Trifunctional sphingomyelin derivatives enable nanoscale resolution of sphingomyelin turnover in physiological and infection processes via expansion microscopy
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
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Trifunctional sphingomyelin derivatives enable nanoscale resolution of sphingomyelin turnover in physiological and infection processes via expansion microscopy ; volume:15 ; number:1 ; day:28 ; month:8 ; year:2024 ; pages:1-16 ; date:12.2024
Nature Communications ; 15, Heft 1 (28.8.2024), 1-16, 12.2024
- Creator
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Rühling, Marcel
Kersting, Louise
Wagner, Fabienne
Schumacher, Fabian
Wigger, Dominik
Helmerich, Dominic A.
Pfeuffer, Tom
Elflein, Robin
Kappe, Christian
Sauer, Markus
Arenz, Christoph
Kleuser, Burkhard
Rudel, Thomas
Fraunholz, Martin
Seibel, Jürgen
- Contributor
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SpringerLink (Online service)
- DOI
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10.1038/s41467-024-51874-w
- URN
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urn:nbn:de:101:1-2411132129537.069137431969
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:22 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Rühling, Marcel
- Kersting, Louise
- Wagner, Fabienne
- Schumacher, Fabian
- Wigger, Dominik
- Helmerich, Dominic A.
- Pfeuffer, Tom
- Elflein, Robin
- Kappe, Christian
- Sauer, Markus
- Arenz, Christoph
- Kleuser, Burkhard
- Rudel, Thomas
- Fraunholz, Martin
- Seibel, Jürgen
- SpringerLink (Online service)
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Sphingomyelin synthase 2 promotes an aggressive breast cancer phenotype by disrupting the homoeostasis of ceramide and sphingomyelin
Sphingomyelin Synthases in Neuropsychiatric Health and Disease
Deficiency of sphingomyelin synthase 1 but not sphingomyelin synthase 2 reduces bone formation due to impaired osteoblast differentiation
Exploring the physiological roles of sphingomyelin synthase family members by proteolytic inactivation and mistargeting strategies
Über die enzymatische Hydrolyse von reinem Sphingomyelin aus Gehirn
Subcellular Targeting Domains of Sphingomyelin Synthase 1 and 2
The Role of Sphingomyelin Breakdown in Measles Virus Immunmodulation
Antidepressants act by inducing autophagy controlled by sphingomyelin–ceramide
Ceramide from sphingomyelin hydrolysis induces neuronal differentiation, whereas de novo ceramide synthesis and sphingomyelin hydrolysis initiate apoptosis after NGF withdrawal in PC12 Cells
Cholesterol-modified sphingomyelin chimeric lipid bilayer for improved therapeutic delivery
GM 1 Ganglioside Inhibits β‐Amyloid Oligomerization Induced by Sphingomyelin
Zur enzymatischen Analytik des HDL-Sphingomyelin
Sphingomyelin synthase 2 promotes an aggressive breast cancer phenotype by disrupting the homoeostasis of ceramide and sphingomyelin
Sphingomyelin Synthases in Neuropsychiatric Health and Disease
Deficiency of sphingomyelin synthase 1 but not sphingomyelin synthase 2 reduces bone formation due to impaired osteoblast differentiation
Exploring the physiological roles of sphingomyelin synthase family members by proteolytic inactivation and mistargeting strategies
Über die enzymatische Hydrolyse von reinem Sphingomyelin aus Gehirn
Subcellular Targeting Domains of Sphingomyelin Synthase 1 and 2
The Role of Sphingomyelin Breakdown in Measles Virus Immunmodulation
Antidepressants act by inducing autophagy controlled by sphingomyelin–ceramide
Ceramide from sphingomyelin hydrolysis induces neuronal differentiation, whereas de novo ceramide synthesis and sphingomyelin hydrolysis initiate apoptosis after NGF withdrawal in PC12 Cells
Cholesterol-modified sphingomyelin chimeric lipid bilayer for improved therapeutic delivery