| scholarly article | Q13442814 |
| P50 | author | Daniel Axelrod | Q88473018 |
| Ronald W Holz | Q90028777 | ||
| Kevin P Bohannon | Q96235786 | ||
| Daniel A. Lawrence | Q39600113 | ||
| P2093 | author name string | Mary A Bittner | |
| P2860 | cites work | Processing of chromogranin A by plasmin provides a novel mechanism for regulating catecholamine secretion | Q40735839 |
| 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 | ||
| Transient transfection studies of secretion in bovine chromaffin cells and PC12 cells. Generation of kainate-sensitive chromaffin cells. | Q41552954 | ||
| Polarized TIRFM reveals changes in plasma membrane topology before and during granule fusion | Q42201429 | ||
| Localization and regulation of the tissue plasminogen activator-plasmin system in the hippocampus. | Q43918819 | ||
| Protonation state of a single histidine residue contributes significantly to the kinetics of the reaction of plasminogen activator inhibitor-1 with tissue-type plasminogen activator | Q44807445 | ||
| Matrix-degrading enzymes tissue plasminogen activator and matrix metalloprotease-3 in the hypothalamo-neurohypophysial system | Q46693077 | ||
| Influence of the Alu-repeat I/D polymorphism in t-PA gene intron 8 on the stimulated t-PA release after venous occlusion | Q48028278 | ||
| Recapture after exocytosis causes differential retention of protein in granules of bovine chromaffin cells. | Q50796308 | ||
| Increased plasminogen activator inhibitor results in a hypofibrinolytic state in adolescents with obesity: in vivo and ex vivo evidence. | Q51630897 | ||
| Evidence that the H+ electrochemical gradient across membranes of chromaffin granules is not involved in exocytosis | Q71766795 | ||
| Serpin-protease complexes are trapped as stable acyl-enzyme intermediates | Q71823584 | ||
| Identification of eight novel single-nucleotide polymorphisms at human tissue-type plasminogen activator (t-PA) locus: association with vascular t-PA release in vivo | Q74225970 | ||
| Plasminogen activator inhibitor-1 contains a cryptic high affinity binding site for the low density lipoprotein receptor-related protein | Q74299355 | ||
| Resolution of Michaelis complex, acylation, and conformational change steps in the reactions of the serpin, plasminogen activator inhibitor-1, with tissue plasminogen activator and trypsin | Q74552310 | ||
| Selective recapture of secretory granule components after full collapse exocytosis in neuroendocrine chromaffin cells | Q85109926 | ||
| A cost-effective approach to microporate mammalian cells with the Neon Transfection System | Q85216644 | ||
| NIH Image to ImageJ: 25 years of image analysis | Q23319322 | ||
| Patterns of synaptic activity in neural networks recorded by light emission from synaptolucins | Q28307290 | ||
| The anti-fibrinolytic SERPIN, plasminogen activator inhibitor 1 (PAI-1), is targeted to and released from catecholamine storage vesicles | Q28579043 | ||
| Proteomics. Tissue-based map of the human proteome | Q29617248 | ||
| Localized topological changes of the plasma membrane upon exocytosis visualized by polarized TIRFM. | Q33643745 | ||
| Lumenal protein within secretory granules affects fusion pore expansion | Q33990912 | ||
| Carbocyanine dye orientation in red cell membrane studied by microscopic fluorescence polarization | Q34254410 | ||
| Beyond endocytosis: LRP function in cell migration, proliferation and vascular permeability | Q34443186 | ||
| Structure-function relationships of plasminogen activator inhibitor-1 and its potential as a therapeutic agent | Q34693493 | ||
| Post-fusion structural changes and their roles in exocytosis and endocytosis of dense-core vesicles. | Q34713448 | ||
| Secretory granules are recaptured largely intact after stimulated exocytosis in cultured endocrine cells. | Q34763388 | ||
| A new role for the dynamin GTPase in the regulation of fusion pore expansion | Q35011226 | ||
| Protein mobility within secretory granules | Q35775194 | ||
| A nibbling mechanism for clathrin-mediated retrieval of secretory granule membrane after exocytosis | Q36725018 | ||
| LRP1 assembles unique co-receptor systems to initiate cell signaling in response to tissue-type plasminogen activator and myelin-associated glycoprotein. | Q37333802 | ||
| Update on intravenous recombinant tissue plasminogen activator for acute ischemic stroke | Q38207776 | ||
| Structure-function studies of the SERPIN plasminogen activator inhibitor type 1. Analysis of chimeric strained loop mutants | Q38338256 | ||
| Tissue plasminogen activator | Q39605345 | ||
| Unique secretory dynamics of tissue plasminogen activator and its modulation by plasminogen activator inhibitor-1 in vascular endothelial cells | Q39929087 | ||
| Mechanisms of dense core vesicle recapture following "kiss and run" ("cavicapture") exocytosis in insulin-secreting cells | Q40522071 | ||
| Stability characterization and formulation development of alteplase, a recombinant tissue plasminogen activator | Q40665888 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 10 | |
| P304 | page(s) | 921-934 | |
| P577 | publication date | 2017-09-07 | |
| P1433 | published in | The Journal of General Physiology | Q1092259 |
| P1476 | title | Slow fusion pore expansion creates a unique reaction chamber for co-packaged cargo | |
| P478 | volume | 149 |
| Q48359379 | Chemistry in a vesicle. |
| Q90028784 | Chromogranin A, the major lumenal protein in chromaffin granules, controls fusion pore expansion |
| Q89715497 | Synaptotagmin-7 enhances calcium-sensing of chromaffin cell granules and slows discharge of granule cargos |
| Q89110786 | The fusion pore, 60 years after the first cartoon |
| Q55239707 | The synaptotagmin C2B domain calcium-binding loops modulate the rate of fusion pore expansion. |
| Q91723384 | Unraveling the mechanisms of calcium-dependent secretion |
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