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A Major Facilitator Superfamily Transporter Plays a Dual Role in Polar Auxin Transport and Drought Stress Tolerance in Arabidopsis

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1006/bbrc.2002.6691openalex-snapshot
Saccharomyces cerevisiae Resistance to Chlorinated Phenoxyacetic Acid Herbicides Involves Pdr1p-Mediated Transcriptional Activation of TPO1 and PDR5 Genes
inferredcites →https://doi.org/10.1007/bf00241470openalex-snapshot
Characterization of the plasma membrane ATPase of Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1007/bf00262639openalex-snapshot
Comparison of mechanisms controlling uptake and accumulation of 2,4-dichlorophenoxy acetic acid, naphthalene-1-acetic acid, and indole-3-acetic acid in suspension-cultured tobacco cells
inferredcites →https://doi.org/10.1007/bf00385573openalex-snapshot
Transport of indoleacetic acid in intact roots of Phaseolus coccineus
inferredcites →https://doi.org/10.1007/bf00388387openalex-snapshot
Carrier-mediated auxin transport
inferredcites →https://doi.org/10.1007/s00018-006-6116-5openalex-snapshot
Spatiotemporal asymmetric auxin distribution: a means to coordinate plant development
inferredcites →https://doi.org/10.1007/s00253-009-2025-5openalex-snapshot
Heterologous expression of a Tpo1 homolog from Arabidopsis thaliana confers resistance to the herbicide 2,4-D and other chemical stresses in yeast
inferredcites →https://doi.org/10.1007/s00709-012-0448-9openalex-snapshot
On the physiological significance of alternative splicing events in higher plants
inferredcites →https://doi.org/10.1007/s11103-006-9041-yopenalex-snapshot
Response diversity of Arabidopsis thaliana ecotypes in elevated [CO2] in the field
inferredcites →https://doi.org/10.1016/j.cub.2006.04.029openalex-snapshot
High-Affinity Auxin Transport by the AUX1 Influx Carrier Protein
inferredcites →https://doi.org/10.1016/j.cub.2007.01.052openalex-snapshot
Clathrin-Mediated Constitutive Endocytosis of PIN Auxin Efflux Carriers in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2008.03.021openalex-snapshot
ARF GEF-Dependent Transcytosis and Polar Delivery of PIN Auxin Carriers in Arabidopsis
inferredcites →https://doi.org/10.1016/j.devcel.2010.05.008openalex-snapshot
Nitrate-Regulated Auxin Transport by NRT1.1 Defines a Mechanism for Nutrient Sensing in Plants
inferredcites →https://doi.org/10.1016/j.febslet.2005.08.061openalex-snapshot
MDR‐like ABC transporter AtPGP4 is involved in auxin‐mediated lateral root and root hair development
inferredcites →https://doi.org/10.1016/j.febslet.2007.03.016openalex-snapshot
The monosaccharide transporter(‐like) gene family in Arabidopsis
inferredcites →https://doi.org/10.1016/j.febslet.2007.04.047openalex-snapshot
Nitrate transporters and peptide transporters
inferredcites →https://doi.org/10.1016/j.gene.2004.10.016openalex-snapshot
Drag&Drop cloning in yeast
inferredcites →https://doi.org/10.1016/j.mod.2012.02.003openalex-snapshot
Posttranslational modification and trafficking of PIN auxin efflux carriers
inferredcites →https://doi.org/10.1016/j.tplants.2007.03.006openalex-snapshot
Molecular and cellular aspects of auxin-transport-mediated development
inferredcites →https://doi.org/10.1016/s0092-8674(00)81535-4openalex-snapshot
An Auxin-Dependent Distal Organizer of Pattern and Polarity in the Arabidopsis Root
inferredcites →https://doi.org/10.1016/s0960-9822(00)00861-7openalex-snapshot
Post-transcriptional control of the Arabidopsis auxin efflux carrier EIR1 requires AXR1
inferredcites →https://doi.org/10.1016/s1360-1385(02)02251-3openalex-snapshot
GATEWAY™ vectors for Agrobacterium-mediated plant transformation
inferredcites →https://doi.org/10.1038/221281a0openalex-snapshot
Stomatal Closure and Inhibition of Transpiration induced by (RS)-Abscisic Acid
inferredcites →https://doi.org/10.1038/35096571openalex-snapshot
Auxin transport inhibitors block PIN1 cycling and vesicle trafficking
inferredcites →https://doi.org/10.1038/415806aopenalex-snapshot
Lateral relocation of auxin efflux regulator PIN3 mediates tropism in Arabidopsis
inferredcites →https://doi.org/10.1038/emboj.2012.310openalex-snapshot
SCFTIR1/AFB‐auxin signalling regulates PIN vacuolar trafficking and auxin fluxes during root gravitropism
inferredcites →https://doi.org/10.1038/nature02081openalex-snapshot
Regulation of phyllotaxis by polar auxin transport
inferredcites →https://doi.org/10.1038/nature03184openalex-snapshot
The PIN auxin efflux facilitator network controls growth and patterning in Arabidopsis roots
inferredcites →https://doi.org/10.1038/nature03633openalex-snapshot
Auxin inhibits endocytosis and promotes its own efflux from cells
inferredcites →https://doi.org/10.1038/ncb1316openalex-snapshot
Root gravitropism requires lateral root cap and epidermal cells for transport and response to a mobile auxin signal
inferredcites →https://doi.org/10.1038/ncb1369openalex-snapshot
Intracellular trafficking and proteolysis of the Arabidopsis auxin-efflux facilitator PIN2 are involved in root gravitropism
inferredcites →https://doi.org/10.1038/ncb1754openalex-snapshot
The auxin influx carrier LAX3 promotes lateral root emergence
inferredcites →https://doi.org/10.1038/nprot.2006.15openalex-snapshot
Immunocytochemical techniques for whole-mount in situ protein localization in plants
inferredcites →https://doi.org/10.1038/nprot.2007.199openalex-snapshot
Arabidopsis mesophyll protoplasts: a versatile cell system for transient gene expression analysis
inferredcites →https://doi.org/10.1038/nprot.2009.1openalex-snapshot
Measurement of auxin transport in Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00304.xopenalex-snapshot
A GFP‐mouse talin fusion protein labels plant actin filamentsin vivoand visualizes the actin cytoskeleton in growing pollen tubes
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01676.xopenalex-snapshot
Retracted: An enhanced transient expression system in plants based on suppression of gene silencing by the p19 protein of tomato bushy stunt virus
inferredcites →https://doi.org/10.1046/j.1469-8137.2000.00704.xopenalex-snapshot
Tansley Review No. 113
inferredcites →https://doi.org/10.1055/s-2006-923965openalex-snapshot
How Does Auxin Enhance Cell Elongation? Roles of Auxin-Binding Proteins and Potassium Channels in Growth Control
inferredcites →https://doi.org/10.1055/s-2006-924121openalex-snapshot
Ion Channels Meet Auxin Action
inferredcites →https://doi.org/10.1073/pnas.0509512102openalex-snapshot
Up-regulation of a H + -pyrophosphatase (H + -PPase) as a strategy to engineer drought-resistant crop plants
inferredcites →https://doi.org/10.1073/pnas.0808073105openalex-snapshot
Differential degradation of PIN2 auxin efflux carrier by retromer-dependent vacuolar targeting
inferredcites →https://doi.org/10.1073/pnas.76.5.2295openalex-snapshot
Relation between leaf senescence and stomatal closure: Senescence in light
inferredcites →https://doi.org/10.1073/pnas.95.25.15112openalex-snapshot
The Arabidopsis thaliana AGRAVITROPIC 1 gene encodes a component of the polar-auxin-transport efflux carrier
inferredcites →https://doi.org/10.1074/jbc.m109.030247openalex-snapshot
The Arabidopsis ATP-binding Cassette Protein AtMRP5/AtABCC5 Is a High Affinity Inositol Hexakisphosphate Transporter Involved in Guard Cell Signaling and Phytate Storage
inferredcites →https://doi.org/10.1074/jbc.m607926200openalex-snapshot
The ATP Binding Cassette Transporter AtMRP5 Modulates Anion and Calcium Channel Activities in Arabidopsis Guard Cells
inferredcites →https://doi.org/10.1093/aob/mci083openalex-snapshot
Auxin: Regulation, Action, and Interaction
inferredcites →https://doi.org/10.1093/emboj/17.23.6903openalex-snapshot
AtPIN2 defines a locus of Arabidopsis for root gravitropism control
inferredcites →https://doi.org/10.1093/emboj/18.8.2066openalex-snapshot
AUX1 regulates root gravitropism in Arabidopsis by facilitating auxin uptake within root apical tissues
inferredcites →https://doi.org/10.1093/emboj/20.8.1875openalex-snapshot
The Arabidopsis thaliana ABC transporter AtMRP5 controls root development and stomata movement
inferredcites →https://doi.org/10.1093/emboj/cdf312openalex-snapshot
A viral protein suppresses RNA silencing and binds silencing‐generated, 21‐ to 25‐nucleotide double‐stranded RNAs
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/nar/29.1.102openalex-snapshot
The Arabidopsis Information Resource (TAIR): a comprehensive database and web-based information retrieval, analysis, and visualization system for a model plant
inferredcites →https://doi.org/10.1093/nar/gkh016openalex-snapshot
TransportDB: a relational database of cellular membrane transport systems
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a029419openalex-snapshot
Differential Effects of 1-Naphthaleneacetic Acid, Indole-3-Acetic Acid and 2,4-Dichlorophenoxyacetic Acid on the Gravitropic Response of Roots in an Auxin-Resistant Mutant of Arabidopsis, auxl
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a075700openalex-snapshot
Transport of 14C-lableled indoleacetic acid in Vicia root segments
inferredcites →https://doi.org/10.1101/gad.12.14.2175openalex-snapshot
EIR1, a root-specific protein involved in auxin transport, is required for gravitropism inArabidopsis thaliana
inferredcites →https://doi.org/10.1101/gad.210501openalex-snapshot
Localization of the auxin permease AUX1 suggests two functionally distinct hormone transport pathways operate in the Arabidopsis root apex
inferredcites →https://doi.org/10.1101/gad.9.14.1797openalex-snapshot
Patterns of gene action in plant development revealed by enhancer trap and gene trap transposable elements.
inferredcites →https://doi.org/10.1101/gr.134106.111openalex-snapshot
Transcriptome survey reveals increased complexity of the alternative splicing landscape in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.010519openalex-snapshot
Identification, Purification, and Molecular Cloning of N-1-Naphthylphthalmic Acid-Binding Plasma Membrane-Associated Aminopeptidases from Arabidopsis
inferredcites →https://doi.org/10.1104/pp.103.022582openalex-snapshot
Transport of the Two Natural Auxins, Indole-3-Butyric Acid and Indole-3-Acetic Acid, in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.104.046672openalex-snapshot
Cesium Toxicity in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.105.061572openalex-snapshot
Two Homologous ATP-Binding Cassette Transporter Proteins, AtMDR1 and AtPGP1, Regulate Arabidopsis Photomorphogenesis and Root Development by Mediating Polar Auxin Transport
inferredcites →https://doi.org/10.1104/pp.106.084533openalex-snapshot
A Gain-of-Function Mutation in the Arabidopsis Pleiotropic Drug Resistance Transporter PDR9 Confers Resistance to Auxinic Herbicides
inferredcites →https://doi.org/10.1104/pp.106.092015openalex-snapshot
A Novel Major Facilitator Superfamily Protein at the Tonoplast Influences Zinc Tolerance and Accumulation in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.109.138180openalex-snapshot
Two Alternatively Spliced Isoforms of the Arabidopsis SR45 Protein Have Distinct Roles during Normal Plant Development
inferredcites →https://doi.org/10.1104/pp.110.167981openalex-snapshot
Loss-of-Function and Gain-of-Function Mutations in FAB1A/B Impair Endomembrane Homeostasis, Conferring Pleiotropic Developmental Abnormalities in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.122.2.481openalex-snapshot
Basipetal Auxin Transport Is Required for Gravitropism in Roots of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.122.4.999openalex-snapshot
Plant Cells Are Not Just Green Yeast
inferredcites →https://doi.org/10.1105/tpc.010350openalex-snapshot
Multidrug Resistance –like Genes of Arabidopsis Required for Auxin Transport and Auxin-Mediated Development
inferredcites →https://doi.org/10.1105/tpc.015560openalex-snapshot
ALTERED RESPONSE TO GRAVITY Is a Peripheral Membrane Protein That Modulates Gravity-Induced Cytoplasmic Alkalinization and Lateral Auxin Transport in Plant Statocytes
inferredcites →https://doi.org/10.1105/tpc.021501openalex-snapshot
Variation in Expression and Protein Localization of the PIN Family of Auxin Efflux Facilitator Proteins in Flavonoid Mutants with Altered Auxin Transport in Arabidopsis thaliana [W]
inferredcites →https://doi.org/10.1105/tpc.104.024380openalex-snapshot
Transcript Profiling in thechl1-5Mutant of Arabidopsis Reveals a Role of the Nitrate Transporter NRT1.1 in the Regulation of Another Nitrate Transporter, NRT2.1[W]
inferredcites →https://doi.org/10.1105/tpc.105.034637openalex-snapshot
Maintenance of Embryonic Auxin Distribution for Apical-Basal Patterning by PIN-FORMED–Dependent Auxin Transport in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.105.035816openalex-snapshot
PGP4, an ATP Binding Cassette P-Glycoprotein, Catalyzes Auxin Transport in Arabidopsis thaliana Roots
inferredcites →https://doi.org/10.1105/tpc.106.040782openalex-snapshot
Interactions among PIN-FORMED and P-Glycoprotein Auxin Transporters in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.106.042770openalex-snapshot
Subcellular Trafficking of the Arabidopsis Auxin Influx Carrier AUX1 Uses a Novel Pathway Distinct from PIN1
inferredcites →https://doi.org/10.1105/tpc.106.048777openalex-snapshot
Mutations inArabidopsis Multidrug Resistance-LikeABC Transporters Separate the Roles of Acropetal and Basipetal Auxin Transport in Lateral Root Development
inferredcites →https://doi.org/10.1105/tpc.107.051599openalex-snapshot
Separating the Roles of Acropetal and Basipetal Auxin Transport on Gravitropism with Mutations in Two Arabidopsis Multidrug Resistance-Like ABC Transporter Genes
inferredcites →https://doi.org/10.1105/tpc.110.073957openalex-snapshot
Natural Variation of Transcriptional Auxin Response Networks inArabidopsis thaliana
inferredcites →https://doi.org/10.1105/tpc.110.075317openalex-snapshot
Gravitropism ofArabidopsis thalianaRoots Requires the Polarization of PIN2 toward the Root Tip in Meristematic Cortical Cells
inferredcites →https://doi.org/10.1105/tpc.13.11.2441openalex-snapshot
Multidrug Resistance-like Genes of Arabidopsis Required for Auxin Transport and Auxin-Mediated Development
inferredcites →https://doi.org/10.1105/tpc.3.7.677openalex-snapshot
Requirement of the Auxin Polar Transport System in Early Stages of Arabidopsis Floral Bud Formation.
inferredcites →https://doi.org/10.1105/tpc.9.11.1963openalex-snapshot
Aux/IAA proteins repress expression of reporter genes containing natural and highly active synthetic auxin response elements.
inferredcites →https://doi.org/10.1111/j.1365-313x.1994.00421.xopenalex-snapshot
Transient transformation of Arabidopsis leaf protoplasts: a versatile experimental system to study gene expression
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.2004.02230.xopenalex-snapshot
Potassium carrier TRH1 is required for auxin transport in Arabidopsis roots
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02369.xopenalex-snapshot
Complex regulation of Arabidopsis AGR1/PIN2‐mediated root gravitropic response and basipetal auxin transport by cantharidin‐sensitive protein phosphatases
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02519.xopenalex-snapshot
Cellular efflux of auxin catalyzed by the Arabidopsis MDR/PGP transporter AtPGP1
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02615.xopenalex-snapshot
ABA‐induced NO generation and stomatal closure in Arabidopsis are dependent on H 2 O 2 synthesis
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02617.xopenalex-snapshot
Gateway‐compatible vectors for plant functional genomics and proteomics
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03068.xopenalex-snapshot
Auxin, actin and growth of the Arabidopsis thaliana primary root
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03158.xopenalex-snapshot
MODULATOR OF PIN genes control steady‐state levels of Arabidopsis PIN proteins
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03212.xopenalex-snapshot
A multicolored set of in vivo organelle markers for co‐localization studies in Arabidopsis and other plants
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03668.xopenalex-snapshot
ABCB19/PGP19 stabilises PIN1 in membrane microdomains in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03856.xopenalex-snapshot
Functional expression and characterization of Arabidopsis ABCB, AUX 1 and PIN auxin transporters in Schizosaccharomyces pombe
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04302.xopenalex-snapshot
AtALMT12 represents an R-type anion channel required for stomatal movement in Arabidopsis guard cells
inferredcites →https://doi.org/10.1111/j.1399-3054.1962.tb08052.xopenalex-snapshot
A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures
inferredcites →https://doi.org/10.1111/j.1399-3054.1975.tb03171.xopenalex-snapshot
Evidence for Three Different Systems of Movement of Indoleacetic Acid in Intact Roots of Phaseolus coccineus
inferredcites →https://doi.org/10.1111/j.1469-8137.1975.tb02602.xopenalex-snapshot
TRANSPORT OF INDOLEACETIC ACID IN PLANT CELLS IN RELATION TO pH AND ELECTRICAL POTENTIAL GRADIENTS, AND ITS SIGNIFICANCE FOR POLAR IAA TRANSPORT
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/nph.12092openalex-snapshot
Root gravitropism and root hair development constitute coupled developmental responses regulated by auxin homeostasis in the Arabidopsis root apex
inferredcites →https://doi.org/10.1126/science.1115711openalex-snapshot
Arabidopsis H + -PPase AVP1 Regulates Auxin-Mediated Organ Development
inferredcites →https://doi.org/10.1126/science.1121356openalex-snapshot
Polar PIN Localization Directs Auxin Flow in Plants
inferredcites →https://doi.org/10.1126/science.1123542openalex-snapshot
PIN Proteins Perform a Rate-Limiting Function in Cellular Auxin Efflux
inferredcites →https://doi.org/10.1126/science.273.5277.948openalex-snapshot
Arabidopsis AUX1 Gene: A Permease-Like Regulator of Root Gravitropism
inferredcites →https://doi.org/10.1128/ec.00290-06openalex-snapshot
Saccharomyces cerevisiae Multidrug Resistance Transporter Qdr2 Is Implicated in Potassium Uptake, Providing a Physiological Advantage to Quinidine-Stressed Cells
inferredcites →https://doi.org/10.1128/mmbr.62.1.1-34.1998openalex-snapshot
Major Facilitator Superfamily
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105406openalex-snapshot
Plant ATP-Binding Cassette Transporters
inferredcites →https://doi.org/10.1146/annurev.physiol.010908.163204openalex-snapshot
Plant Ion Channels: Gene Families, Physiology, and Functional Genomics Analyses
inferredcites →https://doi.org/10.1146/annurev.pp.28.060177.002255openalex-snapshot
The Polar Transport of Auxin
inferredcites →https://doi.org/10.1242/dev.02027openalex-snapshot
Functional redundancy of PIN proteins is accompanied by auxin-dependent cross-regulation of PIN expression
inferredcites →https://doi.org/10.1242/dev.021071openalex-snapshot
Interaction of PIN and PGP transport mechanisms in auxin distribution-dependent development
inferredcites →https://doi.org/10.1242/dev.030353openalex-snapshot
Auxin transport routes in plant development
inferredcites →https://doi.org/10.1242/dev.124.1.33openalex-snapshot
Organization and cell differentiation in lateral roots of Arabidopsis thaliana
inferredcites →https://doi.org/10.1242/jcs.02910openalex-snapshot
Auxin signaling
inferredcites →https://doi.org/10.1371/journal.pone.0001510openalex-snapshot
Light Plays an Essential Role in Intracellular Distribution of Auxin Efflux Carrier PIN2 in Arabidopsis thaliana
inferredcites →https://doi.org/10.2307/3869249openalex-snapshot
Requirement of the Auxin Polar Transport System in Early Stages of Arabidopsis Floral Bud Formation
inferredcites →https://doi.org/10.2307/3870557openalex-snapshot
Aux/IAA Proteins Repress Expression of Reporter Genes Containing Natural and Highly Active Synthetic Auxin Response Elements
inferredcites →https://doi.org/10.4161/psb.6.9.16425openalex-snapshot
Control of stomatal aperture

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1002/9781118889022.ch2openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781119800156.ch9openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201308972openalex-snapshot
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Real‐Time Monitoring of Auxin Vesicular Exocytotic Efflux from Single Plant Protoplasts by Amperometry at Microelectrodes Decorated with Nanowires
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Role of Arabidopsis RAB5 GEF vps9a in maintaining potassium levels under sodium chloride stress
inferred← citeshttps://doi.org/10.1002/pld3.289openalex-snapshot
The commitment of barley microspores into embryogenesis correlates with miRNA‐directed regulation of members of the SPL, GRF and HD‐ZIPIII transcription factor families
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Post‐transcriptional regulation in root development
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Alternative splicing: An efficient regulatory approach towards plant developmental plasticity
inferred← citeshttps://doi.org/10.1007/978-1-4939-2211-6_11openalex-snapshot
Emerging Roles of Auxin in Abiotic Stress Responses
inferred← citeshttps://doi.org/10.1007/978-3-030-13035-0_1openalex-snapshot
Physiological Genomics of Multistress Resistance in the Yeast Cell Model and Factory: Focus on MDR/MXR Transporters
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Climate Smart Crops: Flood and Drought-Tolerant Crops
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Potassium (K+) Regulation by Phytohormones Under Abiotic Stress
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Mapping-by-sequencing of Ligon-lintless-1 (Li 1 ) reveals a cluster of neighboring genes with correlated expression in developing fibers of Upland cotton (Gossypium hirsutum L.)
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Structural genome analysis in cultivated potato taxa
inferred← citeshttps://doi.org/10.1007/s00122-025-05095-4openalex-snapshot
Comparative genomic analysis of QTL for resistance to Aphanomyces euteiches between pea, lentil, faba bean, and the model species Medicago truncatula
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Dissection of local haplotype diversity at soybean rust loci reveals resistance-associated and context-dependent variation patterns in diverse germplasm
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Overexpression of OsZHD1, a zinc finger homeodomain class homeobox transcription factor, induces abaxially curled and drooping leaf in rice
inferred← citeshttps://doi.org/10.1007/s00425-021-03642-zopenalex-snapshot
Zinc toxicity in plants: a review
inferred← citeshttps://doi.org/10.1007/s00438-017-1330-4openalex-snapshot
Transcriptome analysis of drought-responsive genes regulated by hydrogen sulfide in wheat (Triticum aestivum L.) leaves
inferred← citeshttps://doi.org/10.1007/s10142-023-01066-4openalex-snapshot
Alternative splicing shapes the transcriptome complexity in blackgram [Vigna mungo (L.) Hepper]
inferred← citeshttps://doi.org/10.1007/s10142-024-01420-0openalex-snapshot
Integrative analyses of long and short-read RNA sequencing reveal the spliced isoform regulatory network of seedling growth dynamics in upland cotton
inferred← citeshttps://doi.org/10.1007/s10681-018-2152-0openalex-snapshot
Comparative alternative splicing analysis of two contrasting rice cultivars under drought stress and association of differential splicing genes with drought response QTLs
inferred← citeshttps://doi.org/10.1007/s10725-019-00541-yopenalex-snapshot
RNA sequencing and functional analyses reveal regulation of novel drought-responsive, long-non-coding RNA in Zanthoxylum bungeanum Maxim
inferred← citeshttps://doi.org/10.1007/s10725-020-00684-3openalex-snapshot
Plant transporters: roles in stress responses and effects on growth and development
inferred← citeshttps://doi.org/10.1007/s11033-019-05225-4openalex-snapshot
Genome-wide association mapping for adult resistance to powdery mildew in common wheat
inferred← citeshttps://doi.org/10.1007/s11033-020-05396-5openalex-snapshot
Transcriptome analysis of drought-tolerant sorghum genotype SC56 in response to water stress reveals an oxidative stress defense strategy
inferred← citeshttps://doi.org/10.1007/s11295-016-1035-6openalex-snapshot
PtFCA from precocious trifoliate orange is regulated by alternative splicing and affects flowering time and root development in transgenic Arabidopsis
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/b978-0-12-817958-1.00017-7openalex-snapshot
Regulation of membrane transporters in plants in response to drought stress
inferred← citeshttps://doi.org/10.1016/b978-0-12-819773-8.00018-6openalex-snapshot
Ion-uptake mechanisms of individual cells and roots: short-distance transport
inferred← citeshttps://doi.org/10.1016/bs.ampbs.2026.02.002openalex-snapshot
From feeding cell to fruiting body: Multidrug transport in the life cycle of Dictyostelium discoideum
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2017.10.010openalex-snapshot
The rice cold-responsive calcium-dependent protein kinase OsCPK17 is regulated by alternative splicing and post-translational modifications
inferred← citeshttps://doi.org/10.1016/j.bbrc.2021.04.120openalex-snapshot
Functional overlap of two major facilitator superfamily transporter, ZIF1, and ZIFL1 in zinc and iron homeostasis
inferred← citeshttps://doi.org/10.1016/j.copbio.2015.03.001openalex-snapshot
Yeast toxicogenomics: lessons from a eukaryotic cell model and cell factory
inferred← citeshttps://doi.org/10.1016/j.cpb.2025.100556openalex-snapshot
Integrated whole genome and transcriptome analysis reveals the molecular mechanisms for enhanced salt tolerance in an introgression line of rice
inferred← citeshttps://doi.org/10.1016/j.cropd.2022.01.001openalex-snapshot
Divergence of two cultivated allotetraploid cottons unveiled by single-molecule long-read expression sequencing
inferred← citeshttps://doi.org/10.1016/j.cub.2015.05.053openalex-snapshot
A Recently Evolved Alternative Splice Site in the BRANCHED1a Gene Controls Potato Plant Architecture
inferred← citeshttps://doi.org/10.1016/j.devcel.2014.06.017openalex-snapshot
Long Noncoding RNA Modulates Alternative Splicing Regulators in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2014.01.003openalex-snapshot
Grape contains 4 ICE genes whose expression includes alternative polyadenylation, leading to transcripts encoding at least 7 different ICE proteins
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2019.103810openalex-snapshot
Transcriptomic and alternative splicing analyses reveal mechanisms of the difference in salt tolerance between barley and rice
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2022.03.179openalex-snapshot
Genomic & structural diversity and functional role of potassium (K+) transport proteins in plants
inferred← citeshttps://doi.org/10.1016/j.isci.2023.108112openalex-snapshot
Physiology and transcriptomics highlight the underlying mechanism of sunflower responses to drought stress and rehydration
inferred← citeshttps://doi.org/10.1016/j.jare.2022.04.008openalex-snapshot
Expression complementation of gene presence/absence polymorphisms in hybrids contributes importantly to heterosis in sunflower
inferred← citeshttps://doi.org/10.1016/j.jare.2022.09.008openalex-snapshot
Genome resequencing and transcriptome profiling reveal molecular evidence of tolerance to water deficit in barley
inferred← citeshttps://doi.org/10.1016/j.jgg.2015.08.001openalex-snapshot
Dynamic and Coordinated Expression Changes of Rice Small RNAs in Response to Xanthomonas oryzae pv. oryzae
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2026.143357openalex-snapshot
The gene homologous to OsCd1, designated as ABNORMAL SHOOT IN YOUTH (OsASY), functions as a cadmium influx transporter in rice
inferred← citeshttps://doi.org/10.1016/j.jplph.2021.153432openalex-snapshot
Potassium physiology from Archean to Holocene: A higher-plant perspective
inferred← citeshttps://doi.org/10.1016/j.micres.2026.128703openalex-snapshot
Localized root colonization by Trichoderma afroharzianum T22 is associated with host transcriptional reprogramming and beneficial bacterial enrichment under salinity stress in sorghum
inferred← citeshttps://doi.org/10.1016/j.molp.2019.07.003openalex-snapshot
More Transporters, More Substrates: The Arabidopsis Major Facilitator Superfamily Revisited
inferred← citeshttps://doi.org/10.1016/j.molp.2021.12.008openalex-snapshot
Zinc in plants: Integrating homeostasis and biofortification
inferred← citeshttps://doi.org/10.1016/j.ncrops.2024.100012openalex-snapshot
ZmMYB56 regulates stomatal closure and drought tolerance in maize seedlings through the transcriptional regulation of ZmTOM7
inferred← citeshttps://doi.org/10.1016/j.pbi.2015.04.007openalex-snapshot
Genetic approaches for improvement of the crop potassium acquisition and utilization efficiency
inferred← citeshttps://doi.org/10.1016/j.plantsci.2015.06.014openalex-snapshot
Expression of peach sucrose transporters in heterologous systems points out their different physiological role
inferred← citeshttps://doi.org/10.1016/j.plaphy.2019.11.021openalex-snapshot
Genome-wide expression of low temperature response genes in Rosa hybrida L.
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.01.016openalex-snapshot
Identification of cassava alternative splicing-related genes and functional characterization of MeSCL30 involvement in drought stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.03.030openalex-snapshot
The PIN gene family in relic plant L. chinense: Genome-wide identification and gene expression profiling in different organizations and abiotic stress responses
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109011openalex-snapshot
TaMYB-CC5 gene specifically expressed in root improve tolerance of phosphorus deficiency and drought stress in wheat
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109839openalex-snapshot
Phytohormones: Heart of plants’ signaling network under biotic, abiotic, and climate change stresses
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110554openalex-snapshot
Identification of MFS gene family in tomato and functional characterization of SlZIF1/SlMFS4 under salt stress
inferred← citeshttps://doi.org/10.1016/j.plgene.2019.100179openalex-snapshot
Global study of MFS superfamily transporters in arabidopsis and grapes reveals their functional diversity in plants
inferred← citeshttps://doi.org/10.1016/j.sajb.2022.05.016openalex-snapshot
Delineating genome-wide alternative splicing landscapes and their functional significance in orchids
inferred← citeshttps://doi.org/10.1016/j.scienta.2018.09.056openalex-snapshot
Comparative transcriptome analysis of genes involved in the response of resistant and susceptible peach cultivars to water stress
inferred← citeshttps://doi.org/10.1016/j.scienta.2024.113449openalex-snapshot
Identification and characterization of SmPIC30, an important gene that controls resistance to the auxin herbicide picloram in eggplant
inferred← citeshttps://doi.org/10.1016/j.scienta.2026.114883openalex-snapshot
Banana WOX6 synergizes with WUS2 to induce hormone-free regeneration via LAFL activation and metabolic reprogramming
inferred← citeshttps://doi.org/10.1016/j.tplants.2017.09.019openalex-snapshot
Alternative Splicing Control of Abiotic Stress Responses
inferred← citeshttps://doi.org/10.1016/j.tplants.2018.05.011openalex-snapshot
Out of Shape During Stress: A Key Role for Auxin
inferred← citeshttps://doi.org/10.1016/j.xplc.2020.100052openalex-snapshot
The Potassium Transporter OsHAK5 Alters Rice Architecture via ATP-Dependent Transmembrane Auxin Fluxes
inferred← citeshttps://doi.org/10.1017/qpb.2022.9openalex-snapshot
How alternative splicing changes the properties of plant proteins
inferred← citeshttps://doi.org/10.1021/acs.jproteome.9b00420openalex-snapshot
Comparative Proteomics Unravels the Differences in Salt Stress Response of Own-Rooted and 110R-Grafted Thompson Seedless Grapevines
inferred← citeshttps://doi.org/10.1038/ncomms11708openalex-snapshot
Unveiling the complexity of the maize transcriptome by single-molecule long-read sequencing
inferred← citeshttps://doi.org/10.1038/ncomms9138openalex-snapshot
ABA signalling is fine-tuned by antagonistic HAB1 variants
inferred← citeshttps://doi.org/10.1038/ncomms9139openalex-snapshot
An Arabidopsis PWI and RRM motif-containing protein is critical for pre-mRNA splicing and ABA responses
inferred← citeshttps://doi.org/10.1038/s41598-017-04534-7openalex-snapshot
Heterologous expression of the yeast Tpo1p or Pdr5p membrane transporters in Arabidopsis confers plant xenobiotic tolerance
inferred← citeshttps://doi.org/10.1038/s41598-020-79770-5openalex-snapshot
The application of a biostimulant based on tannins affects root architecture and improves tolerance to salinity in tomato plants
inferred← citeshttps://doi.org/10.1038/s41598-022-10299-5openalex-snapshot
Scavenging of nitric oxide up-regulates photosynthesis under drought in Festuca arundinacea and F. glaucescens but reduces their drought tolerance
inferred← citeshttps://doi.org/10.1038/srep46106openalex-snapshot
Identified of a novel cis-element regulating the alternative splicing of LcDREB2
inferred← citeshttps://doi.org/10.1051/fruits/2016010openalex-snapshot
Pineapple harvest index and fruit quality improvement by application of gibberellin and cytokinin
inferred← citeshttps://doi.org/10.1073/pnas.2100136118openalex-snapshot
An ABCC-type transporter endowing glyphosate resistance in plants
inferred← citeshttps://doi.org/10.1073/pnas.2535250123openalex-snapshot
Population genomics reveals ginseng domestication and ginsenoside biosynthesis
inferred← citeshttps://doi.org/10.1080/15592324.2021.1917170openalex-snapshot
Normal, novel or none: versatile regulation from alternative splicing
inferred← citeshttps://doi.org/10.1093/dnares/dsz010openalex-snapshot
The complexity of alternative splicing and landscape of tissue-specific expression in lotus (Nelumbo nucifera) unveiled by Illumina- and single-molecule real-time-based RNA-sequencing
inferred← citeshttps://doi.org/10.1093/jxb/eraa241openalex-snapshot
Auxin-mediated responses under salt stress: from developmental regulation to biotechnological applications
inferred← citeshttps://doi.org/10.1093/jxb/eraf304openalex-snapshot
The RNA recognition motif (RRM) of the Arabidopsis RS2Z32 and RS2Z33 splicing factors coordinates protein–protein and protein–RNA interactions, and contributes to their nucleocytoplasmic dynamics
inferred← citeshttps://doi.org/10.1093/jxb/eru486openalex-snapshot
Differential gene expression and alternative splicing between diploid and tetraploid watermelon
inferred← citeshttps://doi.org/10.1093/jxb/erv189openalex-snapshot
RNA processing in auxin and cytokinin pathways
inferred← citeshttps://doi.org/10.1093/nar/gkac338openalex-snapshot
Missplicing suppressor alleles of Arabidopsis PRE-MRNA PROCESSING FACTOR 8 increase splicing fidelity by reducing the use of novel splice sites
inferred← citeshttps://doi.org/10.1093/pcp/pcu157openalex-snapshot
The Major Facilitator Superfamily Transporter ZIFL2 Modulates Cesium and Potassium Homeostasis in Arabidopsis
inferred← citeshttps://doi.org/10.1093/pcp/pcz068openalex-snapshot
Biological Function of Changes in RNA Metabolism in Plant Adaptation to Abiotic Stress
inferred← citeshttps://doi.org/10.1093/plcell/koac047openalex-snapshot
The maize single-nucleus transcriptome comprehensively describes signaling networks governing movement and development of grass stomata
inferred← citeshttps://doi.org/10.1093/treephys/tpaf114openalex-snapshot
Boron reduces the damage of copper toxicity to Citrus sinensis cell wall structure and function via maintaining copper, calcium, magnesium, potassium and phosphorus homeostasis in subcellular fractions
inferred← citeshttps://doi.org/10.1101/2021.03.04.433936openalex-snapshot
Auxin-triggered changes in the Arabidopsis root tip (phospho)proteome reveal novel root growth regulators
inferred← citeshttps://doi.org/10.1101/718890openalex-snapshot
Alternative splicing of circadian clock genes correlates with temperature in field-grown sugarcane
inferred← citeshttps://doi.org/10.1104/pp.113.217778openalex-snapshot
Genome-Wide Detection of Condition-Sensitive Alternative Splicing in Arabidopsis Roots
inferred← citeshttps://doi.org/10.1104/pp.16.00240openalex-snapshot
Role of SKD1 Regulators LIP5 and IST1-LIKE1 in Endosomal Sorting and Plant Development
inferred← citeshttps://doi.org/10.1104/pp.16.01949openalex-snapshot
The Membrane Transport System of the Guard Cell and Its Integration for Stomatal Dynamics
inferred← citeshttps://doi.org/10.1104/pp.17.01260openalex-snapshot
Subcellular Compartmentation of Alternatively Spliced Transcripts Defines SERINE/ARGININE-RICH PROTEIN30 Expression
inferred← citeshttps://doi.org/10.1105/tpc.113.113803openalex-snapshot
Alternative Splicing at the Intersection of Biological Timing, Development, and Stress Responses
inferred← citeshttps://doi.org/10.1105/tpc.113.115881openalex-snapshot
Cellular Auxin Homeostasis under High Temperature Is Regulated through a SORTING NEXIN1–Dependent Endosomal Trafficking Pathway
inferred← citeshttps://doi.org/10.1105/tpc.113.117523openalex-snapshot
Complexity of the Alternative Splicing Landscape in Plants
inferred← citeshttps://doi.org/10.1105/tpc.113.250312openalex-snapshot
Alternative Splicing Confers a Dual Role in Polar Auxin Transport and Drought Stress Tolerance to the Major Facilitator Superfamily Transporter ZIFL1
inferred← citeshttps://doi.org/10.1105/tpc.114.131417openalex-snapshot
Arabidopsis Ensemble Reverse-Engineered Gene Regulatory Network Discloses Interconnected Transcription Factors in Oxidative Stress
inferred← citeshttps://doi.org/10.1105/tpc.16.00961openalex-snapshot
Changes in Gene Expression in Space and Time Orchestrate Environmentally Mediated Shaping of Root Architecture
inferred← citeshttps://doi.org/10.1105/tpc.18.00528openalex-snapshot
Phosphatidic Acid Directly Regulates PINOID-Dependent Phosphorylation and Activation of the PIN-FORMED2 Auxin Efflux Transporter in Response to Salt Stress
inferred← citeshttps://doi.org/10.1111/1462-2920.14952openalex-snapshot
The auxin‐inducible phosphate transporter AsPT5 mediates phosphate transport and is indispensable for arbuscule formation in Chinese milk vetch at moderately high phosphate supply
inferred← citeshttps://doi.org/10.1111/jipb.12327openalex-snapshot
Genome‐wide identification, expression analysis of auxin‐responsive GH3 family genes in maize ( Zea mays L.) under abiotic stresses
inferred← citeshttps://doi.org/10.1111/jipb.13365openalex-snapshot
Cowpea NAC1/NAC2 transcription factors improve growth and tolerance to drought and heat in transgenic cowpea through combined activation of photosynthetic and antioxidant mechanisms
inferred← citeshttps://doi.org/10.1111/mec.15289openalex-snapshot
Seedling response to water stress in valley oak (Quercus lobata) is shaped by different gene networks across populations
inferred← citeshttps://doi.org/10.1111/mec.16758openalex-snapshot
Transcriptome‐based analyses of adaptive divergence between two closely related spruce species on the Qinghai–Tibet plateau and adjacent regions
inferred← citeshttps://doi.org/10.1111/nph.12836openalex-snapshot
Characterization of FAB 1 phosphatidylinositol kinases in A rabidopsis pollen tube growth and fertilization
inferred← citeshttps://doi.org/10.1111/nph.17792openalex-snapshot
Mutually opposing activity of PIN7 splicing isoforms is required for auxin‐mediated tropic responses in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/nph.18799openalex-snapshot
C atsnap : a user‐friendly algorithm for determining the conservation of protein variants reveals extensive parallelisms in the evolution of alternative splicing
inferred← citeshttps://doi.org/10.1111/pce.13683openalex-snapshot
Genetic components of root architecture and anatomy adjustments to water‐deficit stress in spring barley
inferred← citeshttps://doi.org/10.1111/pce.13829openalex-snapshot
Functions and regulatory framework of ZmNST3 in maize under lodging and drought stress
inferred← citeshttps://doi.org/10.1111/pce.14256openalex-snapshot
Root traits for low input agroecosystems in Africa: Lessons from three case studies
inferred← citeshttps://doi.org/10.1111/ppl.12165openalex-snapshot
Regulation of potassium transport in plants under hostile conditions: implications for abiotic and biotic stress tolerance
inferred← citeshttps://doi.org/10.1111/tpj.14608openalex-snapshot
Arabidopsis PIC30 encodes a major facilitator superfamily transporter responsible for the uptake of picolinate herbicides
inferred← citeshttps://doi.org/10.1146/annurev-arplant-083123-090055openalex-snapshot
Alternative Splicing Dynamics in Plant Adaptive Responses to Stress
inferred← citeshttps://doi.org/10.1155/2015/419428openalex-snapshot
Shaping the Arabidopsis Transcriptome through Alternative Splicing
inferred← citeshttps://doi.org/10.1186/s12284-019-0273-2openalex-snapshot
Dissecting molecular mechanisms underlying salt tolerance in rice: a comparative transcriptional profiling of the contrasting genotypes
inferred← citeshttps://doi.org/10.1186/s12864-015-2283-9openalex-snapshot
Genome-wide transcriptome analyses of developing seeds from low and normal phytic acid soybean lines
inferred← citeshttps://doi.org/10.1186/s12864-017-3901-5openalex-snapshot
The PIN gene family in cotton (Gossypium hirsutum): genome-wide identification and gene expression analyses during root development and abiotic stress responses
inferred← citeshttps://doi.org/10.1186/s12864-017-4054-2openalex-snapshot
Identification and analysis of alternative splicing events in Phaseolus vulgaris and Glycine max
inferred← citeshttps://doi.org/10.1186/s12867-019-0139-6openalex-snapshot
Overlapping transcriptional expression response of wheat zinc-induced facilitator-like transporters emphasize important role during Fe and Zn stress
inferred← citeshttps://doi.org/10.1186/s12870-018-1339-9openalex-snapshot
Transcriptome analysis of alternative splicing in peanut (Arachis hypogaea L.)
inferred← citeshttps://doi.org/10.1186/s12870-020-02460-xopenalex-snapshot
The differential expression patterns of paralogs in response to stresses indicate expression and sequence divergences
inferred← citeshttps://doi.org/10.1186/s12870-021-03108-0openalex-snapshot
Transcriptomic analysis to reveal the differentially expressed miRNA targets and their miRNAs in response to Ralstonia solanacearum in ginger species
inferred← citeshttps://doi.org/10.1186/s12870-022-03489-wopenalex-snapshot
Linking genome wide RNA sequencing with physio-biochemical and cytological responses to catalogue key genes and metabolic pathways for alkalinity stress tolerance in lentil (Lens culinaris Medikus)
inferred← citeshttps://doi.org/10.1186/s12870-024-05749-3openalex-snapshot
Dissecting genomic regions and underlying candidate genes in groundnut MAGIC population for drought tolerance
inferred← citeshttps://doi.org/10.1186/s12870-024-05951-3openalex-snapshot
Functional study of ZmHDZ4 in maize (Zea mays) seedlings under drought stress
inferred← citeshttps://doi.org/10.1371/journal.pgen.1004375openalex-snapshot
Intron Retention in the 5′UTR of the Novel ZIF2 Transporter Enhances Translation to Promote Zinc Tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1371/journal.pone.0102301openalex-snapshot
Alternative Splicing of Arabidopsis IBR5 Pre-mRNA Generates Two IBR5 Isoforms with Distinct and Overlapping Functions
inferred← citeshttps://doi.org/10.1371/journal.pone.0147849openalex-snapshot
Transcriptome Sequencing in Response to Salicylic Acid in Salvia miltiorrhiza
inferred← citeshttps://doi.org/10.1371/journal.pone.0164280openalex-snapshot
Overexpression of Grain Amaranth (Amaranthus hypochondriacus) AhERF or AhDOF Transcription Factors in Arabidopsis thaliana Increases Water Deficit- and Salt-Stress Tolerance, Respectively, via Contrasting Stress-Amelioration Mechanisms
inferred← citeshttps://doi.org/10.1534/g3.118.200573openalex-snapshot
Transcriptome Analysis of Four Arabidopsis thaliana Mediator Tail Mutants Reveals Overlapping and Unique Functions in Gene Regulation
inferred← citeshttps://doi.org/10.18174/385576openalex-snapshot
Exploring the genetics underlying the responses to consecutive combinations of biotic stresses and drought in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.21203/rs.3.rs-115945/v1openalex-snapshot
Unravelling the Differential Expression of Potential microRNAs in Bacterial Wilt-resistant and Susceptible Ginger Species
inferred← citeshttps://doi.org/10.21203/rs.3.rs-35539/v1openalex-snapshot
Genome-wide identification and expression profiling of the PIN auxin transporter gene family in L. chinense
inferred← citeshttps://doi.org/10.21203/rs.3.rs-846593/v1openalex-snapshot
Genome-Wide Association Study (GWAS) Reveals The Genetic Basis of Brace Root Angle and Diameter in Maize
inferred← citeshttps://doi.org/10.21273/hortsci13278-18openalex-snapshot
Investigation on Various Aboveground Traits to Identify Drought Tolerance in Cowpea Seedlings
inferred← citeshttps://doi.org/10.23919/ccc55666.2022.9902755openalex-snapshot
Gene Differential Co-expression Network Analysis Reveals Drought-responsive Crucial Genes in Sorghum
inferred← citeshttps://doi.org/10.31742/isgpb.84.1.15openalex-snapshot
Unraveling the inheritance of powdery mildew disease resistance in blackgram [Vigna mungo L. Hepper]
inferred← citeshttps://doi.org/10.32604/phyton.2022.021698openalex-snapshot
Growth, ROS Markers, Antioxidant Enzymes, Osmotic Regulators and Metabolic Changes in Tartary Buckwheat Subjected to Short Drought
inferred← citeshttps://doi.org/10.32615/bp.2019.092openalex-snapshot
Molecular and physiological analysis of drought stress responses in Zea mays treated with plant growth promoting rhizobacteria
inferred← citeshttps://doi.org/10.3389/fagro.2021.648694openalex-snapshot
Potential Role of Plant Growth Regulators in Administering Crucial Processes Against Abiotic Stresses
inferred← citeshttps://doi.org/10.3389/fgene.2017.00014openalex-snapshot
The Evolutionary Relationship between Alternative Splicing and Gene Duplication
inferred← citeshttps://doi.org/10.3389/fgene.2022.822516openalex-snapshot
Identification of Candidate Genes for Salinity and Anaerobic Tolerance at the Germination Stage in Rice by Genome-Wide Association Analyses
inferred← citeshttps://doi.org/10.3389/fphys.2014.00201openalex-snapshot
Beyond cellular detoxification: a plethora of physiological roles for MDR transporter homologs in plants
inferred← citeshttps://doi.org/10.3389/fpls.2014.00151openalex-snapshot
Tolerance to drought and salt stress in plants: Unraveling the signaling networks
inferred← citeshttps://doi.org/10.3389/fpls.2014.00687openalex-snapshot
Membrane transporters and drought resistance – a complex issue
inferred← citeshttps://doi.org/10.3389/fpls.2015.00057openalex-snapshot
Post-transcriptional and post-translational regulations of drought and heat response in plants: a spider’s web of mechanisms
inferred← citeshttps://doi.org/10.3389/fpls.2015.00506openalex-snapshot
Identification of novel drought-responsive microRNAs and trans-acting siRNAs from Sorghum bicolor (L.) Moench by high-throughput sequencing analysis
inferred← citeshttps://doi.org/10.3389/fpls.2016.00519openalex-snapshot
Transcriptional Profiles of Drought-Related Genes in Modulating Metabolic Processes and Antioxidant Defenses in Lolium multiflorum
inferred← citeshttps://doi.org/10.3389/fpls.2017.00292openalex-snapshot
RBM25 Mediates Abiotic Responses in Plants
inferred← citeshttps://doi.org/10.3389/fpls.2017.00461openalex-snapshot
A Genome-Scale Analysis of the PIN Gene Family Reveals Its Functions in Cotton Fiber Development
inferred← citeshttps://doi.org/10.3389/fpls.2017.01308openalex-snapshot
Perturbation of Auxin Homeostasis and Signaling by PINOID Overexpression Induces Stress Responses in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2017.01924openalex-snapshot
Alternative Splicing of CIPK3 Results in Distinct Target Selection to Propagate ABA Signaling in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2019.00299openalex-snapshot
Overexpression of Cotton a DTX/MATE Gene Enhances Drought, Salt, and Cold Stress Tolerance in Transgenic Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2019.01614openalex-snapshot
Alternative Splicing of Circadian Clock Genes Correlates With Temperature in Field-Grown Sugarcane
inferred← citeshttps://doi.org/10.3389/fpls.2020.00776openalex-snapshot
Identification of QTLs Containing Resistance Genes for Sclerotinia Stem Rot in Brassica napus Using Comparative Transcriptomic Studies
inferred← citeshttps://doi.org/10.3389/fpls.2021.632676openalex-snapshot
Abscisic Acid Regulates the Root Growth Trajectory by Reducing Auxin Transporter PIN2 Protein Levels in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3389/fpls.2022.970113openalex-snapshot
The early response of oil palm (Elaeis guineensis Jacq.) plants to water deprivation: Expression analysis of miRNAs and their putative target genes, and similarities with the response to salinity stress
inferred← citeshttps://doi.org/10.3389/fpls.2023.1182074openalex-snapshot
Ticarcillin degradation product thiophene acetic acid is a novel auxin analog that promotes organogenesis in tomato
inferred← citeshttps://doi.org/10.3389/fpls.2023.1220928openalex-snapshot
Response of the organellar and nuclear (post)transcriptomes of Arabidopsis to drought
inferred← citeshttps://doi.org/10.3389/fpls.2023.1250588openalex-snapshot
Multilayered regulation of iron homeostasis in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2024.1329065openalex-snapshot
Dissection of the E8 locus in two early maturing Canadian soybean populations
inferred← citeshttps://doi.org/10.3389/fpls.2025.1652482openalex-snapshot
Nitric oxide regulates photosynthesis and the capacity of the antioxidant system under water deficit and rehydration in Lolium multiflorum/Festuca arundinacea introgression forms
inferred← citeshttps://doi.org/10.3390/cells10071665openalex-snapshot
The Arabidopsis Root Tip (Phospho)Proteomes at Growth-Promoting versus Growth-Repressing Conditions Reveal Novel Root Growth Regulators
inferred← citeshttps://doi.org/10.3390/genes11111286openalex-snapshot
Hybrid of Restricted and Penalized Maximum Likelihood Method for Efficient Genome-Wide Association Study
inferred← citeshttps://doi.org/10.3390/horticulturae9020175openalex-snapshot
Improved Annotation of the Peach (Prunus persica) Genome and Identification of Tissue- or Development Stage-Specific Alternative Splicing through the Integration of Iso-Seq and RNA-Seq Data
inferred← citeshttps://doi.org/10.3390/ijms150610424openalex-snapshot
Alternative Splicing in Plant Immunity
inferred← citeshttps://doi.org/10.3390/ijms18071427openalex-snapshot
Plants under Stress: Involvement of Auxin and Cytokinin
inferred← citeshttps://doi.org/10.3390/ijms20163867openalex-snapshot
Identification of Sugarcane Host Factors Interacting with the 6K2 Protein of the Sugarcane Mosaic Virus
inferred← citeshttps://doi.org/10.3390/ijms21093361openalex-snapshot
Genome-Wide Association and Prediction of Traits Related to Salt Tolerance in Autotetraploid Alfalfa (Medicago sativa L.)
inferred← citeshttps://doi.org/10.3390/ijms21196984openalex-snapshot
Two Alternative Splicing Variants of AtERF73/HRE1, HRE1α and HRE1β, Have Differential Transactivation Activities in Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms21239019openalex-snapshot
Adaptation Strategies of Halophytic Barley Hordeum marinum ssp. marinum to High Salinity and Osmotic Stress
inferred← citeshttps://doi.org/10.3390/ijms222011032openalex-snapshot
Mining Fiskeby III and Mandarin (Ottawa) Expression Profiles to Understand Iron Stress Tolerant Responses in Soybean
inferred← citeshttps://doi.org/10.3390/ijms25073859openalex-snapshot
Genome-Wide Identification, Expression Analysis under Abiotic Stress and Co-Expression Analysis of MATE Gene Family in Torreya grandis
inferred← citeshttps://doi.org/10.3390/jof7110892openalex-snapshot
Phosphorus Starvation- and Zinc Excess-Induced Astragalus sinicus AsZIP2 Zinc Transporter Is Suppressed by Arbuscular Mycorrhizal Symbiosis
inferred← citeshttps://doi.org/10.3390/plants10010148openalex-snapshot
Haplotype- and SNP-Based GWAS for Growth and Wood Quality Traits in Eucalyptus cladocalyx Trees under Arid Conditions
inferred← citeshttps://doi.org/10.3390/plants11010102openalex-snapshot
Diverse Functions of Plant Zinc-Induced Facilitator-like Transporter for Their Emerging Roles in Crop Trait Enhancement
inferred← citeshttps://doi.org/10.3390/plants12142708openalex-snapshot
Transcriptional Profiling Reveals the Wheat Defences against Fusarium Head Blight Disease Regulated by a NAC Transcription Factor
inferred← citeshttps://doi.org/10.3390/plants12203542openalex-snapshot
Transcriptome and Proteome Association Analysis to Screen Candidate Genes Related to Salt Tolerance in Reaumuria soongorica Leaves under Salt Stress
inferred← citeshttps://doi.org/10.3390/plants13060837openalex-snapshot
Transcriptome Profiling of a Salt Excluder Hybrid Grapevine Rootstock ‘Ruggeri’ throughout Salinity
inferred← citeshttps://doi.org/10.3390/plants14071064openalex-snapshot
Exploring Alternative Splicing in Response to Salinity: A Tissue-Level Comparative Analysis Using Arabidopsis thaliana Public Transcriptomic Data
inferred← citeshttps://doi.org/10.3390/plants2040650openalex-snapshot
Calcium: The Missing Link in Auxin Action
inferred← citeshttps://doi.org/10.3390/plants9070868openalex-snapshot
In Vivo Reporters for Visualizing Alternative Splicing of Hormonal Genes
inferred← citeshttps://doi.org/10.3390/plants9101311openalex-snapshot
Auxin Homeostasis and Distribution of the Auxin Efflux Carrier PIN2 Require Vacuolar NHX-Type Cation/H+ Antiporter Activity
inferred← citeshttps://doi.org/10.4161/psb.25688openalex-snapshot
ZIFL1.1 transporter modulates polar auxin transport by stabilizing membrane abundance of multiple PINs inArabidopsisroot tip
inferred← citeshttps://doi.org/10.5539/jps.v6n1p58openalex-snapshot
Interaction of Nitric Oxide with Phytohormones under Drought Stress
inferred← citeshttps://doi.org/10.5586/asbp.2014.035openalex-snapshot
The Old and New RNA World
inferred← citeshttps://doi.org/10.6084/m9.figshare.12495509openalex-snapshot
Additional file 10 of The differential expression patterns of paralogs in response to stresses indicate expression and sequence divergences
inferred← citeshttps://doi.org/10.6084/m9.figshare.12495518openalex-snapshot
Additional file 11 of The differential expression patterns of paralogs in response to stresses indicate expression and sequence divergences
inferred← citeshttps://doi.org/10.6084/m9.figshare.12495524openalex-snapshot
Additional file 12 of The differential expression patterns of paralogs in response to stresses indicate expression and sequence divergences
inferred← citeshttps://doi.org/10.6084/m9.figshare.12495530openalex-snapshot
Additional file 13 of The differential expression patterns of paralogs in response to stresses indicate expression and sequence divergences
inferred← citeshttps://doi.org/10.6084/m9.figshare.12495536openalex-snapshot
Additional file 14 of The differential expression patterns of paralogs in response to stresses indicate expression and sequence divergences
inferred← citeshttps://doi.org/10.6084/m9.figshare.12495542openalex-snapshot
Additional file 15 of The differential expression patterns of paralogs in response to stresses indicate expression and sequence divergences
inferred← citeshttps://doi.org/10.6084/m9.figshare.12495548openalex-snapshot
Additional file 1 of The differential expression patterns of paralogs in response to stresses indicate expression and sequence divergences
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