Exit of newly synthesized membrane proteins from the trans cisterna of the Golgi complex to the plasma membrane.
about
Association of the Hermansky-Pudlak syndrome type-3 protein with clathrin.VAMP4 is required to maintain the ribbon structure of the Golgi apparatusComplexes of syndapin II with dynamin II promote vesicle formation at the trans-Golgi networkInteractions of NK cell receptor KIR3DL1*004 with chaperones and conformation-specific antibody reveal a functional folded state as well as predominant intracellular retentionDistribution and function of AP-1 clathrin adaptor complexes in polarized epithelial cellsRab8, a small GTPase involved in vesicular traffic between the TGN and the basolateral plasma membraneRab17, a novel small GTPase, is specific for epithelial cells and is induced during cell polarizationTraffic of Kv4 K+ channels mediated by KChIP1 is via a novel post-ER vesicular pathwayCloning of cDNAs encoding two related 100-kD coated vesicle proteins (alpha-adaptins)Spatial partitioning of secretory cargo from Golgi resident proteins in live cells.A novel imaging method for quantitative Golgi localization reveals differential intra-Golgi trafficking of secretory cargoes.The number of identical kringle IV repeats in apolipoprotein(a) affects its processing and secretion by HepG2 cellsMicrotubules and actin filaments are not critically involved in the biogenesis of epithelial cell surface polarityMorphology and dynamics of clathrin/GGA1-coated carriers budding from the trans-Golgi networkVectorial insertion of apical and basolateral membrane proteins in polarized epithelial cells revealed by quantitative 3D live cell imaging.Mechanism of constitutive export from the golgi: bulk flow via the formation, protrusion, and en bloc cleavage of large trans-golgi network tubular domains.A distinct trans-Golgi network subcompartment for sorting of synaptic and granule proteins in neurons and neuroendocrine cells.Role of Na+/H+ exchanger regulatory factor 1 in forward trafficking of the type IIa Na+-Pi cotransporter.Acquisition of Lubrol insolubility, a common step for growth hormone and prolactin in the secretory pathway of neuroendocrine cells.Dissection of Semliki Forest virus glycoprotein delivery from the trans-Golgi network to the cell surface in permeabilized BHK cells.Transport of soluble proteins through the Golgi occurs by diffusion via continuities across cisternae.Transport of horseradish peroxidase from the cell surface to the Golgi in insulin-secreting cells: preferential labelling of cisternae located in an intermediate position in the stack.Reconstitution of vesicle fusions occurring in endocytosis with a cell-free system.Structure of the Golgi and distribution of reporter molecules at 20 degrees C reveals the complexity of the exit compartments.The mannose 6-phosphate receptor cytoplasmic domain is not sufficient to alter the cellular distribution of a chimeric EGF receptorSphingomyelin synthases regulate protein trafficking and secretionIdentification, sequencing and expression of an integral membrane protein of the trans-Golgi network (TGN38)The delta subunit of AP-3 is required for efficient transport of VSV-G from the trans-Golgi network to the cell surface.A mitotic form of the Golgi apparatus in HeLa cells.Distinct pathogenic processes between Fig4-deficient motor and sensory neurons.Differential, phosphorylation dependent trafficking of AQP2 in LLC-PK1 cellsPalmitoylated Ras proteins traffic through recycling endosomes to the plasma membrane during exocytosis.Src regulates Golgi structure and KDEL receptor-dependent retrograde transport to the endoplasmic reticulum.MLN64 transport to the late endosome is regulated by binding to 14-3-3 via a non-canonical binding siteSimultaneous rather than ordered cleavage of two sites within the BMP4 prodomain leads to loss of ligand in miceRenal vacuolar H+-ATPase.The palmitoyltransferase of the cation-dependent mannose 6-phosphate receptor cycles between the plasma membrane and endosomesMaintenance of the diacylglycerol level in the Golgi apparatus by the Nir2 protein is critical for Golgi secretory function.Two naturally occurring alpha2,6-sialyltransferase forms with a single amino acid change in the catalytic domain differ in their catalytic activity and proteolytic processing.Adaptor and clathrin exchange at the plasma membrane and trans-Golgi network.
P2860
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P2860
Exit of newly synthesized membrane proteins from the trans cisterna of the Golgi complex to the plasma membrane.
description
1985 nî lūn-bûn
@nan
1985年の論文
@ja
1985年論文
@yue
1985年論文
@zh-hant
1985年論文
@zh-hk
1985年論文
@zh-mo
1985年論文
@zh-tw
1985年论文
@wuu
1985年论文
@zh
1985年论文
@zh-cn
name
Exit of newly synthesized memb ...... omplex to the plasma membrane.
@en
type
label
Exit of newly synthesized memb ...... omplex to the plasma membrane.
@en
prefLabel
Exit of newly synthesized memb ...... omplex to the plasma membrane.
@en
P2093
P2860
P356
P1476
Exit of newly synthesized memb ...... omplex to the plasma membrane.
@en
P2093
P2860
P304
P356
10.1083/JCB.101.3.949
P407
P50
P577
1985-09-01T00:00:00Z