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  • 1
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Sphingolipids. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (786 pages)
    Edition: 1st ed.
    ISBN: 9780080496689
    Series Statement: Issn Series
    Language: English
    Note: Front Cover -- Sphingolipid Metabolism and Cell Signaling -- Copyright Page -- Table of Contents -- Contributors to Volume 311 -- Preface -- Volumes in Series -- Section I: Sphingolipid Metabolism -- A. Biosynthesis -- Chapter 1. Serine Palmitoyltransferase -- Chapter 2. Assay of the Saccharomyces cerevisiae Dihydrosphingosine C-4 Hydroxylase -- Chapter 3. Ceramide Synthase -- Chapter 4. Dihydroceramide Desaturase -- Chapter 5. Assays for the Biosynthesis of Sphingomyelin and Ceramide- Phosphoethanolamine -- Chapter 6. Glucosylceramide Synthase: Assay and Properties -- Chapter 7. Methods for Studying Glucosylceramide Synthase -- Chapter 8. Analysis of Galactolipids and UDP-Galactose: Ceramide Galactosyltransferase -- Chapter 9. Assay of Lactosylceramide Synthase and Comments on Its Potential Role in Signal Transduction -- Chapter 10. In Vitro Assays for Enzymes of Ganglioside Synthesis -- Chapter 11. Analyses of Sulfatide and Enzymes of Sulfatide Metabolism -- Chapter 12. 1-O-Acylceramide Synthase -- Chapter 13. N-Acetylation of Sphingosine by Platelet-Activating Factor: Sphingosine Transacetylase -- Chapter 14. Inositolphosphoryl Ceramide Synthase from Yeast -- Chapter 15. Enzymes of Sphingolipid Metabolism in Plants -- B. Turnover -- Chapter 16. Purification and Characterization of Recombinant Human Acid Sphingomyelinase Expressed in Insect Sf 21 Cells -- Chapter 17. Purification of Rat Brain Membrane Neutral Sphingomyelinase -- Chapter 18. Sphingomyelinase Assay Using Radiolabeled Substrate -- Chapter 19. Robotic Assay of Sphingomyelinase for High Throughput Screening -- Chapter 20. A High Throughput Sphingomyelinase Assay -- Chapter 21. Analyses of Sphingomyelin Hydrolysis in Caveolar Membranes -- Chapter 22. Ceramidases -- Chapter 23. Purification of Acid Ceramidase from Human Placenta -- Chapter 24. Ceramide Kinase. , Chapter 25. Assaying Sphingosine Kinase Activity -- Chapter 26. Yeast Sphingosine-1-Phosphate Phosphatases: Assay, Expression, Deletion, Purification, and Cellular Localization by GFP Tagging -- Chapter 27. Analysis of Ceramide 1-Phosphate and Sphingosine-1-Phosphate Phosphatase Activities -- Chapter 28. Sphingosine-1-Phosphate Lyase -- Chapter 29. Sphingolipid Hydrolases and Activator Proteins -- Chapter 30. Sphingolipid Hydrolyzing Enzymes in the Gastrointestinal Tract -- Chapter 31. Properties of Animal Ceramide Glycanases -- C. Genetic Approaches -- Chapter 32. Enzymatic N-Deacylation of Sphingolipids -- Chapter 33. Genetic Approaches for Studies of Glycolipid Synthetic Enzymes -- Chapter 34. Use of Yeast as a Model System for Studies of Sphingolipid Metabolism and Signaling -- Section II: Inhibitors of Sphingolipid Biosynthesis -- Chapter 35. Isolation and Characterization of Novel Inhibitors of Sphingolipid Biosynthesis: Australifungin, Viridiofungins, Rustmicin, and Khafrefungin -- Chapter 36. Fermentation, Partial Purification, and Use of Serine Palmitoyltransferase Inhibitors from Isaria (=Cordyceps) sinclairii -- Chapter 37. Isolation and Characterization of Fumonisins -- Chapter 38. Inhibitors of Glucosylceramide Synthase -- Section III: Chemical and Enzymatic Synthesis -- Chapter 39. Synthesis of Sphingosine and Sphingoid Bases -- Chapter 40. Synthesis of Sphingosine, Radiolabeled Sphingosine, 4-Methyl-cis-Sphingosine, and 1-Amino Derivatives of Sphingosine via Their Azido Derivatives -- Chapter 41. Total Synthesis of Sphingosine and Its Analogs -- Chapter 42. Radiolabeling of the Sphingolipid Backbone -- Chapter 43. Preparation of Radiolabeled Ceramides and Phosphosphingolipids -- Chapter 44. Synthesis of Key Precursors of Radiolabeled Sphingolipids. , Chapter 45. Practical Synthesis of N-Palmitoylsphingomyelin and N-Palmitoyldihydrosphingomyelin -- Chapter 46. Synthesis and Biological Activity of Glycolipids, with a Focus on Gangliosides and Sulfatide Analogs -- Chapter 47. Sphingolipid Photoaffinity Labels -- Chapter 48. Synthesis and Characterization of Metabolically Stable Sphingolipids -- Chapter 49. Synthetic Soluble Analogs of Glycolipids for Studies of Virus-Glycolipid Interactions -- Chapter 50. Preparation of Radioactive Gangliosides 3H or 14C Isotopically Labeled at the Oligosaccharide or Ceramide Moieties -- Chapter 51. Estimating Sphingolipid Metabolism and Trafficking in Cultured Cells Using Radiolabeled Compounds -- Chapter 52. Enzymatic Synthesis of [14C]Ceramide, [14C]Glycosphingolipids, and w-Aminoceramide -- Author Index -- Subject Index.
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  • 2
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Clinical enzymology. ; Electronic books.
    Description / Table of Contents: This volume contains information on analyzing sphingolipids, sphingolipid transport and trafficking, and sphingolipid-protein interactions and cellular targets. Its companion Volume 311 presents methods used in studying enzymes of sphingolipid biosynthesis and turnover, including inhibitors of some of these enzymes, genetic approaches, and organic and enzymatic syntheses of sphingolipids and analogs. The critically acclaimed laboratory standard for more than forty years, Methods in Enzymology is one of the most highly respected publications in the field of biochemistry. Since 1955, each volume has been eagerly awaited, frequently consulted, and praised by researchers and reviewers alike. Now with more than 300 volumes (all of them still in print), the series contains much material still relevant today--truly an essential publication for researchers in all fields of life sciences.
    Type of Medium: Online Resource
    Pages: 1 online resource (687 pages)
    Edition: 1st ed.
    ISBN: 9780080496696
    Series Statement: Issn Series ; v.Volume 312
    DDC: 571.6
    Language: English
    Note: Front Cover -- Sphingolipid Metabolism and Cell Signaling -- Copyright Page -- Table of Contents -- Contributors to Volume 312 -- Preface -- Volumes in Series -- Section I: Methods for Analyzing Sphingolipids -- Chapter 1. Analysis of Sphingoid Bases and Sphingoid Base 1-Phosphates by High-Performance Liquid Chromatography -- Chapter 2. Enzymatic Method for Measurement of Sphingosine 1-Phosphate -- Chapter 3. Ceramide Mass Analysis by Normal-Phase High-Performance Liquid Chromatography -- Chapter 4. Quantitative Determination of Ceramide Using Diglyceride Kinase -- Chapter 5. Analysis of Sphingomyelin, Glucosylceramide, Ceramide, Sphingosine, and Sphingosine 1-Phosphate by Tandem Mass Spectrometry -- Chapter 6. Analyses of Glycosphingolipids by High-Performance Liquid Chromatography -- Chapter 7. Sphingolipid Extraction and Analysis by Thin-Layer Chromatography -- Chapter 8. Extraction and Analysis of Multiple Sphingolipids from a Single Sample -- Chapter 9. Purification of Sphingolipid Classes by Solid-Phase Extraction with Aminopropyl and Weak Cation Exchanger Cartridges -- Chapter 10. Ganglioside Analysis by High-Performance Thin-Layer Chromatography -- Chapter 11. Purification and Analysis of Gangliosides -- Chapter 12. Thin-Layer Chromatography Blotting Using Polyvinylidene Difluoride Membrane (Far-Eastern Blotting) and Its Applications -- Chapter 13. Thin-Layer Chromatography Immunostaining -- Chapter 14. Monoclonal Anti-Glycosphingolipid Antibodies -- Chapter 15. Immunolocalization of Gangliosides by Light Microscopy Using Anti-Ganglioside Antibodies -- Chapter 16. Cloud-Point Extraction of Gangliosides Using Nonionic Detergent C14EO6 -- Chapter 17. Analyses of Glycosphingolipids Using Clam, Mercenaria mercenaria, Ceramide Glycanase. , Chapter 18. Quantitative Analyses of Binding Affinity and Specificity for Glycolipid Receptors by Surface Plasmon Resonance -- Chapter 19. Use of Circular Dichroism for Assigning Stereochemistry of Sphingosine and Other Long-Chain Bases -- Chapter 20. Infrared Determination of Conformational Order and Phase Behavior in Ceramides and Stratum Corneum Models -- Chapter 21. Use of Nuclear Magnetic Resonance Spectroscopy in Evaluation of Ganglioside Structure, Conformation, and Dynamics -- Chapter 22. Fluorescence Quenching Assay of Sphingolipid/ Phospholipid Phase Separation in Model Membranes -- Section II: Methods for Analyzing Aspects of Sphingolipid Metabolism in Intact Cells -- Chapter 23. Synthesis of Fluorescent Substrates and Their Application to Study of Sphingolipid Metabolism in Vitro and in Intact Cells -- Chapter 24. Selection of Mammalian Cell Mutants in Sphingolipid Biosynthesis -- Chapter 25. Selection of Yeast Mutants in Sphingolipid Metabolism -- Chapter 26. Fluorescence-Based Selection of Gene-Corrected Hematopoietic Stem and Progenitor Cells Based on Acid Sphingomyelinase Expression -- Chapter 27. Mammalian Ganglioside Sialidases: Preparation and Activity Assays -- Section III: Sphingolipid-Protein Interactions and Cellular Targets -- Chapter 28. Effects of Sphingosine and Other Sphingolipids on Protein Kinase C -- Chapter 29. Kinetic Analysis of Sphingoid Base Inhibition of Yeast Phosphatidate Phosphatase -- Chapter 30. Assays of Sphingosine-Dependent Kinase for 14-3-3 Protein -- Chapter 31. Synthesis and Use of Caged Sphingolipids -- Chapter 32. Binding of Sphingosine 1-Phosphate to Cell Surface Receptors -- Chapter 33. Use of Short-Chain Ceramides -- Chapter 34. Analysis of Ceramide-Activated Protein Phosphatases. , Chapter 35. Use of Affinity Chromatography and TID-Ceramide Photoaffinity Labeling for Detection of Ceramide-Binding Proteins -- Chapter 36. Lectin-Mediated Cell Adhesion to Immobilized Glycosphingolipids -- Chapter 37. Analysis of Glycolipid-Dependent Cell Adhesion Based on Carbohydrate-Carbohydrate Interaction -- Chapter 38. Analysis of Interactions between Glycosphingolipids and Microbial Toxins -- Chapter 39. Oxidation of Aglycone of Glycosphingolipids: Serine and Ceramide Acid Precursors for Soluble Glycoconjugates -- Chapter 40. Separation of Glycosphingolipid-Enriched Microdomains from Caveolae Characterized by Presence of Caveolin -- Chapter 41. Reconstitution of Sphingolipid-Cholesterol Plasma Membrane Microdomains for Studies of Virus-Glycolipid Interactions -- Chapter 42. Analysis of Ceramides Present in Glycosylphosphatidylinositol Anchored Proteins of Saccharomyces cerevisiae -- Chapter 43. Preparation of Functionalized Lipid Tubules for Electron Crystallography of Macromolecules -- Section IV: Sphingolipid Transport and Trafficking -- Chapter 44. Applications of BODIPY-Sphingolipid Analogs to Study Lipid Traffic and Metabolism in Cells -- Chapter 45. Using Biotinylated Gangliosides to Study Their Distribution and Traffic in Cells by Immunoelectron Microscopy -- Chapter 46. Assays for Transmembrane Movement of Sphingolipids -- Section V: Other Methods -- Chapter 47. Compilation of Methods Published in Previous Volumes of Methods in Enzymology -- Author Index -- Subject Index.
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  • 3
    Online Resource
    Online Resource
    Berlin, Heidelberg :Springer Berlin / Heidelberg,
    Keywords: Sphingolipids-Physiological effect. ; Sphingolipids-Metabolism. ; Cellular signal transduction. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (199 pages)
    Edition: 1st ed.
    ISBN: 9783662224250
    Series Statement: Molecular Biology Intelligence Unit Series
    DDC: 571.6
    Language: English
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  • 4
    Online Resource
    Online Resource
    Cham :Springer International Publishing AG,
    Keywords: Medical laboratories. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (491 pages)
    Edition: 1st ed.
    ISBN: 9783319207506
    DDC: 612.01577
    Language: English
    Note: Intro -- Dedication -- Preface -- Contents -- Basics of Sphingolipid Metabolism and Signalling -- 1 Introduction: Sphingolipids Are Bioactive Metabolites -- 2 How Are Sphingolipids Formed, Transformed and Degraded? -- 3 How Do Sphingolipids Signal and Mediate Biological Effects? -- 3.1 History of Signalling Sphingolipids: Where Are We One Generation Later? -- 3.2 Sphingosine 1-Phosphate: A Paradigmatic Signalling Molecule -- 3.3 How Are Other Sphingolipids Bioactive? -- 4 Current and Future Challenges -- References -- Part I: Roles and Functions of Sphingolipids in the Development of Different Types of Cancers -- Role of Sphingolipids in Hematological Malignancies: Lymphoproliferative Disorders -- 1 Introduction -- 1.1 Sphingolipids in Lymphoid Cell Functions -- 1.1.1 Apoptosis and the Mechanisms by Which Ceramide Induces Apoptosis -- 1.1.2 Rb -- 1.1.3 Ras and Raf-1 -- 1.1.4 Protein Kinase C -- 1.1.5 Bcl-2 and Bcl-xL -- 1.1.6 ROS -- 1.1.7 Caspase -- 1.1.8 p53 -- 1.1.9 Lipid Rafts -- 1.1.10 Autophagy -- 1.1.11 Regulated Necrosis/Necroptosis -- 1.1.12 Migration -- 1.1.13 Differentiation -- 1.1.14 Proliferation -- 1.1.15 Secretion -- 1.2 Mechanisms of Ceramide Generation -- 1.2.1 Acid Sphingomyelinase (ASMase) -- 1.2.2 Neutral Sphingomyelinase (NSMase) -- 1.2.3 De Novo Ceramide Synthesis -- 1.2.4 Sphingomyelin Synthase (SMS) -- 1.2.5 Glucosylceramide Synthase (GCS) -- 1.3 Sphingolipids Other than Ceramide in Lymphoid Cell Functions -- 1.3.1 Sphingosine (Sph) -- 1.3.2 Sphingosine 1-Phosphate (S1P) -- 1.3.3 Sphingomyelin (SM) -- 1.3.4 GD3/GM3 -- 1.4 Clinical Aspects of Sphingolipids -- 1.4.1 Leukemia [Acute Lymphoid Leukemia (ALL) and Chronic Lymphoid Leukemia (CLL)] -- 1.4.2 Malignant Lymphoma -- 1.4.3 Multiple Myeloma -- 2 Concluding Remarks -- References -- Role of Sphingolipids in Hematological Malignancies: Myeloproliferative Disorders. , 1 Introduction -- 1.1 Myeloproliferative Neoplasms (MPNs) -- 1.1.1 Chronic Myelogenous Leukemia, BCR-ABL1 Positive (CML) -- Role of Sphingolipids in CML -- 1.1.2 Sphingolipids and Other MPNs -- 1.2 Myelodysplastic Syndrome (MDS) -- 1.3 Acute Myeloid Leukemia (AML) and Other Related Neoplasms -- 1.3.1 Sphingolipids and Regulation of Differentiation of AML Cells and Other Cell Models of Related Neoplasms -- 1.3.2 Sphingolipids and Regulation of Apoptosis in AML Cells -- 2 Conclusions -- References -- Sphingolipids as Mediators of Breast Cancer Progression, Metastasis, Response and Resistance to Chemotherapy -- 1 Introduction to Breast Cancer -- 2 Molecular Genetic Portraits of Breast Cancer -- 3 Sphingolipids in Breast Cancer -- 4 Sphingolipids in Luminal Type Breast Cancers -- 4.1 Glucosylceramide Transferase -- 4.2 The Ceramide Synthases -- 4.3 The Sphingomyelinases -- 4.4 The Ceramidases -- 4.5 The Sphingosine Kinases -- 4.6 Ceramide Kinase -- 5 Sphingolipids in Basal Type Breast Cancer -- 6 Sphingolipids in Her2-Like Breast Cancer -- 7 Conclusions -- References -- Role of Sphingolipids in Non-melanoma Skin Cancer -- 1 Cellular Origins of BCC and SCC -- 2 BCC and SCC Incidence -- 3 Causal Factors of BCC and SCC -- 4 Genetic Mutations in BCC and SCC -- 5 Epidermal Homeostasis -- 6 Extracellular Ceramides Are a Major Constituent of the Epidermal Permeability Barrier -- 7 NMSC Results from an Imbalance Between Keratinocyte Proliferation and Differentiation in the Epidermis -- 8 Intracellular Ceramides and Their Metabolites Regulate Epidermal Keratinocyte Proliferation and Differentiation -- 9 Role for Sphingolipid-Metabolizing Enzymes in Regulating Keratinocyte Proliferation and Differentiation -- 10 Roles of Bioactive Sphingolipids in Mediating UVR-­Induced Proliferation Inhibition and Apoptosis of Keratinocytes. , 11 Potential Roles of Sphingolipids in NMSC Therapy -- 12 Conclusions and Future Directions -- References -- Dysregulation of Sphingolipid Metabolism in Melanoma: Roles in Pigmentation, Cell Survival and Tumor Progression -- 1 Melanoma: A Dreadful Cancer -- 2 SL Metabolism Is Deregulated in Melanoma -- 3 Role of SLs in Melanogenesis -- 4 Role of SLs in Melanoma-Stroma Interactions -- 4.1 Effect of S1P on Angiogenesis -- 4.2 Role of S1P in Fibroblast Differentiation -- 5 Role of SLs on Melanoma Growth and Survival -- 6 Concluding Remarks -- References -- Colon Cancer: The Role of Sphingolipid Metabolic Enzymes -- 1 Introduction -- 2 Modulation of Sphingomyelin and Ceramide: Sphingomyelinases -- 3 Modulation of Ceramide and Sphingosine: Ceramidases and Ceramide Synthases -- 3.1 Ceramidases (CDases) -- 3.2 Ceramide Synthases (CerS) -- 4 Modulation of Sphingosine and Sphingosine-1-Phosphate: Kinases, Lyase and Phosphatases, Sphingosine-1-­Phosphate Receptors -- 4.1 Sphingosine Kinases (SphKs) -- 4.2 Sphingosine-1-Phosphate Lyase and Phosphatases (SPL and SPPs) -- 4.3 Sphingosine-1-Phosphate Receptors (S1PRs) -- 5 Conclusion -- References -- Dietary Sphingolipids in Colon Cancer Prevention -- 1 Introduction -- 2 Colon Cancer -- 3 Sphingolipids in the Diet: Release of Bioactive Metabolites into the Intestinal Tract -- 4 Sphingolipids in the Diet: Impact on Colon Cancer -- 4.1 Sphingomyelin -- 4.2 Ceramides, Cerebrosides and Gangliosides -- 4.3 Free Sphingoid Bases -- 5 Cancers of Distant Organs as Targets for Dietary Sphingolipids -- 6 Mechanisms of Colon Cancer Suppression by Dietary Sphingolipids -- 6.1 Regulation of Proliferation and Apoptosis -- 6.2 APC-ß-Catenin Signaling Pathways as Targets for Colon Cancer Suppression -- 7 Microenvironment Intestinal Tract -- 7.1 Modulating the Inflammatory Intestinal Microenvironment. , 7.2 Inflammation-Driven Colon Cancer -- 8 Emerging Target: Intestinal Microbiota -- 9 Summary -- References -- Role of Sphingolipids in Liver Cancer -- 1 Chronic Liver Disease: A Driving Path to Liver Cancer Development -- 2 Pathways of Ceramide Generation and Metabolism -- 3 Role and Mechanisms of Sphingolipids in Cell Death -- 3.1 Mitochondrial Targeting -- 3.2 ER Stress, Autophagy and Lysosomal Membrane Permeabilization -- 4 Sphingolipids in Liver Disease Preceding HCC -- 4.1 ASMase Promotes NASH and Liver Fibrosis -- 4.2 GD3 Acetylation Regulates Fibrosis -- 5 Role of Sphingolipids in HCC and Metastasis -- 5.1 Acid Ceramidase -- 5.2 Inhibition of CerS by Fumonisin B1 -- 5.3 Neutral and Acid Sphingomyelinases -- 5.4 Gangliosides -- 5.5 Nanoliposomal Ceramide -- 6 Concluding Remarks -- References -- Pancreatic Cancer and Sphingolipids -- 1 Pancreatic Cancer: Historical Perspective -- 2 Epidemiology in Brief -- 3 Treatment Options -- 4 Pancreas Anatomy and Function and Pancreatic Cancer Progression -- 5 Sphingolipid Biology and Chemistry -- 6 Anticancer Drugs and Sphingolipid Metabolism in Pancreatic Cancer -- 7 Ceramide and Targeting Ceramide Metabolism as Therapeutic Approach in Pancreatic Cancer -- 8 Nanoliposomal Ceramide as an Emerging Therapeutic in Pancreatic Cancer -- 9 Future Directions -- References -- Sphingolipids in the Pathogenesis of Head and Neck and Lung Cancers: Translational Aspects for Therapy and Biomarker Development -- 1 Head and Neck Squamous Cell Carcinoma (HNSCC) and Lung Cancer Epidemiology -- 2 Sphingolipid Chemistry and Metabolism -- 3 Ceramides and Their Analogs in HNSCC and Lung Cancer Therapy -- 3.1 Role of Endogenous Ceramides in Mediating Cancer Therapy -- 3.2 Anti-Cancer Mechanism of Ceramides -- 3.3 Sphingolipid Analogs in Cancer Therapy -- 3.4 Role of Ceramide Metabolizing Enzyme Inhibitors in Cancer Therapy. , 3.5 Sphingosine-1-Phosphate and S1P Receptor Signaling -- 4 Sphingolipids as Biomarkers in HNSCC and Lung Cancer -- 5 Conclusions and Future Directions -- References -- The Role and Function of Sphingolipids in Glioblastoma Multiforme -- 1 Overview of GBM and Sphingolipids -- 2 Sphingolipid Aberrations in GBM -- 3 Sphingolipid Molecules in the Hallmark Traits of GBM -- 4 Sphingolipids in GBM Proliferation -- 5 Sphingolipids and GBM Invasive Behavior -- 6 S1P in GBM Stemness -- 7 Sphingolipids in GBM Angiogenesis -- 8 Sphingolipids in GBM Cell Death -- 8.1 Ceramide in GBM Apoptosis -- 8.1.1 Ceramide in the Extrinsic Apoptotic Pathway of GBM Cells -- 8.1.2 Ceramide in the Apoptotic Intrinsic Pathway of GBM Cells -- 8.2 Ceramide in Necrotic and Autophagic Death of GBM Cells -- 9 Sphingolipids in GBM Cell Survival and Death Resistance -- 10 Clinical Aspects -- 10.1 Sphingolipids and Sphingolipid-Related Enzymes as Possible Diagnostic/Prognostic Markers -- 10.2 GBM Therapy: The Potential Application of Sphingolipid Targeting Drugs in GBM -- 11 Conclusions -- References -- Part II: Emerging Technologies for Sphingolipid Detection and Prediction of Modulation of Sphingolipid Metabolism -- Systems Biology Approaches for Studying Sphingolipid Signaling -- 1 Introduction -- 2 Strategies of System Biology Study of Sphingolipid Signaling -- 3 Systematic Perturbations Creates Sufficient Conditions to Deconvolute Signaling Roles of Sphingolipids -- 4 Distinct Signaling Roles of Sphingolipids are Revealed by Identifying Specific Transcriptomic Responses -- 5 Functional Analyses Support the Notion That Distinct Sphingolipids Regulate Specific Signaling Pathways -- 6 Identify Novel Players of the Sphingolipid Pathway from the Ontology Fingerprint Derived Gene Networks -- 7 Discussion and Future Directions -- References. , Qualitative and Quantitative Measurements of Sphingolipids by Mass Spectrometry.
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  • 5
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The molecular machinery responsible for the generation of transport carriers moving from the Golgi complex to the plasma membrane relies on a tight interplay between proteins and lipids. Among the lipid-binding proteins of this machinery, we previously identified the four-phosphate adaptor protein ...
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Mathematical models have become a necessary tool for organizing the rapidly increasing amounts of large-scale data on biochemical pathways and for advanced evaluation of their structure and regulation. Most of these models have addressed specific pathways using either stoichiometric or ...
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Cancer and metastasis reviews 13 (1994), S. 411-431 
    ISSN: 1573-7233
    Keywords: protein kinase C ; isoenzymes ; cancer ; differentiation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Protein kinase C (PKC) is a family of closely related lipid-dependent and diacyglycerol-activated isoenzymes known to play an important role in the signal transduction pathways involved in hormone release, mitogenesis and tumor promotion. Reversible activation of PKC by the second messengers diacylglycerol and calcium is an established model for the short term regulation of PKC in the immediate events of signal transduction. PKC can also be modulated long term by changes in the levels of activators or inhibitors for a prolonged period or by changes in the levels of functional PKC isoenzymes in the cell during development or in response to hormones and/or differentiation factors. Indeed, studies have indicated that the sustained activation or inhibition of PKC activityin vivo may play a critical role in regulation of long term cellular events such as proliferation, differentiation and tumorigenesis. In addition, these regulatory events are important in colon cancer, where a decrease in PKC activators and activity suggests PKC acts as an anti-oncogene, in breast cancer, where an increase in PKC activity suggests an oncogenic role for PKC, and in multidrug resistance (MDR) and metastasis where an increase in PKC activity correlates with increased resistance and metastatic potential. These studies highlight the importance and significance of regulation of PKC activityin vivo.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 58 (1995), S. 191-198 
    ISSN: 0730-2312
    Keywords: sphingomyelin cycle ; signal transduction ; leukemia ; membrane lipids ; apoptosis ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: A novel pathway termed the sphingomyelin cycle has been identified whereby membrane sphingomyelin is hydrolyzed in response to multiple extracellular stimuli (such as tumor necrosis factor α) which cause activation of regulated sphingomyelinases. The product, ceramide, has emerged as a second messenger that mediates many of the cellular effects of these extracellular stimuli. An intriguing relation exists between activation of the sphingomyelin cycle and the action of multiple stress stimuli that induce growth arrest and programmed cell death. Exogenously administered ceramide mimics these growth-suppressing effects, including the induction of apoptosis. This review will highlight the role of the sphingomyelin cycle in signal transduction and will focus on the role and function of ceramide in the regulation of cell growth in general and apoptosis specifically.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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