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ICE1: a regulator of cold-induced transcriptome and freezing tolerance in Arabidopsis

https://doi.org/10.1101/gad.1077503
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What this work says

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

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AnArabidopsisGene Family Encoding DRE/CRT Binding Proteins Involved in Low-Temperature-Responsive Gene Expression
inferredcites →https://doi.org/10.1007/bf00017731openalex-snapshot
Cloning and characterization of a cold-and ABA-inducible Arabidopsis gene
inferredcites →https://doi.org/10.1007/bf00018452openalex-snapshot
cDNA sequence analysis and expression of two cold-regulated genes ofArabidopsis thaliana
inferredcites →https://doi.org/10.1016/s1369-5266(00)00167-9openalex-snapshot
Temperature sensing and cold acclimation
inferredcites →https://doi.org/10.1023/a:1013316816955openalex-snapshot
Bar-expressing peppermint (Mentha × Piperita L. var. Black Mitcham) plants are highly resistant to the glufosinate herbicide Liberty
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Low temperature regulation of theArabidopsisCBF family of AP2 transcriptional activators as an early step in cold‐inducedCORgene expression
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00709.xopenalex-snapshot
Three ethylene‐responsive transcription factors in tobacco with distinct transactivation functions
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.01048.xopenalex-snapshot
Antisense inhibition of protein phosphatase 2C accelerates cold acclimation in Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1432-1327.1999.00349.xopenalex-snapshot
Transcription factors and their genes in higher plants
inferredcites →https://doi.org/10.1073/pnas.112040099openalex-snapshot
An Arabidopsis mutation in translation elongation factor 2 causes superinduction of CBF/DREB1 transcription factor genes but blocks the induction of their downstream targets under low temperatures
inferredcites →https://doi.org/10.1073/pnas.172399299openalex-snapshot
RNA helicase-like protein as an early regulator of transcription factors for plant chilling and freezing tolerance
inferredcites →https://doi.org/10.1073/pnas.94.3.1035openalex-snapshot
Arabidopsis thaliana CBF1 encodes an AP2 domain-containing transcriptional activator that binds to the C-repeat/DRE, a cis-acting DNA regulatory element that stimulates transcription in response to low temperature and water deficit
inferredcites →https://doi.org/10.1073/pnas.95.13.7799openalex-snapshot
eskimo1 mutants of Arabidopsis are constitutively freezing-tolerant
inferredcites →https://doi.org/10.1074/jbc.273.41.26857openalex-snapshot
Unique Mode of GCC Box Recognition by the DNA-binding Domain of Ethylene-responsive Element-binding Factor (ERF Domain) in Plant
inferredcites →https://doi.org/10.1093/emboj/21.11.2692openalex-snapshot
LOS2, a genetic locus required for cold‐responsive gene transcription encodes a bi‐functional enolase
inferredcites →https://doi.org/10.1093/genetics/138.3.849openalex-snapshot
Molecular evolution of the plant R regulatory gene family.
inferredcites →https://doi.org/10.1093/jxb/47.3.291openalex-snapshot
The molecular biology of plant acclimation to low temperature
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a078903openalex-snapshot
Plant Transcription Factors
inferredcites →https://doi.org/10.1101/gad.866801openalex-snapshot
The Arabidopsis HOS1 gene negatively regulates cold signal transduction and encodes a RING finger protein that displays cold-regulated nucleo–cytoplasmic partitioning
inferredcites →https://doi.org/10.1104/pp.003442openalex-snapshot
Heterology Expression of the Arabidopsis C-Repeat/Dehydration Response Element Binding Factor 1 Gene Confers Elevated Tolerance to Chilling and Oxidative Stresses in Transgenic Tomato
inferredcites →https://doi.org/10.1104/pp.114.2.591openalex-snapshot
Proline Accumulation and Salt-Stress-Induced Gene Expression in a Salt-Hypersensitive Mutant of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.89.1.375openalex-snapshot
Molecular Cloning and Relationship to Freezing Tolerance of Cold-Acclimation-Specific Genes of Alfalfa
inferredcites →https://doi.org/10.1104/pp.99.2.519openalex-snapshot
DNA Sequence Analysis of a Complementary DNA for Cold-Regulated Arabidopsis Gene cor15 and Characterization of the COR 15 Polypeptide
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.010127openalex-snapshot
Repression Domains of Class II ERF Transcriptional Repressors Share an Essential Motif for Active Repression
inferredcites →https://doi.org/10.1105/tpc.10.7.1151openalex-snapshot
HOS1, a Genetic Locus Involved in Cold-Responsive Gene Expression in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.10.8.1391openalex-snapshot
Two Transcription Factors, DREB1 and DREB2, with an EREBP/AP2 DNA Binding Domain Separate Two Cellular Signal Transduction Pathways in Drought- and Low-Temperature-Responsive Gene Expression, Respectively, in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.11.5.875openalex-snapshot
The sfr6 Mutation in Arabidopsis Suppresses Low-Temperature Induction of Genes Dependent on the CRT/DRE Sequence Motif
inferredcites →https://doi.org/10.1105/tpc.11.7.1337openalex-snapshot
The TRANSPARENT TESTA GLABRA1 Locus, Which Regulates Trichome Differentiation and Anthocyanin Biosynthesis in Arabidopsis, Encodes a WD40 Repeat Protein
inferredcites →https://doi.org/10.1105/tpc.12.9.1619openalex-snapshot
anthocyanin1 of Petunia Encodes a Basic Helix-Loop-Helix Protein That Directly Activates Transcription of Structural Anthocyanin Genes
inferredcites →https://doi.org/10.1105/tpc.13.8.1959openalex-snapshot
Repression Domains of Class II ERF Transcriptional Repressors Share an Essential Motif for Active Repression
inferredcites →https://doi.org/10.1105/tpc.6.2.251openalex-snapshot
A novel cis-acting element in an Arabidopsis gene is involved in responsiveness to drought, low-temperature, or high-salt stress.
inferredcites →https://doi.org/10.1105/tpc.9.11.1935openalex-snapshot
Genetic analysis of osmotic and cold stress signal transduction in Arabidopsis: interactions and convergence of abscisic acid-dependent and abscisic acid-independent pathways.
inferredcites →https://doi.org/10.1126/science.280.5360.104openalex-snapshot
Arabidopsis CBF1 Overexpression Induces COR Genes and Enhances Freezing Tolerance
inferredcites →https://doi.org/10.1126/stke.2002.140.pl10openalex-snapshot
Screening for Gene Regulation Mutants by Bioluminescence Imaging
inferredcites →https://doi.org/10.1146/annurev.arplant.41.1.187openalex-snapshot
Cold Acclimation And Freezing Stress Tolerance: Role Of Protein Metabolism
inferredcites →https://doi.org/10.1146/annurev.arplant.50.1.571openalex-snapshot
PLANT COLD ACCLIMATION: Freezing Tolerance Genes and Regulatory Mechanisms
inferredcites →https://doi.org/10.1146/annurev.cellbio.16.1.653openalex-snapshot
The Myc/Max/Mad Network and the Transcriptional Control of Cell Behavior

What points at this work

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

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inferred← citeshttps://doi.org/10.1007/978-981-13-1244-1_1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00018-008-7535-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00122-003-1378-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00122-004-1867-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00122-005-0144-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00122-005-0185-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00122-010-1288-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00122-010-1458-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00122-019-03482-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00122-022-04097-wopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00122-023-04506-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00122-026-05220-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00299-006-0204-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00299-007-0459-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00299-010-0883-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00299-011-1136-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00299-012-1288-yopenalex-snapshot
The constitutive expression of Chrysanthemum dichrum ICE1 in Chrysanthemum grandiflorum improves the level of low temperature, salinity and drought tolerance
inferred← citeshttps://doi.org/10.1007/s00299-014-1655-yopenalex-snapshot
Identification of wheat non-specific lipid transfer proteins involved in chilling tolerance
inferred← citeshttps://doi.org/10.1007/s00299-014-1659-7openalex-snapshot
A wheat aminocyclopropane-1-carboxylate oxidase gene, TaACO1, negatively regulates salinity stress in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00299-016-1980-4openalex-snapshot
Isolation and functional characterization of a cold responsive phosphatidylinositol transfer-associated protein, ZmSEC14p, from maize (Zea may L.)
inferred← citeshttps://doi.org/10.1007/s00299-016-2036-5openalex-snapshot
Wheat bHLH-type transcription factor gene TabHLH1 is crucial in mediating osmotic stresses tolerance through modulating largely the ABA-associated pathway
inferred← citeshttps://doi.org/10.1007/s00299-016-2073-0openalex-snapshot
Breeding approaches and genomics technologies to increase crop yield under low-temperature stress
inferred← citeshttps://doi.org/10.1007/s00299-019-02376-3openalex-snapshot
Cold acclimation by the CBF–COR pathway in a changing climate: Lessons from Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00299-019-02398-xopenalex-snapshot
The ICE-like transcription factor HbICE2 is involved in jasmonate-regulated cold tolerance in the rubber tree (Hevea brasiliensis)
inferred← citeshttps://doi.org/10.1007/s00299-019-02399-wopenalex-snapshot
Cold-inducible MaC2H2s are associated with cold stress response of banana fruit via regulating MaICE1
inferred← citeshttps://doi.org/10.1007/s00299-022-02890-xopenalex-snapshot
StATL2-like could affect growth and cold tolerance of plant by interacting with StCBFs
inferred← citeshttps://doi.org/10.1007/s00299-022-02894-7openalex-snapshot
Abscisic acid induces the expression of AsKIN during the recovery period of garlic cryopreservation
inferred← citeshttps://doi.org/10.1007/s00299-022-02949-9openalex-snapshot
StICE1 enhances plant cold tolerance by directly upregulating StLTI6A expression
inferred← citeshttps://doi.org/10.1007/s00299-023-03117-3openalex-snapshot
A novel R2R3-MYB transcription factor PbMYB1L of Pyrus bretschneideri regulates cold tolerance and anthocyanin accumulation
inferred← citeshttps://doi.org/10.1007/s00299-024-03382-wopenalex-snapshot
Ectopic expression of HvbHLH132 from hulless barley reduces cold tolerance in transgenic Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00299-026-03797-7openalex-snapshot
CsPRR7 negatively regulates cold tolerance by repressing CsCBF3 in tea plants
inferred← citeshttps://doi.org/10.1007/s00299-026-03807-8openalex-snapshot
Vernalization-responsive intronless genes in faba bean and the development of KASP markers
inferred← citeshttps://doi.org/10.1007/s00299-026-03973-9openalex-snapshot
Genome-wide identification and evolutionary analysis of the ERF-VII gene family in the tea plant (Camellia sinensis) and functional characterization of CsRAP2.2 in response to cold stress
inferred← citeshttps://doi.org/10.1007/s00344-020-10252-8openalex-snapshot
Genome-Wide Identification and Expression Analysis of the Barrel Medic (Medicago truncatula) and Alfalfa (Medicago sativa L.) Basic Helix-Loop-Helix Transcription Factor Family Under Salt and Drought Stresses
inferred← citeshttps://doi.org/10.1007/s00344-021-10437-9openalex-snapshot
Comparative Transcriptome Analysis Reveals Potential Gene Modules Associated with Cold Tolerance in Sugarcane (Saccharum officinarum L.)
inferred← citeshttps://doi.org/10.1007/s00344-022-10611-7openalex-snapshot
An Acer palmatum R2R3-MYB Gene, ApMYB77, Confers Freezing and Drought Tolerance in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00344-024-11322-xopenalex-snapshot
Cold Acclimation and Deacclimation Processes in Grapevine Buds: Insights into the Regulation of Cod Hardiness and ICE-CBF-COR Gene Expression
inferred← citeshttps://doi.org/10.1007/s00344-026-12314-9openalex-snapshot
Plant Signal Cross-Talk during Abiotic Stress
inferred← citeshttps://doi.org/10.1007/s00425-004-1351-1openalex-snapshot
Physcomitrella patens is highly tolerant against drought, salt and osmotic stress
inferred← citeshttps://doi.org/10.1007/s00425-004-1475-3openalex-snapshot
Low temperature promotes intron retention in two e-cor genes of durum wheat
inferred← citeshttps://doi.org/10.1007/s00425-005-0012-3openalex-snapshot
SKS6, a multicopper oxidase-like gene, participates in cotyledon vascular patterning during Arabidopsis thaliana development
inferred← citeshttps://doi.org/10.1007/s00425-005-0200-1openalex-snapshot
Expression of SK3-type dehydrin in transporting organs is associated with cold acclimation in Solanum species
inferred← citeshttps://doi.org/10.1007/s00425-006-0446-2openalex-snapshot
Isolation and characterization of a GCN5-interacting protein from Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00425-007-0528-9openalex-snapshot
ERF protein JERF1 that transcriptionally modulates the expression of abscisic acid biosynthesis-related gene enhances the tolerance under salinity and cold in tobacco
inferred← citeshttps://doi.org/10.1007/s00425-010-1279-6openalex-snapshot
Dwarf apple MbDREB1 enhances plant tolerance to low temperature, drought, and salt stress via both ABA-dependent and ABA-independent pathways
inferred← citeshttps://doi.org/10.1007/s00425-011-1353-8openalex-snapshot
Genomic organization, induced expression and promoter activity of a resistance gene analog (PmTNL1) in western white pine (Pinus monticola)
inferred← citeshttps://doi.org/10.1007/s00425-011-1358-3openalex-snapshot
Ectopic expression of a novel peach (Prunus persica) CBF transcription factor in apple (Malus × domestica) results in short-day induced dormancy and increased cold hardiness
inferred← citeshttps://doi.org/10.1007/s00425-011-1416-xopenalex-snapshot
Comparative studies on tolerance of Medicago truncatula and Medicago falcata to freezing
inferred← citeshttps://doi.org/10.1007/s00425-012-1641-yopenalex-snapshot
Physiological and molecular changes in plants grown at low temperatures
inferred← citeshttps://doi.org/10.1007/s00425-013-1944-7openalex-snapshot
Molecular characterization of cold-responsive basic helix-loop-helix transcription factors MabHLHs that interact with MaICE1 in banana fruit
inferred← citeshttps://doi.org/10.1007/s00425-015-2299-zopenalex-snapshot
Early transcriptional changes in Beta vulgaris in response to low temperature
inferred← citeshttps://doi.org/10.1007/s00425-015-2445-7openalex-snapshot
Functional analysis of the Arabidopsis thaliana MUTE promoter reveals a regulatory region sufficient for stomatal-lineage expression
inferred← citeshttps://doi.org/10.1007/s00425-016-2592-5openalex-snapshot
Molecular characterization and evolution of carnivorous sundew (Drosera rotundifolia L.) class V β-1,3-glucanase
inferred← citeshttps://doi.org/10.1007/s00425-019-03222-2openalex-snapshot
Genomic identification of AP2/ERF transcription factors and functional characterization of two cold resistance-related AP2/ERF genes in celery (Apium graveolens L.)
inferred← citeshttps://doi.org/10.1007/s00425-019-03281-5openalex-snapshot
Energy metabolism involved in fertility of the wheat TCMS line YS3038
inferred← citeshttps://doi.org/10.1007/s00425-021-03615-2openalex-snapshot
Identification and functional characterization of a new flavonoid synthase gene MdFLS1 from apple
inferred← citeshttps://doi.org/10.1007/s00425-021-03686-1openalex-snapshot
Elevation of GhDREB1B transcription by a copy number variant significantly improves chilling tolerance in cotton
inferred← citeshttps://doi.org/10.1007/s00425-021-03694-1openalex-snapshot
What if the cold days return? Epigenetic mechanisms in plants to cold tolerance
inferred← citeshttps://doi.org/10.1007/s00425-022-03858-7openalex-snapshot
The network centered on ICEs play roles in plant cold tolerance, growth and development
inferred← citeshttps://doi.org/10.1007/s00425-022-04007-wopenalex-snapshot
Bolstered plant tolerance to low temperatures by overexpressing NAC transcription factors: identification of critical variables by meta-analysis
inferred← citeshttps://doi.org/10.1007/s00425-023-04232-xopenalex-snapshot
A pervasive phosphorylation cascade modulation of plant transcription factors in response to abiotic stress
inferred← citeshttps://doi.org/10.1007/s00425-026-05055-2openalex-snapshot
VaWRKY26 transcription factor from Vitis amurensis negatively regulates plant cold tolerance
inferred← citeshttps://doi.org/10.1007/s00438-005-0047-yopenalex-snapshot
The expression of several Cbf genes at the Fr-A2 locus is linked to frost resistance in wheat
inferred← citeshttps://doi.org/10.1007/s00438-005-0076-6openalex-snapshot
A cluster of 11 CBF transcription factors is located at the frost tolerance locus Fr-A m 2 in Triticum monococcum
inferred← citeshttps://doi.org/10.1007/s00438-008-0335-4openalex-snapshot
Isolation and characterization of cold-regulated transcriptional activator LpCBF3 gene from perennial ryegrass (Lolium perenne L.)
inferred← citeshttps://doi.org/10.1007/s00438-009-0451-9openalex-snapshot
Comparative expression of Cbf genes in the Triticeae under different acclimation induction temperatures
inferred← citeshttps://doi.org/10.1007/s00438-009-0481-3openalex-snapshot
Functional characterization of the Arabidopsis bHLH92 transcription factor in abiotic stress
inferred← citeshttps://doi.org/10.1007/s00438-015-1161-0openalex-snapshot
Dynamic transcriptome analysis reveals AP2/ERF transcription factors responsible for cold stress in rapeseed (Brassica napus L.)
inferred← citeshttps://doi.org/10.1007/s00438-016-1273-1openalex-snapshot
Molecular characterization and functional analysis of the OsPsbR gene family in rice
inferred← citeshttps://doi.org/10.1007/s00468-013-0950-5openalex-snapshot
The ethylene response factor (ERF) genes from Tamarix hispida respond to salt, drought and ABA treatment
inferred← citeshttps://doi.org/10.1007/s00468-016-1463-9openalex-snapshot
Characterization of a cold responsive HbICE1 gene from rubber trees
inferred← citeshttps://doi.org/10.1007/s00468-020-01991-yopenalex-snapshot
Comparative transcriptome combined with morpho-physiological analyses revealed candidate genes potentially for differential cold tolerance in two contrasting apricot (Prunus armeniaca L.) cultivars
inferred← citeshttps://doi.org/10.1007/s00468-020-01994-9openalex-snapshot
Characterization of transcription activation domain of EcaICE1 and its interaction with EcaSIZ1 in Eucalyptus camaldulensis
inferred← citeshttps://doi.org/10.1007/s00497-025-00520-6openalex-snapshot
Potential regulation of cleistogamy in pigeonpea through jasmonic acid and bHLH transcription factor interactions
inferred← citeshttps://doi.org/10.1007/s00709-012-0429-zopenalex-snapshot
Construction of cold induced subtracted cDNA library from Cicer microphyllum and transcript characterization of identified novel wound induced gene
inferred← citeshttps://doi.org/10.1007/s00709-016-1004-9openalex-snapshot
Stress-responsive gene RsICE1 from Raphanus sativus increases cold tolerance in rice
inferred← citeshttps://doi.org/10.1007/s00709-020-01531-yopenalex-snapshot
Hydrogen sulfide is required for salicylic acid–induced chilling tolerance of cucumber seedlings
inferred← citeshttps://doi.org/10.1007/s10059-011-0031-9openalex-snapshot
Regulation of Abiotic Stress Signal Transduction by E3 Ubiquitin Ligases in Arabidopsis
inferred← citeshttps://doi.org/10.1007/s10059-012-0230-zopenalex-snapshot
Genes Encoding Plant-Specific Class III Peroxidases Are Responsible for Increased Cold Tolerance of the brassinosteroid-insensitive 1 Mutant
inferred← citeshttps://doi.org/10.1007/s10142-005-0014-zopenalex-snapshot
Monitoring expression profiles of Arabidopsis genes during cold acclimation and deacclimation using DNA microarrays
inferred← citeshttps://doi.org/10.1007/s10142-006-0030-7openalex-snapshot
Identification of quantitative trait loci and associated candidate genes for low-temperature tolerance in cold-hardy winter wheat
inferred← citeshttps://doi.org/10.1007/s10142-016-0500-5openalex-snapshot
Deep-sequencing transcriptome analysis of field-grown Medicago sativa L. crown buds acclimated to freezing stress
inferred← citeshttps://doi.org/10.1007/s10142-018-0608-xopenalex-snapshot
Transcriptome-wide identification and expression profile analysis of the bHLH family genes in Camellia sinensis
inferred← citeshttps://doi.org/10.1007/s10142-018-0615-yopenalex-snapshot
Transcriptome profiling of short-term response to chilling stress in tolerant and sensitive Oryza sativa ssp. Japonica seedlings
inferred← citeshttps://doi.org/10.1007/s10142-022-00890-4openalex-snapshot
Genome-wide identification and characterization of bHLH family genes from orchardgrass and the functional characterization of DgbHLH46 and DgbHLH128 in drought and salt tolerance
inferred← citeshttps://doi.org/10.1007/s10142-026-01910-3openalex-snapshot
Genome-wide identification and cold stress expression of inducer of CBF expression (ICE) transcription factors in Taraxacum kok-saghyz
inferred← citeshttps://doi.org/10.1007/s10265-020-01195-yopenalex-snapshot
AP2/ERF transcription factors regulate salt-induced chloroplast division in the moss Physcomitrella patens
inferred← citeshttps://doi.org/10.1007/s10265-026-01762-9openalex-snapshot
Overexpression of the Vitis amurensis gene VabHLH015 in Arabidopsis thaliana and grape calli suppresses cold tolerance
inferred← citeshttps://doi.org/10.1007/s10529-006-9214-4openalex-snapshot
Isolated and characterization of a cDNA encoding ethylene-responsive element binding protein (EREBP)/AP2-type protein, RCBF2, in Oryza sativa L.
inferred← citeshttps://doi.org/10.1007/s10535-008-0120-6openalex-snapshot
The relationship between vernalization-and photoperiodically-regulated genes and the development of frost tolerance in wheat and barley
inferred← citeshttps://doi.org/10.1007/s10535-010-0038-7openalex-snapshot
Transcription factors in plants and ABA dependent and independent abiotic stress signalling
inferred← citeshttps://doi.org/10.1007/s10535-010-0113-0openalex-snapshot
Functional characterization of the apple MdSAMDC2 gene by ectopic promoter analysis and over-expression in tobacco
inferred← citeshttps://doi.org/10.1007/s10535-015-0497-yopenalex-snapshot
ICE genes in Arabidopsis thaliana: clinal variation in DNA polymorphism and sequence diversification
inferred← citeshttps://doi.org/10.1007/s10535-016-0648-9openalex-snapshot
Some key physiological and molecular processes of cold acclimation
inferred← citeshttps://doi.org/10.1007/s10535-016-0683-6openalex-snapshot
Signal transduction and biotechnology in response to environmental stresses
inferred← citeshttps://doi.org/10.1007/s10658-015-0745-1openalex-snapshot
Cold Stress-Induced Disease Resistance (SIDR): indirect effects of low temperatures on host-pathogen interactions and disease progress in the grapevine powdery mildew pathosystem
inferred← citeshttps://doi.org/10.1007/s10725-009-9434-4openalex-snapshot
DREB1C from Medicago truncatula enhances freezing tolerance in transgenic M. truncatula and China Rose (Rosa chinensis Jacq.)
inferred← citeshttps://doi.org/10.1007/s10725-014-9985-xopenalex-snapshot
The Arabidopsis E3 ubiquitin ligase HOS1 contributes to auxin biosynthesis in the control of hypocotyl elongation
inferred← citeshttps://doi.org/10.1007/s10725-019-00485-3openalex-snapshot
Identification of the grape basic helix–loop–helix transcription factor family and characterization of expression patterns in response to different stresses
inferred← citeshttps://doi.org/10.1007/s10725-020-00583-7openalex-snapshot
SlHY5 is a necessary regulator of the cold acclimation response in tomato
inferred← citeshttps://doi.org/10.1007/s10725-022-00834-9openalex-snapshot
Genome-wide analysis of invertase gene family in wheat (Triticum aestivum L.) indicates involvement of TaCWINVs in pollen development
inferred← citeshttps://doi.org/10.1007/s10725-024-01248-5openalex-snapshot
Research progress on low-temperature stress response mechanisms and mitigation strategies in plants
inferred← citeshttps://doi.org/10.1007/s10725-024-01253-8openalex-snapshot
Advances in plant response to low-temperature stress
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