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A new potentially toxic A zadinium species ( D inophyceae) from the M editerranean Sea, A . dexteroporum sp. nov.

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What this work says

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

inferredcites →https://doi.org/10.1002/rcm.1164openalex-snapshot

Studies on azaspiracid biotoxins. III. Instrumental validation for rapid quantification of AZA 1 in complex biological matrices

inferredcites →https://doi.org/10.1007/bf00349240openalex-snapshot

Microphytoplankton in the Strait of Otranto (eastern Mediterranean)

inferredcites →https://doi.org/10.1007/s00299-001-0399-7openalex-snapshot

Regeneration and molecular characterization of intergeneric somatic hybrids between Citrus reticulata and Poncirus trifoliata

inferredcites →https://doi.org/10.1016/0168-9525(90)90186-aopenalex-snapshot

PCR protocols — A guide to methods and applications

inferredcites →https://doi.org/10.1016/j.chroma.2003.10.045openalex-snapshot

Liquid chromatography—multiple tandem mass spectrometry for the determination of ten azaspiracids, including hydroxyl analogues in shellfish

inferredcites →https://doi.org/10.1016/j.hal.2005.09.002openalex-snapshot

Potentially toxic and harmful microalgae from coastal waters of the Campania region (Tyrrhenian Sea, Mediterranean Sea)

inferredcites →https://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

inferredcites →https://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

inferredcites →https://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

inferredcites →https://doi.org/10.1016/j.hal.2012.10.001openalex-snapshot

First record of the genus Azadinium (Dinophyceae) from the Shetland Islands, including the description of Azadinium polongum sp. nov.

inferredcites →https://doi.org/10.1016/j.protis.2011.10.005openalex-snapshot

Amphidoma languida sp. nov. (Dinophyceae) Reveals a Close Relationship between Amphidoma and Azadinium

inferredcites →https://doi.org/10.1016/j.toxicon.2008.05.006openalex-snapshot

First report on azaspiracid and yessotoxin groups detection in French shellfish

inferredcites →https://doi.org/10.1016/j.toxicon.2009.02.008openalex-snapshot

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

inferredcites →https://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

inferredcites →https://doi.org/10.1016/j.toxicon.2009.09.009openalex-snapshot

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

inferredcites →https://doi.org/10.1016/j.toxicon.2012.05.007openalex-snapshot

New azaspiracids in Amphidomataceae (Dinophyceae)

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(03)00105-3openalex-snapshot

The first identification of azaspiracids in shellfish from France and Spain

inferredcites →https://doi.org/10.1017/s002531540002066xopenalex-snapshot

Check-list of British marine algae-third revision

inferredcites →https://doi.org/10.1017/s0967026202003608openalex-snapshot

Toxic Pseudo-nitzschia multistriata (Bacillariophyceae) from the Gulf of Naples: morphology, toxin analysis and phylogenetic relationships with other Pseudo-nitzschia species

inferredcites →https://doi.org/10.1021/es020246zopenalex-snapshot

Geographical, Temporal, and Species Variation of the Polyether Toxins, Azaspiracids, in Shellfish

inferredcites →https://doi.org/10.1080/00071618900650121openalex-snapshot

Scanning electron microscopy ofHeterocapsa minimasp. nov. (Dinophyceae) and its seasonal distribution in the Celtic Sea

inferredcites →https://doi.org/10.1080/09670260802578534openalex-snapshot

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

inferredcites →https://doi.org/10.1080/09670262.2011.556753openalex-snapshot

A new non-toxic species in the dinoflagellate genusAzadinium:A. poporumsp. nov.

inferredcites →https://doi.org/10.1093/bioinformatics/14.9.817openalex-snapshot

MODELTEST: testing the model of DNA substitution.

inferredcites →https://doi.org/10.1093/bioinformatics/btn575openalex-snapshot

TOPALi v2: a rich graphical interface for evolutionary analyses of multiple alignments on HPC clusters and multi-core desktops

inferredcites →https://doi.org/10.1093/molbev/msr121openalex-snapshot

MEGA5: Molecular Evolutionary Genetics Analysis Using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods

inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot

MUSCLE: multiple sequence alignment with high accuracy and high throughput

inferredcites →https://doi.org/10.1093/plankt/22.9.1735openalex-snapshot

Seasonal variability of phytoplankton populations in the middle Adriatic sub-basin

inferredcites →https://doi.org/10.1111/j.1529-8817.1987.tb04217.xopenalex-snapshot

MEDIA FOR THE CULTURE OF OCEANIC ULTRAPHYTOPLANKTON 1,2

inferredcites →https://doi.org/10.1111/j.1529-8817.2012.01159.xopenalex-snapshot

TAXONOMIC REVISION OF THE DINOFLAGELLATE AMPHIDOMA CAUDATA : TRANSFER TO THE GENUS AZADINIUM (DINOPHYCEAE) AND PROPOSAL OF TWO VARIETIES, BASED ON MORPHOLOGICAL AND MOLECULAR PHYLOGENETIC ANALYSES 1

inferredcites →https://doi.org/10.1111/j.1550-7408.2011.00600.xopenalex-snapshot

First Report of the Photosynthetic Dinoflagellate Genus A zadinium in the P acific O cean: Morphology and Molecular Characterization of A zadinium cf. poporum

inferredcites →https://doi.org/10.1111/j.1574-6941.2006.00060.xopenalex-snapshot

Comparison of prokaryotic diversity at offshore oceanic locations reveals a different microbiota in the Mediterranean Sea

inferredcites →https://doi.org/10.14601/phytopathol_mediterr-14998u1.29openalex-snapshot

BIOEDIT: A USER-FRIENDLY BIOLOGICAL SEQUENCE ALIGNMENT EDITOR AND ANALYSIS PROGRAM FOR WINDOWS 95/98/ NT

inferredcites →https://doi.org/10.2216/08-61.1openalex-snapshot

Unarmoured and thin-walled dinoflagellates from the Gulf of Naples, with the description ofWoloszynskia cinctasp. nov. (Dinophyceae, Suessiales)

inferredcites →https://doi.org/10.2216/i0031-8884-34-2-166.1openalex-snapshot

Analysis of the thecal plate pattern in the dinoflagellate Heterocapsa rotundata (Lohmann) comb. nov. (=Katodinium rotundatum (Lohmann) Loeblich)

inferredcites →https://doi.org/10.2216/i0031-8884-41-1-22.1openalex-snapshot

Diel changes in pyrenoid and starch reserves in dinoflagellates

inferredcites →https://doi.org/10.2216/i0031-8884-41-1-29.1openalex-snapshot

Prorocentrum nux sp. nov. (Dinophyceae), a small planktonic dinoflagellate from the Mediterranean Sea, and discussion of P. nanum and P. pusillum

inferredcites →https://doi.org/10.2216/i0031-8884-43-4-394.1openalex-snapshot

Investigations of body scales in twelve Heterocapsa species (Peridiniales, Dinophyceae), including a new species H. pseudotriquetra sp. nov.

inferredcites →https://doi.org/10.2216/ph09-35.1openalex-snapshot

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

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

inferredcites →https://doi.org/10.3390/md10061360openalex-snapshot

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

inferredcites →https://doi.org/10.3390/md6020039openalex-snapshot

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

inferredcites →https://doi.org/10.3989/scimar.2004.68s165openalex-snapshot

Seasonal patterns in plankton communities in a pluriannual time series at a coastal Mediterranean site (Gulf of Naples): an attempt to discern recurrences and trends

inferredcites →https://doi.org/10.5194/bg-9-4553-2012openalex-snapshot

Diversity of cultured photosynthetic flagellates in the northeast Pacific and Arctic Oceans in summer

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.4591756openalex-extracted

inferred← citeshttps://doi.org/10.1002/9781118500354.ch18openalex-snapshot

Ichthyotoxins

inferred← citeshttps://doi.org/10.1002/9781118994672.ch16openalex-snapshot

Harmful Algal Species Fact Sheets

inferred← citeshttps://doi.org/10.1002/9781118994672.ch16bopenalex-snapshot

Harmful Algal Species Fact Sheet: Amphidomataceae

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/10.1007/978-94-007-6419-4_20openalex-snapshot

Azaspiracid Toxins: Toxicological Profile

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

Azaspiracid Toxins: Toxicological Profile

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/10.1007/s10811-015-0667-5openalex-snapshot

Detection of Azadinium poporum in New Zealand: the use of molecular tools to assist with species isolations

inferred← citeshttps://doi.org/10.1007/s40415-017-0435-7openalex-snapshot

First detection of species of the potentially toxic genus Azadinium (Amphidomataceae, Dinophyceae) in tropical coastal waters of Brazil

inferred← citeshttps://doi.org/10.1016/b978-0-12-811405-6.00013-xopenalex-snapshot

Microalgae and Toxins

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

Structural Diversity of Microalgal Marine Toxins

inferred← citeshttps://doi.org/10.1016/j.ecoenv.2016.01.017openalex-snapshot

Growth and toxin production of Azadinium poporum strains in batch cultures under different nutrient conditions

inferred← citeshttps://doi.org/10.1016/j.ecss.2021.107622openalex-snapshot

Insights into the discrepancy between Azadinium spp. and azaspiracid toxins near strategically important aquaculture operations in the west and southwest of Ireland

inferred← citeshttps://doi.org/10.1016/j.ecss.2025.109416openalex-snapshot

Differential accumulation of dissolved azaspiracids and diarrhetic shellfish toxins in Manila clam (Ruditapes philippinarum): effects of temperature and tissue-specific uptake

inferred← citeshttps://doi.org/10.1016/j.ejop.2026.126182openalex-snapshot

Azadinium fusiforme, a new species of Amphidomataceae from Korean and Japanese coastal waters that lacks azaspiracid production

inferred← citeshttps://doi.org/10.1016/j.fct.2019.04.041openalex-snapshot

Bioaccessibility of lipophilic and hydrophilic marine biotoxins in seafood: An in vitro digestion approach

inferred← citeshttps://doi.org/10.1016/j.hal.2014.04.012openalex-snapshot

Azaspiracid variability of Azadinium poporum (Dinophyceae) from the China Sea

inferred← citeshttps://doi.org/10.1016/j.hal.2015.11.001openalex-snapshot

Azadinium poporum from the Argentine Continental Shelf, Southwestern Atlantic, produces azaspiracid-2 and azaspiracid-2 phosphate

inferred← citeshttps://doi.org/10.1016/j.hal.2016.02.006openalex-snapshot

Morphology, molecular phylogeny and azaspiracid profile of Azadinium poporum (Dinophyceae) from the Gulf of Mexico

inferred← citeshttps://doi.org/10.1016/j.hal.2016.02.012openalex-snapshot

Toxigenic algae and associated phycotoxins in two coastal embayments in the Ebro Delta (NW Mediterranean)

inferred← citeshttps://doi.org/10.1016/j.hal.2016.12.001openalex-snapshot

Amphidoma languida (Amphidomatacea, Dinophyceae) with a novel azaspiracid toxin profile identified as the cause of molluscan contamination at the Atlantic coast of southern Spain

inferred← citeshttps://doi.org/10.1016/j.hal.2017.05.001openalex-snapshot

Adding new pieces to the Azadinium (Dinophyceae) diversity and biogeography puzzle: Non-toxigenic Azadinium zhuanum sp. nov. from China, toxigenic A. poporum from the Mediterranean, and a non-toxigenic A. dalianense from the French Atlantic

inferred← citeshttps://doi.org/10.1016/j.hal.2017.08.004openalex-snapshot

Identification of Azadinium species and a new azaspiracid from Azadinium poporum in Puget Sound, Washington State, USA

inferred← citeshttps://doi.org/10.1016/j.hal.2018.08.003openalex-snapshot

Sympatric occurrence of two Azadinium poporum ribotypes in the Eastern Mediterranean Sea

inferred← citeshttps://doi.org/10.1016/j.hal.2018.11.005openalex-snapshot

Role of temperature and nutrients on the growth and toxin production of Prorocentrum hoffmannianum (Dinophyceae) from the Florida Keys

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.hal.2019.101629openalex-snapshot

Variability and profiles of lipophilic toxins in bivalves from Great Britain during five and a half years of monitoring: azaspiracids and yessotoxins

inferred← citeshttps://doi.org/10.1016/j.hal.2019.101637openalex-snapshot

Occurrence and distribution of Amphidomataceae (Dinophyceae) in Danish coastal waters of the North Sea, the Limfjord and the Kattegat/Belt area

inferred← citeshttps://doi.org/10.1016/j.hal.2019.101665openalex-snapshot

The effect of temperature and salinity on growth rate and azaspiracid cell quotas in two strains of Azadinium poporum (Dinophyceae) from Puget Sound, Washington State

inferred← citeshttps://doi.org/10.1016/j.hal.2020.101843openalex-snapshot

Toxic marine microalgae and noxious blooms in the Mediterranean Sea: A contribution to the Global HAB Status Report

inferred← citeshttps://doi.org/10.1016/j.hal.2020.101874openalex-snapshot

Temporal and spatial distribution of Azadinium species in the inland and coastal waters of the Pacific northwest in 2014–2018

inferred← citeshttps://doi.org/10.1016/j.hal.2021.101976openalex-snapshot

Diversity and regional distribution of harmful algal events along the Atlantic margin of Europe

inferred← citeshttps://doi.org/10.1016/j.hal.2021.102066openalex-snapshot

Molecular characterization of harmful algal blooms in the Bohai Sea using metabarcoding analysis

inferred← citeshttps://doi.org/10.1016/j.hal.2021.102077openalex-snapshot

Diverse harmful microalgal community assemblages in the Johor Strait and the environmental effects on its community dynamics

inferred← citeshttps://doi.org/10.1016/j.hal.2023.102404openalex-snapshot

Metabarcoding revealed a high diversity of Amphidomataceae (Dinophyceae) and the seasonal distribution of their toxigenic species in the Taiwan Strait

inferred← citeshttps://doi.org/10.1016/j.hal.2023.102471openalex-snapshot

Production of the dinoflagellate Amphidoma languida in a large scale photobioreactor and structure elucidation of its main metabolite AZA-39

inferred← citeshttps://doi.org/10.1016/j.hal.2023.102560openalex-snapshot

Marine phycotoxin levels in shellfish—14 years of data gathered along the Italian coast

inferred← citeshttps://doi.org/10.1016/j.hal.2024.102701openalex-snapshot

Phylogeny and ultrastructure of a non-toxigenic dinoflagellate Amphidoma fulgens sp. nov. (Amphidomataceae, Dinophyceae), with a wide distribution across Asian Pacific

inferred← citeshttps://doi.org/10.1016/j.hal.2025.102969openalex-snapshot

Diversity of amphidomatacean dinoflagellates in Japan, with a description of Azadinium inconspicuum sp. nov. and azaspiracid components in Azadinium poporum ribotypes

inferred← citeshttps://doi.org/10.1016/j.hal.2026.103103openalex-snapshot

Unlocking species and subspecies diversity of harmful microalgae using HiFi long-read metabarcoding: insights from Amphidomataceae (Dinophyceae) in the China Sea

inferred← citeshttps://doi.org/10.1016/j.hal.2026.103196openalex-snapshot

Intracellular ultrastructural characterization of Azadinium and Amphidoma (Amphidomataceae, Dinophyceae), including toxigenic and non-toxigenic strains

inferred← citeshttps://doi.org/10.1016/j.jchromb.2024.124065openalex-snapshot

New azaspiracid analogues detected as bi-charged ions in Azadinium poporum (Amphidomataceae, Dinophyceae) isolated from Japanese coastal waters

inferred← citeshttps://doi.org/10.1016/j.marenvres.2020.104891openalex-snapshot

Distribution and potential toxicity of benthic harmful dinoflagellates in waters of Florida Bay and the Florida Keys

inferred← citeshttps://doi.org/10.1016/j.protis.2014.04.004openalex-snapshot

Morphological and Molecular Characterization of Three New Azadinium Species (Amphidomataceae, Dinophyceae) from the Irminger Sea

inferred← citeshttps://doi.org/10.1016/j.toxicon.2015.10.002openalex-snapshot

Two-year study of lipophilic marine toxin profile in mussels of the North-central Adriatic Sea: First report of azaspiracids in Mediterranean seafood

inferred← citeshttps://doi.org/10.1016/j.toxicon.2017.07.025openalex-snapshot

Presence of azaspiracids in bivalve molluscs from Northern Spain

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.toxicon.2022.09.002openalex-snapshot

Development of harmful algal blooms species responsible for lipophilic and amnesic shellfish poisoning intoxications in southwestern Mediterranean coastal waters

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/s1755267215001128openalex-snapshot

First records of Amphidoma languida and Azadinium dexteroporum (Amphidomataceae, Dinophyceae) from the Irminger Sea off Iceland

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/10.1071/mf19124openalex-snapshot

Field observations of the dinoflagellate genus Azadinium and azaspiracid toxins in the south-west Atlantic Ocean

inferred← citeshttps://doi.org/10.1080/00318884.2019.1670013openalex-snapshot

Amphidomataceae (Dinophyceae) in the western Greenland area, including description of Azadinium perforatum sp. nov.

inferred← citeshttps://doi.org/10.1080/00318884.2023.2204681openalex-snapshot

A new small thecate dinoflagellate Azadinium anteroporum sp. nov . (Amphidomataceae, Dinophyceae) isolated from the Asian Pacific

inferred← citeshttps://doi.org/10.1080/17451000.2013.866252openalex-snapshot

Azadinium caudatumvar.margalefii, a poorly known member of the toxigenic genusAzadinium(Dinophyceae)

inferred← citeshttps://doi.org/10.1093/plankt/fbag029openalex-snapshot

Molecular detections of 14 amphidomatacean species (Dinophyceae) and their temperature-associated distribution in subarctic waters off eastern Hokkaido, Japan

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/10.1111/1462-2920.13039openalex-snapshot

Global patterns of pelagic dinoflagellate diversity across protist size classes unveiled by metabarcoding

inferred← citeshttps://doi.org/10.1111/jpy.12464openalex-snapshot

Ostreopsis fattorussoisp. nov. (Dinophyceae), a new benthic toxicOstreopsisspecies from the eastern Mediterranean Sea

inferred← citeshttps://doi.org/10.1111/maec.12758openalex-snapshot

Metabarcoding reveals marked seasonality and a distinctive winter assemblage of dinoflagellates at a coastal LTER site in the Gulf of Naples

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/10.1111/pre.12448openalex-snapshot

Morphological and molecular characterization of multiple new Azadinium strains revealed a high diversity of non‐toxigenic species of Amphidomataceae (Dinophyceae ) including two new Azadinium species in Irish waters, North East Atlantic

inferred← citeshttps://doi.org/10.1111/pre.12455openalex-snapshot

Toxigenic strains of Azadinium poporum (Amphidomataceae, Dinophyceae) from Japan and Vietnam, with first reports of A. poporum (ribotype A) and A. trinitatum in Asian Pacific

inferred← citeshttps://doi.org/10.1111/pre.12567openalex-snapshot

First report of toxigenic Amphidoma languida (Amphidomataceae, Dinophyceae) from the Pacific, with reference to intracellular ultrastructure and azaspiracid compounds

inferred← citeshttps://doi.org/10.1111/pre.70001openalex-snapshot

Diversity of Amphidomataceae (Dinophyceae) in the Black Sea, including description of Amphidoma pontica sp. nov.

inferred← citeshttps://doi.org/10.1201/b16662-26openalex-snapshot

AZA: The Producing Organisms—Biology and Trophic Transfer

inferred← citeshttps://doi.org/10.1371/journal.pone.0235015openalex-snapshot

Distribution and abundance of azaspiracid-producing dinophyte species and their toxins in North Atlantic and North Sea waters in summer 2018

inferred← citeshttps://doi.org/10.2216/13-178.1openalex-snapshot

Azadinium dalianense , a new dinoflagellate species from the Yellow Sea, China

inferred← citeshttps://doi.org/10.3390/appliedchem3010012openalex-snapshot

Metabolomics Approach to Reveal the Effects of Ocean Acidification on the Toxicity of Harmful Microalgae: A Review of the Literature

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/md15120393openalex-snapshot

Biotechnological and Pharmacological Applications of Biotoxins and Other Bioactive Molecules from Dinoflagellates

inferred← citeshttps://doi.org/10.3390/md17100595openalex-snapshot

Biological Effects of the Azaspiracid-Producing Dinoflagellate Azadinium dexteroporum in Mytilus galloprovincialis from the Mediterranean Sea

inferred← citeshttps://doi.org/10.3390/md20040271openalex-snapshot

Phytoplankton Toxins and Their Potential Therapeutic Applications: A Journey toward the Quest for Potent Pharmaceuticals

inferred← citeshttps://doi.org/10.3897/mbmg.5.72371openalex-snapshot

Plankton biodiversity and species co-occurrence based on environmental DNA – a multiple marker study

inferred← citeshttps://doi.org/10.3897/natureconservation.34.30789openalex-snapshot

Time series and beyond: multifaceted plankton research at a marine Mediterranean LTER site

inferred← citeshttps://doi.org/10.5670/oceanog.2018.403openalex-snapshot

Occurrence of Marine Biotoxins and Shellfish Poisoning Events and Their Causative Organisms in Argentine Marine Waters

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