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Genome-wide identification of soybean potassium transporter KUP/HAK/KT gene family and functional characterization of GmHAK5 under salt stress

https://doi.org/10.2139/ssrn.7412517
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inferredcites →https://doi.org/10.1002/ece3.299openalex-snapshot
Genome‐wide and molecular evolution analysis of the P oplar KT / HAK / KUP potassium transporter gene family
inferredcites →https://doi.org/10.1007/bf00331014openalex-snapshot
The promoter of TL-DNA gene 5 controls the tissue-specific expression of chimaeric genes carried by a novel type of Agrobacterium binary vector
inferredcites →https://doi.org/10.1007/s00438-008-0377-7openalex-snapshot
KT/HAK/KUP potassium transporters gene family and their whole-life cycle expression profile in rice (Oryza sativa)
inferredcites →https://doi.org/10.1007/s10725-020-00684-3openalex-snapshot
Plant transporters: roles in stress responses and effects on growth and development
inferredcites →https://doi.org/10.1007/s11033-012-1700-2openalex-snapshot
Genome-wide analysis and identification of HAK potassium transporter gene family in maize (Zea mays L.)
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.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.2023.09.010openalex-snapshot
TBtools-II: A “one for all, all for one” bioinformatics platform for biological big-data mining
inferredcites →https://doi.org/10.1016/j.plantsci.2020.110736openalex-snapshot
GmAKT1 is involved in K+ uptake and Na+/K+ homeostasis in Arabidopsis and soybean plants
inferredcites →https://doi.org/10.1016/j.plantsci.2025.112734openalex-snapshot
Over-expression of CsHAK4 from tea plant (Camellia sinensis L.) negatively regulates high salt tolerance in transgenic Arabidopsis
inferredcites →https://doi.org/10.1016/j.plaphy.2021.12.019openalex-snapshot
Light regulation of potassium in 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.2022.07.011openalex-snapshot
Potassium in plant physiological adaptation to abiotic stresses
inferredcites →https://doi.org/10.1016/j.tplants.2011.08.002openalex-snapshot
The role of mitochondrial respiration in salinity tolerance
inferredcites →https://doi.org/10.1016/j.xplc.2020.100052openalex-snapshot
The Potassium Transporter OsHAK5 Alters Rice Architecture via ATP-Dependent Transmembrane Auxin Fluxes
inferredcites →https://doi.org/10.1017/qpb.2025.10openalex-snapshot
Potassium homeostasis and signalling: from the whole plant to the subcellular level
inferredcites →https://doi.org/10.1038/nature08670openalex-snapshot
Genome sequence of the palaeopolyploid soybean
inferredcites →https://doi.org/10.1038/nprot.2006.286openalex-snapshot
Rapid, transient expression of fluorescent fusion proteins in tobacco plants and generation of stably transformed plants
inferredcites →https://doi.org/10.1038/nprot.2007.141openalex-snapshot
Agrobacterium rhizogenes-mediated transformation of soybean to study root biology
inferredcites →https://doi.org/10.1038/s41467-024-45086-5openalex-snapshot
The mechanism of low blue light-induced leaf senescence mediated by GmCRY1s in soybean
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/s43016-021-00322-9openalex-snapshot
A meta-analysis of projected global food demand and population at risk of hunger for the period 2010–2050
inferredcites →https://doi.org/10.1042/ebc20230089openalex-snapshot
Malate dehydrogenase in plants: evolution, structure, and a myriad of functions
inferredcites →https://doi.org/10.1073/pnas.0707912104openalex-snapshot
A protein phosphorylation/dephosphorylation network regulates a plant potassium channel
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/erw288openalex-snapshot
Functional characterization of the ribosome biogenesis factors PES, BOP1, and WDR12 (PeBoW), and mechanisms of defective cell growth and proliferation caused by PeBoW deficiency in Arabidopsis
inferredcites →https://doi.org/10.1093/mp/sss125openalex-snapshot
Characterization of Ion Contents and Metabolic Responses to Salt Stress of Different Arabidopsis AtHKT1;1 Genotypes and Their Parental Strains
inferredcites →https://doi.org/10.1093/plphys/kiab028openalex-snapshot
Insights into the mechanisms of transport and regulation of the arabidopsis high-affinity K+ transporter HAK51
inferredcites →https://doi.org/10.1104/pp.017004openalex-snapshot
Legumes: Importance and Constraints to Greater Use
inferredcites →https://doi.org/10.1104/pp.104.057216openalex-snapshot
The Potassium Transporter AtHAK5 Functions in K+ Deprivation-Induced High-Affinity K+ Uptake and AKT1 K+ Channel Contribution to K+ Uptake Kinetics in Arabidopsis Roots
inferredcites →https://doi.org/10.1104/pp.110.154369openalex-snapshot
High-Affinity K+ Transport in Arabidopsis: AtHAK5 and AKT1 Are Vital for Seedling Establishment and Postgermination Growth under Low-Potassium Conditions
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/10.1105/tpc.10.1.51openalex-snapshot
AtKUP1: An Arabidopsis Gene Encoding High-Affinity Potassium Transport Activity
inferredcites →https://doi.org/10.1111/j.1744-7909.2008.00760.xopenalex-snapshot
Salt Tolerance in Soybean
inferredcites →https://doi.org/10.1111/nph.14920openalex-snapshot
Elucidating the molecular mechanisms mediating plant salt‐stress responses
inferredcites →https://doi.org/10.1111/nph.15864openalex-snapshot
Energy costs of salt tolerance in crop plants
inferredcites →https://doi.org/10.1111/nph.20207openalex-snapshot
Potassium extrusion by plant cells: evolution from an emergency valve to a driver of long‐distance transport
inferredcites →https://doi.org/10.1111/pbi.70042openalex-snapshot
GmAKT1 ‐mediated K + absorption positively modulates soybean salt tolerance by GmCBL9 ‐ GmCIPK6 complex
inferredcites →https://doi.org/10.1111/pce.70398openalex-snapshot
Root Epidermis‐Specific Expression of Potassium Transporter AtHAK5 Enhances Potassium Acquisition and Salt Tolerance
inferredcites →https://doi.org/10.1111/tpj.12302openalex-snapshot
Pescadillo plays an essential role in plant cell growth and survival by modulating ribosome biogenesis
inferredcites →https://doi.org/10.1146/annurev-arplant-042916-040936openalex-snapshot
Genomics, Physiology, and Molecular Breeding Approaches for Improving Salt Tolerance
inferredcites →https://doi.org/10.3390/ijms19123969openalex-snapshot
Genome-Wide Identification and Analysis of HAK/KUP/KT Potassium Transporters Gene Family in Wheat (Triticum aestivum L.)
inferredcites →https://doi.org/10.3390/metabo11110724openalex-snapshot
Soil Salinity, a Serious Environmental Issue and Plant Responses: A Metabolomics Perspective
inferredcites →https://doi.org/10.3410/b1-47openalex-snapshot
The role of malate in plant homeostasis
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