On the public citation graph
Salt tolerance inNitellopsis obtusa
0 signed · 69 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known work and none has been retracted — and get a dated CiteStamped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/10.1007/978-94-009-5111-2_1openalex-snapshot
Adaptation to salinity at the plant cell level
inferredcites →https://doi.org/10.1007/bf00397424openalex-snapshot
Adenine-nucleotide levels and metabolism-dependent membrane potential in cells of Nitellopsis obtusa Groves
inferredcites →https://doi.org/10.1007/bf01282121openalex-snapshot
Membrane characteristics as revealed by water and ionic relations of algal cells
inferredcites →https://doi.org/10.1007/bf01604093openalex-snapshot
Der Erregungsvorgang bei Nitella mucronata
inferredcites →https://doi.org/10.1007/bf02182230openalex-snapshot
Adaptation to salinity at the plant cell level
inferredcites →https://doi.org/10.1071/bi9660385openalex-snapshot
The Electrical Measurement of Chloride Fluxes in Nitella
inferredcites →https://doi.org/10.1085/jgp.42.6.1167openalex-snapshot
PROTOPLASMIC STREAMING OF AN INTERNODAL CELL OF NITELLA FLEXILIS
inferredcites →https://doi.org/10.1093/jxb/18.1.1openalex-snapshot
The Membrane Potential ofNitella translucens
inferredcites →https://doi.org/10.1093/jxb/37.2.238openalex-snapshot
The Membrane Potential of Enzymatically IsolatedNitella expansaProtoplasts as Compared with their Intact Cells
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.a076860openalex-snapshot
Intracellular Distribution of Free Amino Acids between the Vacuolar and Extravacuolar Compartments in Internodal Cells of Chara australis
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a077107openalex-snapshot
Quantitative Analysis of ATP-Dependent H+ Efflux and Pump Current Driven by an Electrogenic Pump in Nitellopsis obtusa 1
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a079120openalex-snapshot
IONIC COMPOSITION OF THE CYTOPLASM OF NITELLA FLEXILIS 1
inferredcites →https://doi.org/10.1097/00010694-198509000-00011openalex-snapshot
Salinity Tolerance in Plants
inferredcites →https://doi.org/10.1104/pp.19.3.466openalex-snapshot
CALCIUM AND OTHER POLYVALENT CATIONS AS ACCELERATORS OF ION ACCUMULATION BY EXCISED BARLEY ROOTS
inferredcites →https://doi.org/10.1104/pp.36.4.437openalex-snapshot
The essential role of calcium in selective cation transport by plant cells
inferredcites →https://doi.org/10.1104/pp.72.3.685openalex-snapshot
Aspects of Salt Tolerance in a NaCl-Selected Stable Cell Line of Citrus sinensis
inferredcites →https://doi.org/10.1104/pp.73.3.624openalex-snapshot
Comparison between a Stable NaCl-Selected Nicotiana Cell Line and the Wild Type
inferredcites →https://doi.org/10.1104/pp.78.1.144openalex-snapshot
Relation between Ion Accumulation of Salt-Sensitive and Isolated Stable Salt-Tolerant Cell Lines of Citrus aurantium
inferredcites →https://doi.org/10.1104/pp.79.1.118openalex-snapshot
Adaptation of Tobacco Cells to NaCl
inferredcites →https://doi.org/10.1104/pp.79.1.207openalex-snapshot
Displacement of Ca2+ by Na+ from the Plasmalemma of Root Cells
inferredcites →https://doi.org/10.1111/j.1365-3040.1985.tb01223.xopenalex-snapshot
Germination and seedling growth of cotton: salinity‐calcium interactions
inferredcites →https://doi.org/10.1111/j.1399-3054.1971.tb01430.xopenalex-snapshot
Calcium and Salt Toleration by Bean Plants
inferredcites →https://doi.org/10.1126/science.166.3903.395openalex-snapshot
Salt Toleration by Plants: Enhancement with Calcium
inferredcites →https://doi.org/10.1146/annurev.pp.17.060166.000403openalex-snapshot
Role of Mineral Elements with Emphasis on the Univalent Cations
inferredcites →https://doi.org/10.1146/annurev.pp.28.060177.000513openalex-snapshot
The Mechanism of Salt Tolerance in Halophytes
inferredcites →https://doi.org/10.1146/annurev.pp.31.060180.001053openalex-snapshot
Mechanisms of Salt Tolerance in Nonhalophytes
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.5252/geodiversitas2018v40a10zenodo-depositor-declared
Charophyte flora from the Miocene of Zahle (Beeka Valley, Lebanon). Biostratigraphic, palaeoenvironmental and palaeobiogeographical implications
inferred← citeshttps://doi.org/10.1002/tox.2530100108openalex-snapshot
Wastewater toxicity assessment using the electrophysiological response of a charophyte Nitellopsis obtusa
inferred← citeshttps://doi.org/10.1007/978-3-642-13145-5_1openalex-snapshot
Sixty Years Research with Characean Cells: Fascinating Material for Plant Cell Biology
inferred← citeshttps://doi.org/10.1007/978-3-642-84619-9_11openalex-snapshot
Ion Channels in the Plasma Membrane of Plant Cells
inferred← citeshttps://doi.org/10.1007/bf00233382openalex-snapshot
D2O-induced ion channel activation in Characeae at low ionic strength
inferred← citeshttps://doi.org/10.1007/bf01281029openalex-snapshot
ATP is essential for calcium-induced salt tolerance inNitellopsis obtusa
inferred← citeshttps://doi.org/10.1007/bf01869308openalex-snapshot
Demonstration and characterization of Ca2+ channel in tonoplast-free cells ofNitellopsis obtusa
inferred← citeshttps://doi.org/10.1007/s00232-009-9182-4openalex-snapshot
The Role of H+/OH− Channels in the Salt Stress Response of Chara australis
inferred← citeshttps://doi.org/10.1007/s43538-022-00102-4openalex-snapshot
First report on late Miocene (Tortonian: ~ 11–10 Ma) charophyte gyrogonites from Tapar, Kachchh District, Gujarat State, western India
inferred← citeshttps://doi.org/10.1016/0033-5894(91)90026-2openalex-snapshot
Charophyte remains from Wadi Howar as evidence for deep mid-Holocene freshwater lakes in the eastern Sahara of Northwest Sudan
inferred← citeshttps://doi.org/10.1016/0899-5362(91)90083-bopenalex-snapshot
Charophytes as lacustrine biomarkers during the quaternary in North Africa
inferred← citeshttps://doi.org/10.1016/j.revpalbo.2022.104784openalex-snapshot
Eocene to Miocene Charophytes from the Qaidam Basin on the northern Tibetan Plateau and its calibration to the Geomagnetic Polarity Time Scale
inferred← citeshttps://doi.org/10.1016/j.revpalbo.2023.104848openalex-snapshot
Early Pleistocene charophyte flora from Dursunlu (Ilgın Basin, Turkey): palaeoecological implications
inferred← citeshttps://doi.org/10.1016/s0005-2736(00)00135-8openalex-snapshot
Sodium transport in plant cells
inferred← citeshttps://doi.org/10.1016/s0301-4622(02)00365-4openalex-snapshot
Theoretical and experimental studies on freezing point depression and vapor pressure deficit as methods to measure osmotic pressure of aqueous polyethylene glycol and bovine serum albumin solutions
inferred← citeshttps://doi.org/10.1071/pp01027openalex-snapshot
How characean cells have contributed to the progress of plant membrane biophysics
inferred← citeshttps://doi.org/10.1080/08912963.2022.2106861openalex-snapshot
Palaeoecology of Middle Miocene charophytes from the Vallès‒Penedès and Vilanova basins (Catalonia, Spain)
inferred← citeshttps://doi.org/10.1093/jexbot/52.355.223openalex-snapshot
Ca 2+ and phosphate releases from calcified Chara cell walls in concentrated KCl solution
inferred← citeshttps://doi.org/10.1093/jxb/45.5.657openalex-snapshot
Na+fluxes inCharaunder salt stress
inferred← citeshttps://doi.org/10.1093/oxfordjournals.pcp.a029521openalex-snapshot
Cycloprodigiosin Hydrochloride Inhibits Acidification of the Plant Vacuole
inferred← citeshttps://doi.org/10.1098/rstb.1992.0125openalex-snapshot
Calcium -regulated channels and their bearing on physiological activities in Characean cells
inferred← citeshttps://doi.org/10.1104/pp.90.3.1102openalex-snapshot
Salt Stress-Induced Cytoplasmic Acidification and Vacuolar Alkalization in Nitellopsis obtusa Cells
inferred← citeshttps://doi.org/10.1104/pp.93.1.343openalex-snapshot
ATP-Regulated Ion Channels in the Plasma Membrane of a Characeae Alga, Nitellopsis obtusa
inferred← citeshttps://doi.org/10.1111/1365-3040.ep11604878openalex-snapshot
Changes in sodium and potassium in Nitellopsis cells treated with transient salt stress
inferred← citeshttps://doi.org/10.1111/j.1365-3040.1988.tb01120.xopenalex-snapshot
Changes in sodium and potassium in Nitellopsis cells treated with transient salt stress
inferred← citeshttps://doi.org/10.1111/j.1365-3040.1988.tb01785.xopenalex-snapshot
The effect of divalent cations on Na+ tolerance in Charophytes. II: Chara corallina
inferred← citeshttps://doi.org/10.1111/j.1365-3040.1990.tb01290.xopenalex-snapshot
Mechanism of calcium‐dependent salt tolerance in cells of Nitellopsis obtusa: role of intracellular adenine nucleotides
inferred← citeshttps://doi.org/10.1111/j.1365-3040.1990.tb01324.xopenalex-snapshot
Survival and death of Chara internodal cells in electrolyte solutions and calcium release from the cell wall
inferred← citeshttps://doi.org/10.1111/j.1365-3040.1992.tb01015.xopenalex-snapshot
Calcium‐salinity interactions affect ion transport in Chara corallina
inferred← citeshttps://doi.org/10.1111/j.1365-3040.1992.tb01454.xopenalex-snapshot
Zinc and salinity effects on membrane transport in Chara connivens
inferred← citeshttps://doi.org/10.1111/j.1365-3040.1993.tb00902.xopenalex-snapshot
Effects of salinity and turgor on calcium influx in Chara
inferred← citeshttps://doi.org/10.1111/j.1365-3040.1996.tb00390.xopenalex-snapshot
Short‐term regulation of cytosolic Ca2+, cytosolic pH and vacuolar pH under NaCl stress in the charophyte alga Nitellopsis obtusa
inferred← citeshttps://doi.org/10.1111/j.1365-3040.1996.tb00407.xopenalex-snapshot
Control of sodium influx by calcium and turgor in two charophytes differing in salinity tolerance
inferred← citeshttps://doi.org/10.1111/j.1399-3054.1993.tb05204.xopenalex-snapshot
Loss of ionic and osmotic regulation in Chara internodal cells in concentrated KCl solutions
inferred← citeshttps://doi.org/10.1111/j.1399-3054.1996.tb00495.xopenalex-snapshot
Ionic processes underlying the decrease in osmotic potential of Chara L‐cell fragments in dilute electrolyte solutions
inferred← citeshttps://doi.org/10.1111/j.1438-8677.1995.tb00833.xopenalex-snapshot
Concanamycin 4‐B: A Potent Inhibitor of Vacuolar pH Regulation in Chara Cells
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2009.03169.xopenalex-snapshot
42K analysis of sodium‐induced potassium efflux in barley: mechanism and relevance to salt tolerance
inferred← citeshttps://doi.org/10.1111/j.1574-6968.1991.tb04443.x-i1openalex-snapshot
Calcium-induced salt tolerance inRhizobium leguminosarumbiovarviciaestrain C124b
inferred← citeshttps://doi.org/10.1139/g09-041openalex-snapshot
Characterization of Salt Overly Sensitive 1 (SOS1) gene homoeologs in quinoa (Chenopodium quinoa Willd.)
inferred← citeshttps://doi.org/10.1201/9780824746728.pt2openalex-snapshot
Mechanisms Involved in Salt Tolerance of Plants
inferred← citeshttps://doi.org/10.3389/fpls.2019.00082openalex-snapshot
Modeling the Action Potential in Characeae Nitellopsis obtusa: Effect of Saline Stress
inferred← citeshttps://doi.org/10.3906/vet-1305-10openalex-snapshot
Effects of spirulina in arsenic poisoning in the Black Bengal goat
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.