On the public citation graph

A new class of plant lipid is essential for protection against phosphorus depletion

0 signed · 300 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.
Claim with ORCID
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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/978-1-4020-6863-8_10openalex-snapshot
Sulfolipid Biosynthesis and Function in Plants
inferredcites →https://doi.org/10.1007/bf00333575openalex-snapshot
Auxin-resistant mutants of Arabidopsis thaliana with an altered morphology
inferredcites →https://doi.org/10.1007/s004250050375openalex-snapshot
Uridine-diphospho-sulfoquinovose: diacylglycerol sulfoquinovosyltransferase activity is concentrated in the inner membrane of chloroplast envelopes
inferredcites →https://doi.org/10.1007/s11103-009-9589-4openalex-snapshot
Involvement of auxin signaling mediated by IAA14 and ARF7/19 in membrane lipid remodeling during phosphate starvation
inferredcites →https://doi.org/10.1007/s11120-007-9195-8openalex-snapshot
Chloroplast envelope membranes: a dynamic interface between plastids and the cytosol
inferredcites →https://doi.org/10.1007/s11306-011-0318-zopenalex-snapshot
Plant lipidomics based on hydrophilic interaction chromatography coupled to ion trap time-of-flight mass spectrometry
inferredcites →https://doi.org/10.1016/0005-2760(68)90141-0openalex-snapshot
Glycosyl diglycerides from Pseudomonas rubescens
inferredcites →https://doi.org/10.1016/0005-2760(69)90046-0openalex-snapshot
Lipids of Pseudomonas diminuta
inferredcites →https://doi.org/10.1016/0076-6879(66)08014-5openalex-snapshot
[10] Assay of inorganic phosphate, total phosphate and phosphatases
inferredcites →https://doi.org/10.1016/j.carres.2009.07.012openalex-snapshot
Characterization of glucuronic acid containing glycolipid in Aspergillus fumigatus mycelium
inferredcites →https://doi.org/10.1016/j.chemosphere.2011.02.032openalex-snapshot
Towards global phosphorus security: A systems framework for phosphorus recovery and reuse options
inferredcites →https://doi.org/10.1016/j.plipres.2007.05.001openalex-snapshot
Structure and function of glycoglycerolipids in plants and bacteria
inferredcites →https://doi.org/10.1016/j.plipres.2011.02.003openalex-snapshot
Biosynthesis and functions of the plant sulfolipid
inferredcites →https://doi.org/10.1016/s0005-2760(97)00060-xopenalex-snapshot
Unusual lipid composition of the gram-negative, freshwater, stalked bacterium Caulobacter bacteroides NP-105
inferredcites →https://doi.org/10.1016/s0014-5793(03)00109-1openalex-snapshot
Phosphate‐deficient oat replaces a major portion of the plasma membrane phospholipids with the galactolipid digalactosyldiacylglycerol
inferredcites →https://doi.org/10.1016/s0031-9422(00)89069-xopenalex-snapshot
The sugar components of the galactosyl diglycerides from green plants
inferredcites →https://doi.org/10.1016/s0031-9422(97)00201-xopenalex-snapshot
Lipids of Pavlova lutheri: Cellular site and metabolic role of DGCC
inferredcites →https://doi.org/10.1016/s0176-1617(11)81186-7openalex-snapshot
Diacylglyceryl-α-D-glucuronide from Ochromonas danica (Chrysophyceae)
inferredcites →https://doi.org/10.1016/s1369-5266(00)00062-5openalex-snapshot
Phosphate transport and signaling
inferredcites →https://doi.org/10.1016/s1369-5266(00)80063-1openalex-snapshot
Phosphate transport and signaling
inferredcites →https://doi.org/10.1021/ac0713510openalex-snapshot
Visualization of GC/TOF-MS-Based Metabolomics Data for Identification of Biochemically Interesting Compounds Using OPLS Class Models
inferredcites →https://doi.org/10.1038/249268a0openalex-snapshot
Replacement of acidic phospholipids by acidic glycolipids in Pseudomonas diminuta
inferredcites →https://doi.org/10.1038/461716aopenalex-snapshot
Environment: The disappearing nutrient
inferredcites →https://doi.org/10.1042/bj2350025openalex-snapshot
Fluxes through the prokaryotic and eukaryotic pathways of lipid synthesis in the ‘16:3’ plant Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01918.xopenalex-snapshot
Anionic lipids are required for chloroplast structure and function in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0600863103openalex-snapshot
Phospholipase DZ2 plays an important role in extraplastidic galactolipid biosynthesis and phosphate recycling in Arabidopsis roots
inferredcites →https://doi.org/10.1073/pnas.082696499openalex-snapshot
Arabidopsis disrupted in SQD2 encoding sulfolipid synthase is impaired in phosphate-limited growth
inferredcites →https://doi.org/10.1073/pnas.0907173106openalex-snapshot
Arabidopsis lipins mediate eukaryotic pathway of lipid metabolism and cope critically with phosphate starvation
inferredcites →https://doi.org/10.1073/pnas.180320497openalex-snapshot
DGD1-independent biosynthesis of extraplastidic galactolipids after phosphate deprivation in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.181331498openalex-snapshot
Two types of MGDG synthase genes, found widely in both 16:3 and 18:3 plants, differentially mediate galactolipid syntheses in photosynthetic and nonphotosynthetic tissues in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.90.4.1561openalex-snapshot
The sulfolipid sulfoquinovosyldiacylglycerol is not required for photosynthetic electron transport in Rhodobacter sphaeroides but enhances growth under phosphate limitation.
inferredcites →https://doi.org/10.1073/pnas.95.4.1950openalex-snapshot
Phosphate availability affects the thylakoid lipid composition and the expression of SQD1 , a gene required for sulfolipid biosynthesis in Arabidopsis thaliana
inferredcites →https://doi.org/10.1074/jbc.271.13.7501openalex-snapshot
A Null Mutant of Synechococcus sp. PCC7942 Deficient in the Sulfolipid Sulfoquinovosyl Diacylglycerol
inferredcites →https://doi.org/10.1074/jbc.m008200200openalex-snapshot
Recombinant Arabidopsis SQD1 Converts UDP-glucose and Sulfite to the Sulfolipid Head Group Precursor UDP-sulfoquinovose in Vitro
inferredcites →https://doi.org/10.1074/jbc.m110066200openalex-snapshot
DGD2, an Arabidopsis Gene Encoding a UDP-Galactose-dependent Digalactosyldiacylglycerol Synthase Is Expressed during Growth under Phosphate-limiting Conditions
inferredcites →https://doi.org/10.1074/jbc.m408799200openalex-snapshot
A Novel Phosphatidylcholine-hydrolyzing Phospholipase C Induced by Phosphate Starvation in Arabidopsis
inferredcites →https://doi.org/10.1074/jbc.m503273200openalex-snapshot
Phosphate-limited Oat
inferredcites →https://doi.org/10.1074/jbc.r400032200openalex-snapshot
Three Enzyme Systems for Galactoglycerolipid Biosynthesis Are Coordinately Regulated in Plants
inferredcites →https://doi.org/10.1083/jcb.200407022openalex-snapshot
Phosphate deprivation induces transfer of DGDG galactolipid from chloroplast to mitochondria
inferredcites →https://doi.org/10.1099/00221287-54-2-195openalex-snapshot
Studies on the Cell Walls of Pseudomonas Species Resistant to Ethylenediaminetetra-acetic Acid
inferredcites →https://doi.org/10.1104/pp.002725openalex-snapshot
The pgp1 Mutant Locus of Arabidopsis Encodes a Phosphatidylglycerolphosphate Synthase with Impaired Activity
inferredcites →https://doi.org/10.1104/pp.010331openalex-snapshot
Symbiotic Nitrogen Fixation and Phosphorus Acquisition. Plant Nutrition in a World of Declining Renewable Resources
inferredcites →https://doi.org/10.1104/pp.106.079707openalex-snapshot
PHO2, MicroRNA399, and PHR1 Define a Phosphate-Signaling Pathway in Plants
inferredcites →https://doi.org/10.1104/pp.106.085647openalex-snapshot
Quantitative Profiling of Arabidopsis Polar Glycerolipids in Response to Phosphorus Starvation. Roles of Phospholipases Dζ1 and Dζ2 in Phosphatidylcholine Hydrolysis and Digalactosyldiacylglycerol Accumulation in Phosphorus-Starved Plants
inferredcites →https://doi.org/10.1104/pp.72.2.273openalex-snapshot
Similarities and Differences in Lipid Metabolism of Chloroplasts Isolated from 18:3 and 16:3 Plants
inferredcites →https://doi.org/10.1105/tpc.108.063925openalex-snapshot
A Chloroplastic UDP-Glucose Pyrophosphorylase from Arabidopsis Is the Committed Enzyme for the First Step of Sulfolipid Biosynthesis
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02778.xopenalex-snapshot
Membrane lipid alteration during phosphate starvation is regulated by phosphate signaling and auxin/cytokinin cross‐talk
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03582.xopenalex-snapshot
Phospholipase C5 (NPC5) is involved in galactolipid accumulation during phosphate limitation in leaves of Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03692.xopenalex-snapshot
Type‐B monogalactosyldiacylglycerol synthases are involved in phosphate starvation‐induced lipid remodeling, and are crucial for low‐phosphate adaptation
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04538.xopenalex-snapshot
Characterization of the Arabidopsis glycerophosphodiester phosphodiesterase (GDPD) family reveals a role of the plastid‐localized AtGDPD1 in maintaining cellular phosphate homeostasis under phosphate starvation
inferredcites →https://doi.org/10.1111/j.1399-3054.1962.tb08052.xopenalex-snapshot
A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures
inferredcites →https://doi.org/10.1111/j.1432-1033.1989.tb15037.xopenalex-snapshot
Synthesis of different nucleoside 5′‐diphospho‐sulfoquinovoses and their use for studies on sulfolipid biosynthesis in chloroplasts
inferredcites →https://doi.org/10.1111/j.1432-1033.1995.016_c.xopenalex-snapshot
Impaired Photosystem II in a Mutant of Chlamydomonas Reinhardtii Defective in Sulfoquinovosyl Diacylglycerol
inferredcites →https://doi.org/10.1111/j.1438-8677.1992.tb00287.xopenalex-snapshot
Enzymatic Characteristics of UDP‐sulfoquinovose: Diacylglycerol Sulfoquinovosyltransferase from Chloroplast Envelopes*
inferredcites →https://doi.org/10.1126/science.1086391openalex-snapshot
Genome-Wide Insertional Mutagenesis of Arabidopsis thaliana
inferredcites →https://doi.org/10.1139/o59-099openalex-snapshot
A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION
inferredcites →https://doi.org/10.1146/annurev-arplant-042110-103921openalex-snapshot
Sulfur Assimilation in Photosynthetic Organisms: Molecular Functions and Regulations of Transporters and Assimilatory Enzymes
inferredcites →https://doi.org/10.1146/annurev.arplant.49.1.53openalex-snapshot
BIOSYNTHESIS AND FUNCTION OF THE SULFOLIPID SULFOQUINOVOSYL DIACYLGLYCEROL
inferredcites →https://doi.org/10.1248/cpb.29.1475openalex-snapshot
New methods and reagents in organic synthesis. 14. A simple efficient preparation of methyl esters with trimethylsilyldiazomethane (TMSCHN2) and its application to gas chromatographic analysis of fatty acids.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4837258openalex-extracted
Genome-Wide Characterization and Expression of the Myb-Cc Gene Family in Salvia Miltiorrhiza Andsmmyb-Cc7-Mediated Response to Phosphate Starvation in Arabidopsis
inferred← citeshttps://doi.org/10.1002/9781118958841.ch3openalex-snapshot
‘Omics’ Approaches Towards Understanding Plant Phosphorus Acquisition and Use
inferred← citeshttps://doi.org/10.1002/9781118958841.ch8openalex-snapshot
Metabolomics of plant phosphorus‐starvation response
inferred← citeshttps://doi.org/10.1002/9781118958841.ch9openalex-snapshot
Membrane remodelling in phosphorus‐deficient plants
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0518openalex-snapshot
‘Omics’ Approaches Towards Understanding Plant Phosphorus Acquisition and Use
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0523openalex-snapshot
Metabolomics of Plant Phosphorus‐Starvation Response
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0524openalex-snapshot
Membrane Remodelling in Phosphorus‐Deficient Plants
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0627openalex-snapshot
Advances of Metabolite Profiling of Plants in Challenging Environments
inferred← citeshttps://doi.org/10.1002/9783527836512.ch22openalex-snapshot
Lipidomics in Plant Science
inferred← citeshttps://doi.org/10.1002/cppb.20109openalex-snapshot
Liquid Chromatography–Mass Spectrometry (LC‐MS)‐Based Analysis for Lipophilic Compound Profiling in Plants
inferred← citeshttps://doi.org/10.1002/pld3.393openalex-snapshot
Sorghum root epigenetic landscape during limiting phosphorus conditions
inferred← citeshttps://doi.org/10.1007/978-1-0716-2716-7_5openalex-snapshot
Mass Spectroscopy as an Analytical Tool to Harness the Production of Secondary Plant Metabolites: The Way Forward for Drug Discovery
inferred← citeshttps://doi.org/10.1007/978-1-0716-4799-8_16openalex-snapshot
Hydroponic Cultivation Systems to Study Nutrient-Dependent Changes in Inositol Polyphosphate Metabolism in Plants
inferred← citeshttps://doi.org/10.1007/978-1-4939-7819-9_11openalex-snapshot
Plant Lipidomics Using UPLC-QTOF-MS
inferred← citeshttps://doi.org/10.1007/978-1-4939-7819-9_12openalex-snapshot
Targeted LC-MS Analysis for Plant Secondary Metabolites
inferred← citeshttps://doi.org/10.1007/978-3-030-37510-2_21openalex-snapshot
Metabolomics for Rice Grain Quality
inferred← citeshttps://doi.org/10.1007/978-3-319-25979-6_2openalex-snapshot
Roles of Lipids in Photosynthesis
inferred← citeshttps://doi.org/10.1007/978-3-319-25979-6_3openalex-snapshot
DGDG and Glycolipids in Plants and Algae
inferred← citeshttps://doi.org/10.1007/978-3-319-55729-8_12openalex-snapshot
Physiological and Molecular Mechanisms and Adaptation Strategies in Soybean (Glycine max) Under Phosphate Deficiency
inferred← citeshttps://doi.org/10.1007/978-3-319-55729-8_6openalex-snapshot
Transport and Metabolism of Nitrogen in Legume Nodules Under Phosphorus Deficiency
inferred← citeshttps://doi.org/10.1007/978-3-319-59192-6_1openalex-snapshot
Phytochemical Genomics of Ashwagandha
inferred← citeshttps://doi.org/10.1007/978-981-15-4120-9_5openalex-snapshot
Improvement of Rice Quality: The New Revolution
inferred← citeshttps://doi.org/10.1007/978-981-16-9037-2_5openalex-snapshot
Lipid Metabolism in Plants Under Low-Temperature Stress: A Review
inferred← citeshttps://doi.org/10.1007/s00122-022-04095-yopenalex-snapshot
Prospects of genetics and breeding for low-phosphate tolerance: an integrated approach from soil to cell
inferred← citeshttps://doi.org/10.1007/s00216-013-6869-2openalex-snapshot
Metabolomics for unknown plant metabolites
inferred← citeshttps://doi.org/10.1007/s00299-014-1719-zopenalex-snapshot
Specific role of phosphatidylglycerol and functional overlaps with other thylakoid lipids in Arabidopsis chloroplast biogenesis
inferred← citeshttps://doi.org/10.1007/s00299-025-03461-6openalex-snapshot
Genome-wide identification of the SmPHR gene family in Salvia miltiorrhiza and SmPHR7-mediated response to phosphate starvation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00425-022-03834-1openalex-snapshot
Remodeling and protecting the membrane system to resist phosphorus deficiency in wild soybean (Glycine soja) seedling leaves
inferred← citeshttps://doi.org/10.1007/s00425-026-04981-5openalex-snapshot
Future perspectives in mass spectrometry of plant lipids
inferred← citeshttps://doi.org/10.1007/s10265-016-0827-yopenalex-snapshot
Role of membrane glycerolipids in photosynthesis, thylakoid biogenesis and chloroplast development
inferred← citeshttps://doi.org/10.1007/s10265-024-01545-0openalex-snapshot
Recent advances in research on phosphate starvation signaling in plants
inferred← citeshttps://doi.org/10.1007/s10265-024-01546-zopenalex-snapshot
Modulation of plant immunity and biotic interactions under phosphate deficiency
inferred← citeshttps://doi.org/10.1007/s10342-020-01289-1openalex-snapshot
Foliar P nutrition of European beech (Fagus sylvatica L.) depends on the season but remains unaffected by co-cultivation with silver fir (Abies alba Mill.)
inferred← citeshttps://doi.org/10.1007/s10646-021-02479-2openalex-snapshot
Changes in the fatty acid composition of pine needle lipids under the aluminum smelter emissions
inferred← citeshttps://doi.org/10.1007/s10725-023-01014-zopenalex-snapshot
NUTCRACKER-overexpressing Arabidopsis thaliana grows better under phosphate starvation
inferred← citeshttps://doi.org/10.1007/s10811-024-03420-wopenalex-snapshot
Unraveling the lipidome of Pavlova gyrans, a natural reservoir of bioactive lipids for biotechnological applications
inferred← citeshttps://doi.org/10.1007/s11103-023-01364-2openalex-snapshot
The regulation of sulfolipids under sulfur starvation
inferred← citeshttps://doi.org/10.1007/s11104-022-05316-5openalex-snapshot
Membrane lipid phosphorus reusing and antioxidant protecting played key roles in wild soybean resistance to phosphorus deficiency compared with cultivated soybean
inferred← citeshttps://doi.org/10.1007/s11104-022-05602-2openalex-snapshot
How do tropical tree species maintain high growth rates on low-phosphorus soils?
inferred← citeshttps://doi.org/10.1007/s11306-018-1446-5openalex-snapshot
Crop metabolomics: from diagnostics to assisted breeding
inferred← citeshttps://doi.org/10.1007/s11306-020-01665-3openalex-snapshot
Environmental lipidomics: understanding the response of organisms and ecosystems to a changing world
inferred← citeshttps://doi.org/10.1007/s11306-026-02525-2openalex-snapshot
Comparative metabolomic profiling reveals salinity tolerance mechanisms in a rice introgression line
inferred← citeshttps://doi.org/10.1007/s12298-022-01255-8openalex-snapshot
Adaptive strategies of plants to conserve internal phosphorus under P deficient condition to improve P utilization efficiency
inferred← citeshttps://doi.org/10.1007/s13562-021-00715-8openalex-snapshot
Phosphorus starvation response dynamics and management in plants for sustainable agriculture
inferred← citeshttps://doi.org/10.1007/s40502-021-00624-xopenalex-snapshot
Phosphate deficiency response and membrane lipid remodeling in plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14823-1openalex-snapshot
Top-Down Metabolomics Approaches: Nitrogen- and Sulfur-Omics by Ultrahigh-Resolution Fourier Transform Ion Cyclotron Resonance-Mass Spectrometry
inferred← citeshttps://doi.org/10.1016/b978-0-12-816451-8.00016-2openalex-snapshot
Role of Mineral Nutrients in Abiotic Stress Tolerance
inferred← citeshttps://doi.org/10.1016/b978-0-323-90631-9.00011-9openalex-snapshot
Lipids produced by microalgae and thraustochytrids
inferred← citeshttps://doi.org/10.1016/b978-0-323-90943-3.00005-5openalex-snapshot
Physiological and molecular strategies of plant adaptationin phosphorus-deficient soils
inferred← citeshttps://doi.org/10.1016/b978-0-443-15313-6.00016-8openalex-snapshot
Phospholipase-mediated regulation of plant's response to nutrient deficiency
inferred← citeshttps://doi.org/10.1016/b978-0-443-16082-0.00014-xopenalex-snapshot
Current understanding and interface between micro- and macronutrients in the plant–soil system: an overview
inferred← citeshttps://doi.org/10.1016/j.aca.2018.03.062openalex-snapshot
A high-resolution HPLC-QqTOF platform using parallel reaction monitoring for in-depth lipid discovery and rapid profiling
inferred← citeshttps://doi.org/10.1016/j.algal.2022.102756openalex-snapshot
Chrysotila pseudoroscoffensis as a source of high-value polar lipids with antioxidant activity: A lipidomic approach
inferred← citeshttps://doi.org/10.1016/j.bbabio.2013.09.007openalex-snapshot
Glycerolipids in photosynthesis: Composition, synthesis and trafficking
inferred← citeshttps://doi.org/10.1016/j.bbalip.2016.04.015openalex-snapshot
Tangled evolutionary processes with commonality and diversity in plastidial glycolipid synthesis in photosynthetic organisms
inferred← citeshttps://doi.org/10.1016/j.bbalip.2017.04.005openalex-snapshot
Green light for lipid fingerprinting
inferred← citeshttps://doi.org/10.1016/j.bbalip.2019.158522openalex-snapshot
Adaptation of Synechococcus sp. PCC 7942 to phosphate starvation by glycolipid accumulation and membrane lipid remodeling
inferred← citeshttps://doi.org/10.1016/j.bbamem.2022.184037openalex-snapshot
Sulfoquinovosyldiacylglycerol and phosphatidylglycerol bilayers share biophysical properties and are good mutual substitutes in photosynthetic membranes
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.09.094openalex-snapshot
Arabidopsis PECP1 and PS2 are phosphate starvation-inducible phosphocholine phosphatases
inferred← citeshttps://doi.org/10.1016/j.biochi.2016.06.004openalex-snapshot
Using lipidomics for expanding the knowledge on lipid metabolism in plants
inferred← citeshttps://doi.org/10.1016/j.biochi.2026.10.011openalex-snapshot
Sulfoquinovosyldiacylglycerol (SQDG) in Chloroplast-Poor Tissues: What Can Lipidomics Tell Us?
inferred← citeshttps://doi.org/10.1016/j.biortech.2019.122299openalex-snapshot
Highest accumulated microalgal lipids (polar and non-polar) for biodiesel production with advanced wastewater treatment: Role of lipidomics
inferred← citeshttps://doi.org/10.1016/j.carres.2022.108556openalex-snapshot
A comprehensive review on natural occurrence, synthesis and biological activities of glycolipids
inferred← citeshttps://doi.org/10.1016/j.chroma.2015.01.035openalex-snapshot
A fast liquid chromatography-mass Spectrometry methodology for membrane lipid profiling through hydrophilic interaction liquid chromatography
inferred← citeshttps://doi.org/10.1016/j.chroma.2025.466165openalex-snapshot
Evaluation of separation performance and quantification accuracy in lipidomics methods
inferred← citeshttps://doi.org/10.1016/j.coisb.2019.03.005openalex-snapshot
A new era in plant functional genomics
inferred← citeshttps://doi.org/10.1016/j.copbio.2015.10.010openalex-snapshot
Omics data input for metabolic modeling
inferred← citeshttps://doi.org/10.1016/j.copbio.2017.08.012openalex-snapshot
Control of plant phosphate homeostasis by inositol pyrophosphates and the SPX domain
inferred← citeshttps://doi.org/10.1016/j.cpb.2025.100505openalex-snapshot
Integrative multi-omics analysis of rice grown continuously under P-starvation stress unravels Pup1-mediated regulatory complex for resilience to phosphorus deficiency
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2019.03.017openalex-snapshot
Improved photosynthesis and growth of poplar during nitrogen fertilization is accompanied by phosphorus depletion that indicates phosphorus remobilization from older stem tissues
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105653openalex-snapshot
Differences in membrane lipid homeostasis confer contrast tolerance to low phosphorus in two wheat (Triticum aestivum L.) cultivars
inferred← citeshttps://doi.org/10.1016/j.foodchem.2022.132968openalex-snapshot
Portulaca oleracea, a rich source of polar lipids: Chemical profile by LC-ESI/LTQOrbitrap/MS/MS and in vitro preliminary anti-inflammatory activity
inferred← citeshttps://doi.org/10.1016/j.indcrop.2026.123385openalex-snapshot
Phosphate availability shapes source–sink dynamics and nitrogen balance in dual-purpose hemp (Cannabis sativa L.): Insights from physiological and transcriptomic analyses
inferred← citeshttps://doi.org/10.1016/j.indcrop.2026.123865openalex-snapshot
Integrated multi-omics analysis reveals the involvement of glycerolipid and glycerophospholipid metabolism in cotton phosphorus starvation responses
inferred← citeshttps://doi.org/10.1016/j.indcrop.2026.124415openalex-snapshot
Physiological and molecular mechanisms of arbuscular mycorrhizal inoculation and soil-available phosphorus in regulating photosynthesis of alfalfa
inferred← citeshttps://doi.org/10.1016/j.jgg.2024.09.018openalex-snapshot
Phosphorus acquisition, translocation, and redistribution in maize
inferred← citeshttps://doi.org/10.1016/j.molp.2014.11.010openalex-snapshot
Using Metabolomic Approaches to Explore Chemical Diversity in Rice
inferred← citeshttps://doi.org/10.1016/j.molp.2021.12.005openalex-snapshot
Plant adaptation to low phosphorus availability: Core signaling, crosstalks, and applied implications
inferred← citeshttps://doi.org/10.1016/j.orggeochem.2021.104315openalex-snapshot
Targeted and untargeted lipidomic analysis of haptophyte cultures reveals novel and divergent nutrient-stress adaptations
inferred← citeshttps://doi.org/10.1016/j.pbi.2013.04.001openalex-snapshot
Phytochemical genomics — a new trend
inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111636openalex-snapshot
Phosphate deficiency modifies lipid composition and seed oil production in camelina
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113013openalex-snapshot
Seed treatment technologies: Effects on physical, functional, and physiological seed quality
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113187openalex-snapshot
Molecular basis of delayed leaf senescence induced by short-term treatment with low phosphate in rice
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109838openalex-snapshot
Phosphorus and sulphur crosstalk in cereals: Unraveling the molecular interplay, agronomic impacts on yield and heavy metal tolerance
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111116openalex-snapshot
A novel role of the SQDG synthase gene in Eucommia ulmoides SQD2 in drought tolerance: Lipid remodeling, chloroplast protection, and antioxidant regulation in transgenic tobaccos
inferred← citeshttps://doi.org/10.1016/j.plipres.2019.100990openalex-snapshot
Lipidomic studies of membrane glycerolipids in plant leaves under heat stress
inferred← citeshttps://doi.org/10.1016/j.plipres.2023.101266openalex-snapshot
Biosynthesis of phosphatidylglycerol in photosynthetic organisms
inferred← citeshttps://doi.org/10.1016/j.plipres.2024.101290openalex-snapshot
Plant and algal lipidomes: Analysis, composition, and their societal significance
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.161646openalex-snapshot
Mechanistic insights into the selective adsorption of phosphorus from wastewater by MgO(100)-functionalized cellulose sponge
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.06.034openalex-snapshot
Synthesis of polyunsaturated fatty acid-containing glucuronosyl-diacylglycerol through direct glycosylation
inferred← citeshttps://doi.org/10.1016/j.tplants.2019.02.002openalex-snapshot
Catch You on the Flip Side: A Critical Review of Flippase Mutant Phenotypes
inferred← citeshttps://doi.org/10.1017/qpb.2025.1openalex-snapshot
Mobilization and recycling of intracellular phosphorus in response to availability
inferred← citeshttps://doi.org/10.1021/ac502511aopenalex-snapshot
LipidBlast Templates As Flexible Tools for Creating New in-Silico Tandem Mass Spectral Libraries
inferred← citeshttps://doi.org/10.1021/acs.jafc.2c07988openalex-snapshot
Comparative Lipidomics Study of Four Edible Red Seaweeds Based on RPLC–Q-TOF
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c06927openalex-snapshot
Combined Analysis of the Leaf Metabolome, Lipidome, and Candidate Gene Function: Insights into Genotypic Variation in Phosphorus Utilization Efficiency in Stylosanthes guianensis
inferred← citeshttps://doi.org/10.1021/acscentsci.8b00453openalex-snapshot
Structural and Biochemical Insights into the Function and Evolution of Sulfoquinovosidases
inferred← citeshttps://doi.org/10.1021/jasms.1c00162openalex-snapshot
Characterization of Glucuronosyl-diacyl/monoacylglycerols and Discovery of Their Acylated Derivatives in Tomato Lipid Extracts by Reversed-Phase Liquid Chromatography with Electrospray Ionization and Tandem Mass Spectrometry
inferred← citeshttps://doi.org/10.1038/s41467-025-66437-wopenalex-snapshot
Mycobacterium tuberculosis overcomes phosphate starvation by extensively remodelling its lipidome with phosphorus-free lipids
inferred← citeshttps://doi.org/10.1038/s41477-019-0537-2openalex-snapshot
HIGH STEROL ESTER 1 is a key factor in plant sterol homeostasis
inferred← citeshttps://doi.org/10.1038/s41598-017-04002-2openalex-snapshot
The Sulfoquinovosyltransferase-like Enzyme SQD2.2 is Involved in Flavonoid Glycosylation, Regulating Sugar Metabolism and Seed Setting in Rice
inferred← citeshttps://doi.org/10.1038/s41598-018-25686-0openalex-snapshot
Metabolic Reprogramming in Leaf Lettuce Grown Under Different Light Quality and Intensity Conditions Using Narrow-Band LEDs
inferred← citeshttps://doi.org/10.1038/s41598-020-63551-1openalex-snapshot
Nutrient availability affects the polar lipidome of Halimione portulacoides leaves cultured in hydroponics
inferred← citeshttps://doi.org/10.1038/s41598-022-16887-9openalex-snapshot
Metabolomics analysis of milk thistle lipids to identify drought-tolerant genes
inferred← citeshttps://doi.org/10.1039/c4ob01602eopenalex-snapshot
Anionic glycolipids related to glucuronosyldiacylglycerol inhibit protein kinase Akt
inferred← citeshttps://doi.org/10.1039/c8cs00209fopenalex-snapshot
Gold-catalyzed glycosylation in the synthesis of complex carbohydrate-containing natural products
inferred← citeshttps://doi.org/10.1039/c9sc05248hopenalex-snapshot
α-Glucuronosyl and α-glucosyl diacylglycerides, natural killer T cell-activating lipids from bacteria and fungi
inferred← citeshttps://doi.org/10.1039/d1mo00196eopenalex-snapshot
The state of the art in plant lipidomics
inferred← citeshttps://doi.org/10.1039/d3ob00891fopenalex-snapshot
Synthesis of N -oxyamide analogues of protein kinase B (Akt) targeting anionic glycoglycerolipids and their antiproliferative activity on human ovarian carcinoma cells
inferred← citeshttps://doi.org/10.1042/bcj20160508openalex-snapshot
Sulfoquinovose in the biosphere: occurrence, metabolism and functions
inferred← citeshttps://doi.org/10.1071/fp19082openalex-snapshot
Characterisation of genes involved in galactolipids and sulfolipids metabolism in maize and Arabidopsis and their differential responses to phosphate deficiency
inferred← citeshttps://doi.org/10.1073/pnas.2400711121openalex-snapshot
Nitrogen and sulfur for phosphorus: Lipidome adaptation of anaerobic sulfate-reducing bacteria in phosphorus-deprived conditions
inferred← citeshttps://doi.org/10.1074/jbc.m113.519298openalex-snapshot
A Bifunctional Glycosyltransferase from Agrobacterium tumefaciens Synthesizes Monoglucosyl and Glucuronosyl Diacylglycerol under Phosphate Deprivation
inferred← citeshttps://doi.org/10.1074/jbc.ra120.013796openalex-snapshot
Two bacterial glycosphingolipid synthases responsible for the synthesis of glucuronosylceramide and α-galactosylceramide
inferred← citeshttps://doi.org/10.1079/9781800624597.0001openalex-snapshot
Plant Nutrient Requirements and Nutrient Homeostasis in Plants
inferred← citeshttps://doi.org/10.1080/00380768.2016.1223521openalex-snapshot
Identification and selection of low-phosphate-tolerant germplasm in barley (Hordeum vulgare L.)
inferred← citeshttps://doi.org/10.1080/00380768.2017.1369362openalex-snapshot
The membrane lipid bilayer as a regulated barrier to cope with detrimental ionic conditions: making new tolerant plant lines with altered membrane lipid bilayer
inferred← citeshttps://doi.org/10.1080/00380768.2024.2408307openalex-snapshot
The strategies for improving phosphorus-use efficiency in plant cell
inferred← citeshttps://doi.org/10.1080/00380768.2025.2539724openalex-snapshot
Low phosphorus tolerance of plants forming root clusters: can the specialized functions be used to resolve the phosphorus crisis?
inferred← citeshttps://doi.org/10.1080/10408398.2015.1084992openalex-snapshot
Progress and challenges in improving the nutritional quality of rice ( Oryza sativa L.)
inferred← citeshttps://doi.org/10.1080/15230430.2017.1420246openalex-snapshot
Plant and soil P determine functional attributes of subalpine Australian plants
inferred← citeshttps://doi.org/10.1080/15592324.2015.1049791openalex-snapshot
A new insight into root responses to external cues: Paradigm shift in nutrient sensing
inferred← citeshttps://doi.org/10.1080/15592324.2019.1657339openalex-snapshot
Different regulations of cell-type transcription by UV-B in multicellular green alga Volvox carteri
inferred← citeshttps://doi.org/10.1093/femsre/fuag034openalex-snapshot
Bacterial sulfoquinovose cycling across aquatic ecosystems
inferred← citeshttps://doi.org/10.1093/hr/uhac011openalex-snapshot
Improving phosphate use efficiency in the aquatic crop watercress (Nasturtium officinale)
inferred← citeshttps://doi.org/10.1093/jxb/erab026openalex-snapshot
Hydrolysis of organophosphorus by diatom purple acid phosphatase and sequential regulation of cell metabolism
inferred← citeshttps://doi.org/10.1093/jxb/erab300openalex-snapshot
Sulfoquinovosyl diacylglycerol synthase 1 impairs glycolipid accumulation and photosynthesis in phosphate-deprived rice
inferred← citeshttps://doi.org/10.1093/jxb/erab335openalex-snapshot
Inoculation of barley withTrichoderma harzianumT-22 modifies lipids and metabolites to improve salt tolerance
inferred← citeshttps://doi.org/10.1093/jxb/erab559openalex-snapshot
Metabolite shift in Medicago truncatula occurs in phosphorus deprivation
inferred← citeshttps://doi.org/10.1093/jxb/eraf048openalex-snapshot
LIPID RICH 1 modulates allocation of carbon between starch and triacylglycerol in Arabidopsis leaves
inferred← citeshttps://doi.org/10.1093/jxb/eraf482openalex-snapshot
Lipid-mediated responses to nutrient and other stresses: roles in plant adaptation and signaling
inferred← citeshttps://doi.org/10.1093/jxb/ert306openalex-snapshot
The evolution of autotrophy in relation to phosphorus requirement
inferred← citeshttps://doi.org/10.1093/jxb/erv056openalex-snapshot
Linking phosphorus availability with photo-oxidative stress in plants
inferred← citeshttps://doi.org/10.1093/pcp/pcaf130openalex-snapshot
Membrane lipid-driven thylakoid biogenesis coordinating chlorophyll synthesis and expression of photosynthetic proteins
inferred← citeshttps://doi.org/10.1093/pcp/pct156openalex-snapshot
Nitrate and Phosphate Regimes Induced Lipidomic and Biochemical Changes in the Intertidal Macroalga Ulva lactuca (Ulvophyceae, Chlorophyta)
inferred← citeshttps://doi.org/10.1093/plcell/koaa054openalex-snapshot
Nonspecific phospholipase C4 hydrolyzes phosphosphingolipids and sustains plant root growth during phosphate deficiency
inferred← citeshttps://doi.org/10.1093/plcell/koaa057openalex-snapshot
Nonspecific phospholipase C4 hydrolyzes phosphosphingolipids and sustains plant root growth during phosphate deficiency
inferred← citeshttps://doi.org/10.1093/plcell/koad326openalex-snapshot
Milestones in understanding transport, sensing, and signaling of the plant nutrient phosphorus
inferred← citeshttps://doi.org/10.1093/plcell/koaf138openalex-snapshot
Regulation of glucosylceramide synthase and sphingolipid remodeling in the plant response to phosphate deficiency
inferred← citeshttps://doi.org/10.1093/plphys/kiad212openalex-snapshot
Chloroplastic Sec14-like proteins modulate growth and phosphate deficiency responses inArabidopsisand rice
inferred← citeshttps://doi.org/10.1093/plphys/kiad604openalex-snapshot
Anionic lipids facilitate membrane development and protochlorophyllide biosynthesis in etioplasts
inferred← citeshttps://doi.org/10.1093/plphys/kiae382openalex-snapshot
From sensing to acclimation: The role of membrane lipid remodeling in plant responses to low temperatures
inferred← citeshttps://doi.org/10.1093/plphys/kiag585openalex-snapshot
Phospholipid homeostasis and gametophyte development require the glycerophosphodiester phosphodiesterases GDPD5 and GDPD6
inferred← citeshttps://doi.org/10.1099/mic.0.001588openalex-snapshot
Pectobacterium atrosepticum SCRI1043 flagella mediate adherence to potato plants indirectly through motility
inferred← citeshttps://doi.org/10.1101/2020.10.19.346056openalex-snapshot
Investigation of biochemical changes in barley inoculated with Trichoderma harzianum T-22 under salt stress
inferred← citeshttps://doi.org/10.1101/2022.05.11.491395openalex-snapshot
Characterization and visualization of global metabolomic responses of Brachypodium distachyon to environmental changes
inferred← citeshttps://doi.org/10.1101/2023.05.16.541020openalex-snapshot
Plastid anionic lipids are required for membrane development and protochlorophyllide synthesis in etioplasts
inferred← citeshttps://doi.org/10.1101/2024.02.24.581867openalex-snapshot
A missense mutation in the Xan-h gene encoding the Mg-chelatase subunit I leads to a viable pale green line with phenotypic features of potential interest for barley breeding programs
inferred← citeshttps://doi.org/10.1101/2024.09.27.615480openalex-snapshot
Mycobacterium tuberculosis overcomes phosphate starvation by extensively remodelling its lipidome with phosphorus-free lipids
inferred← citeshttps://doi.org/10.1101/2025.09.18.677093openalex-snapshot
METABOLIC AND TRANSCRIPTOMIC ANALYSES IDENTIFY COORDINATED RESOURCE REALLOCATION IN RESPONSE TO PHOSPHATE SUPPLY IN HEMP
inferred← citeshttps://doi.org/10.1104/pp.18.01469openalex-snapshot
Phosphate Starvation Alters Abiotic-Stress-Induced Cytosolic Free Calcium Increases in Roots
inferred← citeshttps://doi.org/10.1111/1462-2920.12315openalex-snapshot
Flagella interact with ionic plant lipids to mediate adherence of pathogenic Escherichia coli to fresh produce plants
inferred← citeshttps://doi.org/10.1111/jipb.12163openalex-snapshot
Molecular mechanisms underlying phosphate sensing, signaling, and adaptation in plants
inferred← citeshttps://doi.org/10.1111/pce.13191openalex-snapshot
Molecular mechanisms underpinning phosphorus‐use efficiency in rice
inferred← citeshttps://doi.org/10.1111/pce.13554openalex-snapshot
Rice sulfoquinovosyltransferase SQD2.1 mediates flavonoid glycosylation and enhances tolerance to osmotic stress
inferred← citeshttps://doi.org/10.1111/pce.13764openalex-snapshot
OsSQD1 at the crossroads of phosphate and sulfur metabolism affects plant morphology and lipid composition in response to phosphate deprivation
inferred← citeshttps://doi.org/10.1111/pce.15110openalex-snapshot
Hydrogen sulphide alleviates root growth inhibition induced by phosphate starvation
inferred← citeshttps://doi.org/10.1111/pce.15122openalex-snapshot
Non‐specific Phospholipase C4 Improves Phosphorus Remobilization From Old to Young Leaves in Camelina
inferred← citeshttps://doi.org/10.1111/pce.70080openalex-snapshot
Polar Lipid and Fatty Acid Profiles of Oat Groats Substantially Influenced by Field Management: A Comparison of Cultivars, Sowing Times and Fertilizer Composition
inferred← citeshttps://doi.org/10.1111/pce.70262openalex-snapshot
From Soil to Cell: Systemic Signalling and Regulatory Networks in Zea mays Under Phosphorus Deprivation
inferred← citeshttps://doi.org/10.1111/ppl.12334openalex-snapshot
Induced accumulation of glucuronosyldiacylglycerol in tomato and soybean under phosphorus deprivation
inferred← citeshttps://doi.org/10.1111/ppl.12601openalex-snapshot
Does triacylglycerol (TAG) serve a photoprotective function in plant leaves? An examination of leaf lipids under shading and drought
inferred← citeshttps://doi.org/10.1111/ppl.12699openalex-snapshot
Ancient rice cultivar extensively replaces phospholipids with non‐phosphorus glycolipid under phosphorus deficiency
inferred← citeshttps://doi.org/10.1111/tpj.12522openalex-snapshot
The metabolic flux phenotype of heterotrophic Arabidopsis cells reveals a flexible balance between the cytosolic and plastidic contributions to carbohydrate oxidation in response to phosphate limitation
inferred← citeshttps://doi.org/10.1111/tpj.12556openalex-snapshot
Roles of lipids as signaling molecules and mitigators during stress response in plants
inferred← citeshttps://doi.org/10.1111/tpj.13013openalex-snapshot
An enhanced plant lipidomics method based on multiplexed liquid chromatography–mass spectrometry reveals additional insights into cold‐ and drought‐induced membrane remodeling
inferred← citeshttps://doi.org/10.1111/tpj.13281openalex-snapshot
Molecular characterization and targeted quantitative profiling of the sphingolipidome in rice
inferred← citeshttps://doi.org/10.1111/tpj.15078openalex-snapshot
Phosphate and phosphite have a differential impact on the proteome and phosphoproteome of Arabidopsis suspension cell cultures
inferred← citeshttps://doi.org/10.1111/tpj.16160openalex-snapshot
Information theory and machine learning illuminate large‐scale metabolomic responses of Brachypodium distachyon to environmental change
inferred← citeshttps://doi.org/10.1111/tpj.16737openalex-snapshot
Genome‐wide association identifies a BAHD acyltransferase activity that assembles an ester of glucuronosylglycerol and phenylacetic acid
inferred← citeshttps://doi.org/10.1111/tpj.17227openalex-snapshot
Phosphorus starvation induces the synthesis of novel lipid class diacylglyceryl glucuronide and diacylglyceryl‐ N,N,N ‐trimethylhomoserine in two species of cold‐adapted microalgae Raphidonema (Chlorophyta)
inferred← citeshttps://doi.org/10.1111/tpj.70969openalex-snapshot
Chloroplast glycerolipid metabolism during maintenance and under stress
inferred← citeshttps://doi.org/10.1128/jb.02004-14openalex-snapshot
Accumulation of Novel Glycolipids and Ornithine Lipids in Mesorhizobium loti under Phosphate Deprivation
inferred← citeshttps://doi.org/10.1134/s1021443721050162openalex-snapshot
Proteome and Lipidome of Plant Cell Membranes during Development
inferred← citeshttps://doi.org/10.1134/s1021443724610061openalex-snapshot
Study of the Regulatory Mechanisms of Phosphorus Homeostasis and Phosphate (Pi)-Starvation Rescue in Rice
inferred← citeshttps://doi.org/10.1134/s1063074022040034openalex-snapshot
The Influence of Endophyte Laminariocolax aecidioides (Rosenvinge) A.F. Peters, 1998 (Phaeophyceae, Ectocarpales) on the Lipid Composition of the Brown Alga Undaria pinnatifida (Harvey) Suringar, 1873 (Phaeophyceae: Laminariales)
inferred← citeshttps://doi.org/10.1146/annurev-arplant-050718-100202openalex-snapshot
Chloroplast Lipids and Their Biosynthesis
inferred← citeshttps://doi.org/10.1186/s12870-016-0825-1openalex-snapshot
Physiological and comparative proteome analyses reveal low-phosphate tolerance and enhanced photosynthesis in a maize mutant owing to reinforced inorganic phosphate recycling
inferred← citeshttps://doi.org/10.1186/s12870-020-02590-2openalex-snapshot
Transcriptomic analysis at organ and time scale reveals gene regulatory networks controlling the sulfate starvation response of Solanum lycopersicum
inferred← citeshttps://doi.org/10.1186/s12870-020-2237-5openalex-snapshot
Deconstructing the genetic architecture of iron deficiency chlorosis in soybean using genome-wide approaches
inferred← citeshttps://doi.org/10.1186/s12870-021-03015-4openalex-snapshot
Characterization of contrasting rice (Oryza sativa L.) genotypes reveals the Pi-efficient schema for phosphate starvation tolerance
inferred← citeshttps://doi.org/10.1186/s12870-021-03124-0openalex-snapshot
The role of strigolactones in P deficiency induced transcriptional changes in tomato roots
inferred← citeshttps://doi.org/10.1186/s12870-025-07193-3openalex-snapshot
Effects of phosphorus deficiency on lipid composition and photosynthesis process in Zygophyllum xanthoxylum
inferred← citeshttps://doi.org/10.1248/yakushi.17-00193openalex-snapshot
Development of Plant Metabolomics and Medicinal Plant Genomics
inferred← citeshttps://doi.org/10.1271/kagakutoseibutsu.60.420openalex-snapshot
植物の低リン適応戦略
inferred← citeshttps://doi.org/10.1271/kagakutoseibutsu.61.394openalex-snapshot
植物の脂質合成の起源と進化
inferred← citeshttps://doi.org/10.1271/kagakutoseibutsu.62.579openalex-snapshot
The Metabolic Change for Phosphate Starvation Stress in Plant Cell
inferred← citeshttps://doi.org/10.12794/metadc1833476openalex-snapshot
Effect of Phosphorus Starvation on Metabolism and Spatial Distribution of Phosphatidylcholine in Medicago truncatula Wild-Type and PDIL3 Genotypes
inferred← citeshttps://doi.org/10.1371/journal.pbio.2004310openalex-snapshot
Arabidopsis choline transporter-like 1 (CTL1) regulates secretory trafficking of auxin transporters to control seedling growth
inferred← citeshttps://doi.org/10.1371/journal.pone.0218690openalex-snapshot
Re-modeling of foliar membrane lipids in a seagrass allows for growth in phosphorus-deplete conditions
inferred← citeshttps://doi.org/10.15446/rcciquifa.v51n1.102693openalex-snapshot
Metabolomics studies of allelopathy: a review
inferred← citeshttps://doi.org/10.1584/jpestics.w23-38openalex-snapshot
ホスファチジルグリセロールとシアノバクテリア—光合成に関与するリン脂質の機能—
inferred← citeshttps://doi.org/10.17557/tjfc.974756openalex-snapshot
THE EFFECT OF DIFFERENT PHOSPHORUS DOSES ON SEED YIELD AND QUALITY PARAMETERS OF BLACK CUMIN (Nigella sp.)
inferred← citeshttps://doi.org/10.21203/rs.3.rs-8022751/v1openalex-snapshot
Lipid stoichiometry and biomarkers reflect microbial acclimation and nutrient stress across the Atlantic Ocean
inferred← citeshttps://doi.org/10.22271/phyto.2020.v9.i6r.13115openalex-snapshot
Comparative metabolic profile of maize genotypes reveals the tolerance mechanism associated in combined stresses
inferred← citeshttps://doi.org/10.3389/fmicb.2015.00912openalex-snapshot
Manipulation of oil synthesis in Nannochloropsis strain NIES-2145 with a phosphorus starvation–inducible promoter from Chlamydomonas reinhardtii
inferred← citeshttps://doi.org/10.3389/fphar.2024.1378249openalex-snapshot
Supplementation of Saussurea costus root alleviates sodium nitrite-induced hepatorenal toxicity by modulating metabolic profile, inflammation, and apoptosis
inferred← citeshttps://doi.org/10.3389/fpls.2013.00469openalex-snapshot
Differential regulation of two types of monogalactosyldiacylglycerol synthase in membrane lipid remodeling under phosphate-limited conditions in sesame plants
inferred← citeshttps://doi.org/10.3389/fpls.2015.01014openalex-snapshot
Metabolic Adaptations of White Lupin Roots and Shoots under Phosphorus Deficiency
inferred← citeshttps://doi.org/10.3389/fpls.2015.01127openalex-snapshot
Boosting Sensitivity in Liquid Chromatography–Fourier Transform Ion Cyclotron Resonance–Tandem Mass Spectrometry for Product Ion Analysis of Monoterpene Indole Alkaloids
inferred← citeshttps://doi.org/10.3389/fpls.2015.01184openalex-snapshot
Comparative Morphophysiological Analyses and Molecular Profiling Reveal Pi-Efficient Strategies of a Traditional Rice Genotype
showing the first 200 of 241 · page through all 241
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.