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Journal Article
The FASEB journal, ISSN 1530-6860, 2014, Volume 28, Issue 8, pp. 3325 - 3338
Dysfunctions in Wnt signaling increase β‐catenin stability and are associated with cancers, including colorectal cancer. In addition, β‐catenin degradation is... 
ETD‐MS/MS | Wnt signaling | cancer | ETD-MS/MS | Cancer | LACTIC-ACID | ACTIVATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | RISK | INCIDENT COLORECTAL-CANCER | CELL-GROWTH | TUMORS | CELL BIOLOGY | PATHWAY | BIOLOGY | 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 | Research Communications | ETD-MS
Journal Article
Science (American Association for the Advancement of Science), ISSN 1095-9203, 2013, Volume 342, Issue 6163, pp. 1235 - 1239
Journal Article
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 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 | MULTIDISCIPLINARY SCIENCES | glycosylation | EXTRACELLULAR DOMAIN | ELECTRON-TRANSFER DISSOCIATION | GLUCOSE-METABOLISM | CLONING | DISEASE | CROSSTALK | 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 | 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
PLoS ONE, ISSN 1932-6203, 04/2013, Volume 8, Issue 4, p. e58224
... to overconsumption of lipids, associated to low physical activity. Absorption by the small intestine has a key role in this metabolism being the exclusive site of absorption... 
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 | Lipids | Adipocytes | Lipase | Small intestine | Proteins | Absorption | Intestine | Rodents | Atherosclerosis | Coenzyme A | Droplets | Localization | Intestinal absorption | Lipoproteins (high density) | Spectroscopy | Taurocholic acid | Duodenum | 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 | Organic chemistry | Chemical Sciences
Journal Article
Nature communications, ISSN 2041-1723, 2018, Volume 9, Issue 1, pp. 3287 - 17
Leukocytes are coated with a layer of heterogeneous carbohydrates (glycans) that modulate immune function, in part by governing specific interactions with... 
LYN | IMMUNITY | PROTEIN | MULTIDISCIPLINARY SCIENCES | RED-CELLS | SIALIC ACIDS | BINDING | T-CELLS | CD22 | ANTIGEN | LYMPHOCYTES | Phosphorylation | Cell Proliferation | Leukocyte Common Antigens - metabolism | Humans | Receptors, Antigen, B-Cell - metabolism | Endocytosis | Lymphocyte Activation - immunology | Cell Nucleus - metabolism | Sialic Acid Binding Ig-like Lectin 2 - metabolism | src-Family Kinases - metabolism | Polysaccharides - chemistry | B-Lymphocytes - metabolism | Calcium Signaling | Cell Line | N-Acetylhexosaminyltransferases - metabolism | Signal Transduction | Lymphoid Tissue - metabolism | N-Acetylneuraminic Acid - metabolism | Polysaccharides - metabolism | Germinal Center - metabolism | Protein Tyrosine Phosphatase, Non-Receptor Type 6 - metabolism | Models, Biological | Protein Binding | Galectins - blood | Immunologic Memory | Amino Sugars - chemistry | Immunologic Factors - metabolism | Galectins - metabolism | Lymphocyte receptors | SHP-1 protein | Calcium | N-Acetylglucosinyldiphosphodolichol N-acetylglucosaminyltransferase | Activation | Leukocytes | B-cell receptor | CD45 antigen | Calcium signalling | Proteins | Galectin-9 | Cell activation | Polysaccharides | Germinal centers | Sugars | Binding | Carbohydrates | Immunological memory | Memory cells | Immune response | Tonsil | Immunoregulation | T cell receptors | N-glycans | Glycan | Membrane proteins | White blood cells | CD22 antigen | Lymphocytes B | Lectins
Journal Article
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
Journal Article
Nature (London), ISSN 1476-4687, 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 | EPEC | apoptosis | caspase-8 | death domain
Journal Article