553 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. Symbol Nomenclature for Graphical Representations of Glycans.
5. Gene therapy with AAV-S1S3 improves disease in mucolipidosis type II mice
6. Recycling of Golgi glycosyltransferases requires direct binding to coatomer
7. Reduced PU.1 Expression Causes Myeloid Progenitor Expansion and Increased Leukemia Penetrance in Mice Expressing PML-RARα
8. The Molecular Basis of Ferroportin-Linked Hemochromatosis
9. Mouse Na + / K + - ATPase β1-Subunit Has a K + -Dependent Cell Adhesion Activity for β-GlcNAc-Terminating Glycans
10. Induction of Peripheral Lymph Node Addressin in Human Gastric Mucosa Infected by Helicobacter pylori
11. Mammalian GGAs Act Together to Sort Mannose 6-Phosphate Receptors
12. AP-1 Binding to Sorting Signals and Release from Clathrin-Coated Vesicles Is Regulated by Phosphorylation
13. Engineering of GlcNAc-1-Phosphotransferase for Production of Highly Phosphorylated Lysosomal Enzymes for Enzyme Replacement Therapy
14. Cooperation of GGAs and AP-1 in Packaging MPRs at the Trans-Golgi Network
15. Autoinhibition of the Ligand-Binding Site of GGA1/3 VHS Domains by an Internal Acidic Cluster-Dileucine Motif
16. ADP-Ribosylation Factor 1 Dependent Clathrin-Coat Assembly on Synthetic Liposomes
17. Mannose 6-Phosphate/Insulin-Like Growth Factor-II Receptor Targets the Urokinase Receptor to Lysosomes via a Novel Binding Interaction
18. AP-2-Containing Clathrin Coats Assemble on Mature Lysosomes
19. The Biogenesis of the MHC Class II Compartment in Human I-Cell Disease B Lymphoblasts
20. 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
21. The Targeting of Lamp1 to Lysosomes Is Dependent on the Spacing of Its Cytoplasmic Tail Tyrosine Sorting Motif Relative to the Membrane
22. Multiple Domains of GlcNAc-1-phosphotransferase Mediate Recognition of Lysosomal Enzymes
23. Phil Majerus : Champion of low-dose aspirin therapy
24. N-Acetylglucosamine-1-Phosphodiester Alpha-N-Acetylglucosaminidase (NAGPA)
25. 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
26. Binding of GGA2 to the Lysosomal Enzyme Sorting Motif of the Mannose 6-Phosphate Receptor
27. Mislocalization of phosphotransferase as a cause of mucolipidosis III αβ
28. Structure and Function of the DUF2233 Domain in Bacteria and in the Human Mannose 6-Phosphate Uncovering Enzyme
29. The DMAP interaction domain of UDP-GlcNAc:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase is a substrate recognition module
30. Training the next generation of biomedical investigators in glycosciences
31. Core 1-derived O-glycans are essential E-selectin ligands on neutrophils
32. Molecular basis for peptidoglycan recognition by a bactericidal lectin
33. LRP6 overexpression defines a class of breast cancer subtype and is a target for therapy
34. Tumor Suppressor Function of Laminin-Binding α-Dystroglycan Requires a Distinct β3-N-Acetylglucosaminyltransferase
35. Identification of mRNA Splicing Factors as the Endothelial Receptor for Carbohydrate-Dependent Lung Colonization of Cancer Cells
36. The P53-Cathepsin Axis Cooperates with ROS to Activate Programmed Necrotic Death upon DNA Damage
37. Binding of Cargo Sorting Signals to AP-1 Enhances Its Association with ADP Ribosylation Factor 1-GTP
38. Analysis of Mannose 6-Phosphate Uncovering Enzyme Mutations Associated with Persistent Stuttering
39. The Iminosugar Isofagomine Increases the Activity of N370S Mutant Acid β-Glucosidase in Gaucher Fibroblasts by Several Mechanisms
40. Role of spacer‐1 in the maturation and function of GlcNAc‐1‐phosphotransferase
41. Mucolipidosis III GNPTG Missense Mutations Cause Misfolding of the γ Subunit of GlcNAc-1-Phosphotransferase
42. Functions of the α, β, and γ Subunits of UDP-GlcNAc:Lysosomal Enzyme N-Acetylglucosamine-1-phosphotransferase
43. Co-expression of S1S3 phosphotransferase in production cell line improves mannose 6-phosphorylation and cellular uptake of alpha--acetylglucosaminidase (Sanfilippo syndrome type B)
44. Glycan Microarray Analysis of P-type Lectins Reveals Distinct Phosphomannose Glycan Recognition
45. Tuberous sclerosis, polycystic kidney disease and mucolipidosis III gamma caused by a microdeletion unmasking a recessive mutation
46. 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
47. Biochemical Dissection of AP-1 Recruitment onto Golgi Membranes
48. Mannose 6-Phosphate-Independent Targeting of Lysosomal Enzymes in I-Cell Disease B Lymphoblasts
49. Intracellular Movement of Two Mannose 6-Phosphate Receptors: Return to the Golgi Apparatus
50. Renin, a Secretory Glycoprotein, Acquires Phosphomannosyl Residues
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