Compartmentation of asparagine-linked oligosaccharide processing in the Golgi apparatus
about
Recycling of golgi-resident glycosyltransferases through the ER reveals a novel pathway and provides an explanation for nocodazole-induced Golgi scatteringIntracellular maturation of mumps virus hemagglutinin-neuraminidase glycoprotein: conformational changes detected with monoclonal antibodiesCell type-dependent variations in the subcellular distribution of alpha-mannosidase I and IIERS-24, a mammalian v-SNARE implicated in vesicle traffic between the ER and the GolgiOverexpression of CALNUC (nucleobindin) increases agonist and thapsigargin releasable Ca2+ storage in the GolgiMolecular cloning and expression of cDNA encoding the rat UDP-N-acetylglucosamine:alpha-6-D-mannoside beta-1,2-N-acetylglucosaminyltransferase IIGlycoproteins of the lysosomal membraneLocalization of Tctex-1, a cytoplasmic dynein light chain, to the Golgi apparatus and evidence for dynein complex heterogeneityCarboxy-terminal SEKDEL sequences retard but do not retain two secretory proteins in the endoplasmic reticulum.Intracellular transport of membrane glycoproteins: two closely related histocompatibility antigens differ in their rates of transit to the cell surfaceTransport through the Golgi apparatus by rapid partitioning within a two-phase membrane system.Membrane organization of bluetongue virus nonstructural glycoprotein NS3.Reduction in Golgi apparatus dimension in the absence of a residential protein, N-acetylglucosaminyltransferase V.Functional complexity of the axonal growth cone: a proteomic analysis.The future of Golgi research.The distribution of 215-kilodalton mannose 6-phosphate receptors within cis (heavy) and trans (light) Golgi subfractions varies in different cell types.Immunoelectron microscopic studies of the intracellular transport of the membrane glycoprotein (G) of vesicular stomatitis virus in infected Chinese hamster ovary cells.Evidence for both prelysosomal and lysosomal intermediates in endocytic pathways.Co-translational excision of alpha-glucose and alpha-mannose in nascent vesicular stomatitis virus G protein.Intracellular translocation of fluorescent sphingolipids in cultured fibroblasts: endogenously synthesized sphingomyelin and glucocerebroside analogues pass through the Golgi apparatus en route to the plasma membraneIntracellular movement of cell surface receptors after endocytosis: resialylation of asialo-transferrin receptor in human erythroleukemia cells.Characterization of cytoplasmically oriented Golgi proteins with a monoclonal antibodyProcessing of the asparagine-linked oligosaccharides of secreted and intracellular forms of the vesicular stomatitis virus G protein: in vivo evidence of Golgi apparatus compartmentalizationBiogenesis of the polymeric IgA receptor in rat hepatocytes. I. Kinetic studies of its intracellular forms.Transferrin receptors recycle to cis and middle as well as trans Golgi cisternae in Ig-secreting myeloma cellsMembrane traffic in animal cells: cellular glycoproteins return to the site of Golgi mannosidase I.Reconstitution of transport of vesicular stomatitis virus G protein from the endoplasmic reticulum to the Golgi complex using a cell-free system.Postendocytic maturation of acid hydrolases: evidence of prelysosomal processing.Antibodies to rat pancreas Golgi subfractions: identification of a 58-kD cis-Golgi protein.Selective retention of monoglucosylated high mannose oligosaccharides by a class of mutant vesicular stomatitis virus G proteinsOverlapping distribution of two glycosyltransferases in the Golgi apparatus of HeLa cellsThe small GTP-binding protein rab6 functions in intra-Golgi transport.The G protein-activating peptide, mastoparan, and the synthetic NH2-terminal ARF peptide, ARFp13, inhibit in vitro Golgi transport by irreversibly damaging membranesIntercompartmental transport in the Golgi complex is a dissociative process: facile transfer of membrane protein between two Golgi populations.Transport of protein between cytoplasmic membranes of fused cells: correspondence to processes reconstituted in a cell-free system.Redistribution of mannose-6-phosphate receptors induced by tunicamycin and chloroquine.The isolated ER-Golgi intermediate compartment exhibits properties that are different from ER and cis-Golgi.Cytoplasmic dynein participates in the centrosomal localization of the Golgi complex.A Golgi retention signal in a membrane-spanning domain of coronavirus E1 proteinTemperature-sensitive steps in the transport of secretory proteins through the Golgi complex in exocrine pancreatic cells.
P2860
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P2860
Compartmentation of asparagine-linked oligosaccharide processing in the Golgi apparatus
description
1983 nî lūn-bûn
@nan
1983年の論文
@ja
1983年論文
@yue
1983年論文
@zh-hant
1983年論文
@zh-hk
1983年論文
@zh-mo
1983年論文
@zh-tw
1983年论文
@wuu
1983年论文
@zh
1983年论文
@zh-cn
name
Compartmentation of asparagine-linked oligosaccharide processing in the Golgi apparatus
@ast
Compartmentation of asparagine-linked oligosaccharide processing in the Golgi apparatus
@en
type
label
Compartmentation of asparagine-linked oligosaccharide processing in the Golgi apparatus
@ast
Compartmentation of asparagine-linked oligosaccharide processing in the Golgi apparatus
@en
prefLabel
Compartmentation of asparagine-linked oligosaccharide processing in the Golgi apparatus
@ast
Compartmentation of asparagine-linked oligosaccharide processing in the Golgi apparatus
@en
P2860
P356
P1476
Compartmentation of asparagine-linked oligosaccharide processing in the Golgi apparatus
@en
P2093
J E Rothman
W G Dunphy
P2860
P304
P356
10.1083/JCB.97.1.270
P407
P577
1983-07-01T00:00:00Z