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Suffer from drought to withstand the cold

0 signed · 18 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.

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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/s13595-021-01052-5openalex-snapshot

Interaction of drought and frost in tree ecophysiology: rethinking the timing of risks

inferredcites →https://doi.org/10.1016/j.plantsci.2018.02.012openalex-snapshot

ShCIGT, a Trihelix family gene, mediates cold and drought tolerance by interacting with SnRK1 in tomato

inferredcites →https://doi.org/10.1016/j.tplants.2016.07.009openalex-snapshot

Recognizing Plant Defense Priming

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/10.1093/plphys/kiab050openalex-snapshot

Transcription-associated metabolomic adjustments in maize occur during combined drought and cold stress

inferredcites →https://doi.org/10.1104/pp.104.040295openalex-snapshot

From Laboratory to Field. Using Information from Arabidopsis to Engineer Salt, Cold, and Drought Tolerance in Crops

inferredcites →https://doi.org/10.1104/pp.16.01815openalex-snapshot

Monitoring of Freezing Dynamics in Trees: A Simple Phase Shift Causes Complexity

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/10.3389/fpls.2014.00170openalex-snapshot

The transcriptional regulatory network in the drought response and its crosstalk in abiotic stress responses including drought, cold, and heat

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.4693224openalex-extracted

1+1<2: Evidence from Combined Stress of Sesuvium Portulacastrum L

inferred← citeshttps://doi.org/10.1016/j.fcr.2023.109083openalex-snapshot

Enhancing crop resilience: Understanding the role of drought priming in wheat stress response

inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109404openalex-snapshot

1+1<2: Combined effect of low temperature stress and salt stress on Sesuvium portulacastrum L.

inferred← citeshttps://doi.org/10.1080/15592324.2026.2716979openalex-snapshot

Laying the blueprint of abiotic stress tolerance: an analysis on the complexities of the stress matrix

inferred← citeshttps://doi.org/10.1093/jxb/erac089openalex-snapshot

Molecular basis of priming-induced acquired tolerance to multiple abiotic stresses in plants

inferred← citeshttps://doi.org/10.1111/gcb.16400openalex-snapshot

Projections of leaf turgor loss point shifts under future climate change scenarios

inferred← citeshttps://doi.org/10.1111/nph.70218openalex-snapshot

A guide to understanding and measuring photosynthetic induction: considerations and recommendations

inferred← citeshttps://doi.org/10.3389/fpls.2025.1635078openalex-snapshot

Advanced imaging-enabled understanding of cell wall remodeling mechanisms mediating plant drought stress tolerance

inferred← citeshttps://doi.org/10.3390/agronomy13092368openalex-snapshot

Combined Cold and Drought Stress-Induced Response of Photosynthesis and Osmotic Adjustment in Elymus nutans Griseb.

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