scholarly article | Q13442814 |
P50 | author | David Perrais | Q41808473 |
P2093 | author name string | Justin W Taraska | |
Wolfhard Almers | |||
Ingo C Kleppe | |||
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Multiple forms of endocytosis in bovine adrenal chromaffin cells | Q42837428 | ||
A membrane marker leaves synaptic vesicles in milliseconds after exocytosis in retinal bipolar cells | Q44158659 | ||
Regulation of dense core release from neuroendocrine cells revealed by imaging single exocytic events | Q48213707 | ||
Local Ca2+ release from internal stores controls exocytosis in pituitary gonadotrophs | Q48819860 | ||
Compensatory and excess retrieval: two types of endocytosis following single step depolarizations in bovine adrenal chromaffin cells | Q49102815 | ||
Effects of pH and Ca2+ on heterodimer and heterotetramer formation by chromogranin A and chromogranin B. | Q52301253 | ||
Delay in vesicle fusion revealed by electrochemical monitoring of single secretory events in adrenal chromaffin cells | Q52423917 | ||
The exocytotic event in chromaffin cells revealed by patch amperometry. | Q53963862 | ||
Direct observation of membrane retrieval in chromaffin cells by capacitance measurements | Q57362965 | ||
Ca2+-Triggered Peptide Secretion in Single Cells Imaged with Green Fluorescent Protein and Evanescent-Wave Microscopy | Q58450914 | ||
Transport, docking and exocytosis of single secretory granules in live chromaffin cells | Q59065064 | ||
Properties of the fusion pore that forms during exocytosis of a mast cell secretory vesicle | Q68795597 | ||
Release of NPY-like immunoreactive material from primary cultures of chromaffin cells prepared from bovine adrenal medulla | Q69803569 | ||
Multiple calcium-dependent processes related to secretion in bovine chromaffin cells | Q70547407 | ||
Flux of catecholamines through chromaffin vesicles in cultured bovine adrenal medullary cells | Q71357649 | ||
Docked granules, the exocytic burst, and the need for ATP hydrolysis in endocrine cells | Q71783396 | ||
Exocytotic fusion pores exhibit semi-stable states | Q72804151 | ||
Exocytosis of single chromaffin granules in cell-free inside-out membrane patches | Q73161655 | ||
Transport, capture and exocytosis of single synaptic vesicles at active zones | Q74265534 | ||
The last few milliseconds in the life of a secretory granule. Docking, dynamics and fusion visualized by total internal reflection fluorescence microscopy (TIRFM) | Q74410292 | ||
The primary structure of human dopamine-beta-hydroxylase: insights into the relationship between the soluble and the membrane-bound forms of the enzyme | Q24298559 | ||
The primary structure of human secretogranin II, a widespread tyrosine-sulfated secretory granule protein that exhibits low pH- and calcium-induced aggregation | Q24339539 | ||
Temporally resolved catecholamine spikes correspond to single vesicle release from individual chromaffin cells | Q24559973 | ||
The 2.3 A crystal structure of the catalytic domain of recombinant two-chain human tissue-type plasminogen activator | Q27732669 | ||
Crystal structure of the Aequorea victoria green fluorescent protein | Q27733214 | ||
A variant of yellow fluorescent protein with fast and efficient maturation for cell-biological applications | Q28213193 | ||
Visualizing secretion and synaptic transmission with pH-sensitive green fluorescent proteins | Q28276992 | ||
Dynamin-dependent and dynamin-independent processes contribute to the regulation of single vesicle release kinetics and quantal size | Q30165438 | ||
Bilayers merge even when exocytosis is transient | Q30597894 | ||
A real-time view of life within 100 nm of the plasma membrane | Q31890399 | ||
High calcium concentrations shift the mode of exocytosis to the kiss-and-run mechanism | Q33880066 | ||
Use of the green fluorescent protein and its mutants in quantitative fluorescence microscopy | Q33907871 | ||
Rapid endocytosis coupled to exocytosis in adrenal chromaffin cells involves Ca2+, GTP, and dynamin but not clathrin | Q33969084 | ||
Rapid fluctuations in transmitter release from single vesicles in bovine adrenal chromaffin cells | Q34017485 | ||
Sustained stimulation shifts the mechanism of endocytosis from dynamin-1-dependent rapid endocytosis to clathrin- and dynamin-2-mediated slow endocytosis in chromaffin cells | Q34029233 | ||
Green fluorescent protein as a noninvasive intracellular pH indicator | Q34167493 | ||
Imaging direct, dynamin-dependent recapture of fusing secretory granules on plasma membrane lawns from PC12 cells | Q34430018 | ||
Measurement of cytosolic, mitochondrial, and Golgi pH in single living cells with green fluorescent proteins | Q34470955 | ||
Secretory granules are recaptured largely intact after stimulated exocytosis in cultured endocrine cells. | Q34763388 | ||
A triggered mechanism retrieves membrane in seconds after Ca(2+)-stimulated exocytosis in single pituitary cells | Q36233809 | ||
Real-time imaging of the axonal transport of granules containing a tissue plasminogen activator/green fluorescent protein hybrid | Q36905781 | ||
64 The measurement of membrane potential and ΔpH in cells, organelles, and vesicles | Q39258641 | ||
Punctate appearance of dopamine-beta-hydroxylase on the chromaffin cell surface reflects the fusion of individual chromaffin granules upon exocytosis | Q39451872 | ||
The molecular function of adrenal chromaffin granules: established facts and unresolved topics | Q39479340 | ||
Exocytosis: The Common Release Mechanism of Secretory Granules in Glandular Cells, Neurosecretory Cells, Neurons and Paraneurons | Q39758209 | ||
Exocytosis of catecholamine (CA)-containing and CA-free granules in chromaffin cells | Q40689422 | ||
Processing of chromogranin A by plasmin provides a novel mechanism for regulating catecholamine secretion | Q40735839 | ||
Delay between fusion pore opening and peptide release from large dense-core vesicles in neuroendocrine cells | Q40755810 | ||
Simultaneous evanescent wave imaging of insulin vesicle membrane and cargo during a single exocytotic event | Q40843756 | ||
Fast steps in exocytosis and endocytosis studied by capacitance measurements in endocrine cells | Q41103298 | ||
Tissue plasminogen activator (t-PA) is targeted to the regulated secretory pathway. Catecholamine storage vesicles as a reservoir for the rapid release of t-PA. | Q41133880 | ||
Exocytotic exposure and retrieval of membrane antigens of chromaffin granules: quantitative evaluation of immunofluorescence on the surface of chromaffin cells | Q41456200 | ||
Exocytotic exposure and recycling of membrane antigens of chromaffin granules: ultrastructural evaluation after immunolabeling | Q41498377 | ||
Vesicle recycling revisited: rapid endocytosis may be the first step | Q41720900 | ||
Neuronal plasminogen activators: cell surface binding sites and involvement in neurite outgrowth | Q41767690 | ||
P433 | issue | Pt 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | exocytosis | Q323426 |
P304 | page(s) | 413-428 | |
P577 | publication date | 2004-08-05 | |
P1433 | published in | Journal of Physiology | Q7743612 |
P1476 | title | Recapture after exocytosis causes differential retention of protein in granules of bovine chromaffin cells. | |
P478 | volume | 560 |
Q41808432 | A Central Small Amino Acid in the VAMP2 Transmembrane Domain Regulates the Fusion Pore in Exocytosis. |
Q27322004 | A new role for myosin II in vesicle fission |
Q35011226 | A new role for the dynamin GTPase in the regulation of fusion pore expansion |
Q50609954 | Actin and dynamin recruitment and the lack thereof at exo- and endocytotic sites in PC12 cells. |
Q42482478 | Activity-dependent differential transmitter release in mouse adrenal chromaffin cells. |
Q36182432 | Activity-dependent fusion pore expansion regulated by a calcineurin-dependent dynamin-syndapin pathway in mouse adrenal chromaffin cells |
Q48231153 | An acto-myosin II constricting ring initiates the fission of activity-dependent bulk endosomes in neurosecretory cells. |
Q64080789 | Anaphylactic Degranulation of Mast Cells: Focus on Compound Exocytosis |
Q83134550 | Chapter 7: Total internal reflection fluorescence microscopy |
Q91121458 | Chromaffin Cells of the Adrenal Medulla: Physiology, Pharmacology, and Disease |
Q90028784 | Chromogranin A, the major lumenal protein in chromaffin granules, controls fusion pore expansion |
Q37246337 | Cortical F-actin, the exocytic mode, and neuropeptide release in mouse chromaffin cells is regulated by myristoylated alanine-rich C-kinase substrate and myosin II |
Q37362012 | Differential activity-dependent secretion of brain-derived neurotrophic factor from axon and dendrite |
Q27345923 | Differential cargo mobilisation within Weibel-Palade bodies after transient fusion with the plasma membrane |
Q34081432 | Distinct fusion properties of synaptotagmin-1 and synaptotagmin-7 bearing dense core granules |
Q42412601 | Dynamic regulation of the large exocytotic fusion pore in pancreatic acinar cells |
Q41329702 | Dynamin I plays dual roles in the activity-dependent shift in exocytic mode in mouse adrenal chromaffin cells |
Q37808139 | Dynamin and Myosin Regulate Differential Exocytosis from Mouse Adrenal Chromaffin Cells |
Q58104637 | Dynamin-1 restrains vesicular release to a sub-quantal mode in mammalian adrenal chromaffin cells |
Q38143006 | Dynamin-2 function and dysfunction along the secretory pathway. |
Q34935558 | Dynamin-2 regulates fusion pore expansion and quantal release through a mechanism that involves actin dynamics in neuroendocrine chromaffin cells |
Q30491898 | Efficient copackaging and cotransport yields postsynaptic colocalization of neuromodulators associated with synaptic plasticity |
Q24313584 | Endosomal WASH and exocyst complexes control exocytosis of MT1-MMP at invadopodia |
Q37210505 | Exocytosis and endocytosis in neuroendocrine cells: inseparable membranes! |
Q34657846 | Exocytosis and endocytosis: modes, functions, and coupling mechanisms |
Q46152267 | Fluorescent cargo proteins in peptidergic endocrine cells: cell type determines secretion kinetics at exocytosis |
Q83232831 | Fusion pore regulation by cAMP/Epac2 controls cargo release during insulin exocytosis |
Q39123295 | Fusion pores and their control of neurotransmitter and hormone release. |
Q42514168 | How does the stimulus define exocytosis in adrenal chromaffin cells? |
Q38639370 | How intravesicular composition affects exocytosis |
Q38724299 | How the stimulus defines the dynamics of vesicle pool recruitment, fusion mode, and vesicle recycling in neuroendocrine cells |
Q98513739 | Imaging endocytic vesicle formation at high spatial and temporal resolutions with the pulsed-pH protocol |
Q30523626 | Imaging of lytic granule exocytosis in CD8+ cytotoxic T lymphocytes reveals a modified form of full fusion |
Q30529773 | Imaging the post-fusion release and capture of a vesicle membrane protein |
Q37139164 | Imaging the recruitment and loss of proteins and lipids at single sites of calcium-triggered exocytosis |
Q42838114 | Intravesicular factors controlling exocytosis in chromaffin cells |
Q34194018 | Involvement of Rab3A in vesicle priming during exocytosis: interaction with Munc13-1 and Munc18-1. |
Q34268757 | Is PACAP the major neurotransmitter for stress transduction at the adrenomedullary synapse? |
Q33990993 | It's what's inside that matters |
Q47616783 | Ketamine Inhibits ATP-Evoked Exocytotic Release of Brain-Derived Neurotrophic Factor from Vesicles in Cultured Rat Astrocytes |
Q58806150 | Local protein dynamics during microvesicle exocytosis in neuroendocrine cells |
Q33643745 | Localized topological changes of the plasma membrane upon exocytosis visualized by polarized TIRFM. |
Q24657724 | Loose coupling between calcium channels and sites of exocytosis in chromaffin cells |
Q33990912 | Lumenal protein within secretory granules affects fusion pore expansion |
Q40262984 | Matching native electrical stimulation by graded chemical stimulation in isolated mouse adrenal chromaffin cells |
Q50607017 | Matrix-dependent local retention of secretory vesicle cargo in cortical neurons. |
Q37012410 | Mechanisms of granule membrane recapture following exocytosis in intact mast cells |
Q30277941 | Monitoring C-Peptide Storage and Secretion in Islet β-Cells In Vitro and In Vivo. |
Q30486472 | Myosin 2 maintains an open exocytic fusion pore in secretory epithelial cells |
Q83994642 | Near simultaneous release of classical and peptide cotransmitters from chromaffin cells |
Q42162321 | New insights into the control of secretion |
Q36485197 | Orai-STIM-mediated Ca2+ release from secretory granules revealed by a targeted Ca2+ and pH probe. |
Q47069326 | PKC-1 regulates secretion of neuropeptides |
Q43115363 | Platelet granule exocytosis: a comparison with chromaffin cells |
Q34713448 | Post-fusion structural changes and their roles in exocytosis and endocytosis of dense-core vesicles. |
Q43099990 | Prediction of local pH variations during amperometric monitoring of vesicular exocytotic events at chromaffin cells |
Q35775194 | Protein mobility within secretory granules |
Q27302963 | Quantifying exocytosis by combination of membrane capacitance measurements and total internal reflection fluorescence microscopy in chromaffin cells |
Q44433942 | Rab3a ablation related changes in morphology of secretory vesicles in major endocrine pancreatic cells, pituitary melanotroph cells and adrenal gland chromaffin cells in mice |
Q37806688 | Rapid Endocytosis and Vesicle Recycling in Neuroendocrine Cells |
Q50466227 | Rapid recovery of releasable vesicles and formation of nonreleasable endosomes follow intense exocytosis in chromaffin cells. |
Q26861207 | Real-time imaging of plasma membrane deformations reveals pre-fusion membrane curvature changes and a role for dynamin in the regulation of fusion pore expansion |
Q33814740 | Real-time visualization of complexin during single exocytic events |
Q48280805 | Recycling endosomes undergo rapid closure of a fusion pore on exocytosis in neuronal dendrites. |
Q30427201 | Regulation of fusion pore closure and compound exocytosis in neuroendocrine PC12 cells by SCAMP1 |
Q42483730 | Sequential compound exocytosis of large dense-core vesicles in PC12 cells studied with TEPIQ (two-photon extracellular polar-tracer imaging-based quantification) analysis |
Q46310573 | Slow fusion pore expansion creates a unique reaction chamber for co-packaged cargo |
Q48194442 | Small molecules demonstrate the role of dynamin as a bi-directional regulator of the exocytosis fusion pore and vesicle release |
Q35178306 | Static retention of the lumenal monotopic membrane protein torsinA in the endoplasmic reticulum |
Q48187995 | Subnanometer fusion pores in spontaneous exocytosis of peptidergic vesicles |
Q35668838 | Survey of Red Fluorescence Proteins as Markers for Secretory Granule Exocytosis |
Q37125115 | Sustained Exocytosis after Action Potential-Like Stimulation at Low Frequencies in Mouse Chromaffin Cells Depends on a Dynamin-Dependent Fast Endocytotic Process |
Q90012237 | Synaptic Vesicle Endocytosis in Different Model Systems |
Q41413294 | Synaptotagmin-1 utilizes membrane bending and SNARE binding to drive fusion pore expansion |
Q28505296 | Synaptotagmin-IV modulates synaptic function and long-term potentiation by regulating BDNF release |
Q30009484 | Syndapin 3 modulates fusion pore expansion in mouse neuroendocrine chromaffin cells. |
Q30497547 | Syntaxin clusters assemble reversibly at sites of secretory granules in live cells |
Q89110786 | The fusion pore, 60 years after the first cartoon |
Q62512847 | The high-affinity calcium sensor synaptotagmin-7 serves multiple roles in regulated exocytosis |
Q30483372 | The mouth of a dense-core vesicle opens and closes in a concerted action regulated by calcium and amphiphysin |
Q42075070 | Three distinct modes of exocytosis revealed by amperometry in neuroendocrine cells |
Q37083841 | Trafficking and fusion of neuropeptide Y-containing dense-core granules in astrocytes |
Q91723384 | Unraveling the mechanisms of calcium-dependent secretion |
Q92659614 | Vesicle Shrinking and Enlargement Play Opposing Roles in the Release of Exocytotic Contents |
Q26851822 | Vesicular trafficking and signaling for cytokine and chemokine secretion in mast cells |
Q53833435 | Visualization of Membrane Pore in Live Cells Reveals a Dynamic-Pore Theory Governing Fusion and Endocytosis. |
Q36906319 | cAMP-mediated stabilization of fusion pores in cultured rat pituitary lactotrophs |
Q41757696 | α-Synuclein promotes dilation of the exocytotic fusion pore. |
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