| P50 | author | Carolyn Bertozzi | Q7442 |
| P2093 | author name string | Mark M Davis | |
| | Peder J Lund | |
| | Sharon Pitteri | |
| | Christina M Woo | |
| | Andrew C Huang | |
| P2860 | cites work | Requirement for O-linked N-acetylglucosaminyltransferase in lymphocytes activation | Q24294511 |
| | Phosphofructokinase 1 glycosylation regulates cell growth and metabolism | Q24297510 |
| | Phosphoinositide signalling links O-GlcNAc transferase to insulin resistance | Q24315875 |
| | Structure of human O-GlcNAc transferase and its complex with a peptide substrate | Q24337218 |
| | Reduced O-GlcNAcylation links lower brain glucose metabolism and tau pathology in Alzheimer's disease | Q24656640 |
| | The O-GlcNAc transferase gene resides on the X chromosome and is essential for embryonic stem cell viability and mouse ontogeny | Q24685967 |
| | Proteome wide purification and identification of O-GlcNAc-modified proteins using click chemistry and mass spectrometry | Q27334695 |
| | Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources | Q27860739 |
| | Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists | Q28131785 |
| | GRAIL: an E3 ubiquitin ligase that inhibits cytokine gene transcription is expressed in anergic CD4+ T cells | Q28155998 |
| | The ubiquitin ligase SCFFbw7 antagonizes apoptotic JNK signaling | Q28240232 |
| | Cycling of O-linked beta-N-acetylglucosamine on nucleocytoplasmic proteins | Q28299550 |
| | O-GlcNAcylation of cofilin promotes breast cancer cell invasion | Q28564207 |
| | Global identification and characterization of both O-GlcNAcylation and phosphorylation at the murine synapse | Q28594444 |
| | 2016 update of the PRIDE database and its related tools | Q28603110 |
| | Regulation of calcium/calmodulin-dependent kinase IV by O-GlcNAc modification. | Q30490721 |
| | Metabolic cross-talk allows labeling of O-linked beta-N-acetylglucosamine-modified proteins via the N-acetylgalactosamine salvage pathway | Q30498243 |
| | Novel LC-MS² product dependent parallel data acquisition function and data analysis workflow for sequencing and identification of intact glycopeptides | Q30814409 |
| | Glycoform composition profiling of O-glycopeptides derived from human serum IgA1 by matrix-assisted laser desorption ionization-time of flight-mass spectrometry. | Q30832695 |
| | Modification of p53 with O-linked N-acetylglucosamine regulates p53 activity and stability | Q33256999 |
| | O-linked beta-N-acetylglucosamine (O-GlcNAc): Extensive crosstalk with phosphorylation to regulate signaling and transcription in response to nutrients and stress | Q33625265 |
| | S-acylation of LCK protein tyrosine kinase is essential for its signalling function in T lymphocytes | Q33887288 |
| | Quantification of O-glycosylation stoichiometry and dynamics using resolvable mass tags | Q34075637 |
| | A metabolic labeling approach toward proteomic analysis of mucin-type O-linked glycosylation | Q34386471 |
| | O-GlcNAc transferase integrates metabolic pathways to regulate the stability of c-MYC in human prostate cancer cells. | Q34747232 |
| | Chemical reporters for fluorescent detection and identification of O-GlcNAc-modified proteins reveal glycosylation of the ubiquitin ligase NEDD4-1 | Q35002612 |
| | The active site of O-GlcNAc transferase imposes constraints on substrate sequence | Q35735257 |
| | Regulation of CK2 by phosphorylation and O-GlcNAcylation revealed by semisynthesis | Q35783386 |
| | Cross talk between O-GlcNAcylation and phosphorylation: roles in signaling, transcription, and chronic disease | Q35804446 |
| | E3 ubiquitin ligases as T cell anergy factors. | Q35873265 |
| | Isotope-targeted glycoproteomics (IsoTaG): a mass-independent platform for intact N- and O-glycopeptide discovery and analysis. | Q36142717 |
| | O-GlcNAc modification blocks the aggregation and toxicity of the protein α-synuclein associated with Parkinson's disease | Q36200921 |
| | Ogt-dependent X-chromosome-linked protein glycosylation is a requisite modification in somatic cell function and embryo viability | Q36233025 |
| | Post-translational O-GlcNAcylation is essential for nuclear pore integrity and maintenance of the pore selectivity filter | Q36455332 |
| | Sulfated ligands for the copper(I)-catalyzed azide-alkyne cycloaddition | Q36598813 |
| | The nutrient sensor OGT in PVN neurons regulates feeding. | Q36755203 |
| | Glucose and glutamine fuel protein O-GlcNAcylation to control T cell self-renewal and malignancy | Q36988176 |
| | Tailoring T-cell receptor signals by proximal negative feedback mechanisms | Q37252710 |
| | Genome-wide analysis of histone methylation reveals chromatin state-based regulation of gene transcription and function of memory CD8+ T cells | Q37259809 |
| | Global Analysis of O-GlcNAc Glycoproteins in Activated Human T Cells | Q37321175 |
| | Lymphocyte activation induces rapid changes in nuclear and cytoplasmic glycoproteins | Q37413972 |
| | The intersections between O-GlcNAcylation and phosphorylation: implications for multiple signaling pathways | Q37479201 |
| | Emerging roles for protein S-palmitoylation in immunity from chemical proteomics | Q38075225 |
| | Combining high-energy C-trap dissociation and electron transfer dissociation for protein O-GlcNAc modification site assignment | Q38403960 |
| | O-GlcNAcase is essential for embryonic development and maintenance of genomic stability | Q38465648 |
| | A mutant O-GlcNAcase enriches Drosophila developmental regulators. | Q38730380 |
| | High Glucose Stimulates Tumorigenesis in Hepatocellular Carcinoma Cells Through AGER-Dependent O-GlcNAcylation of c-Jun | Q38798215 |
| | EOGT and O-GlcNAc on secreted and membrane proteins | Q39241488 |
| | Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions | Q39811057 |
| | Elucidating crosstalk mechanisms between phosphorylation and O-GlcNAcylation | Q41613862 |
| | Systematic analysis of barrier-forming FG hydrogels from Xenopus nuclear pore complexes | Q41828480 |
| | Human T cell activation results in extracellular signal-regulated kinase (ERK)-calcineurin-dependent exposure of Tn antigen on the cell surface and binding of the macrophage galactose-type lectin (MGL). | Q41840726 |
| | Direct in-gel fluorescence detection and cellular imaging of O-GlcNAc-modified proteins | Q42040937 |
| | O-linked N-acetylglucosamine proteomics of postsynaptic density preparations using lectin weak affinity chromatography and mass spectrometry | Q42679419 |
| | O-linked-N-acetylglucosamine on extracellular protein domains mediates epithelial cell-matrix interactions. | Q44729096 |
| | Development of IsoTaG, a Chemical Glycoproteomics Technique for Profiling Intact N- and O-Glycopeptides from Whole Cell Proteomes. | Q45985041 |
| | Hyper-O-GlcNAcylation activates nuclear factor κ-light-chain-enhancer of activated B cells (NF-κB) signaling through interplay with phosphorylation and acetylation. | Q46015847 |
| | O-GlcNAc occurs cotranslationally to stabilize nascent polypeptide chains | Q48216207 |
| | Topography and polypeptide distribution of terminal N-acetylglucosamine residues on the surfaces of intact lymphocytes. Evidence for O-linked GlcNAc | Q70466786 |
| P577 | publication date | 2018-01-19 | |
| P1433 | published in | Molecular & Cellular Proteomics | Q6895932 |
| P1476 | title | Mapping and quantification of over 2,000 O-linked glycopeptides in activated human T cells with isotope-targeted glycoproteomics (IsoTaG). | |