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An appraisal of the variable response of microalgal lipids to culture salinity
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Nutraceutical Fatty Acids from Oleaginous Microalgae
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Interactive effects of salinity, high light, and nitrogen starvation on fatty acid and carotenoid profiles in Nannochloropsis oceanica CCALA 804
inferredcites →https://doi.org/10.1002/ejlt.201700152openalex-snapshot
Production of chemicals from microalgae lipids – status and perspectives
inferredcites →https://doi.org/10.1002/elsc.201100204openalex-snapshot
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inferredcites →https://doi.org/10.1002/jcp.21715openalex-snapshot
Osmotic responses of Dunaliella to the changes of salinity
inferredcites →https://doi.org/10.1002/jsfa.6470openalex-snapshot
Optimisation of the critical medium components for better growth of Picochlorum sp. and the role of stressful environments for higher lipid production
inferredcites →https://doi.org/10.1007/978-0-387-89366-2_1openalex-snapshot
Algal lipids and effect of the environment on their biochemistry
inferredcites →https://doi.org/10.1007/978-3-319-25979-6_6openalex-snapshot
Role of MGDG and Non-bilayer Lipid Phases in the Structure and Dynamics of Chloroplast Thylakoid Membranes
inferredcites →https://doi.org/10.1007/bf00003531openalex-snapshot
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inferredcites →https://doi.org/10.1007/bf00023373openalex-snapshot
Environmental control of lipid and biomass production in two diatom species
inferredcites →https://doi.org/10.1007/bf01131597openalex-snapshot
Osmotic Acclimation and Turgor Pressure Regulation in Algae
inferredcites →https://doi.org/10.1007/bf02179778openalex-snapshot
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inferredcites →https://doi.org/10.1007/bf02181949openalex-snapshot
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inferredcites →https://doi.org/10.1007/s00248-017-0983-1openalex-snapshot
Common and Species-Specific Effects of Phosphate on Marine Microalgae Fatty Acids Shape Their Function in Phytoplankton Trophic Ecology
inferredcites →https://doi.org/10.1007/s00253-011-3170-1openalex-snapshot
The effect of light, salinity, and nitrogen availability on lipid production by Nannochloropsis sp.
inferredcites →https://doi.org/10.1007/s00253-012-4570-6openalex-snapshot
Carotenoid and lipid production by the autotrophic microalga Chlorella protothecoides under nutritional, salinity, and luminosity stress conditions
inferredcites →https://doi.org/10.1007/s00253-013-4749-5openalex-snapshot
Screening and characterization of Isochrysis strains and optimization of culture conditions for docosahexaenoic acid production
inferredcites →https://doi.org/10.1007/s00253-013-5092-6openalex-snapshot
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inferredcites →https://doi.org/10.1007/s00284-019-01860-zopenalex-snapshot
Effect of Salinity Stress on Lipid Accumulation in Scenedesmus sp. and Chlorella sp.: Feasibility of Stepwise Culturing
inferredcites →https://doi.org/10.1007/s00449-013-0919-1openalex-snapshot
Biomass, lipid content, and fatty acid composition of freshwater Chlamydomonas mexicana and Scenedesmus obliquus grown under salt stress
inferredcites →https://doi.org/10.1007/s00449-018-1935-yopenalex-snapshot
Combined production of fucoxanthin and EPA from two diatom strains Phaeodactylum tricornutum and Cylindrotheca fusiformis cultures
inferredcites →https://doi.org/10.1007/s00449-020-02293-wopenalex-snapshot
Enhanced lipid productivity of Chlamydomonas reinhardtii with combination of NaCl and CaCl2 stresses
inferredcites →https://doi.org/10.1007/s00792-003-0360-5openalex-snapshot
Salt-induced changes in lipid composition and membrane fluidity of halophilic yeast-like melanized fungi
inferredcites →https://doi.org/10.1007/s00792-009-0275-xopenalex-snapshot
Molecular cloning and stress-dependent expression of a gene encoding Δ12-fatty acid desaturase in the Antarctic microalga Chlorella vulgaris NJ-7
inferredcites →https://doi.org/10.1007/s10126-010-9309-8openalex-snapshot
A Novel Omega-3 Fatty Acid Desaturase Involved in Acclimation Processes of Polar Condition from Antarctic Ice Algae Chlamydomonas sp. ICE-L
inferredcites →https://doi.org/10.1007/s10265-004-0183-1openalex-snapshot
Roles of the acidic lipids sulfoquinovosyl diacylglycerol and phosphatidylglycerol in photosynthesis: their specificity and evolution
inferredcites →https://doi.org/10.1007/s10529-006-9026-6openalex-snapshot
Response of Growth and Fatty Acid Compositions of Nannochloropsis sp. to Environmental Factors Under Elevated CO2 Concentration
inferredcites →https://doi.org/10.1007/s10535-012-0144-9openalex-snapshot
Plasma membrane permeability as an indicator of salt tolerance in plants
inferredcites →https://doi.org/10.1007/s10750-005-0982-yopenalex-snapshot
Physiological and Optical Responses of the Harmful Dinoflagellate Heterocapsa circularisquama to a Range of Salinity
inferredcites →https://doi.org/10.1007/s10811-010-9532-8openalex-snapshot
Effect of salinity on the biochemical composition of the alga Botryococcus braunii Kütz IPPAS H-252
inferredcites →https://doi.org/10.1007/s10811-011-9732-xopenalex-snapshot
Environmental controls on growth and lipid content for the freshwater diatom, Fragilaria capucina: A candidate for biofuel production
inferredcites →https://doi.org/10.1007/s10811-012-9956-4openalex-snapshot
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inferredcites →https://doi.org/10.1007/s10811-013-0060-1openalex-snapshot
Physiological response of Nannochloropsis sp. to saline stress in laboratory batch cultures
inferredcites →https://doi.org/10.1007/s10811-013-0156-7openalex-snapshot
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inferredcites →https://doi.org/10.1007/s10811-015-0560-2openalex-snapshot
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inferredcites →https://doi.org/10.1007/s10811-015-0666-6openalex-snapshot
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inferredcites →https://doi.org/10.1007/s10811-017-1377-yopenalex-snapshot
The effect of gradual increase in salinity on the biomass productivity and biochemical composition of several marine, halotolerant, and halophilic microalgae
inferredcites →https://doi.org/10.1007/s10811-018-1619-7openalex-snapshot
Effects of salinity changes on growth, photosynthetic activity, biochemical composition, and lipid productivity of marine microalga Tetraselmis suecica
inferredcites →https://doi.org/10.1007/s10811-018-1718-5openalex-snapshot
Co-cultivation and stepwise cultivation of Chaetoceros muelleri and Amphora sp. for fucoxanthin production under gradual salinity increase
inferredcites →https://doi.org/10.1007/s10811-020-02258-2openalex-snapshot
Lipid dynamics and nutritional value of the estuarine strain Isochrysis galbana VLP grown from hypo to hyper salinity
inferredcites →https://doi.org/10.1007/s10811-020-02273-3openalex-snapshot
Photosynthetic pigment production and metabolic and lipidomic alterations in the marine cyanobacteria Synechocystis sp. PCC 7338 under various salinity conditions
inferredcites →https://doi.org/10.1007/s10973-010-1247-1openalex-snapshot
Influence of pH shift and salting on the energetics of microalgae Chlorella vulgaris and Dunaliella maritima
inferredcites →https://doi.org/10.1007/s11120-008-9334-xopenalex-snapshot
Salt stress inhibits photosystems II and I in cyanobacteria
inferredcites →https://doi.org/10.1007/s11120-011-9633-5openalex-snapshot
Molecular dynamics of the diatom thylakoid membrane under different light conditions
inferredcites →https://doi.org/10.1007/s11240-014-0655-5openalex-snapshot
Salinity-dependent changes in growth and fatty acid composition of new Arctic Chlamydomonas species, ArM0029A
inferredcites →https://doi.org/10.1007/s11274-008-9879-zopenalex-snapshot
NaCl induced metabolic changes in the diazotrophic cyanobacterium Anabaena cylindrica
inferredcites →https://doi.org/10.1007/s11356-017-8875-yopenalex-snapshot
Effect of salinity stress on growth, lipid productivity, fatty acid composition, and biodiesel properties in Acutodesmus obliquus and Chlorella vulgaris
inferredcites →https://doi.org/10.1007/s11738-013-1477-5openalex-snapshot
Salt-induced photoinhibition of PSII is alleviated in halophyte Thellungiella halophila by increases of unsaturated fatty acids in membrane lipids
inferredcites →https://doi.org/10.1007/s11814-015-0089-8openalex-snapshot
Enhancement of lipid production in marine microalga Tetraselmis sp. through salinity variation
inferredcites →https://doi.org/10.1007/s12155-013-9360-1openalex-snapshot
Transcriptome and Gene Expression Analysis of an Oleaginous Diatom Under Different Salinity Conditions
inferredcites →https://doi.org/10.1007/s12155-019-10077-8openalex-snapshot
Synergistic Effect of Nutrient and Salt Stress on Lipid Productivity of Chlorella vulgaris Through Two-Stage Cultivation
inferredcites →https://doi.org/10.1007/s12229-015-9156-4openalex-snapshot
Role of the Plasma Membrane in Saline Conditions: Lipids and Proteins
inferredcites →https://doi.org/10.1007/s12237-019-00629-8openalex-snapshot
Fatty Acids to Quantify Phytoplankton Functional Groups and Their Spatiotemporal Dynamics in a Highly Turbid Estuary
inferredcites →https://doi.org/10.1007/s12257-019-0432-8openalex-snapshot
Comparative Primary Metabolic and Lipidomic Profiling of Freshwater and Marine Synechocystis Strains Using by GC-MS and NanoESI-MS Analyses
inferredcites →https://doi.org/10.1007/s12275-018-7488-6openalex-snapshot
Application of high-salinity stress for enhancing the lipid productivity of Chlorella sorokiniana HS1 in a two-phase process
inferredcites →https://doi.org/10.1007/s12601-010-0001-8openalex-snapshot
The effect of decrease in salinity on the dynamics of abundance and the cell size of Corethron Hystrix (Bacillariophyta) in laboratory culture
inferredcites →https://doi.org/10.1007/s13131-012-0183-2openalex-snapshot
Acclimatory responses to high-salt stress in Chlamydomonas (Chlorophyta, Chlorophyceae) from Antarctica
inferredcites →https://doi.org/10.1007/s13131-019-1354-1openalex-snapshot
Identification and characterization of a delta-12 fatty acid desaturase gene from marine microalgae Isochrysis galbana
inferredcites →https://doi.org/10.1007/s13213-013-0645-6openalex-snapshot
Effects of photoperiod, salinity and pH on cell growth and lipid content of Pavlova lutheri
inferredcites →https://doi.org/10.1007/s13762-018-1720-0openalex-snapshot
Salinity-induced oxidative stress-mediated change in fatty acids composition of cyanobacterium Synechococcus sp. PCC7942
inferredcites →https://doi.org/10.1016/0003-9861(90)90577-lopenalex-snapshot
Membrane lipid composition, fluidity, and surface charge changes in response to growth of the fresh water cyanobacterium Synechococcus 6311 under high salinity
inferredcites →https://doi.org/10.1016/0163-7827(95)00009-7openalex-snapshot
Betaine ether-linked glycerolipids: Chemistry and biology
inferredcites →https://doi.org/10.1016/j.algal.2015.05.013openalex-snapshot
Pavlova lutheri is a high-level producer of phytosterols
inferredcites →https://doi.org/10.1016/j.algal.2017.03.027openalex-snapshot
Evaluating Marinichlorella kaistiae KAS603 cell size variation, growth and TAG accumulation resulting from rapid adaptation to highly diverse trophic and salinity cultivation regimes
inferredcites →https://doi.org/10.1016/j.algal.2018.12.003openalex-snapshot
Elucidating the unique physiological responses of halotolerant Scenedesmus sp. cultivated in sea water for biofuel production
inferredcites →https://doi.org/10.1016/j.aquaculture.2005.02.051openalex-snapshot
Growth and biochemical composition of the diatom Chaetoceros cf. wighamii brightwell under different temperature, salinity and carbon dioxide levels. I. Protein, carbohydrates and lipids
inferredcites →https://doi.org/10.1016/j.aquaculture.2005.09.011openalex-snapshot
New microalgae for the Pacific oyster Crassostrea gigas larvae
inferredcites →https://doi.org/10.1016/j.bbalip.2016.02.008openalex-snapshot
Stress-induced neutral lipid biosynthesis in microalgae — Molecular, cellular and physiological insights
inferredcites →https://doi.org/10.1016/j.biombioe.2013.03.026openalex-snapshot
Effects of salinity on growth and lipid accumulation of biofuel microalga Nannochloropsis salina and invading organisms
inferredcites →https://doi.org/10.1016/j.biombioe.2015.12.026openalex-snapshot
Chlorella sorokiniana HS1, a novel freshwater green algal strain, grows and hyperaccumulates lipid droplets in seawater salinity
inferredcites →https://doi.org/10.1016/j.biortech.2006.02.007openalex-snapshot
Effect of salinity on growth of green alga Botryococcus braunii and its constituents
inferredcites →https://doi.org/10.1016/j.biortech.2009.12.139openalex-snapshot
Phytosterols from Dunaliella tertiolecta and Dunaliella salina: A potentially novel industrial application
inferredcites →https://doi.org/10.1016/j.biortech.2011.01.089openalex-snapshot
Bioprospecting for oil producing microalgal strains: Evaluation of oil and biomass production for ten microalgal strains
inferredcites →https://doi.org/10.1016/j.biortech.2011.07.025openalex-snapshot
Effect of light, nutrient, cultivation time and salinity on lipid production of newly isolated strain of the green microalga, Botryococcus braunii KMITL 2
inferredcites →https://doi.org/10.1016/j.biortech.2013.06.112openalex-snapshot
Photoautotrophic outdoor two-stage cultivation for oleaginous microalgae Scenedesmus obtusus XJ-15
inferredcites →https://doi.org/10.1016/j.biortech.2013.09.027openalex-snapshot
Expression of fatty acid desaturase genes and fatty acid accumulation in Chlamydomonas sp. ICE-L under salt stress
inferredcites →https://doi.org/10.1016/j.biortech.2013.10.084openalex-snapshot
Significance evaluation of the effects of environmental factors on the lipid accumulation of Chlorella minutissima UTEX 2341 under low-nutrition heterotrophic condition
inferredcites →https://doi.org/10.1016/j.biortech.2014.03.063openalex-snapshot
NaCl as an effective inducer for lipid accumulation in freshwater microalgae Desmodesmus abundans
inferredcites →https://doi.org/10.1016/j.biortech.2014.08.066openalex-snapshot
Rapid neutral lipid accumulation of the alkali-resistant oleaginous Monoraphidium dybowskii LB50 by NaCl induction
inferredcites →https://doi.org/10.1016/j.biortech.2014.10.140openalex-snapshot
Water use and its recycling in microalgae cultivation for biofuel application
inferredcites →https://doi.org/10.1016/j.biortech.2015.04.017openalex-snapshot
Salinity induced oxidative stress enhanced biofuel production potential of microalgae Scenedesmus sp. CCNM 1077
inferredcites →https://doi.org/10.1016/j.biortech.2016.07.022openalex-snapshot
Salinity stress increases lipid, secondary metabolites and enzyme activity in Amphora subtropica and Dunaliella sp. for biodiesel production
inferredcites →https://doi.org/10.1016/j.biortech.2017.03.175openalex-snapshot
Salinity induced lipid production in microalgae and cluster analysis (ICCB 16-BR_047)
inferredcites →https://doi.org/10.1016/j.biortech.2017.05.003openalex-snapshot
Salinity induced oxidative stress alters the physiological responses and improves the biofuel potential of green microalgae Acutodesmus dimorphus
inferredcites →https://doi.org/10.1016/j.biortech.2017.06.035openalex-snapshot
Evolutionary engineering of salt-resistant Chlamydomonas sp. strains reveals salinity stress-activated starch-to-lipid biosynthesis switching
inferredcites →https://doi.org/10.1016/j.biortech.2017.06.081openalex-snapshot
Effect of salt type and concentration on the growth and lipid content of Chlorella vulgaris in synthetic saline wastewater for biofuel production
inferredcites →https://doi.org/10.1016/j.biortech.2017.11.067openalex-snapshot
Salinity-induced cellular cross-talk in carbon partitioning reveals starch-to-lipid biosynthesis switching in low-starch freshwater algae
inferredcites →https://doi.org/10.1016/j.biortech.2018.01.062openalex-snapshot
Temporal acclimation of Microchloropsis gaditana CCMP526 in response to hypersalinity
inferredcites →https://doi.org/10.1016/j.biortech.2018.09.065openalex-snapshot
Sodium chloride incites reactive oxygen species in green algae Chlorococcum humicola and Chlorella vulgaris: Implication on lipid synthesis, mineral nutrients and antioxidant system
inferredcites →https://doi.org/10.1016/j.copbio.2012.08.008openalex-snapshot
Lipid metabolism in microalgae distinguishes itself
inferredcites →https://doi.org/10.1016/j.ejar.2016.10.006openalex-snapshot
Induction of the synthesis of bioactive compounds of the marine alga Tetraselmis tetrathele (West) Butcher grown under salinity stress
inferredcites →https://doi.org/10.1016/j.envexpbot.2004.01.009openalex-snapshot
Cellular basis of salinity tolerance in plants
inferredcites →https://doi.org/10.1016/j.enzmictec.2005.05.014openalex-snapshot
Metabolic relationships between macro- and micronutrients, and the eicosapentaenoic acid and docosahexaenoic acid contents of Pavlova lutheri
inferredcites →https://doi.org/10.1016/j.esd.2011.07.010openalex-snapshot
Indigenous algae for local bioresource production: Phycoprospecting
inferredcites →https://doi.org/10.1016/j.hal.2007.09.002openalex-snapshot
Effect of salinity, temperature, organic and inorganic nutrients on growth of cultured Fibrocapsa japonica (Raphidophyceae) from the northern Adriatic Sea
inferredcites →https://doi.org/10.1016/j.heliyon.2019.e01553openalex-snapshot
Growth performance, biochemical composition and sedimentation velocity of Tetraselmis sp. CTP4 under different salinities using low-cost lab- and pilot-scale systems
inferredcites →https://doi.org/10.1016/j.jbiosc.2017.04.009openalex-snapshot
Acclimation to NaCl and light stress of heterotrophic Chlamydomonas reinhardtii for lipid accumulation
inferredcites →https://doi.org/10.1016/j.jbiotec.2016.04.025openalex-snapshot
Salt stress induced lipid accumulation in heterotrophic culture cells of Chlorella protothecoides : Mechanisms based on the multi-level analysis of oxidative response, key enzyme activity and biochemical alteration
inferredcites →https://doi.org/10.1016/j.jbiotec.2016.11.029openalex-snapshot
Biomass and oil production by Chlorella vulgaris and four other microalgae — Effects of salinity and other factors
inferredcites →https://doi.org/10.1016/j.jbiotec.2021.03.001openalex-snapshot
Effect of salt stress on physiological parameters of microalgae Vischeria punctata strain IPPAS H-242, a superproducer of eicosapentaenoic acid
inferredcites →https://doi.org/10.1016/j.jphotobiol.2013.04.007openalex-snapshot
Alteration of photochemistry and protein degradation of photosystem II from Chlamydomonas reinhardtii under high salt grown cells
inferredcites →https://doi.org/10.1016/j.jplph.2004.11.010openalex-snapshot
Changes in content and fatty acid profiles of total lipids and sulfolipids in the halophyte Crithmum maritimum under salt stress
inferredcites →https://doi.org/10.1016/j.phytochem.2004.06.021openalex-snapshot
Salt-induced lipid changes in Catharanthus roseus cultured cell suspensions
inferredcites →https://doi.org/10.1016/j.phytochem.2013.07.024openalex-snapshot
Differences in betaine lipids and fatty acids between Pseudoisochrysis paradoxa VLP and Diacronema vlkianum VLP isolates (Haptophyta)
inferredcites →https://doi.org/10.1016/j.phytochem.2016.02.007openalex-snapshot
Exploring occurrence and molecular diversity of betaine lipids across taxonomy of marine microalgae
inferredcites →https://doi.org/10.1016/j.phytochem.2016.12.014openalex-snapshot
Acclimation to salt modifies the activation of several osmotic stress-activated lipid signalling pathways in Chlamydomonas
inferredcites →https://doi.org/10.1016/j.plipres.2017.06.002openalex-snapshot
Emerging roles for conjugated sterols in plants
inferredcites →https://doi.org/10.1016/j.plipres.2019.01.003openalex-snapshot
The lipid biochemistry of eukaryotic algae
inferredcites →https://doi.org/10.1016/j.procbio.2006.08.002openalex-snapshot
Changes of lipid content and fatty acid composition of Schizochytrium limacinum in response to different temperatures and salinities
inferredcites →https://doi.org/10.1016/j.procbio.2012.04.011openalex-snapshot
Regulation of lipid metabolism in the snow alga Chlamydomonas nivalis in response to NaCl stress: An integrated analysis by cytomic and lipidomic approaches
inferredcites →https://doi.org/10.1016/j.renene.2015.02.002openalex-snapshot
Cultivation of four microalgae for biomass and oil production using a two-stage culture strategy with salt stress
inferredcites →https://doi.org/10.1016/j.rser.2019.109621openalex-snapshot
Two-stage cultivation strategy for simultaneous increases in growth rate and lipid content of microalgae: A review
inferredcites →https://doi.org/10.1016/j.sjbs.2020.07.027openalex-snapshot
Combined effect of salinity and pH on lipid content and fatty acid composition of Tisochrysis lutea
inferredcites →https://doi.org/10.1016/j.tca.2007.03.003openalex-snapshot
The effect of changes in salinity on the energy yielding processes of Chlorella vulgaris and Dunaliella maritima cells
inferredcites →https://doi.org/10.1016/s0031-9422(96)00868-0openalex-snapshot
Effect of salinity on fatty acid composition of a green microalga from an antarctic hypersaline lake
inferredcites →https://doi.org/10.1016/s1369-5274(02)00306-5openalex-snapshot
Regulation of the desaturation of fatty acids and its role in tolerance to cold and salt stress
inferredcites →https://doi.org/10.1021/acs.iecr.7b00841openalex-snapshot
Insights into the Enhanced Lipid Production Characteristics of a Fresh Water Microalga under High Salinity Conditions
inferredcites →https://doi.org/10.1021/acs.jafc.7b00552openalex-snapshot
Effects of Salt Concentrations and Nitrogen and Phosphorus Starvations on Neutral Lipid Contents in the Green Microalga Dunaliella tertiolecta
inferredcites →https://doi.org/10.1021/jp0750708openalex-snapshot
Effect of NaCl and KCl on Phosphatidylcholine and Phosphatidylethanolamine Lipid Membranes: Insight from Atomic-Scale Simulations for Understanding Salt-Induced Effects in the Plasma Membrane
inferredcites →https://doi.org/10.1023/a:1007128315049openalex-snapshot
Plant Lipid Biosynthesis. Fundamentals and Agricultural Applications
inferredcites →https://doi.org/10.1038/s41598-017-07540-xopenalex-snapshot
Bioenergy application of Dunaliella salina SA 134 grown at various salinity levels for lipid production
inferredcites →https://doi.org/10.1038/s41598-018-23340-3openalex-snapshot
Scale-up and large-scale production of Tetraselmis sp. CTP4 (Chlorophyta) for CO2 mitigation: from an agar plate to 100-m3 industrial photobioreactors
inferredcites →https://doi.org/10.1038/s41598-020-79950-3openalex-snapshot
Lipid accumulation patterns and role of different fatty acid types towards mitigating salinity fluctuations in Chlorella vulgaris
inferredcites →https://doi.org/10.1038/sj.jim.2900759openalex-snapshot
Effects of salinity on cell growth and docosahexaenoic acid content of the heterotrophic marine microalga Crypthecodinium cohnii
inferredcites →https://doi.org/10.1038/srep25825openalex-snapshot
Hyperosmosis and its combination with nutrient-limitation are novel environmental stressors for induction of triacylglycerol accumulation in cells of Chlorella kessleri
inferredcites →https://doi.org/10.1038/srep45471openalex-snapshot
Dynamic metabolic profiling together with transcription analysis reveals salinity-induced starch-to-lipid biosynthesis in alga Chlamydomonas sp. JSC4
inferredcites →https://doi.org/10.1039/c6ra23933aopenalex-snapshot
An integrated salinity-driven workflow for rapid lipid enhancement in green microalgae for biodiesel application
inferredcites →https://doi.org/10.1046/j.1432-1033.2002.02896.xopenalex-snapshot
Role of sulfoquinovosyl diacylglycerol for the maintenance of photosystem II in Chlamydomonas reinhardtii
inferredcites →https://doi.org/10.1046/j.1440-1835.2001.00227.xopenalex-snapshot
Effects of sodium chloride on the fatty acids composition in Boekelovia hooglandii (Ochromonadales, Chrysophyceae)
inferredcites →https://doi.org/10.1073/pnas.94.10.4872openalex-snapshot
Redesign of soluble fatty acid desaturases from plants for altered substrate specificity and double bond position
inferredcites →https://doi.org/10.1074/jbc.r700042200openalex-snapshot
Intracellular Organic Osmolytes: Function and Regulation
inferredcites →https://doi.org/10.1080/01490451.2011.581331openalex-snapshot
The Physiological Response ofSynechococcus elongatusto Salinity: A Potential Biomarker for Ancient Salinity in Evaporative Environments
inferredcites →https://doi.org/10.1080/09593330.2013.812668openalex-snapshot
Effects of calcium, magnesium and sodium chloride in enhancing lipid accumulation in two green microalgae
inferredcites →https://doi.org/10.1080/09593330.2013.871350openalex-snapshot
The effects of salinity on the growth and biochemical properties ofChlamydomonas mexicanaGU732420 cultivated in municipal wastewater
inferredcites →https://doi.org/10.1080/09670262.2019.1637547openalex-snapshot
Hyperosmotic stress in Chlamydomonas induces metabolomic changes in biosynthesis of complex lipids
inferredcites →https://doi.org/10.1080/15435075.2020.1727480openalex-snapshot
Assessment of different carbon and salinity level on growth kinetics, lipid, and starch composition of Chlorella vulgaris SAG 211-12
inferredcites →https://doi.org/10.1093/femsre/fuy009openalex-snapshot
Strategies of adaptation of microorganisms of the three domains of life to high salt concentrations
inferredcites →https://doi.org/10.1093/jxb/ern348openalex-snapshot
Salt stress-induced cell death in the unicellular green alga Micrasterias denticulata
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a078271openalex-snapshot
Betaine Lipids in Lower Plants. Biosynthesis of DGTS and DGTA in Ochromonas danica (Chrysophyceae) and the Possible Role of DGTS in Lipid Metabolism
inferredcites →https://doi.org/10.1093/pcp/pcu015openalex-snapshot
Ca2+ Signal Transduction Related to Neutral Lipid Synthesis in an Oil-Producing Green Alga Chlorella sp. C2
inferredcites →https://doi.org/10.1093/plankt/fbw034openalex-snapshot
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inferredcites →https://doi.org/10.1093/plankt/fbx064openalex-snapshot
Effects of salinity on cellular growth and exopolysaccharide production of freshwater Synechococcus strain CCAP1405
inferredcites →https://doi.org/10.1099/00221287-133-9-2607openalex-snapshot
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inferredcites →https://doi.org/10.1099/00221287-144-6-1557openalex-snapshot
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inferredcites →https://doi.org/10.1099/mic.0.2007/009563-0openalex-snapshot
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inferredcites →https://doi.org/10.1104/pp.001909openalex-snapshot
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inferredcites →https://doi.org/10.1104/pp.125.4.1842openalex-snapshot
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inferredcites →https://doi.org/10.1104/pp.19.00666openalex-snapshot
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inferredcites →https://doi.org/10.1104/pp.89.3.970openalex-snapshot
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inferredcites →https://doi.org/10.1104/pp.94.4.1512openalex-snapshot
Changes in Membrane Lipid Composition during Saline Growth of the Fresh Water Cyanobacterium Synechococcus 6311
inferredcites →https://doi.org/10.1111/j.0022-3646.1985.00072.xopenalex-snapshot
CHEMICAL PROFILE OF SELECTED SPECIES OF MICROALGAE WITH EMPHASIS ON LIPIDS1
inferredcites →https://doi.org/10.1111/j.1365-2109.2009.02423.xopenalex-snapshot
Effects of salinity on the growth and proximate composition of selected tropical marine periphytic diatoms and cyanobacteria
inferredcites →https://doi.org/10.1111/j.1529-8817.2008.00565.xopenalex-snapshot
SALT‐INDUCED ALTERATIONS IN LIPID COMPOSITION OF DIATOM NITZSCHIA LAEVIS (BACILLARIOPHYCEAE) UNDER HETEROTROPHIC CULTURE CONDITION1
inferredcites →https://doi.org/10.1111/j.1574-6976.2010.00234.xopenalex-snapshot
Molecular biology of cyanobacterial salt acclimation
inferredcites →https://doi.org/10.1111/jpy.12300openalex-snapshot
Indirect and direct effects of salinity on the quantity and quality of total amino acids in Ulva ohnoi (Chlorophyta)
inferredcites →https://doi.org/10.1111/jpy.12547openalex-snapshot
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inferredcites →https://doi.org/10.1111/jpy.12929openalex-snapshot
Acclimation of the Marine Diatom Pseudo‐nitzschia australis to Different Salinity Conditions: Effects on Growth, Photosynthetic Activity, and Domoic Acid Content1
inferredcites →https://doi.org/10.1111/jpy.12995openalex-snapshot
Carbon Partitioning and Lipid Remodeling During Phosphorus and Nitrogen Starvation in the Marine Microalga Diacronema lutheri (Haptophyta)
inferredcites →https://doi.org/10.1111/nph.14179openalex-snapshot
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inferredcites →https://doi.org/10.1111/raq.12244openalex-snapshot
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inferredcites →https://doi.org/10.1146/annurev.arplant.41.1.21openalex-snapshot
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inferredcites →https://doi.org/10.1186/1475-2859-13-3openalex-snapshot
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inferredcites →https://doi.org/10.1186/s12864-020-6507-2openalex-snapshot
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inferredcites →https://doi.org/10.1186/s13068-020-01714-yopenalex-snapshot
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inferredcites →https://doi.org/10.1201/b19464openalex-snapshot
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inferredcites →https://doi.org/10.1285/i1825229xv2n1p31openalex-snapshot
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inferredcites →https://doi.org/10.1557/jmr.2006.0333openalex-snapshot
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inferredcites →https://doi.org/10.3923/pjbs.2007.2286.2291openalex-snapshot
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