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https://doi.org/10.2139/ssrn.4076676

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inferredcites →https://doi.org/10.1002/(sici)1522-7189(199905/06)7:3<99::aid-nt46>3.0.co;2-lopenalex-extracted
Two analogs of azaspiracid isolated from mussels, Mytilus edulis, involved in human intoxication in Ireland
inferredcites →https://doi.org/10.1002/1522-7189(199911/12)7:6<247::aid-nt68>3.0.co;2-topenalex-extracted
A sensitive and specific determination method for azaspiracids by liquid chromatography mass spectrometry
inferredcites →https://doi.org/10.1002/ange.200351826openalex-extracted
Total Synthesis of the Proposed Azaspiracid‐1 Structure, Part 2: Coupling of the C1–C20, C21–C27, and C28–C40 Fragments and Completion of the Synthesis
inferredcites →https://doi.org/10.1002/anie.200351825openalex-extracted
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.200351826openalex-extracted
Total Synthesis of the Proposed Azaspiracid‐1 Structure, Part 2: Coupling of the C1–C20, C21–C27, and C28–C40 Fragments and Completion of the Synthesis
inferredcites →https://doi.org/10.1007/s00216-010-4161-2openalex-extracted
The preparation of certified calibration solutions for azaspiracid-1, -2, and -3, potent marine biotoxins found in shellfish
inferredcites →https://doi.org/10.1007/s00216-011-4803-zopenalex-extracted
A mussel tissue certified reference material for multiple phycotoxins. Part 2: liquid chromatography–mass spectrometry, sample extraction and quantitation procedures
inferredcites →https://doi.org/10.1007/s00216-014-8250-5openalex-extracted
A mussel (Mytilus edulis) tissue certified reference material for the marine biotoxins azaspiracids
inferredcites →https://doi.org/10.1007/s00216-016-0004-0openalex-extracted
A mussel tissue certified reference material for multiple phycotoxins. Part 4: certification
inferredcites →https://doi.org/10.1007/s00216-020-03133-2openalex-extracted
A mussel tissue certified reference material for multiple phycotoxins. Part 5: profiling by liquid chromatography–high-resolution mass spectrometry
inferredcites →https://doi.org/10.1016/j.chroma.2010.09.020openalex-extracted
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
inferredcites →https://doi.org/10.1016/j.hal.2008.06.003openalex-extracted
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.2012.11.009openalex-extracted
Morphology, phylogeny and azaspiracid profile of Azadinium poporum (Dinophyceae) from the China Sea
inferredcites →https://doi.org/10.1016/j.hal.2014.04.012openalex-extracted
Azaspiracid variability of Azadinium poporum (Dinophyceae) from the China Sea
inferredcites →https://doi.org/10.1016/j.jchromb.2017.07.017openalex-extracted
Selectivity of commercial immunoaffinity columns for modified forms of the mycotoxin 4-deoxynivalenol (DON)
inferredcites →https://doi.org/10.1016/j.snb.2018.02.046openalex-extracted
Detection of azaspiracids in mussels using electrochemical immunosensors for fast screening in monitoring programs
inferredcites →https://doi.org/10.1016/j.toxicon.2007.08.008openalex-extracted
Structural confirmation and occurrence of azaspiracids in Scandinavian brown crabs (Cancer pagurus)
inferredcites →https://doi.org/10.1016/j.toxicon.2008.05.006openalex-extracted
First report on azaspiracid and yessotoxin groups detection in French shellfish
inferredcites →https://doi.org/10.1016/j.toxicon.2009.02.008openalex-extracted
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-extracted
First identification of azaspiracid and spirolides in Mesodesma donacium and Mulinia edulis from Northern Chile
inferredcites →https://doi.org/10.1016/j.toxicon.2009.10.020openalex-extracted
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
inferredcites →https://doi.org/10.1016/j.toxicon.2012.05.007openalex-extracted
New azaspiracids in Amphidomataceae (Dinophyceae)
inferredcites →https://doi.org/10.1016/s0021-9258(19)52451-6openalex-extracted
PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT
inferredcites →https://doi.org/10.1016/s0041-0101(02)00082-xopenalex-extracted
First evidence of an extensive northern European distribution of azaspiracid poisoning (AZP) toxins in shellfish
inferredcites →https://doi.org/10.1016/s0041-0101(03)00105-3openalex-extracted
The first identification of azaspiracids in shellfish from France and Spain
inferredcites →https://doi.org/10.1021/acs.jafc.5b02513openalex-extracted
Development of an ELISA for the Detection of Azaspiracids
inferredcites →https://doi.org/10.1021/acs.jafc.8b00346openalex-extracted
Selective Extraction and Purification of Azaspiracids from Blue Mussels (Mytilus edulis) Using Boric Acid Gel
inferredcites →https://doi.org/10.1021/acs.jafc.8b05652openalex-extracted
A Practical ELISA for Azaspiracids in Shellfish via Development of a New Plate-Coating Antigen
inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00973openalex-extracted
Identification of 21,22-Dehydroazaspiracids in Mussels (Mytilus edulis) and in Vitro Toxicity of Azaspiracid-26
inferredcites →https://doi.org/10.1021/es020246zopenalex-extracted
Geographical, Temporal, and Species Variation of the Polyether Toxins, Azaspiracids, in Shellfish
inferredcites →https://doi.org/10.1021/ja066971hopenalex-extracted
Antibodies with Broad Specificity to Azaspiracids by Use of Synthetic Haptens
inferredcites →https://doi.org/10.1021/ja981413ropenalex-extracted
Azaspiracid, a New Marine Toxin Having Unique Spiro Ring Assemblies, Isolated from Irish Mussels, Mytilus edulis
inferredcites →https://doi.org/10.1021/jf2048788openalex-extracted
Improved Isolation Procedure for Azaspiracids from Shellfish, Structural Elucidation of Azaspiracid-6, and Stability Studies
inferredcites →https://doi.org/10.1080/09670260802578534openalex-extracted
Azadinium spinosumgen. et sp. nov. (Dinophyceae) identified as a primary producer of azaspiracid toxins
inferredcites →https://doi.org/10.1093/jaoac/88.3.761openalex-extracted
Multiresidue Method for Determination of Algal Toxins in Shellfish: Single-Laboratory Validation and Interlaboratory Study
inferredcites →https://doi.org/10.1201/b16662-27openalex-extracted
Azaspiracids: Chemistry, Biosynthesis, Metabolism, and Detection
inferredcites →https://doi.org/10.1271/bbb.65.740openalex-extracted
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-extracted
FIRST DETECTION OF AZASPIRACIDS IN MUSSELS IN NORTH WEST AFRICA
inferredcites →https://doi.org/10.3390/md20080004openalex-extracted
Azaspiracid Shellfish Poisoning: A Review on the Chemistry, Ecology, and Toxicology with an Emphasis on Human Health Impacts
inferredcites →https://doi.org/10.3390/md6020039openalex-extracted
Azaspiracid Shellfish Poisoning: A Review on the Chemistry, Ecology, and Toxicology with an Emphasis on Human Health Impacts
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