On the public citation graph

Tahak1 Promotes Salt Tolerance Via Synergistic Modulation of Auxin Signaling

https://doi.org/10.2139/ssrn.5239872
0 signed · 55 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/s11738-019-2918-6openalex-snapshot
Exogenous hydrogen sulfide alleviates salt stress by improving antioxidant defenses and the salt overly sensitive pathway in wheat seedlings
inferredcites →https://doi.org/10.1016/0014-5793(95)00853-2openalex-snapshot
NTR1 encodes a high affinity oligopeptide transporter in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cell.2009.03.001openalex-snapshot
Auxin: A Trigger for Change in Plant Development
inferredcites →https://doi.org/10.1016/j.cj.2024.06.011openalex-snapshot
Advances in the study of auxin early response genes: Aux/IAA, GH3, and SAUR
inferredcites →https://doi.org/10.1016/j.cub.2018.01.023openalex-snapshot
The FERONIA Receptor Kinase Maintains Cell-Wall Integrity during Salt Stress through Ca2+ Signaling
inferredcites →https://doi.org/10.1016/j.ecoenv.2022.113533openalex-snapshot
Exogenous melatonin mitigates cadmium toxicity through ascorbic acid and glutathione pathway in wheat
inferredcites →https://doi.org/10.1016/j.envexpbot.2021.104689openalex-snapshot
A novel salt responsive PvHAK16 negatively regulates salt tolerance in transgenic Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.envexpbot.2023.105354openalex-snapshot
Hydrogen sulfide alleviates salt stress through auxin signaling in Arabidopsis
inferredcites →https://doi.org/10.1016/j.isci.2024.108830openalex-snapshot
Soil salinization in agriculture: Mitigation and adaptation strategies combining nature-based solutions and bioengineering
inferredcites →https://doi.org/10.1016/j.jbiosc.2010.10.014openalex-snapshot
Rice sodium-insensitive potassium transporter, OsHAK5, confers increased salt tolerance in tobacco BY2 cells
inferredcites →https://doi.org/10.1016/j.jhazmat.2024.136070openalex-snapshot
High-affinity potassium transporter TaHAK1 implicates in cesium tolerance and phytoremediation
inferredcites →https://doi.org/10.1016/j.molp.2016.01.012openalex-snapshot
Potassium Transporter KUP7 Is Involved in K + Acquisition and Translocation in Arabidopsis Root under K + -Limited Conditions
inferredcites →https://doi.org/10.1016/j.molp.2024.01.007openalex-snapshot
Structures and ion transport mechanisms of plant high-affinity potassium transporters
inferredcites →https://doi.org/10.1016/j.plantsci.2020.110465openalex-snapshot
A leucine-rich repeat receptor-like kinase, OsSTLK, modulates salt tolerance in rice
inferredcites →https://doi.org/10.1016/j.plaphy.2010.08.016openalex-snapshot
Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants
inferredcites →https://doi.org/10.1016/j.plaphy.2022.01.001openalex-snapshot
Potassium in plants: Growth regulation, signaling, and environmental stress tolerance
inferredcites →https://doi.org/10.1016/j.plaphy.2022.04.022openalex-snapshot
Salt stress triggers augmented levels of Na+, K+ and ROS alters salt-related gene expression in leaves and roots of tall wheatgrass (Agropyron elongatum)
inferredcites →https://doi.org/10.1016/j.plaphy.2023.107832openalex-snapshot
Wheat type one protein phosphatase promotes salt and osmotic stress tolerance in arabidopsis via auxin-mediated remodelling of the root system
inferredcites →https://doi.org/10.1016/j.plaphy.2023.107921openalex-snapshot
Multiple roles of wheat ferritin genes during stress treatment and TaFER5D-1 as a positive regulator in response to drought and salt tolerance
inferredcites →https://doi.org/10.1016/j.semcdb.2017.07.009openalex-snapshot
Plant HAK/KUP/KT K+ transporters: Function and regulation
inferredcites →https://doi.org/10.1016/j.stress.2024.100652openalex-snapshot
Integrative mechanisms of plant salt tolerance: Biological pathways, phytohormonal regulation, and technological innovations
inferredcites →https://doi.org/10.1016/j.tplants.2020.01.009openalex-snapshot
The CBL–CIPK Calcium Signaling Network: Unified Paradigm from 20 Years of Discoveries
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.xinn.2020.100017openalex-snapshot
Mechanisms of Plant Responses and Adaptation to Soil Salinity
inferredcites →https://doi.org/10.1016/s1369-5266(03)00085-2openalex-snapshot
Regulation of ion homeostasis under salt stress
inferredcites →https://doi.org/10.1023/a:1015207114117openalex-snapshot
Auxin-responsive gene expression: genes, promoters and regulatory factors
inferredcites →https://doi.org/10.1038/s41467-021-26907-3openalex-snapshot
Global predictions of primary soil salinization under changing climate in the 21st century
inferredcites →https://doi.org/10.1038/s41467-024-52963-6openalex-snapshot
Arabidopsis HAK5 under low K+ availability operates as PMF powered high-affinity K+ transporter
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/10.1093/jxb/eraa212openalex-snapshot
Arabidopsis K+ transporter HAK5-mediated high-affinity root K+ uptake is regulated by protein kinases CIPK1 and CIPK9
inferredcites →https://doi.org/10.1093/jxb/eraa241openalex-snapshot
Auxin-mediated responses under salt stress: from developmental regulation to biotechnological applications
inferredcites →https://doi.org/10.1093/plcell/koac292openalex-snapshot
The cell biology of primary cell walls during salt stress
inferredcites →https://doi.org/10.1093/plcell/koad317openalex-snapshot
Root branching under high salinity requires auxin-independent modulation of LATERAL ORGAN BOUNDARY DOMAIN 16 function
inferredcites →https://doi.org/10.1104/pp.114.246520openalex-snapshot
The Role of a Potassium Transporter OsHAK5 in Potassium Acquisition and Transport from Roots to Shoots in Rice at Low Potassium Supply Levels
inferredcites →https://doi.org/10.1104/pp.17.01713openalex-snapshot
The ARF7 and ARF19 Transcription Factors Positively Regulate PHOSPHATE STARVATION RESPONSE1 in Arabidopsis Roots
inferredcites →https://doi.org/10.1105/tpc.9.12.2281openalex-snapshot
The HAK1 gene of barley is a member of a large gene family and encodes a high-affinity potassium transporter.
inferredcites →https://doi.org/10.1111/j.1365-3040.2009.02041.xopenalex-snapshot
Reactive oxygen species homeostasis and signalling during drought and salinity stresses
inferredcites →https://doi.org/10.1111/jpi.12727openalex-snapshot
Melatonin promotes potassium deficiency tolerance by regulating HAK1 transporter and its upstream transcription factor NAC71 in wheat
inferredcites →https://doi.org/10.1111/nph.14920openalex-snapshot
Elucidating the molecular mechanisms mediating plant salt‐stress responses
inferredcites →https://doi.org/10.1111/pbi.13699openalex-snapshot
The genome sequence provides insights into salt tolerance of Achnatherum splendens (Gramineae), a constructive species of alkaline grassland
inferredcites →https://doi.org/10.1111/pce.12585openalex-snapshot
Rice potassium transporter O s HAK 1 is essential for maintaining potassium‐mediated growth and functions in salt tolerance over low and high potassium concentration ranges
inferredcites →https://doi.org/10.1111/pce.14180openalex-snapshot
OsHyPRP06 / R3L1 regulates root system development and salt tolerance via apoplastic ROS homeostasis in rice ( Oryza sativa L.)
inferredcites →https://doi.org/10.1111/ppl.13453openalex-snapshot
Molecular insights into the role of plant transporters in salt stress response
inferredcites →https://doi.org/10.2307/3870585openalex-snapshot
The HAK1 Gene of Barley Is a Member of a Large Gene Family and Encodes a High-Affinity Potassium Transporter
inferredcites →https://doi.org/10.3389/fphys.2017.00509openalex-snapshot
The Role of Na+ and K+ Transporters in Salt Stress Adaptation in Glycophytes
inferredcites →https://doi.org/10.3389/fpls.2019.00080openalex-snapshot
Plant Salinity Stress: Many Unanswered Questions Remain
inferredcites →https://doi.org/10.3389/fpls.2019.01361openalex-snapshot
Tissue-Specific Regulation of Na+ and K+ Transporters Explains Genotypic Differences in Salinity Stress Tolerance in Rice
inferredcites →https://doi.org/10.3389/fpls.2020.00139openalex-snapshot
Characterization of the bZIP Transcription Factor Family in Pepper (Capsicum annuum L.): CabZIP25 Positively Modulates the Salt Tolerance
inferredcites →https://doi.org/10.3390/agronomy10070938openalex-snapshot
Insights into the Physiological and Biochemical Impacts of Salt Stress on Plant Growth and Development
inferredcites →https://doi.org/10.3390/cells11172761openalex-snapshot
Roles of Auxin in the Growth, Development, and Stress Tolerance of Horticultural Plants
inferredcites →https://doi.org/10.3390/ijms19010259openalex-snapshot
Aux/IAA Gene Family in Plants: Molecular Structure, Regulation, and Function
inferredcites →https://doi.org/10.3390/ijms21155292openalex-snapshot
Halophytic Hordeum brevisubulatum HbHAK1 Facilitates Potassium Retention and Contributes to Salt Tolerance
inferredcites →https://doi.org/10.3390/ijms22084089openalex-snapshot
OsARF11 Promotes Growth, Meristem, Seed, and Vein Formation during Rice Plant Development
inferredcites →https://doi.org/10.3390/ijms23105551openalex-snapshot
Genome-Wide Identification of Gramineae Brassinosteroid-Related Genes and Their Roles in Plant Architecture and Salt Stress Adaptation
inferredcites →https://doi.org/10.3390/metabo11110724openalex-snapshot
Soil Salinity, a Serious Environmental Issue and Plant Responses: A Metabolomics Perspective
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.