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How characean cells have contributed to the progress of plant membrane biophysics
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/j.1460-2075.1995.tb07271.xopenalex-snapshot
Gadolinium‐sensitive, voltage‐dependent calcium release channels in the endoplasmic reticulum of a higher plant mechanoreceptor organ.
inferredcites →https://doi.org/10.1007/bf00195329openalex-snapshot
Role of cytoplasmic inorganic phosphate in light-induced activation of H+-pumps in the plasma membrane and tonoplast of Chara corallina
inferredcites →https://doi.org/10.1007/bf00195729openalex-snapshot
Responses of wheat plants to nutrient deprivation may involve the regulation of water-channel function
inferredcites →https://doi.org/10.1007/bf00233475openalex-snapshot
Microscopic elements of electrical excitation in Chara: Transient activity of Cl? channels in the plasma membrane
inferredcites →https://doi.org/10.1007/bf00393642openalex-snapshot
Dependence of the membrane potential on intracellular ATP concentration in tonoplast-free cells of Nitellopsis obtusa
inferredcites →https://doi.org/10.1007/bf01248199openalex-snapshot
Neue Methode zur Messung des osmotischen Wertes einer Zelle
inferredcites →https://doi.org/10.1007/bf01248890openalex-snapshot
Studies on water permeability of a single plant cell by means of transcellular osmosis
inferredcites →https://doi.org/10.1007/bf01252056openalex-snapshot
The polar permeability of plant cell membranes to water
inferredcites →https://doi.org/10.1007/bf01273256openalex-snapshot
Turgor regulation and cytoplasmic free Ca2+ in the algaLamprothamnium
inferredcites →https://doi.org/10.1007/bf01275803openalex-snapshot
Participation of Ca2+ in cessation of cytoplasmic streaming induced by membrane excitation inCharaceae internodal cells
inferredcites →https://doi.org/10.1007/bf01276370openalex-snapshot
Demonstration of two proton translocating systems in tonoplast of permeabilizedNitella cell
inferredcites →https://doi.org/10.1007/bf01276378openalex-snapshot
Ca2+ antagonist nifedipine inhibits turgor regulation upon hypotonic treatment in internodal cells ofLamprothamnium
inferredcites →https://doi.org/10.1007/bf01276604openalex-snapshot
Plant vacuole degrades exogenous proteins
inferredcites →https://doi.org/10.1007/bf01277008openalex-snapshot
Salt tolerance inNitellopsis obtusa
inferredcites →https://doi.org/10.1007/bf01281029openalex-snapshot
ATP is essential for calcium-induced salt tolerance inNitellopsis obtusa
inferredcites →https://doi.org/10.1007/bf01282988openalex-snapshot
Tonoplast origin of the envelope membrane of cytoplasmic droplets prepared fromChara internodal cells
inferredcites →https://doi.org/10.1007/bf01868083openalex-snapshot
The relationship between ATP and an electrogenic pump in the plasma membrane ofNeurospora crassa
inferredcites →https://doi.org/10.1007/bf01868954openalex-snapshot
Tonoplast action potential inNitella in relation to vacuolar chloride concentration
inferredcites →https://doi.org/10.1007/bf01869213openalex-snapshot
Calcium ion and turgor regulation in plant cells
inferredcites →https://doi.org/10.1007/bf01870313openalex-snapshot
Excitation ofCharaceae cell membranes as a result of activation of calcium and chloride channels
inferredcites →https://doi.org/10.1007/bf01871233openalex-snapshot
Ca2+-activated Cl− channel in plasmalemma ofNitellopsis obtusa
inferredcites →https://doi.org/10.1007/bf01871669openalex-snapshot
Nature of the water channels in the internodal cells ofNitellopsis
inferredcites →https://doi.org/10.1007/bf02344296openalex-snapshot
Membrane control of cytoplasmic streaming in characean cells
inferredcites →https://doi.org/10.1007/s004250050239openalex-snapshot
Aquaporin function, structure, and expression: are there more surprises to surface in water relations?
inferredcites →https://doi.org/10.1007/s004250050656openalex-snapshot
Osmotic water permeability of isolated vacuoles
inferredcites →https://doi.org/10.1016/0005-2736(73)90197-1openalex-snapshot
Studies of excitable membrane formed on the surface of protoplasmic drops isolated from Nitella II. Tension at the surface of protoplasmic drops
inferredcites →https://doi.org/10.1016/0022-5193(63)90063-8openalex-snapshot
Irreversible thermodynamics and frictional models of membrane processes, with particular reference to the cell membrane
inferredcites →https://doi.org/10.1016/0926-6577(64)90043-9openalex-snapshot
The measurement of hydraulic conductivity (osmotic permeability to water) of internodal characean cells by means of trancellular osmosis
inferredcites →https://doi.org/10.1016/s0005-2736(00)00137-1openalex-snapshot
Calcium channels in higher plants
inferredcites →https://doi.org/10.1016/s0005-2736(00)00147-4openalex-snapshot
The role of aquaporins in cellular and whole plant water balance
inferredcites →https://doi.org/10.1016/s0005-2736(99)00037-1openalex-snapshot
Molecular cloning and sequencing of the cDNA for vacuolar H+-pyrophosphatase from Chara corallina
inferredcites →https://doi.org/10.1016/s1360-1385(99)01438-7openalex-snapshot
Aquaporins and water homeostasis in plants
inferredcites →https://doi.org/10.1038/191811a0openalex-snapshot
The Action Potential in Cells of Chara
inferredcites →https://doi.org/10.1038/296647a0openalex-snapshot
Free Ca2+ and cytoplasmic streaming in the alga Chara
inferredcites →https://doi.org/10.1046/j.1365-3040.2000.00524.xopenalex-snapshot
Phosphate uptake in Chara: membrane transport via Na/Pi cotransport
inferredcites →https://doi.org/10.1046/j.1365-3040.2000.00571.xopenalex-snapshot
Turgor regulation in the salt‐tolerant alga Chara longifolia
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00019.xopenalex-snapshot
The action potential in Chara: Ca2+ release from internal stores visualized by Mn2+‐induced quenching of fura‐dextran
inferredcites →https://doi.org/10.1071/bi9640062openalex-snapshot
Ionic Relations of Cells of Ohara Australis VII. The Separate Electrical Oharacteristics of the Plasmalemma and Tonoplast
inferredcites →https://doi.org/10.1071/bi9640388openalex-snapshot
Ionic Relations of Cells of Chara Australis VIII. Membrane Currents During a Voltage Clamp
inferredcites →https://doi.org/10.1071/bi9640400openalex-snapshot
Ionic Relations of Cells of Chara Australis IX. Analysis of Transient Membrane Currents
inferredcites →https://doi.org/10.1071/bi9660399openalex-snapshot
Water Permeability of a Characean Internodal Cell with Special Reference to Its Polarity
inferredcites →https://doi.org/10.1071/bi9701033openalex-snapshot
Membrane Electrical Behaviour in Nitellopsis Obtusa
inferredcites →https://doi.org/10.1073/pnas.92.10.4124openalex-snapshot
Effects of mechanical signaling on plant cell cytosolic calcium.
inferredcites →https://doi.org/10.1085/jgp.17.1.87openalex-snapshot
ANESTHESIA PRODUCED BY DISTILLED WATER
inferredcites →https://doi.org/10.1093/jxb/31.5.1223openalex-snapshot
Lamprothamnium, a Euryhaline Charophyte
inferredcites →https://doi.org/10.1093/jxb/46.2.199openalex-snapshot
Reversible closing of water channels in Chara internodes provides evidence for a composite transport model of the plasma membrane
inferredcites →https://doi.org/10.1093/jxb/46.9.1067openalex-snapshot
Water channels in plants: do basic concepts of water transport change?
inferredcites →https://doi.org/10.1093/jxb/47.4.589openalex-snapshot
Plasma membrane isolation from freshwater and salt-tolerant species ofChara: antibody cross-reactions and phosphohydrolase activities
inferredcites →https://doi.org/10.1093/jxb/48.8.1511openalex-snapshot
Water channels inChara corallina
inferredcites →https://doi.org/10.1093/jxb/48.special_issue.609openalex-snapshot
Ion channel activity during the action potential in Chara: new insights with new techniques
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a074969openalex-snapshot
Potassium, sodium and Chloride in the protoplasm of characeae
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a075025openalex-snapshot
Osmotic and ionic regulation in Nitella
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a076747openalex-snapshot
Turgor Regulation in a Brackish Charophyte, Lamprothamnium succinctum II. Changes in K$, Na$ and Cl− Concentrations, Membrane Potential and Membrane Resistance during Turgor Regulation
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a077346openalex-snapshot
Dependence of Plasmalemma Conductance and Potential on Intracellular Free Ca2+ in Tonoplast-Removed Cells of a Brackish Water Characeae Lamprothamnium
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a077382openalex-snapshot
Characterization of Two Proton Transport Systems in the Tonoplast of Plasmalemma-Permeabilized Nitella Cells
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a077774openalex-snapshot
Patch-Clamp Study on a Ca2+-Regulated K+ Channel in the Tonoplast of the Brackish Characeae Lamprothamnium succinctum
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a078964openalex-snapshot
WATER PERMEABILITY OF THE CELL WALL IN NITELLA 1
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a078969openalex-snapshot
CHANGES IN RESTING POTENTIAL AND ION ABSORPTION INDUCED BY LIGHT IN A SINGLE PLANT CELL
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a079354openalex-snapshot
Light-induced changes of bioelectric potential in Chara
inferredcites →https://doi.org/10.1104/pp.105.1.9openalex-snapshot
Aquaporins: The Molecular Basis of Facilitated Water Movement Through Living Plant Cells?
inferredcites →https://doi.org/10.1104/pp.120.1.1openalex-snapshot
Le Calcium, C'est la Vie: Calcium Makes Waves1
inferredcites →https://doi.org/10.1104/pp.61.2.158openalex-snapshot
Pressure Probe Technique for Measuring Water Relations of Cells in Higher Plants
inferredcites →https://doi.org/10.1104/pp.74.2.252openalex-snapshot
Osmoregulation or Turgor Regulation in Chara ?
inferredcites →https://doi.org/10.1104/pp.77.1.46openalex-snapshot
Proton-Translocating Inorganic Pyrophosphatase in Red Beet (Beta vulgaris L.) Tonoplast Vesicles
inferredcites →https://doi.org/10.1104/pp.78.4.673openalex-snapshot
Metabolic Conversion of Amino Acids Loaded in the Vacuole of Chara australis Internodal Cells
inferredcites →https://doi.org/10.1111/j.1365-3040.1996.tb00420.xopenalex-snapshot
Turgor regulation in Lamprothamnium papulosum. I. I/V analysis and pharmacological dissection of the hypotonic effect
inferredcites →https://doi.org/10.1111/j.1438-8677.1996.tb00588.xopenalex-snapshot
Characteristics of Hg‐ and Zn‐sensitive Water Channels in the Plasma Membrane of Chara Cells*
inferredcites →https://doi.org/10.1146/annurev.pp.34.060183.000443openalex-snapshot
Photosynthetic Assimilation of Exogenous HCO3 by Aquatic Plants
inferredcites →https://doi.org/10.1146/annurev.pp.38.060187.000523openalex-snapshot
Membrane Control in the Characeae
inferredcites →https://doi.org/10.1242/jcs.17.3.655openalex-snapshot
Cytoplasmic streaming in Chara: A cell model activated by atp and inhibited by cytochalasin b
inferredcites →https://doi.org/10.1247/csf.19.263openalex-snapshot
Characean Cells as a Tool for Studying Electrophysiological Characteristics of Plant Cells.
inferredcites →https://doi.org/10.1247/csf.9.225openalex-snapshot
Vacuolar pH regulation in Chara australis.
inferredcites →https://doi.org/10.2183/pjab1945.47.549openalex-snapshot
Properties of Excitable Membrane Produced on the Surface of Protoplasmic Drop in Nitella
inferredcites →https://doi.org/10.2183/pjab1945.47.554openalex-snapshot
Excitability of Surface Membrane of Protoplasmic Drop Produced from Protoplasm in Nitella
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/ejic.201300697openalex-snapshot
Biogenic Manganese–Calcium Oxides on the Cell Walls of the Algae Chara Corallina: Elemental Composition, Atomic Structure, and Water‐Oxidation Catalysis
inferred← citeshttps://doi.org/10.1007/1-4020-4927-7_3openalex-snapshot
Coherent domains in the streaming cytoplasm of a giant algal cell
inferred← citeshttps://doi.org/10.1007/978-3-319-32669-6_40-1openalex-snapshot
Charophyceae (Charales)
inferred← citeshttps://doi.org/10.1007/978-3-319-32669-6_40-2openalex-snapshot
Charophyceae (Charales)
inferred← citeshttps://doi.org/10.1007/s10265-003-0109-3openalex-snapshot
Cell physiological aspects of the plasma membrane electrogenic H + pump
inferred← citeshttps://doi.org/10.1007/s10265-004-0157-3openalex-snapshot
Studies on semipermeability and electrical characteristics in membranes of Chara cells fixed with glutaraldehyde
inferred← citeshttps://doi.org/10.1007/s10265-006-0061-0openalex-snapshot
The sliding theory of cytoplasmic streaming: fifty years of progress
inferred← citeshttps://doi.org/10.1007/s10265-008-0147-yopenalex-snapshot
Primary effect of bromoxynil to induce plant cell death may be cytosol acidification
inferred← citeshttps://doi.org/10.1007/s10265-009-0297-6openalex-snapshot
Unique cellular effect of the herbicide bromoxynil revealed by electrophysiological studies using characean cells
inferred← citeshttps://doi.org/10.1007/s10265-010-0391-9openalex-snapshot
Involvement of protein synthesis in recovery from refractory period of electrical depolarization induced by osmotic stimulation in Chara corallina
inferred← citeshttps://doi.org/10.1016/b978-0-12-800179-0.00006-4openalex-snapshot
Characean Internodal Cells as a Model System for the Study of Cell Organization
inferred← citeshttps://doi.org/10.1016/j.bpc.2024.107199openalex-snapshot
Dependence of cell's membrane potential on extracellular voltage observed in Chara globularis
inferred← citeshttps://doi.org/10.1016/j.jplph.2016.02.009openalex-snapshot
Auxin effects on ion transport in Chara corallina
inferred← citeshttps://doi.org/10.1071/pp01152openalex-snapshot
Membrane transport: mechanisms and processes from organelles to whole plants
inferred← citeshttps://doi.org/10.1093/jxb/ert322openalex-snapshot
Molecular and biochemical analysis of the first ARA6 homologue, a RAB5 GTPase, from green algae
inferred← citeshttps://doi.org/10.1093/pcp/pcf182openalex-snapshot
Electrical Perception of “Death Message” in Chara: Analysis of Rapid Component and Ionic Process
inferred← citeshttps://doi.org/10.1093/pcp/pcg065openalex-snapshot
Is Ca2+ Release from Internal Stores Involved in Membrane Excitation in Characean Cells?
inferred← citeshttps://doi.org/10.1093/pcp/pcg070openalex-snapshot
Low-Temperature Induced Transmembrane Potential Changes in the Liverwort Conocephalum conicum
inferred← citeshttps://doi.org/10.1093/pcp/pcg120openalex-snapshot
Studies on Alkaline Band Formation in Chara corallina: Ameliorating Effect of Ca2+ on Inhibition Induced by Osmotic Shock
inferred← citeshttps://doi.org/10.1093/pcp/pcg151openalex-snapshot
Studies on Mechano-perception in the Characeae: Transduction of Pressure Signals into Electrical Signals
inferred← citeshttps://doi.org/10.1093/pcp/pci200openalex-snapshot
Electrical Perception of the ‘Death Message’ in Chara: Analysis of K+-sensitive Depolarization
inferred← citeshttps://doi.org/10.1093/pcp/pcn002openalex-snapshot
Electrophysiological Characterization of the Node in Chara corallina: Functional Differentiation for Wounding Response
inferred← citeshttps://doi.org/10.1093/pcp/pcn136openalex-snapshot
Involvement of Membrane Potential in Alkaline Band Formation by Internodal Cells of Chara corallina
inferred← citeshttps://doi.org/10.1093/pcp/pcr074openalex-snapshot
Plasma Membrane Domains Participate in pH Banding of Chara Internodal Cells
inferred← citeshttps://doi.org/10.1104/pp.113.231688openalex-snapshot
Polarity of Water Transport across Epidermal Cell Membranes in Tradescantia virginiana
inferred← citeshttps://doi.org/10.1111/j.1365-2818.2011.03572.xopenalex-snapshot
The characean internodal cell as a model system for studying wound healing
inferred← citeshttps://doi.org/10.1111/j.1365-3040.2008.01866.xopenalex-snapshot
Mechano‐perception in Chara cells: the influence of salinity and calcium on touch‐activated receptor potentials, action potentials and ion transport
inferred← citeshttps://doi.org/10.1111/tra.12267openalex-snapshot
Molecular Analysis and Localization of CaARA7 a Conventional RAB5 GTPase from Characean Algae
inferred← citeshttps://doi.org/10.1134/s0006350924700118openalex-snapshot
Electrogenesis in the Root Environment of Various Lettuce Varieties
inferred← citeshttps://doi.org/10.1139/o05-019openalex-snapshot
Removal of the nitro and phenyl groups from NPPB decreases its inhibitory effect on cytoplasmic streaming in the alga Nitella hookeri
inferred← citeshttps://doi.org/10.31857/s0006302924010113openalex-snapshot
Electrogenesis in the Root Environment of Various Lettuce Varieties
inferred← citeshttps://doi.org/10.4149/gpb_2011_01_52openalex-snapshot
Effect of cadmium and lead on the membrane potential and photoelectric reaction of Nitellopsis obtusa cells
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