about
Characterization of four plasma membrane aquaporins in tulip petals: a putative homolog is regulated by phosphorylation.Yeast functional screen to identify genes conferring salt stress tolerance in Salicornia europaeaOsHKT1;4-mediated Na(+) transport in stems contributes to Na(+) exclusion from leaf blades of rice at the reproductive growth stage upon salt stress.Genome-Wide Characterization of Major Intrinsic Proteins in Four Grass Plants and Their Non-Aqua Transport Selectivity Profiles with Comparative Perspective.The photosynthetic response of tobacco plants overexpressing ice plant aquaporin McMIPB to a soil water deficit and high vapor pressure deficit.CO2 transport by PIP2 aquaporins of barley.An aluminum-activated citrate transporter in barley.A novel cyanobacterial SmtB/ArsR family repressor regulates the expression of a CPx-ATPase and a metallothionein in response to both Cu(I)/Ag(I) and Zn(II)/Cd(II).Drought stress alters water relations and expression of PIP-type aquaporin genes in Nicotiana tabacum plants.Rice sodium-insensitive potassium transporter, OsHAK5, confers increased salt tolerance in tobacco BY2 cells.A novel histidine-rich CPx-ATPase from the filamentous cyanobacterium Oscillatoria brevis related to multiple-heavy-metal cotoleranceDifferential sodium and potassium transport selectivities of the rice OsHKT2;1 and OsHKT2;2 transporters in plant cells.OsHKT2;2/1-mediated Na(+) influx over K(+) uptake in roots potentially increases toxic Na(+) accumulation in a salt-tolerant landrace of rice Nona Bokra upon salinity stress.Control of the Water Transport Activity of Barley HvTIP3;1 Specifically Expressed in Seeds.Salinity tolerance mechanisms in glycophytes: An overview with the central focus on rice plantsExogenous application of abscisic acid (ABA) increases root and cell hydraulic conductivity and abundance of some aquaporin isoforms in the ABA-deficient barley mutant Az34.The BnALMT1 Protein That is an Aluminum-Activated Malate Transporter is Localized in the Plasma MembraneFunctional analysis of water channels in barley roots.Dynamic regulation of the root hydraulic conductivity of barley plants in response to salinity/osmotic stress.Overexpression of the barley aquaporin HvPIP2;1 increases internal CO(2) conductance and CO(2) assimilation in the leaves of transgenic rice plants.The BnALMT1 and BnALMT2 genes from rape encode aluminum-activated malate transporters that enhance the aluminum resistance of plant cells.Over-expression of a barley aquaporin increased the shoot/root ratio and raised salt sensitivity in transgenic rice plants.T-DNA Tagging-Based Gain-of-Function of OsHKT1;4 Reinforces Na Exclusion from Leaves and Stems but Triggers Na Toxicity in Roots of Rice Under Salt Stress.Identification of an H2 O2 permeable PIP aquaporin in barley and a serine residue promoting H2 O2 transport.Aquaporin OsPIP1;1 promotes rice salt resistance and seed germination.K+ transport by the OsHKT2;4 transporter from rice with atypical Na+ transport properties and competition in permeation of K+ over Mg2+ and Ca2+ ions.Mechanisms of water transport mediated by PIP aquaporins and their regulation via phosphorylation events under salinity stress in barley roots.Abiotic stresses modulate expression of major intrinsic proteins in barley (Hordeum vulgare).Influence of low air humidity and low root temperature on water uptake, growth and aquaporin expression in rice plants.Insights into the salt tolerance mechanism in barley (Hordeum vulgare) from comparisons of cultivars that differ in salt sensitivity.High-affinity K+ transporters from a halophyte, Sporobolus virginicus, mediate both K+ and Na+ transport in transgenic Arabidopsis, X. laevis oocytes, and yeastA Cyclic Nucleotide-Gated Channel, HvCNGC2-3, Is Activated by the Co-Presence of Na⁺ and K⁺ and Permeable to Na⁺ and K⁺ Non-Selectively.Salt Stress-Induced Cytoplasmic Acidification and Vacuolar Alkalization in Nitellopsis obtusa Cells : In VivoP-Nuclear Magnetic Resonance StudyATP-Regulated Ion Channels in the Plasma Membrane of a Characeae Alga, Nitellopsis obtusaHydrogen peroxide permeability of plasma membrane aquaporins of Arabidopsis thalianaOverexpression of alternative oxidase gene confers aluminum tolerance by altering the respiratory capacity and the response to oxidative stress in tobacco cellsOsmotic stress decreases PIP aquaporin transcripts in barley roots but H2O2 is not involved in this processThe mechanism of SO2 -induced stomatal closure differs from O3 and CO2 responses and is mediated by nonapoptotic cell death in guard cellsFunctional screening of salt tolerance genes from a halophyte Sporobolus virginicus and transcriptomic and metabolomic analysis of salt tolerant plants expressing glycine-rich RNA-binding proteinEnergy costs of salinity tolerance in crop plants
P50
Q34787813-2DDFDED0-09D6-45C7-ADFD-7E7DB89BDF92Q35844708-5E30F992-7FCC-4466-B209-B78A044FE169Q35898347-3E10EEC1-1F75-4AC6-9F66-9B6AAE6B98C6Q36058003-C97703B7-E5F0-4626-BC65-7ABE579C2679Q36962533-19CCE1A3-60A5-438B-B546-511FE359B773Q37553751-C4123E65-DA1D-40AD-9823-C4DFE72D34CAQ38299985-18EF4A34-1749-46A2-8396-DFA8C49BE05AQ38344821-CC302BC6-D74F-4507-8813-9944383C53D5Q39203885-E0C6FA71-66A6-48B9-9B09-3EECF09B2D1DQ39630657-E3BA39DA-720E-4B89-989D-D2FDAB6A6AF7Q39680275-857E9B9D-66FA-45DD-9B8D-0711D6839B3DQ39778875-DB0581AA-44B7-4257-B950-B1A074C5D9EDQ40311171-6B80B30B-7C00-477A-BEC8-6554DEC6FC6FQ40733360-F6A43070-12BC-4CA2-9E5D-160B790F8A98Q41083549-8C4DD569-BEB5-4FB0-9CD6-9268DD375034Q41632302-78340C05-376C-4ECB-8D3B-0058A4164CD6Q41898037-A8008A77-BB51-4B5B-A402-FA423695F7C6Q44116198-37429681-7818-4FC8-AFE5-9D6AD39ACD90Q46780058-73ADBA1D-5175-4AC4-A47C-9637F3B667A3Q47414111-C39C7EEB-D709-47F3-8E3D-F5E7CA8DB2EFQ48084239-8B10A02E-FCC9-4277-B7C8-C9CC143B58BFQ48212887-3E852EBE-8194-4BF4-91FC-EA05FA560B93Q48253061-E6788DCA-B49F-47B0-8C9D-E3F6CCDB17BCQ48370205-289A0686-DACC-47FD-8CB5-50DB8282B796Q48633933-F35229CB-0A30-4BB1-9184-2C492C6741F6Q48672668-07D6391E-9665-4497-ACEA-22F042BB3A9DQ48678309-05F132DC-B49F-4F9F-B48C-06065A566960Q48681114-76A721A2-F373-4E2C-9309-D22C44831FFAQ53163638-E567F802-C481-4DD2-AFA5-051AB06AB1FDQ54455203-FCC7C38A-60BA-4984-8323-A14B2561BD85Q57459824-8C430EC3-940A-493F-A4EF-F657B0DA80F2Q64969159-CC6C4E01-9055-4923-B5B7-D90C0B8165F5Q83268480-193BECCB-1907-466A-A782-6B7E34683447Q83269930-C4AD3EAF-EA69-4F41-B2B7-18C0BED8D697Q83577255-3B7127C2-DE4E-401F-A81A-EE161D4DE7F5Q84958630-5F0AB885-9A15-40DA-BFA2-EEDBD3C4015BQ85259629-71019BB7-6E00-4F1E-8FB5-8BEC383CAADBQ90266596-00FE2669-9130-4669-80CB-7495B08FBC33Q93341759-7999651B-4BA8-4E6C-94AD-3BC03E8DE2F8Q93387429-E17C0D0C-CEE9-475B-B91A-E2E3F4CC66B3
P50
description
researcher
@en
wetenschapper
@nl
name
Maki Katsuhara
@en
Maki Katsuhara
@nl
type
label
Maki Katsuhara
@en
Maki Katsuhara
@nl
prefLabel
Maki Katsuhara
@en
Maki Katsuhara
@nl
P106
P31
P496
0000-0002-8264-3063