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Journal Article
Nature, ISSN 0028-0836, 2013, Volume 501, Issue 7466, pp. 242 - 246
The tumour necrosis factor (TNF) family is crucial for immune homeostasis, cell death and inflammation. These cytokines are recognized by members of the TNF... 
PATHWAYS | TOLL-LIKE-RECEPTORS | NECROSIS-FACTOR RECEPTOR | PROTEIN | TRADD | MULTIDISCIPLINARY SCIENCES | ESCHERICHIA-COLI | SUPERFAMILY | BACTERIAL EFFECTOR | FAMILY | NLEB | Receptor-Interacting Protein Serine-Threonine Kinases - metabolism | Tumor Necrosis Factor-alpha - metabolism | Protein Biosynthesis | Humans | Virulence | Receptor-Interacting Protein Serine-Threonine Kinases - chemistry | Male | NF-kappa B - metabolism | Receptors, Tumor Necrosis Factor, Type I - metabolism | fas Receptor - metabolism | Multiprotein Complexes - metabolism | Enteropathogenic Escherichia coli - metabolism | Enteropathogenic Escherichia coli - pathogenicity | Receptors, Tumor Necrosis Factor, Type I - chemistry | TNF Receptor-Associated Death Domain Protein - metabolism | Acylation | Disease Models, Animal | Protein Structure, Tertiary | Signal Transduction | Mice, Inbred C57BL | Fas-Associated Death Domain Protein - metabolism | Escherichia coli Infections - microbiology | Escherichia coli Proteins - metabolism | Escherichia coli Infections - metabolism | TNF-Related Apoptosis-Inducing Ligand - metabolism | Fas-Associated Death Domain Protein - chemistry | N-Acetylglucosaminyltransferases - metabolism | Multiprotein Complexes - chemistry | Animals | TNF Receptor-Associated Death Domain Protein - chemistry | Escherichia coli Infections - pathology | Virulence Factors - metabolism | Mice | HeLa Cells | Arginine - metabolism | Apoptosis | Death Domain Receptor Signaling Adaptor Proteins - metabolism | Arginine | Cytokines | Cell death | Tumor necrosis factor | Escherichia coli | Genetic aspects | Research | Properties | Salmonella | Microbiology | Kinases | Bacteriology | Index Medicus
Journal Article
Science, ISSN 0036-8075, 8/2012, Volume 337, Issue 6097, pp. 975 - 980
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 5/2012, Volume 109, Issue 19, pp. 7280 - 7285
O-linked N-acetylglucosamine (O-GlcNAc) is a reversible posttranslational modification of Ser and Thr residues on cytosolic and nuclear proteins of higher... 
Datasets | Brain | Phosphorylation | Proteomics | Mass spectroscopy | Gene expression regulation | Physiological regulation | Grants | Proteomes | Alzheimers disease | Chemical/enzymatic photochemical cleavage enrichment | Glycosylation | Mouse cerebral cortex | mouse cerebral cortex | LINKED-N-ACETYLGLUCOSAMINE | chemical/enzymatic photochemical cleavage enrichment | PHOSPHORYLATION | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | glycosylation | EXTRACELLULAR DOMAIN | ELECTRON-TRANSFER DISSOCIATION | UBIQUITIN LIGASE NEDD4-1 | GLUCOSE-METABOLISM | NOTCH RECEPTORS | PROTEOMICS | Amino Acid Sequence | Glycoproteins - metabolism | Brain - enzymology | Molecular Sequence Data | Cytoplasm - metabolism | Epidermal Growth Factor - metabolism | N-Acetylglucosaminyltransferases - metabolism | Acetylglucosamine - metabolism | Brain - metabolism | Animals | Cell Nucleus - metabolism | Peptides - metabolism | Cell Membrane - metabolism | Mice | Proteomics - methods | Binding Sites | Organelles - metabolism | Proteome - metabolism | Tandem Mass Spectrometry - methods | Proteins | Peptides | Catalysis | Mass spectrometry | Photochemistry | Index Medicus | Epidermal growth factor | Core protein | N-Acetylglucosamine | Neurodegenerative diseases | Cortex | versican | Tryptic peptides | Alzheimer's disease | Membrane proteins | MEMBRANE PROTEINS | CEPC enrichment | BASIC BIOLOGICAL SCIENCES | SUBSTRATES | HCD | MASS SPECTROSCOPY | TRANSFERASES | CLEAVAGE | 60 APPLIED LIFE SCIENCES | O-GlcNAc | MODIFICATIONS | DISEASES | PEPTIDES | ETD | Environmental Molecular Sciences Laboratory | TARGETS | mass spectrometry | PROTEINS | RESIDUES | BRAIN | CID | Biological Sciences | enzymatic photochemical cleavage enrichment | chemical
Journal Article
FASEB Journal, ISSN 0892-6638, 2014, Volume 28, Issue 8, pp. 3325 - 3328
Dysfunctions in Wnt signaling increase beta-catenin stability and are associated with cancers, including colorectal cancer. In addition, beta-catenin... 
Wnt signaling | ETD-MS/MS | Cancer | LACTIC-ACID | ACTIVATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | RISK | INCIDENT COLORECTAL-CANCER | CELL-GROWTH | TUMORS | CELL BIOLOGY | PATHWAY | BIOLOGY | cancer | GLCNAC GLYCOSYLATION | MUTATIONS | CARBOHYDRATE-METABOLISM | Intestinal Mucosa - metabolism | Phosphorylation | Threonine - chemistry | alpha Catenin - metabolism | Adenocarcinoma - etiology | Humans | Hyperglycemia - complications | Molecular Sequence Data | Male | Dietary Carbohydrates - metabolism | Neoplasm Proteins - metabolism | Adherens Junctions - metabolism | Acetylglucosamine - metabolism | Colorectal Neoplasms - etiology | Adenocarcinoma - metabolism | MCF-7 Cells | Proteolysis | HEK293 Cells | beta Catenin - chemistry | Protein Stability | Dietary Carbohydrates - toxicity | Colorectal Neoplasms - metabolism | Wnt Signaling Pathway | Amino Acid Sequence | Mice, Inbred C57BL | RNA, Small Interfering - pharmacology | Enzyme Inhibitors - pharmacology | Neoplasm Proteins - chemistry | beta-N-Acetylhexosaminidases - antagonists & inhibitors | Glycosylation | beta Catenin - metabolism | Colon - metabolism | Adherens Junctions - pathology | Protein Interaction Mapping | Hyperglycemia - metabolism | Animals | beta-N-Acetylhexosaminidases - physiology | Glucose - metabolism | N-Acetylglucosaminyltransferases - antagonists & inhibitors | N-Acetylglucosaminyltransferases - physiology | Mice | Protein Processing, Post-Translational | Index Medicus | Research Communications | ETD-MS
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2013, Volume 8, Issue 4, pp. e58224 - e58224
Intestinal absorption of dietary fat is a complex process mediated by enterocytes leading to lipid assembly and secretion of circulating lipoproteins as... 
CHOLESTEROL ABSORPTION | TRANSPORT | PROTEIN | HUMAN PLASMA | ENTEROCYTES | PHYSIOLOGICAL REGULATION | MULTIDISCIPLINARY SCIENCES | ENDOPLASMIC-RETICULUM | SECRETION | TOF-SIMS | LIPOPROTEINS | Dietary Fats - metabolism | Enterocytes - metabolism | Taurocholic Acid - metabolism | Sterol Esterase - metabolism | Lipoproteins, HDL - metabolism | N-Acetylglucosaminyltransferases - genetics | Intestinal Absorption | Biological Transport | Duodenum - cytology | Duodenum - metabolism | Sterol O-Acyltransferase - metabolism | Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | Fatty Acids - metabolism | Gene Expression | Enterocytes - cytology | Mice, Inbred C57BL | Lipid Metabolism | Lipase - metabolism | Cholesterol - metabolism | N-Acetylglucosaminyltransferases - metabolism | Triglycerides - metabolism | Acetyl-CoA C-Acetyltransferase - genetics | Carrier Proteins - genetics | Chylomicrons - metabolism | Animals | Carrier Proteins - metabolism | Sterol Esterase - genetics | Mice | Sterol O-Acyltransferase - genetics | Acetyl-CoA C-Acetyltransferase - metabolism | Lipase - genetics | Dietary fat | Usage | Research | Health aspects | Mass spectrometry | Lecithin | Liver | Lipids | Adipocytes | Lipase | Small intestine | Proteins | Absorption | Intestine | Rodents | Atherosclerosis | Coenzyme A | Droplets | Localization | Intestinal absorption | Lipoproteins (high density) | Spectroscopy | Taurocholic acid | Duodenum | Secretion | Chylomicrons | Mass spectroscopy | Secondary ion mass spectrometry | Triglycerides | Digestion | Metabolism | Fatty acids | Cholesterol | Esterification | Lipoproteins (very low density) | Lipoproteins | Enterocytes | Diet | Arteriosclerosis | Sphingomyelin | Oils & fats | Scientific imaging | Fats | Acylglycerols | Endoplasmic reticulum | Bile | Index Medicus | Organic chemistry | Chemical Sciences
Journal Article
Nature, ISSN 0028-0836, 2013, Volume 501, Issue 7466, pp. 247 - 251
Successful infection by enteric bacterial pathogens depends on the ability of the bacteria to colonize the gut, replicate in host tissues and disseminate to... 
SYSTEM | INDUCED APOPTOSIS | ROLES | MULTIDISCIPLINARY SCIENCES | DISEASE | CITROBACTER-RODENTIUM | VIRULENCE | PROTEINS | NLEB | Receptor-Interacting Protein Serine-Threonine Kinases - metabolism | Fas Ligand Protein - metabolism | Humans | fas Receptor - deficiency | Caspase 8 - metabolism | Receptor-Interacting Protein Serine-Threonine Kinases - chemistry | Male | Citrobacter rodentium - pathogenicity | fas Receptor - metabolism | Enteropathogenic Escherichia coli - metabolism | Enteropathogenic Escherichia coli - pathogenicity | Cell Death | HEK293 Cells | Female | TNF Receptor-Associated Death Domain Protein - metabolism | Protein Structure, Tertiary | Citrobacter rodentium - physiology | Signal Transduction | Fas-Associated Death Domain Protein - metabolism | Escherichia coli Infections - microbiology | Gastrointestinal Tract - microbiology | Escherichia coli Proteins - metabolism | Escherichia coli Infections - metabolism | Fas-Associated Death Domain Protein - chemistry | N-Acetylglucosaminyltransferases - metabolism | Fas Ligand Protein - antagonists & inhibitors | Animals | TNF Receptor-Associated Death Domain Protein - chemistry | Escherichia coli Infections - pathology | Virulence Factors - metabolism | Mice | Enzyme Activation | HeLa Cells | Cell receptors | Bacterial infections | Pathogenic microorganisms | Microbiology | Physiological aspects | Research | Stomach diseases | Proteins | Yeast | Microscopy | Rodents | Infections | Kinases | Apoptosis | Index Medicus | EPEC | apoptosis | caspase-8 | death domain
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 10/2007, Volume 282, Issue 42, pp. 31038 - 31045
Methylglyoxal is a highly reactive dicarbonyl degradation product formed from triose phosphates during glycolysis. Methylglyoxal forms stable adducts primarily... 
DIABETIC-RETINOPATHY | ACTIVATION | ADVANCED GLYCATION | SP1 | BIOCHEMISTRY & MOLECULAR BIOLOGY | O-GLYCOSYLATION | MICE | 3 MAJOR PATHWAYS | EXPRESSION | HYPERGLYCEMIC DAMAGE | GLYOXALASE-I | Tumor Necrosis Factor-alpha - metabolism | Transcription, Genetic - drug effects | Kidney - pathology | Sweetening Agents - metabolism | Angiopoietin-2 - genetics | Protein Processing, Post-Translational - genetics | Diabetes Mellitus, Experimental - genetics | N-Acetylglucosaminyltransferases - genetics | Glycolysis - drug effects | Acetylglucosamine - metabolism | Glycolysis - genetics | Pyruvaldehyde - metabolism | Kidney - metabolism | Diabetic Angiopathies - pathology | Protein Processing, Post-Translational - drug effects | Arginine - genetics | Intercellular Adhesion Molecule-1 - biosynthesis | Vascular Cell Adhesion Molecule-1 - genetics | Response Elements - genetics | Diabetes Mellitus, Experimental - metabolism | Diabetic Angiopathies - genetics | Repressor Proteins - metabolism | Sp3 Transcription Factor - metabolism | Diabetic Angiopathies - metabolism | Sweetening Agents - pharmacology | Endothelial Cells - metabolism | Gene Expression Regulation - genetics | Sp3 Transcription Factor - genetics | Angiopoietin-2 - biosynthesis | Repressor Proteins - genetics | Glucose - pharmacology | Acetylglucosamine - genetics | N-Acetylglucosaminyltransferases - metabolism | Gene Expression Regulation - drug effects | Tumor Necrosis Factor-alpha - pharmacology | Animals | Intercellular Adhesion Molecule-1 - genetics | Diabetes Mellitus, Experimental - pathology | Glucose - metabolism | Vascular Cell Adhesion Molecule-1 - biosynthesis | Mice | Endothelial Cells - pathology | Arginine - metabolism | Cell Line, Transformed | Index Medicus
Journal Article
Journal Article
The EMBO Journal, ISSN 0261-4189, 03/2013, Volume 32, Issue 5, pp. 645 - 655
Journal Article
Journal Article
Journal Article