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231225s2020 xx |||||o 00| ||eng c |
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|a 10.1093/jxb/eraa004
|2 doi
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|a pubmed24n1021.xml
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|a (DE-627)NLM306474387
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|a (NLM)32053194
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Tagliani, Andrea
|e verfasserin
|4 aut
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| 245 |
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|a The calcineurin β-like interacting protein kinase CIPK25 regulates potassium homeostasis under low oxygen in Arabidopsis
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|c 2020
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
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|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 14.05.2021
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|a Date Revised 11.11.2023
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|a published: Print
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|a Citation Status MEDLINE
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|a © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Experimental Biology.
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|a Hypoxic conditions often arise from waterlogging and flooding, affecting several aspects of plant metabolism, including the uptake of nutrients. We identified a member of the CALCINEURIN β-LIKE INTERACTING PROTEIN KINASE (CIPK) family in Arabidopsis, CIPK25, which is induced in the root endodermis under low-oxygen conditions. A cipk25 mutant exhibited higher sensitivity to anoxia in conditions of potassium limitation, suggesting that this kinase is involved in the regulation of potassium uptake. Interestingly, we found that CIPK25 interacts with AKT1, the major inward rectifying potassium channel in Arabidopsis. Under anoxic conditions, cipk25 mutant seedlings were unable to maintain potassium concentrations at wild-type levels, suggesting that CIPK25 likely plays a role in modulating potassium homeostasis under low-oxygen conditions. In addition, cipk25 and akt1 mutants share similar developmental defects under waterlogging, further supporting an interplay between CIPK25 and AKT1
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Anoxia
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|a Arabidopsis
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|a CIPK25
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|a calcineurin β-like interacting protein kinase
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|a hypoxia
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|a potassium homeostasis
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|a Arabidopsis Proteins
|2 NLM
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|a Potassium Channels
|2 NLM
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|a AT5G25110 protein, Arabidopsis
|2 NLM
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|a EC 2.7.11.1
|2 NLM
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|a Protein Serine-Threonine Kinases
|2 NLM
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|a EC 2.7.11.1
|2 NLM
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| 650 |
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|a Calcineurin
|2 NLM
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| 650 |
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|a EC 3.1.3.16
|2 NLM
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| 650 |
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|a Potassium
|2 NLM
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| 650 |
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|a RWP5GA015D
|2 NLM
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| 650 |
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|a Oxygen
|2 NLM
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| 650 |
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|a S88TT14065
|2 NLM
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| 700 |
1 |
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|a Tran, Anh Nguyet
|e verfasserin
|4 aut
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| 700 |
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|a Novi, Giacomo
|e verfasserin
|4 aut
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| 700 |
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|a Di Mambro, Riccardo
|e verfasserin
|4 aut
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| 700 |
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|a Pesenti, Michele
|e verfasserin
|4 aut
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| 700 |
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|a Sacchi, Gian Attilio
|e verfasserin
|4 aut
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| 700 |
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|a Perata, Pierdomenico
|e verfasserin
|4 aut
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| 700 |
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|a Pucciariello, Chiara
|e verfasserin
|4 aut
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| 773 |
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|i Enthalten in
|t Journal of experimental botany
|d 1985
|g 71(2020), 9 vom: 09. Mai, Seite 2678-2689
|w (DE-627)NLM098182706
|x 1460-2431
|7 nnns
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| 773 |
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|g volume:71
|g year:2020
|g number:9
|g day:09
|g month:05
|g pages:2678-2689
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|u http://dx.doi.org/10.1093/jxb/eraa004
|3 Volltext
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|d 71
|j 2020
|e 9
|b 09
|c 05
|h 2678-2689
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