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Phosphorylation regulation of nitrogen, phosphorus, and potassium uptake systems in plants
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1873-3468.13473openalex-snapshot
A reevaluation of the contribution of NRT 1.1 to nitrate uptake in Arabidopsis under low‐nitrate supply
inferredcites →https://doi.org/10.1002/jsfa.4700openalex-snapshot
Changes in the efficiency of fertiliser use in China
inferredcites →https://doi.org/10.1002/pmic.200701104openalex-snapshot
Identification of novel proteins and phosphorylation sites in a tonoplast enriched membrane fraction of Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/b84168openalex-snapshot
Molecular Mechanisms Controlling Transmembrane Transport
inferredcites →https://doi.org/10.1007/b95775openalex-snapshot
Regulation and function of ammonium carriers in bacteria, fungi, and plants
inferredcites →https://doi.org/10.1007/s00299-014-1709-1openalex-snapshot
The rice OsAMT1;1 is a proton-independent feedback regulated ammonium transporter
inferredcites →https://doi.org/10.1007/s00425-019-03194-3openalex-snapshot
Rice OsHAK16 functions in potassium uptake and translocation in shoot, maintaining potassium homeostasis and salt tolerance
inferredcites →https://doi.org/10.1007/s10705-006-9042-xopenalex-snapshot
Crop yield, nitrogen uptake and nitrate-nitrogen accumulation in soil as affected by 23 annual applications of fertilizer and manure in the rainfed region of Northwestern China
inferredcites →https://doi.org/10.1007/s11103-004-1965-5openalex-snapshot
Transcriptional regulation and functional properties of Arabidopsis Pht1;4, a high affinity transporter contributing greatly to phosphate uptake in phosphate deprived plants
inferredcites →https://doi.org/10.1007/s11427-018-9503-xopenalex-snapshot
Genetic dissection of root morphological traits as related to potassium use efficiency in rapeseed under two contrasting potassium levels by hydroponics
inferredcites →https://doi.org/10.1016/b978-0-12-473542-2.x5000-7openalex-snapshot
Mineral Nutrition of Higher Plants
inferredcites →https://doi.org/10.1016/j.bbrc.2007.08.177openalex-snapshot
Novel subsets of the Arabidopsis plasmalemma phosphoproteome identify phosphorylation sites in secondary active transporters
inferredcites →https://doi.org/10.1016/j.bbrc.2012.06.019openalex-snapshot
Phosphorylation of the transcriptional regulator MYB44 by mitogen activated protein kinase regulates Arabidopsis seed germination
inferredcites →https://doi.org/10.1016/j.bbrc.2015.01.009openalex-snapshot
AtTGA4, a bZIP transcription factor, confers drought resistance by enhancing nitrate transport and assimilation in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.bpj.2019.10.018openalex-snapshot
Feedforward Control of Plant Nitrate Transporter NRT1.1 Biphasic Adaptive Activity
inferredcites →https://doi.org/10.1016/j.ceca.2021.102447openalex-snapshot
The expression of constitutively active CPK3 impairs potassium uptake and transport in Arabidopsis under low K+ stress
inferredcites →https://doi.org/10.1016/j.cell.2006.06.011openalex-snapshot
A Protein Kinase, Interacting with Two Calcineurin B-like Proteins, Regulates K+ Transporter AKT1 in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cell.2009.07.004openalex-snapshot
CHL1 Functions as a Nitrate Sensor in Plants
inferredcites →https://doi.org/10.1016/j.cj.2022.03.011openalex-snapshot
Rice transcription factors OsLBD37/38/39 regulate nitrate uptake by repressing OsNRT2.1/2.2/2.3 under high-nitrogen conditions
inferredcites →https://doi.org/10.1016/j.cub.2018.08.004openalex-snapshot
Understanding the Molecular Basis of Salt Sequestration in Epidermal Bladder Cells of Chenopodium quinoa
inferredcites →https://doi.org/10.1016/j.devcel.2007.06.009openalex-snapshot
An Essential Role for 14-3-3 Proteins in Brassinosteroid Signal Transduction in Arabidopsis
inferredcites →https://doi.org/10.1016/j.febslet.2007.03.034openalex-snapshot
Molecular mechanisms of ammonium transport and accumulation in plants
inferredcites →https://doi.org/10.1016/j.gloenvcha.2008.10.009openalex-snapshot
The story of phosphorus: Global food security and food for thought
inferredcites →https://doi.org/10.1016/j.jclepro.2019.118718openalex-snapshot
Assessment of greenhouse gas mitigation options for the iron, gold, and potash mining sectors
inferredcites →https://doi.org/10.1016/j.jgg.2016.11.001openalex-snapshot
The OsAMT1.1 gene functions in ammonium uptake and ammonium–potassium homeostasis over low and high ammonium concentration ranges
inferredcites →https://doi.org/10.1016/j.jplph.2014.01.011openalex-snapshot
Molecular biology of K+ transport across the plant cell membrane: What do we learn from comparison between plant species?
inferredcites →https://doi.org/10.1016/j.molp.2015.12.012openalex-snapshot
Complex Regulation of Plant Phosphate Transporters and the Gap between Molecular Mechanisms and Practical Application: What Is Missing?
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.2016.05.004openalex-snapshot
Nitrate Transport, Sensing, and Responses in Plants
inferredcites →https://doi.org/10.1016/j.molp.2021.02.005openalex-snapshot
A transceptor–channel complex couples nitrate sensing to calcium signaling in Arabidopsis
inferredcites →https://doi.org/10.1016/j.molp.2021.06.024openalex-snapshot
A transcription factor STOP1-centered pathway coordinates ammonium and phosphate acquisition in Arabidopsis
inferredcites →https://doi.org/10.1016/j.molp.2022.11.007openalex-snapshot
Genetic improvement toward nitrogen-use efficiency in rice: Lessons and perspectives
inferredcites →https://doi.org/10.1016/j.molp.2022.11.010openalex-snapshot
The MEKK1-MKK1/2-MPK4 cascade phosphorylates and stabilizes STOP1 to confer aluminum resistance in Arabidopsis
inferredcites →https://doi.org/10.1016/j.pbi.2007.08.015openalex-snapshot
Multiple mechanisms modulate brassinosteroid signaling
inferredcites →https://doi.org/10.1016/j.pbi.2009.04.003openalex-snapshot
Physiological functions of mineral macronutrients
inferredcites →https://doi.org/10.1016/j.pbi.2009.05.003openalex-snapshot
Potassium nutrition, sodium toxicity, and calcium signaling: connections through the CBL–CIPK network
inferredcites →https://doi.org/10.1016/j.pbi.2013.03.002openalex-snapshot
Improvement of phosphorus efficiency in rice on the basis of understanding phosphate signaling and homeostasis
inferredcites →https://doi.org/10.1016/j.pbi.2021.102048openalex-snapshot
Fe acquisition at the crossroad of calcium and reactive oxygen species signaling
inferredcites →https://doi.org/10.1016/j.plaphy.2021.08.026openalex-snapshot
The CBL1/9-CIPK23-AKT1 complex is essential for low potassium response in cassava
inferredcites →https://doi.org/10.1016/j.scitotenv.2020.139113openalex-snapshot
Development of fertilizers for enhanced nitrogen use efficiency – Trends and perspectives
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.tplants.2012.04.006openalex-snapshot
Uptake, allocation and signaling of nitrate
inferredcites →https://doi.org/10.1016/j.tplants.2013.08.008openalex-snapshot
A unified nomenclature of NITRATE TRANSPORTER 1/PEPTIDE TRANSPORTER family members in plants
inferredcites →https://doi.org/10.1016/j.tplants.2021.06.011openalex-snapshot
Synergistic and antagonistic pleiotropy of STOP1 in stress tolerance
inferredcites →https://doi.org/10.1016/s0014-5793(01)02096-8openalex-snapshot
An Arabidopsis T‐DNA mutant affected in Nrt2 genes is impaired in nitrate uptake
inferredcites →https://doi.org/10.1016/s0038-0717(00)00209-1openalex-snapshot
Competition for amino acids between wheat roots and rhizosphere microorganisms and the role of amino acids in plant N acquisition
inferredcites →https://doi.org/10.1016/s1360-1385(98)01311-9openalex-snapshot
Molecular and physiological aspects of nitrate uptake in plants
inferredcites →https://doi.org/10.1016/s1534-5807(02)00229-0openalex-snapshot
A Calcium Sensor and Its Interacting Protein Kinase Are Global Regulators of Abscisic Acid Signaling in Arabidopsis
inferredcites →https://doi.org/10.1016/s1671-2927(08)60091-7openalex-snapshot
Recent Advances on the Technologies to Increase Fertilizer Use Efficiency
inferredcites →https://doi.org/10.1016/s1672-6308(08)60096-7openalex-snapshot
Molecular Basis and Regulation of Ammonium Transporter in Rice
inferredcites →https://doi.org/10.1016/s2095-3119(17)61709-xopenalex-snapshot
Transgenic approaches for improving use efficiency of nitrogen, phosphorus and potassium in crops
inferredcites →https://doi.org/10.1023/a:1004744903556openalex-snapshot
A dynamic whole-plant model of integrated metabolism of nitrogen and carbon. 2. Balanced growth driven by C fluxes and regulated by signals from C and N substrate
inferredcites →https://doi.org/10.1038/nature04681openalex-snapshot
Downstream nuclear events in brassinosteroid signalling
inferredcites →https://doi.org/10.1038/nature05579openalex-snapshot
A cytosolic trans-activation domain essential for ammonium uptake
inferredcites →https://doi.org/10.1038/nature13074openalex-snapshot
Crystal structure of the plant dual-affinity nitrate transporter NRT1.1
inferredcites →https://doi.org/10.1038/nature13116openalex-snapshot
Molecular basis of nitrate uptake by the plant nitrate transporter NRT1.1
inferredcites →https://doi.org/10.1038/nplants.2015.15openalex-snapshot
Multiple mechanisms of nitrate sensing by Arabidopsis nitrate transceptor NRT1.1
inferredcites →https://doi.org/10.1038/s41467-022-33420-8openalex-snapshot
Structural basis for the activity regulation of a potassium channel AKT1 from Arabidopsis
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/10.1038/s41477-021-00870-9openalex-snapshot
A type 2C protein phosphatase activates high-affinity nitrate uptake by dephosphorylating NRT2.1
inferredcites →https://doi.org/10.1038/s41477-022-01236-5openalex-snapshot
Regulatory functions of cellular energy sensor SnRK1 for nitrate signalling through NLP7 repression
inferredcites →https://doi.org/10.1038/s41586-018-0415-5openalex-snapshot
Modulating plant growth–metabolism coordination for sustainable agriculture
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01356.xopenalex-snapshot
Expression analysis suggests novel roles for members of the Pht1 family of phosphate transporters in Arabidopsis
inferredcites →https://doi.org/10.1071/fp03087openalex-snapshot
Kinetics of ammonium and nitrate uptake by eucalypt roots and associated proton fluxes measured using ion selective microelectrodes
inferredcites →https://doi.org/10.1073/pnas.0504219102openalex-snapshot
The putative high-affinity nitrate transporter NRT2.1 represses lateral root initiation in response to nutritional cues
inferredcites →https://doi.org/10.1073/pnas.0706386104openalex-snapshot
Functions of OsBZR1 and 14-3-3 proteins in brassinosteroid signaling in rice
inferredcites →https://doi.org/10.1073/pnas.0707912104openalex-snapshot
A protein phosphorylation/dephosphorylation network regulates a plant potassium channel
inferredcites →https://doi.org/10.1073/pnas.0803996105openalex-snapshot
Integration of auxin and brassinosteroid pathways by Auxin Response Factor 2
inferredcites →https://doi.org/10.1073/pnas.1007879107openalex-snapshot
In planta changes in protein phosphorylation induced by the plant hormone abscisic acid
inferredcites →https://doi.org/10.1073/pnas.1404654111openalex-snapshot
SPX1 is a phosphate-dependent inhibitor of PHOSPHATE STARVATION RESPONSE 1 in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1404680111openalex-snapshot
Rice SPX1 and SPX2 inhibit phosphate starvation responses through interacting with PHR2 in a phosphate-dependent manner
inferredcites →https://doi.org/10.1073/pnas.1411375111openalex-snapshot
Nitrate foraging by Arabidopsis roots is mediated by the transcription factor TCP20 through the systemic signaling pathway
inferredcites →https://doi.org/10.1073/pnas.1507810112openalex-snapshot
Calcium sensor kinase activates potassium uptake systems in gland cells of Venus flytraps
inferredcites →https://doi.org/10.1073/pnas.1525184113openalex-snapshot
Overexpression of a pH-sensitive nitrate transporter in rice increases crop yields
inferredcites →https://doi.org/10.1073/pnas.2114347118openalex-snapshot
An endoplasmic reticulum–localized cytochrome b 5 regulates high-affinity K + transport in response to salt stress in rice
inferredcites →https://doi.org/10.1074/jbc.m109.020842openalex-snapshot
Pore Mutations in Ammonium Transporter AMT1 with Increased Electrogenic Ammonium Transport Activity
inferredcites →https://doi.org/10.1074/mcp.m112.021220openalex-snapshot
Quantitative Phosphoproteomics after Auxin-stimulated Lateral Root Induction Identifies an SNX1 Protein Phosphorylation Site Required for Growth
inferredcites →https://doi.org/10.1074/mcp.m600429-mcp200openalex-snapshot
Quantitative Phosphoproteomics of Early Elicitor Signaling in Arabidopsis
inferredcites →https://doi.org/10.1080/15592324.2018.1554468openalex-snapshot
Contribution of KUPs to potassium and cesium accumulation appears complementary in Arabidopsis
inferredcites →https://doi.org/10.1093/emboj/cdg118openalex-snapshot
Switching between the two action modes of the dual‐affinity nitrate transporter CHL1 by phosphorylation
inferredcites →https://doi.org/10.1093/jxb/48.special_issue.451openalex-snapshot
Regulation of K+ absorption in plant root cells by external K+: interplay of different plasma membrane K+ transporters
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/eraa249openalex-snapshot
CALCIUM-DEPENDENT PROTEIN KINASE 32-mediated phosphorylation is essential for the ammonium transport activity of AMT1;1 in Arabidopsis roots
inferredcites →https://doi.org/10.1093/jxb/eraa361openalex-snapshot
NRT1.1-centered nitrate signaling in plants
inferredcites →https://doi.org/10.1093/jxb/erac059openalex-snapshot
Ammonium transporters cooperatively regulate rice crown root formation responding to ammonium nitrogen
inferredcites →https://doi.org/10.1093/jxb/erac456openalex-snapshot
The transcription factor OsWRKY10 inhibits phosphate uptake via suppressingOsPHT1;2expression under phosphate-replete conditions in rice
inferredcites →https://doi.org/10.1093/jxb/erad277openalex-snapshot
Arabidopsis calcium-dependent protein kinase CPK6 regulates drought tolerance under high nitrogen by the phosphorylation of NRT1.1
inferredcites →https://doi.org/10.1093/jxb/erh147openalex-snapshot
Regulatory levels for the transport of ammonium in plant roots
inferredcites →https://doi.org/10.1093/jxb/erj034openalex-snapshot
Plant responses to potassium deficiencies: a role for potassium transport proteins
inferredcites →https://doi.org/10.1093/jxb/erm330openalex-snapshot
The high affinity K+transporter AtHAK5 plays a physiological rolein plantaat very low K+concentrations and provides a caesium uptake pathway inArabidopsis
inferredcites →https://doi.org/10.1093/jxb/erq297openalex-snapshot
Understanding plant response to nitrogen limitation for the improvement of crop nitrogen use efficiency
inferredcites →https://doi.org/10.1093/jxb/ert402openalex-snapshot
Molecular mechanisms involved in plant adaptation to low K+ availability
inferredcites →https://doi.org/10.1093/jxb/ert458openalex-snapshot
AMT1;1 transgenic rice plants with enhanced NH4+ permeability show superior growth and higher yield under optimal and suboptimal NH4+ conditions
inferredcites →https://doi.org/10.1093/jxb/eru001openalex-snapshot
Nitrate transport and signalling in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/erx073openalex-snapshot
Post-translational regulation of nitrogen transporters in plants and microorganisms
inferredcites →https://doi.org/10.1093/jxb/erx101openalex-snapshot
Nitrogen use efficiency in crops: lessons from Arabidopsis and rice
inferredcites →https://doi.org/10.1093/jxb/ery182openalex-snapshot
A protein phosphatase 2C, AP2C1, interacts with and negatively regulates the function of CIPK9 under potassium-deficient conditions in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/erz113openalex-snapshot
A role for the OsHKT 2;1 sodium transporter in potassium use efficiency in rice
inferredcites →https://doi.org/10.1093/jxb/erz230openalex-snapshot
Ammonium and nitrate regulate NH4+ uptake activity of Arabidopsis ammonium transporter AtAMT1;3 via phosphorylation at multiple C-terminal sites
inferredcites →https://doi.org/10.1093/jxb/erz458openalex-snapshot
Emerging concepts of potassium homeostasis in plants
inferredcites →https://doi.org/10.1093/jxb/erz554openalex-snapshot
NRT1.1s in plants: functions beyond nitrate transport
inferredcites →https://doi.org/10.1093/mp/ssp102openalex-snapshot
The Arabidopsis thaliana HAK5 K+ Transporter Is Required for Plant Growth and K+ Acquisition from Low K+ Solutions under Saline Conditions
inferredcites →https://doi.org/10.1093/mp/ssr031openalex-snapshot
Mechanistic Analysis of AKT1 Regulation by the CBL–CIPK–PP2CA Interactions
inferredcites →https://doi.org/10.1093/mp/sst125openalex-snapshot
A Calcium-Dependent Protein Kinase Interacts with and Activates A Calcium Channel to Regulate Pollen Tube Growth
inferredcites →https://doi.org/10.1093/pcp/pcac104openalex-snapshot
OsAMT1;1 and OsAMT1;2 Coordinate Root Morphological and Physiological Responses to Ammonium for Efficient Nitrogen Foraging in Rice
inferredcites →https://doi.org/10.1093/pcp/pcg083openalex-snapshot
Distinct Expression and Function of Three Ammonium Transporter Genes (OsAMT1;1 – 1;3) in Rice
inferredcites →https://doi.org/10.1093/pcp/pcn186openalex-snapshot
AtAMT1;4, a Pollen-Specific High-Affinity Ammonium Transporter of the Plasma Membrane in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcs056openalex-snapshot
HAK Transporters from Physcomitrella patens and Yarrowia lipolytica Mediate Sodium Uptake
inferredcites →https://doi.org/10.1093/pcp/pct094openalex-snapshot
Identification and Characterization of Transcription Factors Regulating Arabidopsis HAK5
inferredcites →https://doi.org/10.1093/pcp/pcy038openalex-snapshot
MpAMT1;2 from Marchantia polymorpha is a High-Affinity, Plasma Membrane Ammonium Transporter
inferredcites →https://doi.org/10.1093/plcell/koab226openalex-snapshot
STOP1 activates NRT1.1-mediated nitrate uptake to create a favorable rhizospheric pH for plant adaptation to acidity
inferredcites →https://doi.org/10.1093/plphys/kiab047openalex-snapshot
Genome-wide analysis in response to nitrogen and carbon identifies regulators for root AtNRT2 transporters
inferredcites →https://doi.org/10.1093/plphys/kiac030openalex-snapshot
The rice phosphate transporter OsPHT1;7 plays a dual role in phosphorus redistribution and anther development
inferredcites →https://doi.org/10.1093/plphys/kiac178openalex-snapshot
The rice transcription factor Nhd1 regulates root growth and nitrogen uptake by activating nitrogen transporters
inferredcites →https://doi.org/10.1093/plphys/kiac250openalex-snapshot
Phosphate transporter PHT1;1 is a key determinant of phosphorus acquisition in Arabidopsis natural accessions
inferredcites →https://doi.org/10.1093/plphys/kiac315openalex-snapshot
Abscisic acid influences ammonium transport via regulation of kinase CIPK23 and ammonium transporters
inferredcites →https://doi.org/10.1098/rstb.2018.0006openalex-snapshot
Naturalizing pollution: a critical social science view on the link between potash mining and salinization in the Llobregat river basin, northeast Spain
inferredcites →https://doi.org/10.1101/2020.01.08.898254openalex-snapshot
A phospho-switch in the N-terminus of NRT2.1 affects nitrate uptake by controlling the interaction of NRT2.1 with NAR2.1
inferredcites →https://doi.org/10.1101/244467openalex-snapshot
Revisiting the functional properties of NPF6.3/NRT1.1/CHL1 in xenopus oocytes
inferredcites →https://doi.org/10.1101/gad.204401openalex-snapshot
A conserved MYB transcription factor involved in phosphate starvation signaling both in vascular plants and in unicellular algae
inferredcites →https://doi.org/10.1104/pp.008599openalex-snapshot
Characterization of Arabidopsis AtAMT2, a High-Affinity Ammonium Transporter of the Plasma Membrane
inferredcites →https://doi.org/10.1104/pp.103.029538openalex-snapshot
Modeling Nitrogen Uptake in Oilseed Rape cv Capitol during a Growth Cycle Using Influx Kinetics of Root Nitrate Transport Systems and Field Experimental Data
inferredcites →https://doi.org/10.1104/pp.103.4.1259openalex-snapshot
Ammonium Uptake by Rice Roots (II. Kinetics of 13NH4+ Influx across the Plasmalemma)
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.105.069757openalex-snapshot
Arabidopsis Calcium-Dependent Protein Kinase AtCPK32 Interacts with ABF4, a Transcriptional Regulator of Abscisic Acid-Responsive Gene Expression, and Modulates Its Activity
inferredcites →https://doi.org/10.1104/pp.106.091223openalex-snapshot
Dissection of the AtNRT2.1 : AtNRT2.2 Inducible High-Affinity Nitrate Transporter Gene Cluster
inferredcites →https://doi.org/10.1104/pp.106.093237openalex-snapshot
Nitrogen-Dependent Posttranscriptional Regulation of the Ammonium Transporter AtAMT1;1
inferredcites →https://doi.org/10.1104/pp.106.094243openalex-snapshot
Regulation of NH4 + Transport by Essential Cross Talk between AMT Monomers through the Carboxyl Tails
inferredcites →https://doi.org/10.1104/pp.107.111443openalex-snapshot
OsPHR2 Is Involved in Phosphate-Starvation Signaling and Excessive Phosphate Accumulation in Shoots of Plants
inferredcites →https://doi.org/10.1104/pp.109.1.319openalex-snapshot
Kinetics of NO3- Influx in Spruce
inferredcites →https://doi.org/10.1104/pp.109.138677openalex-snapshot
Large-Scale Arabidopsis Phosphoproteome Profiling Reveals Novel Chloroplast Kinase Substrates and Phosphorylation Networks
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.111.174805openalex-snapshot
Arabidopsis Pht1;5 Mobilizes Phosphate between Source and Sink Organs and Influences the Interaction between Phosphate Homeostasis and Ethylene Signaling
inferredcites →https://doi.org/10.1104/pp.111.175240openalex-snapshot
The Phosphate Transporter Gene OsPht1;8 Is Involved in Phosphate Homeostasis in Rice
inferredcites →https://doi.org/10.1104/pp.111.188532openalex-snapshot
Regulation of High-Affinity Nitrate Uptake in Roots of Arabidopsis Depends Predominantly on Posttranscriptional Control of the NRT2.1/NAR2.1 Transport System
inferredcites →https://doi.org/10.1104/pp.112.196345openalex-snapshot
A Constitutive Expressed Phosphate Transporter, OsPht1;1, Modulates Phosphate Uptake and Translocation in Phosphate-Replete Rice
inferredcites →https://doi.org/10.1104/pp.113.215913openalex-snapshot
Capacity and Plasticity of Potassium Channels and High-Affinity Transporters in Roots of Barley and Arabidopsis
inferredcites →https://doi.org/10.1104/pp.113.229161openalex-snapshot
A Reevaluation of the Role of Arabidopsis NRT1.1 in High-Affinity Nitrate Transport
inferredcites →https://doi.org/10.1104/pp.113.235077openalex-snapshot
Arabidopsis WRKY45 Transcription Factor Activates PHOSPHATE TRANSPORTER1;1 Expression in Response to Phosphate Starvation
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.114.252338openalex-snapshot
Reducing the Genetic Redundancy of Arabidopsis PHOSPHATE TRANSPORTER1 Transporters to Study Phosphate Uptake and Signaling
inferredcites →https://doi.org/10.1104/pp.116.2.447openalex-snapshot
Phosphorus Uptake by Plants: From Soil to Cell
inferredcites →https://doi.org/10.1104/pp.127.1.262openalex-snapshot
Major Alterations of the Regulation of Root NO3 − Uptake Are Associated with the Mutation of Nrt2.1 and Nrt2.2 Genes in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.16.00035openalex-snapshot
The Raf-like kinase ILK1 and the high affinity K+ transporter HAK5 are required for Innate Immunity and Abiotic Stress Response
inferredcites →https://doi.org/10.1104/pp.18.01097openalex-snapshot
OsPHT1;3 Mediates Uptake, Translocation, and Remobilization of Phosphate under Extremely Low Phosphate Regimes
inferredcites →https://doi.org/10.1104/pp.19.00346openalex-snapshot
Phosphorylation-Mediated Dynamics of Nitrate Transceptor NRT1.1 Regulate Auxin Flux and Nitrate Signaling in Lateral Root Growth
inferredcites →https://doi.org/10.1104/pp.19.01084openalex-snapshot
Recognition and Activation of the Plant AKT1 Potassium Channel by the Kinase CIPK23
inferredcites →https://doi.org/10.1104/pp.93.4.1426openalex-snapshot
Studies of the Uptake of Nitrate in Barley
inferredcites →https://doi.org/10.1105/tpc.010126openalex-snapshot
The Arabidopsis Dual-Affinity Nitrate Transporter Gene AtNRT1.1 (CHL1) Is Activated and Functions in Nascent Organ Development during Vegetative and Reproductive Growth
inferredcites →https://doi.org/10.1105/tpc.104.023150openalex-snapshot
Phosphoproteomics of the Arabidopsis Plasma Membrane and a New Phosphorylation Site Database[W]
inferredcites →https://doi.org/10.1105/tpc.107.052134openalex-snapshot
The Organization of High-Affinity Ammonium Uptake in Arabidopsis Roots Depends on the Spatial Arrangement and Biochemical Properties of AMT1-Type Transporters
inferredcites →https://doi.org/10.1105/tpc.109.068593openalex-snapshot
Feedback Inhibition of Ammonium Uptake by a Phospho-Dependent Allosteric Mechanism in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.11.5.865openalex-snapshot
CHL1 Is a Dual-Affinity Nitrate Transporter of Arabidopsis Involved in Multiple Phases of Nitrate Uptake
inferredcites →https://doi.org/10.1105/tpc.110.081067openalex-snapshot
Arabidopsis thaliana High-Affinity Phosphate Transporters Exhibit Multiple Levels of Posttranslational Regulation
inferredcites →https://doi.org/10.1105/tpc.111.084996openalex-snapshot
Phosphorylation of a WRKY Transcription Factor by Two Pathogen-Responsive MAPKs Drives Phytoalexin Biosynthesis in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.111.092221openalex-snapshot
The Arabidopsis Nitrate Transporter NRT2.4 Plays a Double Role in Roots and Shoots of Nitrogen-Starved Plants
inferredcites →https://doi.org/10.1105/tpc.112.105700openalex-snapshot
Osmotic Stress Responses and Plant Growth Controlled by Potassium Transporters in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.108027openalex-snapshot
Allosteric Regulation of Transport Activity by Heterotrimerization of Arabidopsis Ammonium Transporter Complexes in Vivo
inferredcites →https://doi.org/10.1105/tpc.114.123455openalex-snapshot
The Os-AKT1 Channel Is Critical for K + Uptake in Rice Roots and Is Modulated by the Rice CBL1-CIPK23 Complex
inferredcites →https://doi.org/10.1105/tpc.114.135335openalex-snapshot
The Rice CK2 Kinase Regulates Trafficking of Phosphate Transporters in Response to Phosphate Levels
inferredcites →https://doi.org/10.1105/tpc.15.00213openalex-snapshot
WRKY Transcription Factors Phosphorylated by MAPK Regulate a Plant Immune NADPH Oxidase in Nicotiana benthamiana
inferredcites →https://doi.org/10.1105/tpc.16.00684openalex-snapshot
Phosphorylation of ARF2 Relieves Its Repression of Transcription of the K + Transporter Gene HAK5 in Response to Low Potassium Stress
inferredcites →https://doi.org/10.1105/tpc.16.00806openalex-snapshot
The Kinase CIPK23 Inhibits Ammonium Transport in Arabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.19.00685openalex-snapshot
PROTEIN PHOSPHATASE95 Regulates Phosphate Homeostasis by Affecting Phosphate Transporter Trafficking in Rice
inferredcites →https://doi.org/10.1105/tpc.19.00971openalex-snapshot
Differential Phosphorylation of the Transcription Factor WRKY33 by the Protein Kinases CPK5/CPK6 and MPK3/MPK6 Cooperatively Regulates Camalexin Biosynthesis in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.20.00361openalex-snapshot
The Transcription Factor NIGT1.2 Modulates Both Phosphate Uptake and Nitrate Influx during Phosphate Starvation in Arabidopsis and Maize
inferredcites →https://doi.org/10.1111/j.1365-3040.1987.tb01824.xopenalex-snapshot
Multiphasic uptake of phosphate by corn roots
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02161.xopenalex-snapshot
Phosphate transport in Arabidopsis : Pht1;1 and Pht1;4 play a major role in phosphate acquisition from both low‐ and high‐phosphate environments
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02887.xopenalex-snapshot
Additive contribution of AMT1;1 and AMT1;3 to high‐affinity ammonium uptake across the plasma membrane of nitrogen‐deficient Arabidopsis roots
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03443.xopenalex-snapshot
Nitrate signalling mediated by the NRT1.1 nitrate transporter antagonises l ‐glutamate‐induced changes in root architecture
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03726.xopenalex-snapshot
Two rice phosphate transporters, OsPht1;2 and OsPht1;6, have different functions and kinetic properties in uptake and translocation
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.04029.xopenalex-snapshot
A grapevine Shaker inward K+channel activated by the calcineurin B-like calcium sensor 1–protein kinase CIPK23 network is expressed in grape berries under drought stress conditions
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04170.xopenalex-snapshot
OsSPX1 suppresses the function of OsPHR2 in the regulation of expression of OsPT2 and phosphate homeostasis in shoots of rice
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04218.xopenalex-snapshot
Comparative analysis of phytohormone-responsive phosphoproteins in Arabidopsis thaliana using TiO2-phosphopeptide enrichment and mass accuracy precursor alignment
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04848.xopenalex-snapshot
Nitrate and ammonium lead to distinct global dynamic phosphorylation patterns when resupplied to nitrogen‐starved Arabidopsis seedlings
inferredcites →https://doi.org/10.1111/j.1399-3054.2008.01168.xopenalex-snapshot
Relative contribution of AtHAK5 and AtAKT1 to K + uptake in the high‐affinity range of concentrations
inferredcites →https://doi.org/10.1111/j.1399-3054.2010.01354.xopenalex-snapshot
Studies on Arabidopsis athak5, atakt1 double mutants disclose the range of concentrations at which AtHAK5, AtAKT1 and unknown systems mediate K+ uptake
inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04094.xopenalex-snapshot
Nitrate transport capacity of the Arabidopsis thaliana NRT2 family members and their interactions with AtNAR2.1
inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04167.xopenalex-snapshot
The Pht1;9 and Pht1;8 transporters mediate inorganic phosphate acquisition by the Arabidopsis thaliana root during phosphorus starvation
inferredcites →https://doi.org/10.1111/jipb.12756openalex-snapshot
ZmHAK5 and ZmHAK1 function in K + uptake and distribution in maize under low K + conditions
inferredcites →https://doi.org/10.1111/jipb.12858openalex-snapshot
Phosphorylation at Ser28 stabilizes the Arabidopsis nitrate transporter NRT2.1 in response to nitrate limitation
inferredcites →https://doi.org/10.1111/jipb.13057openalex-snapshot
Abscisic acid signaling negatively regulates nitrate uptake via phosphorylation of NRT1.1 by SnRK2s in Arabidopsis
inferredcites →https://doi.org/10.1111/nph.12075openalex-snapshot
I ndeterminate domain 10regulates ammonium‐mediated gene expression in rice roots
inferredcites →https://doi.org/10.1111/nph.15155openalex-snapshot
Rice SPX6 negatively regulates the phosphate starvation response through suppression of the transcription factor PHR2
inferredcites →https://doi.org/10.1111/nph.16710openalex-snapshot
NRT2.1 C‐terminus phosphorylation prevents root high affinity nitrate uptake activity in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/nph.16931openalex-snapshot
OsWRKY21 and OsWRKY108 function redundantly to promote phosphate accumulation through maintaining the constitutive expression of OsPHT1;1 under phosphate‐replete conditions
inferredcites →https://doi.org/10.1111/nph.17017openalex-snapshot
Plasma membrane calcineurin B‐like calcium‐ion sensor proteins function in regulating primary root growth and nitrate uptake by affecting global phosphorylation patterns and microdomain protein distribution
inferredcites →https://doi.org/10.1111/nph.17589openalex-snapshot
MYB77 regulates high‐affinity potassium uptake by promoting expression of HAK5
inferredcites →https://doi.org/10.1111/nph.17679openalex-snapshot
Three polarly localized ammonium transporter 1 members are cooperatively responsible for ammonium uptake in rice under low ammonium condition
inferredcites →https://doi.org/10.1111/pbi.13414openalex-snapshot
Maize ZmPT7 regulates Pi uptake and redistribution which is modulated by phosphorylation
inferredcites →https://doi.org/10.1111/pce.12224openalex-snapshot
Phosphate transporters OsPHT1 ;9 and OsPHT1 ;10 are involved in phosphate uptake in rice
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.12586openalex-snapshot
The potassium transporter O s HAK 21 functions in the maintenance of ion homeostasis and tolerance to salt stress in rice
inferredcites →https://doi.org/10.1111/ppl.13831openalex-snapshot
Phosphorylation of S11 in PHR1 negatively controls its transcriptional activity
inferredcites →https://doi.org/10.1111/tpj.12123openalex-snapshot
Calcineurin B‐like protein CBL 10 directly interacts with AKT 1 and modulates K + homeostasis in Arabidopsis
inferredcites →https://doi.org/10.1111/tpj.12618openalex-snapshot
Systems approach identifies TGA 1 and TGA 4 transcription factors as important regulatory components of the nitrate response of A rabidopsis thaliana roots
inferredcites →https://doi.org/10.1111/tpj.12626openalex-snapshot
The Arabidopsis nitrate transporter NRT 2.5 plays a role in nitrate acquisition and remobilization in nitrogen‐starved plants
inferredcites →https://doi.org/10.1111/tpj.12804openalex-snapshot
Involvement of O s P ht1;4in phosphate acquisition and mobilization facilitates embryo development in rice
inferredcites →https://doi.org/10.1111/tpj.13272openalex-snapshot
Early nitrogen‐deprivation responses in Arabidopsis roots reveal distinct differences on transcriptome and (phospho‐) proteome levels between nitrate and ammonium nutrition
showing the first 200 of 237 · page through all 237
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