review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0167-4889(97)00050-5 |
P698 | PubMed publication ID | 9296516 |
P50 | author | Sharon Tooze | Q21264645 |
Francis A. Barr | Q37378170 | ||
P2093 | author name string | S Urbé | |
P2860 | cites work | Human ADP-ribosylation factor-activated phosphatidylcholine-specific phospholipase D defines a new and highly conserved gene family | Q24312818 |
Carboxypeptidase E is a regulated secretory pathway sorting receptor: genetic obliteration leads to endocrine disorders in Cpe(fat) mice | Q24317472 | ||
The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase | Q24336782 | ||
ICA 512, an autoantigen of type I diabetes, is an intrinsic membrane protein of neurosecretory granules | Q24563069 | ||
Sorting by COP I-coated vesicles under interphase and mitotic conditions | Q24671510 | ||
COPII: a membrane coat formed by Sec proteins that drive vesicle budding from the endoplasmic reticulum | Q27930804 | ||
Requirement for a GTPase-activating protein in vesicle budding from the endoplasmic reticulum | Q27931640 | ||
The Saccharomyces cerevisiae SEC14 gene encodes a cytosolic factor that is required for transport of secretory proteins from the yeast Golgi complex | Q27935633 | ||
SEC12 encodes a guanine-nucleotide-exchange factor essential for transport vesicle budding from the ER. | Q27937857 | ||
An essential role for a phospholipid transfer protein in yeast Golgi function | Q27938456 | ||
Coatomer is essential for retrieval of dilysine-tagged proteins to the endoplasmic reticulum | Q27938624 | ||
The protein deficient in Lowe syndrome is a phosphatidylinositol-4,5-bisphosphate 5-phosphatase | Q28118769 | ||
Involvement of GTP-binding "G" proteins in transport through the Golgi stack. | Q44841845 | ||
COPI- and COPII-coated vesicles bud directly from the endoplasmic reticulum in yeast. | Q45973926 | ||
Uncoupled packaging of targeting and cargo molecules during transport vesicle budding from the endoplasmic reticulum | Q46122896 | ||
Purification of Golgi cisternae-derived non-clathrin-coated vesicles | Q46800952 | ||
Regulation of granule size in human and horse eosinophils by number of fusion events among unit granules | Q47359456 | ||
Phosphoinositide 3-kinases and membrane traffic | Q47986385 | ||
Pathways of protein secretion in eukaryotes | Q48446174 | ||
Regulated formation of Golgi secretory vesicles containing Alzheimer beta-amyloid precursor protein. | Q53200160 | ||
Receptor and protein kinase C-mediated regulation of ARF binding to the Golgi complex. | Q54237450 | ||
ATP-dependent inositide phosphorylation required for Ca2+-activated secretion | Q56689852 | ||
Requirement for GTP hydrolysis in the formation of secretory vesicles | Q57269837 | ||
Phospholipase D: a downstream effector of ARF in granulocytes | Q57956412 | ||
Inhibition by brefeldin A of a Golgi membrane enzyme that catalyses exchange of guanine nucleotide bound to ARF | Q59066677 | ||
Ringing necks with dynamin | Q60073639 | ||
Proteolytic maturation of insulin is a post-Golgi event which occurs in acidifying clathrin-coated secretory vesicles | Q68956740 | ||
Proteolytic processing of pro-ACTH/endorphin begins in the Golgi complex of pituitary corticotropes and AtT-20 cells | Q69356258 | ||
Purification of a novel class of coated vesicles mediating biosynthetic protein transport through the Golgi stack | Q69664046 | ||
Fatty acyl-coenzyme A is required for budding of transport vesicles from Golgi cisternae | Q69747227 | ||
Reconstitution of the transport of protein between successive compartments of the Golgi measured by the coupled incorporation of N-acetylglucosamine | Q70669685 | ||
Secretory granule content proteins and the luminal domains of granule membrane proteins aggregate in vitro at mildly acidic pH | Q70870919 | ||
A role for ADP-ribosylation factor 1, but not COP I, in secretory vesicle biogenesis from the trans-Golgi network | Q71513453 | ||
pH-dependent interaction of an intraluminal loop of inositol 1,4,5-trisphosphate receptor with chromogranin A | Q72315455 | ||
Stepwise assembly of functionally active transport vesicles | Q72636717 | ||
Protein sorting and secretion granule formation in regulated secretory cells | Q75292716 | ||
Trimeric G proteins and vesicle formation | Q75294190 | ||
Mechanisms of intracellular protein transport | Q28131681 | ||
ADP-Ribosylation factor is a subunit of the coat of Golgi-derived COP-coated vesicles: A novel role for a GTP-binding protein | Q28248936 | ||
Phosphatidylinositol transfer protein required for ATP-dependent priming of Ca(2+)-activated secretion | Q28257147 | ||
Coated vesicle assembly in the Golgi requires only coatomer and ARF proteins from the cytosol | Q28261740 | ||
The ARF1 GTPase-activating protein: zinc finger motif and Golgi complex localization | Q28271461 | ||
A role of amphiphysin in synaptic vesicle endocytosis suggested by its binding to dynamin in nerve terminals | Q28272772 | ||
The granin (chromogranin/secretogranin) family | Q28284590 | ||
Bimodal interaction of coatomer with the p24 family of putative cargo receptors | Q28284591 | ||
'Coatomer': a cytosolic protein complex containing subunits of non-clathrin-coated Golgi transport vesicles | Q28300053 | ||
Requirement for phosphatidylinositol transfer protein in epidermal growth factor signaling | Q28302121 | ||
Arf proteins: the membrane traffic police? | Q28302542 | ||
Signal transduction and membrane traffic: the PITP/phosphoinositide connection | Q28302672 | ||
The internal pH and membrane potential of the insulin-secretory granule | Q28365767 | ||
A presynaptic inositol-5-phosphatase | Q28565411 | ||
Formation of nascent secretory vesicles from the trans-Golgi network of endocrine cells is inhibited by tyrosine kinase and phosphatase inhibitors | Q28567654 | ||
Molecular cloning of phogrin, a protein-tyrosine phosphatase homologue localized to insulin secretory granule membranes | Q28583729 | ||
ADP-ribosylation factor, a small GTP-binding protein, is required for binding of the coatomer protein beta-COP to Golgi membranes | Q28609784 | ||
Coatomer interaction with di-lysine endoplasmic reticulum retention motifs | Q28609806 | ||
Coat proteins and vesicle budding | Q28645867 | ||
Intracellular Aspects of the Process of Protein Synthesis | Q29615237 | ||
Brefeldin A inhibits Golgi membrane-catalysed exchange of guanine nucleotide onto ARF protein | Q29618202 | ||
Mannose 6-phosphate receptors in sorting and transport of lysosomal enzymes | Q30417552 | ||
Evidence for phosphatidylinositol 3-kinase as a regulator of endocytosis via activation of Rab5. | Q33826723 | ||
A possible role for Na+,K+-ATPase in regulating ATP-dependent endosome acidification | Q33831586 | ||
Regulation of endocytic pH by the Na+,K+-ATPase in living cells | Q33831627 | ||
Rapid endocytosis coupled to exocytosis in adrenal chromaffin cells involves Ca2+, GTP, and dynamin but not clathrin | Q33969084 | ||
Reduction of the disulfide bond of chromogranin B (secretogranin I) in the trans-Golgi network causes its missorting to the constitutive secretory pathways. | Q34051310 | ||
Use of a synthetic peptide antigen to generate antisera reactive with a proteolytic processing site in native human proinsulin: demonstration of cleavage within clathrin-coated (pro)secretory vesicles | Q34343129 | ||
Distinct coated vesicles labeled for p200 bud from trans-Golgi network membranes. | Q34511811 | ||
The trans Golgi network: sorting at the exit site of the Golgi complex. | Q34562583 | ||
Biological membranes as bilayer couples. A molecular mechanism of drug-erythrocyte interactions | Q35116324 | ||
Biogenesis of secretory granules | Q35567704 | ||
Isolation and sequence analysis of cDNA for rat carboxypeptidase E [EC 3.4.17.10], a neuropeptide processing enzyme | Q36038594 | ||
PROTEIN SYNTHESIS, STORAGE, AND DISCHARGE IN THE PANCREATIC EXOCRINE CELL. AN AUTORADIOGRAPHIC STUDY | Q36186067 | ||
The exocrine protein trypsinogen is targeted into the secretory granules of an endocrine cell line: studies by gene transfer | Q36212613 | ||
Conversion of proinsulin to insulin occurs coordinately with acidification of maturing secretory vesicles | Q36216775 | ||
Patch-clamp measurements reveal multimodal distribution of granule sizes in rat mast cells | Q36222762 | ||
Prohormone processing in the trans-Golgi network: endoproteolytic cleavage of prosomatostatin and formation of nascent secretory vesicles in permeabilized cells | Q36233508 | ||
Distinct molecular mechanisms for protein sorting within immature secretory granules of pancreatic beta-cells | Q36234350 | ||
pH-independent and -dependent cleavage of proinsulin in the same secretory vesicle | Q36234623 | ||
HVEM tomography of the trans-Golgi network: structural insights and identification of a lace-like vesicle coat | Q36234682 | ||
Transport via the regulated secretory pathway in semi-intact PC12 cells: role of intra-cisternal calcium and pH in the transport and sorting of secretogranin II. | Q36234806 | ||
Association of a dynamin-like protein with the Golgi apparatus in mammalian cells. | Q36236862 | ||
Evidence that phospholipase D mediates ADP ribosylation factor-dependent formation of Golgi coated vesicles | Q36236974 | ||
Dynamic measurement of the pH of the Golgi complex in living cells using retrograde transport of the verotoxin receptor | Q36237417 | ||
Role for phosphatidylinositol 3-kinase in the sorting and transport of newly synthesized lysosomal enzymes in mammalian cells | Q36382633 | ||
What the granins tell us about the formation of secretory granules in neuroendocrine cells | Q36724876 | ||
Metabolism of Alzheimer beta-amyloid precursor protein: regulation by protein kinase A in intact cells and in a cell-free system | Q37629098 | ||
Chromogranin B (secretogranin I) promotes sorting to the regulated secretory pathway of processing intermediates derived from a peptide hormone precursor | Q37639506 | ||
The absence of Emp24p, a component of ER-derived COPII-coated vesicles, causes a defect in transport of selected proteins to the Golgi. | Q37695497 | ||
Phosphatidylinositol transfer protein dictates the rate of inositol trisphosphate production by promoting the synthesis of PIP2 | Q38293933 | ||
ADP-ribosylation factor-1 stimulates formation of nascent secretory vesicles from the trans-Golgi network of endocrine cells | Q38360636 | ||
The insulin factory: a tour of the plant surroundings and a visit to the assembly line. The Minkowski lecture 1973 revisited | Q38591483 | ||
Cellular and molecular biology of neuropeptide processing and packaging | Q38772879 | ||
Biosynthetic protein transport and sorting by the endoplasmic reticulum and Golgi | Q39664981 | ||
Regulated secretion. Helper proteins for neuroendocrine secretion | Q40544514 | ||
The role of clathrin, adaptors and dynamin in endocytosis | Q40647427 | ||
About turn for the COPs? | Q40655615 | ||
Sorting and processing of secretory proteins | Q40744676 | ||
Biogenesis of constitutive secretory vesicles, secretory granules and synaptic vesicles | Q40788803 | ||
Phosphoinositides as regulators in membrane traffic | Q40968891 | ||
Dynamin and receptor-mediated endocytosis | Q41017094 | ||
Receptor-mediated protein sorting to the vacuole in yeast: roles for a protein kinase, a lipid kinase and GTP-binding proteins | Q41020937 | ||
Molecular mechanisms in synaptic vesicle endocytosis and recycling | Q41094245 | ||
pH-dependent processing of secretogranin II by the endopeptidase PC2 in isolated immature secretory granules. | Q41142545 | ||
The in vitro generation of post-Golgi vesicles carrying viral envelope glycoproteins requires an ARF-like GTP-binding protein and a protein kinase C associated with the Golgi apparatus | Q41185133 | ||
A novel adaptor-related protein complex | Q41202077 | ||
The AP-1 adaptor complex binds to immature secretory granules from PC12 cells, and is regulated by ADP-ribosylation factor | Q41233302 | ||
A role for phosphatidylinositol transfer protein in secretory vesicle formation | Q41283307 | ||
Phosphatidylinositol 3-kinase regulation of fluid phase endocytosis | Q41327182 | ||
Identification of the sorting signal motif within pro-opiomelanocortin for the regulated secretory pathway | Q41350449 | ||
Direct measurement of trans-Golgi pH in living cells and regulation by second messengers | Q41360787 | ||
Density of newly synthesized plasma membrane proteins in intracellular membranes II. Biochemical studies | Q41450671 | ||
Vesicular stomatitis virus glycoprotein is sorted and concentrated during export from the endoplasmic reticulum | Q41481250 | ||
Clathrin-coated vesicular transport of secretory proteins during the formation of ACTH-containing secretory granules in AtT20 cells | Q41508036 | ||
ADP-ribosylation factor, a small GTP-dependent regulatory protein, stimulates phospholipase D activity | Q41508317 | ||
An antibody specific for an endoproteolytic cleavage site provides evidence that pro-opiomelanocortin is packaged into secretory granules in AtT20 cells before its cleavage | Q41541196 | ||
Milieu-induced, selective aggregation of regulated secretory proteins in the trans-Golgi network | Q41654828 | ||
Characterization of the immature secretory granule, an intermediate in granule biogenesis | Q41654836 | ||
Wortmannin causes mistargeting of procathepsin D. evidence for the involvement of a phosphatidylinositol 3-kinase in vesicular transport to lysosomes | Q41680092 | ||
A targeting sequence for dense secretory granules resides in the active renin protein moiety of human preprorenin | Q41713300 | ||
Prosomatostatin processing in permeabilized cells. Calcium is required for prohormone cleavage but not formation of nascent secretory vesicles | Q42513868 | ||
Phosphatidylinositol kinase. A component of the chromaffin-granule membrane | Q42559326 | ||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 6-22 | |
P577 | publication date | 1997-08-01 | |
P1433 | published in | Biochimica et Biophysica Acta | Q864239 |
P1476 | title | Formation of secretory vesicles in the biosynthetic pathway | |
P478 | volume | 1358 |
Q34264518 | Concentrating hormones into secretory granules: layers of control |
Q38331526 | Determinants in the cytoplasmic domain of P-selectin required for sorting to secretory granules |
Q42477805 | Differences in the ways sympathetic neurons and endocrine cells process, store, and secrete exogenous neuropeptides and peptide-processing enzymes. |
Q36328578 | Homotypic fusion of immature secretory granules during maturation in a cell-free assay |
Q30682134 | Identification of putative proteins involved in granule biogenesis of tick salivary glands |
Q39566395 | Kinetic evidence that newly-synthesized endogenous lysosome-associated membrane protein-1 (LAMP-1) first transits early endosomes before it is delivered to lysosomes |
Q35623188 | Molecular aspects of membrane trafficking in paramecium |
Q42992153 | Molecular aspects of the endocytic pathway |
Q78525421 | Proprotein processing within secretory dense core granules of Tetrahymena thermophila |
Q43946084 | Routing of membrane proteins to large dense core vesicles in PC12 cells |
Q28565137 | Signaling mediated by the cytosolic domain of peptidylglycine alpha-amidating monooxygenase |
Q77545818 | Synthesis, processing and secretion of surfactant proteins B and C |
Q35131420 | The diffuse endocrine system: from embryogenesis to carcinogenesis. |
Q36255436 | The protozoan parasite Toxoplasma gondii targets proteins to dense granules and the vacuolar space using both conserved and unusual mechanisms |
Q47169436 | UNC-16/JIP3 regulates early events in synaptic vesicle protein trafficking via LRK-1/LRRK2 and AP complexes. |
Q27972823 | etramps, a new Plasmodium falciparum gene family coding for developmentally regulated and highly charged membrane proteins located at the parasite-host cell interface |
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