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Cell Death and Differentiation, ISSN 1350-9047, 08/2011, Volume 18, Issue 8, pp. 1356 - 1365
We have recently reported that the bioactive lipid sphingosine-1-phosphate (S1P), usually signaling proliferation and anti-apoptosis induces neuronal death... 
neurodegeneration | calpain | apoptosis | cis-4-methylsphingosine | release | Sphingosine-1-phosphate | Ca2+-release | ALZHEIMERS-DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | FUNCTIONAL-CHARACTERIZATION | SPHINGOSINE 1-PHOSPHATE | CELL BIOLOGY | SPHINGOLIPID METABOLISM | CYTOCHROME-C | POSTMITOTIC NEURONS | AMYLOID-BETA | CELL-CYCLE | MOLECULAR-CLONING | Lysophospholipids - metabolism | Neurons - pathology | Calpain - metabolism | Caspase 9 - metabolism | Calcium - metabolism | tau Proteins - metabolism | Calpain - genetics | Nerve Degeneration - chemically induced | Nerve Degeneration - metabolism | Neurons - physiology | Sphingosine - metabolism | Aldehyde-Lyases - genetics | Neurons - drug effects | Mice, Inbred C57BL | Phosphotransferases (Alcohol Group Acceptor) - genetics | Mitochondria - metabolism | Caspase 12 - metabolism | Nerve Degeneration - pathology | Cyclin-Dependent Kinase 5 - metabolism | Mice, Knockout | Phosphotransferases (Alcohol Group Acceptor) - metabolism | Sphingosine - pharmacology | Sphingosine - analogs & derivatives | Animals | Cerebellum - cytology | Aldehyde-Lyases - metabolism | Cell Cycle - physiology | Glycosphingolipids - metabolism | Signal Transduction - physiology | Mice | Apoptosis - physiology | Sphingosine - chemistry | Cerebellum | Phosphorylation | Calcium | Central nervous system | Cysteine proteinase | Caspase | Calpain | Lipids | Anatomy | Metabolism | Cyclin-dependent kinase 5 | Sphingosine 1-phosphate | Neurotoxicity | Glycosphingolipids | Tau protein | Neurodegeneration | Phosphate | Cell cycle | Endoplasmic reticulum | Index Medicus | Original Paper
Journal Article
Nature medicine, ISSN 1546-170X, 2008, Volume 14, Issue 11, pp. 1247 - 1255
Journal Article
American journal of respiratory cell and molecular biology, ISSN 1535-4989, 2004, Volume 30, Issue 5, pp. 627 - 634
Journal Article
Molecular biology of the cell, ISSN 1059-1524, 09/2009, Volume 20, Issue 17, pp. 3792 - 3800
In polarized hepatocytes, the predominant route for apical resident proteins to reach the apical bile canalicular membrane is transcytosis. Apical proteins are... 
ENDOSOMES | MEMBRANE MICRODOMAINS | HEPATOCYTES | GLYCOSPHINGOLIPIDS | ENDOCYTIC PATHWAY | CHOLESTEROL | DISTINCT | TRAFFICKING | CAVEOLAE | CHOLERA-TOXIN | CELL BIOLOGY | Cell Polarity | Dipeptidyl Peptidase 4 - metabolism | Dynamins - metabolism | Membrane Microdomains - metabolism | Glycosylphosphatidylinositols - genetics | Humans | Protein Transport - physiology | cdc42 GTP-Binding Protein - metabolism | Intracellular Signaling Peptides and Proteins - metabolism | Hepatocytes - metabolism | Phosphoproteins - metabolism | Recombinant Fusion Proteins - metabolism | Hepatocytes - cytology | Membrane Proteins - metabolism | Intracellular Signaling Peptides and Proteins - genetics | Calcium-Binding Proteins - metabolism | Cell Line | Membrane Proteins - genetics | CD59 Antigens - genetics | Caveolin 1 - genetics | Dynamins - genetics | Dipeptidyl Peptidase 4 - genetics | Clathrin - genetics | Phosphoproteins - genetics | CD13 Antigens - metabolism | Clathrin - metabolism | Endocytosis - physiology | Caveolin 1 - metabolism | Adaptor Proteins, Signal Transducing | Animals | CD13 Antigens - genetics | Glycosylphosphatidylinositols - metabolism | cdc42 GTP-Binding Protein - genetics | Recombinant Fusion Proteins - genetics | CD59 Antigens - metabolism | Calcium-Binding Proteins - genetics | Organic chemistry | Chemical Sciences
Journal Article
The Plant cell, ISSN 1040-4651, 5/2013, Volume 25, Issue 5, pp. 1881 - 1894
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 2014, Volume 111, Issue 35, pp. 12895 - 12900
Glycosphingolipids are important structural constituents of cellular membranes. They are involved in the formation of nanodomains ("lipid rafts"), which serve... 
Epithelial cells | Rafts | Actins | Lipids | Bacteria | Pseudomonas aeruginosa | Cell membranes | Cholesterols | Endothelial cells | P branes | entry | rafts | e-cadherin | receptor | host-cells | pa-i | human endothelial-cells | epithelial-cells | pseudomonas-aeruginosa lectin | membrane invaginations | Infection | Membrane curvature | Glycolipid | membrane curvature | glycolipid | infection | PSEUDOMONAS-AERUGINOSA LECTIN | ENTRY | MULTIDISCIPLINARY SCIENCES | PA-I | RECEPTOR | E-CADHERIN | ADHERENCE | EPITHELIAL-CELLS | RAFTS | BINDING | MEMBRANE INVAGINATIONS | Epithelial Cells - metabolism | Membrane Microdomains - metabolism | Actins - metabolism | Sphingolipids - metabolism | Glycolipids - metabolism | Pseudomonas Infections - microbiology | Adhesins, Bacterial - metabolism | Bacterial Adhesion - physiology | Models, Biological | Pseudomonas aeruginosa - metabolism | Epithelial Cells - microbiology | Glycosphingolipids - metabolism | Signal Transduction - physiology | Cell Membrane - metabolism | Cell Membrane - microbiology | Lipid Bilayers - metabolism | Membrane Microdomains - microbiology | Protein research | Host-parasite relationships | Sphingolipids | Lipid metabolism | Research | Health aspects | Biological Sciences | HOST-CELLS | P822 | HUMAN ENDOTHELIAL-CELLS | I E | 1991 | Multidisciplinary Sciences | V59 | INFECTION AND IMMUNITY
Journal Article
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, ISSN 1422-0067, 12/2019, Volume 20, Issue 23, p. 6051
...) composition in colon tumors. A number of enzymes involved in the SL metabolism have been found to be deregulated in human colon tumors, in experimental rodent studies, and in human colon cancer cells in vitro... 
NEUTRAL CERAMIDASE | APOPTOSIS | colorectal cancer | SPHINGOSINE KINASE 1 | sphingolipid | BIOCHEMISTRY & MOLECULAR BIOLOGY | DNA-DAMAGE | glycosphingolipid | INTESTINAL TUMORIGENESIS | CHEMISTRY, MULTIDISCIPLINARY | lactosylceramide | CELL-DEATH | colon cancer cells | colon cancer (CRC) sphingolipidomics | sphingosine-1-phosphate | ALKALINE SPHINGOMYELINASE | UP-REGULATION | MEMBRANE-ASSOCIATED SIALIDASE | Lysophospholipids - metabolism | Colonic Neoplasms - genetics | Humans | Gene Expression Regulation, Neoplastic | Alkaline Ceramidase - metabolism | Proto-Oncogene Proteins c-akt - genetics | Neutral Ceramidase - metabolism | Lipid Metabolism - genetics | Sphingosine - metabolism | Tumor Cells, Cultured | Proto-Oncogene Proteins c-akt - metabolism | Acid Ceramidase - metabolism | Disease Models, Animal | Sphingosine N-Acyltransferase - metabolism | Acid Ceramidase - genetics | Ceramides - metabolism | Lactosylceramides - metabolism | Phosphotransferases (Alcohol Group Acceptor) - genetics | Sphingolipids - metabolism | Alkaline Ceramidase - genetics | Phosphotransferases (Alcohol Group Acceptor) - metabolism | Neutral Ceramidase - genetics | Sphingosine - analogs & derivatives | Animals | Sphingosine N-Acyltransferase - genetics | Colonic Neoplasms - pathology | Colonic Neoplasms - enzymology
Journal Article
PloS one, ISSN 1932-6203, 2013, Volume 8, Issue 3, p. e58979
Platelets respond to vascular damage and contribute to inflammation, but their role in the neurodegenerative diseases is unknown. We found that the systemic... 
ALZHEIMER-DISEASE | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | MULTIPLE-SCLEROSIS | MULTIDISCIPLINARY SCIENCES | MICROVASCULAR ENDOTHELIAL-CELLS | SPINAL-CORD | GANGLIOSIDES | SIALIC-ACID | ISCHEMIC-STROKE | PERTUSSIS TOXIN | BLOOD | Blood Platelets - immunology | Central Nervous System - metabolism | Encephalomyelitis, Autoimmune, Experimental - metabolism | Membrane Microdomains - metabolism | Encephalomyelitis, Autoimmune, Experimental - immunology | Cerebrovascular Disorders - metabolism | Central Nervous System - immunology | Brain - metabolism | Membrane Microdomains - immunology | Inflammation - metabolism | Astrocytes - immunology | Biological Transport | Cerebrovascular Disorders - immunology | Anaphylaxis - immunology | Neurons - metabolism | Disease Models, Animal | Cell Degranulation | Neurons - immunology | Membrane Microdomains - chemistry | Receptors, Cell Surface - metabolism | Inflammation - immunology | Glycolipids - metabolism | Gangliosides - immunology | Blood-Brain Barrier - metabolism | Animals | Blood Platelets - metabolism | Glycolipids - immunology | Protein Binding | Mice | Anaphylaxis - metabolism | Brain - immunology | Astrocytes - metabolism | Nervous system diseases | Inflammation | B cells | Neurons | Gangliosides | Brain | Cardiac arrhythmia | Disease | Pathogenesis | Central nervous system | Rafts | Parenchyma | Lipids | Lipid rafts | Medical schools | Receptors | Dyspnea | Anaphylaxis | Blood platelets | Cascades | Immune system | Rigid structures | Phenotypes | Immune response | Neurodegenerative diseases | Neurological diseases | Hospitals | Glycosphingolipids | Womens health | Structural damage | Degranulation | Brain damage | Platelets | P-selectin
Journal Article
The Journal of biological chemistry, ISSN 0021-9258, 05/2012, Volume 287, Issue 19, pp. 15523 - 15532
Journal Article
PLoS biology, ISSN 1545-7885, 2018, Volume 16, Issue 11, pp. e2006951 - e2006951
Glycosylation is a fundamental modification of proteins and membrane lipids. Toxins that utilize glycans as their receptors have served as powerful tools to... 
SPHINGOLIPID METABOLISM | LAPTM4B | CLONING | RETROGRADE TRANSPORT | BIOCHEMISTRY & MOLECULAR BIOLOGY | ESCHERICHIA-COLI | BIOLOGY | MEMBRANE-PROTEIN | DISORDERS | REQUIRES | MULTIDRUG-RESISTANCE | EXPRESSION | Shiga Toxins - genetics | Trihexosylceramides - metabolism | Humans | Oncogene Proteins - metabolism | Glycosylation | Golgi Apparatus - physiology | Glycolipids - metabolism | Endosomes - metabolism | Membrane Transport Proteins - physiology | Protein Transport | Bacterial Toxins - metabolism | Shiga Toxins - metabolism | Glycosphingolipids | Trihexosylceramides - physiology | Ricin - metabolism | CRISPR-Cas Systems | HEK293 Cells | Golgi Apparatus - metabolism | Membrane Transport Proteins - metabolism | Ricin - genetics | Membrane Proteins - metabolism | HeLa Cells | Genome-Wide Association Study - methods | Loss of Function Mutation - genetics | Bacterial toxins | Genome-wide association studies | Physiological aspects | Genetic aspects | Nucleotide sequencing | Methods | DNA sequencing | Golgi apparatus | Globotriaosylceramide | Health sciences | Toxicity | Lipids | Homology | Biology | Biochemistry | Genomes | Biosynthesis | Urology | Medical schools | Defects | Cell adhesion & migration | Proteins | Receptors | Polysaccharides | Surgery | University colleges | Crystal structure | CRISPR | Therapeutic applications | Ricin | Mass spectroscopy | Screens | Membrane proteins | Domains | Hospitals | Insects | Glycolipids | Scientific imaging | Toxins | Mass spectrometry | Endoplasmic reticulum | Binding sites | Index Medicus
Journal Article
Nature cell biology, ISSN 1476-4679, 2011, Volume 13, Issue 10, pp. 1189 - 1201
Metazoan internal organs are assembled from polarized tubular epithelia that must set aside an apical membrane domain as a lumenal surface. In a global... 
EPITHELIAL-CELLS | POLARITY | FATTY-ACID | TRAFFICKING | BRANCHED-CHAIN | C-ELEGANS | ENDOPLASMIC-RETICULUM | NEMATODE CAENORHABDITIS-ELEGANS | SPHINGOLIPIDS | GOLGI-COMPLEX | CELL BIOLOGY | Intestinal Mucosa - metabolism | Epithelial Cells - metabolism | Coenzyme A Ligases - genetics | Caenorhabditis elegans Proteins - metabolism | Serine C-Palmitoyltransferase - genetics | Acetyl-CoA Carboxylase - genetics | Coenzyme A Ligases - metabolism | Alcohol Oxidoreductases - genetics | Glucosyltransferases - metabolism | RNA Interference | Time Factors | Intestinal Mucosa - enzymology | Cell Membrane - metabolism | Glucosyltransferases - genetics | Caenorhabditis elegans - metabolism | Hydroxylation | Intestinal Mucosa - ultrastructure | Caenorhabditis elegans - genetics | Glycosphingolipids - biosynthesis | Epithelial Cells - ultrastructure | Alcohol Oxidoreductases - metabolism | Genotype | Cell Membrane - ultrastructure | Cell Enlargement | Serine C-Palmitoyltransferase - metabolism | Caenorhabditis elegans - ultrastructure | Cell Membrane - enzymology | Cell Polarity - genetics | Microscopy, Confocal | Phenotype | Animals | Transport Vesicles - metabolism | Epithelial Cells - enzymology | Caenorhabditis elegans Proteins - genetics | Acetyl-CoA Carboxylase - metabolism | Caenorhabditis elegans - enzymology | Microscopy, Fluorescence | Physiological aspects | Enzymes | Cell membranes | Sphingolipids | Research
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 0027-8424, 5/2012, Volume 109, Issue 19, pp. 7475 - 7480
The interaction between HIV and dendritic cells (DCs) is an important early event in HIV-1 pathogenesis that leads to efficient viral dissemination. Here we... 
T lymphocytes | Dendritic cells | HIV | Virions | Viruses | Lipids | Cell membranes | Liposomes | Gangliosides | HIV 1 | IN-VITRO | PARTICLES | DC-SIGN | MULTIDISCIPLINARY SCIENCES | LIPID RAFTS | TRANS-INFECTION | HUMAN-IMMUNODEFICIENCY-VIRUS | TYPE-1 | MATURATION | GANGLIOSIDE GM3 | T-CELLS | Lipopeptides - pharmacology | Dendritic Cells - immunology | Humans | Monocytes - metabolism | Galactosyltransferases - genetics | Host-Pathogen Interactions - drug effects | Monocytes - immunology | Glycosphingolipids - immunology | Host-Pathogen Interactions - immunology | Glucosyltransferases - metabolism | Flow Cytometry | G(M1) Ganglioside - immunology | HIV-1 - physiology | RNA Interference | N-Acetylgalactosaminyltransferases - genetics | HEK293 Cells | G(M3) Ganglioside - metabolism | N-Acetylgalactosaminyltransferases - metabolism | Dendritic Cells - virology | Dendritic Cells - metabolism | Glucosyltransferases - genetics | Liposomes - immunology | Virion - immunology | Cell Line | Cells, Cultured | Galactosyltransferases - metabolism | Virion - metabolism | Monocytes - virology | HIV-1 - immunology | G(M3) Ganglioside - immunology | Ganglioside Galactosyltransferase | Glycosphingolipids - metabolism | Liposomes - metabolism | HeLa Cells | G(M1) Ganglioside - metabolism | Physiological aspects | Research | HIV (Viruses) | Health aspects | Biological Sciences
Journal Article