207 results on '"Kornfeld, Stuart"'
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2. Structure of the human GlcNAc-1-phosphotransferase αβ subunits reveals regulatory mechanism for lysosomal enzyme glycan phosphorylation
3. Increased phosphorylation of HexM improves lysosomal uptake and potential for managing GM2 gangliosidoses
4. Recycling of Golgi glycosyltransferases requires direct binding to coatomer
5. Reduced PU.1 Expression Causes Myeloid Progenitor Expansion and Increased Leukemia Penetrance in Mice Expressing PML-RARα
6. The Molecular Basis of Ferroportin-Linked Hemochromatosis
7. Mouse Na + / K + - ATPase β1-Subunit Has a K + -Dependent Cell Adhesion Activity for β-GlcNAc-Terminating Glycans
8. Induction of Peripheral Lymph Node Addressin in Human Gastric Mucosa Infected by Helicobacter pylori
9. Mammalian GGAs Act Together to Sort Mannose 6-Phosphate Receptors
10. AP-1 Binding to Sorting Signals and Release from Clathrin-Coated Vesicles Is Regulated by Phosphorylation
11. Engineering of GlcNAc-1-Phosphotransferase for Production of Highly Phosphorylated Lysosomal Enzymes for Enzyme Replacement Therapy
12. Cooperation of GGAs and AP-1 in Packaging MPRs at the Trans-Golgi Network
13. Autoinhibition of the Ligand-Binding Site of GGA1/3 VHS Domains by an Internal Acidic Cluster-Dileucine Motif
14. ADP-Ribosylation Factor 1 Dependent Clathrin-Coat Assembly on Synthetic Liposomes
15. Mannose 6-Phosphate/Insulin-Like Growth Factor-II Receptor Targets the Urokinase Receptor to Lysosomes via a Novel Binding Interaction
16. AP-2-Containing Clathrin Coats Assemble on Mature Lysosomes
17. The Biogenesis of the MHC Class II Compartment in Human I-Cell Disease B Lymphoblasts
18. Cysteine34 of the Cytoplasmic Tail of the Cation-Dependent Mannose 6-Phosphate Receptor Is Reversibly Palmitoylated and Required for Normal Trafficking and Lysosomal Enzyme Sorting
19. The Targeting of Lamp1 to Lysosomes Is Dependent on the Spacing of Its Cytoplasmic Tail Tyrosine Sorting Motif Relative to the Membrane
20. Multiple Domains of GlcNAc-1-phosphotransferase Mediate Recognition of Lysosomal Enzymes
21. Phil Majerus : Champion of low-dose aspirin therapy
22. Analysis of Mucolipidosis II/III GNPTAB Missense Mutations Identifies Domains of UDP-GlcNAc:lysosomal Enzyme GlcNAc-1-phosphotransferase Involved in Catalytic Function and Lysosomal Enzyme Recognition
23. Binding of GGA2 to the Lysosomal Enzyme Sorting Motif of the Mannose 6-Phosphate Receptor
24. Mislocalization of phosphotransferase as a cause of mucolipidosis III αβ
25. Structure and Function of the DUF2233 Domain in Bacteria and in the Human Mannose 6-Phosphate Uncovering Enzyme
26. The DMAP interaction domain of UDP-GlcNAc:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase is a substrate recognition module
27. Core 1-derived O-glycans are essential E-selectin ligands on neutrophils
28. Molecular basis for peptidoglycan recognition by a bactericidal lectin
29. LRP6 overexpression defines a class of breast cancer subtype and is a target for therapy
30. Tumor Suppressor Function of Laminin-Binding α-Dystroglycan Requires a Distinct β3-N-Acetylglucosaminyltransferase
31. Identification of mRNA Splicing Factors as the Endothelial Receptor for Carbohydrate-Dependent Lung Colonization of Cancer Cells
32. The P53-Cathepsin Axis Cooperates with ROS to Activate Programmed Necrotic Death upon DNA Damage
33. Binding of Cargo Sorting Signals to AP-1 Enhances Its Association with ADP Ribosylation Factor 1-GTP
34. Analysis of Mannose 6-Phosphate Uncovering Enzyme Mutations Associated with Persistent Stuttering
35. The Iminosugar Isofagomine Increases the Activity of N370S Mutant Acid β-Glucosidase in Gaucher Fibroblasts by Several Mechanisms
36. Role of spacer‐1 in the maturation and function of GlcNAc‐1‐phosphotransferase
37. Mucolipidosis III GNPTG Missense Mutations Cause Misfolding of the γ Subunit of GlcNAc-1-Phosphotransferase
38. Functions of the α, β, and γ Subunits of UDP-GlcNAc:Lysosomal Enzyme N-Acetylglucosamine-1-phosphotransferase
39. Glycan Microarray Analysis of P-type Lectins Reveals Distinct Phosphomannose Glycan Recognition
40. Symbol Nomenclature for Graphical Representations of Glycans
41. Tuberous sclerosis, polycystic kidney disease and mucolipidosis III gamma caused by a microdeletion unmasking a recessive mutation
42. Retention of p63 in an ER-Golgi Intermediate Compartment Depends on the Presence of All Three of Its Domains and on Its Ability to Form Oligomers
43. Biochemical Dissection of AP-1 Recruitment onto Golgi Membranes
44. Mannose 6-Phosphate-Independent Targeting of Lysosomal Enzymes in I-Cell Disease B Lymphoblasts
45. Intracellular Movement of Two Mannose 6-Phosphate Receptors: Return to the Golgi Apparatus
46. Renin, a Secretory Glycoprotein, Acquires Phosphomannosyl Residues
47. Expression of Human Cathepsin D in Xenopus Oocytes: Phosphorylation and Intracellular Targeting
48. Studies of the Biosynthesis of the Mannose 6-Phosphate Receptor in Receptor-Positive and -Deficient Cell Lines
49. Two Enzymes Involved in the Synthesis of O-Linked Oligosaccharides Are Localized on Membranes of Different Densities in Mouse Lymphoma BW5147 Cells
50. Targeting of β-Glucuronidase to Lysosomes in Mannose 6-Phosphate Receptor-Deficient MOPC 315 Cells
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