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Sphingolipid and Glycosphingolipid Metabolic Pathways in the Era of Sphingolipidomics

https://doi.org/10.1021/cr2002917

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

inferredcites →https://doi.org/10.1001/jama.1963.03700230140039openalex-snapshot

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inferredcites →https://doi.org/10.1002/mnfr.200800102openalex-snapshot

Regulation of β‐catenin and connexin‐43 expression: Targets for sphingolipids in colon cancer prevention

inferredcites →https://doi.org/10.1002/pmic.200900708openalex-snapshot

Symbol nomenclature for glycan representation

inferredcites →https://doi.org/10.1002/rcm.1043openalex-snapshot

Observation of different ceramide species from crude cellular extracts by normal‐phase high‐performance liquid chromatography coupled to atmospheric pressure chemical ionization mass spectrometry

inferredcites →https://doi.org/10.1002/rcm.1373openalex-snapshot

Quantitative measurement of different ceramide species from crude cellular extracts by normal‐phase high‐performance liquid chromatography coupled to atmospheric pressure ionization mass spectrometry

inferredcites →https://doi.org/10.1002/rcm.505openalex-snapshot

Comparative analysis of glycosylinositol phosphorylceramides from fungi by electrospray tandem mass spectrometry with low‐energy collision‐induced dissociation of Li + adduct ions

inferredcites →https://doi.org/10.1002/rcm.878openalex-snapshot

Analysis of ceramides in cosmetics by reversed‐phase liquid chromatography/electrospray ionization mass spectrometry with collision‐induced dissociation

inferredcites →https://doi.org/10.1006/bbrc.1995.1827openalex-snapshot

Serine Palmitoyltransferase Is the Primary Target of a Sphingosine-like Immunosuppressant, ISP-1/Myriocin

inferredcites →https://doi.org/10.1006/bbrc.2000.3370openalex-snapshot

Neutral/Alkaline and Acid Ceramidase Activities Are Actively Released by Murine Endothelial Cells

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Glucosylceramide in Humans

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Cancer Treatment Strategies Targeting Sphingolipid Metabolism

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Biosynthesis of Sphingolipids in Plants (and Some of Their Functions)

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Computational Analysis of Sphingolipid Pathway Systems

inferredcites →https://doi.org/10.1007/978-1-4419-6741-1_4openalex-snapshot

Ceramide Synthases: Roles in Cell Physiology and Signaling

inferredcites →https://doi.org/10.1007/978-1-4419-6741-1_5openalex-snapshot

Tales and Mysteries of the Enigmatic Sphingomyelin Synthase Family

inferredcites →https://doi.org/10.1007/978-1-4419-6741-1_8openalex-snapshot

Ceramide-1-Phosphate in Cell Survival and Inflammatory Signaling

inferredcites →https://doi.org/10.1007/978-1-4419-7877-6_14openalex-snapshot

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Acetylation of Sphingosine by PAF-Dependent Transacetylase

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Sphingolipids in Macroautophagy

inferredcites →https://doi.org/10.1007/978-3-540-30880-5_16openalex-snapshot

Kahalalide F and ES285: Potent Anticancer Agents from Marine Molluscs

inferredcites →https://doi.org/10.1007/978-4-431-54240-7_162openalex-snapshot

Map 3: Biosynthetic Pathways of Glycosphingolipids

inferredcites →https://doi.org/10.1007/978-4-431-67877-9openalex-snapshot

Handbook of Glycosyltransferases and Related Genes

inferredcites →https://doi.org/10.1007/978-4-431-67877-9_8openalex-snapshot

GalCer Synthase (Ceramide Galactosyltransferase, CGT)

inferredcites →https://doi.org/10.1007/bf01810681openalex-snapshot

Sulfated glycoconjugate determinants recognized by monoclonal antibody, SG-1, correlate with the experimental metastatic ability of KHT fibrosarcoma cells

inferredcites →https://doi.org/10.1007/bf01919147openalex-snapshot

The presence of free D-serine, D-alanine and D-proline in human plasma

inferredcites →https://doi.org/10.1007/bf02531119openalex-snapshot

Sphingolipid long chain bases

inferredcites →https://doi.org/10.1007/bf02535642openalex-snapshot

Differences in the long chain (sphingoid) base composition of sphingomyelin from rats bearing Morris hepatoma 7777

inferredcites →https://doi.org/10.1007/bf02854910openalex-snapshot

Brain tissue lipidomics: Direct probing using matrix-assisted laser desorption/ionization mass spectrometry

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Recently discovered functions of glucosylceramides in plants and fungi

inferredcites →https://doi.org/10.1007/s00018-004-4254-1openalex-snapshot

Enzymes of Sphingolipid metabolism in Drosophila melanogaster

inferredcites →https://doi.org/10.1007/s00018-005-5543-zopenalex-snapshot

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inferredcites →https://doi.org/10.1007/s00277-011-1212-5openalex-snapshot

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inferredcites →https://doi.org/10.1007/s00392-004-0146-5openalex-snapshot

P-selectin in arterial thrombosis

inferredcites →https://doi.org/10.1007/s00418-007-0344-0openalex-snapshot

Differential expression of (dihydro)ceramide synthases in mouse brain: oligodendrocyte-specific expression of CerS2/Lass2

inferredcites →https://doi.org/10.1007/s00795-008-0427-6openalex-snapshot

Layer-specific sulfatide localization in rat hippocampus middle molecular layer is revealed by nanoparticle-assisted laser desorption/ionization imaging mass spectrometry

inferredcites →https://doi.org/10.1007/s10147-010-0141-yopenalex-snapshot

Inhibitory effects of dietary glucosylceramides on squamous cell carcinoma of the head and neck in NOD/SCID mice

inferredcites →https://doi.org/10.1007/s10637-010-9529-9openalex-snapshot

A phase I dose-escalating study of ES-285, a marine sphingolipid-derived compound, with repeat dose administration in patients with advanced solid tumors

inferredcites →https://doi.org/10.1007/s10719-008-9215-8openalex-snapshot

Role of very long fatty acid-containing glycosphingolipids in membrane organization and cell signaling: the model of lactosylceramide in neutrophils

inferredcites →https://doi.org/10.1007/s10719-011-9325-6openalex-snapshot

Systematic analyses of free ceramide species and ceramide species comprising neutral glycosphingolipids by MALDI-TOF MS with high-energy CID

inferredcites →https://doi.org/10.1007/s11064-010-0286-0openalex-snapshot

In Search of a Solution to the Sphinx-Like Riddle of GM1

inferredcites →https://doi.org/10.1007/s11745-009-3316-4openalex-snapshot

Characterization of Mutant Serine Palmitoyltransferase 1 in LY‐B Cells

inferredcites →https://doi.org/10.1007/s11745-010-3417-0openalex-snapshot

Identification of Glucosylceramides Containing Sphingatrienine in Maize and Rice Using Ion Trap Mass Spectrometry

inferredcites →https://doi.org/10.1007/s12017-010-8120-zopenalex-snapshot

Mammalian Neutral Sphingomyelinases: Regulation and Roles in Cell Signaling Responses

inferredcites →https://doi.org/10.1007/s12017-010-8132-8openalex-snapshot

An Introduction to Sphingolipid Metabolism and Analysis by New Technologies

inferredcites →https://doi.org/10.1007/s12035-008-8022-3openalex-snapshot

The Role and Metabolism of Sulfatide in the Nervous System

inferredcites →https://doi.org/10.1007/s13361-011-0117-9openalex-snapshot

Electron Transfer Dissociation of Milk Oligosaccharides

inferredcites →https://doi.org/10.1016/0003-9861(84)90069-9openalex-snapshot

Enzymology of long-chain base synthesis by liver: Characterization of serine palmitoyltransferase in rat liver microsomes

inferredcites →https://doi.org/10.1016/0005-2736(81)90512-5openalex-snapshot

Exfoliation of membrane ecto-enzymes in the form of micro-vesicles

inferredcites →https://doi.org/10.1016/0005-2760(68)90187-2openalex-snapshot

Metabolism of sphingomyelin in the intestinal tract of the rat

inferredcites →https://doi.org/10.1016/0005-2760(69)90138-6openalex-snapshot

Metabolism of cerebroside in the intestinal tract of the rat

inferredcites →https://doi.org/10.1016/0005-2760(85)90210-3openalex-snapshot

The synthesis of sphingomyelin in the Morris hepatomas 7777 and 5123D is restricted to the plasma membrane

inferredcites →https://doi.org/10.1016/0005-2760(89)90142-2openalex-snapshot

Structural and compositional difference in the neutral glycolipids between epithelial and non-epithelial tissue of the mouse small intestine

inferredcites →https://doi.org/10.1016/0006-291x(89)91827-5openalex-snapshot

Enzymatic synthesis of N,N-dimethyl-sphingosine: Demonstration of the sphingosine: N-methyltransferase in mouse brain

inferredcites →https://doi.org/10.1016/0009-3084(70)90008-3openalex-snapshot

On the chemistry and occurrence of sphingolipid long-chain bases

inferredcites →https://doi.org/10.1016/0009-3084(76)90032-3openalex-snapshot

Fatty acids and long-chain bases of gangliosides of human gastrointestinal mucosa

inferredcites →https://doi.org/10.1016/0009-3084(91)90033-8openalex-snapshot

Aggregation properties of GD1b, II3Neu5Ac2GgOse4Cer, and of GD1b-lactone, II3[α-Neu5Ac-(2→8, 1→9)-α-Neu5Ac]GgOse4Cer, in aqueous solution

inferredcites →https://doi.org/10.1016/0014-5793(90)80659-7openalex-snapshot

Sphingomyelin is synthesized in the cis Golgi

inferredcites →https://doi.org/10.1016/0014-5793(92)80769-dopenalex-snapshot

Modulation of cell growth and differentiation by ceramide

inferredcites →https://doi.org/10.1016/0014-5793(94)80591-1openalex-snapshot

Lactosylceramide is synthesized in the lumen of the Golgi apparatus

inferredcites →https://doi.org/10.1016/0304-3835(91)90155-bopenalex-snapshot

Distinctive glycolipid patterns in Wilms' tumor and renal cell carcinoma

inferredcites →https://doi.org/10.1016/0378-1119(96)00309-5openalex-snapshot

Sphingolipid synthesis: Identification and characterization of mammalian cDNAs encoding the Lcb2 subunit of serine palmitoyltransferase

inferredcites →https://doi.org/10.1016/0962-8924(96)10021-0openalex-snapshot

Fumonisins: fungal toxins that shed light on sphingolipid function

inferredcites →https://doi.org/10.1016/j.ab.2004.11.003openalex-snapshot

Isolation and mass spectrometry characterization of molecular species of lactosylceramides using liquid chromatography-electrospray ion trap mass spectrometry

inferredcites →https://doi.org/10.1016/j.ab.2010.01.033openalex-snapshot

Quantitation of ceramide phosphorylethanolamines containing saturated and unsaturated sphingoid base cores

inferredcites →https://doi.org/10.1016/j.aca.2009.02.051openalex-snapshot

MALDI mass spectrometry imaging of gangliosides in mouse brain using ionic liquid matrix

inferredcites →https://doi.org/10.1016/j.advenzreg.2009.10.024openalex-snapshot

Sphingosine 1-phosphate lyase, a key regulator of sphingosine 1-phosphate signaling and function

inferredcites →https://doi.org/10.1016/j.advenzreg.2010.09.016openalex-snapshot

The neutral sphingomyelinase family: Identifying biochemical connections

inferredcites →https://doi.org/10.1016/j.ajhg.2010.09.010openalex-snapshot

Mutations in the SPTLC2 Subunit of Serine Palmitoyltransferase Cause Hereditary Sensory and Autonomic Neuropathy Type I

inferredcites →https://doi.org/10.1016/j.bbagen.2007.08.010openalex-snapshot

The Yin and Yang of lactosylceramide metabolism: Implications in cell function

inferredcites →https://doi.org/10.1016/j.bbagen.2007.09.001openalex-snapshot

Lysenin: A sphingomyelin specific pore-forming toxin

inferredcites →https://doi.org/10.1016/j.bbagen.2007.10.016openalex-snapshot

The medium is the message: Glycosphingolipids and their soluble analogues

inferredcites →https://doi.org/10.1016/j.bbalip.2005.08.006openalex-snapshot

Serine palmitoyl-CoA transferase (SPT) deficiency and sphingolipid levels in mice

inferredcites →https://doi.org/10.1016/j.bbalip.2006.02.021openalex-snapshot

Distribution of cholesterol and galactosylceramide in rat cerebellar white matter

inferredcites →https://doi.org/10.1016/j.bbalip.2006.03.007openalex-snapshot

Alkaline sphingomyelinase: An old enzyme with novel implications

inferredcites →https://doi.org/10.1016/j.bbalip.2006.04.010openalex-snapshot

Sphingolipids of the nucleus and their role in nuclear signaling

inferredcites →https://doi.org/10.1016/j.bbalip.2007.01.009openalex-snapshot

CERT and intracellular trafficking of ceramide

inferredcites →https://doi.org/10.1016/j.bbalip.2007.01.011openalex-snapshot

Glycolipid transfer proteins

inferredcites →https://doi.org/10.1016/j.bbalip.2008.05.005openalex-snapshot

Sphingosine-1-phosphate lyase in development and disease: Sphingolipid metabolism takes flight

inferredcites →https://doi.org/10.1016/j.bbalip.2008.06.002openalex-snapshot

Ceramidases: regulators of cellular responses mediated by ceramide, sphingosine, and sphingosine-1-phosphate

inferredcites →https://doi.org/10.1016/j.bbalip.2009.02.011openalex-snapshot

Export and functions of sphingosine-1-phosphate

inferredcites →https://doi.org/10.1016/j.bbalip.2009.03.016openalex-snapshot

Serine palmitoyltransferase subunit 1 is present in the endoplasmic reticulum, nucleus and focal adhesions, and functions in cell morphology

inferredcites →https://doi.org/10.1016/j.bbalip.2010.01.010openalex-snapshot

Multi-dimensional mass spectrometry-based shotgun lipidomics and the altered lipids at the mild cognitive impairment stage of Alzheimer's disease

inferredcites →https://doi.org/10.1016/j.bbalip.2010.11.003openalex-snapshot

Sphingolipid profiling of human plasma and FPLC-separated lipoprotein fractions by hydrophilic interaction chromatography tandem mass spectrometry

inferredcites →https://doi.org/10.1016/j.bbalip.2011.03.004openalex-snapshot

Imaging mass spectrometry for lipidomics

inferredcites →https://doi.org/10.1016/j.bbalip.2011.06.027openalex-snapshot

Analysis of mammalian sphingolipids by liquid chromatography tandem mass spectrometry (LC-MS/MS) and tissue imaging mass spectrometry (TIMS)

inferredcites →https://doi.org/10.1016/j.bbamcr.2003.10.002openalex-snapshot

Cycloserine and threo-dihydrosphingosine inhibit TNF-α-induced cytotoxicity: evidence for the importance of de novo ceramide synthesis in TNF-α signaling

inferredcites →https://doi.org/10.1016/j.bbamcr.2008.09.020openalex-snapshot

Principles of lysosomal membrane degradation

inferredcites →https://doi.org/10.1016/j.bbamcr.2009.04.006openalex-snapshot

Ceramide synthase 1 is regulated by proteasomal mediated turnover

inferredcites →https://doi.org/10.1016/j.bbamem.2006.05.011openalex-snapshot

Ceramide 1-phosphate/ceramide, a switch between life and death

inferredcites →https://doi.org/10.1016/j.bbamem.2006.08.009openalex-snapshot

Ceramides and other bioactive sphingolipid backbones in health and disease: Lipidomic analysis, metabolism and roles in membrane structure, dynamics, signaling and autophagy

inferredcites →https://doi.org/10.1016/j.bbamem.2006.08.012openalex-snapshot

Glycosphingolipids and drug resistance

inferredcites →https://doi.org/10.1016/j.bbamem.2006.09.011openalex-snapshot

Biophysics of sphingolipids I. Membrane properties of sphingosine, ceramides and other simple sphingolipids

inferredcites →https://doi.org/10.1016/j.bbamem.2006.09.026openalex-snapshot

Lysophospholipid receptors: Signalling, pharmacology and regulation by lysophospholipid metabolism

inferredcites →https://doi.org/10.1016/j.bbamem.2007.05.007openalex-snapshot

Effect of ceramide N-acyl chain and polar headgroup structure on the properties of ordered lipid domains (lipid rafts)

inferredcites →https://doi.org/10.1016/j.bbamem.2008.09.002openalex-snapshot

Effects of ceramide and other simple sphingolipids on membrane lateral structure

inferredcites →https://doi.org/10.1016/j.bbamem.2008.11.010openalex-snapshot

How the molecular features of glycosphingolipids affect domain formation in fluid membranes

inferredcites →https://doi.org/10.1016/j.bbapap.2011.02.005openalex-snapshot

Mechanistic enzymology of serine palmitoyltransferase

inferredcites →https://doi.org/10.1016/j.bbrc.2009.01.075openalex-snapshot

A lipid binding domain in sphingosine kinase 2

inferredcites →https://doi.org/10.1016/j.bbrc.2009.11.035openalex-snapshot

Increased ceramide synthase 2 and 6 mRNA levels in breast cancer tissues and correlation with sphingosine kinase expression

inferredcites →https://doi.org/10.1016/j.bcp.2010.08.012openalex-snapshot

Activation of ceramide synthase 6 by celecoxib leads to a selective induction of C16:0-ceramide

inferredcites →https://doi.org/10.1016/j.bcp.2010.12.002openalex-snapshot

Cis-4-methylsphingosine is a sphingosine-1-phosphate receptor modulator

inferredcites →https://doi.org/10.1016/j.biochi.2006.10.014openalex-snapshot

Exosome lipidomics unravels lipid sorting at the level of multivesicular bodies

inferredcites →https://doi.org/10.1016/j.biochi.2007.07.001openalex-snapshot

Myristic acid increases the activity of dihydroceramide Δ4-desaturase 1 through its N-terminal myristoylation

inferredcites →https://doi.org/10.1016/j.biomaterials.2007.09.037openalex-snapshot

Thermoresponsive and biodegradable linear-dendritic nanoparticles for targeted and sustained release of a pro-apoptotic drug

inferredcites →https://doi.org/10.1016/j.canlet.2003.08.034openalex-snapshot

Ceramide synthesis and metabolism as a target for cancer therapy

inferredcites →https://doi.org/10.1016/j.canlet.2006.10.026openalex-snapshot

Anticancer activity of a ceramide analog containing a disulfide linkage

inferredcites →https://doi.org/10.1016/j.canlet.2007.06.003openalex-snapshot

Clinical relevance of ceramide metabolism in the pathogenesis of human head and neck squamous cell carcinoma (HNSCC): Attenuation of C18-ceramide in HNSCC tumors correlates with lymphovascular invasion and nodal metastasis

inferredcites →https://doi.org/10.1016/j.carres.2009.03.001openalex-snapshot

Comprehensive analysis of glycosyltransferases in eukaryotic genomes for structural and functional characterization of glycans

inferredcites →https://doi.org/10.1016/j.carres.2010.02.006openalex-snapshot

Enzymatic synthesis of Gb3 and iGb3 ceramides

inferredcites →https://doi.org/10.1016/j.cbi.2009.04.012openalex-snapshot

Transport of lipids by ABC proteins: Interactions and implications for cellular toxicity, viability and function

inferredcites →https://doi.org/10.1016/j.cellsig.2007.12.006openalex-snapshot

The sphingolipid salvage pathway in ceramide metabolism and signaling

inferredcites →https://doi.org/10.1016/j.cellsig.2010.04.006openalex-snapshot

Ceramide synthases 2, 5, and 6 confer distinct roles in radiation-induced apoptosis in HeLa cells

inferredcites →https://doi.org/10.1016/j.cellsig.2010.08.001openalex-snapshot

Activation of mTOR and RhoA is a major mechanism by which ceramide 1-phosphate stimulates macrophage proliferation

inferredcites →https://doi.org/10.1016/j.cellsig.2010.11.012openalex-snapshot

Ceramide kinase: The first decade

inferredcites →https://doi.org/10.1016/j.chemphyslip.2011.04.013openalex-snapshot

A view on sphingolipids and disease

inferredcites →https://doi.org/10.1016/j.chroma.2005.08.016openalex-snapshot

High performance liquid chromatography-tandem mass spectrometry of phospholipid molecular species in eggs from hens fed diets enriched in seal blubber oil

inferredcites →https://doi.org/10.1016/j.chroma.2007.01.108openalex-snapshot

Liquid chromatography with dual parallel mass spectrometry and 31P nuclear magnetic resonance spectroscopy for analysis of sphingomyelin and dihydrosphingomyelin

inferredcites →https://doi.org/10.1016/j.ejphar.2008.02.011openalex-snapshot

Spisulosine (ES-285) induces prostate tumor PC-3 and LNCaP cell death by de novo synthesis of ceramide and PKCζ activation

inferredcites →https://doi.org/10.1016/j.febslet.2004.08.060openalex-snapshot

Identification of an essential sequence for dihydroceramide C‐4 hydroxylase activity of mouse DES2

inferredcites →https://doi.org/10.1016/j.febslet.2006.08.039openalex-snapshot

Epidermal sphingolipids: Metabolism, function, and roles in skin disorders

inferredcites →https://doi.org/10.1016/j.febslet.2007.10.018openalex-snapshot

Kinetic characterization of mammalian ceramide synthases: Determination of K m values towards sphinganine

inferredcites →https://doi.org/10.1016/j.febslet.2009.06.048openalex-snapshot

Activity of plasma membrane β‐galactosidase and β‐glucosidase

inferredcites →https://doi.org/10.1016/j.febslet.2009.10.021openalex-snapshot

Lysosomal degradation of membrane lipids

inferredcites →https://doi.org/10.1016/j.febslet.2009.10.043openalex-snapshot

Significance of glycosphingolipid fatty acid chain length on membrane microdomain‐mediated signal transduction

inferredcites →https://doi.org/10.1016/j.febslet.2009.10.058openalex-snapshot

Sphingomyelin metabolism at the plasma membrane: Implications for bioactive sphingolipids

inferredcites →https://doi.org/10.1016/j.febslet.2009.11.019openalex-snapshot

Altered sphingolipid metabolism induced by tumor hypoxia – New vistas in glycolipid tumor markers

inferredcites →https://doi.org/10.1016/j.febslet.2009.11.020openalex-snapshot

Fine tuning of cell functions through remodeling of glycosphingolipids by plasma membrane‐associated glycohydrolases

inferredcites →https://doi.org/10.1016/j.febslet.2009.11.074openalex-snapshot

Participation of galactosylceramide and sulfatide in glycosynapses between oligodendrocyte or myelin membranes

inferredcites →https://doi.org/10.1016/j.febslet.2009.11.083openalex-snapshot

Acid sphingomyelinase, cell membranes and human disease: Lessons from Niemann–Pick disease

inferredcites →https://doi.org/10.1016/j.febslet.2009.11.089openalex-snapshot

Globotriaosyl ceramide receptor function – Where membrane structure and pathology intersect

inferredcites →https://doi.org/10.1016/j.febslet.2009.12.032openalex-snapshot

Very long chain sphingolipids: Tissue expression, function and synthesis

inferredcites →https://doi.org/10.1016/j.ijms.2008.04.005openalex-snapshot

A minimalist approach to MALDI imaging of glycerophospholipids and sphingolipids in rat brain sections

inferredcites →https://doi.org/10.1016/j.immuni.2007.05.022openalex-snapshot

Toll-like Receptor 4 Is a Sensor for Autophagy Associated with Innate Immunity

inferredcites →https://doi.org/10.1016/j.jasms.2005.02.001openalex-snapshot

Structural characterization of the GM1 ganglioside by infrared multiphoton dissociation, electron capture dissociation, and electron detachment dissociation electrospray ionization FT-ICR MS/MS

inferredcites →https://doi.org/10.1016/j.jasms.2005.05.003openalex-snapshot

Ganglioside analysis by thin-layer chromatography matrix-assisted laser desorption/ionization orthogonal time-of-flight mass spectrometry

inferredcites →https://doi.org/10.1016/j.jasms.2007.12.003openalex-snapshot

Desorption electrospray ionization (DESI) mass spectrometry and tandem mass spectrometry (MS/MS) of phospholipids and sphingolipids: Ionization, adduct formation, and fragmentation

inferredcites →https://doi.org/10.1016/j.jasms.2008.04.017openalex-snapshot

UV-MALDI mass spectrometry analysis of NBD-glycosphingolipids without an external matrix

inferredcites →https://doi.org/10.1016/j.jasms.2010.08.002openalex-snapshot

The detection of glycosphingolipids in brain tissue sections by imaging mass spectrometry using gold nanoparticles

inferredcites →https://doi.org/10.1016/j.jbi.2010.03.006openalex-snapshot

Drug target identification in sphingolipid metabolism by computational systems biology tools: Metabolic control analysis and metabolic pathway analysis

inferredcites →https://doi.org/10.1016/j.jchromb.2006.06.025openalex-snapshot

Liquid chromatography–tandem mass spectrometric determination of ceramides and related lipid species in cellular extracts

inferredcites →https://doi.org/10.1016/j.jchromb.2006.07.022openalex-snapshot

Determination of d-serine and related neuroactive amino acids in human plasma by high-performance liquid chromatography with fluorimetric detection

inferredcites →https://doi.org/10.1016/j.jchromb.2007.02.030openalex-snapshot

Separation and mass spectrometric characterization of covalently bound skin ceramides using LC/APCI-MS and Nano-ESI-MS/MS

inferredcites →https://doi.org/10.1016/j.jchromb.2008.06.001openalex-snapshot

High-sensitivity analysis of glycosphingolipids by matrix-assisted laser desorption/ionization quadrupole ion trap time-of-flight imaging mass spectrometry on transfer membranes

inferredcites →https://doi.org/10.1016/j.jchromb.2008.12.057openalex-snapshot

Sphingolipidomics: Methods for the comprehensive analysis of sphingolipids

inferredcites →https://doi.org/10.1016/j.jchromb.2009.02.037openalex-snapshot

High-throughput shotgun lipidomics by quadrupole time-of-flight mass spectrometry

inferredcites →https://doi.org/10.1016/j.jchromb.2009.07.008openalex-snapshot

Normal phase liquid chromatography coupled to quadrupole time of flight atmospheric pressure chemical ionization mass spectrometry for separation, detection and mass spectrometric profiling of neutral sphingolipids and cholesterol

inferredcites →https://doi.org/10.1016/j.jdermsci.2009.04.006openalex-snapshot

A possible mechanism underlying the ceramide deficiency in atopic dermatitis: Expression of a deacylase enzyme that cleaves the N-acyl linkage of sphingomyelin and glucosylceramide

inferredcites →https://doi.org/10.1016/j.jmb.2007.04.086openalex-snapshot

The Structure of Serine Palmitoyltransferase; Gateway to Sphingolipid Biosynthesis

inferredcites →https://doi.org/10.1016/j.jnutbio.2010.09.017openalex-snapshot

Suppression of intestinal inflammation and inflammation-driven colon cancer in mice by dietary sphingomyelin: importance of peroxisome proliferator-activated receptor γ expression

inferredcites →https://doi.org/10.1016/j.jtbi.2003.08.010openalex-snapshot

Integration of kinetic information on yeast sphingolipid metabolism in dynamical pathway models

inferredcites →https://doi.org/10.1016/j.mito.2006.03.002openalex-snapshot

Ceramide forms channels in mitochondrial outer membranes at physiologically relevant concentrations

inferredcites →https://doi.org/10.1016/j.molmed.2008.06.002openalex-snapshot

Sialic acids in human health and disease

inferredcites →https://doi.org/10.1016/j.molmed.2011.03.002openalex-snapshot

Translational aspects of sphingosine 1-phosphate biology

inferredcites →https://doi.org/10.1016/j.plipres.2007.11.001openalex-snapshot

The multi-functional role of sphingosylphosphorylcholine

inferredcites →https://doi.org/10.1016/j.plipres.2010.02.004openalex-snapshot

Control of metabolism and signaling of simple bioactive sphingolipids: Implications in disease

inferredcites →https://doi.org/10.1016/j.plipres.2010.10.006openalex-snapshot

Group XV phospholipase A2, a lysosomal phospholipase A2

inferredcites →https://doi.org/10.1016/j.prostaglandins.2004.09.010openalex-snapshot

Sphingosine kinases, sphingosine-1-phosphate and sphingolipidomics

inferredcites →https://doi.org/10.1016/j.sbi.2009.06.001openalex-snapshot

Gangliosides in cell recognition and membrane protein regulation

inferredcites →https://doi.org/10.1016/j.sbi.2009.06.003openalex-snapshot

Sialic acids as regulators of molecular and cellular interactions

inferredcites →https://doi.org/10.1016/j.semcdb.2004.03.007openalex-snapshot

The cell biology of glycosphingolipids

inferredcites →https://doi.org/10.1016/j.smim.2009.10.003openalex-snapshot

Lipid and glycolipid antigens of CD1d-restricted natural killer T cells

inferredcites →https://doi.org/10.1016/j.tcb.2005.04.006openalex-snapshot

The ins and outs of sphingolipid synthesis

inferredcites →https://doi.org/10.1016/j.tcb.2010.09.009openalex-snapshot

Autophagy: a broad role in unconventional protein secretion?

inferredcites →https://doi.org/10.1016/j.tibs.2007.09.004openalex-snapshot

(Glyco)sphingolipidology: an amazing challenge and opportunity for systems biology

inferredcites →https://doi.org/10.1016/j.tox.2004.05.001openalex-snapshot

d-Serine-induced nephrotoxicity: possible interaction with tyrosine metabolism

inferredcites →https://doi.org/10.1016/j.tox.2006.02.012openalex-snapshot

The role of tumor necrosis factor α and the peroxisome proliferator-activated receptor α in modulating the effects of fumonisin in mouse liver

inferredcites →https://doi.org/10.1016/j.yexcr.2009.09.027openalex-snapshot

Stress-induced ER to Golgi translocation of ceramide synthase 1 is dependent on proteasomal processing

showing the first 200 of 624

What points at this work

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

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A Sphingolipid-mTORC1 Nutrient-Sensing Machinery Enables Animal Development by Suppression of the Intestinal Peroxisome Relocation, Hormone Secretion and the Gut-Brain Crosstalk

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(1-Deoxy)Ceramides in Bilayers Containing Sphingomyelin and Cholesterol

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NuclearDrosophilaCerS Schlank regulates lipid homeostasis via the homeodomain, independent of the lag1p motif

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The role of sphingolipids in endoplasmic reticulum stress

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Organization of gangliosides into membrane nanodomains

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In situ glucosylceramide synthesis and its pharmacological inhibition analysed in cells by 13C5‐sphingosine precursor feeding and mass spectrometry

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Sphingolipid metabolism in the development and progression of cancer: one cancer's help is another's hindrance

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The structure of gangliosides hides a code for determining neuronal functions

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Cross‐talk between CFTR and sphingolipids in cystic fibrosis

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Cis ‐unsaturated sphingolipids support growth of sphingoid base‐deficient yeast but impair plasma membrane integrity

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Animal Glycolipids

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Lysosomal Storage Diseases. For Better or Worse: Adapting to Defective Lysosomal Glycosphingolipid Breakdown

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Polyketides

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SYNTHESIS OF GLYCOSPHINGOLIPIDS

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Bioinformatics in Lipidomics

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Fragmentation Patterns of Sphingolipids

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Sphingolipid α‐Hydroxylase ( Scs7p )

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Enzyme Technology for Detoxification of Mycotoxins in Animal Feed

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Microbial Lipidomics

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Phospholipid Remodeling and Tri‐Layer Membrane Reconstruction Mediate Cognitive Effects of Humanized Milk Fat Globules in Neonatal Rats

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A FRET Probe for Cell‐Based Imaging of Ganglioside‐Processing Enzyme Activity and High‐Throughput Screening

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Quantitative Screening of Cell‐Surface Gangliosides by Nondestructive Extraction and Hydrophobic Collection

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Unterscheidung von isomeren Sphingolipiden mittels kryogener Infrarotspektroskopie

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Detection of Bacterial Neutral Ceramidase in Diabetic Foot Ulcers with an Optimized Substrate and Chemoenzymatic Probes

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Strukturrevision von Halisphingosin A durch Totalsynthese und Bioaktivitätsstudien

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Sugar Auxiliary Group Assisted Diversity‐Oriented Enzymatic Modular Synthesis of 0‐Series Ganglioside Glycans

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A FRET Probe for Cell‐Based Imaging of Ganglioside‐Processing Enzyme Activity and High‐Throughput Screening

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Quantitative Screening of Cell‐Surface Gangliosides by Nondestructive Extraction and Hydrophobic Collection

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Resolving Sphingolipid Isomers Using Cryogenic Infrared Spectroscopy

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Detection of Bacterial Neutral Ceramidase in Diabetic Foot Ulcers with an Optimized Substrate and Chemoenzymatic Probes

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Structure Revision of Halisphingosine A via Total Synthesis and Bioactivity Studies

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Sugar Auxiliary Group Assisted Diversity‐Oriented Enzymatic Modular Synthesis of 0‐Series Ganglioside Glycans

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The Marine Starfish Acanthaster planci : Secondary Metabolites and Pharmacological Activities

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Organic Fluorophores for Studying Lipid Membrane Structures and Dynamics

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Metabolic channeling of lipids via the contact zones between different organelles

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Cellular Metabolomics Reveals Hepatoprotective Mechanisms of Platycoside Metabolites Against Acetaminophen‐Induced Liver Injury

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Species‐Specific Activity of Glycolipid Ligands for Invariant NKT Cells

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C‐Glycosphingolipids with an exo‐Methylene Substituent: Stereocontrolled Synthesis and Immunostimulation of Mouse and Human Natural Killer T Lymphocytes

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Thermodynamic and Structural Behavior of α‐Galactosylceramide and C6‐Functionalized α‐GalCer in 2D Layers at the Air–Liquid Interface

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Ketodeoxynonulosonic Acid Hydroxylase (Kdnase) Assisted Site‐Specific Enzymatic α2,6‐Sialylation

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Identification of novel glycolipid ligands activating a sulfatide‐reactive, CD1d‐restricted, type II natural killer T lymphocyte

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A personal journey with bioactive lipids

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Integral Membrane Fatty Acid Desaturases: A Review of Biochemical, Structural, and Biotechnological Advances

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Glycosphingolipidomics of donkey milk by hydrophilic interaction liquid chromatography coupled to ESI and multistage MS

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iso‐Fatty Acid Metabolism in Caenorhabditis elegans’ Ceramide Biosynthesis

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Lysosphingolipid Quantitation in Plasma and Dried‐Blood Spots Using Targeted High‐Resolution Mass Spectrometry

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The role of sphingosine 1 phosphate in coronary artery disease and ischemia reperfusion injury

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Quantitative Lipid Analysis of Extracellular Vesicle Preparations: A Perspective

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Sphingolipids role in the regulation of inflammatory response: From leukocyte biology to bacterial infection

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Perspective on innovative therapies for globoid cell leukodystrophy

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Analysis of carbohydrates and glycoconjugates by matrix‐assisted laser desorption/ionization mass spectrometry: An update for the period 2005–2006

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Analysis of carbohydrates and glycoconjugates by matrix‐assisted laser desorption/ionization mass spectrometry: An update for 2011–2012

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The Role of Cholesterol in α‐Synuclein and Lewy Body Pathology in GBA1 Parkinson's Disease

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A Phase 1B Trial in GBA1 ‐ Associated Parkinson's Disease of BIA‐28‐6156, a Glucocerebrosidase Activator

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A Biomarker Study in Patients with GBA1 ‐Parkinson's Disease and Healthy Controls

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Quantitative metabolic profiling of lipid mediators

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Ursprung und Funktionen der Sphingolipide

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Structural characterization of sphingomyelins from tissue using electron‐induced dissociation

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Minor plasma lipids modulate clotting factor activities and may affect thrombosis risk

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Stochastic simulation algorithms for computational systems biology: Exact, approximate, and hybrid methods

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Isolation and Analysis of Lipid Rafts from Neural Cells and Tissues

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Thin-Layer Chromatography in Structure and Recognition Studies of Shiga Toxin Glycosphingolipid Receptors

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Plasma Lysosphingolipid Biomarker Measurement by Liquid Chromatography Tandem Mass Spectrometry

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Mass Spectrometry of Neutral Glycosphingolipids

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NMR Analysis of Mammalian Glycolipids

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Sphingolipid Analysis in Clinical Research

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Assaying Ceramide Synthase Activity In Vitro and in Living Cells Using Liquid Chromatography-Mass Spectrometry

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Fluorescent Assays for Ceramide Synthase Activity

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Sphingolipid Analysis in Clinical Research

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Methods for Assay of Ganglioside Catabolic Enzymes

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Gangliosides of the Nervous System

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Ganglioside Metabolism and Its Inherited Diseases

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Overview of Lipid Mass Spectrometry and Lipidomics

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Chemistry of the Secondary Metabolites of Termites

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Roles of Ceramides and Other Sphingolipids in Immune Cell Function and Inflammation

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Druggable Sphingolipid Pathways: Experimental Models and Clinical Opportunities

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Glycosphingolipids

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Gangliosides in Neurodegenerative Diseases

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Sphingolipids in Intestinal Inflammation and Tumorigenesis

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Sphingolipids in the Pathogenesis of Head and Neck and Lung Cancers: Translational Aspects for Therapy and Biomarker Development

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Bioactive Lipids

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Bioactive Lipids

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Sphingolipid Metabolism and Neutral Sphingomyelinases

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Regulation of the Sphingosine Kinase/Sphingosine 1-Phosphate Pathway

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Neuronal Forms of Gaucher Disease

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Lung Cancer and Lung Injury: The Dual Role of Ceramide

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The Role of Sphingolipids in Modulating Pluripotency of Stem Cells

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Elevation of Ceramide in Senescence: Role of Sphingolipid Metabolism

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Ceramides

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Phosphosphingolipids

inferred← citeshttps://doi.org/10.1007/978-94-007-7864-1_82-1openalex-snapshot

Liquid Chromatography-Mass Spectrometry of Sphingolipids

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Abiraterone and Ionizing Radiation Alter the Sphingolipid Homeostasis in Prostate Cancer Cells

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Glycosphingolipids (GSLs)

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Mammal GSL Synthesis Via ER and Golgi Network

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The GSL-Dependent Signaling

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Bacterial Toxin Protein Interaction with Host Cells GSL

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Drug Development in the Field of Sphinogolipid Metabolism

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Facing glycosphingolipid–Shiga toxin interaction: dire straits for endothelial cells of the human vasculature

inferred← citeshttps://doi.org/10.1007/s00018-013-1441-yopenalex-snapshot

Cell density-induced changes in lipid composition and intracellular trafficking

inferred← citeshttps://doi.org/10.1007/s00018-022-04524-7openalex-snapshot

Novel lectin-based chimeric antigen receptors target Gb3-positive tumour cells

inferred← citeshttps://doi.org/10.1007/s00018-026-06186-1openalex-snapshot

From molecular mechanisms of glycosphingolipid function to bio-therapeutic applications

inferred← citeshttps://doi.org/10.1007/s00204-020-02896-yopenalex-snapshot

A lipidomics approach reveals new insights into Crotalus durissus terrificus and Bothrops moojeni snake venoms

inferred← citeshttps://doi.org/10.1007/s00216-015-8822-zopenalex-snapshot

Development of a mass-spectrometry-based lipidomics platform for the profiling of phospholipids and sphingolipids in brain tissues

inferred← citeshttps://doi.org/10.1007/s00216-016-9425-zopenalex-snapshot

Development and validation of a high-throughput LC–MS/MS assay for routine measurement of molecular ceramides

inferred← citeshttps://doi.org/10.1007/s00216-021-03860-0openalex-snapshot

Sequential lipidomic, metabolomic, and proteomic analyses of serum, liver, and heart tissue specimens from peroxisomal biogenesis factor 11α knockout mice

inferred← citeshttps://doi.org/10.1007/s00216-025-06186-3openalex-snapshot

Noncovalent crown ether–assisted separation of stereoisomeric glycosphingosines using cyclic ion mobility spectrometry

inferred← citeshttps://doi.org/10.1007/s00418-016-1518-4openalex-snapshot

Lipid glycosylation: a primer for histochemists and cell biologists

inferred← citeshttps://doi.org/10.1007/s10517-019-04389-0openalex-snapshot

Involvement of Actin Filaments in the Cytotoxic Effect of GD2-Specific Antibodies

inferred← citeshttps://doi.org/10.1007/s10555-020-09872-zopenalex-snapshot

The role of lipid species in membranes and cancer-related changes

inferred← citeshttps://doi.org/10.1007/s10719-013-9511-9openalex-snapshot

Individual profiles of free ceramide species and the constituent ceramide species of sphingomyelin and neutral glycosphingolipid and their alteration according to the sequential changes of environmental oxygen content in human colorectal cancer Caco-2 cells

inferred← citeshttps://doi.org/10.1007/s10719-014-9563-5openalex-snapshot

Simplifying complexity: genetically resculpting glycosphingolipid synthesis pathways in mice to reveal function

inferred← citeshttps://doi.org/10.1007/s10719-016-9706-yopenalex-snapshot

Glycosphingolipids of human embryonic stem cells

inferred← citeshttps://doi.org/10.1007/s10719-018-9841-8openalex-snapshot

Neuronal membrane dynamics as fine regulator of sphingolipid composition

inferred← citeshttps://doi.org/10.1007/s10753-026-02458-xopenalex-snapshot

The Acid sphingomyelinase/ceramide System in Idiopathic Inflammatory Myopathies: a Potential Treatment Target

inferred← citeshttps://doi.org/10.1007/s11010-025-05334-8openalex-snapshot

Cerebrospinal fluid sphingolipid and sterol metabolite profiles of neurologically normal subjects

inferred← citeshttps://doi.org/10.1007/s11306-016-1160-0openalex-snapshot

Prepartal overfeeding alters the lipidomic profiles in the liver and the adipose tissue of transition dairy cows

inferred← citeshttps://doi.org/10.1007/s11626-020-00435-8openalex-snapshot

Simulated microgravity significantly altered metabolism in epidermal stem cells

inferred← citeshttps://doi.org/10.1007/s11745-014-3969-5openalex-snapshot

A Three‐Step Assay for Ceramide Synthase Activity Using a Fluorescent Substrate and HPLC

inferred← citeshttps://doi.org/10.1007/s12017-016-8424-8openalex-snapshot

Biological Effects of Naturally Occurring Sphingolipids, Uncommon Variants, and Their Analogs

inferred← citeshttps://doi.org/10.1007/s12035-013-8614-4openalex-snapshot

Lipid Rafts in Neurodegeneration and Neuroprotection

inferred← citeshttps://doi.org/10.1007/s12035-023-03524-3openalex-snapshot

Sphingosine 1-Phosphate Lyase in the Developing and Injured Nervous System: a Dichotomy?

inferred← citeshttps://doi.org/10.1007/s12551-017-0297-zopenalex-snapshot

The many faces (and phases) of ceramide and sphingomyelin I – single lipids

inferred← citeshttps://doi.org/10.1007/s12672-025-02302-yopenalex-snapshot

Glycosphingolipids as emerging attack points in bladder cancer

inferred← citeshttps://doi.org/10.1007/s12672-026-04819-2openalex-snapshot

Deciphering the role of glycolipids as emerging therapeutic targets in EMT-driven cancer progression

inferred← citeshttps://doi.org/10.1007/s13361-017-1772-2openalex-snapshot

Structural Analysis of Unsaturated Glycosphingolipids Using Shotgun Ozone-Induced Dissociation Mass Spectrometry

inferred← citeshttps://doi.org/10.1007/s13361-018-1928-8openalex-snapshot

AP-MALDI Mass Spectrometry Imaging of Gangliosides Using 2,6-Dihydroxyacetophenone

inferred← citeshttps://doi.org/10.1007/s13361-019-02267-7openalex-snapshot

Fragmentation Behavior and Gas-Phase Structures of Cationized Glycosphingolipids in Ozone-Induced Dissociation Mass Spectrometry

inferred← citeshttps://doi.org/10.1007/s43032-025-01898-4openalex-snapshot

Sphingolipids and Male Reproductive Health: A Narrative Review of Their Roles in Spermatogenesis, Fertility, and Dysfunction

inferred← citeshttps://doi.org/10.1007/s43393-026-00467-3openalex-snapshot

Characterization of sphinganine acyltransferase and ceramide reductase in Bacteroides thetaiotaomicron

inferred← citeshttps://doi.org/10.1016/b978-0-12-394274-6.00003-0openalex-snapshot

Ceramide Glycosylation Catalyzed by Glucosylceramide Synthase and Cancer Drug Resistance

inferred← citeshttps://doi.org/10.1016/b978-0-12-394447-4.10022-7openalex-snapshot

Glycolipids

inferred← citeshttps://doi.org/10.1016/b978-0-12-394447-4.10024-0openalex-snapshot

Lipidomics

inferred← citeshttps://doi.org/10.1016/b978-0-12-800111-0.00003-5openalex-snapshot

Lipid Metabolism and Oxidation in Neurons and Glial Cells

inferred← citeshttps://doi.org/10.1016/b978-0-12-800128-8.00004-2openalex-snapshot

Mechanism-Based Inhibitors of Glycosidases

inferred← citeshttps://doi.org/10.1016/b978-0-12-819404-1.00023-3openalex-snapshot

Altered lipid metabolic homeostasis in the pathogenesis of Alzheimer’s disease

inferred← citeshttps://doi.org/10.1016/b978-0-12-819475-1.00013-4openalex-snapshot

Congenital Disorders of Glycosylation

inferred← citeshttps://doi.org/10.1016/b978-0-12-819587-1.00003-3openalex-snapshot

The lipids

inferred← citeshttps://doi.org/10.1016/b978-0-12-821618-7.00070-5openalex-snapshot

Lipidomics

inferred← citeshttps://doi.org/10.1016/b978-0-12-821618-7.00142-5openalex-snapshot

Glycolipids

inferred← citeshttps://doi.org/10.1016/b978-0-12-824048-9.00009-2openalex-snapshot

Sphingolipids

inferred← citeshttps://doi.org/10.1016/b978-0-443-16156-8.00002-xopenalex-snapshot

Glycosphingolipid structure and metabolism

inferred← citeshttps://doi.org/10.1016/b978-0-443-16156-8.00003-1openalex-snapshot

Analysis of glycosphingolipids in the central nervous system

inferred← citeshttps://doi.org/10.1016/b978-0-443-16156-8.00004-3openalex-snapshot

Glycosphingolipid distribution in the central nervous system

inferred← citeshttps://doi.org/10.1016/b978-0-443-18578-6.00009-xopenalex-snapshot

Sphingosine-1-phosphate, its receptors, and their role in multiple sclerosis

inferred← citeshttps://doi.org/10.1016/b978-0-443-21658-9.00016-4openalex-snapshot

Basics and types of microbial biosensors

inferred← citeshttps://doi.org/10.1016/b978-0-444-63438-2.00010-9openalex-snapshot

Sphingolipids

inferred← citeshttps://doi.org/10.1016/bs.acr.2018.04.017openalex-snapshot

Side Effects in Cancer Therapy: Are Sphingolipids to Blame?

inferred← citeshttps://doi.org/10.1016/bs.mie.2025.11.007openalex-snapshot

Multi-structural profiling of neutral glycosphingolipids using selective enrichment and the Paternò–Büchi derivatization

inferred← citeshttps://doi.org/10.1016/bs.pmbts.2017.12.004openalex-snapshot

Glycan Chains of Gangliosides: Functional Ligands for Tissue Lectins (Siglecs/Galectins)

inferred← citeshttps://doi.org/10.1016/j.ab.2017.01.010openalex-snapshot

Assessment of ganglioside age-related and topographic specificity in human brain by Orbitrap mass spectrometry

inferred← citeshttps://doi.org/10.1016/j.ab.2019.03.014openalex-snapshot

Approaches for probing and evaluating mammalian sphingolipid metabolism

inferred← citeshttps://doi.org/10.1016/j.ab.2021.114361openalex-snapshot

Profiling of glycosphingolipids with SCDase digestion and HPLC-FLD-MS

inferred← citeshttps://doi.org/10.1016/j.ab.2026.116157openalex-snapshot

Novel HEXB variant and first evidence of urinary Gb4 isoforms in Sandhoff disease: Biochemical and bioinformatic characterization in two Moroccan families

inferred← citeshttps://doi.org/10.1016/j.aca.2017.11.005openalex-snapshot

Lipid metabolism in mouse embryonic fibroblast cells in response to autophagy induced by nutrient stress

inferred← citeshttps://doi.org/10.1016/j.aca.2020.05.051openalex-snapshot

Recent advances in the mass spectrometric analysis of glycosphingolipidome – A review

inferred← citeshttps://doi.org/10.1016/j.addr.2020.03.002openalex-snapshot

An emerging focus on lipids in extracellular vesicles

inferred← citeshttps://doi.org/10.1016/j.addr.2020.04.009openalex-snapshot

Sphingolipids as prognostic biomarkers of neurodegeneration, neuroinflammation, and psychiatric diseases and their emerging role in lipidomic investigation methods

inferred← citeshttps://doi.org/10.1016/j.aninu.2026.04.011openalex-snapshot

Ursolic acid alleviates high starch induced hepatic glucose and lipid metabolism disorders in largemouth bass (Micropterus salmoides) via the CERK/PI3K/AKT signaling pathway

inferred← citeshttps://doi.org/10.1016/j.atherosclerosis.2018.02.025openalex-snapshot

Lipid phosphate phosphatase 3 in vascular pathophysiology

inferred← citeshttps://doi.org/10.1016/j.atherosclerosis.2026.120774openalex-snapshot

Emerging role of ceramides and other sphingolipids in atherosclerosis

inferred← citeshttps://doi.org/10.1016/j.bbadis.2018.12.012openalex-snapshot

Sphk2−/− mice are protected from obesity and insulin resistance

inferred← citeshttps://doi.org/10.1016/j.bbadis.2019.07.005openalex-snapshot

Global glycosphingolipid analysis in urine and plasma of female Fabry disease patients

inferred← citeshttps://doi.org/10.1016/j.bbagen.2026.130997openalex-snapshot

B3GNT5-associated glycosylation remodeling in tumor-associated macrophages supports TGF-β-related glioma progression

inferred← citeshttps://doi.org/10.1016/j.bbalip.2013.06.006openalex-snapshot

Co-evolution of sphingomyelin and the ceramide transport protein CERT

inferred← citeshttps://doi.org/10.1016/j.bbalip.2013.08.006openalex-snapshot

Sphingolipids and lifespan regulation

inferred← citeshttps://doi.org/10.1016/j.bbalip.2013.10.014openalex-snapshot

Sphingolipid homeostasis in the web of metabolic routes

inferred← citeshttps://doi.org/10.1016/j.bbalip.2014.05.006openalex-snapshot

Characterisation of sphingolipids in the human lens by thin layer chromatography–desorption electrospray ionisation mass spectrometry

inferred← citeshttps://doi.org/10.1016/j.bbalip.2014.08.017openalex-snapshot

Ceramide modulates pre-mRNA splicing to restore the expression of wild-type tumor suppressor p53 in deletion-mutant cancer cells

inferred← citeshttps://doi.org/10.1016/j.bbalip.2015.02.001openalex-snapshot

Lipid membrane domains in the brain

inferred← citeshttps://doi.org/10.1016/j.bbalip.2017.01.009openalex-snapshot

Opinion article on lipidomics: Inherent challenges of lipidomic analysis of sphingolipids

inferred← citeshttps://doi.org/10.1016/j.bbalip.2018.12.013openalex-snapshot

1-Deoxysphingolipids

inferred← citeshttps://doi.org/10.1016/j.bbalip.2019.06.015openalex-snapshot

The role of ceramide in regulating endoplasmic reticulum function

inferred← citeshttps://doi.org/10.1016/j.bbalip.2020.158708openalex-snapshot

S1P-lyase deficiency uncouples ganglioside formation – Potential contribution to tumorigenic capacity

inferred← citeshttps://doi.org/10.1016/j.bbalip.2023.159444openalex-snapshot

Ceramide regulation of autophagy: A biophysical approach

inferred← citeshttps://doi.org/10.1016/j.bbalip.2024.159591openalex-snapshot

Loss of SUR2 alters the composition of ceramides and shortens chronological lifespan of Saccharomyces cerevisiae

inferred← citeshttps://doi.org/10.1016/j.bbamcr.2013.04.010openalex-snapshot

The complexity of sphingolipid biosynthesis in the endoplasmic reticulum

inferred← citeshttps://doi.org/10.1016/j.bbamem.2014.02.021openalex-snapshot

Sphingolipid symmetry governs membrane lipid raft structure

inferred← citeshttps://doi.org/10.1016/j.bbamem.2015.10.012openalex-snapshot

Pore-forming toxins: Properties, diversity, and uses as tools to image sphingomyelin and ceramide phosphoethanolamine

inferred← citeshttps://doi.org/10.1016/j.bbamem.2021.183701openalex-snapshot

The role of the ‘sphingoid motif’ in shaping the molecular interactions of sphingolipids in biomembranes

inferred← citeshttps://doi.org/10.1016/j.bbamem.2021.183731openalex-snapshot

Molecular and mesoscopic geometries in autophagosome generation. A review

inferred← citeshttps://doi.org/10.1016/j.bbapap.2019.01.005openalex-snapshot

Transmembrane topology of mammalian ORMDL proteins in the endoplasmic reticulum as revealed by the substituted cysteine accessibility method (SCAM™)

inferred← citeshttps://doi.org/10.1016/j.biochi.2016.05.009openalex-snapshot

Tools for the analysis of metabolic flux through the sphingolipid pathway

inferred← citeshttps://doi.org/10.1016/j.biochi.2019.05.017openalex-snapshot

Gangliosidome of human anencephaly: A high resolution multistage mass spectrometry study

inferred← citeshttps://doi.org/10.1016/j.biochi.2022.09.016openalex-snapshot

Exosomal lipids from membrane organization to biomarkers: Focus on an endolysosomal-specific lipid

inferred← citeshttps://doi.org/10.1016/j.bj.2016.01.003openalex-snapshot

Antigen specificity of invariant natural killer T-cells

inferred← citeshttps://doi.org/10.1016/j.bmc.2012.08.035openalex-snapshot

Novel fluorescent ceramide derivatives for probing ceramidase substrate specificity

inferred← citeshttps://doi.org/10.1016/j.bmc.2018.06.031openalex-snapshot

Synthesis and characterization of some atypical sphingoid bases

inferred← citeshttps://doi.org/10.1016/j.bmcl.2013.06.030openalex-snapshot

Structure guided design of a series of sphingosine kinase (SphK) inhibitors

inferred← citeshttps://doi.org/10.1016/j.bmcl.2013.12.091openalex-snapshot

Synthesis of neoglycosphingolipid from methoxyamino-functionalized ceramide

inferred← citeshttps://doi.org/10.1016/j.bmcl.2016.08.053openalex-snapshot

Design and synthesis of fluorescent glycolipid photoaffinity probes and their photoreactivity

inferred← citeshttps://doi.org/10.1016/j.bpj.2014.10.010openalex-snapshot

Biophysical Properties of Novel 1-Deoxy-(Dihydro)ceramides Occurring in Mammalian Cells

inferred← citeshttps://doi.org/10.1016/j.bpj.2016.09.021openalex-snapshot

Influence of Ganglioside GM1 Concentration on Lipid Clustering and Membrane Properties and Curvature

inferred← citeshttps://doi.org/10.1016/j.carres.2016.01.009openalex-snapshot

Marine cytotoxic jaspine B and its stereoisomers: biological activity and syntheses

inferred← citeshttps://doi.org/10.1016/j.carres.2018.08.001openalex-snapshot

Synthesis of the cytotoxic phytosphingosines and their isomeric analogues

inferred← citeshttps://doi.org/10.1016/j.carres.2018.08.008openalex-snapshot

A stereoselective approach towards a small library of cytotoxic isomeric sphingoid bases

inferred← citeshttps://doi.org/10.1016/j.carres.2018.09.008openalex-snapshot

Stereoselective synthesis and antiproliferative activity of the isomeric sphinganine analogues

inferred← citeshttps://doi.org/10.1016/j.carres.2019.06.016openalex-snapshot

Synthetic analogues of marine cytotoxic jaspine B and its stereoisomers

inferred← citeshttps://doi.org/10.1016/j.carres.2023.108789openalex-snapshot

Straightforward access to novel cytotoxic phytosphingosine-like aminotriols from l-erythrose chiron

inferred← citeshttps://doi.org/10.1016/j.carres.2023.108874openalex-snapshot

Divergent access to a novel 3,4-diaminophytosphingosine-like ceramide via sequential Overman rearrangement

inferred← citeshttps://doi.org/10.1016/j.carres.2024.109158openalex-snapshot

A ‘Chiron’ approach to novel phytosphingosine mimetics based on a cascade [3,3]-sigmatropic rearrangement

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