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Snakin-1 affects reactive oxygen species and ascorbic acid levels and hormone balance in potato
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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/bf00268703openalex-snapshot
On the specificity of the alcoholic, acidic silver nitrate reagent for the histochemical localization of ascorbic acid
inferredcites →https://doi.org/10.1007/s10059-010-0082-3openalex-snapshot
Methods for detection and measurement of hydrogen peroxide inside and outside of cells
inferredcites →https://doi.org/10.1007/s12230-016-9494-8openalex-snapshot
Genome-wide Analysis of the Snakin/GASA Gene Family in Solanum tuberosum cv. Kennebec
inferredcites →https://doi.org/10.1007/s12374-014-0497-zopenalex-snapshot
Salt- and ABA-inducible OsGASR1 is involved in salt tolerance
inferredcites →https://doi.org/10.1016/j.bbagen.2014.12.020openalex-snapshot
ROS-mediated redox signaling during cell differentiation in plants
inferredcites →https://doi.org/10.1016/j.cub.2011.03.013openalex-snapshot
Hormone Signalling Crosstalk in Plant Growth Regulation
inferredcites →https://doi.org/10.1016/j.jplph.2011.06.010openalex-snapshot
Overexpression of GASA5 increases the sensitivity of Arabidopsis to heat stress
inferredcites →https://doi.org/10.1016/j.molp.2015.09.011openalex-snapshot
A Pivotal Role of DELLAs in Regulating Multiple Hormone Signals
inferredcites →https://doi.org/10.1016/j.pbi.2015.11.009openalex-snapshot
Redox regulation in shoot growth, SAM maintenance and flowering
inferredcites →https://doi.org/10.1016/j.plantsci.2013.07.004openalex-snapshot
Redox control of plant growth and development
inferredcites →https://doi.org/10.1016/j.plaphy.2004.05.012openalex-snapshot
New aspects of sterol biosynthesis in growth and development of higher plants
inferredcites →https://doi.org/10.1016/j.plaphy.2016.02.021openalex-snapshot
Differential hormonal and gene expression dynamics in two inbred sunflower lines with contrasting dormancy level
inferredcites →https://doi.org/10.1016/j.redox.2016.11.006openalex-snapshot
Reactive oxygen species signaling and stomatal movement: Current updates and future perspectives
inferredcites →https://doi.org/10.1016/j.tplants.2004.08.009openalex-snapshot
Reactive oxygen gene network of plants
inferredcites →https://doi.org/10.1016/j.tplants.2011.03.007openalex-snapshot
ROS signaling: the new wave?
inferredcites →https://doi.org/10.1016/s0163-7827(02)00047-4openalex-snapshot
The role of sterols in plant growth and development
inferredcites →https://doi.org/10.1016/s0304-3940(02)01423-4openalex-snapshot
Assumption-free analysis of quantitative real-time polymerase chain reaction (PCR) data
inferredcites →https://doi.org/10.1016/s1369-5266(00)00069-8openalex-snapshot
Ascorbic acid: metabolism and functions of a multi-facetted molecule
inferredcites →https://doi.org/10.1016/s1369-5266(00)80070-9openalex-snapshot
Ascorbic acid: metabolism and functions of a multi-facetted molecule
inferredcites →https://doi.org/10.1021/cr300163eopenalex-snapshot
Cysteine-Mediated Redox Signaling: Chemistry, Biology, and Tools for Discovery
inferredcites →https://doi.org/10.1023/a:1005938624418openalex-snapshot
Expression patterns of GASA genes in Arabidopsis thaliana: the GASA4 gene is up-regulated by gibberellins in meristematic regions
inferredcites →https://doi.org/10.1038/nbt.2450openalex-snapshot
Differential analysis of gene regulation at transcript resolution with RNA-seq
inferredcites →https://doi.org/10.1038/nmeth.1226openalex-snapshot
Mapping and quantifying mammalian transcriptomes by RNA-Seq
inferredcites →https://doi.org/10.1042/bst0150017openalex-snapshot
The use of the Escherichia coli β-glucuronidase gene as a gene fusion marker for studies of gene expression in higher plants
inferredcites →https://doi.org/10.1046/j.1365-3040.2002.00859.xopenalex-snapshot
Activation of an oxidative burst is a general feature of sensitive plants exposed to the air pollutant ozone
inferredcites →https://doi.org/10.1046/j.1365-313x.1997.11061187.xopenalex-snapshot
Subcellular localization of H2O2 in plants. H2O2 accumulation in papillae and hypersensitive response during the barley—powdery mildew interaction
inferredcites →https://doi.org/10.1080/07352689.2018.1528409openalex-snapshot
Function and Compensatory Mechanisms Among the Components of the Chloroplastic Redox Network
inferredcites →https://doi.org/10.1080/10409230008984166openalex-snapshot
Ascorbic Acid in Plants: Biosynthesis and Function
inferredcites →https://doi.org/10.1093/jxb/eri285openalex-snapshot
Housekeeping gene selection for real-time RT-PCR normalization in potato during biotic and abiotic stress
inferredcites →https://doi.org/10.1093/jxb/erl010openalex-snapshot
Modulation of plant morphology, root architecture, and cell structure by low vitamin C in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/jxb/ert021openalex-snapshot
GASA14 regulates leaf expansion and abiotic stress resistance by modulating reactive oxygen species accumulation
inferredcites →https://doi.org/10.1093/jxb/erv089openalex-snapshot
Interplay between reactive oxygen species and hormones in the control of plant development and stress tolerance
inferredcites →https://doi.org/10.1093/mp/ssp040openalex-snapshot
New GATEWAY vectors for High Throughput Analyses of Protein–Protein Interactions by Bimolecular Fluorescence Complementation
inferredcites →https://doi.org/10.1093/mp/sst141openalex-snapshot
The Arabidopsis Cysteine-Rich GASA5 Is a Redox-Active Metalloprotein that Suppresses Gibberellin Responses
inferredcites →https://doi.org/10.1093/nar/30.9.e36openalex-snapshot
Relative expression software tool (REST(C)) for group-wise comparison and statistical analysis of relative expression results in real-time PCR
inferredcites →https://doi.org/10.1093/nar/gkw1138openalex-snapshot
PANTHER version 11: expanded annotation data from Gene Ontology and Reactome pathways, and data analysis tool enhancements
inferredcites →https://doi.org/10.1094/mpmi-03-12-0075-ropenalex-snapshot
Transgenic Expression ofTobacco mosaic virusCapsid and Movement Proteins Modulate Plant Basal Defense and Biotic Stress Responses inNicotiana tabacum
inferredcites →https://doi.org/10.1094/mpmi-23-3-0340openalex-snapshot
Ascorbic Acid Deficiency in Arabidopsis Induces Constitutive Priming That is Dependent on Hydrogen Peroxide, Salicylic Acid, and the NPR1 Gene
inferredcites →https://doi.org/10.1094/mpmi.1999.12.1.16openalex-snapshot
Snakin-1, a Peptide from Potato That Is Active Against Plant Pathogens
inferredcites →https://doi.org/10.1104/pp.007062openalex-snapshot
l -Ascorbic Acid Is Accumulated in Source Leaf Phloem and Transported to Sink Tissues in Plants
inferredcites →https://doi.org/10.1104/pp.109.139352openalex-snapshot
Evidence for a Role of Gibberellins in Salicylic Acid-Modulated Early Plant Responses to Abiotic Stress in Arabidopsis Seeds
inferredcites →https://doi.org/10.1104/pp.111.186544openalex-snapshot
Potato Snakin-1 Gene Silencing Affects Cell Division, Primary Metabolism, and Cell Wall Composition
inferredcites →https://doi.org/10.1104/pp.119.3.897openalex-snapshot
The Arabidopsis dwarf1 Mutant Is Defective in the Conversion of 24-Methylenecholesterol to Campesterol in Brassinosteroid Biosynthesis1
inferredcites →https://doi.org/10.1104/pp.122.3.657openalex-snapshot
Expression of Aluminum-Induced Genes in Transgenic Arabidopsis Plants Can Ameliorate Aluminum Stress and/or Oxidative Stress
inferredcites →https://doi.org/10.1105/tpc.10.10.1677openalex-snapshot
The Arabidopsis DIMINUTO/DWARF1 Gene Encodes a Protein Involved in Steroid Synthesis
inferredcites →https://doi.org/10.1105/tpc.140930openalex-snapshot
Arabidopsis Mutants Reveal Multiple Roles for Sterols in Plant Development
inferredcites →https://doi.org/10.1111/j.1364-3703.2008.00469.xopenalex-snapshot
Overexpression of snakin‐1 gene enhances resistance to Rhizoctonia solani and Erwinia carotovora in transgenic potato plants
inferredcites →https://doi.org/10.1111/j.1365-2621.1989.tb08607.xopenalex-snapshot
Ascorbic Acid and Protein Content of Potatoes in Relation to Tuber Anatomy
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02917.xopenalex-snapshot
The gibberellin‐induced, cysteine‐rich protein GIP2 from Petunia hybrida exhibits in planta antioxidant activity
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03707.xopenalex-snapshot
OsGSR1 is involved in crosstalk between gibberellins and brassinosteroids in rice
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04390.xopenalex-snapshot
The Arabidopsis cysteine-rich protein GASA4 promotes GA responses and exhibits redox activity in bacteria and in planta
inferredcites →https://doi.org/10.1111/j.1399-3054.2009.01313.xopenalex-snapshot
ROS in plant development
inferredcites →https://doi.org/10.1111/j.1399-3054.2009.01326.xopenalex-snapshot
ROS in biotic interactions
inferredcites →https://doi.org/10.1146/annurev-cellbio-101011-155741openalex-snapshot
Hormonal Interactions in the Regulation of Plant Development
inferredcites →https://doi.org/10.1146/annurev.arplant.55.031903.141616openalex-snapshot
BIOSYNTHESIS AND ACCUMULATION OF STEROLS
inferredcites →https://doi.org/10.1146/annurev.arplant.55.031903.141701openalex-snapshot
REACTIVE OXYGEN SPECIES: Metabolism, Oxidative Stress, and Signal Transduction
inferredcites →https://doi.org/10.1155/2013/795964openalex-snapshot
L-Ascorbic Acid: A Multifunctional Molecule Supporting Plant Growth and Development
inferredcites →https://doi.org/10.1186/1471-2164-11-681openalex-snapshot
De novo assembled expressed gene catalog of a fast-growing Eucalyptus tree produced by Illumina mRNA-Seq
inferredcites →https://doi.org/10.1371/journal.pbio.0020311openalex-snapshot
Hormonal Regulation of Plant Growth and Development
inferredcites →https://doi.org/10.1371/journal.pone.0041008openalex-snapshot
Nuclear Import and Dimerization of Tomato ASR1, a Water Stress-Inducible Protein Exclusive to Plants
inferredcites →https://doi.org/10.1371/journal.pone.0061987openalex-snapshot
Reducing AsA Leads to Leaf Lesion and Defence Response in Knock-Down of the AsA Biosynthetic Enzyme GDP-D-Mannose Pyrophosphorylase Gene in Tomato Plant
inferredcites →https://doi.org/10.3389/fpls.2016.01299openalex-snapshot
Reactive Oxygen Species (ROS): Beneficial Companions of Plants’ Developmental Processes
inferredcites →https://doi.org/10.3389/fpls.2018.02006openalex-snapshot
Vitamin C Content in Fruits: Biosynthesis and Regulation
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Mapping and Validation of a New Quantitative Trait Loci (Qtl) for Fruit Size in Watermelon (Citrullus Lanatus)
inferred← citeshttps://doi.org/10.1007/s00299-020-02557-5openalex-snapshot
Potato Snakin-1: an antimicrobial player of the trade-off between host defense and development
inferred← citeshttps://doi.org/10.1007/s00299-023-03108-4openalex-snapshot
Unveiling the defensive role of Snakin-3, a member of the subfamily III of Snakin/GASA peptides in potatoes
inferred← citeshttps://doi.org/10.1007/s00344-023-11194-7openalex-snapshot
Plant Peptides Involved in Abiotic and Biotic Stress Responses and Reactive Oxygen Species (ROS) Signaling
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inferred← citeshttps://doi.org/10.1007/s11033-023-08734-5openalex-snapshot
Snakins: antimicrobial potential and prospects of genetic engineering for enhanced disease resistance in plants
inferred← citeshttps://doi.org/10.1007/s11816-020-00652-3openalex-snapshot
Expression of antimicrobial peptide snakin-1 confers effective protection in rice against sheath blight pathogen, Rhizoctonia solani
inferred← citeshttps://doi.org/10.1016/b978-0-12-822137-2.00018-7openalex-snapshot
Wild Relatives and Modern Plant Breeding Technologies
inferred← citeshttps://doi.org/10.1016/j.alit.2019.10.007openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cj.2026.09.010openalex-snapshot
Small phytopeptides: rising stars in broad-spectrum plant defense and sustainable crop protection
inferred← citeshttps://doi.org/10.1016/j.genrep.2020.100766openalex-snapshot
Antimicrobial peptides Snakin/GASA gene family in sorghum (Sorghum bicolor): Genome-wide identification and bioinformatics analyses
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.139058openalex-snapshot
Identification of the cysteine-rich transmembrane module CYSTM family in upland cotton and functional analysis of GhCYSTM5_A in cold and drought stresses
inferred← citeshttps://doi.org/10.1016/j.indcrop.2020.112902openalex-snapshot
Panax notoginseng snakin gene increases resistance to Fusarium solani in transgenic tobacco
inferred← citeshttps://doi.org/10.1016/j.jplph.2022.153696openalex-snapshot
Subcellular dynamics and protein-protein interactions of plant sucrose transporters
inferred← citeshttps://doi.org/10.1016/j.molimm.2019.07.023openalex-snapshot
Isolation of cypress gibberellin-regulated protein: Analysis of its structural features and IgE binding competition with homologous allergens
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112576openalex-snapshot
SlHBP2 enhances tomato defense through OPDA signaling by boosting antioxidant machinery and regulating ROS in Pseudomonas infection
inferred← citeshttps://doi.org/10.1016/j.scienta.2023.112054openalex-snapshot
Mapping and validation of a new quantitative trait locus (QTL) for fruit size in watermelon (Citrullus lanatus)
inferred← citeshttps://doi.org/10.1021/acsomega.4c11339openalex-snapshot
Plant Defense Peptides: Exploring the Structure–Function Correlation for Potential Applications in Drug Design and Therapeutics
inferred← citeshttps://doi.org/10.1093/hr/uhab060openalex-snapshot
Snakin-2 interacts with cytosolic glyceraldehyde-3-phosphate dehydrogenase 1 to inhibit sprout growth in potato tubers
inferred← citeshttps://doi.org/10.1093/jxb/erab265openalex-snapshot
Stress effects on the reactive oxygen species-dependent regulation of plant growth and development
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Argentinian potato leafroll virus P0 protein: Novel activities for a previously known suppressor
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The StABI5-StCAT1 Module Regulates Potato Resistance to Early Blight Through the ROS Signaling Pathway
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The Cysteine-Rich Peptide Snakin-2 Negatively Regulates Tubers Sprouting through Modulating Lignin Biosynthesis and H2O2 Accumulation in Potato
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A GASA Protein Family Gene, CmGEG, Inhibits Petal Growth in Chrysanthemum
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The Stylo Cysteine-Rich Peptide SgSnakin1 Is Involved in Aluminum Tolerance through Enhancing Reactive Oxygen Species Scavenging
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Overexpression of DWF1 Enhances Low-Nitrogen Stress Tolerance in Potato Plants
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Additional file 1 of The study on interacting factors and functions of GASA6 in Jatropha curcas L.
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Additional file 2 of The study on interacting factors and functions of GASA6 in Jatropha curcas L.
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