferredcites →https://doi.org/10.1042/bj20131080openalex-snapshot
The calmodulin-like protein CML43 functions as a salicylic-acid-inducible root-specific Ca2+ sensor in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1916548117openalex-snapshot
Multifeature analyses of vascular cambial cells reveal longevity mechanisms in old Ginkgo biloba trees
inferredcites →https://doi.org/10.1073/pnas.2022547118openalex-snapshot
The receptor-like kinases BAM1 and BAM2 are required for root xylem patterning
inferredcites →https://doi.org/10.1080/07352689.2011.605739openalex-snapshot
Gene Expression Profiling of Plants under Salt Stress
inferredcites →https://doi.org/10.1080/15476286.2019.1697487openalex-snapshot
Dynamic architecture and regulatory implications of the miRNA network underlying the response to stress in melon
inferredcites →https://doi.org/10.1089/omi.2011.0073openalex-snapshot
Dehydration Stress-Responsive miRNA in Brachypodium distachyon : Evident by Genome-Wide Screening of microRNAs Expression
inferredcites →https://doi.org/10.1093/aob/mcn205openalex-snapshot
Differential expression of miRNAs in response to salt stress in maize roots
inferredcites →https://doi.org/10.1093/jxb/erq063openalex-snapshot
microRNA, seeds, and Darwin?: diverse function of miRNA in seed biology and plant responses to stress
inferredcites →https://doi.org/10.1093/jxb/erv013openalex-snapshot
MicroRNA: a new target for improving plant tolerance to abiotic stress
inferredcites →https://doi.org/10.1093/jxb/erx475openalex-snapshot
The GhmiR157a–GhSPL10 regulatory module controls initial cellular dedifferentiation and callus proliferation in cotton by modulating ethylene-mediated flavonoid biosynthesis
inferredcites →https://doi.org/10.1093/pcp/pcu058openalex-snapshot
miR396a-Mediated Basic Helix–Loop–Helix Transcription Factor bHLH74 Repression Acts as a Regulator for Root Growth in Arabidopsis Seedlings
inferredcites →https://doi.org/10.1093/pcp/pcz042openalex-snapshot
Plasma Membrane-Associated Ca2+-Binding Protein PCaP1 is Involved in Root Hydrotropism of Arabidopsis thaliana
inferredcites →https://doi.org/10.1101/gad.1004402openalex-snapshot
MicroRNAs in plants
inferredcites →https://doi.org/10.1101/gr.270918.120openalex-snapshot
Genome-wide analysis of plant miRNA action clarifies levels of regulatory dynamics across developmental contexts
inferredcites →https://doi.org/10.1104/pp.104.041442openalex-snapshot
Pathogen- and NaCl-Induced Expression of the SCaM-4 Promoter Is Mediated in Part by a GT-1 Box That Interacts with a GT-1-Like Transcription Factor
inferredcites →https://doi.org/10.1104/pp.106.094292openalex-snapshot
Modulation of Ethylene Responses Affects Plant Salt-Stress Responses
inferredcites →https://doi.org/10.1104/pp.111.188789openalex-snapshot
Transcriptional Regulation of ArabidopsisMIR168aandARGONAUTE1Homeostasis in Abscisic Acid and Abiotic Stress Responses
inferredcites →https://doi.org/10.1104/pp.112.193649openalex-snapshot
The Arabidopsis MicroRNA396-GRF1/GRF3 Regulatory Module Acts as a Developmental Regulator in the Reprogramming of Root Cells during Cyst Nematode Infection
inferredcites →https://doi.org/10.1104/pp.15.01407openalex-snapshot
Arabidopsis CML38, a Calcium Sensor That Localizes to Ribonucleoprotein Complexes under Hypoxia Stress
inferredcites →https://doi.org/10.1104/pp.20.00196openalex-snapshot
Calmodulin HvCaM1 Negatively Regulates Salt Tolerance via Modulation of HvHKT1s and HvCAMTA4
inferredcites →https://doi.org/10.1105/tpc.108.059444openalex-snapshot
The Arabidopsis NFYA5 Transcription Factor Is Regulated Transcriptionally and Posttranscriptionally to Promote Drought Resistance
inferredcites →https://doi.org/10.1105/tpc.112.101014openalex-snapshot
Gibberellin Regulates the Arabidopsis Floral Transition through miR156-Targeted SQUAMOSA PROMOTER BINDING–LIKE Transcription Factors
inferredcites →https://doi.org/10.1105/tpc.112.105478openalex-snapshot
Arabidopsis bZIP16 Transcription Factor Integrates Light and Hormone Signaling Pathways to Regulate Early Seedling Development
inferredcites →https://doi.org/10.1105/tpc.113.110668openalex-snapshot
Interacting Glutamate Receptor-Like Proteins in Phloem Regulate Lateral Root Initiation in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.114.134163openalex-snapshot
The RING Finger Ubiquitin E3 Ligase SDIR1 Targets SDIR1-INTERACTING PROTEIN1 for Degradation to Modulate the Salt Stress Response and ABA Signaling in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1753-4887.1981.tb06752.xopenalex-snapshot
Proceedings of the National Academy of Sciences of the United States of America
inferredcites →https://doi.org/10.1111/jac.12585openalex-snapshot
Exogenous calcium application enhances salt tolerance of sweet sorghum seedlings
inferredcites →https://doi.org/10.1111/jipb.12013openalex-snapshot
Physiological and Molecular Features of Puccinellia tenuiflora Tolerating Salt and Alkaline‐Salt Stress
inferredcites →https://doi.org/10.1111/jipb.13054openalex-snapshot
Contribution of phenylpropanoid metabolism to plant development and plant–environment interactions
inferredcites →https://doi.org/10.1111/nph.13699openalex-snapshot
Identification and regulation of host genes related to Rice stripe virus symptom production
inferredcites →https://doi.org/10.1111/nph.14920openalex-snapshot
Elucidating the molecular mechanisms mediating plant salt‐stress responses
inferredcites →https://doi.org/10.1111/nph.15331openalex-snapshot
A brassinosteroid responsive miRNA‐target module regulates gibberellin biosynthesis and plant development
inferredcites →https://doi.org/10.1111/pbi.12512openalex-snapshot
Integration of small RNA s, degradome and transcriptome sequencing in hyperaccumulator Sedum alfredii uncovers a complex regulatory network and provides insights into cadmium phytoremediation
inferredcites →https://doi.org/10.1111/pbi.12940openalex-snapshot
Chromosome‐based survey sequencing reveals the genome organization of wild wheat progenitor Triticum dicoccoides
inferredcites →https://doi.org/10.1111/pbi.13026openalex-snapshot
Integrated transcriptome, small RNA and degradome sequencing approaches provide insights into Ascochyta blight resistance in chickpea
inferredcites →https://doi.org/10.1111/pce.14119openalex-snapshot
The phenylpropanoid pathway inhibitor piperonylic acid induces broad‐spectrum pest and disease resistance in plants
inferredcites →https://doi.org/10.1111/ppl.12067openalex-snapshot
Glycine betaine‐mediated potentiation of HSP gene expression involves calcium signaling pathways in tobacco exposed to NaCl stress
inferredcites →https://doi.org/10.1111/ppl.12724openalex-snapshot
An apple NAC transcription factor enhances salt stress tolerance by modulating the ethylene response
inferredcites →https://doi.org/10.1111/tpj.13637openalex-snapshot
micro RNA 159‐targetedSl GAMYB transcription factors are required for fruit set in tomato
inferredcites →https://doi.org/10.1126/science.1085242openalex-snapshot
Role of MicroRNAs in Plant and Animal Development
inferredcites →https://doi.org/10.1146/annurev-arplant-050718-100005openalex-snapshot
Salt Tolerance Mechanisms of Plants
inferredcites →https://doi.org/10.1146/annurev.arplant.53.091401.143329openalex-snapshot
S ALT AND D ROUGHT S TRESS S IGNAL T RANSDUCTION IN P LANTS
inferredcites →https://doi.org/10.1186/1471-2229-13-210openalex-snapshot
miR394 and LCR are involved in Arabidopsis salt and drought stress responses in an abscisic acid-dependent manner
inferredcites →https://doi.org/10.1186/s12864-015-1760-5openalex-snapshot
Identification and transcriptomic profiling of genes involved in increasing sugar content during salt stress in sweet sorghum leaves
inferredcites →https://doi.org/10.1242/dev.043067openalex-snapshot
Control of cell proliferation in Arabidopsis thaliana by microRNA miR396
inferredcites →https://doi.org/10.1371/journal.pone.0141888openalex-snapshot
GsCML27, a Gene Encoding a Calcium-Binding Ef-Hand Protein from Glycine soja, Plays Differential Roles in Plant Responses to Bicarbonate, Salt and Osmotic Stresses
inferredcites →https://doi.org/10.14348/molcells.2016.2188openalex-snapshot
A Role for Arabidopsis miR399f in Salt, Drought, and ABA Signaling
inferredcites →https://doi.org/10.15252/embr.201642704openalex-snapshot
The NLR protein SUMM2 senses the disruption of an immune signaling MAP kinase cascade via CRCK3
inferredcites →https://doi.org/10.3389/fpls.2018.01038openalex-snapshot
Plant Small Non-coding RNAs and Their Roles in Biotic Stresses
inferredcites →https://doi.org/10.3389/fpls.2019.00716openalex-snapshot
Abscisic Acid Regulates Auxin Distribution to Mediate Maize Lateral Root Development Under Salt Stress
inferredcites →https://doi.org/10.3389/fpls.2019.01169openalex-snapshot
The Glutamate Receptor-Like Protein GLR3.7 Interacts With 14-3-3ω and Participates in Salt Stress Response in Arabidopsis thaliana
inferredcites →https://doi.org/10.3389/fpls.2021.665439openalex-snapshot
Identification and Functional Characterization of Plant MiRNA Under Salt Stress Shed Light on Salinity Resistance Improvement Through MiRNA Manipulation in Crops
inferredcites →https://doi.org/10.3390/agronomy11091751openalex-snapshot
Molecular Manipulation of the MiR396/GRF Expression Module Alters the Salt Stress Response of Arabidopsis thaliana
inferredcites →https://doi.org/10.3390/ijmsopenalex-snapshot
International Journal of Molecular Sciences
inferredcites →https://doi.org/10.3390/ijms19103206openalex-snapshot
Plant Hormone Signaling Crosstalks between Biotic and Abiotic Stress Responses
inferredcites →https://doi.org/10.3390/ijms23115917openalex-snapshot
Integrate Small RNA and Degradome Sequencing to Reveal Drought Memory Response in Wheat (Triticum aestivum L.)

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Transgenic Poplar with the Zygophyllum Xanthoxylon Zinc Finger Protein Transcription Factor Zxzf Gene Shows Improved Drought Resistance by Regulating Hormone Signal
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inferred← citeshttps://doi.org/10.1016/j.cj.2025.09.004openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cj.2025.11.018openalex-snapshot
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microRNAs and stress adaptation in grasses: A systematic review
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