| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Liangyi Chen | Q55641102 |
| Lisi Wei | Q64025689 | ||
| P2093 | author name string | Kuo Liang | |
| P2860 | cites work | Super-resolution fluorescence microscopy | Q24630861 |
| CLASPs attach microtubule plus ends to the cell cortex through a complex with LL5beta | Q28250713 | ||
| The exocytotic event in chromaffin cells revealed by patch amperometry. | Q53963862 | ||
| Two modes of fusion pore opening revealed by cell-attached recordings at a synapse. | Q55042647 | ||
| The Effects of Vesicular Volume on Secretion through the Fusion Pore in Exocytotic Release from PC12 Cells | Q57391720 | ||
| Amperometric detection of quantal secretion from patch-clamped rat pancreatic beta-cells | Q70870864 | ||
| Glucagon-like peptide 1 regulates sequential and compound exocytosis in pancreatic islet beta-cells | Q81118511 | ||
| Vesicular proteins exocytosed and subsequently retrieved by compensatory endocytosis are nonidentical | Q28252426 | ||
| Single vesicle millisecond fusion kinetics reveals number of SNARE complexes optimal for fast SNARE-mediated membrane fusion | Q30434163 | ||
| The dynamic control of kiss-and-run and vesicular reuse probed with single nanoparticles | Q30488206 | ||
| Syntaxin clusters assemble reversibly at sites of secretory granules in live cells | Q30497547 | ||
| Bilayers merge even when exocytosis is transient | Q30597894 | ||
| Calcineurin is universally involved in vesicle endocytosis at neuronal and nonneuronal secretory cells | Q33804443 | ||
| High calcium concentrations shift the mode of exocytosis to the kiss-and-run mechanism | Q33880066 | ||
| Lumenal protein within secretory granules affects fusion pore expansion | Q33990912 | ||
| 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 | ||
| Duration of fusion pore opening and the amount of hormone released are regulated by myosin II during kiss-and-run exocytosis. | Q34119438 | ||
| Turnover of transmitter and synaptic vesicles at the frog neuromuscular junction | Q34207387 | ||
| Membrane protein sequestering by ionic protein-lipid interactions | Q34226601 | ||
| Transmembrane segments of syntaxin line the fusion pore of Ca2+-triggered exocytosis. | Q34305380 | ||
| Currents through the fusion pore that forms during exocytosis of a secretory vesicle | Q34397957 | ||
| The dephosphins: dephosphorylation by calcineurin triggers synaptic vesicle endocytosis | Q34416249 | ||
| Imaging direct, dynamin-dependent recapture of fusing secretory granules on plasma membrane lawns from PC12 cells | Q34430018 | ||
| Dynamin-1 deletion enhances post-tetanic potentiation and quantal size after tetanic stimulation at the calyx of Held. | Q34528445 | ||
| Release of small transmitters through kiss-and-run fusion pores in rat pancreatic beta cells. | Q34570202 | ||
| Kiss-and-run, collapse and 'readily retrievable' vesicles | Q34654997 | ||
| Exocytosis and endocytosis: modes, functions, and coupling mechanisms | Q34657846 | ||
| Secretory granules are recaptured largely intact after stimulated exocytosis in cultured endocrine cells. | Q34763388 | ||
| Control of neurotransmitter release by an internal gel matrix in synaptic vesicles | Q34871028 | ||
| Compound vesicle fusion increases quantal size and potentiates synaptic transmission | Q34961216 | ||
| The phospho-dependent dynamin-syndapin interaction triggers activity-dependent bulk endocytosis of synaptic vesicles | Q34987475 | ||
| A new role for the dynamin GTPase in the regulation of fusion pore expansion | Q35011226 | ||
| The DISABLED protein functions in CLATHRIN-mediated synaptic vesicle endocytosis and exoendocytic coupling at the active zone | Q35064284 | ||
| The fusion pore | Q35197986 | ||
| Molecular control of compound Exocytosis: A key role for VAMP8 | Q35793461 | ||
| Rapid bulk endocytosis and its kinetics of fission pore closure at a central synapse | Q35840503 | ||
| Regulation of exocytosis in neurons and neuroendocrine cells | Q35909212 | ||
| Dominant negative SNARE peptides stabilize the fusion pore in a narrow, release-unproductive state. | Q35983158 | ||
| Syndapin I is the phosphorylation-regulated dynamin I partner in synaptic vesicle endocytosis | Q36151361 | ||
| Beginning of exocytosis captured by rapid-freezing of Limulus amebocytes | Q36204939 | ||
| Structural changes after transmitter release at the frog neuromuscular junction | Q36208626 | ||
| Uncoupling the roles of synaptotagmin I during endo- and exocytosis of synaptic vesicles. | Q36212557 | ||
| Dynamin 2 regulates biphasic insulin secretion and plasma glucose homeostasis | Q36266525 | ||
| Sequential exocytosis of insulin granules is associated with redistribution of SNAP25 | Q36321911 | ||
| Compound exocytosis: mechanisms and functional significance | Q36371669 | ||
| Protein kinase activation increases insulin secretion by sensitizing the secretory machinery to Ca2+. | Q36445740 | ||
| Fusion pore formation and expansion induced by Ca2+ and synaptotagmin 1. | Q36567991 | ||
| Exocytotic fusion pores are composed of both lipids and proteins | Q36589148 | ||
| Flickering fusion pores comparable with initial exocytotic pores occur in protein-free phospholipid bilayers | Q36818766 | ||
| Bulk-like endocytosis plays an important role in the recycling of insulin granules in pancreatic beta cells | Q36922900 | ||
| The role of the C terminus of the SNARE protein SNAP-25 in fusion pore opening and a model for fusion pore mechanics | Q36926938 | ||
| Ca(2+) and calmodulin initiate all forms of endocytosis during depolarization at a nerve terminal. | Q36951925 | ||
| Selective saturation of slow endocytosis at a giant glutamatergic central synapse lacking dynamin 1 | Q36965571 | ||
| Tissue-specific dynamin-1 deletion at the calyx of Held decreases short-term depression through a mechanism distinct from vesicle resupply. | Q36978090 | ||
| The mystery of the fusion pore | Q37013086 | ||
| Hemi-fused structure mediates and controls fusion and fission in live cells | Q37059676 | ||
| PIP2 is a necessary cofactor for ion channel function: how and why? | Q37197976 | ||
| Ultrafast endocytosis at mouse hippocampal synapses. | Q37642826 | ||
| Complexin synchronizes primed vesicle exocytosis and regulates fusion pore dynamics. | Q37677607 | ||
| A guide to super-resolution fluorescence microscopy | Q37774153 | ||
| Coupling exo- and endocytosis: an essential role for PIP₂ at the synapse. | Q37990335 | ||
| Perspectives on kiss-and-run: role in exocytosis, endocytosis, and neurotransmission | Q38067906 | ||
| Dynasore - not just a dynamin inhibitor. | Q38427839 | ||
| The Active and Periactive Zone Organization and the Functional Properties of Small and Large Synapses | Q38851271 | ||
| Synaptic Vesicle Endocytosis Occurs on Multiple Timescales and Is Mediated by Formin-Dependent Actin Assembly. | Q38945813 | ||
| Clathrin-mediated endocytosis is the dominant mechanism of vesicle retrieval at hippocampal synapses. | Q39751968 | ||
| Actin Is Crucial for All Kinetically Distinguishable Forms of Endocytosis at Synapses | Q39757117 | ||
| Ca2+ triggers a novel clathrin-independent but actin-dependent fast endocytosis in pancreatic beta cells | Q40006555 | ||
| Mechanisms of dense core vesicle recapture following "kiss and run" ("cavicapture") exocytosis in insulin-secreting cells | Q40522071 | ||
| Two pathways of synaptic vesicle retrieval revealed by single-vesicle imaging | Q41997492 | ||
| Fast, Temperature-Sensitive and Clathrin-Independent Endocytosis at Central Synapses | Q42362658 | ||
| Sequential compound exocytosis of large dense-core vesicles in PC12 cells studied with TEPIQ (two-photon extracellular polar-tracer imaging-based quantification) analysis | Q42483730 | ||
| One SNARE complex is sufficient for membrane fusion | Q42531466 | ||
| Synaptotagmin modulation of fusion pore kinetics in regulated exocytosis of dense-core vesicles | Q43787533 | ||
| Fusion pore dynamics and insulin granule exocytosis in the pancreatic islet | Q44113066 | ||
| Multiple forms of "kiss-and-run" exocytosis revealed by evanescent wave microscopy | Q44390677 | ||
| Calcium dependence of exo- and endocytotic coupling at a glutamatergic synapse. | Q45916727 | ||
| GTP-independent rapid and slow endocytosis at a central synapse | Q46861221 | ||
| Small molecules demonstrate the role of dynamin as a bi-directional regulator of the exocytosis fusion pore and vesicle release | Q48194442 | ||
| Fast vesicle fusion in living cells requires at least three SNARE complexes. | Q50541149 | ||
| Diacylglycerol Guides the Hopping of Clathrin-Coated Pits along Microtubules for Exo-Endocytosis Coupling. | Q53320957 | ||
| P921 | main subject | exocytosis | Q323426 |
| P304 | page(s) | 109 | |
| P577 | publication date | 2017-04-19 | |
| P1433 | published in | Frontiers in Molecular Neuroscience | Q27721913 |
| P1476 | title | Exocytosis, Endocytosis, and Their Coupling in Excitable Cells | |
| P478 | volume | 10 |
| Q41841597 | Kiss-and-Run Is a Significant Contributor to Synaptic Exocytosis and Endocytosis in Photoreceptors |
| Q91789589 | Knockdown Of CCDC132 Attenuates Gastric Cancer Cells Proliferation And Tumorigenesis By Facilitating DNA Damage Signaling |
| Q93339570 | Papillae revisited and the nature of the adhesive secreting collocytes |
| Q55446462 | Sensing Exocytosis and Triggering Endocytosis at Synapses: Synaptic Vesicle Exocytosis-Endocytosis Coupling. |
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