| scholarly article | Q13442814 |
| P356 | DOI | 10.1101/CSHPERSPECT.A005199 |
| P953 | full work available at URL | http://cshperspectives.cshlp.org/content/3/4/a005199.full.pdf |
| https://doi.org/10.1101/cshperspect.a005199 | ||
| https://europepmc.org/articles/PMC3062213 | ||
| https://europepmc.org/articles/PMC3062213?pdf=render | ||
| https://syndication.highwire.org/content/doi/10.1101/cshperspect.a005199 | ||
| P932 | PMC publication ID | 3062213 |
| P698 | PubMed publication ID | 21441588 |
| P5875 | ResearchGate publication ID | 50868037 |
| P2093 | author name string | Pamela Stanley | |
| P2860 | cites work | Dynamic association between the catalytic and lectin domains of human UDP-GalNAc:polypeptide alpha-N-acetylgalactosaminyltransferase-2 | Q24301958 |
| GPHR is a novel anion channel critical for acidification and functions of the Golgi apparatus | Q24313257 | ||
| Core 2 branching beta1,6-N-acetylglucosaminyltransferase and high endothelial venule-restricted sulfotransferase collaboratively control lymphocyte homing | Q44639255 | ||
| Glycosyltransferase activity of Fringe modulates Notch-Delta interactions. | Q45345395 | ||
| Molecular insights into beta-galactoside alpha2,6-sialyltransferase secretion in vivo | Q46158890 | ||
| O-linked N-acetylglucosamine is present on the extracellular domain of notch receptors | Q46299933 | ||
| Lunatic fringe protein processing by proprotein convertases may contribute to the short protein half-life in the segmentation clock | Q46427203 | ||
| In vitro reconstitution of the modulation of Drosophila Notch-ligand binding by Fringe | Q46960525 | ||
| Functional Characterization of Drosophila Sialyltransferase | Q47070983 | ||
| Windbeutel is required for function and correct subcellular localization of the Drosophila patterning protein Pipe. | Q47071742 | ||
| Medial Golgi but not late Golgi glycosyltransferases exist as high molecular weight complexes. Role of luminal domain in complex formation and localization | Q47241756 | ||
| The role of the membrane-spanning domain and stalk region of N-acetylglucosaminyltransferase I in retention, kin recognition and structural maintenance of the Golgi apparatus in HeLa cells | Q48062442 | ||
| The steady-state distribution of glycosyltransferases between the Golgi apparatus and the endoplasmic reticulum is approximately 90:10. | Q50752875 | ||
| A polarized epithelial cell mutant deficient in translocation of UDP-galactose into the Golgi complex | Q54373337 | ||
| Molecular evolution of protein O-fucosyltransferase genes and splice variants | Q56568617 | ||
| Glycosyl transferases of baby hamster kidney cells and ricin-resistant mutants. O-glycan biosynthesis | Q70462485 | ||
| Kin recognition. A model for the retention of Golgi enzymes | Q72921207 | ||
| Multiple signals are required for alpha2,6-sialyltransferase (ST6Gal I) oligomerization and Golgi localization | Q81103914 | ||
| Identification of glycosyltransferase 8 family members as xylosyltransferases acting on O-glucosylated notch epidermal growth factor repeats | Q24321548 | ||
| LDLC encodes a brefeldin A-sensitive, peripheral Golgi protein required for normal Golgi function | Q24337267 | ||
| Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylation | Q24337849 | ||
| The extracellular region of ErbB4 adopts a tethered conformation in the absence of ligand | Q24536067 | ||
| A unique molecular chaperone Cosmc required for activity of the mammalian core 1 beta 3-galactosyltransferase | Q24543917 | ||
| An investigation of the role of transmembrane domains in Golgi protein retention | Q24598282 | ||
| The Carbohydrate-Active EnZymes database (CAZy): an expert resource for Glycogenomics | Q24655377 | ||
| Insights into the molecular basis of leukocyte tethering and rolling revealed by structures of P- and E-selectin bound to SLe(X) and PSGL-1 | Q27628438 | ||
| Fringe is a glycosyltransferase that modifies Notch | Q28143123 | ||
| Notch ligands are substrates for protein O-fucosyltransferase-1 and Fringe | Q28201516 | ||
| Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan | Q28206027 | ||
| Identification and characterization of abeta1,3-glucosyltransferase that synthesizes the Glc-beta1,3-Fuc disaccharide on thrombospondin type 1 repeats | Q28267777 | ||
| Molecular recognition by LARGE is essential for expression of functional dystroglycan | Q28267964 | ||
| Cosmc is an essential chaperone for correct protein O-glycosylation | Q28506209 | ||
| Multiple isozymes of heparan sulfate/heparin GlcNAc N-deacetylase/GlcN N-sulfotransferase. Structure and activity of the fourth member, NDST4 | Q28591320 | ||
| A testis-specific regulator of complex and hybrid N-glycan synthesis | Q29347272 | ||
| Structure and function in rhodopsin: high-level expression of rhodopsin with restricted and homogeneous N-glycosylation by a tetracycline-inducible N-acetylglucosaminyltransferase I-negative HEK293S stable mammalian cell line | Q29616392 | ||
| N-Glycans of Caenorhabditis elegans are specific to developmental stages | Q30784293 | ||
| Glycosylation site prediction using ensembles of Support Vector Machine classifiers | Q30837456 | ||
| Conservation of peptide acceptor preferences between Drosophila and mammalian polypeptide-GalNAc transferase ortholog pairs | Q30845587 | ||
| Glycomics profiling of Chinese hamster ovary cell glycosylation mutants reveals N-glycans of a novel size and complexity | Q30937269 | ||
| Dynamic developmental elaboration of N-linked glycan complexity in the Drosophila melanogaster embryo | Q33270987 | ||
| Divergent evolution of fucosyltransferase genes from vertebrates, invertebrates, and bacteria | Q33544296 | ||
| The endoplasmic reticulum chaperone Cosmc directly promotes in vitro folding of T-synthase | Q33593911 | ||
| Proteoglycans and pattern formation: sugar biochemistry meets developmental genetics | Q33899439 | ||
| Role of glycosylation of Notch in development | Q33969519 | ||
| Roles of Glycosylation in Notch Signaling | Q34023789 | ||
| Inhibition of Golgi apparatus glycosylation causes endoplasmic reticulum stress and decreased protein synthesis | Q34042596 | ||
| Nucleotide sugar transporters of the Golgi apparatus | Q34066521 | ||
| Dissecting the Biological Role of Mucin-type O-Glycosylation Using RNA Interference in Drosophila Cell Culture | Q34251127 | ||
| Transmembrane BAX Inhibitor Motif Containing (TMBIM) Family Proteins Perturbs a trans-Golgi Network Enzyme, Gb3 Synthase, and Reduces Gb3 Biosynthesis | Q34285102 | ||
| What can yeast tell us about N-linked glycosylation in the Golgi apparatus? | Q34286143 | ||
| Mapping the distribution of Golgi enzymes involved in the construction of complex oligosaccharides | Q34300298 | ||
| Neural-specific α3-fucosylation of N-linked glycans in the Drosophila embryo requires fucosyltransferase A and influences developmental signaling associated with O-glycosylation | Q34308024 | ||
| An evolving view of the eukaryotic oligosaccharyltransferase | Q34471377 | ||
| Rumi is a CAP10 domain glycosyltransferase that modifies Notch and is required for Notch signaling. | Q34744616 | ||
| Role of the conserved oligomeric Golgi (COG) complex in protein glycosylation | Q34763238 | ||
| Mutational and functional analysis of Large in a novel CHO glycosylation mutant | Q34983110 | ||
| Structural remodeling of GPI anchors during biosynthesis and after attachment to proteins | Q35010940 | ||
| Glycosylation engineering | Q36215708 | ||
| Overlapping distribution of two glycosyltransferases in the Golgi apparatus of HeLa cells | Q36232261 | ||
| Transport of vesicular stomatitis virus glycoprotein in a cell-free extract | Q36396443 | ||
| Lectin-resistant CHO glycosylation mutants | Q36657268 | ||
| ProteinC-Mannosylation Is Enzyme-catalysed and Uses Dolichyl-Phosphate-Mannose as a Precursor | Q36851292 | ||
| Notch signaling in normal and disease States: possible therapies related to glycosylation | Q36855548 | ||
| The diversity of O-linked glycans expressed during Drosophila melanogaster development reflects stage- and tissue-specific requirements for cell signaling | Q36949362 | ||
| Deficiencies in subunits of the Conserved Oligomeric Golgi (COG) complex define a novel group of Congenital Disorders of Glycosylation | Q36955423 | ||
| Characterization of mouse sialyltransferase genes: their evolution and diversity | Q37156202 | ||
| Endoplasmic reticulum/golgi nucleotide sugar transporters contribute to the cellular release of UDP-sugar signaling molecules | Q37169570 | ||
| Dystroglycan glycosylation and muscular dystrophy. | Q37261423 | ||
| COG defects, birth and rise! | Q37333173 | ||
| Identification of a glycosylphosphatidylinositol anchor-modifying beta1-3 N-acetylglucosaminyl transferase in Trypanosoma brucei | Q37336926 | ||
| A human embryonic kidney 293T cell line mutated at the Golgi alpha-mannosidase II locus | Q37372109 | ||
| Post-translational modification of thrombospondin type-1 repeats in ADAMTS-like 1/punctin-1 by C-mannosylation of tryptophan | Q37431621 | ||
| Protein quality control in the ER: the recognition of misfolded proteins | Q37719977 | ||
| Mammalian glycosylation mutants as tools for the analysis and reconstitution of protein transport | Q37731585 | ||
| The glycomics of glycan glucuronylation in Drosophila melanogaster | Q37785136 | ||
| The Acidic Environment of the Golgi Is Critical for Glycosylation and Transport | Q37785147 | ||
| Mechanisms of Protein Retention in the Golgi | Q37869708 | ||
| Lysosomal enzyme targeting | Q37886057 | ||
| Five Lec1 CHO cell mutants have distinct Mgat1 gene mutations that encode truncated N-acetylglucosaminyltransferase I. | Q38356775 | ||
| Regulation of O-glycosylation through Golgi-to-ER relocation of initiation enzymes | Q39700918 | ||
| Differences in gene expression of human xylosyltransferases and determination of acceptor specificities for various proteoglycans | Q39769873 | ||
| Identification of N-glycosylated proteins from the central nervous system of Drosophila melanogaster | Q40170831 | ||
| Kin recognition between medial Golgi enzymes in HeLa cells. | Q40790740 | ||
| The lectin domain of UDP-N-acetyl-D-galactosamine: polypeptide N-acetylgalactosaminyltransferase-T4 directs its glycopeptide specificities | Q40855480 | ||
| The signal anchor and stem regions of the beta-galactoside alpha 2,6-sialyltransferase may each act to localize the enzyme to the Golgi apparatus | Q41628848 | ||
| A novel, high endothelial venule-specific sulfotransferase expresses 6-sulfo sialyl Lewis(x), an L-selectin ligand displayed by CD34. | Q41683619 | ||
| Extracellular sugar modifications provide instructive and cell-specific information for axon-guidance choices | Q42047138 | ||
| Drosophila Dystroglycan is a target of O-mannosyltransferase activity of two protein O-mannosyltransferases, Rotated Abdomen and Twisted | Q42109798 | ||
| Precision mapping of an in vivo N-glycoproteome reveals rigid topological and sequence constraints. | Q43050786 | ||
| N-terminal residues in murine P-selectin glycoprotein ligand-1 required for binding to murine P-selectin | Q44189748 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | glycosylation | Q898365 |
| P577 | publication date | 2011-04-01 | |
| P13046 | publication type of scholarly work | review article | Q7318358 |
| P1433 | published in | Cold Spring Harbor Perspectives in Biology | Q3927509 |
| P1476 | title | Golgi glycosylation | |
| Golgi Glycosylation | |||
| P478 | volume | 3 |
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