C16 Sphingomyelin

C16 Sphingomyelin is a lipid of Sphingolipids (SP) class. The involved functions are known as Drug Interactions, Molecular Dynamics, Force, Energy Transfer and Signal Transduction. C16 sphingomyelin often locates in Membrane, Tissue membrane, Cell membrane, biological membrane and lipid raft. The related lipids are 1,2-oleoylphosphatidylcholine, Sphingolipids, lipid structure, Sterols and campesterol.

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Introduction

To understand associated biological information of C16 Sphingomyelin, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.

What diseases are associated with C16 Sphingomyelin?

There are no associated biomedical information in the current reference collection.

No disease MeSH terms mapped to the current reference collection.

PubChem Associated disorders and diseases

What pathways are associated with C16 Sphingomyelin

There are no associated biomedical information in the current reference collection.

PubChem Biomolecular Interactions and Pathways

Link to PubChem Biomolecular Interactions and Pathways

What cellular locations are associated with C16 Sphingomyelin?

Related references are published most in these journals:

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What functions are associated with C16 Sphingomyelin?


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What lipids are associated with C16 Sphingomyelin?

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What genes are associated with C16 Sphingomyelin?

There are no associated biomedical information in the current reference collection.

What common seen animal models are associated with C16 Sphingomyelin?

There are no associated biomedical information in the current reference collection.

NCBI Entrez Crosslinks

All references with C16 Sphingomyelin

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Authors Title Published Journal PubMed Link
Edler E et al. Membrane localization and dynamics of geranylgeranylated Rab5 hypervariable region. 2017 Biochim. Biophys. Acta pmid:28455099
Palacios-Ortega J et al. Regulation of Sticholysin II-Induced Pore Formation by Lipid Bilayer Composition, Phase State, and Interfacial Properties. 2016 Langmuir pmid:27003246
Lee J et al. CHARMM-GUI Input Generator for NAMD, GROMACS, AMBER, OpenMM, and CHARMM/OpenMM Simulations Using the CHARMM36 Additive Force Field. 2016 J Chem Theory Comput pmid:26631602
Sodt AJ et al. Hexagonal Substructure and Hydrogen Bonding in Liquid-Ordered Phases Containing Palmitoyl Sphingomyelin. 2015 Biophys. J. pmid:26331252
Sakamoto S et al. Effect of glycyrrhetinic acid on lipid raft model at the air/water interface. 2015 Biochim. Biophys. Acta pmid:25445675
Venable RM et al. CHARMM all-atom additive force field for sphingomyelin: elucidation of hydrogen bonding and of positive curvature. 2014 Biophys. J. pmid:24988348
Yang Y et al. Lipidomic analyses of female mice lacking hepatic lipase and endothelial lipase indicate selective modulation of plasma lipid species. 2014 Lipids pmid:24777581
Depner CM et al. A metabolomic analysis of omega-3 fatty acid-mediated attenuation of western diet-induced nonalcoholic steatohepatitis in LDLR-/- mice. 2013 PLoS ONE pmid:24358308
Sergelius C et al. Cholesterol's interactions with serine phospholipids - a comparison of N-palmitoyl ceramide phosphoserine with dipalmitoyl phosphatidylserine. 2013 Biochim. Biophys. Acta pmid:23159809
Quinn PJ Structure of sphingomyelin bilayers and complexes with cholesterol forming membrane rafts. 2013 Langmuir pmid:23863113