On the public citation graph
Carbon dioxide and water transport through plant aquaporins
0 signed · 478 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/cphc.200900270openalex-snapshot
110 Years of the Meyer–Overton Rule: Predicting Membrane Permeability of Gases and Other Small Compounds
inferredcites →https://doi.org/10.1002/cphc.201100034openalex-snapshot
Intrinsic CO2 Permeability of Cell Membranes and Potential Biological Relevance of CO2 Channels
inferredcites →https://doi.org/10.1002/j.1460-2075.1993.tb05877.xopenalex-snapshot
The vacuolar membrane protein gamma‐TIP creates water specific channels in Xenopus oocytes.
inferredcites →https://doi.org/10.1007/978-94-007-6988-5openalex-snapshot
Photosynthesis in Bryophytes and Early Land Plants
inferredcites →https://doi.org/10.1007/bf00206296openalex-snapshot
The kinetics of ribulose-1,5-bisphosphate carboxylase/oxygenase in vivo inferred from measurements of photosynthesis in leaves of transgenic tobacco
inferredcites →https://doi.org/10.1007/bf00384257openalex-snapshot
Some relationships between the biochemistry of photosynthesis and the gas exchange of leaves
inferredcites →https://doi.org/10.1007/pl00008138openalex-snapshot
Chemical composition of apoplastic transport barriers in relation to radial hydraulic conductivity of corn roots (Zea mays L.)
inferredcites →https://doi.org/10.1007/s00018-009-0075-6openalex-snapshot
Plant aquaporin selectivity: where transport assays, computer simulations and physiology meet
inferredcites →https://doi.org/10.1007/s00232-010-9240-yopenalex-snapshot
Nonenzymatic Augmentation of Lactate Transport via Monocarboxylate Transporter Isoform 4 by Carbonic Anhydrase II
inferredcites →https://doi.org/10.1007/s002329900120openalex-snapshot
Phylogenetic Characterization of the MIP Family of Transmembrane Channel Proteins
inferredcites →https://doi.org/10.1007/s00299-015-1796-7openalex-snapshot
AcPIP2, a plasma membrane intrinsic protein from halophyte Atriplex canescens, enhances plant growth rate and abiotic stress tolerance when overexpressed in Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/s00299-015-1891-9openalex-snapshot
An aquaporin gene from halophyte Sesuvium portulacastrum, SpAQP1, increases salt tolerance in transgenic tobacco
inferredcites →https://doi.org/10.1007/s00425-003-1105-5openalex-snapshot
Plant responses to drought, salinity and extreme temperatures: towards genetic engineering for stress tolerance
inferredcites →https://doi.org/10.1007/s00425-007-0520-4openalex-snapshot
Overexpression of a Panax ginseng tonoplast aquaporin alters salt tolerance, drought tolerance and cold acclimation ability in transgenic Arabidopsis plants
inferredcites →https://doi.org/10.1007/s00425-013-1988-8openalex-snapshot
Differential tissue-specific expression of NtAQP1 in Arabidopsis thaliana reveals a role for this protein in stomatal and mesophyll conductance of CO2 under standard and salt-stress conditions
inferredcites →https://doi.org/10.1007/s004250000390openalex-snapshot
Expression and distribution of a vacuolar aquaporin in young and mature leaf tissues of Brassica napus in relation to water fluxes
inferredcites →https://doi.org/10.1007/s00438-014-0874-9openalex-snapshot
Genome-wide identification and characterization of aquaporin genes (AQPs) in Chinese cabbage (Brassica rapa ssp. pekinensis)
inferredcites →https://doi.org/10.1007/s00438-015-1038-2openalex-snapshot
Genome-wide identification and characterization of aquaporin gene family in common bean (Phaseolus vulgaris L.)
inferredcites →https://doi.org/10.1007/s10142-007-0065-4openalex-snapshot
The PIP and TIP aquaporins in wheat form a large and diverse family with unique gene structures and functionally important features
inferredcites →https://doi.org/10.1007/s10265-007-0130-zopenalex-snapshot
Expression of the Vicia faba VfPIP1 gene in Arabidopsis thaliana plants improves their drought resistance
inferredcites →https://doi.org/10.1007/s10265-011-0413-2openalex-snapshot
Hydrogen peroxide permeability of plasma membrane aquaporins of Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/s10265-013-0548-4openalex-snapshot
The photosynthetic response of tobacco plants overexpressing ice plant aquaporin McMIPB to a soil water deficit and high vapor pressure deficit
inferredcites →https://doi.org/10.1007/s11103-005-0352-1openalex-snapshot
Whole Gene Family Expression and Drought Stress Regulation of Aquaporins
inferredcites →https://doi.org/10.1007/s11103-006-9022-1openalex-snapshot
Localization and Quantification of Plasma Membrane Aquaporin Expression in Maize Primary Root: A Clue to Understanding their Role as Cellular Plumbers
inferredcites →https://doi.org/10.1007/s11103-007-9181-8openalex-snapshot
Transgenic Arabidopsis and tobacco plants overexpressing an aquaporin respond differently to various abiotic stresses
inferredcites →https://doi.org/10.1007/s11103-008-9373-xopenalex-snapshot
The expression pattern of plasma membrane aquaporins in maize leaf highlights their role in hydraulic regulation
inferredcites →https://doi.org/10.1007/s11103-010-9658-8openalex-snapshot
Intracellular pH sensing is altered by plasma membrane PIP aquaporin co-expression
inferredcites →https://doi.org/10.1007/s11103-013-0084-6openalex-snapshot
Involvement of rose aquaporin RhPIP1;1 in ethylene-regulated petal expansion through interaction with RhPIP2;1
inferredcites →https://doi.org/10.1007/s11103-014-0232-7openalex-snapshot
Expression and characterization of plasma membrane aquaporins in stomatal complexes of Zea mays
inferredcites →https://doi.org/10.1007/s11103-015-0305-2openalex-snapshot
Constitutive and stress-inducible overexpression of a native aquaporin gene (MusaPIP2;6) in transgenic banana plants signals its pivotal role in salt tolerance
inferredcites →https://doi.org/10.1007/s11104-014-2070-4openalex-snapshot
Nitrogen availability affects hydraulic conductivity of rice roots, possibly through changes in aquaporin gene expression
inferredcites →https://doi.org/10.1007/s11105-015-0881-yopenalex-snapshot
Overexpression of AcNIP5;1, a Novel Nodulin-Like Intrinsic Protein from Halophyte Atriplex canescens, Enhances Sensitivity to Salinity and Improves Drought Tolerance in Arabidopsis
inferredcites →https://doi.org/10.1007/s11248-012-9600-8openalex-snapshot
Members of rice plasma membrane intrinsic proteins subfamily are involved in arsenite permeability and tolerance in plants
inferredcites →https://doi.org/10.1007/s12033-008-9084-1openalex-snapshot
Indian Mustard Aquaporin Improves Drought and Heavy-metal Resistance in Tobacco
inferredcites →https://doi.org/10.1016/bs.mie.2014.12.006openalex-snapshot
Major Intrinsic Protein Superfamily
inferredcites →https://doi.org/10.1016/j.bbagen.2013.09.037openalex-snapshot
Aquaporins and membrane diffusion of CO2 in living organisms
inferredcites →https://doi.org/10.1016/j.bbagen.2013.11.012openalex-snapshot
Unraveling aquaporin interaction partners
inferredcites →https://doi.org/10.1016/j.bbagen.2013.12.001openalex-snapshot
Diversity and evolution of membrane intrinsic proteins
inferredcites →https://doi.org/10.1016/j.bbamem.2006.03.012openalex-snapshot
Functional aquaporin diversity in plants
inferredcites →https://doi.org/10.1016/j.bbamem.2009.03.009openalex-snapshot
Aquaporins are multifunctional water and solute transporters highly divergent in living organisms
inferredcites →https://doi.org/10.1016/j.bbamem.2013.08.011openalex-snapshot
Maize plasma membrane aquaporin ZmPIP2;5, but not ZmPIP1;2, facilitates transmembrane diffusion of hydrogen peroxide
inferredcites →https://doi.org/10.1016/j.bbamem.2015.03.013openalex-snapshot
Intra-helical salt-bridge and helix destabilizing residues within the same helical turn: Role of functionally important loop E half-helix in channel regulation of major intrinsic proteins
inferredcites →https://doi.org/10.1016/j.bpj.2016.01.026openalex-snapshot
PIP Water Transport and Its pH Dependence Are Regulated by Tetramer Stoichiometry
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.febslet.2005.06.082openalex-snapshot
Water channel activities of Mimosa pudica plasma membrane intrinsic proteins are regulated by direct interaction and phosphorylation
inferredcites →https://doi.org/10.1016/j.febslet.2005.09.076openalex-snapshot
Novel type aquaporin SIPs are mainly localized to the ER membrane and show cell‐specific expression in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.febslet.2008.06.012openalex-snapshot
Molecular determinants of ammonia and urea conductance in plant aquaporin homologs
inferredcites →https://doi.org/10.1016/j.febslet.2008.11.002openalex-snapshot
AtTIP1;3 and AtTIP5;1 , the only highly expressed Arabidopsis pollen‐specific aquaporins, transport water and urea
inferredcites →https://doi.org/10.1016/j.febslet.2013.02.038openalex-snapshot
Structural basis for pH gating of plant aquaporins
inferredcites →https://doi.org/10.1016/j.febslet.2013.05.046openalex-snapshot
Assessment of the requirement for aquaporins in the thylakoid membrane of plant chloroplasts to sustain photosynthetic water oxidation
inferredcites →https://doi.org/10.1016/j.febslet.2015.10.018openalex-snapshot
PIP1 aquaporins: Intrinsic water channels or PIP2 aquaporin modulators?
inferredcites →https://doi.org/10.1016/j.jmb.2005.05.001openalex-snapshot
The 5Å Structure of Heterologously Expressed Plant Aquaporin SoPIP2;1
inferredcites →https://doi.org/10.1016/j.jmb.2009.01.065openalex-snapshot
Structural and Functional Analysis of SoPIP2;1 Mutants Adds Insight into Plant Aquaporin Gating
inferredcites →https://doi.org/10.1016/j.jplph.2016.02.001openalex-snapshot
Responses of hybrid aspen over-expressing a PIP2;5 aquaporin to low root temperature
inferredcites →https://doi.org/10.1016/j.jprot.2015.07.029openalex-snapshot
RNAi-mediated downregulation of poplar plasma membrane intrinsic proteins (PIPs) changes plasma membrane proteome composition and affects leaf physiology
inferredcites →https://doi.org/10.1016/j.jsb.2006.11.008openalex-snapshot
Exploring gas permeability of cellular membranes and membrane channels with molecular dynamics
inferredcites →https://doi.org/10.1016/j.molp.2016.04.006openalex-snapshot
Single Mutations in the Transmembrane Domains of Maize Plasma Membrane Aquaporins Affect the Activity of Monomers within a Heterotetramer
inferredcites →https://doi.org/10.1016/j.molp.2016.04.012openalex-snapshot
Interactions between Transmembrane Helices within Monomers of the Aquaporin AtPIP2;1 Play a Crucial Role in Tetramer Formation
inferredcites →https://doi.org/10.1016/j.pbi.2009.08.002openalex-snapshot
The exploring root—root growth responses to local environmental conditions
inferredcites →https://doi.org/10.1016/j.pbi.2012.01.011openalex-snapshot
Mechanisms underlying CO2 diffusion in leaves
inferredcites →https://doi.org/10.1016/j.pbi.2013.11.002openalex-snapshot
Gene duplication as a driver of plant morphogenetic evolution
inferredcites →https://doi.org/10.1016/j.pbi.2016.04.003openalex-snapshot
Strategies for improving C4 photosynthesis
inferredcites →https://doi.org/10.1016/j.pbiomolbio.2014.01.002openalex-snapshot
Insights into structural mechanisms of gating induced regulation of aquaporins
inferredcites →https://doi.org/10.1016/j.plantsci.2005.04.013openalex-snapshot
Sense and antisense expression of plasma membrane aquaporin BnPIP1 from Brassica napus in tobacco and its effects on plant drought resistance
inferredcites →https://doi.org/10.1016/j.plantsci.2012.05.009openalex-snapshot
Mesophyll diffusion conductance to CO2: An unappreciated central player in photosynthesis
inferredcites →https://doi.org/10.1016/j.plantsci.2015.06.002openalex-snapshot
Metalloido-porins: Essentiality of Nodulin 26-like intrinsic proteins in metalloid transport
inferredcites →https://doi.org/10.1016/j.plaphy.2011.06.002openalex-snapshot
Identification and characterization of two plasma membrane aquaporins in durum wheat (Triticum turgidum L. subsp. durum) and their role in abiotic stress tolerance
inferredcites →https://doi.org/10.1016/j.plaphy.2013.10.025openalex-snapshot
Genome-wide analysis and expression profiling of the Solanum tuberosum aquaporins
inferredcites →https://doi.org/10.1016/j.plgene.2014.12.002openalex-snapshot
Genome-wide identification and characterization of the aquaporin gene family in Sorghum bicolor (L.)
inferredcites →https://doi.org/10.1016/j.sbi.2015.08.004openalex-snapshot
Structural insights into aquaporin selectivity and regulation
inferredcites →https://doi.org/10.1016/j.tplants.2012.12.003openalex-snapshot
Insights into plant plasma membrane aquaporin trafficking
inferredcites →https://doi.org/10.1016/j.tracli.2006.02.006openalex-snapshot
Rh proteins vs Amt proteins: an organismal and phylogenetic perspective on CO2 and NH3 gas channels
inferredcites →https://doi.org/10.1016/j.tracli.2006.03.001openalex-snapshot
Biological gas channels for NH3 and CO2: evidence that Rh (Rhesus) proteins are CO2 channels
inferredcites →https://doi.org/10.1016/s0014-5793(02)03581-0openalex-snapshot
New potent inhibitors of aquaporins: silver and gold compounds inhibit aquaporins of plant and human origin
inferredcites →https://doi.org/10.1016/s0168-9452(99)00269-1openalex-snapshot
Molecular cloning of a novel water channel from rice: its products expression in Xenopus oocytes and involvement in chilling tolerance
inferredcites →https://doi.org/10.1016/s1673-8527(09)60057-6openalex-snapshot
Overexpression of the tonoplast aquaporin AtTIP5;1 conferred tolerance to boron toxicity in Arabidopsis
inferredcites →https://doi.org/10.1017/s0033583506004458openalex-snapshot
The structure of aquaporins
inferredcites →https://doi.org/10.1021/bi051132dopenalex-snapshot
A Novel Carbonic Anhydrase II Binding Site Regulates NHE1 Activity
inferredcites →https://doi.org/10.1021/jp809152copenalex-snapshot
To Gate or Not To Gate: Using Molecular Dynamics Simulations To Morph Gated Plant Aquaporins into Constitutively Open Conformations
inferredcites →https://doi.org/10.1023/a:1026439226716openalex-snapshot
Water uptake by plant roots: an integration of views
inferredcites →https://doi.org/10.1023/b:plan.0000040900.61345.a6openalex-snapshot
An Expression Analysis of a Gene Family Encoding Plasma Membrane Aquaporins in Response to Abiotic Stresses in Arabidopsis Thaliana
inferredcites →https://doi.org/10.1038/361549a0openalex-snapshot
Cloning and expression of apical membrane water channel of rat kidney collecting tubule
inferredcites →https://doi.org/10.1038/nature01853openalex-snapshot
Cytosolic pH regulates root water transport during anoxic stress through gating of aquaporins
inferredcites →https://doi.org/10.1038/nature02027openalex-snapshot
The tobacco aquaporin NtAQP1 is a membrane CO2 pore with physiological functions
inferredcites →https://doi.org/10.1038/nature04316openalex-snapshot
Structural mechanism of plant aquaporin gating
inferredcites →https://doi.org/10.1038/nature09916openalex-snapshot
Ancestral polyploidy in seed plants and angiosperms
inferredcites →https://doi.org/10.1038/sj.cr.7310035openalex-snapshot
Expression and functional analysis of the rice plasma-membrane intrinsic protein gene family
inferredcites →https://doi.org/10.1038/srep00538openalex-snapshot
Gas-tight triblock-copolymer membranes are converted to CO2 permeable by insertion of plant aquaporins
inferredcites →https://doi.org/10.1038/srep06665openalex-snapshot
A refined model of water and CO2 membrane diffusion: Effects and contribution of sterols and proteins
inferredcites →https://doi.org/10.1038/srep17207openalex-snapshot
Harpin Hpa1 Interacts with Aquaporin PIP1;4 to Promote the Substrate Transport and Photosynthesis in Arabidopsis
inferredcites →https://doi.org/10.1038/srep21640openalex-snapshot
Enhanced Boron Tolerance in Plants Mediated by Bidirectional Transport Through Plasma Membrane Intrinsic Proteins
inferredcites →https://doi.org/10.1042/bc20040122openalex-snapshot
Specific plasma membrane aquaporins of the PIP1 subfamily are expressed in sieve elements and guard cells
inferredcites →https://doi.org/10.1042/bj20080275openalex-snapshot
Structure–function analysis of plant aquaporin At PIP2;1 gating by divalent cations and protons
inferredcites →https://doi.org/10.1042/bj20111704openalex-snapshot
A conserved cysteine residue is involved in disulfide bond formation between plant plasma membrane aquaporin monomers
inferredcites →https://doi.org/10.1046/j.0016-8025.2001.00791.xopenalex-snapshot
Plant aquaporins: multifunctional water and solute channels with expanding roles
inferredcites →https://doi.org/10.1046/j.0016-8025.2003.01130.xopenalex-snapshot
Overexpression of a lily PIP1 gene in tobacco increased the osmotic water permeability of leaf cells
inferredcites →https://doi.org/10.1046/j.1365-313x.1994.6020187.xopenalex-snapshot
Water channels in the plant plasma membrane cloned by immunoselection from a mammalian expression system
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00111.xopenalex-snapshot
Significance of plasmalemma aquaporins for water‐transport in Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00474.xopenalex-snapshot
The Nicotiana tabacum plasma membrane aquaporin NtAQP1 is mercury‐insensitive and permeable for glycerol
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01268.xopenalex-snapshot
The water permeability of Arabidopsis plasma membrane is regulated by divalent cations and pH
inferredcites →https://doi.org/10.1071/fp07130openalex-snapshot
Expanding roles of plant aquaporins in plasma membranes and cell organelles
inferredcites →https://doi.org/10.1071/fp09117openalex-snapshot
Identification and functional characterisation of aquaporins in the grapevine, Vitis vinifera
inferredcites →https://doi.org/10.1071/pp9880541openalex-snapshot
Water Pathways in Wheat Leaves. IV. The Interpretation of Images of a Fluorescent Apoplastic Tracer
inferredcites →https://doi.org/10.1073/pnas.0401809101openalex-snapshot
Lack of the Rhesus protein Rh1 impairs growth of the green alga Chlamydomonas reinhardtii at high CO 2
inferredcites →https://doi.org/10.1073/pnas.0701180104openalex-snapshot
FRET imaging in living maize cells reveals that plasma membrane aquaporins interact to regulate their subcellular localization
inferredcites →https://doi.org/10.1073/pnas.0809606106openalex-snapshot
Passive transport across bilayer lipid membranes: Overton continues to rule
inferredcites →https://doi.org/10.1073/pnas.0813231106openalex-snapshot
Relative CO 2 /NH 3 selectivities of AQP1, AQP4, AQP5, AmtB, and RhAG
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.112225599openalex-snapshot
Rhesus expression in a green alga is regulated by CO 2
inferredcites →https://doi.org/10.1073/pnas.1316537111openalex-snapshot
Heteromerization of PIP aquaporins affects their intrinsic permeability
inferredcites →https://doi.org/10.1073/pnas.88.24.11110openalex-snapshot
Isolation of the cDNA for erythrocyte integral membrane protein of 28 kilodaltons: member of an ancient channel family.
inferredcites →https://doi.org/10.1073/pnas.94.13.7103openalex-snapshot
Purified vesicles of tobacco cell vacuolar and plasma membranes exhibit dramatically different water permeability and water channel activity
inferredcites →https://doi.org/10.1074/jbc.m110.101790openalex-snapshot
Identification of a Residue in Helix 2 of Rice Plasma Membrane Intrinsic Proteins That Influences Water Permeability
inferredcites →https://doi.org/10.1074/jbc.m110.115881openalex-snapshot
Aquaporin Tetramer Composition Modifies the Function of Tobacco Aquaporins
inferredcites →https://doi.org/10.1074/jbc.m110.135657openalex-snapshot
Interaction of Cytosolic Glutamine Synthetase of Soybean Root Nodules with the C-terminal Domain of the Symbiosome Membrane Nodulin 26 Aquaglyceroporin
inferredcites →https://doi.org/10.1074/jbc.m603761200openalex-snapshot
Specific Aquaporins Facilitate the Diffusion of Hydrogen Peroxide across Membranes
inferredcites →https://doi.org/10.1074/jbc.m700066200openalex-snapshot
Carbonic Anhydrase II Increases the Activity of the Human Electrogenic Na+/ HCO3- Cotransporter
inferredcites →https://doi.org/10.1074/jbc.m800096200openalex-snapshot
Carbon Dioxide Transport through Membranes
inferredcites →https://doi.org/10.1074/jbc.m802134200openalex-snapshot
Nonenzymatic Proton Handling by Carbonic Anhydrase II during H+-Lactate Cotransport via Monocarboxylate Transporter 1
inferredcites →https://doi.org/10.1074/jbc.m803865200openalex-snapshot
On the pH Regulation of Plant Aquaporins
inferredcites →https://doi.org/10.1074/mcp.m113.028241openalex-snapshot
Coordinated Post-translational Responses of Aquaporins to Abiotic and Nutritional Stimuli in Arabidopsis Roots
inferredcites →https://doi.org/10.1074/mcp.m700566-mcp200openalex-snapshot
Multiple Phosphorylations in the C-terminal Tail of Plant Plasma Membrane Aquaporins
inferredcites →https://doi.org/10.1074/mcp.m800016-mcp200openalex-snapshot
Consequences of C4 Differentiation for Chloroplast Membrane Proteomes in Maize Mesophyll and Bundle Sheath Cells
inferredcites →https://doi.org/10.1074/mcp.m900325-mcp200openalex-snapshot
AT_CHLORO, a Comprehensive Chloroplast Proteome Database with Subplastidial Localization and Curated Information on Envelope Proteins
inferredcites →https://doi.org/10.1080/07352689.2011.615705openalex-snapshot
Phylogeny and Molecular Evolution of the Green Algae
inferredcites →https://doi.org/10.1085/jgp.79.5.791openalex-snapshot
Diffusional water permeability of human erythrocytes and their ghosts.
inferredcites →https://doi.org/10.1086/bblv229n1p6openalex-snapshot
Evolution and Functional Diversity of Aquaporins
inferredcites →https://doi.org/10.1091/mbc.e14-03-0812openalex-snapshot
Increased water flux induced by an aquaporin-1/carbonic anhydrase II interaction
inferredcites →https://doi.org/10.1093/aob/mcf199openalex-snapshot
The Role of Aquaporins in Root Water Uptake
inferredcites →https://doi.org/10.1093/aob/mci186openalex-snapshot
Leaf Evolution: Gases, Genes and Geochemistry
inferredcites →https://doi.org/10.1093/aob/mcv021openalex-snapshot
Stomatal density and aperture in non-vascular land plants are non-responsive to above-ambient atmospheric CO2concentrations
inferredcites →https://doi.org/10.1093/jexbot/51.342.61openalex-snapshot
Root hydraulic conductance: diurnal aquaporin expression and the effects of nutrient stress
inferredcites →https://doi.org/10.1093/jxb/eri009openalex-snapshot
PIP1 and PIP2 aquaporins are differentially expressed during tobacco anther and stigma development
inferredcites →https://doi.org/10.1093/jxb/eri294openalex-snapshot
Differential responses of maize MIP genes to salt stress and ABA
inferredcites →https://doi.org/10.1093/jxb/erl183openalex-snapshot
Vacuolar transporters and their essential role in plant metabolism
inferredcites →https://doi.org/10.1093/jxb/erp117openalex-snapshot
Resistances along the CO2 diffusion pathway inside leaves
inferredcites →https://doi.org/10.1093/jxb/erp171openalex-snapshot
Role of aquaporins in leaf physiology
inferredcites →https://doi.org/10.1093/jxb/erq210openalex-snapshot
Cloning, functional characterization, and co-expression studies of a novel aquaporin (FaPIP2;1) of strawberry fruit
inferredcites →https://doi.org/10.1093/jxb/err175openalex-snapshot
Developmental pattern of aquaporin expression in barley (Hordeum vulgare L.) leaves
inferredcites →https://doi.org/10.1093/jxb/err404openalex-snapshot
Insights into Populus XIP aquaporins: evolutionary expansion, protein functionality, and environmental regulation
inferredcites →https://doi.org/10.1093/jxb/ert096openalex-snapshot
Transpirational demand affects aquaporin expression in poplar roots
inferredcites →https://doi.org/10.1093/jxb/ert204openalex-snapshot
A force of nature: molecular mechanisms of mechanoperception in plants
inferredcites →https://doi.org/10.1093/jxb/ert448openalex-snapshot
The grape aquaporin VvSIP1 transports water across the ER membrane
inferredcites →https://doi.org/10.1093/jxb/eru360openalex-snapshot
Active water transport in unicellular algae: where, why, and how
inferredcites →https://doi.org/10.1093/jxb/erv244openalex-snapshot
Arabidopsis seed-specific vacuolar aquaporins are involved in maintaining seed longevity under the control of ABSCISIC ACID INSENSITIVE 3
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a004101openalex-snapshot
A New Subfamily of Major Intrinsic Proteins in Plants
inferredcites →https://doi.org/10.1093/pcp/pce085openalex-snapshot
MIP Genes are Down-regulated Under Drought Stress in Nicotiana glauca
inferredcites →https://doi.org/10.1093/pcp/pcf001openalex-snapshot
Effects of HgCl2 on CO2 Dependence of Leaf Photosynthesis: Evidence Indicating Involvement of Aquaporins in CO2 Diffusion across the Plasma Membrane
inferredcites →https://doi.org/10.1093/pcp/pcf102openalex-snapshot
Functional Analysis of Water Channels in Barley Roots
inferredcites →https://doi.org/10.1093/pcp/pcg167openalex-snapshot
Over-expression of a Barley Aquaporin Increased the Shoot/Root Ratio and Raised Salt Sensitivity in Transgenic Rice Plants
inferredcites →https://doi.org/10.1093/pcp/pcg168openalex-snapshot
Diurnal Regulation of Water Transport and Aquaporin Gene Expression in Maize Roots: Contribution of PIP2 Proteins
inferredcites →https://doi.org/10.1093/pcp/pch058openalex-snapshot
The Role of Aquaporin RWC3 in Drought Avoidance in Rice
inferredcites →https://doi.org/10.1093/pcp/pch070openalex-snapshot
Overexpression of the Barley Aquaporin HvPIP2;1 Increases Internal CO2 Conductance and CO2 Assimilation in the Leaves of Transgenic Rice Plants
inferredcites →https://doi.org/10.1093/pcp/pch120openalex-snapshot
Water Channel Activity of Radish Plasma Membrane Aquaporins Heterologously Expressed in Yeast and Their Modification by Site-Directed Mutagenesis
inferredcites →https://doi.org/10.1093/pcp/pci172openalex-snapshot
Identification of 33 Rice Aquaporin Genes and Analysis of Their Expression and Function
inferredcites →https://doi.org/10.1093/pcp/pcm162openalex-snapshot
Tissue and Cell-Specific Localization of Rice Aquaporins and Their Water Transport Activities
inferredcites →https://doi.org/10.1093/pcp/pcn054openalex-snapshot
Drought Stress Alters Water Relations and Expression of PIP-Type Aquaporin Genes in Nicotiana tabacum Plants
inferredcites →https://doi.org/10.1093/pcp/pcn095openalex-snapshot
Characterization of Four Plasma Membrane Aquaporins in Tulip Petals: A Putative Homolog is Regulated by Phosphorylation
inferredcites →https://doi.org/10.1093/pcp/pcn166openalex-snapshot
Characterization of OsPIP2;7, a Water Channel Protein in Rice
inferredcites →https://doi.org/10.1093/pcp/pcq036openalex-snapshot
Overexpressing a Putative Aquaporin Gene from Wheat, TaNIP, Enhances Salt Tolerance in Transgenic Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcq198openalex-snapshot
The Circadian Clock Modulates Water Dynamics and Aquaporin Expression in Arabidopsis Roots
inferredcites →https://doi.org/10.1093/pcp/pcr027openalex-snapshot
Mechanisms of Water Transport Mediated by PIP Aquaporins and Their Regulation Via Phosphorylation Events Under Salinity Stress in Barley Roots
inferredcites →https://doi.org/10.1093/pcp/pcs154openalex-snapshot
Overexpression of a Wheat Aquaporin Gene, TaAQP8, Enhances Salt Stress Tolerance in Transgenic Tobacco
inferredcites →https://doi.org/10.1093/pcp/pct135openalex-snapshot
Aquaporins and Leaf Hydraulics: Poplar Sheds New Light
inferredcites →https://doi.org/10.1093/pcp/pct166openalex-snapshot
The Thellungiella salsuginea Tonoplast Aquaporin TsTIP1;2 Functions in Protection Against Multiple Abiotic Stresses
inferredcites →https://doi.org/10.1093/pcp/pcu003openalex-snapshot
CO2 Transport by PIP2 Aquaporins of Barley
inferredcites →https://doi.org/10.1093/pcp/pcu203openalex-snapshot
Trafficking of Plant Plasma Membrane Aquaporins: Multiple Regulation Levels and Complex Sorting Signals
inferredcites →https://doi.org/10.1093/treephys/tpp127openalex-snapshot
Effect of overexpression of radish plasma membrane aquaporins on water-use efficiency, photosynthesis and growth of Eucalyptus trees
inferredcites →https://doi.org/10.1094/mpmi-07-12-0178-ropenalex-snapshot
Expression Analysis of Aquaporins from Desert Truffle Mycorrhizal Symbiosis Reveals a Fine-Tuned Regulation Under Drought
inferredcites →https://doi.org/10.1096/fj.04-3300comopenalex-snapshot
Evidence that aquaporin 1 is a major pathway for CO 2 transport across the human erythrocyte membrane
inferredcites →https://doi.org/10.1096/fj.12-209916openalex-snapshot
CO 2 permeability of cell membranes is regulated by membrane cholesterol and protein gas channels
inferredcites →https://doi.org/10.1096/fj.14-263988openalex-snapshot
Low CO 2 permeability of cholesterol‐containing liposomes detected by stopped‐flow fluorescence spectroscopy
inferredcites →https://doi.org/10.1104/pp.008250openalex-snapshot
Temperature Response of Mesophyll Conductance. Implications for the Determination of Rubisco Enzyme Kinetics and for Limitations to Photosynthesis in Vivo
inferredcites →https://doi.org/10.1104/pp.009019openalex-snapshot
Plasma Membrane Aquaporins Play a Significant Role during Recovery from Water Deficit
inferredcites →https://doi.org/10.1104/pp.103.027409openalex-snapshot
Urea Transport by Nitrogen-Regulated Tonoplast Intrinsic Proteins in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.103.027797openalex-snapshot
Plasma Membrane Aquaporins Are Involved in Winter Embolism Recovery in Walnut Tree
inferredcites →https://doi.org/10.1104/pp.104.051268openalex-snapshot
Tonoplast Intrinsic Proteins AtTIP2;1 and AtTIP2;3 Facilitate NH3 Transport into the Vacuole
inferredcites →https://doi.org/10.1104/pp.105.063198openalex-snapshot
A Novel Plant Major Intrinsic Protein in Physcomitrella patens Most Similar to Bacterial Glycerol Channels
inferredcites →https://doi.org/10.1104/pp.105.065029openalex-snapshot
Early Effects of Salinity on Water Transport in Arabidopsis Roots. Molecular and Cellular Features of Aquaporin Expression
inferredcites →https://doi.org/10.1104/pp.106.090092openalex-snapshot
Putative Role of Aquaporins in Variable Hydraulic Conductance of Leaves in Response to Light
inferredcites →https://doi.org/10.1104/pp.106.4.1325openalex-snapshot
The Plasma Membrane of Arabidopsis thaliana Contains a Mercury-Insensitive Aquaporin That Is a Homolog of the Tonoplast Water Channel Protein TIP
inferredcites →https://doi.org/10.1104/pp.107.111351openalex-snapshot
Water Transport by Aquaporins in the Extant Plant Physcomitrella patens
inferredcites →https://doi.org/10.1104/pp.108.120154openalex-snapshot
Rh-PIP2;1, a Rose Aquaporin Gene, Is Involved in Ethylene-Regulated Petal Expansion
inferredcites →https://doi.org/10.1104/pp.108.128645openalex-snapshot
The Role of Plasma Membrane Intrinsic Protein Aquaporins in Water Transport through Roots: Diurnal and Drought Stress Responses Reveal Different Strategies between Isohydric and Anisohydric Cultivars of Grapevine
inferredcites →https://doi.org/10.1104/pp.108.134098openalex-snapshot
Roles of Morphology, Anatomy, and Aquaporins in Determining Contrasting Hydraulic Behavior of Roots
inferredcites →https://doi.org/10.1104/pp.109.1.15openalex-snapshot
Cold Acclimation of Arabidopsis thaliana (Effect on Plasma Membrane Lipid Composition and Freeze-Induced Lesions)
inferredcites →https://doi.org/10.1104/pp.109.145326openalex-snapshot
A PIP1 Aquaporin Contributes to Hydrostatic Pressure-Induced Water Transport in Both the Root and Rosette of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.109.145854openalex-snapshot
The Role of Tobacco Aquaporin1 in Improving Water Use Efficiency, Hydraulic Conductivity, and Yield Production Under Salt Stress
inferredcites →https://doi.org/10.1104/pp.110.159442openalex-snapshot
An mRNA Blueprint for C4 Photosynthesis Derived from Comparative Transcriptomics of Closely Related C3 and C4 Species
inferredcites →https://doi.org/10.1104/pp.112.194506openalex-snapshot
Overexpression of PIP2;5 Aquaporin Alleviates Effects of Low Root Temperature on Cell Hydraulic Conductivity and Growth in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.113.233791openalex-snapshot
Aquaporins: Highly Regulated Channels Controlling Plant Water Relations
inferredcites →https://doi.org/10.1104/pp.114.237511openalex-snapshot
Down-Regulation of Plasma Intrinsic Protein1 Aquaporin in Poplar Trees Is Detrimental to Recovery from Embolism
inferredcites →https://doi.org/10.1104/pp.114.240945openalex-snapshot
A New LxxxA Motif in the Transmembrane Helix3 of Maize Aquaporins Belonging to the Plasma Membrane Intrinsic Protein PIP2 Group Is Required for Their Trafficking to the Plasma Membrane
inferredcites →https://doi.org/10.1104/pp.114.248633openalex-snapshot
The Role of Plasma Membrane Aquaporins in Regulating the Bundle Sheath-Mesophyll Continuum and Leaf Hydraulics
inferredcites →https://doi.org/10.1104/pp.114.4.1347openalex-snapshot
The Major Intrinsic Protein Family of Arabidopsis Has 23 Members That Form Three Distinct Groups with Functional Aquaporins in Each Group
inferredcites →https://doi.org/10.1104/pp.115.2.561openalex-snapshot
Characterization of Water Channels in Wheat Root Membrane Vesicles
inferredcites →https://doi.org/10.1104/pp.122.4.1025openalex-snapshot
Plasma Membrane Intrinsic Proteins from Maize Cluster in Two Sequence Subgroups with Differential Aquaporin Activity
inferredcites →https://doi.org/10.1104/pp.125.1.123openalex-snapshot
Plasmodesmata. A Not So Open-and-Shut Case
showing the first 200 of 300 · page through all 300
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4806951openalex-extracted
Expression of Aquaporin Genes is Down-Regulated in Peel and Up-Regulated in Pulp of Orange Fruit and is Related to Water Loss During Storage
inferred← citeshttps://doi.org/10.2139/ssrn.4814705openalex-extracted
Expression of Aquaporin Genes is Down-Regulated in Peel and Up-Regulated in Pulp of Orange Fruit and is Related to Water Loss During Storage
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0626openalex-snapshot
Regulating Root Aquaporin Function in Response to Changes in Salinity
inferred← citeshttps://doi.org/10.1002/ajb2.1030openalex-snapshot
Vessel‐associated cells in angiosperm xylem: Highly specialized living cells at the symplast–apoplast boundary
inferred← citeshttps://doi.org/10.1002/jcc.70377openalex-snapshot
Characterization and Computational Engineering of Structural Elements Controlling Gas Permeability in PIP2 ;1 Aquaporins
inferred← citeshttps://doi.org/10.1002/pei3.70007openalex-snapshot
Responses of ‘Flordaguard’ and ‘ MP ‐29’ Prunus spp. rootstocks to hypoxia and high root zone temperature
inferred← citeshttps://doi.org/10.1002/pld3.321openalex-snapshot
A consensus on the Aquaporin Gene Family in the Allotetraploid Plant, Nicotiana tabacum
inferred← citeshttps://doi.org/10.1002/sae2.12014openalex-snapshot
Synthetic biology and opportunities within agricultural crops
inferred← citeshttps://doi.org/10.1007/978-3-030-29639-1_2openalex-snapshot
Photosynthesis, Respiration, and Long-Distance Transport: Photosynthesis
inferred← citeshttps://doi.org/10.1007/978-3-319-75671-4_3openalex-snapshot
Targeting Aquaporins for Conferring Salinity Tolerance in Crops
inferred← citeshttps://doi.org/10.1007/978-3-319-93594-2_7openalex-snapshot
CO2 Diffusion Inside Photosynthetic Organs
inferred← citeshttps://doi.org/10.1007/978-981-97-0672-3_4openalex-snapshot
Global Drought Threat: Impact on Food Security
inferred← citeshttps://doi.org/10.1007/s00299-021-02673-wopenalex-snapshot
A bamboo leaf-specific aquaporin gene PePIP2;7 is involved in abiotic stress response
inferred← citeshttps://doi.org/10.1007/s00344-022-10636-yopenalex-snapshot
Biochar and Selenium Nanoparticles Induce Water Transporter Genes for Sustaining Carbon Assimilation and Grain Production in Salt-Stressed Wheat
inferred← citeshttps://doi.org/10.1007/s00344-026-12431-5openalex-snapshot
Aquaporin-Mediated Hydraulic Signalling and Stress Tolerance Mechanisms in Cereal Crops
inferred← citeshttps://doi.org/10.1007/s11120-021-00848-wopenalex-snapshot
Role of bundle sheath conductance in sustaining photosynthesis competence in sugarcane plants under nitrogen deficiency
inferred← citeshttps://doi.org/10.1007/s12042-024-09364-2openalex-snapshot
Comprehensive Analysis of the Aquaporin Genes in Eucalyptus grandis Suggests Potential Targets for Drought Stress Tolerance
inferred← citeshttps://doi.org/10.1007/s12229-021-09249-zopenalex-snapshot
Aquaporins Responses under Challenging Environmental Conditions and Abiotic Stress Tolerance in Plants
inferred← citeshttps://doi.org/10.1007/s40626-023-00284-2openalex-snapshot
Molecular modeling of aquaporins and artificial transmembrane channels: a mini-review and perspective for plants
inferred← citeshttps://doi.org/10.1007/s42729-025-02700-9openalex-snapshot
Biochar and Salicylic Acid Improve Agronomic Performance and Physiological Traits of Vigna Radiata L. Varieties (Ramzan and NIFA2019) Under Induced Salt Stress
inferred← citeshttps://doi.org/10.1016/b978-0-443-21793-7.00021-0openalex-snapshot
Current updates on improving rice photosynthesis and resource-use efficiency through enhanced CO2 diffusion inside leaves
inferred← citeshttps://doi.org/10.1016/bs.ampbs.2021.01.001openalex-snapshot
A protet-based, protonic charge transfer model of energy coupling in oxidative and photosynthetic phosphorylation
inferred← citeshttps://doi.org/10.1016/j.agrformet.2022.109153openalex-snapshot
Quantitative expression of mesophyll conductance temperature response in the FvCB model and impacts on plant gas exchange estimations
inferred← citeshttps://doi.org/10.1016/j.agwat.2026.110398openalex-snapshot
Optimizing irrigation thresholds for water conservation and yield stabilization of maize under varying salinity conditions in Northwest China
inferred← citeshttps://doi.org/10.1016/j.aquabot.2025.103949openalex-snapshot
Transcriptome analysis of the red marine alga Gracilaria vermiculophylla grown under different light intensities
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2025.144304openalex-snapshot
Optimization of carbon membrane performance in reverse osmosis systems for reducing salinity, nitrates, phosphates, and ammonia in aquaculture wastewater
inferred← citeshttps://doi.org/10.1016/j.cj.2023.04.010openalex-snapshot
A cluster of mutagenesis revealed an osmotic regulatory role of the OsPIP1 genes in enhancing rice salt tolerance
inferred← citeshttps://doi.org/10.1016/j.cj.2024.04.005openalex-snapshot
Plant aquaporins: Their roles beyond water transport
inferred← citeshttps://doi.org/10.1016/j.crope.2024.04.001openalex-snapshot
Perspectives of improving rice photosynthesis for higher grain yield
inferred← citeshttps://doi.org/10.1016/j.dendro.2022.126026openalex-snapshot
Wildfires affect tree growth and resilience in Northeastern China natural Dahurian larch forests: A dendrochronological perspective
inferred← citeshttps://doi.org/10.1016/j.devcel.2024.12.026openalex-snapshot
PCP-B peptides and CrRLK1L receptor kinases control pollination via pH gating of aquaporins in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2017.09.011openalex-snapshot
Na+ induces the tolerance to water stress in white clover associated with osmotic adjustment and aquaporins-mediated water transport and balance in root and leaf
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2018.10.013openalex-snapshot
Molybdenum improves water uptake via extensive root morphology, aquaporin expressions and increased ionic concentrations in wheat under drought stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2020.104270openalex-snapshot
Heat shock protein and aquaporin expression enhance water conserving behavior of citrus under water deficits and high temperature conditions
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104425openalex-snapshot
Identification of aquaporin members in Acacia auriculiformis and functional characterization of AaPIP1-2 involved in drought stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.104931openalex-snapshot
Oxidative stress impedes recovery of canola (Brassica napus) plants from waterlogging by inhibiting aquaporin-mediated root water transport
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.104950openalex-snapshot
Assessing photosynthesis in plant systems: A cornerstone to aid in the selection of resistant and productive crops
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.104995openalex-snapshot
Genome-wide identification of plasma-membrane intrinsic proteins in pumpkin and functional characterization of CmoPIP1-4 under salinity stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105985openalex-snapshot
Succulence and aquaporin expression during drought and recovery in the CAM epiphytic bromeliad Acanthostachys strobilacea (Schult. & Schult.f.) Klotzsch
inferred← citeshttps://doi.org/10.1016/j.foodchem.2026.149698openalex-snapshot
Uncovering the effect of drying process on aquaporin proteins and fruit quality of goji berry (Lycium barbarum), a worldwide popular functional food
inferred← citeshttps://doi.org/10.1016/j.hpj.2023.07.005openalex-snapshot
VPD modifies CO2 fertilization effect on tomato plants via abscisic acid and jasmonic acid signaling pathways
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2021.126379openalex-snapshot
A transcriptomic view of cadmium retention in roots of cadmium-safe rice line (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1016/j.jia.2026.04.020openalex-snapshot
SlPIP1;7 enhances tomato acclimation to high VPD through optimizing stomatal morphology and regulating ROS
inferred← citeshttps://doi.org/10.1016/j.jplph.2026.154787openalex-snapshot
The regulation of stomatal closure as a key factor to benefit from rising atmospheric [CO2] in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112036openalex-snapshot
Aquaporin LjNIP1;5 positively modulates drought tolerance by promoting arbuscular mycorrhizal symbiosis in Lotus japonicus
inferred← citeshttps://doi.org/10.1016/j.plaphy.2019.03.017openalex-snapshot
Aquaporin PIP2;1 affects water transport and root growth in rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.108801openalex-snapshot
Variation in photosynthetic capacity of Salvia przewalskii along elevational gradients on the eastern Qinghai-Tibetan Plateau, China
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109060openalex-snapshot
Climate change does not impact the water flow of barley at the vegetative stage, ameliorates at anthesis and worsens after subsequent drought episodes
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110952openalex-snapshot
Comprehensive identification of aquaporins under salt stress, and functional characterization of DoTIP1-1 in Dendrobium officinale
inferred← citeshttps://doi.org/10.1016/j.rsci.2025.01.006openalex-snapshot
Aquaporin OsPIP2;2 Regulates Bakanae Disease Resistance in Rice
inferred← citeshttps://doi.org/10.1016/j.scienta.2021.110122openalex-snapshot
The potential implications of a plasma membrane aquaporin in improving CO2 transport capacity, photosynthetic potential and water use efficiency under contrasting CO2 source in Solanum lycopersicum (tomato)
inferred← citeshttps://doi.org/10.1016/j.scienta.2022.111128openalex-snapshot
A plasma membrane aquaporin is potentially involved in moderating water stress and photosynthetic depression by sustaining water transport and CO2 uptake under high VPD stress conditions in Solanum lycopersicum (tomato)
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.166741openalex-snapshot
Intraspecific variations of leaf hydraulic, economic, and anatomical traits in Cinnamomum camphora along an urban-rural gradient
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.169560openalex-snapshot
Nitrogen enrichment delays the drought threshold responses of leaf photosynthesis in alpine grassland plants
inferred← citeshttps://doi.org/10.1016/j.stress.2025.100825openalex-snapshot
Silicon-driven approaches to salinity stress tolerance: Mechanisms, uptake dynamics, and microbial transformations
inferred← citeshttps://doi.org/10.1016/j.tplants.2018.09.005openalex-snapshot
Embracing 3D Complexity in Leaf Carbon–Water Exchange
inferred← citeshttps://doi.org/10.1017/9781139049979.009openalex-snapshot
Physiology of Photosynthetic Autotrophs in Present-Day Environments
inferred← citeshttps://doi.org/10.1021/acs.jproteome.9b00627openalex-snapshot
Proteomic and Metabolomic Profilings Reveal Crucial Functions of γ-Aminobutyric Acid in Regulating Ionic, Water, and Metabolic Homeostasis in Creeping Bentgrass under Salt Stress
inferred← citeshttps://doi.org/10.1039/d4en00520aopenalex-snapshot
Plant nanobiotechnology: a new strategy to enhance crop photosynthesis
inferred← citeshttps://doi.org/10.1071/fp22260openalex-snapshot
Arabidopsis plasma membrane intrinsic protein (AtPIP2;1) is implicated in a salinity conditional influence on seed germination
inferred← citeshttps://doi.org/10.1073/pnas.2605032123openalex-snapshot
Coordinated stomatal, mesophyll, and biochemical functions in photosynthetic responses to heat and dryness
inferred← citeshttps://doi.org/10.1080/07352689.2026.2687338openalex-snapshot
Advances in biotechnological strategies for improving photosynthetic productivity in C3 and C4 plants: falls and rises
inferred← citeshttps://doi.org/10.1089/ars.2017.7455openalex-snapshot
Reactive Oxygen Species, Photosynthesis, and Environment in the Regulation of Stomata
inferred← citeshttps://doi.org/10.1093/aob/mcac100openalex-snapshot
Cost–benefit analysis of mesophyll conductance: diversities of anatomical, biochemical and environmental determinants
inferred← citeshttps://doi.org/10.1093/jxb/eraa002openalex-snapshot
Drying times: plant traits to improve crop water use efficiency and yield
inferred← citeshttps://doi.org/10.1093/jxb/eraa075openalex-snapshot
A wish list for synthetic biology in photosynthesis research
inferred← citeshttps://doi.org/10.1093/jxb/eraa077openalex-snapshot
Photons to food: genetic improvement of cereal crop photosynthesis
inferred← citeshttps://doi.org/10.1093/jxb/erab144openalex-snapshot
Cell wall thickness and composition are involved in photosynthetic limitation
inferred← citeshttps://doi.org/10.1093/jxb/erac065openalex-snapshot
Mesophyll conductance is unaffected by expression of Arabidopsis PIP1 aquaporins in the plasmalemma of Nicotiana
inferred← citeshttps://doi.org/10.1093/jxb/erae418openalex-snapshot
High water use efficiency due to maintenance of photosynthetic capacity in sorghum under water stress
inferred← citeshttps://doi.org/10.1093/jxb/eraf245openalex-snapshot
Single-nuclei sequencing of Moricandia arvensis reveals bundle sheath cell function in the photorespiratory shuttle of C3-C4 intermediate Brassicaceae
inferred← citeshttps://doi.org/10.1093/jxb/erx206openalex-snapshot
Carbon-concentrating mechanisms in seagrasses
inferred← citeshttps://doi.org/10.1093/jxb/ery148openalex-snapshot
Physiological performance of transplastomic tobacco plants overexpressing aquaporin AQP1 in chloroplast membranes
inferred← citeshttps://doi.org/10.1093/jxb/ery321openalex-snapshot
Is xylem of angiosperm leaves less resistant to embolism than branches? Insights from microCT, hydraulics, and anatomy
inferred← citeshttps://doi.org/10.1093/jxb/ery366openalex-snapshot
The nitrogen cost of photosynthesis
inferred← citeshttps://doi.org/10.1093/jxb/erz208openalex-snapshot
Elevated CO2-induced changes in mesophyll conductance and anatomical traits in wild type and carbohydrate-metabolism mutants of Arabidopsis
inferred← citeshttps://doi.org/10.1093/jxb/erz442openalex-snapshot
Photosynthetic efficiency and mesophyll conductance are unaffected in Arabidopsis thaliana aquaporin knock-out lines
inferred← citeshttps://doi.org/10.1093/jxb/erz555openalex-snapshot
Deciphering aquaporin regulation and roles in seed biology
inferred← citeshttps://doi.org/10.1093/pcp/pcae097openalex-snapshot
Proteomic Insights into Trichome Responses to Elevated Elemental Stress in Cation Exchanger (CAX) Mutants
inferred← citeshttps://doi.org/10.1093/plphys/kiad567openalex-snapshot
Sugarcane mosaic virus employs 6K2 protein to impair ScPIP2;4 transport of H2O2 to facilitate virus infection
inferred← citeshttps://doi.org/10.1093/treephys/tpaf145openalex-snapshot
Photosynthetic performance in mangrove species under salt stress: mesophyll conductance as a key limitation
inferred← citeshttps://doi.org/10.1093/treephys/tpag039openalex-snapshot
Variation in photosynthetic capacity of Sorbus rehderiana and Quercus aquifolioides along elevational gradients on the eastern edge of the Qinghai–Tibetan Plateau, China
inferred← citeshttps://doi.org/10.1101/2020.04.15.042234openalex-snapshot
Aquaporin mediating stomatal closure is associated with water conservation under mild water deficit
inferred← citeshttps://doi.org/10.1101/2021.03.26.437249openalex-snapshot
Exploring the Plant Aquaporin Solute Transport Network: Functional characterisation of Nicotiana tabacum PIP, TIP and NIP isoforms
inferred← citeshttps://doi.org/10.1101/2021.05.07.443185openalex-snapshot
Genetic variation associated with plastic and homeostatic growth responses to drought in Arabidopsis
inferred← citeshttps://doi.org/10.1101/2021.09.22.461327openalex-snapshot
Explicit expression of mesophyll conductance in the traditional leaf photosynthesis–transpiration coupled model and its physiological significances
inferred← citeshttps://doi.org/10.1101/2021.10.03.462792openalex-snapshot
Mesophyll conductance response to short-term changes in CO 2 is related to leaf anatomy and biochemistry in diverse C 4 grasses
inferred← citeshttps://doi.org/10.1101/2022.07.06.498957openalex-snapshot
A cross-scale analysis to understand and quantify effects of photosynthetic enhancement on crop growth and yield
inferred← citeshttps://doi.org/10.1101/2023.10.29.564209openalex-snapshot
Comprehensive analysis of the Aquaporin genes in Eucalyptus grandis suggests potential targets for drought stress tolerance
inferred← citeshttps://doi.org/10.1104/pp.20.00328openalex-snapshot
A Decrease in Mesophyll Conductance by Cell-Wall Thickening Contributes to Photosynthetic Downregulation
inferred← citeshttps://doi.org/10.1111/jipb.13432openalex-snapshot
Coronatine promotes maize water uptake by directly binding to the aquaporin ZmPIP2;5 and enhancing its activity
inferred← citeshttps://doi.org/10.1111/nph.14307openalex-snapshot
Photosynthesis: ancient, essential, complex, diverse … and in need of improvement in a changing world
inferred← citeshttps://doi.org/10.1111/nph.16214openalex-snapshot
The role of leaf water potential in the temperature response of mesophyll conductance
inferred← citeshttps://doi.org/10.1111/nph.17730openalex-snapshot
The α subunit of the heterotrimeric G protein regulates mesophyll CO 2 conductance and drought tolerance in rice
inferred← citeshttps://doi.org/10.1111/nph.18363openalex-snapshot
Contrasting anatomical and biochemical controls on mesophyll conductance across plant functional types
inferred← citeshttps://doi.org/10.1111/nph.18427openalex-snapshot
Mesophyll conductance response to short‐term changes in p CO2 is related to leaf anatomy and biochemistry in diverse C4 grasses
inferred← citeshttps://doi.org/10.1111/nph.18545openalex-snapshot
Enhancing crop yields through improvements in the efficiency of photosynthesis and respiration
inferred← citeshttps://doi.org/10.1111/nph.70283openalex-snapshot
Evidence for a CO 2 ‐concentrating mechanism in the model streptophyte green alga Chara braunii
inferred← citeshttps://doi.org/10.1111/pbi.13830openalex-snapshot
Overexpression of cytoplasmic C4Flaveria bidentis carbonic anhydrase in C3Arabidopsis thaliana increases amino acids, photosynthetic potential, and biomass
inferred← citeshttps://doi.org/10.1111/pce.12997openalex-snapshot
Persistent negative temperature response of mesophyll conductance in red raspberry ( Rubus idaeus L.) leaves under both high and low vapour pressure deficits: a role for abscisic acid?
inferred← citeshttps://doi.org/10.1111/pce.13217openalex-snapshot
Identification of novel interactors and potential phosphorylation substrates of GsSnRK1 from wild soybean ( Glycine soja )
inferred← citeshttps://doi.org/10.1111/pce.13553openalex-snapshot
Potassium mediates coordination of leaf photosynthesis and hydraulic conductance by modifications of leaf anatomy
inferred← citeshttps://doi.org/10.1111/pce.13851openalex-snapshot
Phosphorylation influences water and ion channel function of AtPIP2;1
inferred← citeshttps://doi.org/10.1111/pce.14276openalex-snapshot
The plasma membrane aquaporin ZmPIP2;5 enhances the sensitivity of stomatal closure to water deficit
inferred← citeshttps://doi.org/10.1111/pce.14453openalex-snapshot
A cross‐scale analysis to understand and quantify the effects of photosynthetic enhancement on crop growth and yield across environments
inferred← citeshttps://doi.org/10.1111/pce.15259openalex-snapshot
Enhanced CO 2 Coordinates the Spatial Recruitment of Diazotrophs in Rice Via Root Development
inferred← citeshttps://doi.org/10.1111/ppl.13839openalex-snapshot
Does night‐time transpiration provide any benefit to wheat (Triticum aestivum L.) plants which are exposed to salt stress?
inferred← citeshttps://doi.org/10.1111/ppl.14037openalex-snapshot
Coordination of hydraulic and leaf‐level gas exchange traits during water‐deficit acclimation in apple rootstocks
inferred← citeshttps://doi.org/10.1111/ppl.14384openalex-snapshot
Modulation of physio‐biochemical and photosynthesis parameters by overexpressing SbPIP2 gene improved abiotic stress tolerance of transgenic tobacco
inferred← citeshttps://doi.org/10.1111/ppl.71021openalex-snapshot
Nitrogen‐Centric Molecular Mechanisms in Crop Plants Under Elevated CO 2 : Interactions, Responses, and Implications
inferred← citeshttps://doi.org/10.1111/tpj.14662openalex-snapshot
Ectopic expression of a rice plasma membrane intrinsic protein (OsPIP1;3) promotes plant growth and water uptake
inferred← citeshttps://doi.org/10.1111/tpj.14757openalex-snapshot
Peeling back the layers of crassulacean acid metabolism: functional differentiation between Kalanchoë fedtschenkoi epidermis and mesophyll proteomes
inferred← citeshttps://doi.org/10.1111/tpj.15397openalex-snapshot
Mesophyll conductance variability of rice aquaporin knockout lines at different growth stages and growing environments
inferred← citeshttps://doi.org/10.1111/tpj.16098openalex-snapshot
Leaf anatomy does not explain the large variability of mesophyll conductance across C3 crop species
inferred← citeshttps://doi.org/10.1146/annurev-arplant-081720-013608openalex-snapshot
Adaptable and Multifunctional Ion-Conducting Aquaporins
inferred← citeshttps://doi.org/10.1155/2023/7208341openalex-snapshot
Arbuscular Mycorrhizal Fungi Enhance Drought Stress Tolerance by Regulating Osmotic Balance, the Antioxidant System, and the Expression of Drought-Responsive Genes in Vitis vinifera L.
inferred← citeshttps://doi.org/10.1186/s12870-020-02412-5openalex-snapshot
Genome-wide identification and characterisation of Aquaporins in Nicotiana tabacum and their relationships with other Solanaceae species
inferred← citeshttps://doi.org/10.1186/s12870-022-03594-wopenalex-snapshot
Combined use of specific length amplified fragment sequencing (SLAF-seq) and bulked segregant analysis (BSA) for rapid identification of genes influencing fiber content of hemp (Cannabis sativa L.)
inferred← citeshttps://doi.org/10.1186/s12870-026-08262-xopenalex-snapshot
Characterization of the aquaporin gene family in Pinus massoniana and functional analysis of PmNIP2;1 involved in high-temperature and drought stress
inferred← citeshttps://doi.org/10.1186/s13018-025-05729-9openalex-snapshot
Electroacupuncture attenuates intervertebral disc degeneration by upregulating aquaporins via the cAMP/PKA pathway
inferred← citeshttps://doi.org/10.15377/2409-9813.2023.10.3openalex-snapshot
Priming Bean Seedlings to Boost Natural Plant Defenses Against Common Bacterial Wilt: Leaf Architecture, Leaf area, Foliage Water Content, and Plant Biomass Results (Part 3)
inferred← citeshttps://doi.org/10.15407/frg2019.02.114openalex-snapshot
Nitrogen distribution in the source-sink system of plants and its role in the production process
inferred← citeshttps://doi.org/10.17521/cjpe.2023.0107openalex-snapshot
Tree physiology and major influencing factors under forest fires
inferred← citeshttps://doi.org/10.17816/ecogen637037openalex-snapshot
The role of water-transporting aquaporins of the PIP and TIP subfamilies in plant development and adaptation to stress factors
inferred← citeshttps://doi.org/10.18174/516228openalex-snapshot
Nutrients translocation & plant growth in tissue culture
inferred← citeshttps://doi.org/10.21203/rs.2.20548/v1openalex-snapshot
The rate-limiting step for photosynthetic CO2 utilization under varying atmospheric evaporative demand in Solanum lycopersicum (tomato)
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3712727/v1openalex-snapshot
Electroacupuncture attenuates degeneration by upregulating of aquaporins via the cAMP/PKA pathway in a rabbit model of disc degeneration
inferred← citeshttps://doi.org/10.21203/rs.3.rs-820517/v1openalex-snapshot
Combined use of Specific Length Amplified Fragment Sequencing (SLAF-seq) And Bulked Segregant Analysis (BSA) For Rapid Identification of Genes Influencing Fiber Content of Hemp (Cannabis sativa L.)
inferred← citeshttps://doi.org/10.22541/au.164864942.28872279/v1openalex-snapshot
Overexpression of cytoplasmic C4 Flaveria bidentis carbonic anhydrase in C3 Arabidopsis thaliana increases photosynthetic potential and biomass
inferred← citeshttps://doi.org/10.3103/s0095452724050104openalex-snapshot
The Role of Aquaporins and Carbon Nanomaterials in Abiotic Stress in Plants
inferred← citeshttps://doi.org/10.31031/mcda.2020.07.000661openalex-snapshot
Biotechnological Approaches to Improve Carbon Fixation in Agricultural Crops
inferred← citeshttps://doi.org/10.3389/fmars.2023.1138074openalex-snapshot
Genome-wide identification, structural and evolutionary characteristics, and expression analysis of aquaporin gene family members in Mercenaria mercenaria
inferred← citeshttps://doi.org/10.3389/fphys.2023.1205290openalex-snapshot
Aquaporins and CO2 diffusion across biological membrane
inferred← citeshttps://doi.org/10.3389/fpls.2018.01143openalex-snapshot
Is Nitrogen a Key Determinant of Water Transport and Photosynthesis in Higher Plants Upon Drought Stress?
inferred← citeshttps://doi.org/10.3389/fpls.2021.745110openalex-snapshot
Physiological and Transcriptomic Analyses Revealed the Implications of Abscisic Acid in Mediating the Rate-Limiting Step for Photosynthetic Carbon Dioxide Utilisation in Response to Vapour Pressure Deficit in Solanum Lycopersicum (Tomato)
inferred← citeshttps://doi.org/10.3389/fpls.2021.750805openalex-snapshot
Integrated Analysis of miRNAs Associated With Sugarcane Responses to Low-Potassium Stress
inferred← citeshttps://doi.org/10.3389/fpls.2021.760863openalex-snapshot
Transcriptome and Metabolome Analyses Reveal Potential Salt Tolerance Mechanisms Contributing to Maintenance of Water Balance by the Halophytic Grass Puccinellia nuttalliana
inferred← citeshttps://doi.org/10.3389/fpls.2021.761713openalex-snapshot
Highly Conserved Evolution of Aquaporin PIPs and TIPs Confers Their Crucial Contribution to Flowering Process in Plants
inferred← citeshttps://doi.org/10.3389/fpls.2023.1078220openalex-snapshot
A high-throughput yeast approach to characterize aquaporin permeabilities: Profiling the Arabidopsis PIP aquaporin sub-family
inferred← citeshttps://doi.org/10.3389/fpls.2023.1163451openalex-snapshot
The critical role of biochar to mitigate the adverse impacts of drought and salinity stress in plants
inferred← citeshttps://doi.org/10.3389/fpls.2023.1213454openalex-snapshot
Exploring aquaporin functions during changes in leaf water potential
inferred← citeshttps://doi.org/10.3389/fpls.2024.1448432openalex-snapshot
Root-based inorganic carbon uptake increases the growth of Arabidopsis thaliana and changes transporter expression and nitrogen and sulfur metabolism
inferred← citeshttps://doi.org/10.3389/fpls.2024.1475574openalex-snapshot
Osmolytes and CsAQP expression jointly influence water physiology in the peel and pulp of orange (Citrus sinensis (L.) Osbeck) fruit during postharvest water loss
inferred← citeshttps://doi.org/10.3389/fpls.2025.1623156openalex-snapshot
Stress resilience in Coffea arabica and Coffea canephora under harsh drought and/or heat conditions: selected genes, proteins, and lipid integrated responses
inferred← citeshttps://doi.org/10.3390/agronomy12081830openalex-snapshot
Physiological Factors Limiting Leaf Net Photosynthetic Rate in C3 Crops like Rice and Approaches for Improving It
inferred← citeshttps://doi.org/10.3390/cells13161319openalex-snapshot
Enhancing Photosynthesis and Plant Productivity through Genetic Modification
inferred← citeshttps://doi.org/10.3390/f13040594openalex-snapshot
Leaf and Branch Hydraulic Plasticity of Two Light-Demanding Broadleaved Tree Species Differing in Water-Use Strategy
inferred← citeshttps://doi.org/10.3390/horticulturae12060721openalex-snapshot
The Aquaporin Gene SbPIP1;2 Is Involved in Dormancy Release and Regulated Under Low Temperatures in Lilium ‘Siberia’
inferred← citeshttps://doi.org/10.3390/ijms19010035openalex-snapshot
Role of Aquaporins in Determining Carbon and Nitrogen Status in Higher Plants
inferred← citeshttps://doi.org/10.3390/ijms19051352openalex-snapshot
Transport and Use of Bicarbonate in Plants: Current Knowledge and Challenges Ahead
inferred← citeshttps://doi.org/10.3390/ijms21124335openalex-snapshot
Methyl Jasmonate Affects Photosynthesis Efficiency, Expression of HvTIP Genes and Nitrogen Homeostasis in Barley
inferred← citeshttps://doi.org/10.3390/ijms21249485openalex-snapshot
Versatile Roles of Aquaporins in Plant Growth and Development
inferred← citeshttps://doi.org/10.3390/ijms22020565openalex-snapshot
Ectopic Expression of CrPIP2;3, a Plasma Membrane Intrinsic Protein Gene from the Halophyte Canavalia rosea, Enhances Drought and Salt-Alkali Stress Tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms22147269openalex-snapshot
Genome-Wide Identification, Structure Characterization, and Expression Pattern Profiling of the Aquaporin Gene Family in Betula pendula
inferred← citeshttps://doi.org/10.3390/ijms232415552openalex-snapshot
Unique and Shared Proteome Responses of Rice Plants (Oryza sativa) to Individual Abiotic Stresses
inferred← citeshttps://doi.org/10.3390/ijms242417276openalex-snapshot
Genome-Wide Identification and Expression Pattern Profiling of the Aquaporin Gene Family in Papaya (Carica papaya L.)
inferred← citeshttps://doi.org/10.3390/ijms25021229openalex-snapshot
Salt-Induced Early Changes in Photosynthesis Activity Caused by Root-to-Shoot Signaling in Potato
inferred← citeshttps://doi.org/10.3390/ijms252413574openalex-snapshot
Promoter of Vegetable Pea PsPIP2-4 Responds to Abiotic Stresses in Transgenic Tobacco
inferred← citeshttps://doi.org/10.3390/ijms26199782openalex-snapshot
OsPIP2;1 Positively Regulates Rice Tolerance to Water Stress Under Coupling of Partial Root-Zone Drying and Nitrogen Forms
inferred← citeshttps://doi.org/10.3390/plants14142180openalex-snapshot
Pectins as Brakes? Their Potential Implication in Adjusting Mesophyll Conductance Under Water Deficit and Salt Stresses
inferred← citeshttps://doi.org/10.3390/plants15050720openalex-snapshot
Heterologous Expression of Sorghum bicolor PIP1-3 Gene Improves Drought Tolerance in Arabidopsis and Rapeseed
inferred← citeshttps://doi.org/10.47749/t/unicamp.2018.1061606openalex-snapshot
Transcriptômica de plantas de Eucalyptus globulus e Eucalyptus grandis em resposta à variação de temperatura e CO2
inferred← citeshttps://doi.org/10.6084/m9.figshare.19808042openalex-snapshot
Additional file 1 of Combined use of specific length amplified fragment sequencing (SLAF-seq) and bulked segregant analysis (BSA) for rapid identification of genes influencing fiber content of hemp (Cannabis sativa L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19808048openalex-snapshot
Additional file 2 of Combined use of specific length amplified fragment sequencing (SLAF-seq) and bulked segregant analysis (BSA) for rapid identification of genes influencing fiber content of hemp (Cannabis sativa L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19808051openalex-snapshot
Additional file 3 of Combined use of specific length amplified fragment sequencing (SLAF-seq) and bulked segregant analysis (BSA) for rapid identification of genes influencing fiber content of hemp (Cannabis sativa L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19808054openalex-snapshot
Additional file 4 of Combined use of specific length amplified fragment sequencing (SLAF-seq) and bulked segregant analysis (BSA) for rapid identification of genes influencing fiber content of hemp (Cannabis sativa L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19808057openalex-snapshot
Additional file 5 of Combined use of specific length amplified fragment sequencing (SLAF-seq) and bulked segregant analysis (BSA) for rapid identification of genes influencing fiber content of hemp (Cannabis sativa L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19808060openalex-snapshot
Additional file 6 of Combined use of specific length amplified fragment sequencing (SLAF-seq) and bulked segregant analysis (BSA) for rapid identification of genes influencing fiber content of hemp (Cannabis sativa L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19808063openalex-snapshot
Additional file 7 of Combined use of specific length amplified fragment sequencing (SLAF-seq) and bulked segregant analysis (BSA) for rapid identification of genes influencing fiber content of hemp (Cannabis sativa L.)
inferred← citeshttps://doi.org/10.64898/2026.02.26.708164openalex-snapshot
Trade-offs between photosynthetic capacity, mesophyll conductance stability and leaf anatomy shape heat and water deficit resilience in Gossypium
inferred← citeshttps://doi.org/10.66835/psh.2026.e0011openalex-snapshot
Genomic alterations of early drought responses in eastern white pine (Pinus strobus)
inferred← citeshttps://doi.org/10.70675/c0552058z70b1z45a5z836ez5592f9f12b25openalex-snapshot
The role of mesophyll conductance in the regulation of photosynthesis under ozone-induced oxidative stress in poplar : ecophysiological, anatomical and biochemical aspects
inferred← citeshttps://doi.org/10.7251/eoru2305283oopenalex-snapshot
Stress disorders of woody plants as a consequence of damage from high temperatures and fires
inferred← citeshttps://doi.org/10.7554/elife.70095openalex-snapshot
Expression of a CO2-permeable aquaporin enhances mesophyll conductance in the C4 species Setaria viridis
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.