scholarly article | Q13442814 |
review article | Q7318358 |
P50 | author | Kuo-I Lin | Q90673109 |
P2093 | author name string | Chia-Lin Weng | |
Yi-Hsuan Chang | |||
P2860 | cites work | Molecular cloning and characterization of murine and human N-acetylglucosamine kinase | Q22254147 |
Dynamic O-glycosylation of nuclear and cytosolic proteins: cloning and characterization of a neutral, cytosolic beta-N-acetylglucosaminidase from human brain | Q24290716 | ||
Requirement for O-linked N-acetylglucosaminyltransferase in lymphocytes activation | Q24294511 | ||
Dynamic glycosylation of nuclear and cytosolic proteins. Cloning and characterization of a unique O-GlcNAc transferase with multiple tetratricopeptide repeats | Q24310656 | ||
O-Linked GlcNAc transferase is a conserved nucleocytoplasmic protein containing tetratricopeptide repeats | Q24310686 | ||
LSP1 regulates anti-IgM induced apoptosis in WEHI-231 cells and normal immature B-cells | Q40936146 | ||
Recognition of a glycosylation substrate by the O-GlcNAc transferase TPR repeats | Q40984745 | ||
Modulation of O-linked N-acetylglucosamine levels on nuclear and cytoplasmic proteins in vivo using the peptide O-GlcNAc-beta-N-acetylglucosaminidase inhibitor O-(2-acetamido-2-deoxy-D-glucopyranosylidene)amino-N-phenylcarbamate | Q41061967 | ||
Discovery of a metabolic pathway mediating glucose-induced desensitization of the glucose transport system. Role of hexosamine biosynthesis in the induction of insulin resistance | Q41179543 | ||
A novel disulfide-linked heterodimer on pre-T cells consists of the T cell receptor beta chain and a 33 kd glycoprotein | Q41520076 | ||
Elucidating crosstalk mechanisms between phosphorylation and O-GlcNAcylation | Q41613862 | ||
Structural and functional insight into human O-GlcNAcase | Q41686648 | ||
Structural insights into the substrate binding adaptability and specificity of human O-GlcNAcase | Q41689766 | ||
Myeloid-derived cullin 3 promotes STAT3 phosphorylation by inhibiting OGT expression and protects against intestinal inflammation. | Q41978406 | ||
Protein O-GlcNAc modulates motility-associated signaling intermediates in neutrophils | Q42474134 | ||
Hexosamines are unlikely to function as a nutrient-sensor in 3T3-L1 adipocytes: a comparison of UDP-hexosamine levels after increased glucose flux and glucosamine treatment | Q42830486 | ||
Enhanced Th1 activity and development of chronic enterocolitis in mice devoid of Stat3 in macrophages and neutrophils. | Q44021327 | ||
Mitochondrial and nucleocytoplasmic isoforms of O-linked GlcNAc transferase encoded by a single mammalian gene | Q44264485 | ||
YY1 is regulated by O-linked N-acetylglucosaminylation (O-glcNAcylation). | Q44317031 | ||
Palmitate-induced activation of the hexosamine pathway in human myotubes: increased expression of glutamine:fructose-6-phosphate aminotransferase | Q44328952 | ||
26S proteasome subunits are O-linked N-acetylglucosamine-modified in Drosophila melanogaster | Q44677602 | ||
IL-10 induces IL-10 in primary human monocyte-derived macrophages via the transcription factor Stat3. | Q44723708 | ||
Dynamic actions of glucose and glucosamine on hexosamine biosynthesis in isolated adipocytes: differential effects on glucosamine 6-phosphate, UDP-N-acetylglucosamine, and ATP levels | Q44938128 | ||
Neutrophils exhibit rapid agonist-induced increases in protein-associated O-GlcNAc | Q45025090 | ||
Hyper-O-GlcNAcylation activates nuclear factor κ-light-chain-enhancer of activated B cells (NF-κB) signaling through interplay with phosphorylation and acetylation. | Q46015847 | ||
Profiling of Protein O-GlcNAcylation in Murine CD8+ Effector- and Memory-like T Cells. | Q46076973 | ||
Enzymatic addition of O-GlcNAc to nuclear and cytoplasmic proteins. Identification of a uridine diphospho-N-acetylglucosamine:peptide beta-N-acetylglucosaminyltransferase | Q46669689 | ||
O-GlcNAcylation is required for B cell homeostasis and antibody responses | Q47113112 | ||
The "Big-Bang" for modern glial biology: Translation and comments on Pío del Río-Hortega 1919 series of papers on microglia | Q47658635 | ||
Structures of human O-GlcNAcase and its complexes reveal a new substrate recognition mode. | Q48103560 | ||
Rearrangement and diversity of T cell receptor beta chain genes in thymocytes: a critical role for the beta chain in development | Q48120520 | ||
Lipopolysaccharide (LPS)-stimulated iNOS Induction Is Increased by Glucosamine under Normal Glucose Conditions but Is Inhibited by Glucosamine under High Glucose Conditions in Macrophage Cells | Q48402759 | ||
Thiamet G mediates neuroprotection in experimental stroke by modulating microglia/macrophage polarization and inhibiting NF-κB p65 signaling. | Q48423896 | ||
Macrophage plasticity, polarization and function in health and disease | Q50107325 | ||
O-GlcNAcylation regulates EZH2 protein stability and function | Q24324113 | ||
Structure of human O-GlcNAc transferase and its complex with a peptide substrate | Q24337218 | ||
O-GlcNAc transferase catalyzes site-specific proteolysis of HCF-1 | Q24339060 | ||
Keap1 is a redox-regulated substrate adaptor protein for a Cul3-dependent ubiquitin ligase complex | Q24559743 | ||
Oxidative stress sensor Keap1 functions as an adaptor for Cul3-based E3 ligase to regulate proteasomal degradation of Nrf2 | Q24563807 | ||
Caenorhabditis elegans ortholog of a diabetes susceptibility locus: oga-1 (O-GlcNAcase) knockout impacts O-GlcNAc cycling, metabolism, and dauer | Q24670972 | ||
The O-GlcNAc transferase gene resides on the X chromosome and is essential for embryonic stem cell viability and mouse ontogeny | Q24685967 | ||
A potent mechanism-inspired O-GlcNAcase inhibitor that blocks phosphorylation of tau in vivo | Q27650997 | ||
Human OGA binds substrates in a conserved peptide recognition groove | Q27664652 | ||
HCF-1 Is Cleaved in the Active Site of O-GlcNAc Transferase | Q27680781 | ||
Control of regulatory T cell development by the transcription factor Foxp3 | Q27860489 | ||
The orphan nuclear receptor RORgammat directs the differentiation program of proinflammatory IL-17+ T helper cells | Q27860620 | ||
Foxp3 programs the development and function of CD4+CD25+ regulatory T cells | Q27860714 | ||
Identification and characterization of MAVS, a mitochondrial antiviral signaling protein that activates NF-kappaB and IRF 3 | Q27861127 | ||
Characterization of the essential yeast gene encoding N-acetylglucosamine-phosphate mutase. | Q27932464 | ||
The eukaryotic UDP-N-acetylglucosamine pyrophosphorylases. Gene cloning, protein expression, and catalytic mechanism. | Q27936943 | ||
Functional expression of O-linked GlcNAc transferase. Domain structure and substrate specificity | Q28141169 | ||
Identification and cloning of a novel family of coiled-coil domain proteins that interact with O-GlcNAc transferase | Q28215129 | ||
Glycosylation of nuclear and cytoplasmic proteins. Purification and characterization of a uridine diphospho-N-acetylglucosamine:polypeptide beta-N-acetylglucosaminyltransferase | Q28279453 | ||
Glucose induces an autocrine activation of the Wnt/beta-catenin pathway in macrophage cell lines | Q28295410 | ||
Cloning and characterization of the murine glucosamine-6-phosphate acetyltransferase EMeg32. Differential expression and intracellular membrane association | Q28512111 | ||
Increasing brain protein O-GlcNAc-ylation mitigates breathing defects and mortality of Tau.P301L mice | Q28537913 | ||
Regulation of a cytosolic and nuclear O-GlcNAc transferase. Role of the tetratricopeptide repeats | Q28581400 | ||
STATs in cancer inflammation and immunity: a leading role for STAT3 | Q29547203 | ||
Macrophages, inflammation, and insulin resistance | Q29614351 | ||
The Keap1-BTB protein is an adaptor that bridges Nrf2 to a Cul3-based E3 ligase: oxidative stress sensing by a Cul3-Keap1 ligase | Q29616502 | ||
O-GlcNAc transferase inhibitors: current tools and future challenges. | Q30384281 | ||
Modification of RelA by O-linked N-acetylglucosamine links glucose metabolism to NF-κB acetylation and transcription | Q30419967 | ||
Quantification of O-GlcNAc protein modification in neutrophils by flow cytometry | Q30532863 | ||
A monoclonal antibody against a family of nuclear pore proteins (nucleoporins): O-linked N-acetylglucosamine is part of the immunodeterminant | Q30734241 | ||
Alternative O-glycosylation/O-phosphorylation of serine-16 in murine estrogen receptor beta: post-translational regulation of turnover and transactivation activity | Q31813156 | ||
Modification of p53 with O-linked N-acetylglucosamine regulates p53 activity and stability | Q33256999 | ||
Dynamic interplay between O-linked N-acetylglucosaminylation and glycogen synthase kinase-3-dependent phosphorylation | Q33284870 | ||
Cross-talk between GlcNAcylation and phosphorylation: site-specific phosphorylation dynamics in response to globally elevated O-GlcNAc | Q36893523 | ||
Glucose and glutamine fuel protein O-GlcNAcylation to control T cell self-renewal and malignancy | Q36988176 | ||
Up-regulation of O-GlcNAc transferase with glucose deprivation in HepG2 cells is mediated by decreased hexosamine pathway flux. | Q37081885 | ||
Loss of p53 enhances catalytic activity of IKKbeta through O-linked beta-N-acetyl glucosamine modification | Q37117710 | ||
Temporal regulation of Lsp1 O-GlcNAcylation and phosphorylation during apoptosis of activated B cells | Q37208251 | ||
Lymphocyte activation induces rapid changes in nuclear and cytoplasmic glycoproteins | Q37413972 | ||
Neutrophil function: from mechanisms to disease | Q37973773 | ||
How RIG-I like receptors activate MAVS. | Q38460076 | ||
Necroptosis and Inflammation | Q38729108 | ||
Changes in O-Linked N-Acetylglucosamine (O-GlcNAc) Homeostasis Activate the p53 Pathway in Ovarian Cancer Cells. | Q38758695 | ||
Hijacking a biosynthetic pathway yields a glycosyltransferase inhibitor within cells. | Q38845236 | ||
The Biochemistry of O-GlcNAc Transferase: Which Functions Make It Essential in Mammalian Cells? | Q38863245 | ||
O-GlcNAcylation in Cancer Biology: Linking Metabolism and Signaling | Q38876699 | ||
O-GlcNAcylation and neurodegeneration | Q38920683 | ||
O-GlcNAcylation and p50/p105 binding of c-Rel are dynamically regulated by LPS and glucosamine in BV2 microglia cells | Q39155899 | ||
Protein O-GlcNAcylation: emerging mechanisms and functions | Q39295247 | ||
Denitrosylation of S-nitrosylated OGT is triggered in LPS-stimulated innate immune response | Q39567711 | ||
Glucosamine exerts a neuroprotective effect via suppression of inflammation in rat brain ischemia/reperfusion injury | Q39663614 | ||
The ubiquitin E3 ligase TRIM31 promotes aggregation and activation of the signaling adaptor MAVS through Lys63-linked polyubiquitination | Q39757179 | ||
Complex N-glycan number and degree of branching cooperate to regulate cell proliferation and differentiation. | Q40147884 | ||
Notch promotes survival of pre-T cells at the beta-selection checkpoint by regulating cellular metabolism | Q40390896 | ||
β‐Amyloid precursor protein is modified with O‐linked N‐acetylglucosamine | Q40468759 | ||
Inhibition of the activating signals in NK92 cells by recombinant GST-sHLA-G1a chain | Q40561561 | ||
O-GlcNAc modification is an endogenous inhibitor of the proteasome | Q40607491 | ||
Kinetic characterization of human glutamine-fructose-6-phosphate amidotransferase I: potent feedback inhibition by glucosamine 6-phosphate | Q40751230 | ||
MicroRNA-15b Suppresses Th17 Differentiation and Is Associated with Pathogenesis of Multiple Sclerosis by Targeting O-GlcNAc Transferase. | Q50878107 | ||
Insights into activity and inhibition from the crystal structure of human O-GlcNAcase. | Q51084028 | ||
Macrophages and the Recovery from Acute and Chronic Inflammation. | Q51270292 | ||
Glycosylation of chromosomal proteins: localization of O-linked N-acetylglucosamine in Drosophila chromatin. | Q52452782 | ||
An Overview on the Clinical Development of Tau-Based Therapeutics. | Q52594209 | ||
Increasing O-GlcNAc slows neurodegeneration and stabilizes tau against aggregation. | Q53434499 | ||
The subcellular distribution of terminal N-acetylglucosamine moieties. Localization of a novel protein-saccharide linkage, O-linked GlcNAc. | Q54426511 | ||
The Nutrient-Sensing Hexosamine Biosynthetic Pathway as the Hub of Cancer Metabolic Rewiring. | Q55497180 | ||
Deficient O-GlcNAc Glycosylation Impairs Regulatory T Cell Differentiation and Notch Signaling in Autoimmune Hepatitis | Q57816684 | ||
Natural Killer Cells: Development, Maturation, and Clinical Utilization | Q58785734 | ||
The lineage stability and suppressive program of regulatory T cells require protein O-GlcNAcylation | Q61124946 | ||
Nutrient regulation of signaling and transcription | Q64251360 | ||
Glucosamine prevents polarization of cytotoxic granules in NK-92 cells by disturbing FOXO1/ERK/paxillin phosphorylation. | Q64982206 | ||
An intrinsic membrane glycoprotein of the golgi apparatus with O-linked N-acetylglucosamine facing the cytosol | Q67980880 | ||
Translocation of UDP-N-acetylglucosamine into vesicles derived from rat liver rough endoplasmic reticulum and Golgi apparatus | Q70090012 | ||
O-linked N-acetylglucosamine is attached to proteins of the nuclear pore. Evidence for cytoplasmic and nucleoplasmic glycoproteins | Q70345116 | ||
Erythrocytes contain cytoplasmic glycoproteins. O-linked GlcNAc on Band 4.1. | Q70363440 | ||
Topography and polypeptide distribution of terminal N-acetylglucosamine residues on the surfaces of intact lymphocytes. Evidence for O-linked GlcNAc | Q70466786 | ||
T cell receptor beta chain gene rearrangement and selection during thymocyte development in adult mice | Q71680581 | ||
Mitochondrial and nucleocytoplasmic targeting of O-linked GlcNAc transferase | Q78827061 | ||
Stat5 activation plays a critical role in Th2 differentiation | Q79291245 | ||
The specific and essential role of MAVS in antiviral innate immune responses | Q83817506 | ||
Inhibition of Enhancer of zeste homolog 2 (EZH2) induces natural killer cell-mediated eradication of hepatocellular carcinoma cells | Q88181756 | ||
Metabolic Inhibitors of O-GlcNAc Transferase That Act In Vivo Implicate Decreased O-GlcNAc Levels in Leptin-Mediated Nutrient Sensing | Q88658178 | ||
Deficiency in intestinal epithelial O-GlcNAcylation predisposes to gut inflammation | Q89240862 | ||
Elevated O-GlcNAcylation enhances pro-inflammatory Th17 function by altering the intracellular lipid microenvironment | Q90212429 | ||
O-GlcNAc Transferase Links Glucose Metabolism to MAVS-Mediated Antiviral Innate Immunity | Q90449901 | ||
Therapeutically exploiting STAT3 activity in cancer - using tissue repair as a road map | Q90712078 | ||
Genetic recoding to dissect the roles of site-specific protein O-GlcNAcylation | Q91152191 | ||
Inflammation-induced glycolytic switch controls suppressivity of mesenchymal stem cells via STAT1 glycosylation | Q91212037 | ||
Fueling the fire: emerging role of the hexosamine biosynthetic pathway in cancer | Q91614492 | ||
O-GlcNAc Transferase Suppresses Inflammation and Necroptosis by Targeting Receptor-Interacting Serine/Threonine-Protein Kinase 3 | Q91631677 | ||
Metabolic Regulations in Hematopoietic Stem Cells | Q92140577 | ||
Increased O-GlcNAcylation of c-Myc Promotes Pre-B Cell Proliferation | Q92634106 | ||
MAVS O-GlcNAcylation Is Essential for Host Antiviral Immunity against Lethal RNA Viruses | Q92957671 | ||
Blocked O-GlcNAc cycling disrupts mouse hematopoeitic stem cell maintenance and early T cell development | Q92995104 | ||
Glucosamine improves survival in a mouse model of sepsis and attenuates sepsis-induced lung injury and inflammation | Q93222337 | ||
Intrinsic membrane glycoproteins with cytosol-oriented sugars in the endoplasmic reticulum | Q33552214 | ||
Cellular responses to FMLP challenging: a mini-review | Q33721808 | ||
Activation of the transcriptional function of the NF-κB protein c-Rel by O-GlcNAc glycosylation | Q33791683 | ||
The glucose transporter Glut1 is selectively essential for CD4 T cell activation and effector function | Q33838591 | ||
A Caenorhabditis elegans model of insulin resistance: altered macronutrient storage and dauer formation in an OGT-1 knockout | Q33913856 | ||
Glycosylation of nucleocytoplasmic proteins: signal transduction and O-GlcNAc | Q33939701 | ||
T-bet is rapidly induced by interferon-gamma in lymphoid and myeloid cells | Q33952975 | ||
Requirement for transcription factor NFAT in interleukin-2 expression | Q33957551 | ||
Dynamic O-glycosylation of nuclear and cytosolic proteins: further characterization of the nucleocytoplasmic beta-N-acetylglucosaminidase, O-GlcNAcase | Q34109163 | ||
The transcription factor Myc controls metabolic reprogramming upon T lymphocyte activation | Q34242691 | ||
Mapping of O-GlcNAc sites of 20 S proteasome subunits and Hsp90 by a novel biotin-cystamine tag. | Q34255802 | ||
Purification and characterization of an O-GlcNAc selective N-acetyl-beta-D-glucosaminidase from rat spleen cytosol. | Q34330440 | ||
Glycosylation of the c-Myc transactivation domain | Q34331166 | ||
The superhelical TPR-repeat domain of O-linked GlcNAc transferase exhibits structural similarities to importin alpha | Q34347600 | ||
HLA-G remains a mystery | Q34382901 | ||
The hexosamine biosynthetic pathway couples growth factor-induced glutamine uptake to glucose metabolism | Q34411887 | ||
Transcription factor Foxo1 is a negative regulator of natural killer cell maturation and function | Q34467070 | ||
The thymus as an inductive site for T lymphopoiesis | Q34628878 | ||
Chemotactic signaling pathways in neutrophils: from receptor to actin assembly | Q34713881 | ||
A lipid-droplet-targeted O-GlcNAcase isoform is a key regulator of the proteasome | Q35140884 | ||
Dynamic interplay between O-glycosylation and O-phosphorylation of nucleocytoplasmic proteins: a new paradigm for metabolic control of signal transduction and transcription | Q35185681 | ||
Regulation of TCR alpha and beta gene allelic exclusion during T-cell development | Q35232298 | ||
A little sugar goes a long way: the cell biology of O-GlcNAc | Q35261648 | ||
The active site of O-GlcNAc transferase imposes constraints on substrate sequence | Q35735257 | ||
Antigen receptor-mediated changes in glucose metabolism in B lymphocytes: role of phosphatidylinositol 3-kinase signaling in the glycolytic control of growth | Q35849703 | ||
O-GlcNAcylation of kinases | Q36070732 | ||
Inhibition of in vitro nuclear transport by a lectin that binds to nuclear pores | Q36215912 | ||
Nuclear pore complex glycoproteins contain cytoplasmically disposed O-linked N-acetylglucosamine | Q36216148 | ||
The requirement for Notch signaling at the beta-selection checkpoint in vivo is absolute and independent of the pre-T cell receptor. | Q36227978 | ||
Ogt-dependent X-chromosome-linked protein glycosylation is a requisite modification in somatic cell function and embryo viability | Q36233025 | ||
Ezh2 regulates differentiation and function of natural killer cells through histone methyltransferase activity | Q36435156 | ||
Overexpression of X-linked genes in T cells from women with lupus | Q36755936 | ||
Regulation of the O-linked beta-N-acetylglucosamine transferase by insulin signaling. | Q36798755 | ||
P275 | copyright license | Creative Commons Attribution | Q6905323 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 1 | |
P921 | main subject | N-acetylglucosaminyltransferases | Q76877751 |
P304 | page(s) | 57 | |
P577 | publication date | 2020-04-29 | |
P1433 | published in | Journal of Biomedical Science | Q15759332 |
P1476 | title | O-GlcNAcylation and its role in the immune system | |
P478 | volume | 27 |
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