On the public citation graph

Discovery of new analogs of the marine biotoxin azaspiracid in blue mussels ( Mytilus edulis ) by ultra‐performance liquid chromatography/tandem mass spectrometry

0 signed · 123 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1002/(sici)1522-7189(199905/06)7:3<99::aid-nt46>3.0.co;2-lopenalex-snapshot

Two analogs of azaspiracid isolated from mussels, Mytilus edulis, involved in human intoxication in Ireland

inferredcites →https://doi.org/10.1002/ange.200460696openalex-snapshot

Structural Revision and Total Synthesis of Azaspiracid‐1, Part 2: Definition of the ABCD Domain and Total Synthesis

inferredcites →https://doi.org/10.1002/anie.200351825openalex-snapshot

Total Synthesis of the Proposed Azaspiracid‐1 Structure, Part 1: Construction of the Enantiomerically Pure C1–C20, C21–C27, and C28–C40 Fragments

inferredcites →https://doi.org/10.1002/anie.200460696openalex-snapshot

Structural Revision and Total Synthesis of Azaspiracid‐1, Part 2: Definition of the ABCD Domain and Total Synthesis

inferredcites →https://doi.org/10.1002/rcm.2501openalex-snapshot

Discovery of fatty acid ester metabolites of spirolide toxins in mussels from Norway using liquid chromatography/tandem mass spectrometry

inferredcites →https://doi.org/10.1002/rcm.863openalex-snapshot

Studies on azaspiracid biotoxins. II. Mass spectral behavior and structural elucidation of azaspiracid analogs

inferredcites →https://doi.org/10.1016/s0040-4020(01)96469-5openalex-snapshot

Diarrhetic shellfish toxins

inferredcites →https://doi.org/10.1016/s0041-0101(02)00082-xopenalex-snapshot

First evidence of an extensive northern European distribution of azaspiracid poisoning (AZP) toxins in shellfish

inferredcites →https://doi.org/10.1016/s0041-0101(02)00244-1openalex-snapshot

Ubiquitous ‘benign’ alga emerges as the cause of shellfish contamination responsible for the human toxic syndrome, azaspiracid poisoning

inferredcites →https://doi.org/10.1016/s0041-0101(02)00288-xopenalex-snapshot

Detection of five new hydroxyl analogues of azaspiracids in shellfish using multiple tandem mass spectrometry

inferredcites →https://doi.org/10.1016/s0041-0101(03)00105-3openalex-snapshot

The first identification of azaspiracids in shellfish from France and Spain

inferredcites →https://doi.org/10.1021/ja981413ropenalex-snapshot

Azaspiracid, a New Marine Toxin Having Unique Spiro Ring Assemblies, Isolated from Irish Mussels, Mytilus edulis

inferredcites →https://doi.org/10.1021/jf060396jopenalex-snapshot

Identification of Fatty Acid Esters of Pectenotoxin-2 Seco Acid in Blue Mussels (Mytilus edulis) from Ireland

inferredcites →https://doi.org/10.1271/bbb.65.740openalex-snapshot

Structures of Azaspiracid Analogs, Azaspiracid-4 and Azaspiracid-5, Causative Toxins of Azaspiracid Poisoning in Europe

inferredcites →https://doi.org/10.2983/0730-8000(2006)25[1067:fdoaim]2.0.co;2openalex-snapshot

FIRST DETECTION OF AZASPIRACIDS IN MUSSELS IN NORTH WEST AFRICA

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.4671924openalex-extracted

Assessing Escherichia Coli and Coliform Bacteria in Mussel Mytella Strigata (Hanley, 1843) Collected in Tangub Misamis Occidental and Baroy Lanao Del Norte

inferred← citeshttps://doi.org/10.1002/9781118500354.ch19openalex-snapshot

Pathological clues of phycotoxin ingestion

inferred← citeshttps://doi.org/10.1002/9781118992685.ch11openalex-snapshot

The Determination of Marine Biotoxins in Seafood

inferred← citeshttps://doi.org/10.1002/9781118994672.ch4openalex-snapshot

Harmful Algal Blooms and Shellfish

inferred← citeshttps://doi.org/10.1002/9783527634606.ch8openalex-snapshot

Biomimetic Syntheses of Alkaloids with a Non‐Amino Acid Origin

inferred← citeshttps://doi.org/10.1002/cbic.200900201openalex-snapshot

Monoclonal Antibodies with Orthogonal Azaspiracid Epitopes

inferred← citeshttps://doi.org/10.1002/ejoc.201300991openalex-snapshot

Marine Toxins in Italy: The More You Look, the More You Find

inferred← citeshttps://doi.org/10.1002/jms.1303openalex-snapshot

Current literature in mass spectrometry

inferred← citeshttps://doi.org/10.1002/rcm.4724openalex-snapshot

Food contaminant analysis at ultra‐high mass resolution: application of hybrid linear ion trap – orbitrap mass spectrometry for the determination of the polyether toxins, azaspiracids, in shellfish

inferred← citeshttps://doi.org/10.1002/rcm.6900openalex-snapshot

Simultaneous determination of biotoxins DSP and AZAs in bivalve molluscs and fish by liquid chromatography/tandem mass spectrometry

inferred← citeshttps://doi.org/10.1007/978-1-4939-2684-8_18openalex-snapshot

Analysis of Marine Biotoxins Using LC-MS/MS

inferred← citeshttps://doi.org/10.1007/978-3-642-53971-8_33openalex-snapshot

Marine Dinoflagellates-Associated Human Poisoning

inferred← citeshttps://doi.org/10.1007/978-3-7643-8338-1_3openalex-snapshot

Phycotoxins: chemistry, mechanisms of action and shellfish poisoning

inferred← citeshttps://doi.org/10.1007/978-90-481-3834-0_28openalex-snapshot

Seafood Toxins: Classes, Sources, and Toxicology

inferred← citeshttps://doi.org/10.1007/978-94-007-6419-4_20openalex-snapshot

Azaspiracid Toxins: Toxicological Profile

inferred← citeshttps://doi.org/10.1007/978-94-007-6588-7_17openalex-snapshot

Effect of Dilution Rate on Azadinium spinosum and Azaspiracid (AZA) Production in Pilot Scale Photobioreactors for the Harvest of AZA1 and -2

inferred← citeshttps://doi.org/10.1007/978-94-007-6650-1_20-1openalex-snapshot

Azaspiracid Toxins: Toxicological Profile

inferred← citeshttps://doi.org/10.1007/978-981-10-8261-0_1openalex-snapshot

Algal Blooms: Basic Concepts

inferred← citeshttps://doi.org/10.1007/s00216-008-2221-7openalex-snapshot

LC-MS-MS aboard ship: tandem mass spectrometry in the search for phycotoxins and novel toxigenic plankton from the North Sea

inferred← citeshttps://doi.org/10.1007/s00216-010-4007-yopenalex-snapshot

The development of a rapid method for the isolation of four azaspiracids for use as reference materials for quantitative LC–MS–MS methods

inferred← citeshttps://doi.org/10.1007/s00216-010-4161-2openalex-snapshot

The preparation of certified calibration solutions for azaspiracid-1, -2, and -3, potent marine biotoxins found in shellfish

inferred← citeshttps://doi.org/10.1007/s00216-011-4787-8openalex-snapshot

A mussel tissue certified reference material for multiple phycotoxins. Part 3: homogeneity and stability

inferred← citeshttps://doi.org/10.1007/s00216-012-5849-2openalex-snapshot

Quantitative analysis of azaspiracids in Azadinium spinosum cultures

inferred← citeshttps://doi.org/10.1007/s00216-014-8250-5openalex-snapshot

A mussel (Mytilus edulis) tissue certified reference material for the marine biotoxins azaspiracids

inferred← citeshttps://doi.org/10.1007/s00216-016-0037-4openalex-snapshot

Mediterranean Azadinium dexteroporum (Dinophyceae) produces six novel azaspiracids and azaspiracid-35: a structural study by a multi-platform mass spectrometry approach

inferred← citeshttps://doi.org/10.1016/b978-0-12-416595-3.00007-4openalex-snapshot

Cardiovascular Toxicity from Marine Envenomation

inferred← citeshttps://doi.org/10.1016/b978-0-12-811515-2.00007-xopenalex-snapshot

Occurrence of Natural Toxins in Seafood

inferred← citeshttps://doi.org/10.1016/b978-0-443-36320-7.00005-3openalex-snapshot

Comprehensive applications of marine biotoxins resources

inferred← citeshttps://doi.org/10.1016/bs.coac.2017.07.004openalex-snapshot

Marine Toxins Analysis for Consumer Protection

inferred← citeshttps://doi.org/10.1016/bs.coac.2017.08.002openalex-snapshot

Structural Diversity of Microalgal Marine Toxins

inferred← citeshttps://doi.org/10.1016/bs.coac.2017.08.005openalex-snapshot

LC/MS Analysis of Marine Toxins

inferred← citeshttps://doi.org/10.1016/j.ab.2013.10.035openalex-snapshot

Microsphere-based immunoassay for the detection of azaspiracids

inferred← citeshttps://doi.org/10.1016/j.aca.2010.11.036openalex-snapshot

Screening of lipophilic marine toxins in shellfish and algae: Development of a library using liquid chromatography coupled to orbitrap mass spectrometry

inferred← citeshttps://doi.org/10.1016/j.aquatox.2012.08.016openalex-snapshot

Effect of Azadinium spinosum on the feeding behaviour and azaspiracid accumulation of Mytilus edulis

inferred← citeshttps://doi.org/10.1016/j.chemosphere.2025.144502openalex-snapshot

Bioaccumulations and biotransformations of azaspiracids from Amphidoma languida in the mussel Mytilus edulis

inferred← citeshttps://doi.org/10.1016/j.chroma.2008.10.123openalex-snapshot

Determination of dissolved domoic acid in seawater with reversed-phase extraction disks and rapid resolution liquid chromatography tandem mass spectrometry with head-column trapping

inferred← citeshttps://doi.org/10.1016/j.chroma.2008.12.099openalex-snapshot

Liquid chromatography–tandem mass spectrometry method for the detection of marine lipophilic toxins under alkaline conditions

inferred← citeshttps://doi.org/10.1016/j.chroma.2009.03.062openalex-snapshot

Sensitive method for the determination of lipophilic marine biotoxins in extracts of mussels and processed shellfish by high-performance liquid chromatography–tandem mass spectrometry based on enrichment by solid-phase extraction

inferred← citeshttps://doi.org/10.1016/j.chroma.2010.09.020openalex-snapshot

Strategies for the elimination of matrix effects in the liquid chromatography tandem mass spectrometry analysis of the lipophilic toxins okadaic acid and azaspiracid-1 in molluscan shellfish

inferred← citeshttps://doi.org/10.1016/j.chroma.2011.09.017openalex-snapshot

Derivatization of azaspiracid biotoxins for analysis by liquid chromatography with fluorescence detection

inferred← citeshttps://doi.org/10.1016/j.envres.2026.124339openalex-snapshot

Monitoring of regulated and non-regulated biotoxins in marine organisms using liquid-phase microextraction and liquid chromatography coupled with high-resolution mass spectrometry

inferred← citeshttps://doi.org/10.1016/j.hal.2008.06.003openalex-snapshot

Characterization of azaspiracids in plankton size-fractions and isolation of an azaspiracid-producing dinoflagellate from the North Sea

inferred← citeshttps://doi.org/10.1016/j.hal.2011.06.010openalex-snapshot

The role of Azadinium spinosum (Dinophyceae) in the production of azaspiracid shellfish poisoning in mussels

inferred← citeshttps://doi.org/10.1016/j.hal.2012.05.004openalex-snapshot

Blooms of Azadinium cf. spinosum Elbrächter et Tillmann (Dinophyceae) in northern shelf waters of Argentina, Southwestern Atlantic

inferred← citeshttps://doi.org/10.1016/j.hal.2012.11.009openalex-snapshot

Morphology, phylogeny and azaspiracid profile of Azadinium poporum (Dinophyceae) from the China Sea

inferred← citeshttps://doi.org/10.1016/j.hal.2018.12.005openalex-snapshot

Two novel azaspiracids from Azadinium poporum, and a comprehensive compilation of azaspiracids produced by Amphidomataceae, (Dinophyceae)

inferred← citeshttps://doi.org/10.1016/j.jfca.2025.108684openalex-snapshot

A two-step LC-HRMS strategy for targeted and suspect screening of lipophilic marine biotoxins in bivalve molluscs

inferred← citeshttps://doi.org/10.1016/j.jprot.2009.02.008openalex-snapshot

Proteomic response of human neuroblastoma cells to azaspiracid-1

inferred← citeshttps://doi.org/10.1016/j.tiv.2017.09.018openalex-snapshot

Whole genome mRNA transcriptomics analysis reveals different modes of action of the diarrheic shellfish poisons okadaic acid and dinophysis toxin-1 versus azaspiracid-1 in Caco-2 cells

inferred← citeshttps://doi.org/10.1016/j.toxcx.2020.100059openalex-snapshot

Fatty acid esters of azaspiracids identified in mussels (Mytilus edulis) using liquid chromatography-high resolution mass spectrometry

inferred← citeshttps://doi.org/10.1016/j.toxicon.2009.01.010openalex-snapshot

A convenient and cost-effective method for monitoring marine algal toxins with passive samplers

inferred← citeshttps://doi.org/10.1016/j.toxicon.2009.02.008openalex-snapshot

Isolation of azaspiracid-2 from a marine sponge Echinoclathria sp. as a potent cytotoxin

inferred← citeshttps://doi.org/10.1016/j.toxicon.2009.02.015openalex-snapshot

Performance of the EU-harmonised mouse bioassay for lipophilic toxins for the detection of azaspiracids in naturally contaminated mussel (Mytilus edulis) hepatopancreas tissue homogenates characterised by liquid chromatography coupled to tandem mass spectrometry

inferred← citeshttps://doi.org/10.1016/j.toxicon.2009.07.014openalex-snapshot

First identification of azaspiracid and spirolides in Mesodesma donacium and Mulinia edulis from Northern Chile

inferred← citeshttps://doi.org/10.1016/j.toxicon.2009.09.009openalex-snapshot

Azaspiracid poisoning (AZP) toxins in shellfish: Toxicological and health considerations

inferred← citeshttps://doi.org/10.1016/j.toxicon.2009.10.020openalex-snapshot

First evidence of azaspiracids (AZAs): A family of lipophilic polyether marine toxins in scallops (Argopecten purpuratus) and mussels (Mytilus chilensis) collected in two regions of Chile

inferred← citeshttps://doi.org/10.1016/j.toxicon.2012.04.351openalex-snapshot

Azaspiracid accumulation, detoxification and biotransformation in blue mussels (Mytilus edulis) experimentally fed Azadinium spinosum

inferred← citeshttps://doi.org/10.1016/j.toxicon.2012.05.007openalex-snapshot

New azaspiracids in Amphidomataceae (Dinophyceae)

inferred← citeshttps://doi.org/10.1016/j.toxicon.2013.01.010openalex-snapshot

Dissolved azaspiracids are absorbed and metabolized by blue mussels (Mytilus edulis)

inferred← citeshttps://doi.org/10.1016/j.toxicon.2014.10.012openalex-snapshot

Confirmation of extensive natural distribution of azaspiracids in the tissue compartments of mussels (Mytilus edulis)

inferred← citeshttps://doi.org/10.1016/j.toxicon.2017.12.040openalex-snapshot

Accumulation and transformation of azaspiracids in scallops ( Chlamys farreri ) and mussels ( Mytilus galloprovincialis ) fed with Azadinium poporum, and response of antioxidant enzymes

inferred← citeshttps://doi.org/10.1016/j.toxicon.2021.06.010openalex-snapshot

Complex profiles of azaspiracid analogues in two culture strains of Azadinium poporum (Amphidomataceae, Dinophyceae) isolated from Japanese coastal waters determined by LC-MS/MS

inferred← citeshttps://doi.org/10.1016/j.toxlet.2017.10.016openalex-snapshot

Toxic equivalency factors (TEFs) after acute oral exposure of azaspiracid 1, −2 and −3 in mice

inferred← citeshttps://doi.org/10.1017/s0950268810000853openalex-snapshot

Shellfish toxicity: human health implications of marine algal toxins

inferred← citeshttps://doi.org/10.1021/ac801506dopenalex-snapshot

Evaluation of Various pH and Temperature Conditions on the Stability of Azaspiracids and Their Importance in Preparative Isolation and Toxicological Studies

inferred← citeshttps://doi.org/10.1021/acs.jafc.1c03831openalex-snapshot

In Vitro Metabolism of Azaspiracids 1–3 with a Hepatopancreatic Fraction from Blue Mussels (Mytilus edulis)

inferred← citeshttps://doi.org/10.1021/acs.jafc.5b01320openalex-snapshot

Structure Elucidation, Relative LC–MS Response and In Vitro Toxicity of Azaspiracids 7–10 Isolated from Mussels (Mytilus edulis)

inferred← citeshttps://doi.org/10.1021/acs.jafc.5b04609openalex-snapshot

Effects of Heating on Proportions of Azaspiracids 1–10 in Mussels (Mytilus edulis) and Identification of Carboxylated Precursors for Azaspiracids 5, 10, 13, and 15

inferred← citeshttps://doi.org/10.1021/acs.jafc.8b00346openalex-snapshot

Selective Extraction and Purification of Azaspiracids from Blue Mussels (Mytilus edulis) Using Boric Acid Gel

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00973openalex-snapshot

Identification of 21,22-Dehydroazaspiracids in Mussels (Mytilus edulis) and in Vitro Toxicity of Azaspiracid-26

inferred← citeshttps://doi.org/10.1021/es103612copenalex-snapshot

Mussels Increase Xenobiotic (Azaspiracid) Toxicity Using a Unique Bioconversion Mechanism

inferred← citeshttps://doi.org/10.1021/np500555kopenalex-snapshot

Isolation, Structure Elucidation, Relative LC-MS Response, and in Vitro Toxicity of Azaspiracids from the Dinoflagellate Azadinium spinosum

inferred← citeshttps://doi.org/10.1021/tx200553popenalex-snapshot

Comparative Effects of the Marine Algal Toxins Azaspiracid-1, -2, and -3 on Jurkat T Lymphocyte Cells

inferred← citeshttps://doi.org/10.1021/tx3001785openalex-snapshot

Induction of Apoptosis Pathways in Several Cell Lines following Exposure to the Marine Algal Toxin Azaspiracid

inferred← citeshttps://doi.org/10.1021/tx300283topenalex-snapshot

Marine Algal Toxin Azaspiracid Is an Open-State Blocker of hERG Potassium Channels

inferred← citeshttps://doi.org/10.1021/tx400434bopenalex-snapshot

Epimers of Azaspiracids: Isolation, Structural Elucidation, Relative LC-MS Response, and in Vitro Toxicity of 37-epi-Azaspiracid-1

inferred← citeshttps://doi.org/10.1021/tx800165copenalex-snapshot

Azaspiracid Substituent at C1 Is Relevant to in Vitro Toxicity

inferred← citeshttps://doi.org/10.1080/00288330.2021.1953083openalex-snapshot

Molecular detection and distribution of the genera Amphidoma and Azadinium (Amphidomataceae, Dinophyceae) in the coastal waters of Aotearoa/New Zealand

inferred← citeshttps://doi.org/10.1080/09670260802578534openalex-snapshot

Azadinium spinosumgen. et sp. nov. (Dinophyceae) identified as a primary producer of azaspiracid toxins

inferred← citeshttps://doi.org/10.1080/19440049.2017.1368720openalex-snapshot

Screening for the presence of lipophilic marine biotoxins in shellfish samples using the neuro-2a bioassay

inferred← citeshttps://doi.org/10.1093/chromsci/bmu054openalex-snapshot

Solid-Phase Extraction-Based Ultra-Sensitive Detection of Four Lipophilic Marine Biotoxins in Bivalves by High-Performance Liquid Chromatography-Tandem Mass Spectrometry

inferred← citeshttps://doi.org/10.1093/plankt/fbw099openalex-snapshot

Identification ofAzadinium poporum(Dinophyceae) in the Southeast Pacific: morphology, molecular phylogeny, and azaspiracid profile characterization

inferred← citeshttps://doi.org/10.1093/toxsci/kfp246openalex-snapshot

Cell Volume Decrease as a Link between Azaspiracid-Induced Cytotoxicity and c-Jun-N-Terminal Kinase Activation in Cultured Neurons

inferred← citeshttps://doi.org/10.1111/j.1742-4658.2008.06713.xopenalex-snapshot

Marine toxins and the cytoskeleton: azaspiracids

inferred← citeshttps://doi.org/10.1111/pre.12133openalex-snapshot

Revisiting the 1991 algal bloom in shelf waters off Argentina: Azadinium luciferelloides sp. nov. (Amphidomataceae, Dinophyceae) as the causative species in a diverse community of other amphidomataceans

inferred← citeshttps://doi.org/10.14573/altex.2012.4.359openalex-snapshot

Towards tailored assays for cell-based approaches to toxicity testing

inferred← citeshttps://doi.org/10.14573/altex.2013.4.487openalex-snapshot

A roadmap for hazard monitoring and risk assessment of marine biotoxins on the basis of chemical and biological test systems

inferred← citeshttps://doi.org/10.1533/9781845695576.2.129openalex-snapshot

Algal toxins and their detection

inferred← citeshttps://doi.org/10.21427/d7c30nopenalex-snapshot

Optimisation of Isolation Methods for the AZA Group of Marine Biotoxins and the Development of Accurate and Precise Methods of Analysis

inferred← citeshttps://doi.org/10.2174/1389203715666140221120219openalex-snapshot

High-Throughput Proteomics: A New Tool for Quality and Safety in Fishery Products

inferred← citeshttps://doi.org/10.2216/ph09-35.1openalex-snapshot

Azadinium obesum (Dinophyceae), a new nontoxic species in the genus that can produce azaspiracid toxins

inferred← citeshttps://doi.org/10.2903/j.efsa.2008.723openalex-snapshot

Marine biotoxins in shellfish – Azaspiracid group ‐ Scientific Opinion of the Panel on Contaminants in the Food chain

inferred← citeshttps://doi.org/10.2903/j.efsa.2021.6422openalex-snapshot

Evaluation of the shucking of certain species of scallops contaminated with lipophilic toxins with a view to the production of edible parts meeting the safety requirements foreseen in the Union legislation

inferred← citeshttps://doi.org/10.2903/j.efsa.2021.6809openalex-snapshot

Evaluation of the shucking of certain species of scallops contaminated with domoic acid with a view to the production of edible parts meeting the safety requirements foreseen in the Union legislation

inferred← citeshttps://doi.org/10.3390/md10061360openalex-snapshot

Production and Isolation of Azaspiracid-1 and -2 from Azadinium spinosum Culture in Pilot Scale Photobioreactors

inferred← citeshttps://doi.org/10.3390/md13116687openalex-snapshot

Structure Elucidation and in Vitro Toxicity of New Azaspiracids Isolated from the Marine Dinoflagellate Azadinium poporum

inferred← citeshttps://doi.org/10.3390/md17090489openalex-snapshot

Effects of Temperature, Growth Media, and Photoperiod on Growth and Toxin Production of Azadinium spinosum

inferred← citeshttps://doi.org/10.3390/md6020039openalex-snapshot

Azaspiracid Shellfish Poisoning: A Review on the Chemistry, Ecology, and Toxicology with an Emphasis on Human Health Impacts

inferred← citeshttps://doi.org/10.3390/md8040881openalex-snapshot

Impact of Marine Drugs on Cytoskeleton-Mediated Reproductive Events

inferred← citeshttps://doi.org/10.3390/s21072499openalex-snapshot

Current Trends and Challenges for Rapid SMART Diagnostics at Point-of-Site Testing for Marine Toxins

inferred← citeshttps://doi.org/10.3390/s91109414openalex-snapshot

Use of Biosensors as Alternatives to Current Regulatory Methods for Marine Biotoxins

inferred← citeshttps://doi.org/10.3390/toxins10010002openalex-snapshot

Tectus niloticus (Tegulidae, Gastropod) as a Novel Vector of Ciguatera Poisoning: Detection of Pacific Ciguatoxins in Toxic Samples from Nuku Hiva Island (French Polynesia)

inferred← citeshttps://doi.org/10.3390/toxins11010058openalex-snapshot

The Incidence of Marine Toxins and the Associated Seafood Poisoning Episodes in the African Countries of the Indian Ocean and the Red Sea

inferred← citeshttps://doi.org/10.3390/toxins11070394openalex-snapshot

LC–MS/MS Analysis of the Emerging Toxin Pinnatoxin-G and High Levels of Esterified OA Group Toxins in Galician Commercial Mussels

inferred← citeshttps://doi.org/10.3390/toxins2040878openalex-snapshot

Marine Toxins: Chemistry, Toxicity, Occurrence and Detection, with Special Reference to the Dutch Situation

inferred← citeshttps://doi.org/10.3987/com-08-11555openalex-snapshot

Synthesis of Open-Chain C21-C40 Fragment of Azaspiracid-1

inferred← citeshttps://doi.org/10.5772/intechopen.82438openalex-snapshot

Instrumental Methods for Detection of Lipophilic Marine Toxins in Endemic Species from Pacific Austral Fjords

inferred← citeshttps://doi.org/10.70675/5b31fd9dzc5eez4355z8e0dz130fcee1227copenalex-snapshot

Analyse non ciblée des biotoxines marines dans les produits de la pêche

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.