PLoS ONE, ISSN 1932-6203, 09/2013, Volume 8, Issue 9, p. e73380
Chilling tolerance was increased in seed germination and root growth of wheat seedlings grown in media containing 20 mu g/mL cerebroside C (CC), isolated from...
OXIDATIVE STRESS | XANTHINE-OXIDASE | ABIOTIC STRESS | PHOSPHOLIPASE-D | TEMPERATURE | MEMBRANE | MULTIDISCIPLINARY SCIENCES | FATTY-ACID | INVOLVEMENT | LIPOXYGENASE ACTIVITY | PLANT-GROWTH | Superoxide Dismutase - genetics | Gene Expression - drug effects | Adaptation, Physiological - drug effects | Cell Membrane Permeability | Plant Roots - genetics | Seedlings - genetics | Biomass | Plant Roots - drug effects | Triticum - metabolism | Lipoxygenase - metabolism | Saccharomycetales - chemistry | Plant Leaves - drug effects | Plant Proteins - metabolism | Phospholipids - metabolism | Superoxide Dismutase - metabolism | Germination - drug effects | Glutathione Peroxidase - metabolism | Cold Temperature | Plant Roots - metabolism | Seeds - metabolism | Catalase - genetics | Seeds - drug effects | Seeds - genetics | Cerebrosides - isolation & purification | Fatty Acids, Unsaturated - metabolism | Seedlings - drug effects | Glutathione Peroxidase - genetics | Malondialdehyde | Catalase - metabolism | Triticum - genetics | Plant Proteins - genetics | Plant Leaves - genetics | Plant Leaves - metabolism | Lipoxygenase - genetics | Lipid Peroxidation | Cerebrosides - pharmacology | Seedlings - metabolism | Triticum - drug effects | Lipid peroxidation | Superoxide | Saturated fatty acids | Wheat | Germination | Linolenic acids | Plasma | Lipid composition | Seeds | Media (culture) | Laboratories | Roots | Membrane permeability | Science | Lipids | Superoxide dismutase | Phospholipids | Palmitic acid | Fungi | Antioxidants | Catalase | Metabolites | Education | Chilling | Endophytes | Physiology | Peroxidase | Stearic acid | Glutathione | Peroxidation | Glutathione peroxidase | Enzymes | Cooling | Cold | Cultivation | Pesticides | Programmable logic controllers | Permeability | Fatty acids | Phospholipase D | Seed germination | Seedlings | Linoleic acid | Linolenic acid | Plant growth | Programmable logic devices | Liquid oxygen | Crop diseases | Lipoxygenase
OXIDATIVE STRESS | XANTHINE-OXIDASE | ABIOTIC STRESS | PHOSPHOLIPASE-D | TEMPERATURE | MEMBRANE | MULTIDISCIPLINARY SCIENCES | FATTY-ACID | INVOLVEMENT | LIPOXYGENASE ACTIVITY | PLANT-GROWTH | Superoxide Dismutase - genetics | Gene Expression - drug effects | Adaptation, Physiological - drug effects | Cell Membrane Permeability | Plant Roots - genetics | Seedlings - genetics | Biomass | Plant Roots - drug effects | Triticum - metabolism | Lipoxygenase - metabolism | Saccharomycetales - chemistry | Plant Leaves - drug effects | Plant Proteins - metabolism | Phospholipids - metabolism | Superoxide Dismutase - metabolism | Germination - drug effects | Glutathione Peroxidase - metabolism | Cold Temperature | Plant Roots - metabolism | Seeds - metabolism | Catalase - genetics | Seeds - drug effects | Seeds - genetics | Cerebrosides - isolation & purification | Fatty Acids, Unsaturated - metabolism | Seedlings - drug effects | Glutathione Peroxidase - genetics | Malondialdehyde | Catalase - metabolism | Triticum - genetics | Plant Proteins - genetics | Plant Leaves - genetics | Plant Leaves - metabolism | Lipoxygenase - genetics | Lipid Peroxidation | Cerebrosides - pharmacology | Seedlings - metabolism | Triticum - drug effects | Lipid peroxidation | Superoxide | Saturated fatty acids | Wheat | Germination | Linolenic acids | Plasma | Lipid composition | Seeds | Media (culture) | Laboratories | Roots | Membrane permeability | Science | Lipids | Superoxide dismutase | Phospholipids | Palmitic acid | Fungi | Antioxidants | Catalase | Metabolites | Education | Chilling | Endophytes | Physiology | Peroxidase | Stearic acid | Glutathione | Peroxidation | Glutathione peroxidase | Enzymes | Cooling | Cold | Cultivation | Pesticides | Programmable logic controllers | Permeability | Fatty acids | Phospholipase D | Seed germination | Seedlings | Linoleic acid | Linolenic acid | Plant growth | Programmable logic devices | Liquid oxygen | Crop diseases | Lipoxygenase
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 01/2000, Volume 275, Issue 3, pp. 2191 - 2198
Domains rich in sphingolipids and cholesterol, or rafts, may organize signal transduction complexes at the plasma membrane. Raft lipids are believed to exist...
SIGNAL-TRANSDUCTION | ALPHA-SUBUNITS | MODEL MEMBRANES | MEMBRANE-BINDING | HETEROTRIMERIC G-PROTEINS | ADENYLYL-CYCLASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | T-CELL ACTIVATION | TYROSINE KINASES | PLASMA-MEMBRANE | GPI-ANCHORED PROTEINS | Protein Structure, Tertiary | Sphingomyelins - metabolism | GTP-Binding Proteins - chemistry | Signal Transduction | Sphingolipids - metabolism | Cerebrosides - metabolism | Recombinant Proteins | Cholesterol - metabolism | Phosphatidylcholines - metabolism | Surface-Active Agents - pharmacology | Saccharomyces cerevisiae - metabolism | Animals | Membrane Proteins - chemistry | Escherichia coli - metabolism | Liposomes - metabolism | Cell Membrane - metabolism | Membrane Proteins - metabolism | Octoxynol - pharmacology | Phosphatidylethanolamines - metabolism | Acylation | GTP-Binding Proteins - metabolism
SIGNAL-TRANSDUCTION | ALPHA-SUBUNITS | MODEL MEMBRANES | MEMBRANE-BINDING | HETEROTRIMERIC G-PROTEINS | ADENYLYL-CYCLASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | T-CELL ACTIVATION | TYROSINE KINASES | PLASMA-MEMBRANE | GPI-ANCHORED PROTEINS | Protein Structure, Tertiary | Sphingomyelins - metabolism | GTP-Binding Proteins - chemistry | Signal Transduction | Sphingolipids - metabolism | Cerebrosides - metabolism | Recombinant Proteins | Cholesterol - metabolism | Phosphatidylcholines - metabolism | Surface-Active Agents - pharmacology | Saccharomyces cerevisiae - metabolism | Animals | Membrane Proteins - chemistry | Escherichia coli - metabolism | Liposomes - metabolism | Cell Membrane - metabolism | Membrane Proteins - metabolism | Octoxynol - pharmacology | Phosphatidylethanolamines - metabolism | Acylation | GTP-Binding Proteins - metabolism
Journal Article
Neuron, ISSN 0896-6273, 03/2013, Volume 77, Issue 5, pp. 886 - 898
Mitochondrial dysfunction is a common cause of peripheral neuropathy. Much effort has been devoted to examining the role played by neuronal/axonal...
PERIPHERAL-NERVE | BETA-OXIDATION | MULTIDIMENSIONAL MASS-SPECTROMETRY | DISEASE | GENE-EXPRESSION | MICE | SHOTGUN LIPIDOMICS | LONG-CHAIN ACYLCARNITINE | TRANSCRIPTION FACTOR | DIABETIC-NEUROPATHY | NEUROSCIENCES | Aniline Compounds | Cells, Cultured | Protein-Serine-Threonine Kinases - genetics | Mice, Transgenic | Carnitine - metabolism | Ganglia, Spinal - cytology | Schwann Cells - metabolism | Blotting, Western | Nerve Degeneration - metabolism | Nerve Degeneration - pathology | Mice, Knockout | Peripheral Nervous System Diseases - metabolism | Protein-Serine-Threonine Kinases - biosynthesis | Xanthenes | Animals | Mitochondrial Encephalomyopathies - metabolism | Microarray Analysis | Axons - pathology | Mice | Peripheral Nervous System Diseases - pathology | Carnitine - analogs & derivatives | Fatty Acids - metabolism | Fluorescent Dyes | Lipid Metabolism - physiology | Physiological aspects | Mitochondrial DNA | Synthesis | Fatty acids | Analysis | Cell culture | Disease | Neurons | Lipids | Nervous system | Genomes | Metabolism | Gene expression | Proteins | Pathology | Mitochondria | Hospitals | Rodents | Diabetes | Cancer | sulfatides | heme-regulated inhibitor kinase | diabetic neuropathy | cerebrosides | TFAM | eukaryotic elongation factor 2 alpha | acylcarnitines | integrated stress response
PERIPHERAL-NERVE | BETA-OXIDATION | MULTIDIMENSIONAL MASS-SPECTROMETRY | DISEASE | GENE-EXPRESSION | MICE | SHOTGUN LIPIDOMICS | LONG-CHAIN ACYLCARNITINE | TRANSCRIPTION FACTOR | DIABETIC-NEUROPATHY | NEUROSCIENCES | Aniline Compounds | Cells, Cultured | Protein-Serine-Threonine Kinases - genetics | Mice, Transgenic | Carnitine - metabolism | Ganglia, Spinal - cytology | Schwann Cells - metabolism | Blotting, Western | Nerve Degeneration - metabolism | Nerve Degeneration - pathology | Mice, Knockout | Peripheral Nervous System Diseases - metabolism | Protein-Serine-Threonine Kinases - biosynthesis | Xanthenes | Animals | Mitochondrial Encephalomyopathies - metabolism | Microarray Analysis | Axons - pathology | Mice | Peripheral Nervous System Diseases - pathology | Carnitine - analogs & derivatives | Fatty Acids - metabolism | Fluorescent Dyes | Lipid Metabolism - physiology | Physiological aspects | Mitochondrial DNA | Synthesis | Fatty acids | Analysis | Cell culture | Disease | Neurons | Lipids | Nervous system | Genomes | Metabolism | Gene expression | Proteins | Pathology | Mitochondria | Hospitals | Rodents | Diabetes | Cancer | sulfatides | heme-regulated inhibitor kinase | diabetic neuropathy | cerebrosides | TFAM | eukaryotic elongation factor 2 alpha | acylcarnitines | integrated stress response
Journal Article
Journal of Lipid Research, ISSN 0022-2275, 03/2011, Volume 52, Issue 3, pp. 509 - 517
Alterations in lipid metabolism may contribute to diabetic complications. Sphingolipids are essential components of cell membranes and have essential roles in...
Ceramide | Sphingomyelin cerebrosides | Lipidomics | Nervonic acid | Sphingosine-1-phosphate | ACTIVATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | TANDEM MASS-SPECTROMETRY | ceramide | OBESITY | RECEPTOR SUBTYPES | METABOLISM | INSULIN-RESISTANCE | cerebrosides | nervonic acid | sphingomyelin | sphingosine-1-phosphate | MICE | ACCUMULATION | lipidomics | ADIPOSE-TISSUE | Sphingolipids - chemistry | Lysophospholipids - metabolism | Diabetes Mellitus, Type 1 - metabolism | Male | Diabetes Mellitus, Experimental - blood | Sphingolipids - blood | Liver - drug effects | Myocardium - metabolism | Female | Sphingosine - metabolism | Fatty Acids - blood | Diabetes Mellitus, Experimental - metabolism | Insulin - genetics | Disease Models, Animal | Biomarkers - metabolism | Insulin - pharmacology | Liver - metabolism | Diabetes Mellitus, Type 1 - genetics | Rats | Sphingolipids - metabolism | Biomarkers - blood | Sphingosine - analogs & derivatives | Animals | Diabetes Mellitus, Type 1 - blood | Alleles | Mice | Mutation | Biomarkers - chemistry
Ceramide | Sphingomyelin cerebrosides | Lipidomics | Nervonic acid | Sphingosine-1-phosphate | ACTIVATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | TANDEM MASS-SPECTROMETRY | ceramide | OBESITY | RECEPTOR SUBTYPES | METABOLISM | INSULIN-RESISTANCE | cerebrosides | nervonic acid | sphingomyelin | sphingosine-1-phosphate | MICE | ACCUMULATION | lipidomics | ADIPOSE-TISSUE | Sphingolipids - chemistry | Lysophospholipids - metabolism | Diabetes Mellitus, Type 1 - metabolism | Male | Diabetes Mellitus, Experimental - blood | Sphingolipids - blood | Liver - drug effects | Myocardium - metabolism | Female | Sphingosine - metabolism | Fatty Acids - blood | Diabetes Mellitus, Experimental - metabolism | Insulin - genetics | Disease Models, Animal | Biomarkers - metabolism | Insulin - pharmacology | Liver - metabolism | Diabetes Mellitus, Type 1 - genetics | Rats | Sphingolipids - metabolism | Biomarkers - blood | Sphingosine - analogs & derivatives | Animals | Diabetes Mellitus, Type 1 - blood | Alleles | Mice | Mutation | Biomarkers - chemistry
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 02/2004, Volume 279, Issue 6, pp. 3900 - 3905
Growth of the yeast species Candida albicans and Pichia pastoris is inhibited by RsAFP2, a plant defensin isolated from radish seed ( Raphanus sativus ), at...
protein-synthesis | cells | saccharomyces-cerevisiae | barley endosperm | cerebrosides | candida-albicans | binding-sites | antifungal activity | tandem mass-spectrometry | dahlia dahlia-merckii | CELLS | BARLEY ENDOSPERM | CANDIDA-ALBICANS | BIOCHEMISTRY & MOLECULAR BIOLOGY | ANTIFUNGAL ACTIVITY | CEREBROSIDES | TANDEM MASS-SPECTROMETRY | BINDING-SITES | SACCHAROMYCES-CEREVISIAE | PROTEIN-SYNTHESIS | DAHLIA DAHLIA-MERCKII | Defensins - metabolism | Candida albicans - metabolism | Antimicrobial Cationic Peptides - metabolism | Candida albicans - growth & development | Fungi - metabolism | Pichia - metabolism | Candida albicans - drug effects | Defensins - pharmacology | Antifungal Agents - metabolism | Genes, Fungal | Plant Proteins - metabolism | Fungi - growth & development | Insect Proteins - metabolism | Antifungal Agents - pharmacology | Glucosylceramides - genetics | Pichia - drug effects | Plant Proteins - pharmacology | Fungi - drug effects | Insect Proteins - pharmacology | Glucosylceramides - chemistry | Antimicrobial Cationic Peptides - pharmacology | Animals | Pichia - genetics | Mutation | In Vitro Techniques | Glucosylceramides - metabolism | Pichia - growth & development | glucosylceramides | heliomicin | defensins | AFP2 protein | RsAFP2 protein
protein-synthesis | cells | saccharomyces-cerevisiae | barley endosperm | cerebrosides | candida-albicans | binding-sites | antifungal activity | tandem mass-spectrometry | dahlia dahlia-merckii | CELLS | BARLEY ENDOSPERM | CANDIDA-ALBICANS | BIOCHEMISTRY & MOLECULAR BIOLOGY | ANTIFUNGAL ACTIVITY | CEREBROSIDES | TANDEM MASS-SPECTROMETRY | BINDING-SITES | SACCHAROMYCES-CEREVISIAE | PROTEIN-SYNTHESIS | DAHLIA DAHLIA-MERCKII | Defensins - metabolism | Candida albicans - metabolism | Antimicrobial Cationic Peptides - metabolism | Candida albicans - growth & development | Fungi - metabolism | Pichia - metabolism | Candida albicans - drug effects | Defensins - pharmacology | Antifungal Agents - metabolism | Genes, Fungal | Plant Proteins - metabolism | Fungi - growth & development | Insect Proteins - metabolism | Antifungal Agents - pharmacology | Glucosylceramides - genetics | Pichia - drug effects | Plant Proteins - pharmacology | Fungi - drug effects | Insect Proteins - pharmacology | Glucosylceramides - chemistry | Antimicrobial Cationic Peptides - pharmacology | Animals | Pichia - genetics | Mutation | In Vitro Techniques | Glucosylceramides - metabolism | Pichia - growth & development | glucosylceramides | heliomicin | defensins | AFP2 protein | RsAFP2 protein
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 03/2015, Volume 290, Issue 11, pp. 7040 - 7053
The membrane-bound receptor for platelet-derived growth factor A (PDGFRα) is crucial for controlling the production of oligodendrocytes (OLs) for myelination,...
Exosomes - metabolism | Oligodendroglia - metabolism | Exosomes - genetics | Neural Stem Cells - cytology | Neurogenesis | Myelin Sheath - metabolism | Leukodystrophy, Metachromatic - metabolism | Proteolysis | Transcription, Genetic | Oligodendroglia - cytology | Fatty Acids - metabolism | Leukodystrophy, Metachromatic - pathology | Receptor, Platelet-Derived Growth Factor alpha - metabolism | Signal Transduction | Mice, Inbred C57BL | Cells, Cultured | Neural Stem Cells - pathology | Oligodendroglia - pathology | Leukodystrophy, Metachromatic - genetics | Animals | Receptor, Platelet-Derived Growth Factor alpha - genetics | Sulfoglycosphingolipids - metabolism | Cerebroside-Sulfatase - metabolism | Neural Stem Cells - metabolism | Cerebroside-Sulfatase - genetics | Lipid Raft | PDGFRalpha | Sulfatides | Oligodendrocyte | Exosome | Neural Precursor Cells | Arylsulfatase A | Lysosomal Storage Disease | AKT PKB | Cell Biology | Glycolipid
Exosomes - metabolism | Oligodendroglia - metabolism | Exosomes - genetics | Neural Stem Cells - cytology | Neurogenesis | Myelin Sheath - metabolism | Leukodystrophy, Metachromatic - metabolism | Proteolysis | Transcription, Genetic | Oligodendroglia - cytology | Fatty Acids - metabolism | Leukodystrophy, Metachromatic - pathology | Receptor, Platelet-Derived Growth Factor alpha - metabolism | Signal Transduction | Mice, Inbred C57BL | Cells, Cultured | Neural Stem Cells - pathology | Oligodendroglia - pathology | Leukodystrophy, Metachromatic - genetics | Animals | Receptor, Platelet-Derived Growth Factor alpha - genetics | Sulfoglycosphingolipids - metabolism | Cerebroside-Sulfatase - metabolism | Neural Stem Cells - metabolism | Cerebroside-Sulfatase - genetics | Lipid Raft | PDGFRalpha | Sulfatides | Oligodendrocyte | Exosome | Neural Precursor Cells | Arylsulfatase A | Lysosomal Storage Disease | AKT PKB | Cell Biology | Glycolipid
Journal Article
Journal of Neurochemistry, ISSN 0022-3042, 09/2005, Volume 94, Issue 6, pp. 1696 - 1710
Two different types of low‐density detergent‐insoluble glycosphingolipid‐enriched membrane domain (DIG) fractions were isolated from myelin by extraction with...
galactosylceramide | rafts | oligodendrocytes | cerebroside sulfate | cytoskeleton | caveolin | Cerebroside sulfate | Cytoskeleton | Caveolin | Galactosylceramide | Oligodendrocytes | Rafts | PROTEOLIPID PROTEIN | ACTIVATED PROTEIN-KINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | NERVOUS-SYSTEM MYELIN | PLASMA-MEMBRANE | NEUROSCIENCES | FYN KINASE | LIPID RAFTS | TRITON X-100 | ACTIN CYTOSKELETON | BASIC-PROTEIN | GPI-ANCHORED PROTEINS | Detergents - chemistry | Membrane Microdomains - metabolism | Actins - metabolism | Octoxynol - chemistry | Galactosylceramides - metabolism | Caveolins - metabolism | Membrane Microdomains - ultrastructure | Myelin Sheath - metabolism | Brain - metabolism | Cholesterol - chemistry | Galactosylceramides - isolation & purification | Tubulin - metabolism | Caveolin 1 | Cattle | Axons - ultrastructure | G(M1) Ganglioside - chemistry | Membrane Proteins - metabolism | Glycosphingolipids - isolation & purification | Microscopy, Electron, Transmission | Cholesterol - isolation & purification | Neural Cell Adhesion Molecules - chemistry | Solubility | Axons - metabolism | Membrane Microdomains - chemistry | Axons - chemistry | Cholesterol - metabolism | Galactosylceramides - chemistry | Neural Cell Adhesion Molecules - isolation & purification | Animals | Neural Cell Adhesion Molecules - metabolism | Cytoskeleton - metabolism | Glycosphingolipids - metabolism | Signal Transduction - physiology | Myelin Sheath - ultrastructure | Myelin Sheath - chemistry | G(M1) Ganglioside - metabolism | Subcellular Fractions - chemistry | Glycosphingolipids - chemistry | Proteins | Neurons | Membranes
galactosylceramide | rafts | oligodendrocytes | cerebroside sulfate | cytoskeleton | caveolin | Cerebroside sulfate | Cytoskeleton | Caveolin | Galactosylceramide | Oligodendrocytes | Rafts | PROTEOLIPID PROTEIN | ACTIVATED PROTEIN-KINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | NERVOUS-SYSTEM MYELIN | PLASMA-MEMBRANE | NEUROSCIENCES | FYN KINASE | LIPID RAFTS | TRITON X-100 | ACTIN CYTOSKELETON | BASIC-PROTEIN | GPI-ANCHORED PROTEINS | Detergents - chemistry | Membrane Microdomains - metabolism | Actins - metabolism | Octoxynol - chemistry | Galactosylceramides - metabolism | Caveolins - metabolism | Membrane Microdomains - ultrastructure | Myelin Sheath - metabolism | Brain - metabolism | Cholesterol - chemistry | Galactosylceramides - isolation & purification | Tubulin - metabolism | Caveolin 1 | Cattle | Axons - ultrastructure | G(M1) Ganglioside - chemistry | Membrane Proteins - metabolism | Glycosphingolipids - isolation & purification | Microscopy, Electron, Transmission | Cholesterol - isolation & purification | Neural Cell Adhesion Molecules - chemistry | Solubility | Axons - metabolism | Membrane Microdomains - chemistry | Axons - chemistry | Cholesterol - metabolism | Galactosylceramides - chemistry | Neural Cell Adhesion Molecules - isolation & purification | Animals | Neural Cell Adhesion Molecules - metabolism | Cytoskeleton - metabolism | Glycosphingolipids - metabolism | Signal Transduction - physiology | Myelin Sheath - ultrastructure | Myelin Sheath - chemistry | G(M1) Ganglioside - metabolism | Subcellular Fractions - chemistry | Glycosphingolipids - chemistry | Proteins | Neurons | Membranes
Journal Article
Journal of Lipid Research, ISSN 0022-2275, 02/2012, Volume 53, Issue 2, pp. 273 - 281
Peroxisome proliferator-activated receptor gamma coactivator-1 alpha (PGC-1 alpha), a key regulator of energy metabolism and lipid homeostasis in multiple...
Shotgun lipidomics | Sphingolipidomics | Apolipoprotein E | Alzheimer's disease | 1-ALPHA PGC-1-ALPHA | TRANSCRIPTIONAL COACTIVATOR PGC-1-ALPHA | AMYLOID DEPOSITION | MULTIDIMENSIONAL MASS-SPECTROMETRY | ALZHEIMERS-DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | APOLIPOPROTEIN-E | shotgun lipidomics | PGC-1 COACTIVATORS | apolipoprotein E | sphingolipidomics | CENTRAL-NERVOUS-SYSTEM | LIVER-X-RECEPTOR | Caloric Restriction | Proteolipids - metabolism | Neurodegenerative Diseases - metabolism | Orphan Nuclear Receptors - metabolism | Apolipoproteins E - metabolism | Cerebral Cortex - metabolism | Trans-Activators - physiology | Animals | Mice, Mutant Strains | Liver X Receptors | Myelin and Lymphocyte-Associated Proteolipid Proteins | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Trans-Activators - genetics | Membrane Transport Proteins - metabolism | Sulfotransferases - metabolism | Mice | Transcription Factors | Sulfoglycosphingolipids - metabolism | Myelin Proteins - metabolism | Cerebroside-Sulfatase - metabolism | Retinoid X Receptors - metabolism | Enzymes - metabolism | Homeostasis - genetics
Shotgun lipidomics | Sphingolipidomics | Apolipoprotein E | Alzheimer's disease | 1-ALPHA PGC-1-ALPHA | TRANSCRIPTIONAL COACTIVATOR PGC-1-ALPHA | AMYLOID DEPOSITION | MULTIDIMENSIONAL MASS-SPECTROMETRY | ALZHEIMERS-DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | APOLIPOPROTEIN-E | shotgun lipidomics | PGC-1 COACTIVATORS | apolipoprotein E | sphingolipidomics | CENTRAL-NERVOUS-SYSTEM | LIVER-X-RECEPTOR | Caloric Restriction | Proteolipids - metabolism | Neurodegenerative Diseases - metabolism | Orphan Nuclear Receptors - metabolism | Apolipoproteins E - metabolism | Cerebral Cortex - metabolism | Trans-Activators - physiology | Animals | Mice, Mutant Strains | Liver X Receptors | Myelin and Lymphocyte-Associated Proteolipid Proteins | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Trans-Activators - genetics | Membrane Transport Proteins - metabolism | Sulfotransferases - metabolism | Mice | Transcription Factors | Sulfoglycosphingolipids - metabolism | Myelin Proteins - metabolism | Cerebroside-Sulfatase - metabolism | Retinoid X Receptors - metabolism | Enzymes - metabolism | Homeostasis - genetics
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2010, Volume 5, Issue 2, p. e9079
Membrane lipids play a pivotal role in the pathogenesis of Alzheimer's disease, which is associated with conformational changes, oligomerization and/or...
FORM | SPHINGOLIPID-BINDING DOMAIN | DISEASE | BIOLOGY | MEMBRANES | CEREBROSIDE | GM1 | PRECURSOR PROTEIN | LIPID MONOLAYERS | FIBRILLOGENESIS | HELICOBACTER-PYLORI | Sodium Chloride - pharmacology | Humans | Molecular Conformation | Crystallography, X-Ray | G(M3) Ganglioside - chemistry | Cholesterol - chemistry | Protein Binding - drug effects | Surface Properties | Amyloid beta-Peptides - metabolism | Glycolipids - chemistry | G(M1) Ganglioside - chemistry | G(M3) Ganglioside - metabolism | Molecular Structure | Fatty Acids - metabolism | Peptide Fragments - metabolism | Fatty Acids - chemistry | Models, Molecular | Cholesterol - metabolism | Glycolipids - metabolism | Molecular Dynamics Simulation | Peptide Fragments - chemistry | Alzheimer Disease - metabolism | Glycosphingolipids - metabolism | Amyloid beta-Peptides - chemistry | Lipid Bilayers - chemistry | Lipid Bilayers - metabolism | G(M1) Ganglioside - metabolism | Glycosphingolipids - chemistry | Peptides | Pathogenesis | Molecular dynamics | Lipids | Biochemistry | Crystallography | Cell surface | Proteins | Human immunodeficiency virus--HIV | Ceramide | Inhibition | Alzheimer's disease | Sugar | Antigens | Oligomerization | Neurodegenerative diseases | Fatty acids | Cholesterol | Dilution | Molecular modelling | Glycosphingolipids | Monolayers | β-Amyloid | Lymphomas | Alzheimers disease | Conformation | Life Sciences | Biomolecules | Biochemistry, Molecular Biology | HIV | Human immunodeficiency virus
FORM | SPHINGOLIPID-BINDING DOMAIN | DISEASE | BIOLOGY | MEMBRANES | CEREBROSIDE | GM1 | PRECURSOR PROTEIN | LIPID MONOLAYERS | FIBRILLOGENESIS | HELICOBACTER-PYLORI | Sodium Chloride - pharmacology | Humans | Molecular Conformation | Crystallography, X-Ray | G(M3) Ganglioside - chemistry | Cholesterol - chemistry | Protein Binding - drug effects | Surface Properties | Amyloid beta-Peptides - metabolism | Glycolipids - chemistry | G(M1) Ganglioside - chemistry | G(M3) Ganglioside - metabolism | Molecular Structure | Fatty Acids - metabolism | Peptide Fragments - metabolism | Fatty Acids - chemistry | Models, Molecular | Cholesterol - metabolism | Glycolipids - metabolism | Molecular Dynamics Simulation | Peptide Fragments - chemistry | Alzheimer Disease - metabolism | Glycosphingolipids - metabolism | Amyloid beta-Peptides - chemistry | Lipid Bilayers - chemistry | Lipid Bilayers - metabolism | G(M1) Ganglioside - metabolism | Glycosphingolipids - chemistry | Peptides | Pathogenesis | Molecular dynamics | Lipids | Biochemistry | Crystallography | Cell surface | Proteins | Human immunodeficiency virus--HIV | Ceramide | Inhibition | Alzheimer's disease | Sugar | Antigens | Oligomerization | Neurodegenerative diseases | Fatty acids | Cholesterol | Dilution | Molecular modelling | Glycosphingolipids | Monolayers | β-Amyloid | Lymphomas | Alzheimers disease | Conformation | Life Sciences | Biomolecules | Biochemistry, Molecular Biology | HIV | Human immunodeficiency virus
Journal Article
Molecular Therapy, ISSN 1525-0016, 09/2015, Volume 23, Issue 9, pp. 1519 - 1531
Metachromatic leukodystrophy (MLD) is an inherited lysosomal storage disorder resulting from a functional deficiency of arylsulfatase A (ARSA), an enzyme that...
MEDICINE, RESEARCH & EXPERIMENTAL | PATHOLOGY | DELIVERY | PLURIPOTENT STEM-CELLS | ENZYME | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | NEURONS | GENE-THERAPY | MICE | DYSFUNCTION | DEFICITS | BRAIN | Cell- and Tissue-Based Therapy - methods | Central Nervous System - metabolism | Humans | Cell Survival - genetics | Neurons - cytology | DNA-Binding Proteins - deficiency | Brain - metabolism | Leukodystrophy, Metachromatic - metabolism | Neuroglia - cytology | Lentivirus - genetics | Cell Differentiation | Neurons - metabolism | Induced Pluripotent Stem Cells - cytology | Gene Order | Disease Models, Animal | Induced Pluripotent Stem Cells - metabolism | Gene Expression | Transduction, Genetic | Axons - metabolism | Genetic Vectors - genetics | Mice, Knockout | Leukodystrophy, Metachromatic - genetics | Animals | Neuroglia - metabolism | Mice | Sulfoglycosphingolipids - metabolism | Cerebroside-Sulfatase - metabolism | Cerebroside-Sulfatase - genetics | Genetic Therapy - methods | Original
MEDICINE, RESEARCH & EXPERIMENTAL | PATHOLOGY | DELIVERY | PLURIPOTENT STEM-CELLS | ENZYME | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | NEURONS | GENE-THERAPY | MICE | DYSFUNCTION | DEFICITS | BRAIN | Cell- and Tissue-Based Therapy - methods | Central Nervous System - metabolism | Humans | Cell Survival - genetics | Neurons - cytology | DNA-Binding Proteins - deficiency | Brain - metabolism | Leukodystrophy, Metachromatic - metabolism | Neuroglia - cytology | Lentivirus - genetics | Cell Differentiation | Neurons - metabolism | Induced Pluripotent Stem Cells - cytology | Gene Order | Disease Models, Animal | Induced Pluripotent Stem Cells - metabolism | Gene Expression | Transduction, Genetic | Axons - metabolism | Genetic Vectors - genetics | Mice, Knockout | Leukodystrophy, Metachromatic - genetics | Animals | Neuroglia - metabolism | Mice | Sulfoglycosphingolipids - metabolism | Cerebroside-Sulfatase - metabolism | Cerebroside-Sulfatase - genetics | Genetic Therapy - methods | Original
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 11/2005, Volume 280, Issue 44, pp. 36815 - 36823
The beta-secretase, BACE, is a membrane spanning aspartic protease, which cleaves the amyloid precursor protein (APP) in the first step of proteolytic...
BETA-SECRETASE | RAFTS | ALZHEIMERS-DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | MEMBRANES | NEURONS | ASYMMETRIC VESICLES | RECEPTOR | GENERATION | AMYLOID PRECURSOR PROTEIN | CYTOSOLIC DOMAIN | Recombinant Proteins - metabolism | Endopeptidases - metabolism | Humans | Phosphatidylserines - metabolism | Recombinant Proteins - chemistry | Baculoviridae - genetics | Cerebrosides - metabolism | Recombinant Proteins - genetics | Cholesterol - metabolism | Endopeptidases - genetics | Aspartic Acid Endopeptidases | Amyloid Precursor Protein Secretases | Amyloid beta-Peptides - metabolism | Glycosphingolipids - metabolism | In Vitro Techniques
BETA-SECRETASE | RAFTS | ALZHEIMERS-DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | MEMBRANES | NEURONS | ASYMMETRIC VESICLES | RECEPTOR | GENERATION | AMYLOID PRECURSOR PROTEIN | CYTOSOLIC DOMAIN | Recombinant Proteins - metabolism | Endopeptidases - metabolism | Humans | Phosphatidylserines - metabolism | Recombinant Proteins - chemistry | Baculoviridae - genetics | Cerebrosides - metabolism | Recombinant Proteins - genetics | Cholesterol - metabolism | Endopeptidases - genetics | Aspartic Acid Endopeptidases | Amyloid Precursor Protein Secretases | Amyloid beta-Peptides - metabolism | Glycosphingolipids - metabolism | In Vitro Techniques
Journal Article
Journal of Neurochemistry, ISSN 0022-3042, 10/2016, Volume 139, Issue 1, pp. 40 - 54
Cerebroside sulfotransferase (CST) catalyzes the production of sulfatide, a major class of myelin‐specific lipids. CST knockout (CST−/−) mice in which...
sulfatide | myelin lipidome | proteolipid protein | cerebroside sulfotransferase | myelin‐associated glycoprotein | shotgun lipidomics | myelin-associated glycoprotein | MULTIDIMENSIONAL MASS-SPECTROMETRY | BIOCHEMISTRY & MOLECULAR BIOLOGY | INCREASED NUMBER | MONOCLONAL-ANTIBODY | NEUROSCIENCES | APOLIPOPROTEIN-E | OLIGODENDROCYTE DIFFERENTIATION | EARLY ALZHEIMERS-DISEASE | CENTRAL-NERVOUS-SYSTEM | BASIC-PROTEIN | Oligodendroglia - metabolism | Myelin Sheath - physiology | Mice, Inbred C57BL | Myelin-Associated Glycoprotein - metabolism | Axons - metabolism | Homeostasis | Lipid Metabolism | Male | Myelin Proteins - genetics | Mice, Knockout | Myelin Sheath - metabolism | Phenotype | Animals | Axons - ultrastructure | Myelin Proteolipid Protein - metabolism | Sulfotransferases - metabolism | Mice | Myelin Sheath - ultrastructure | Sulfoglycosphingolipids - metabolism | Myelin Proteins - metabolism | Lipids | Tremor | Analysis | Myelin proteins | Neurochemistry | Proteins | Catalysis
sulfatide | myelin lipidome | proteolipid protein | cerebroside sulfotransferase | myelin‐associated glycoprotein | shotgun lipidomics | myelin-associated glycoprotein | MULTIDIMENSIONAL MASS-SPECTROMETRY | BIOCHEMISTRY & MOLECULAR BIOLOGY | INCREASED NUMBER | MONOCLONAL-ANTIBODY | NEUROSCIENCES | APOLIPOPROTEIN-E | OLIGODENDROCYTE DIFFERENTIATION | EARLY ALZHEIMERS-DISEASE | CENTRAL-NERVOUS-SYSTEM | BASIC-PROTEIN | Oligodendroglia - metabolism | Myelin Sheath - physiology | Mice, Inbred C57BL | Myelin-Associated Glycoprotein - metabolism | Axons - metabolism | Homeostasis | Lipid Metabolism | Male | Myelin Proteins - genetics | Mice, Knockout | Myelin Sheath - metabolism | Phenotype | Animals | Axons - ultrastructure | Myelin Proteolipid Protein - metabolism | Sulfotransferases - metabolism | Mice | Myelin Sheath - ultrastructure | Sulfoglycosphingolipids - metabolism | Myelin Proteins - metabolism | Lipids | Tremor | Analysis | Myelin proteins | Neurochemistry | Proteins | Catalysis
Journal Article