review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Vadim Volkov | Q62058501 |
P2093 | author name string | Vadim Volkov | |
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Evolution of sodium channels predates the origin of nervous systems in animals | Q22337197 | ||
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A genetic system based on split-ubiquitin for the analysis of interactions between membrane proteins in vivo | Q24569545 | ||
The PMR2 gene cluster encodes functionally distinct isoforms of a putative Na+ pump in the yeast plasma membrane | Q24598671 | ||
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Plant High-Affinity Potassium (HKT) Transporters involved in salinity tolerance: structural insights to probe differences in ion selectivity | Q27023803 | ||
X-ray structure of yeast Hal2p, a major target of lithium and sodium toxicity, and identification of framework interactions determining cation sensitivity | Q27621207 | ||
Crystal structure of a potassium ion transporter, TrkH | Q27666958 | ||
Global analysis of protein expression in yeast | Q27860658 | ||
A novel genetic system to detect protein-protein interactions | Q27860915 | ||
TRK1 and TRK2 encode structurally related K+ transporters in Saccharomyces cerevisiae | Q27931482 | ||
Characterization of the NHA1 gene encoding a Na+/H+-antiporter of the yeast Saccharomyces cerevisiae | Q27931500 | ||
TRK1 encodes a plasma membrane protein required for high-affinity potassium transport in Saccharomyces cerevisiae | Q27932066 | ||
The Nha1 antiporter of Saccharomyces cerevisiae mediates sodium and potassium efflux. | Q27933304 | ||
A new family of outwardly rectifying potassium channel proteins with two pore domains in tandem. | Q27933854 | ||
New phenotypes of functional expression of the mKir2.1 channel in potassium efflux-deficient Saccharomyces cerevisiae strains | Q81633564 | ||
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Plasma-membrane hyperpolarization diminishes the cation efflux via Nha1 antiporter and Ena ATPase under potassium-limiting conditions | Q83432339 | ||
Monitoring of real changes of plasma membrane potential by diS-C(3)(3) fluorescence in yeast cell suspensions | Q84586737 | ||
Measuring cell wall thickness in living yeast cells using single molecular rulers | Q84966750 | ||
Hyperactive and hypoactive mutations in Cch1, a yeast homologue of the voltage-gated calcium-channel pore-forming subunit | Q86335896 | ||
The F130S point mutation in the Arabidopsis high-affinity K(+) transporter AtHAK5 increases K(+) over Na(+) and Cs(+) selectivity and confers Na(+) and Cs(+) tolerance to yeast under heterologous expression | Q41878914 | ||
Quantification of endogenous sirtuin metabolite O-acetyl-ADP-ribose | Q41883705 | ||
Yeast adaptation to weak acids prevents futile energy expenditure | Q41955487 | ||
Interactive domains between pore loops of the yeast K+ channel TOK1 associate with extracellular K+ sensitivity | Q42063695 | ||
Direct measurement of potential difference across the human red blood cell membrane | Q42121227 | ||
A systems-level analysis of perfect adaptation in yeast osmoregulation | Q42133339 | ||
Design principles of a conditional futile cycle exploited for regulation | Q42223696 | ||
The transcriptional response of yeast to saline stress | Q42623210 | ||
Random mutagenesis reveals a region important for gating of the yeast K+ channel Ykc1. | Q42627006 | ||
Estimation of the electric plasma membrane potential difference in yeast with fluorescent dyes: comparative study of methods | Q42824372 | ||
Aptamers embedded in polyacrylamide nanoparticles: a tool for in vivo metabolite sensing | Q42929248 | ||
Functional study of the Saccharomyces cerevisiae Nha1p C-terminus | Q43612706 | ||
Ion-exchange properties of cell walls isolated from lupine roots | Q43639759 | ||
Defective H(+)-ATPase of hygromycin B-resistant pma1 mutants fromSaccharomyces cerevisiae | Q43942055 | ||
Early changes in membrane potential of Saccharomyces cerevisiae induced by varying extracellular K(+), Na (+) or H (+) concentrations | Q44618327 | ||
Chloride channel function in the yeast TRK-potassium transporters. | Q44951024 | ||
Determining the mechanical properties of yeast cell walls | Q45165523 | ||
Potassium transport at the plasma membrane of the food spoilage yeast Zygosaccharomyces bailii. | Q45174389 | ||
In vitro bioactivity of 17alpha-estradiol | Q45255555 | ||
Conservation and dispersion of sequence and function in fungal TRK potassium transporters: focus on Candida albicans | Q46143041 | ||
Ion-channel blocker sensitivity of voltage-gated calcium-channel homologue Cch1 in Saccharomyces cerevisiae | Q46220229 | ||
TOK1 is a volatile anesthetic stimulated K+ channel | Q46570947 | ||
Identification of conserved prolyl residue important for transport activity and the substrate specificity range of yeast plasma membrane Na+/H+ antiporters | Q46580657 | ||
The Saccharomyces cerevisiae Ca2+ channel Cch1pMid1p is essential for tolerance to cold stress and iron toxicity. | Q46751509 | ||
Functional expression of the voltage-gated neuronal mammalian potassium channel rat ether à go-go1 in yeast | Q46773187 | ||
Loss of stability: a new look at the physics of cell wall behavior during plant cell growth | Q46974242 | ||
Ectopic potassium uptake in trk1 trk2 mutants of Saccharomyces cerevisiae correlates with a highly hyperpolarized membrane potential | Q48010776 | ||
A pH-sensitive yeast outward rectifier K+ channel with two pore domains and novel gating properties | Q48066130 | ||
Nobel Lecture. The identification of the sodium pump | Q48583824 | ||
Influence of different yeast cell-wall mutants on performance and protection against pathogenic bacteria (Vibrio campbellii) in gnotobiotically-grown Artemia | Q49063848 | ||
A mechanosensitive ion channel in the yeast plasma membrane. | Q50561501 | ||
A TRP homolog in Saccharomyces cerevisiae forms an intracellular Ca(2+)-permeable channel in the yeast vacuolar membrane | Q27935922 | ||
Multiple transduction pathways regulate the sodium-extrusion gene PMR2/ENA1 during salt stress in yeast | Q27935975 | ||
Patchwork organization of the yeast plasma membrane into numerous coexisting domains | Q27936685 | ||
Molecular identification of a eukaryotic, stretch-activated nonselective cation channel. | Q27936715 | ||
Unified inventory of established and putative transporters encoded within the complete genome of Saccharomyces cerevisiae | Q27936745 | ||
Regulation of yeast H(+)-ATPase by protein kinases belonging to a family dedicated to activation of plasma membrane transporters | Q27937938 | ||
Saccharomyces cerevisiae Na+/H+ antiporter Nha1p associates with lipid rafts and requires sphingolipid for stable localization to the plasma membrane | Q27939067 | ||
Characterization of the ion transport activity of the budding yeast Na+/H+ antiporter, Nha1p, using isolated secretory vesicles | Q27939097 | ||
A novel P-type ATPase from yeast involved in sodium transport | Q27939098 | ||
Chloride homeostasis in Saccharomyces cerevisiae: high affinity influx, V-ATPase-dependent sequestration, and identification of a candidate Cl- sensor | Q27939535 | ||
The yeast HAL2 nucleotidase is an in vivo target of salt toxicity | Q27939766 | ||
A prokaryotic voltage-gated sodium channel | Q28211089 | ||
Mechanosensitive channels in microbes | Q28292690 | ||
Na,K-ATPase alpha4 isoform is essential for sperm fertility | Q28506390 | ||
Osmotic stress signaling and osmoadaptation in yeasts | Q29617597 | ||
Membrane potential governs lateral segregation of plasma membrane proteins and lipids in yeast | Q30478876 | ||
Bacterial turgor pressure can be measured by atomic force microscopy. | Q31831161 | ||
Three-dimensional map of the plasma membrane H+-ATPase in the open conformation. | Q32065095 | ||
A fast Na+/Ca2+-based action potential in a marine diatom | Q33420380 | ||
Divalent cation block of inward currents and low-affinity K+ uptake in Saccharomyces cerevisiae. | Q33635043 | ||
A speed limit for conformational change of an allosteric membrane protein | Q33715701 | ||
Cell wall architecture in yeast: new structure and new challenges | Q33734183 | ||
Biogenesis and function of the yeast plasma-membrane H(+)-ATPase. | Q33796236 | ||
Single-molecule atomic force microscopy reveals clustering of the yeast plasma-membrane sensor Wsc1 | Q33912282 | ||
The yeast cell wall and septum as paradigms of cell growth and morphogenesis | Q33942954 | ||
Condition-dependent cell volume and concentration of Escherichia coli to facilitate data conversion for systems biology modeling | Q33988243 | ||
Surface:volume relationship in cardiac myocytes studied with confocal microscopy and membrane capacitance measurements: species-dependence and developmental effects. | Q34017452 | ||
Glycine residues in potassium channel-like selectivity filters determine potassium selectivity in four-loop-per-subunit HKT transporters from plants | Q34029594 | ||
Biophysical properties of Saccharomyces cerevisiae and their relationship with HOG pathway activation | Q34146196 | ||
Activation of H+-ATPase of the plasma membrane of Saccharomyces cerevisiae by glucose: the role of sphingolipid and lateral enzyme mobility. | Q34168099 | ||
K(+)-dependent composite gating of the yeast K(+) channel, Tok1. | Q34171935 | ||
Geometry of the human erythrocyte. I. Effect of albumin on cell geometry | Q34270666 | ||
Biophysical implications of lipid bilayer rheometry for mechanosensitive channels. | Q34280899 | ||
Interaction landscape of membrane-protein complexes in Saccharomyces cerevisiae | Q34297076 | ||
The TRK1 potassium transporter is the critical effector for killing of Candida albicans by the cationic protein, Histatin 5. | Q38335411 | ||
Role of Wall Phosphomannan in Flocculation of Saccharomyces cerevisiae | Q39117962 | ||
Futile Na+ cycling at the root plasma membrane in rice (Oryza sativa L.): kinetics, energetics, and relationship to salinity tolerance | Q39207330 | ||
Structure and function of proton translocating ATPase in plasma membranes of plants and fungi | Q39466498 | ||
The bacterial surface: general considerations towards design and function | Q39533168 | ||
Relationship between intracellular phosphate, proton motive force, and rate of nongrowth energy dissipation (energy spilling) in Streptococcus bovis JB1. | Q39561332 | ||
Incorporation of ionic channels from yeast plasma membranes into black lipid membranes | Q39618833 | ||
Ion Transport in yeast | Q40128315 | ||
Visualization of protein compartmentation within the plasma membrane of living yeast cells. | Q40195858 | ||
Estrogenic effects of natural and synthetic compounds including tibolone assessed in Saccharomyces cerevisiae expressing the human estrogen alpha and beta receptors | Q40276245 | ||
Elastic, flexible peptidoglycan and bacterial cell wall properties | Q40742906 | ||
Salt tolerance in plants and microorganisms: toxicity targets and defense responses. | Q41195796 | ||
A refined atomic scale model of the Saccharomyces cerevisiae K+-translocation protein Trk1p combined with experimental evidence confirms the role of selectivity filter glycines and other key residues | Q41423687 | ||
Time-resolved measurements of intracellular ATP in the yeast Saccharomyces cerevisiae using a new type of nanobiosensor | Q41713897 | ||
A genomic view of yeast membrane transporters | Q34309020 | ||
ATP-sensitive K+ channels in a plasma membrane H+-ATPase mutant of the yeast Saccharomyces cerevisiae | Q34311813 | ||
Quantitative modeling of chloride conductance in yeast TRK potassium transporters | Q34351368 | ||
Interplay of Mg2+, ADP, and ATP in the cytosol and mitochondria: unravelling the role of Mg2+ in cell respiration | Q34442022 | ||
Pressure probe technique for measuring water relations of cells in higher plants | Q34520406 | ||
Action potential generation requires a high sodium channel density in the axon initial segment | Q34587263 | ||
Role of "active" potassium transport in the regulation of cytoplasmic pH by nonanimal cells. | Q34617624 | ||
Action potential in charophytes | Q34653469 | ||
Glucose depletion rapidly inhibits translation initiation in yeast | Q34690058 | ||
Mapping condition-dependent regulation of metabolism in yeast through genome-scale modeling | Q34696017 | ||
Genetics of single-cell protein abundance variation in large yeast populations | Q34846880 | ||
Yeast two-hybrid, a powerful tool for systems biology | Q34990983 | ||
Anion currents in yeast K+ transporters (TRK) characterize a structural homologue of ligand-gated ion channels | Q35150440 | ||
The transient receptor potential channel on the yeast vacuole is mechanosensitive | Q35163125 | ||
Complex modulation of cation channels in the tonoplast and plasma membrane of Saccharomyces cerevisiae: single-channel studies | Q35166194 | ||
The split-ubiquitin membrane-based yeast two-hybrid system | Q35738280 | ||
KSper, a pH-sensitive K+ current that controls sperm membrane potential | Q35759834 | ||
Functional expression of heterologous proteins in yeast: insights into Ca2+ signaling and Ca2+-transporting ATPases | Q35861869 | ||
Removal of Potassium Negative Resistance in Perfused Squid Giant Axons | Q36427585 | ||
Non-invasive microelectrode ion flux measurements to study adaptive responses of microorganisms to the environment | Q36440567 | ||
Sperm channel diversity and functional multiplicity | Q36492847 | ||
Action potentials in a giant algal cell: a comparative approach to mechanisms and evolution of excitability | Q36669271 | ||
Physiological roles of nonselective cation channels in plants: from salt stress to signalling and development | Q36884030 | ||
Substrate cycles in metabolic regulation and in heat generation | Q37163334 | ||
Serum oestrogen receptor alpha and beta bioactivity are independently associated with breast cancer: a proof of principle study. | Q37269668 | ||
The mechanical properties of Saccharomyces cerevisiae | Q37385221 | ||
Mechanical forces of fission yeast growth | Q37464321 | ||
Alkali metal cation transport and homeostasis in yeasts | Q37701634 | ||
The lateral compartmentation of the yeast plasma membrane. | Q37773851 | ||
Ion channels in human red blood cell membrane: actors or relics? | Q37856544 | ||
In defense of "nonmolecular" cell biology | Q38141943 | ||
Advances in metabolic engineering of yeast Saccharomyces cerevisiae for production of chemicals | Q38200072 | ||
Systems biology of monovalent cation homeostasis in yeast: the translucent contribution | Q38209500 | ||
Metabolic futile cycles and their functions: a systems analysis of energy and control. | Q51933046 | ||
Mathematical modeling of calcium homeostasis in yeast cells. | Q51953620 | ||
A role for the AKT1 potassium channel in plant nutrition. | Q52530553 | ||
Low-affinity potassium uptake by Saccharomyces cerevisiae is mediated by NSC1, a calcium-blocked non-specific cation channel. | Q52544947 | ||
Lack of main K+ uptake systems in Saccharomyces cerevisiae cells affects yeast performance in both potassium-sufficient and potassium-limiting conditions. | Q53322794 | ||
Gating and conductance in an outward-rectifying K+ channel from the plasma membrane of Saccharomyces cerevisiae. | Q54050617 | ||
Studies of the cell-wall properties of Saccharomyces cerevisiae during fermentation. | Q54194569 | ||
Physiology of mutants with reduced expression of plasma membrane H+-ATPase. | Q54350704 | ||
NSC1: a novel high-current inward rectifier for cations in the plasma membrane of Saccharomyces cerevisiae. | Q55067787 | ||
Reidentification of Facultatively Alkaliphilic Bacillus sp. C-125 to Bacillus halodurans | Q57088202 | ||
Physiological Characterization of the Yeast Plasma Membrane Outward Rectifying K + Channel, DUK1 (TOK1), In Situ | Q57306911 | ||
Ion-exchange properties of cell walls of Spinacia oleracea L. roots under different environmental salt conditions | Q57379452 | ||
Heterologous Expression of Human Membrane Receptors in the Yeast Saccharomyces cerevisiae | Q57847566 | ||
A comparative study of iron uptake mechanisms in marine microalgae: iron binding at the cell surface is a critical step | Q57901532 | ||
Electrophysiological characterization of pathways for K+uptake into growing and non-growing leaf cells of barley | Q58166263 | ||
The Bulk Elastic Modulus and the Reversible Properties of Cell Walls in Developing Quercus Leaves | Q58763596 | ||
KCl leakage from microelectrodes and its impact on the membrane parameters of a nonexcitable cell | Q62988574 | ||
Membrane potential of guinea-pig spermatozoa | Q67698676 | ||
Overproduction and purification of a functional Na+/H+ antiporter coded by nhaA (ant) from Escherichia coli | Q68238305 | ||
31P NMR measurements of the ADP concentration in yeast cells genetically modified to express creatine kinase | Q68507801 | ||
Ion channels in yeast | Q68969875 | ||
Tight control of the amount of yeast plasma membrane ATPase during changes in growth conditions and gene dosage | Q70041240 | ||
Membrane potentials in yeast cells measured by direct and indirect methods | Q70152114 | ||
Effect of membrane potential on K-Cl transport in human erythrocytes | Q70595362 | ||
Glucose repression/derepression in budding yeast: SNF1 protein kinase is activated by phosphorylation under derepressing conditions, and this correlates with a high AMP:ATP ratio | Q71824307 | ||
Surface area and volume measurements for ram and human spermatozoa | Q71847301 | ||
Quantitative measurements of membrane potential in Escherichia coli | Q72147758 | ||
Comparative physiology of salt tolerance in Candida tropicalis and Saccharomyces cerevisiae | Q73320397 | ||
Glucose induces a Na(+),K(+)-ATPase-dependent transient hyperpolarization in human sperm. I. Induction of changes in plasma membrane potential by the proton ionophore CCCP | Q73571685 | ||
Swelling of root cell walls as an indicator of their functional state | Q73631273 | ||
The Saccharomyces cerevisiae CCH1 gene is involved in calcium influx and mating | Q74038134 | ||
The biophysics of leaf growth in salt-stressed barley. A study at the cell level | Q74099690 | ||
Potassium uptake through the TOK1 K+ channel in the budding yeast | Q74629441 | ||
Measurement of Membrane Potentials in Neurospora | Q76495145 | ||
The structure of the yeast cell wall. I. Identification of charged groups at the surface | Q77167047 | ||
The presumed potassium carrier Trk2p in Saccharomyces cerevisiae determines an H+-dependent, K+-independent current | Q77369991 | ||
Simultaneous determination of potassium and rubidium content in yeast | Q78433836 | ||
Characterization of potassium transport in wild-type and isogenic yeast strains carrying all combinations of trk1, trk2 and tok1 null mutations | Q78816856 | ||
Futile cycling at the plasma membrane: a hallmark of low-affinity nutrient transport | Q79224982 | ||
Measurements of plasma membrane potential changes in Saccharomyces cerevisiae cells reveal the importance of the Tok1 channel in membrane potential maintenance | Q79248877 | ||
Ring test assessment of the mKir2.1 growth based assay in Saccharomyces cerevisiae using parametric models and model-free fits | Q79338110 | ||
Water permeability differs between growing and non-growing barley leaf tissues | Q79378179 | ||
Revised procedures for yeast metabolites extraction: application to a glucose pulse to carbon-limited yeast cultures, which reveals a transient activation of the purine salvage pathway | Q79456757 | ||
The Na+,K+/H+ -antiporter Nha1 influences the plasma membrane potential of Saccharomyces cerevisiae | Q80032247 | ||
Analysis of the mKir2.1 channel activity in potassium influx defective Saccharomyces cerevisiae strains determined as changes in growth characteristics | Q81502117 | ||
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 425 | |
P577 | publication date | 2015-06-11 | |
P1433 | published in | Frontiers in Plant Science | Q27723840 |
P1476 | title | Quantitative description of ion transport via plasma membrane of yeast and small cells | |
P478 | volume | 6 |
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