about
Clathrin-mediated endocytosis of MUC1 is modulated by its glycosylation stateTwo independent targeting signals in the cytoplasmic domain determine trans-Golgi network localization and endosomal trafficking of the proprotein convertase furinMurine mucopolysaccharidosis type VII. Characterization of a mouse with beta-glucuronidase deficiencyLysosomal hydrolase mannose 6-phosphate uncovering enzyme resides in the trans-Golgi networkThe fungal vacuole: composition, function, and biogenesisTransport of mannose-6-phosphate receptors from the trans-Golgi network to endosomes requires Rab31Molecular cloning of cDNAs encoding lamp A, a human lysosomal membrane glycoprotein with apparent Mr approximately equal to 120,000Prolonged expression of a lysosomal enzyme in mouse liver after Sleeping Beauty transposon-mediated gene delivery: implications for non-viral gene therapy of mucopolysaccharidosesEnvelopment of varicella-zoster virus: targeting of viral glycoproteins to the trans-Golgi networkPep7p provides a novel protein that functions in vesicle-mediated transport between the yeast Golgi and endosomeMembrane protein sorting: biosynthesis, transport and processing of yeast vacuolar alkaline phosphataseInhibition of tubercle bacilli in cultured human macrophages by chloroquine used alone and in combination with streptomycin, isoniazid, pyrazinamide, and two metabolites of vitamin D3Genetic contributions to stuttering: the current evidence.Knockout of Lysosomal Enzyme-Targeting Gene Causes Abnormalities in Mouse Pup Isolation CallsAssembly of the ligand-binding conformation of Mr 46,000 mannose 6-phosphate-specific receptor takes place before reaching the Golgi complexGuanidinylated neomycin mediates heparan sulfate-dependent transport of active enzymes to lysosomes.Requirement of N-glycosylation of the prostaglandin E2 receptor EP3beta for correct sorting to the plasma membrane but not for correct folding.Identification of the insulin-like growth factor II receptor as a novel receptor for binding and invasion by Listeria monocytogenes.Endocytosis and recycling of subunit H1 of the asialoglycoprotein receptor is independent of oligomerization with H2.Recognition by the glycoprotein hormone-specific N-acetylgalactosaminetransferase is independent of hormone native conformation.Mutant cells selected during persistent reovirus infection do not express mature cathepsin L and do not support reovirus disassembly.Acute systemic inflammation up-regulates secretory sphingomyelinase in vivo: a possible link between inflammatory cytokines and atherogenesis.The mannose 6-phosphate receptor cytoplasmic domain is not sufficient to alter the cellular distribution of a chimeric EGF receptorMolecular basis of variant pseudo-hurler polydystrophy (mucolipidosis IIIC)Cholesterol dependence of varicella-zoster virion entry into target cellsModifications of glycans: biological significance and therapeutic opportunitiesNew strategies for enzyme replacement therapy for lysosomal storage diseasesUptake of extracellular enzyme by a novel pathway is a major determinant of cathepsin L levels in human macrophagesPutative miRNAs for the diagnosis of dyslexia, dyspraxia, and specific language impairment.Identification of surface residues on Niemann-Pick C2 essential for hydrophobic handoff of cholesterol to NPC1 in lysosomesInduction of hypertrophy in cultured proximal tubule cells by extracellular NH4ClIdentification and characterization of pharmacological chaperones to correct enzyme deficiencies in lysosomal storage disorders.Lysosomal storage disease: gene therapy on both sides of the blood-brain barrier.High resolution crystal structure of human β-glucuronidase reveals structural basis of lysosome targeting.Extensive mannose phosphorylation on leukemia inhibitory factor (LIF) controls its extracellular levels by multiple mechanismsA xylosylphosphotransferase of Cryptococcus neoformans acts in protein O-glycan synthesis.Gene therapy for neurologic manifestations of mucopolysaccharidoses.Latency-associated peptide of transforming growth factor-β1 is not subject to physiological mannose phosphorylationRous-Whipple Award Lecture. Contributions to the physiology and pathology of the Golgi apparatusCorrection of the mineralization defect in hyp mice treated with protease inhibitors CA074 and pepstatin
P2860
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P2860
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
1987年论文
@zh
1987年论文
@zh-cn
name
Trafficking of lysosomal enzymes.
@en
Trafficking of lysosomal enzymes.
@nl
type
label
Trafficking of lysosomal enzymes.
@en
Trafficking of lysosomal enzymes.
@nl
prefLabel
Trafficking of lysosomal enzymes.
@en
Trafficking of lysosomal enzymes.
@nl
P1433
P1476
Trafficking of lysosomal enzymes
@en
P2093
S Kornfeld
P304
P356
10.1096/FASEBJ.1.6.3315809
P407
P577
1987-12-01T00:00:00Z