On the public citation graph

Physiological roles of ERD10 in abiotic stresses and seed germination of Arabidopsis

https://doi.org/10.1007/s00299-009-0813-0
0 signed · 109 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.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/bf00028874openalex-snapshot
Cloning of cDNAs for genes that are early-responsive to dehydration stress (ERDs) inArabidopsis thaliana L.: identification of three ERDs as HSP cognate genes
inferredcites →https://doi.org/10.1007/bf01279351openalex-snapshot
The specialized chalazal endosperm inArabidopsis thaliana andLepidium virginicum (Brassicaceae)
inferredcites →https://doi.org/10.1016/0014-5793(93)80727-copenalex-snapshot
Characterization of two cDNAs (ERD11 and ERD13) for dehydration‐inducible genes that encode putative glutathione S‐transferases in Arabidopsis thaliana L
inferredcites →https://doi.org/10.1016/j.bbrc.2008.11.156openalex-snapshot
Modulations of AtGSTF10 expression induce stress tolerance and BAK1-mediated cell death
inferredcites →https://doi.org/10.1016/j.tplants.2003.10.012openalex-snapshot
POPP the question: what do LEA proteins do?
inferredcites →https://doi.org/10.1016/j.tplants.2004.12.012openalex-snapshot
Organization of cis-acting regulatory elements in osmotic- and cold-stress-responsive promoters
inferredcites →https://doi.org/10.1016/j.tplants.2007.07.002openalex-snapshot
Cold stress regulation of gene expression in plants
inferredcites →https://doi.org/10.1016/s0005-2736(98)00007-8openalex-snapshot
ERD6, a cDNA clone for an early dehydration-induced gene of Arabidopsis, encodes a putative sugar transporter
inferredcites →https://doi.org/10.1016/s1369-5266(01)00219-9openalex-snapshot
Seed dormancy and germination
inferredcites →https://doi.org/10.1016/s1369-5266(03)00092-xopenalex-snapshot
Regulatory network of gene expression in the drought and cold stress responses
inferredcites →https://doi.org/10.1093/jxb/ern155openalex-snapshot
The relationship of drought-related gene expression in Arabidopsis thaliana to hormonal and environmental factors
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a078588openalex-snapshot
Characterization of Two cDNAs (ERD10 and ERD14) Corresponding to Genes That Respond Rapidly to Dehydration Stress in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcj059openalex-snapshot
Endosperm-limited Brassicaceae Seed Germination: Abscisic Acid Inhibits Embryo-induced Endosperm Weakening of Lepidium sativum (cress) and Endosperm Rupture of Cress and Arabidopsis thaliana
inferredcites →https://doi.org/10.1096/fj.04-1584revopenalex-snapshot
The role of structural disorder in the function of RNA and protein chaperones
inferredcites →https://doi.org/10.1104/pp.011171openalex-snapshot
The binding of Maize DHN1 to Lipid Vesicles. Gain of Structure and Lipid Specificity
inferredcites →https://doi.org/10.1104/pp.106.079848openalex-snapshot
Structural Investigation of Disordered Stress Proteins. Comparison of Full-Length Dehydrins with Isolated Peptides of Their Conserved Segments
inferredcites →https://doi.org/10.1104/pp.108.118208openalex-snapshot
Chaperone Activity of ERD10 and ERD14, Two Disordered Stress-Related Plant Proteins
inferredcites →https://doi.org/10.1104/pp.118.4.1233openalex-snapshot
A Gene Encoding Proline Dehydrogenase Is Not Only Induced by Proline and Hypoosmolarity, but Is Also Developmentally Regulated in the Reproductive Organs of Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.003483openalex-snapshot
Arabidopsis Transcriptome Profiling Indicates That Multiple Regulatory Pathways Are Activated during Cold Acclimation in Addition to the CBF Cold Response Pathway[W]
inferredcites →https://doi.org/10.1105/tpc.106.042713openalex-snapshot
Rapid Transcriptome Changes Induced by Cytosolic Ca2+ Transients Reveal ABRE-Related Sequences as Ca2+-Responsive cis Elements in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1095-8339.1971.tb02153.xopenalex-snapshot
Seed structure and the taxonomy of the Cruciferae
inferredcites →https://doi.org/10.1111/j.1365-3040.2005.01348.xopenalex-snapshot
Phosphorylation regulated ion‐binding is a property shared by the acidic subclass dehydrins
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02773.xopenalex-snapshot
Light activates the degradation of PIL5 protein to promote seed germination through gibberellin in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02883.xopenalex-snapshot
Identification of plant cytoskeleton‐interacting proteins by screening for actin stress fiber association in mammalian fibroblasts
inferredcites →https://doi.org/10.1111/j.1399-3054.2009.01304.xopenalex-snapshot
Constitutive activation of stress‐inducible genes in a brassinosteroid‐insensitive 1 (bri1) mutant results in higher tolerance to cold
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/10.1186/1471-2229-8-13openalex-snapshot
Light has a specific role in modulating Arabidopsis gene expression at low temperature
inferredcites →https://doi.org/10.1186/1471-2229-8-87openalex-snapshot
Transcriptional responses of Arabidopsis thaliana plants to As (V) stress
inferredcites →https://doi.org/10.1186/gb-2004-5-8-r53openalex-snapshot
Phylogenetic profiling of the Arabidopsis thalianaproteome: what proteins distinguish plants from other organisms?

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.4135723openalex-extracted
Exploring Drought-Responsive Crucial Genes in Sorghum
inferred← citeshttps://doi.org/10.1002/9783527694570.ch6openalex-snapshot
Abiotic Stress Response in Plants: Role of Cytoskeleton
inferred← citeshttps://doi.org/10.1007/s00299-021-02757-7openalex-snapshot
Alfalfa (Medicago sativa L.) MsCML46 gene encoding calmodulin-like protein confers tolerance to abiotic stress in tobacco
inferred← citeshttps://doi.org/10.1007/s00468-016-1410-9openalex-snapshot
Overexpression of an SKn-dehydrin gene from Eucalyptus globulus and Eucalyptus nitens enhances tolerance to freezing stress in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s00468-017-1529-3openalex-snapshot
Overexpression of three novel CBF transcription factors from Eucalyptus globulus improves cold tolerance on transgenic Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s10142-018-0614-zopenalex-snapshot
Heterologous expression of Brassica juncea annexin, AnnBj2 confers salt tolerance and ABA insensitivity in transgenic tobacco seedlings
inferred← citeshttps://doi.org/10.1007/s10725-019-00563-6openalex-snapshot
Quantitative proteomic analysis of Malus halliana exposed to salt-alkali mixed stress reveals alterations in energy metabolism and stress regulation
inferred← citeshttps://doi.org/10.1007/s11103-015-0423-xopenalex-snapshot
RETRACTED ARTICLE: Brassica RNA binding protein ERD4 is involved in conferring salt, drought tolerance and enhancing plant growth in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11103-016-0574-4openalex-snapshot
Retraction note to: Brassica RNA binding protein ERD4 is involved in conferring salt, drought tolerance and enhancing plant growth in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s11105-013-0642-8openalex-snapshot
Differential Expression of Genes for Tolerance to Salt Stress in Common Bean (Phaseolus vulgaris L.)
inferred← citeshttps://doi.org/10.1007/s11105-026-01720-8openalex-snapshot
A DREB-like Transcription Factor from Ocimum sanctum L., OscDREB1, Regulates Plant Growth and Confers Abiotic Stress Tolerance in Transgenic Tobacco
inferred← citeshttps://doi.org/10.1007/s11240-016-0961-1openalex-snapshot
Establishment of an in vitro propagation and transformation system of Balanites aegyptiaca
inferred← citeshttps://doi.org/10.1007/s11248-011-9577-8openalex-snapshot
Stress-inducible expression of barley Hva1 gene in transgenic mulberry displays enhanced tolerance against drought, salinity and cold stress
inferred← citeshttps://doi.org/10.1007/s11295-015-0938-yopenalex-snapshot
Genome-wide identification, characterization, and expression analysis of the dehydrin gene family in Asian pear (Pyrus pyrifolia)
inferred← citeshttps://doi.org/10.1007/s12104-011-9297-2openalex-snapshot
Full backbone assignment and dynamics of the intrinsically disordered dehydrin ERD14
inferred← citeshttps://doi.org/10.1007/s12374-016-0366-zopenalex-snapshot
Suppressor of bri1-120 mutant allele revealed interrelated and independent actions of brassinosteroid and light signaling
inferred← citeshttps://doi.org/10.1007/s13258-013-0088-2openalex-snapshot
Genome-wide expression profiles of contrasting inbred lines of Chinese cabbage, Chiifu and Kenshin, under temperature stress
inferred← citeshttps://doi.org/10.1016/j.bbagen.2019.129506openalex-snapshot
Dehydrin ERD14 activates glutathione transferase Phi9 in Arabidopsis thaliana under osmotic stress
inferred← citeshttps://doi.org/10.1016/j.compbiomed.2012.02.002openalex-snapshot
Extracting plants core genes responding to abiotic stresses by penalized matrix decomposition
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2020.104223openalex-snapshot
Ectopic expression of BrALDH7B2 gene encoding an antiquitin from Brassica rapa confers tolerance to abiotic stresses and improves photosynthetic performance under salt stress in tobacco
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.105143openalex-snapshot
Overexpression of MsNAC51 from alfalfa confers drought tolerance in tobacco
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2025.106266openalex-snapshot
Barley nuclear cap-binding complex subunits, HvCBP20 and HvCBP80, play distinct roles in drought adaptation at reproductive phase of development
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.131020openalex-snapshot
AmDHN4, a winter accumulated SKn-type dehydrin from Ammopiptanthus mongolicus, and regulated by AmWRKY45, enhances the tolerance of Arabidopsis to low temperature and osmotic stress
inferred← citeshttps://doi.org/10.1016/j.jia.2026.02.028openalex-snapshot
VvGA2ox5 positively improves drought tolerance in grapevine by activating the hormone signal transduction pathway
inferred← citeshttps://doi.org/10.1016/j.jprot.2018.11.008openalex-snapshot
Temporal proteomics of Arabidopsis plasma membrane during cold- and de-acclimation
inferred← citeshttps://doi.org/10.1016/j.plantsci.2015.05.009openalex-snapshot
Cold tolerance in rice germinating seeds revealed by deep RNAseq analysis of contrasting indica genotypes
inferred← citeshttps://doi.org/10.1016/j.plantsci.2016.06.006openalex-snapshot
ABI3 mediates dehydration stress recovery response in Arabidopsis thaliana by regulating expression of downstream genes
inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.02.022openalex-snapshot
Wheat expansin gene TaEXPA2 is involved in conferring plant tolerance to Cd toxicity
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112441openalex-snapshot
Genome-wide analysis of apple histone acetyltransferases reveals the regulatory roles of MdHAG1 and MdHAM1 in response to abiotic stresses
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112536openalex-snapshot
Co-overexpression of OsSIZ1 and LtRCA in Arabidopsis thaliana improves heat, drought, and salt tolerance
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110598openalex-snapshot
WITHDRAWN: PgGRAS52, a stress-responsive GRAS transcription factor from pearl millet, enhances drought and salinity tolerance via functional interplay with PgIDDs
inferred← citeshttps://doi.org/10.1016/j.scienta.2021.109930openalex-snapshot
Genome-wide identification and expression profiling of the dehydrin gene family in Actinidia chinensis
inferred← citeshttps://doi.org/10.1016/j.scienta.2021.110848openalex-snapshot
Overexpression of watermelon ClWRKY20 in transgenic Arabidopsis improves salt and low-temperature tolerance
inferred← citeshttps://doi.org/10.1016/j.scienta.2022.111822openalex-snapshot
SWATH-based quantitative proteomics gives insight into a significant proteome shift in UCB-1 pistachio rootstock under salt stress
inferred← citeshttps://doi.org/10.1038/s41598-017-15986-2openalex-snapshot
In vivo evidence for homo- and heterodimeric interactions of Arabidopsis thaliana dehydrins AtCOR47, AtERD10, and AtRAB18
inferred← citeshttps://doi.org/10.1038/srep28306openalex-snapshot
Comparative proteomic study of Arabidopsis mutants mpk4 and mpk6
inferred← citeshttps://doi.org/10.1080/15592324.2022.2105021openalex-snapshot
Characteristics analysis of Early Responsive to Dehydration genes in Arabidopsis thaliana ( AtERD )
inferred← citeshttps://doi.org/10.1093/pcp/pcu118openalex-snapshot
A Subset of Arabidopsis RAV Transcription Factors Modulates Drought and Salt Stress Responses Independent of ABA
inferred← citeshttps://doi.org/10.1101/2025.10.27.684818openalex-snapshot
Identification of dehydrin protein complexes in vivo reveals functional interactions of LEA5 with OSCA3, PIP2B and PLD α 1 in plant water-deficit stress
inferred← citeshttps://doi.org/10.1111/jipb.12149openalex-snapshot
Retracted: Identification, Occurrence, and Validation of DRE and ABRE Cis‐Regulatory Motifs in the Promoter Regions of Genes of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/nph.20446openalex-snapshot
Dual and spatially resolved drought responses in the Arabidopsis leaf mesophyll revealed by single‐cell transcriptomics
inferred← citeshttps://doi.org/10.1111/pce.12894openalex-snapshot
Multifaceted role of cycling DOF factor 3 (CDF3) in the regulation of flowering time and abiotic stress responses in Arabidopsis
inferred← citeshttps://doi.org/10.1111/pce.14317openalex-snapshot
Ethylene responsive factor34 mediates stress‐induced leaf senescence by regulating salt stress‐responsive genes
inferred← citeshttps://doi.org/10.1111/tpj.12759openalex-snapshot
The GI – CDF module of Arabidopsis affects freezing tolerance and growth as well as flowering
inferred← citeshttps://doi.org/10.1111/tpj.16925openalex-snapshot
The transcription factor ERF110 promotes cold tolerance by directly regulating sugar and sterol biosynthesis in citrus
inferred← citeshttps://doi.org/10.1186/1471-2164-14-764openalex-snapshot
The broccoli (Brassica oleracea) phloem tissue proteome
inferred← citeshttps://doi.org/10.1186/1471-2164-15-431openalex-snapshot
Genome-wide analysis of alternative splicing of pre-mRNA under salt stress in Arabidopsis
inferred← citeshttps://doi.org/10.1186/1471-2229-12-140openalex-snapshot
Identification of the dehydrin gene family from grapevine species and analysis of their responsiveness to various forms of abiotic and biotic stress
inferred← citeshttps://doi.org/10.1186/s12870-020-02418-zopenalex-snapshot
Transcriptomic analysis of poco1, a mitochondrial pentatricopeptide repeat protein mutant in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1371/journal.pone.0161970openalex-snapshot
A Novel Method for Assessing the Chaperone Activity of Proteins
inferred← citeshttps://doi.org/10.1371/journal.pone.0248089openalex-snapshot
Genetic mapping and identification of a QTL determining tolerance to freezing stress in Fragaria vesca L.
inferred← citeshttps://doi.org/10.14232/phd.658openalex-snapshot
An enumeration-based putative dyad predicting algorithm for promoter analysis in plants
inferred← citeshttps://doi.org/10.1515/biolog-2017-0080openalex-snapshot
Identification and expression analyses of two lotus (Nelumbo nucifera) dehydrin genes in response to adverse temperatures, ABA and IAA treatments
inferred← citeshttps://doi.org/10.20868/upm.thesis.35207openalex-snapshot
Cycling Dof Factors: Molecular and functional characterization of Arabidopsis thaliana AtCDF3 and tomato (Solanum lycopersicum L.) SlCDF3 in response to abiotic stress
inferred← citeshttps://doi.org/10.2174/1874294701105010009openalex-snapshot
Diversity of Dehydrins in Oleae europaea Plants Exposed to Stress
inferred← citeshttps://doi.org/10.3389/fpls.2014.00583openalex-snapshot
Dissecting the cryoprotection mechanisms for dehydrins
inferred← citeshttps://doi.org/10.3389/fpls.2017.00297openalex-snapshot
VaERD15, a Transcription Factor Gene Associated with Cold-Tolerance in Chinese Wild Vitis amurensis
inferred← citeshttps://doi.org/10.3389/fpls.2017.01999openalex-snapshot
Functional and Structural Characterization of a Receptor-Like Kinase Involved in Germination and Cell Expansion in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2021.788938openalex-snapshot
AnDHN, a Dehydrin Protein From Ammopiptanthus nanus, Mitigates the Negative Effects of Drought Stress in Plants
inferred← citeshttps://doi.org/10.3389/fpls.2022.866054openalex-snapshot
Divergence in the Regulation of the Salt Tolerant Response Between Arabidopsis thaliana and Its Halophytic Relative Eutrema salsugineum by mRNA Alternative Polyadenylation
inferred← citeshttps://doi.org/10.3389/fpls.2022.936958openalex-snapshot
A Chromosome Level Genome Assembly of a Winter Turnip Rape (Brassica rapa L.) to Explore the Genetic Basis of Cold Tolerance
inferred← citeshttps://doi.org/10.3389/fpls.2022.975073openalex-snapshot
TMT proteomics analysis of a pseudocereal crop, quinoa (Chenopodium quinoa Willd.), during seed maturation
inferred← citeshttps://doi.org/10.3389/fpls.2023.1135552openalex-snapshot
Ectopic expression of DnaJ type-I protein homolog of Vigna aconitifolia (VaDJI) confers ABA insensitivity and multiple stress tolerance in transgenic tobacco plants
inferred← citeshttps://doi.org/10.3390/f11090978openalex-snapshot
Overexpression of BplERD15 Enhances Drought Tolerance in Betula platyphylla Suk.
inferred← citeshttps://doi.org/10.3390/horticulturae7120527openalex-snapshot
Gene Expression Analysis in Cold Stress Conditions Reveals BBX20 and CLO as Potential Biomarkers for Cold Tolerance in Almond
inferred← citeshttps://doi.org/10.3390/horticulturae8111022openalex-snapshot
Low Temperature Conditioning Reduced the Chilling Injury by Regulating Expression of the Dehydrin Genes in Postharvest Huangguan Pear (Pyrus bretschneideri Rehd. cv. Huangguan)
inferred← citeshttps://doi.org/10.3390/ijms20020394openalex-snapshot
Expression Pattern and Function Analysis of AtPPRT1, a Novel Negative Regulator in ABA and Drought Stress Responses in Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms22158172openalex-snapshot
Characterization of the Heat-Stable Proteome during Seed Germination in Arabidopsis with Special Focus on LEA Proteins
inferred← citeshttps://doi.org/10.3390/ijms222312619openalex-snapshot
Plant Dehydrins: Expression, Regulatory Networks, and Protective Roles in Plants Challenged by Abiotic Stress
inferred← citeshttps://doi.org/10.3390/ijms241914655openalex-snapshot
The miRNA-mRNA Regulatory Modules of Pinus massoniana Lamb. in Response to Drought Stress
inferred← citeshttps://doi.org/10.3390/plants10091878openalex-snapshot
Transcriptomic and Proteomic Analysis of Drought Stress Response in Opium Poppy Plants during the First Week of Germination
inferred← citeshttps://doi.org/10.3923/ijb.2018.30.35openalex-snapshot
Genotypic Variation Affects the Efficiency of the Genetic Transformation Process in Balanites aegyptiaca
inferred← citeshttps://doi.org/10.6084/m9.figshare.12291836openalex-snapshot
Additional file 1 of Transcriptomic analysis of poco1, a mitochondrial pentatricopeptide repeat protein mutant in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.6084/m9.figshare.12291845openalex-snapshot
Additional file 2 of Transcriptomic analysis of poco1, a mitochondrial pentatricopeptide repeat protein mutant in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.6084/m9.figshare.12291848openalex-snapshot
Additional file 3 of Transcriptomic analysis of poco1, a mitochondrial pentatricopeptide repeat protein mutant in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.6084/m9.figshare.12291854openalex-snapshot
Additional file 4 of Transcriptomic analysis of poco1, a mitochondrial pentatricopeptide repeat protein mutant in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.6084/m9.figshare.12291860openalex-snapshot
Additional file 5 of Transcriptomic analysis of poco1, a mitochondrial pentatricopeptide repeat protein mutant in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.6084/m9.figshare.12291863openalex-snapshot
Additional file 6 of Transcriptomic analysis of poco1, a mitochondrial pentatricopeptide repeat protein mutant in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.6084/m9.figshare.12291866openalex-snapshot
Additional file 7 of Transcriptomic analysis of poco1, a mitochondrial pentatricopeptide repeat protein mutant in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.6084/m9.figshare.12291869openalex-snapshot
Additional file 8 of Transcriptomic analysis of poco1, a mitochondrial pentatricopeptide repeat protein mutant in Arabidopsis thaliana
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.