| 1 | Boosting photosynthesis opens new opportunities for agriculture sustainability and circular economy: The BEST‐CROP research and innovation action | 4.0 | 7 | Citations (PDF) |
| 2 | Constitutive activation of ABA receptors in Arabidopsis reveals unique regulatory circuitries | 5.3 | 23 | Citations (PDF) |
| 3 | Synthesis and import of GDP‐
l
‐fucose into the Golgi affect plant–water relations | 5.3 | 15 | Citations (PDF) |
| 4 | Stomatal CO2 responses at sub- and above-ambient CO2 levels employ different pathways in Arabidopsis | 4.0 | 11 | Citations (PDF) |
| 5 | MPK12 in stomatal CO2 signaling: function beyond its kinase activity | 5.3 | 19 | Citations (PDF) |
| 6 | A role for ethylene signaling and biosynthesis in regulating and accelerating CO2‐ and abscisic acid‐mediated stomatal movements in Arabidopsis | 5.3 | 30 | Citations (PDF) |
| 7 | ALMT‐independent guard cell R‐type anion currents | 5.3 | 11 | Citations (PDF) |
| 8 | THESEUS1 modulates cell wall stiffness and abscisic acid production in
Arabidopsis thaliana | 5.3 | 133 | Citations (PDF) |
| 9 | Phosphorylation of the plasma membrane H+-ATPase AHA2 by BAK1 is required for ABA-induced stomatal closure in Arabidopsis | 5.8 | 103 | Citations (PDF) |
| 10 | Elevated
CO
2
induces rapid dephosphorylation of plasma membrane H
+
‐
ATPase
in guard cells | 5.3 | 26 | Citations (PDF) |
| 11 | Stomatal CO
2
/bicarbonate sensor consists of two interacting protein kinases, Raf-like HT1 and non-kinase-activity requiring MPK12/MPK4 | 8.2 | 80 | Citations (PDF) |
| 12 | A role for calcium‐dependent protein kinases in differential CO2‐ and ABA‐controlled stomatal closing and low CO2‐induced stomatal opening in Arabidopsis | 5.3 | 68 | Citations (PDF) |
| 13 | Ozone responses in Arabidopsis: beyond stomatal conductance | 4.0 | 43 | Citations (PDF) |
| 14 | Combined action of guard cell plasma membrane rapid- and slow-type anion channels in stomatal regulation | 4.0 | 37 | Citations (PDF) |
| 15 | Jasmonic acid and salicylic acid play minor roles in stomatal regulation by CO2, abscisic acid, darkness, vapor pressure deficit and ozone | 4.0 | 50 | Citations (PDF) |
| 16 | Multiparameter in vivo imaging in plants using genetically encoded fluorescent indicator multiplexing | 4.0 | 18 | Citations (PDF) |
| 17 | Rapid depolarization and cytosolic calcium increase go hand‐in‐hand in mesophyll cells’ ozone response | 5.3 | 5 | Citations (PDF) |
| 18 | Differential role of MAX2 and strigolactones in pathogen, ozone, and stomatal responses | 1.6 | 41 | Citations (PDF) |
| 19 | Genetic controls of short- and long-term stomatal CO2 responses in Arabidopsis thaliana | 2.1 | 13 | Citations (PDF) |
| 20 | STRESS INDUCED FACTOR 2 Regulates Arabidopsis Stomatal Immunity through Phosphorylation of the Anion Channel SLAC1 | 5.8 | 54 | Citations (PDF) |
| 21 | The role of Arabidopsis ABA receptors from the PYR/PYL/RCAR family in stomatal acclimation and closure signal integration | 8.0 | 191 | Citations (PDF) |
| 22 | Calcium signals in guard cells enhance the efficiency by which abscisic acid triggers stomatal closure | 5.3 | 115 | Citations (PDF) |
| 23 | A ligand-independent origin of abscisic acid perception | 5.3 | 130 | Citations (PDF) |
| 24 | Reactive Oxygen Species, Photosynthesis, and Environment in the Regulation of Stomata | 4.2 | 57 | Citations (PDF) |
| 25 | Arabidopsis MLO2 is a negative regulator of sensitivity to extracellular reactive oxygen species | 4.8 | 27 | Citations (PDF) |
| 26 | Stomatal VPD Response: There Is More to the Story Than ABA | 4.0 | 205 | Citations (PDF) |
| 27 | ABA‐mediated regulation of stomatal density is OST1‐independent | 1.6 | 37 | Citations (PDF) |
| 28 | Insights into the Molecular Mechanisms of CO2-Mediated Regulation of Stomatal Movements | 2.5 | 119 | Citations (PDF) |
| 29 | Abscisic acid-independent stomatal CO
2
signal transduction pathway and convergence of CO
2
and ABA signaling downstream of OST1 kinase | 5.3 | 118 | Citations (PDF) |
| 30 | Mitogen‐activated protein kinases MPK4 and MPK12 are key components mediating CO2‐induced stomatal movements | 4.0 | 83 | Citations (PDF) |
| 31 | The Receptor-like Pseudokinase GHR1 Is Required for Stomatal Closure | 5.8 | 135 | Citations (PDF) |
| 32 | Gas exchange-yield relationships of malting barley genotypes treated with fungicides and biostimulants | 4.3 | 11 | Citations (PDF) |
| 33 | The Role of ENHANCED RESPONSES TO ABA1 (ERA1) in Arabidopsis Stomatal Responses Is Beyond ABA Signaling | 4.0 | 33 | Citations (PDF) |
| 34 | Fern Stomatal Responses to ABA and CO2 Depend on Species and Growth Conditions | 4.0 | 96 | Citations (PDF) |
| 35 | A Rationally Designed Agonist Defines Subfamily IIIA Abscisic Acid Receptors As Critical Targets for Manipulating Transpiration | 2.5 | 77 | Citations (PDF) |
| 36 | Isolation of guard-cell enriched tissue for RNA extraction | 0.2 | 7 | Citations (PDF) |
| 37 | A Dominant Mutation in the HT1 Kinase Uncovers Roles of MAP Kinases and GHR1 in CO2-Induced Stomatal Closure | 5.8 | 117 | Citations (PDF) |
| 38 | BODYGUARD is required for the biosynthesis of cutin in Arabidopsis | 5.3 | 62 | Citations (PDF) |
| 39 | Natural Variation in Arabidopsis Cvi-0 Accession Reveals an Important Role of MPK12 in Guard Cell CO2 Signaling | 3.1 | 97 | Citations (PDF) |
| 40 | Guard cell SLAC1‐type anion channels mediate flagellin‐induced stomatal closure | 5.3 | 167 | Citations (PDF) |
| 41 | Large-Scale Phenomics Identifies Primary and Fine-Tuning Roles for CRKs in Responses Related to Oxidative Stress | 2.2 | 213 | Citations (PDF) |
| 42 | A specialized histone H1 variant is required for adaptive responses to complex abiotic stress and related DNA methylation in Arabidopsis | 4.0 | 117 | Citations (PDF) |
| 43 | Abscisic Acid Transport and Homeostasis in the Context of Stomatal Regulation | 18.4 | 122 | Citations (PDF) |
| 44 | The Role of ABA Recycling and Transporter Proteins in Rapid Stomatal Responses to Reduced Air Humidity, Elevated CO2, and Exogenous ABA | 18.4 | 99 | Citations (PDF) |
| 45 | The F-box protein MAX2 contributes to resistance to bacterial phytopathogens in Arabidopsis thaliana | 3.0 | 127 | Citations (PDF) |
| 46 | To open or to close: species‐specific stomatal responses to simultaneously applied opposing environmental factors | 5.3 | 114 | Citations (PDF) |
| 47 | The Arabidopsis thaliana cysteine-rich receptor-like kinases CRK6 and CRK7 protect against apoplastic oxidative stress | 1.5 | 151 | Citations (PDF) |
| 48 | Closing gaps: linking elements that control stomatal movement | 5.3 | 368 | Citations (PDF) |
| 49 | Mutations in the SLAC1 anion channel slow stomatal opening and severely reduce K+ uptake channel activity via enhanced cytosolic [Ca2+] and increased Ca2+ sensitivity of K+ uptake channels | 5.3 | 58 | Citations (PDF) |
| 50 | PYR/RCAR Receptors Contribute to Ozone-, Reduced Air Humidity-, Darkness-, and CO2-Induced Stomatal Regulation | 4.0 | 216 | Citations (PDF) |
| 51 | Calcium-Dependent and -Independent Stomatal Signaling Network and Compensatory Feedback Control of Stomatal Opening via Ca2+ Sensitivity Priming | 4.0 | 53 | Citations (PDF) |
| 52 | Defense‐related transcription factors WRKY70 and WRKY54 modulate osmotic stress tolerance by regulating stomatal aperture in Arabidopsis | 5.3 | 280 | Citations (PDF) |
| 53 | Identification of Cyclic GMP-Activated Nonselective Ca2+-Permeable Cation Channels and Associated CNGC5 and CNGC6 Genes in Arabidopsis Guard Cells
| 4.0 | 138 | Citations (PDF) |
| 54 | The PYL4 A194T Mutant Uncovers a Key Role of PYR1-LIKE4/PROTEIN PHOSPHATASE 2CA Interaction for Abscisic Acid Signaling and Plant Drought Resistance | 4.0 | 198 | Citations (PDF) |
| 55 | Arabidopsis PYR/PYL/RCAR Receptors Play a Major Role in Quantitative Regulation of Stomatal Aperture and Transcriptional Response to Abscisic Acid | 5.8 | 612 | Citations (PDF) |
| 56 | ERD15—An attenuator of plant ABA responses and stomatal aperture | 3.0 | 55 | Citations (PDF) |
| 57 | Anion channels in plant cells | 3.3 | 63 | Citations (PDF) |
| 58 | Central functions of bicarbonate in S‐type anion channel activation and OST1 protein kinase in CO2 signal transduction in guard cell | 5.2 | 190 | Citations (PDF) |
| 59 | Natural variation in ozone sensitivity among Arabidopsis thaliana accessions and its relation to stomatal conductance | 4.8 | 116 | Citations (PDF) |
| 60 | Ozone-triggered rapid stomatal response involves the production of reactive oxygen species, and is controlled by SLAC1 and OST1 | 4.0 | 287 | Citations (PDF) |
| 61 | Stomatal action directly feeds back on leaf turgor: new insights into the regulation of the plant water status from non-invasive pressure probe measurements | 4.0 | 91 | Citations (PDF) |
| 62 | Arabidopsis
GRI is involved in the regulation of cell death induced by extracellular ROS | 5.3 | 83 | Citations (PDF) |
| 63 | Nitric oxide modulates ozone‐induced cell death, hormone biosynthesis and gene expression in Arabidopsis thaliana | 4.0 | 189 | Citations (PDF) |
| 64 | Complex phenotypic profiles leading to ozone sensitivity in Arabidopsis thaliana mutants | 4.8 | 69 | Citations (PDF) |
| 65 | SLAC1 is required for plant guard cell S-type anion channel function in stomatal signalling | 31.3 | 831 | Citations (PDF) |
| 66 | A novel device detects a rapid ozone-induced transient stomatal closure in intact Arabidopsis and its absence in abi2 mutant | 2.2 | 106 | Citations (PDF) |
| 67 | Components of apoplastic ascorbate use in
Betula pendula
leaves exposed to CO
2
and O
3
enrichment | 5.3 | 28 | Citations (PDF) |
| 68 | Signalling and cell death in ozone-exposed plants | 4.8 | 453 | Citations (PDF) |
| 69 | Arabidopsis RADICAL-INDUCED CELL DEATH1 Belongs to the WWE Protein–Protein Interaction Domain Protein Family and Modulates Abscisic Acid, Ethylene, and Methyl Jasmonate Responses | 5.8 | 228 | Citations (PDF) |
| 70 | Mutual antagonism of ethylene and jasmonic acid regulates ozone-induced spreading cell death inArabidopsis | 4.0 | 115 | Citations (PDF) |
| 71 | Acclimation of antioxidant pools to the light environment in a natural forest canopy | 5.3 | 49 | Citations (PDF) |
| 72 | Impact of ozone on monoterpene emissions and evidence for an isoprene-like antioxidant action of monoterpenes emitted by Quercus ilex leaves | 2.3 | 291 | Citations (PDF) |
| 73 | Do the capacity and kinetics for modification of xanthophyll cycle pool size depend on growth irradiance in temperate trees? | 4.8 | 85 | Citations (PDF) |
| 74 | Physiological effects of immune challenge in captive greenfinches (Carduelis chloris) | 0.7 | 39 | Citations (PDF) |
| 75 | Repeatability of condition indices in captive greenfinches (Carduelis chloris) | 0.7 | 90 | Citations (PDF) |
| 76 | Ascorbate transport from the apoplast to the symplast in intact leaves | 2.2 | 27 | Citations (PDF) |
| 77 | Ozone Flux to Plasmalemma in Barley and Wheat is controlled by Stomata rather than by direct Reaction of Ozone with Cell Wall Ascorbate | 2.9 | 41 | Citations (PDF) |
| 78 | FRET kinase sensor development reveals SnRK2/OST1 activation by ABA but not by MeJA and high CO2 during stomatal closure | 1.0 | 94 | Citations (PDF) |
| 79 | MAP4K1 and MAP4K2 regulate ABA-induced and Ca
2+
-mediated stomatal closure in
Arabidopsis | 8.2 | 8 | Citations (PDF) |
| 80 | Arabidopsis
OST1
homologs of barley are involved in stomatal regulation | 3.8 | 1 | Citations (PDF) |
