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Elucidating the chemical structure of native 1-deoxysphingosine

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

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Ozone-induced dissociation on a modified tandem linear ion-trap: Observations of different reactivity for isomeric lipids
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Structure of plasma sphingadienine
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What points at this work

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

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(1-Deoxy)Ceramides in Bilayers Containing Sphingomyelin and Cholesterol
inferred← citeshttps://doi.org/10.1002/ange.201812698openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.202002459openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201812698openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202002459openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jssc.201700919openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-030-50621-6_6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11914-025-00908-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13361-019-02261-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ab.2016.09.014openalex-snapshot
Advances and unresolved challenges in the structural characterization of isomeric lipids
inferred← citeshttps://doi.org/10.1016/j.atherosclerosis.2024.119091openalex-snapshot
Sphingoid Base Diversity
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inferred← citeshttps://doi.org/10.1016/j.bbalip.2023.159335openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmc.2018.06.031openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cellsig.2020.109890openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.chembiol.2018.10.008openalex-snapshot
High-Throughput Plasma Lipidomics: Detailed Mapping of the Associations with Cardiometabolic Risk Factors
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1-deoxysphingolipids dysregulate membrane properties and cargo trafficking in the early secretory pathway
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(1-Deoxy)ceramides in bilayers containing sphingomyelin and cholesterol
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1-deoxysphingolipids bind to COUP-TF to modulate lymphatic and cardiac cell development
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inferred← citeshttps://doi.org/10.1016/j.plipres.2019.100988openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.plipres.2019.100995openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.trac.2019.03.031openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ymgme.2018.07.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.analchem.7b04091openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.analchem.8b00469openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.2c02019openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41586-020-2609-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.26434/chemrxiv.12094041openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fmolb.2023.1112521openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms22115793openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms22158171openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms23031254openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms26020650openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms26209879openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/medicina57070729openalex-snapshot
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inferred← citeshttps://doi.org/10.5167/uzh-181692openalex-snapshot
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